A. Castleman Jr, et al : Superatom Clusters

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**Albert CASTLEMAN,
Jr., *et
al.***

**Superatom Clusters**

---

**<http://en.wikipedia.org/wiki/Superatoms>**

**Superatom**

Superatoms are clusters of atoms that seem to exhibit some of
the properties of elemental atoms.

Sodium atoms, when cooled from vapor, naturally condense into
clusters, more so into clusters of 2, 8, 20, 40, 58 or 82 atoms
(the magic numbers), than into the other numbers. The first two
of these can be recognized as the numbers of electrons needed to
fill s and p orbitals, respectively. The superatom suggestion is
that free electrons in the cluster occupy a new set of orbitals
that are defined by the entire group of atoms, i.e. cluster,
rather than each individual atom separately (non-spherical or
doped clusters show deviations in the number of electrons that
form a closed shell as the potential is defined by the shape of
the positive nuclei.) Superatoms tend to behave chemically in a
way that will allow them to have a closed shell of electrons, in
this new counting scheme. Therefore, a superatom with one more
electron than a full shell should give up that electron very
easily, similar to an alkali metal, and a cluster with one
electron short of full shell should have a large electron
affinity, such as a halogen.

**Aluminium clusters**

Certain aluminium clusters have superatom properties. These
aluminium clusters are generated as anions (Aln- with n =
1,2,3...) in helium gas and reacted with a gas containing
iodine. When analyzed by mass spectrometry one main reaction
product turns out to be Al13I-.[1] These clusters of 13
aluminium atoms with an extra electron added do not appear to
react with oxygen when it is introduced in the same gas stream.
Assuming each atom liberates its 3 valence electrons, this means
that there are 40 electrons present, which is one of the magic
numbers noted above for sodium, and implies that these numbers
are a reflection of the noble gases. Calculations show that the
additional electron is located in the aluminium cluster at the
location directly opposite from the iodine atom. The cluster
must therefore have a higher electron affinity for the electron
than iodine and therefore the aluminium cluster is called a
superhalogen. The cluster component in Al13I- ion is similar to
an iodine ion or better still a bromine atom. The related
Al13I2- cluster is expected to behave chemically like the
triiodide ion.

Similarly it has been noted that Al14 clusters with 42
electrons (2 more than the magic numbers) appear to exhibit the
properties of an alkaline earth metal which typically adopt +2
valence states. This is only known to occur when there are at
least 3 iodine atoms attached to an Al14- cluster, Al14I3-. The
anionic cluster has a total of 43 itinerant electrons, but the
three Iodine atoms each remove one of the itinerant electrons to
leave 40 electrons in the jellium shell.[2][3]

It is particularly easy and reliable to study atomic clusters
of inert gas atoms by computer simulation because interaction
between two atoms can be approximated very well by the
Lennard-Jones potential. Other methods are readily available and
it has been established that the magic numbers are 13, 19, 23,
26, 29, 32, 34, 43, 46, 49, 55, etc. [I. A. Harris et al. Phys.
Rev. Lett. Vol. 53, 2390-94 (1984).]

**Aluminum clusters**

\* Al7 = the property is similar to germanium atoms.   
\* Al13 = the property is similar to halogen atoms, more
specifically, chlorine.   
          o
Al13Ix-, where x = 1-13.[4]   
\* Al14 = the property is similar to alkaline metals.   
          o
Al14Ix-, where x = 1-14.[4]   
\* Al23   
\* Al37

**Other clusters**

\* Li(HF)3Li = the (HF)3 interior causes 2 valence electrons
from the Li to orbit the entire molecule as if it were an atom's
nucleus.[5]   
\* VSi16F = has ionic bonding.[6]   
\* A cluster of 13 platinum becomes magnetic.[7]   
\* A cluster of 2000 Rubidium atoms.[8]

**References**

1. ^ Formation of Al13I-: Evidence for the Superhalogen
Character of Al13 D. E. Bergeron, A.W. Castleman Jr., T.
Morisato, S. N. Khanna Science, Vol 304, Issue 5667, 84-87 , 2
April 2004

2. ^ Philip Ball, "A New Kind of Alchemy", New Scientist,
2005-04-16.

3. ^ Al Cluster Superatoms as Halogens in Polyhalides and as
Alkaline Earths in Iodide Salts D. E. Bergeron, P. J. Roach,
A.W. Castleman Jr., N.O. Jones, S. N. Khanna Science, Vol 307,
Issue 5707, 231-235 , 14 January 2005

4. ^ a b Naiche Owen Jones, 2006. -- **http://etd.vcu.edu/theses/available/etd-01102007-131059/unrestricted/jonesno\_phd.pdf**

5. ^ Extraordinary superatom containing double shell nucleus:
Li(HF)3Li connected mainly by intermolecular interactions, Sun,
Xiao-Ying, Li, Zhi-Ru, Wu, Di, & Sun, Chia-Chung, 2007. -- **http://adsabs.harvard.edu/abs/2007IJQC..107.1215S**

6. ^ Electronic and geometric stabilities of clusters with
transition metal encapsulated by silicon, Kiichirou Koyasu et
al. -- **http://lib.bioinfo.pl/pmid:17201386**

7. ^ Platinum nanoclusters go magnetic, nanotechweb.org, 2007
-- **http://nanotechweb.org/cws/article/tech/26782**

8. ^ Ultra Cold Trap Yields Superatom, NIST, 1995 -- **http://www.nist.gov/public\_affairs/gallery/95subose.htm**

**External links**

\* Expanding the periodic table? The Scientist, 2005 -- **http://www.biomedcentral.com/news/20050114/02/**

\* On the Aluminum Cluster Superatoms acting as Halogens and
Alkaline-earth Metals, Bergeron, Dennis E et.al., 2006 -- **http://adsabs.harvard.edu/abs/2006APS..MARR11013B**

\* Research Reveals Halogen Characteristics innovations report,
2004. Have pictures of Al13. -- **http://www.innovations-report.com/html/reports/materials\_science/report-27795.html**

