Building on our successful synthetic strategy, we have begun
to analyze the growth of these materials using electrospray
mass spectrometry methods (ESMS). This effort represents one
of the first attempts to utilize a traditional biochemical analytical
method to directly probe nano-scale inorganic structures. The
initial results are allowing a broadening of the understanding
of the role of kinetics and thermodynamics in nano-material
growth.
Molecular clusters, as a class of materials, exist as discrete
units with structures that are often related to a fragment of
a bulk solid state lattice. These materials have long held promise
in materials chemistry, biological chemistry, and catalysis,
particularly as models in biological catalytic activity and
more recently for understanding the effects of reduced dimensionality
on bulk materials. Traditionally the structures and metal valence
for metallo-clusters are probed by a correlation of solid state
and solution phase physical techniques such as NMR, X-ray diffraction,
XPS, UV/Visible, Infrared, Raman, and ESR spectroscopies. Recent
efforts on electrospray ionization mass spectrometry (ESI-MS)
of inorganic and bio-inorganic materials have yielded important
insight into both the structure and valency of metallo-proteins
and inorganic clusters in solution by analysis of the fragmentation
behavior, parent ion m/z ratio and daughter ion analysis in
tandem mass spectrometry studies. These early studies on inorganic
materials suggest ESI-MS techniques may provide a unique platform
for analysis of intact clusters under solution conditions without
the need for multiple analytical techniques. The applicability
of electrospray ionization (ESMS) methods to problems in materials
chemistry is demonstrated by our results for mass spectrometry
of these nano-precursor materials. Low-cone voltage ESMS is
a useful technique for the rapid analysis of the organometallic
precursor molecules when both positive and negative ionic modes
are analyzed. This method shows promise as an alternative method
of analysis of the dynamics of growth in nano-scale materials.
The main advantage of ESMS over other mass spectrometry techniques
is the capabilities for direct analyses of mixtures and solvated
molecules.
The analysis of the change in physical properties of nanomaterials
represents the transition from molecular to bulk behavior. The
development of scaling laws for phase transitions, optical bandgaps,
and melting points on CdSe and CdS have provided a significant
body of knowledge on the size dependent behavior of inorganic
semiconductors. Typically size and size dispersity in these
materials are measured by TEM imaging, or estimates from the
optical properties. With these techniques, specific distributions
in the composition, surface compositions and structure of individual
nano-materials are not addressed. The use of mass spectrometry
is an alternative technique that provides exact mass and stability
to fragmentation information by analysis of the mass/charge
ratio of ions in the gas phase. While mass spectrometry is largely
used in biological and polymeric tools, significant advances
in the development of MS techniques have shown soft-ionization
methods, such as electrospray, are ideal for studies of solution
phase species in the gas phase without perturbation of the solution
structures, particularly in biological and inorganic materials
Electrospray ionization (ESI) mass spectrometry is a soft-ionization
technique that allows analysis of exact structure, composition,
and stability of solution phase materials by a gas phase technique.
We have described the first electrospray ionization mass spectrometry
analysis of a 1.5 nm CdS cluster, [Cd32S14(SC6H5)36.DMF4]. The
cluster [Cd32S14(SC6H5)36.DMF4] has been previously analyzed
by X-ray diffraction providing evidence of the ~1.2 nm cluster
core, and described in effect as the smallest nanocrystal for
the CdS series. This size represents the boundary between molecular
cluster and nanomaterial behavior. By using a nanospray mass
spectrometry technique, we are able to carry out a careful mass
spectroscopic analysis of the fragmentation behavior of an 82-atom
CdS cluster that is a roughly spherical piece of cubic sphalerite
lattice (~ 1.2 nm in diameter). With the capping of the four
corners of the lattice by hexagonal wurtzite-like CdS units,
the size of the cluster is ~ 1.5 nm in diameter. Analysis of
the fragmentation, parent ion and daughter ion patterns allows
the stability of the 1.5 nm CdS nanoparticle to be assessed,
as well as evidence for cleavage planes in the crystallite.
To our knowledge, this is the first time that mass spectrometry
has given information on nano-sized metal chalcogenide clusters
(“Cd32” is a 1.5 nm average diameter). Such results
show the versatility of mass spectrometry analysis in determining
the composition of nanomaterials. Specific information concerning
the chemical composition of nanomaterials can be obtained with
high accuracy. Parent ion fragmentation indicates cleavage along
favorable planes in the CdS core of the cluster, that may be
crucial in understanding the fragmentation behavior in ESI-MS
/MS data of larger nanomaterials. We are continuing to apply
ESI-MS and ESI-MS/MS techniques to a wide range of inorganic
clusters including TiO2 and Au nanocrystals to probe the stability
and fragmentation behavior in these materials.
Interested in learning more?
Contact Dr. Strouse
or read the published articles: "Mass Spectrometry Analysis of Organic-Inorganic Nanomaterials
and their Precursors." Gaumet, J.J.; Strouse, G.F. Mat.
Res. Soc. Symp. Proc., 726, Q10.6, 1-6 (2002). [ view
article - PDF ]
"Mass Spectrometry Analysis of the 1.5
nm Sphalerite-CdS core of [Cd32S14(SC6H5)36*DMF4]." Gaumet,
J.J.; Khitrov, G.A.; Strouse, G.F. Nano Lett., 2, 375-379
(2002). [ view article - PDF ]
"Nanospray Mass Spectrometry Technique
for Analyzing Nanomaterials from Molecular Precursors up to
1.5 nm in Diameter Clusters." Gaumet, J.J.; Strouse,
G.F. Mater. Sci. Eng. C, 19, 299-304 (2002). [ view
article - PDF ]
"Power of Mass Spectrometry for Analyzing
Organometallic Molecules as Precursors of Nanomaterials."
Strouse, G.F.; Gaumet, J.J. Mat. Res. Soc. Symp. Proc., 581,
479-484 (2000). [ view article - PDF
]
"Electrospray Mass Spectrometry
of Semiconductor Nanoclusters: Comparative Analysis of Positive
and Negative Ion Mode". Gaumet, J.J.; Strouse, G.F. J.
Amer. Soc. Mass. Spec., 11, 338-344 (2000). [ view
article - PDF ]
|