\* Clusters of Aluminum Atoms Found to Have Properties of Other
Elements Reveal a New Form of Chemistry, innovations report,
2005. Have a picture of Al14. -- **http://www.innovations-report.com/html/reports/life\_sciences/report-38837.html**

\* Beyond The Periodic Table, Computational Chemistry Portal,
2006 -- **http://comchem.edugrid.ac.in/news/discovery/latestInventions-236.html**

\* Clusters of Aluminum Atoms Found to Have Properties of Other
Elements Reveal a New Form of Chemistry, Penn State, Eberly
College of Science, 2005 -- **http://www.science.psu.edu/alert/Castleman1-2005.htm**

---

[**http://pubs.acs.org/doi/abs/10.1021/jp806850h?prevSearch=reber&searchHistoryKey=**](http://pubs.acs.org/doi/abs/10.1021/jp806850h?prevSearch=reber&searchHistoryKey=)  
***J. Phys. Chem. C*, 2009, 113 (7), pp 26642675**   
**January 23, 2009**

**Clusters, Superatoms, and Building Blocks
of New Materials**

**A. W. Castleman, Jr.**   
Departments of Chemistry and Physics, The Pennsylvania State
University, University Park, Pennsylvania 16802

**S. N. Khanna**   
Department of Physics, Virginia Commonwealth University,
Richmond, Virginia 23284   
J. Phys. Chem. C, 2009, 113 (7), pp 26642675   
Publication Date (Web): January 23, 2009

**Biography**

**A. W. Castleman, Jr.** is Evan Pugh Professor of Chemistry
and Physics and Eberly Distinguished Chair in Science at The
Pennsylvania State University, having been professor of
chemistry and member of CIRES at the University of Colorado
(1975?1882) and previously on the staff at the Brookhaven
National Laboratory. He served as a Senior Editor of the Journal
of Physical Chemistry from 1988 to 1998. He is a member of the
National Academy of Sciences, and a fellow of the American
Academy of Arts and Sciences, as well as of the American
Physical Society, the American Association for the Advancement
of Science, the New York Academy of Sciences and the Royal
Society of Chemistry. Included among his many awards and honors
are the Doktors Honoris Causa from the University of Innsbruck,
Austria, the American Chemical Society Award for Creative
Advances in Environmental Science and Technology, the Wilhelm
Jost Memorial Lectureship Award from the German Chemical
Society, U. S. Senior Scientist von Humboldt Award, Fulbright
Senior Scholar award, Senior Fellow of the Japanese Society for
the Promotion of Science, Rensselaer distinguished Thomas W.
Phelan Fellows alumni award, and Sherman Fairchild Distinguished
Scholar at Cal Tech. He is engaged in studies to bridge the gas
and condensed phase and to elucidate the fundamentals of
solvation dynamics through investigation of cluster
photophysics. He is particularly interested in exploring the
properties of matter of finite dimension using ultrafast laser
techniques, elucidating the physical basis for catalysis and
surface phenomena at the molecular level, and developing with
his theoretical collaborator S. N. Khanna of VCU the unique
characteristics of superatom clusters as building blocks to
cluster assembled nanoscale materials. Castleman has published
over 600 papers dealing with these subjects.   
Biography

**Shiv N. Khanna** is a Professor of Physics at Virginia
Commonwealth University, having been a visiting associate
professor at the Northeastern University (1983?84) and a
scientific collaborator at the Swiss Federal Institute of
Technology in Switzerland (1980?1983). He is a Fellow of the
American Physical Society and has been twice the recipient of
the Distinguished Scholar Award of the College of Humanities and
Sciences at VCU. He is a member of the Advisory Board of the
Materials Science Forum from Trans Tech Publications and
Journal of Mathematics and Sciences: Collaborative
Explorations. He has co-authored more than 200 research
publications in refereed journals, has edited six monographs,
and has chaired/co-chaired several International Conferences.
Dr. Khanna and his group are involved in theoretical studies of
the electronic structure, magnetic properties, and catalytic
properties of atomic clusters, cluster assemblies, and nanoscale
materials. Along with A. W. Castleman, Jr. at PSU, they have
proposed superatoms that extend the Periodic Chart to a
third dimension and could lead to novel materials with tunable
properties and potential for applications in numerous areas.   
Abstract

The physical and chemical properties of cluster systems at the
subnano and nanoscale are often found to differ from those of
the bulk and display a unique dependence on size, geometry, and
composition. Indeed, most interesting are systems which have
properties that vary discontinuously with the number of atoms
and composition, rather than scale linearly with size. This
realm of cluster science where one atom makes a difference is
undergoing an explosive growth in activity, and as a result of
extensive collaborative activities through theory at VCU and
experiment at PSU, our groups are recognized as pioneers in this
area in which we have been active for many years. Herein we
provide an overview of the field with primary focus on our joint
undertakings which have spawned the superatom concept, giving
rise to a 3-D periodic table of cluster elements and the
prospect of using these as building blocks of new nanoscale
materials with tailored properties.

---



![](imagePSH.JPG)

**Artists rendition of an aluminum-iodine "Superatom"
identified by the Castleman group at Penn State and the
Khanna group at Virginia Commonwealth University.**

**Credit: D.E. Bergeron, P.J. Roach, A.W. Castleman, N.O.
Jones, and S.N. Khanna**

---

[**http://www.sciencemag.org/cgi/content/abstract/307/5707/231**](http://www.sciencemag.org/cgi/content/abstract/307/5707/231)  
***Science* 14 January 2005: Vol. 307. no. 5707, pp. 231 -
235**   
**DOI: 10.1126/science.1105820**

**Al Cluster Superatoms as Halogens in
Polyhalides and as Alkaline Earths in Iodide Salts**

**D. E. Bergeron, P. J. Roach, A. W.
Castleman, Jr., N. O. Jones, S. N. Khanna**

Two classes of gas-phase aluminum-iodine clusters have been
identified whose stability and reactivity can be understood in
terms of the spherical shell jellium model. Experimental
reactivity studies show that the Al13I x clusters exhibit
pronounced stability for even numbers of I atoms. Theoretical
investigations reveal that the enhanced stability is associated
with complementary pairs of I atoms occupying the on-top sites
on the opposing Al atoms of the Al13 core. We also report the
existence of another series, Al14I x, that exhibits stability
for odd numbers of I atoms. This series can be described as
consisting of an Al14I 3 core upon which the I atoms occupy
on-top locations around the Al atoms. The potential synthetic
utility of superatom chemistry built upon these motifs is
addressed.

---

[**http://pubs.acs.org/action/doSearch?searchText=[all%3A+Castleman+superatom]**](http://pubs.acs.org/action/doSearch?searchText=[all%3A+Castleman+superatom])

***J. Am. Chem. Soc.*, 2008, 130 (1), pp 23**   
**December 08, 2007 (Communication)**   
DOI: 10.1021/ja074225m

**Does the Superatom Exist in Halogenated
Aluminum Clusters?**

**Young-Kyu Han and Jaehoon Jung**

![](ja074225mn00001.gif)

Does the Superatom Exist in Halogenated Aluminum Clusters?
... We have shown that Aln clusters do not show any
characteristics of a superatom ... The enhanced stability of
halogenated Al clusters can be explained by the magic nature of
the clusters, not by superatom chemistry. ...

---

***Inorg. Chem.*, Articles ASAP (As Soon As Publishable)**
  
**February 23, 2009 (Communication)**   
**DOI: 10.1021/ic8024588**

**From Superatomic Au25(SR)18? to
Superatomic M@Au24(SR)18q Core?Shell Clusters**

**De-en Jiang and Sheng Dai**

![](ic-2008-024588_0006.gif)

Au25(SR)18? belongs to a new type of superatom ... This
superatom ... By applying this superatom ...

---

***J. Am. Chem. Soc.*, 2007, 129 (33), pp 1018910194**
  
**Publication Date (Web): July 27, 2007 (Article)**   
**DOI: 10.1021/ja071647n**

**Superatom Compounds, Clusters, and
Assemblies:  Ultra Alkali Motifs and Architectures**

**Arthur C. Reber, Shiv N. Khanna, and A.
Welford Castleman, Jr.**

---

***J. Am. Chem. Soc.*, 2005, 127 (14), pp 49984999**   
**March 18, 2005**   
**DOI: 10.1021/ja045380t**

**Selective Formation of MSi16 (M = Sc, Ti,
and V)**

**Kiichirou Koyasu, Minoru Akutsu, Masaaki
Mitsui, and Atsushi Nakajima**

![](ja045380tn00001.gif)

We present experimental evidence for a highly stable cluster
corresponding to M@Si16 (M = Sc, Ti, and V). Mass spectrometry
and anion photoelectron spectroscopy show that the cluster
features an electronically closed TiSi16 neutral core which
undergoes a change in the number of valence electrons involving
(i) substitution of neighboring metals with Sc and V, or (ii)
addition of a halogen atom to the TiSi16 anion, and that VSi16F
is predicted to form an ionically bound superatom complex. ...

---

***ACS Nano*, 2009, 3 (2), pp 244255**   
**February 5, 2009 (Review)**   
**DOI: 10.1021/nn800820e**

**Cluster-Assembled Materials**

**Shelley A. Claridge, A. W. Castleman, ,
Shiv N. Khanna, Christopher B. Murray, Ayusman Sen and
Paul S. Weiss**

![](imageMNN.JPG)

---

***Inorg. Chem.*, 2008, 47 (21), pp 97739778**   
**October 3, 2008**   
**DOI: 10.1021/ic800184z**

**Compounds of Superatom Clusters: Preferred
Structures and Significant Nonlinear Optical Properties of
the BLi6-X (X = F, LiF2, BeF3, BF4) Motifs**

**Ying Li, Di Wu and Zhi-Ru Li**   
 

![](image4AB.JPG)

---

***J. Am. Chem. Soc.*, 2007, 129 (7), pp 19001901**   
**January 27, 2007**   
**DOI: 10.1021/ja068334x**

**Assembly and Stabilization of a Planar
Tetracoordinated Carbon Radical CAl3Si:  A Way To
Design Spin-Based Molecular Materials**

**Li-ming Yang, Yi-hong Ding, and Chia-chung
Sun**

To capture and stabilize the ptC radical, we proposed a scheme
heterodecked sandwich, in which way CAl3Si can act as a
spin-embedded superatom because of the well conservation of
the radical's spin, structural and electronic integrity during
the cluster assembly. ...

---

***J. Phys. Chem. A*, 2006, 110 (44), pp 1207312076**
  
**October 19, 2006**   
**DOI: 10.1021/jp065161p**

**Experimental and Theoretical
Characterization of Aluminum-Based Binary Superatoms of
Al12X and Their Cluster Salts**

**Minoru Akutsu, Kiichirou Koyasu, Junko
Atobe, Natsuki Hosoya, Ken Miyajima, Masaaki Mitsui, and
Atsushi Nakajima**

![](imageJMB.JPG)

The geometric and electronic structures of aluminum binary
clusters, AlnX (X = Si and P), have been investigated, using
mass spectrometry, anion photoelectron spectroscopy,
photoionization spectroscopy, and theoretical calculations. Both
experimental and ...

---

***J. Am. Chem. Soc.*, 2009, 131 (7), pp 24902492**   
**January 29, 2009**   
**DOI: 10.1021/ja809157f**

**Reversible Switching of Magnetism in
Thiolate-Protected Au25 Superatoms**

**Manzhou Zhu, Christine M. Aikens, Michael
P. Hendrich, Rupal Gupta, Huifeng Qian, George C. Schatz
and Rongchao Jin**

![](imageKUG.JPG)

Interestingly, the HOMO orbital exhibits distinct P-like
character, reminiscent of the superatom model for bare metal
clusters. ...

---

***J. Phys. Chem. A*, 2007, 111 (42), pp 1067510681**
  
**October 3, 2007**   
**DOI: 10.1021/jp071054z**

**Theoretical Study on the Assembly and
Stabilization of a Magic Cluster Al4N-**

**Li-ming Yang, Yi-hong Ding, and Chia-chung
Sun**

The good structural and electronic integrity of the Al4N- unit
within the designed assembled systems leads us to propose that
the magic unit Al4N- might act as a new kind of
superatom8d-f,11 in combinational chemistry. ...

---

***J. Phys. Chem. A*, 2007, 111 (20), pp 43784383**   
**April 21, 2007**   
**DOI: 10.1021/jp068591o**

**Structures and Electronic Properties of
Al7X0,- and Al13X1,2,12- Clusters with XF, Cl, and Br**

**Jiao Sun, Wen-Cai Lu, Li-Zhen Zhao, Wei
Zhang, Ze-Sheng Li, and Chia-Chung Sun**

Among the systems studied, Al7 and Al13 clusters in Al7X and
Al13X- reveal alkali-like and halogen-like superatom characters,
respectively. ... However, when adding more halogens, the
superatom structure would be destroyed, resulting in
low-symmetry compounds with the center Al atom moving toward the
cluster surface. ...

---

***J. Phys. Chem. A*, 2007, 111 (1), pp 4249**   
**December 14, 2006**   
**DOI: 10.1021/jp066757f**

**Electronic and Geometric Stabilities of
Clusters with Transition Metal Encapsulated by Silicon**

**Kiichirou Koyasu, Junko Atobe, Minoru
Akutsu, Masaaki Mitsui, and Atsushi Nakajima**

The reactivity of a halogen atom with the MSi16 clusters
reveals that VSi16F forms a superatom complex with ionic
bonding. ...

---

***J. Am. Chem. Soc*., 2005, 127 (46), pp 1604816053**
  
**October 28, 2005**   
**DOI: 10.1021/ja050338z**

**Stability of Al7I and the Chemical
Significance of Active Centers**

**Denis E. Bergeron, Patrick J. Roach,
A.Welford Castleman, Jr., Naiche O. Jones, J. Ulises
Reveles, and Shiv N. Khanna**

We show that the relative inertness of the cluster is derived
from the stability of the neutral Al7I which can be looked upon
as a jellium compound formed by the interaction between a Al7
superatom and an I atom. ...

---

***J. Phys. Chem. A*, 2008, 112 (51), pp 1331613325**
  
**November 24, 2008**   
**DOI: 10.1021/jp804667d**

**AlnBi Clusters: Transitions Between
Aromatic and Jellium Stability**

**Charles E. Jones, , Pene A. Clayborne, J.
Ulises Reveles, Joshua J. Melko, Ujjwal Gupta, Shiv N.
Khanna and A. W. Castleman,**

The electron count (20) combined with a compact,
three-dimensional geometry makes the stable Al5Bi a possible
superatom candidate. ...

---

***J. Chem. Theory Comput.,* 2008, 4 (12), pp 20112019**
  
**November 5, 2008**   
**DOI: 10.1021/ct800232b**

**Al5O4: A Superatom with Potential for New
Materials Design**

**Ujjal Das and Krishnan Raghavachari**

Al5O4: A Superatom with Potential for New Materials Design ...
For example, Castleman and co-workers have shown that the size
of the Al13 superatom(4) is too big to fit with counterions such
as the alkali metals. ... For example, the HOMO?LUMO energy gap
in Al13K, which also behaves like a stable diatomic ionic
molecule as shown by Bowen and co-workers, is observed to be 1.3
eV.(38) As7K3 is another stable cluster where this gap is
measured to be 2.2 eV by Castleman et al.(15) Using TDDFT
calculations, we have computed the energy required to excite an
electron from the doubly filled HOMO of Al5O4K to the LUMO
without allowing any geometric changes. ...

---

***J. Phys. Chem. A*, 2007, 111 (37), pp 91229129**   
**August 29, 2007**   
**DOI: 10.1021/jp074645y**

**Investigation of the Typical Triangular
Structure B3 in Boron Chemistry:  Insight into Bare
All-Boron Clusters Used as Ligands or Building Blocks**

**Li-ming Yang, Jian Wang, Yi-hong Ding, and
Chia-chung Sun**

Additionally, the electronic and structural properties of B3-
are well conserved during cluster-assembly, characteristic of a
superatom feature. ...

---

***J. Am. Chem. Soc*., 2006, 128 (24), pp 79047908**   
**Publication Date (Web): May 28, 2006 (Article)**   
**DOI: 10.1021/ja060613x**

**Primary Reaction Steps of Al13- Clusters
in an HCl Atmosphere:  Snapshots of the Dissolution
of a Base Metal**

**Ralf Burgert, Sarah T. Stokes, Kit H.
Bowen, and Hansgeorg Schnockel**

![](imageS6O.JPG)

Recently, the icosahedral Al13- cluster has been shown to
possess some unusual characteristics due to its special
stability (Bergeron, D. E.; et al. Science 2004, 304, 84?87;
2005, 307, 231?235). Here we present reactions of isolated Al13-
clusters with ...

---

***J. Phys. Chem. B*, 2006, 110 (41), pp 2009820101**
  
**September 20, 2006**   
**DOI: 10.1021/jp064821n**

**Aromatic Superclusters from All-Metal
Aromatic and Antiaromatic Monomers, [Al4]2- and [Al4]4-**

**Sairam S. Mallajosyula, Ayan Datta, and
Swapan K. Pati**

![](image2S7.JPG)

In fact, within these superclusters, each monomer cluster acts
as a superatom, leading to the formation of highly stable
three-dimensional structures. ...

---

***J. Am. Chem. Soc.*, 2005, 127 (45), pp 1568015681**
  
**October 20, 2005**   
**DOI: 10.1021/ja055407o**

**Gold-Caged Metal Clusters with Large
HOMO?LUMO Gap and High Electron Affinity**

**Yi Gao, Satya Bulusu, and Xiao Cheng Zeng**

![](imageNMC.JPG)

In particular, highly stable clusters with large energy gap
(>1.5 eV) between the highest occupied molecular orbital
(HOMO) and lowest unoccupied molecular orbital (LUMO) may be
perceived as a superatom, analogous to fullerene C60 (with a
large HOMO?LUMO gap ? = 1.57 eV)4 that tends to retain its
structure integrity and chemical identity in cluster-assembled
solids. ...

---

[**http://www.innovations-report.com/html/reports/life\_sciences/report-38837.html**](http://www.innovations-report.com/html/reports/life_sciences/report-38837.html)

**Clusters of Aluminum Atoms Found to Have
Properties of Other Elements Reveal a New Form of
Chemistry**

**Barbara K. Kennedy**

**Source: EurekAlert!**   
**Further information: www.psu.edu**

A research team has discovered clusters of aluminum atoms that
have chemical properties similar to single atoms of metallic and
nonmetallic elements when they react with iodine. The discovery
opens the door to using superatom chemistry based on a new
periodic table of cluster elements to create unique compounds
with distinctive properties never seen before. The results of
the research, headed jointly by Shiv N. Khanna, professor of
physics at Virginia Commonwealth University and A. Welford
Castleman Jr., the Evan Pugh Professor of Chemistry and Physics
and the Eberly Family Distinguished Chair in Science at Penn
State University, will be reported in the 14 January 2005 issue
of the journal Science.

"Depending on the number of aluminum atoms in the cluster, we
have demonstrated superatoms exhibiting the properties of
either halogens or alkaline earth metals," says Castleman. "This
result suggests the intriguing potential of this chemistry in
nanoscale synthesis." The discovery could have practical
applications in the fields of medicine, food production and
photography.

The researchers examined the chemical properties, electronic
structure, and geometry of aluminum clusters both theoretically
and experimentally in chemical compounds with iodine atoms. They
found that a cluster of 13 aluminum atoms behaves like a single
iodine atom, while a cluster of 14 aluminum atoms behaves like
an alkaline earth atom. "The discovery of these new iodine
compounds, which include aluminum clusters, is critical because
it reveals a new form of superatom chemistry," said Khanna.
"In the future, we may apply this chemistry, building on our
previous knowledge, to create new materials for energy
applications and even medical devices."   
To make their discovery, the research team replaced iodine atoms
with the aluminum clusters in naturally occurring chains or
networks of iodine atoms and molecules known as polyiodides.
When the researchers substituted the iodine atom with the
aluminum cluster, Al13, they observed that the entire chemistry
of the compound changed--causing the other iodine molecules to
break apart and bind individually to the cluster. The
researchers then were able to bind 12 iodine atoms to a single
Al13 cluster, forming a completely new class of polyiodides.
"Our production of such a species is a stirring development that
may lead to new compounds with a completely new class of
chemistry and applications," says Castleman. "Along with the
discovery that Al14 clusters appear to behave similarly to
alkaline earth atoms when combined with iodine, these new
results give further evidence that we are really on our way to
the development of a periodic table of the cluster elements."

The researchers conducted experimental reactivity studies that
indicate that certain aluminum-cluster superatoms are highly
stable by nature. The teams related theoretical investigations
reveal that the enhanced stability of these superatoms is
associated with a balance in their atomic and electronic states.
While the clusters resemble atoms of other elements in their
interactions, their chemistry is unique, creating stable
compounds with bonds that are not identical to those of single
atoms.

Using stable clusters provides a possible route to an adaptive
chemistry that introduces the aluminum-cluster species into
nanoscale materials, tailoring them to create desirable
properties. "The flexibility of an Al13 cluster to act as an
iodine atom shows that superatoms can have synthetic utility,
providing an unexplored third dimension to the traditional
periodic table of elements," said Khanna. "Applications using
Al13 clusters instead of iodine in polymers may lead to the
development of improved conducting materials. Assembling Al13I
units may provide aluminum materials that will not oxidize, and
may help overcome a major problem in fuels that burn aluminum
particles."

The theoretical investigations for this project were conducted
by Khanna with N.O. Jones, a graduate student in the physics
department at Virginia Commonwealth University, and the
experimental work was conducted by Castleman with Denis Bergeron
and Patrick J. Roach, graduate students in the chemistry
department at Penn State.

This research was supported by the U. S. Air Force Office of
Scientific Research and the U. S. Department of Energy.

---

[**http://www.biophysica.com/superatom.htm**](http://www.biophysica.com/superatom.htm)  
[**http://www.newscientist.com/channel/fundamentals/mg18624951.800**](http://www.newscientist.com/channel/fundamentals/mg18624951.800)
  
***New Scientist* # 2495 ( 16 April 2005 ), page 30**

**A New Kind of Alchemy**

**Philip Ball**

*The Transformative Power of the nano-clustered Superatom
generates a new form of Chemistry with super-catalytic
effects and implications for metal colloidals.*

LET'S hear it for Dmitri Mendeleev. His periodic table has done
a remarkable job of making sense of the elements, arranging them
neatly into families whose members share similar properties. For
more than a century it has been chemists' guiding light. But
Mendeleev's classic layout is starting to prove inadequate at
describing the unexpected ways in which chemical elements behave
when divvied up into small chunks. And now some chemists think
it may be time to build a whole new table, this time from
something much stranger than atoms: superatoms.

According to Mendeleev's roll call, an element's chemistry can
be deduced from where it sits in the periodic table. Reactive
metals like sodium and calcium occupy the two columns on the
left. The inert "noble" gases make up the column on the far
right, flanked by typical non-metals such as chlorine and
sulphur.

Now this neat picture is being disrupted by superatoms -
clusters of atoms of a particular chemical element that can take
on the properties of entirely different elements. The chemical
behaviour can be altered, sometimes drastically, by the addition
of just one extra atom. "We can take one element and have it
mimic several different elements in the periodic table," says
Welford Castleman, an inorganic chemist at Pennsylvania State
University who has studied the chemistry of aluminium
superatoms.

It is a finding that is challenging our entire understanding of
chemical reactivity. Adding superatoms to the periodic table
would transform it from a flatland to a three-dimensional
landscape in which each element is drawn out into a series of
super-elements. Superatoms could have practical uses too: they
could be combined into super-molecules to make new materials.
And their unusual chemistry could be harnessed to make efficient
fuels.

According to conventional thinking, the chemical properties of
an atom depend on the way the electrons orbiting its nucleus are
arranged in a series of shells. This in turn is determined by
the number of electrons it possesses - just one in the case of
hydrogen, for example, but up to 92 for an atom of the heavy
metal uranium. The structure of the periodic table is explained
by the gradual filling of the shells. Atoms with completely
filled shells - the noble gases, such as helium, argon and xenon
- are particularly unreactive. The most reactive elements are
often those with atoms that are just one electron short of a
filled shell and so occupy the column next to the noble gases in
the periodic table, or those with one electron too many, which
make up the left-most column of the table.

This simple picture was thrown into disarray in the early
1980s, when evidence started appearing that clusters of atoms of
one element could behave like another. Thomas Upton at the
California Institute of Technology in Pasadena discovered that
clusters of six aluminium atoms could catalyse the splitting of
hydrogen molecules in much the same way as ruthenium, a metal
used as a catalyst in the chemical industry. This quickly led to
thoughts of extending the periodic table. "Some of us started
giving talks with Mendeleev in the title," recalls Robert
Whetten, a cluster chemist at the Georgia Institute of
Technology in Atlanta.

What was so special about these six-atom clusters? Research
carried out around the same time by Walter Knight and his
colleagues at the University of California, Berkeley, on another
type of cluster started to provide some clues. Knight's team was
working with a cool gas of sodium atoms and noticed clusters of
atoms condensing out of the gas, rather like water droplets in a
steamy room. Close inspection led to an unexpected discovery:
rather than being made up of random numbers of atoms, the
clusters mostly contained 8, 20, 40, 58 or 92 atoms. But why
these numbers over others?

**Atomic alter ego**

Knight and his colleagues suspected it was down to the
arrangement of electrons in the clusters. In a large lump of any
metal, including sodium, some of each atom's electrons are free
to move through the solid lattice. That's why metals conduct
electricity. But Knight suspected that if these electrons are
confined to a small number of atoms they might behave
differently. To find out more, he borrowed a model used in
nuclear physics and applied it to the cluster of atoms. Known as
the "jellium" model, it treats the cluster of atoms as though
they were a blob of jelly. Inside the blob, one electron from
each sodium atom becomes free to roam through the blob.

According to Knight's calculations, the electrons in the blob
arrange themselves in shells, just as the electrons of a single
atom do, making the cluster behave as a giant atom. And when his
team calculated the number of electrons that would make complete
shells in a jellium cluster, the answer turned out to be 8, 20,
40 and so on. Since each sodium atom contributes one electron to
the jelly, this explains why sodium clusters tended to be made
of 8, 20 and 40 atoms. Clusters of this size can be thought of
as the superatom counterparts of the noble gases, because their
jellium electron shells are completely filled.

Knight's jellium model explains why stable clusters form. But
could it explain why clusters of one element mimic another as
Upton had found? Fast-forward to the mid-1990s, when Castleman
was investigating what happens when oxygen reacts with aluminium
cluster-ions - clusters that had been given an extra electron.
Castleman saw the oxygen stripping away aluminium atoms from the
clusters one at a time, steadily shrinking them down to nothing
as the reaction progressed.

* We can take one element and have it mimic several
different elements in the periodic table *

But when he did the experiment with clusters of various sizes,
he noticed that the reaction would suddenly stop, leaving behind
a depleted cluster. When he looked more closely, he found that
the leftover clusters contained 13, 23 and 37 aluminium atoms.
It seemed that there was something about these clusters that
made them unwilling to react with oxygen.

To understand what that was, Castleman and his colleagues
turned to the jellium model and used it to calculate the
arrangement of electrons in the Al13, Al23 and Al37 clusters.
They found something similar to what Knight had seen in sodium
clusters. Aluminium cluster-ions made of 13, 23 and 37 atoms -
plus an extra electron - have just the right number of electrons
to form closed electron shells. In effect, aluminium cluster
ions with this number of atoms behave more like a noble gas than
aluminium, at least as far as the reaction with oxygen is
concerned. The numbers are different from the numbers in
Knight's clusters because aluminium atoms contribute more
electrons to the jelly than sodium does.

Castleman then wondered what would happen if he removed the
extra electron from the clusters. Elements with one electron
fewer than the noble gases are the halogens - fluorine,
chlorine, bromine and iodine - which are highly reactive. Sure
enough, his team found that if they removed an electron, the
neutral Al13 clusters underwent the same chemical reactions as
the halogens. What's more, they found that Al13 cluster-ions,
with their extra electron, behave much like the bromide ions
that form when bromine atoms gain an electron. So it certainly
looks as if aluminium, which is a typical metal, can be made to
behave like a classic non-metal if it is in superatom form.

How far does the similarity go? To test the chemistry of the
aluminium superatom, Castleman's team investigated how it reacts
with a halogen molecule such as iodine. Bromide ions are known
to stick to iodine gas molecules to create BrI2- ions.
Similarly, iodine ions latch onto iodine molecules to form
tri-iodide ions, I3-, and further iodine molecules can then be
added to create I5- and I7-. Castleman thought that if Al13
cluster-ions really do mimic halide ions, then they should
undergo the same reaction too. So his group tried it. Sure
enough, they found that they could make Al13I2- and Al13I4-.

It certainly looked promising. "We then started to work with
other aluminium clusters," says Castleman, and that's when they
discovered that they could get aluminium to mimic another
element too. In reactions with iodine gas, they found that a
cluster of 14 aluminium atoms behaves like an alkaline earth
metal, the family in the second column of the periodic table
that includes calcium and magnesium.

**Scouring for superatoms**

These discoveries have prompted Castleman and his colleagues to
scour the periodic table for more superatoms. So far, they have
found hints that the chemical reactivity of clusters combining
vanadium and oxygen atoms changes dramatically with the number
of atoms in the cluster.

But curiosity aside, what's the point? What can be gained from
making a compound with a superatom mimicking an element like
bromine, rather than with bromine itself?

One answer is that superatoms could provide entirely new types
of material, including "expanded" crystals. In a solid such as
sodium chloride, the atoms are stacked together like oranges in
a market display. In an expanded crystal, the atoms would be
replaced by a stack of giant superatoms.

Expanded crystals could have useful properties. In the early
1990s, it was discovered that the superconducting properties of
carbon-60 crystals doped with metal ions could be maintained at
ever higher temperatures by squeezing larger and larger ions
into the crystal lattice. Even so, the temperature at which the
material ceased to act as a superconductor was still not very
high - and was certainly a long way from the room-temperature
superconductivity that researchers would love to achieve.
Perhaps superatoms could hold the answer here and in related
applications. Shiv Khanna, a physicist at Virginia Commonwealth
University in Richmond who works with Castleman, hopes that
replacing iodine in conducting polymers with aluminium
superatoms could improve their conductivity.

Not all researchers share his optimism. "There is scepticism,
mostly expressed by physicists and theorists, that a crystalline
material composed of large aluminium clusters could ever be
achieved," Whetten admits. "But my opinion is that one of these
projects will eventually succeed." Castleman is confident that
chemists' ingenuity will win through. "Physicists lack
appreciation for the immense variety of chemical approaches to
synthesising new materials," he says. He looks forward to being
able to use clusters to build materials with tailor-made
properties.

Another of the hopes for superatoms is that they could be used
to disguise an element's normal chemistry. Aluminium could be a
useful additive to solid fuels because it releases huge amounts
of energy when it burns. But there is a problem: fine aluminium
power is so reactive that the grains often oxidise before they
even reach the ignition chamber, making them useless for
boosting fuel.

Castleman thinks the solution might lie with noble-gas-like
Al13 cluster-ions, which do not react with oxygen. His plan is
to combine them with some kind of combustible organic molecule
and mix the resulting compound with the fuel. "It would be
totally stable," he says, "until a flame kicks out the extra
electron." At that moment, the cluster's disguise would fall
away, returning it to its reactive neutral form.

The idea "is just getting started", Castleman says, and he
cautions that he doesn't know yet if it will work. But it is
looking promising enough to have attracted the US air force,
which is funding him to do further research.

Applications like these are not the main point, however, at
least as far as chemists are concerned. For them, superatoms
could provide a means to change something they had previously
accepted as given: the chemical properties of the elements. Now
they are on the verge of being able to control and alter the way
the elements react. It is a kind of alchemy, but it has no need
of magic. All you have to do is count the right number of atoms.

**Size does matter**

FOR nearly two centuries, researchers have known that when
matter is divided into very small lumps it behaves in new and
sometimes surprising ways. One of the most recent examples is
seen in the change in the colour of light produced by some
fluorescent materials if they are diced into nanoscale specks.

When the semiconductor cadmium selenide is illuminated with
white light, it normally fluoresces in the infrared part of the
spectrum. But prepare it in the form of grains just a few tens
of nanometres wide, and the wavelength of the light it emits
becomes shorter, putting it into the red or yellow part of the
visible range.

The light is emitted when electrons in the semiconductor jump
between quantised energy levels. Confining the electrons within
nanoscale particles changes the energy levels, making the gap
between them larger. As a result, the photons of fluorescent
light have more energy, which in turn means that their
wavelength is shorter. This effect allows the colour of the
light emitted by the nanoparticles to be tuned simply by
changing their size. The particles are already being used as
glowing tags for labelling cells and could be turned into tiny
light sources for optical communications.

---

[**http://nanotechweb.org/cws/article/tech/26782**](http://nanotechweb.org/cws/article/tech/26782)
  
**Jan 10, 2007**   
***Phys. Rev. Lett*.**

**Platinum Nanoclusters Go Magnetic**

**Belle Dume**

Platinum atoms, which are not magnetic in the bulk, become
magnetic when grouped together in small clusters, according to
new experiments by physicists in Germany. The result, which
confirms theoretical predictions, is not only of fundamental
interest but could find applications in information storage and
spintronics in the future.

![](imageLTE.JPG)

**13-atom Pt cluster**

Clusters of atoms form a type of matter that is intermediate
between single atoms and bulk matter. Metallic clusters are
widely used as catalysts because they have a very high
surface-to-volume ratio, which allows them to speed up chemical
reactions. Researchers believe that magnetic clusters might also
be used in information storage or in spintronic devices that
exploit the spin of the electron as well as its charge.

Scientists had already predicted that nanosized samples of
platinum are highly paramagnetic (i.e. they are attracted to a
magnet). The new experimental results, from Emil Roduner of the
University of Stuttgart and colleagues, confirm these
predictions and could help us to understand better how magnetism
can develop in a normally non-magnetic element.

Roduner and co-workers began their experiment by preparing the
platinum clusters in the pores of a zeolite  a crystalline
aluminosilicate that resembles a highly regular sponge with a
network of pores measuring 1.3 nm in diameter. They then
stabilized the clusters in these pores so that they did not grow
any further. Next the team identified the clusters using a
special X-ray technique called EXAFS, which is selective for
specific elements (in this case platinum) and is particularly
suitable for small species like these clusters. Finally the
physicists measured the magnetization of the clusters as a
function of temperature and magnetic field using an extremely
sensitive magnetometer known as a superconducting quantum
interference device.

The Germany team found that each cluster, which consists of 13
atoms, has a magnetic moment as high as 0.65 Bohr magnetons per
atom. By comparison the figure for iron is 2.2 Bohr magnetons
per atom.

"The main significance of our work at this point is a
fundamental understanding of magnetism," Roduner told
nanotechweb.org. "However, since small, isolated, high magnetic
moments - in this case corresponding to eight unpaired electrons
per 13-atom cluster - are also of general interest to
information storage or spintronics, these materials might be
further developed to suit such advanced applications."

Another intriguing feature of the platinum clusters is that
they are best described as "superatoms", said Roduner. This
means that each 13-atom cluster has properties that are very
similar to those of individual atoms. "It is fascinating to
imagine that new periodic tables of superatoms might be drawn
and that this may lead to a new chemistry of superatoms,
offering a fantastic perspective for the future of young
chemists," he added.

The researchers reported their work in Phys. Rev. Lett..

---

[**http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1693677**](http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1693677)

***Proc Natl Acad Sci U S A.* 2006 December 5; 103(49):
1840518410.**   
**doi: 10.1073/pnas.0608781103.**

**Multiple valence superatoms**

**J. U. Reveles, S. N. Khanna, P. J. Roach,
and A. W. Castleman, Jr.**

We recently demonstrated that, in gas phase clusters containing
aluminum and iodine atoms, an Al13 cluster behaves like a
halogen atom, whereas an Al14 cluster exhibits properties
analogous to an alkaline earth atom. These observations,
together with our findings that Al13? is inert like a rare gas
atom, have reinforced the idea that chosen clusters can exhibit
chemical behaviors reminiscent of atoms in the periodic table,
offering the exciting prospect of a new dimension of the
periodic table formed by cluster elements, called superatoms. As
the behavior of clusters can be controlled by size and
composition, the superatoms offer the potential to create unique
compounds with tailored properties. In this article, we provide
evidence of an additional class of superatoms, namely Al7?, that
exhibit multiple valences, like some of the elements in the
periodic table, and hence have the potential to form stable
compounds when combined with other atoms. These findings support
the contention that there should be no limitation in finding
clusters, which mimic virtually all members of the periodic
table.

![](imageHRQ.JPG)

**Fig. 2.**

**Structure and energetics of aluminum compound clusters. (a)
Al7C?-optimized geometry. (b) Energy gained by adding an Al
atom to Aln-1C? species and HOMOLUMO gap for the AlnC?
clusters. (c) Electron charge density of the HOMO in Al7C?
clusters. (d) Al7O?-optimized geometry. (e) Energy gained by
adding an Al atom to Aln-1O? species and HOMOLUMO gap for the
AlnO? clusters. (f) Electron charge density of the HOMO in
Al7O?.**

---

[**http://www.sciencedaily.com**](http://www.sciencedaily.com)

# Research Reveals Halogen Characteristics Of Cluster Of Metal Atoms

A stable cluster of aluminum atoms, Al13, acts as a single
entity in chemical reactions, demonstrating properties similar
to those of a halogen, reports a research team led by A Welford
Castleman Jr., the Evan Pugh Professor of Chemistry and Physics
and the Eberly Family Distinguished Chair in Science at Penn
State, in a paper to be published in the 2 April 2004 issue of
the journal Science. Experimental results and theoretical
calculations indicate that the cluster chemically resembles a
"superhalogen" atom, retaining its properties during the
reaction and in reaction products. Other team members include
Denis E. Bergeron of the Penn State departments of chemistry and
physics and Shiv N. Khanna of the Virginia Commonwealth
University department of Physics. One implication of the
research is the possibility of using such clusters as building
blocks in nanoscale fabrication. The project focused on
experimental evidence of the existence of a very stable cluster
anion, Al13I-, prepared by the gas-phase reaction of aluminum
clusters with HI gas. Mass spectrometric analysis indicated that
the reaction produced relatively few products, the most abundant
corresponding to Al13I-. Energy calculations to determine the
bonding mechanism between the aluminum cluster and the iodine
atom indicate that the extra electron is localized on the Al13
cluster, meaning that the cluster maintains its integrity
throughout the reaction. Because the cluster has a greater
electron affinity in the compound, or attraction to the free
electron, than does iodine, it can be considered a
"superhalogen."

"One of the themes of our research is using the clusters as
building blocks for new nanoscale materials," says Castleman.
"In many cases, people have worked from the top down; that is,
subdividing matter to get it smaller and smaller. We're trying
to work with atoms and molecules and put them together--working
our way from the bottom up. If we can retain the properties of
aggregates, as we put them together, perhaps we will be able to
construct new nanoscale materials." The key to using the
aggregates as building blocks is that they retain their
individual properties during the reaction and do not coalesce
into a large aggregate.

One goal of the research is to test the Jellium model of stable
clusters, which treats metal atoms in a small system as positive
cores surrounded by the valence electrons. The model predicts
certain closed-shell arrangements with high stability, called
magic clusters. In the Jellium model, the cluster's atomic
nuclei and inner electrons are seen as a single, spherical,
positively charged core, surrounded by valence electrons in
electronic shells similar to those of atoms. Essentially, the
magic clusters can be viewed as superatoms, capable of forming
compounds.

"When we started looking at reactions, Al13 turned out to be a
very interesting species for several reasons, " says Castleman.
"It behaves very much like a halogen, somewhere between iodine
and bromine the way it wants to bind an electron. If we could
put an iodine atom in contact with Al13, the Al13 has a little
higher electron affinity than iodine, which could allow the Al13
to retain the electron, thereby bonding the Al13 and I
together."

Experimental observations indicated that the stability of the
Al13I- ion is comparable to that of BrI-, a well-known and very
stable molecular halogen ion. The ability of a cluster of
aluminum atoms to behave like a halogen opens up the prospect
that Al13 and other magic clusters can retain their properties
as a building block for assembling new materials.

"This superhalogen is not disrupted even in the presence of the
very reactive iodine atom in close proximity, but still keeps
its properties," says Castleman. "Now that we have shown that
this is possible, we see potential ways to make other clusters,
maybe involving other metals or alloys. It should be possible to
construct something in the Jellium framework that would have the
properties not only of a halogen, but of other types of atoms as
well. For example, the Al13- ion itself resembles a rare gas
atom because it is so unreactive. Ideally, we could have a whole
series of clusters--a 'three dimensional' periodic table, not of
elements but rather of clusters simulating the properties of the
elements." The goal is to use these clusters as building blocks
to tailor the design and formation of nanoscale materials with
selected properties.

This research was supported by the U. S. Air Force Office of
Scientific Research and the U. S. Department of Energy.

![](040402074127.jpg)

*Charge density map of the highest occupied molecular orbital
for the Al13I- cluster. Note the preservation of Al13I-
icosahedral geometry, and the localized charge density on the
  
aluminum cluster moiety. Color code: blue=aluminum;
red=iodine. (Image courtesy Penn State)*

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---