09/28/2018:
In collaboration with researchers from Cornell and NTU, we reported our observation of phase transitions in formamidinium lead iodide (FAPbI3) under pressure. The article was just accepted by
J. Am. Chem. Soc. FAPbI3
is a hybrid compound, consisting of a perovskite alpha-phase and hexagonal (non-perovskite)
delta-phase. Study on the pressure-induced structural evolution of this
organic-inorganic compound is a hot topic. For the first time, the authors
determined that the pressure could accelerate the alpha- to
delta-FAPbI3 transformation.
link
03/31/2016:
A recent publication, "Pressure Dependent Polymorphism and Bandgap Tuning of Methylammonium Lead Iodide Perovskite", was chosen as a Hot article and has been featured in the online collection of "Nanoscale".
Author:
Sarah Millar
Published
Date: 18 January 2014
Source / Publisher: Chemistry - A
European Journal/Wiley-VCH
Copyright: Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
10/17/2012:
Hydrogenation of olefins is often used to test new heterogeneous catalysts,
especially noble metals, such as Pt, Pd, and Au. Each crystallographic facet of
such catalysts has its own role in the catalysis. For example, {111} planes of
Au preferentially activate C=O groups, whereas low-coordinated sites at corners
and edges favor the breaking of C=C bonds. It has also been shown that
hydrogenation of styrene takes place on defect sites (high-index kinks and
steps) of Pd catalysts, rather than their low-index terraces. Thus, the
fabrication of nanocatalysts with high-index crystallographic facets could lead
to more efficient catalysts.
We recently report the simple synthesis of high-quality Pt3Co
nanocubes (NCs) with a concave structure. The NCs were prepared through a
wet-chemical approach, in which the ratio of oleyl amine (OAM)/oleic acid (OA)
was finely tuned. The NCs are terminated with high-index crystallographic planes
containing a combination of several sub-facets.The team proposes that the
formation of Pt3Co seeds is dependent on the concentration of free metallic
atoms during the reaction, whereas the final morphology of NCs was controlled by
selective binding with the appropriate OAM/OA ratio during the crystal-growth
stage.Using hydrogenation of styrene as a model reaction, the NCs showed
enhanced catalytic activity in comparison with low-indexed surface terminated Pt3Co
nanocubes of similar size owing to their more open structure, more stable
composition/morphology, and the increased number of active atomic sites located
on their high-index crystallographic planes.
The manuscript (DOI: 10.1002/chem.201301724) has been chosen to be highlighted
on the ChemistryViews website.
The short news article is available at this link.
10/17/2012:
Watching Nanoscale Octahedra Crystallize:
Assembly of nanoparticles into ordered superlattices opens up many potential applications such as sensors, catalysts, and novel optical materials. Unlike spherical particles, which can normally self-assemble into a close-packed fcc superlattice, systems containing non-spherical building blocks are much less known. We have recently demonstrated how to synthesize monodisperse non-spherical nanocrystals, including nanocubes and nanoctahedra. In recent experiments at D1 station of Cornell High Energy Synchrotron Source (CHESS) at Cornell University, together with CHESS staff scientist Dr. Detlef-M. Smilgies we determined an extremely low packing density superstructure consisting of Pt3Cu2 nanotahdera. Furthermore, for the first time, we observed reversible Kirkwood-Alder transition occurred in this system. The details were just highlighted on CHESS web site
http://news.chess.cornell.edu/articles/2012/Fang10172012.html as well as reported in our recent publication [JACS
134 (34), 14043-14049 (2012)].
12/10/2011:
TOC of our recent publication, "Reversal of Hall-Petch Effect in Structural Stability
of PbTe Nanocrystals and Associated Variation of Phase Transformation", has been
selected and posted as one of "rolling pictures" on
Nano Letters.
05/10/2011:
Our review paper, "self-Assembly of Lead Chalcogenide Nanocrystals" (Chem. Asian
J. 6(5)/2011, page 1126), was recently published, and its art-work was chosen as
a cover picture.
1/18/2011:
Our previous synthesis methodology of Pt nanocubes was cited in
Gelest catalog (click show details), "Metal-Organics" p.
176-177.
Are shape-controlled nanocrystals of Pt-based alloy promising
electrocatalysts?
11/22/2010:
Our previous work,
Pt3M (M=Fe,
Co, Ni and Pt) nanocube synthesis and
ORR study on
Pt3Ni nanoctahedra, has been highlighted by Xia's paper, "
Shaping a Bright Future for Platinum-Based Alloy Electrocatalysts" which will
be published soon.
Can an electrocatalytic investigation be conducted on a
particle shape-controlled level?
08/16/2009:
Our new paper, "Enhancing by Weakening: Electrooxidation of Methanol on Pt3Co and
Pt Nanocubes" was just published in Angew. Chem. Int. Ed. In this work, Pt3Co and
Pt nanocubes were comparatively prepared and studied. The enhanced catalytic activity
on Pt3Co nanocubes was explained by the slower and weaker adsorption of CO onto
the surface of Pt3Co.
8/12/2010:
We just receive word that our communication "Enhancing
by Weakening: Electrooxidation of Methanol on Pt3Co and Pt Nanocubes" has been
chosen as a "Hot Paper" by the Editors of Angewandte Chemie for its importance in
a rapidly evolving field of high current interest.
This announcement will be published in the table of contents entry on Angewandte's
homepage prior to publication of the full paper as soon as possible.
4/27/2010:
It is now possible to assemble binary nanosphere superlattice patterns with various
structures, and it was determined that opposite electrical charges are the major
driving force to result in such patterns. With a success of various nanopolyhedron
syntheses, the question has been extended to a non-spherical nanoparticle colloidal
system: What is the dominant driving force to induce a superlattice assembly in
a non-spherical-particle system? With our recent advances in preparation of shape-
and size-controlled nonspherical nanoparticles, we answered this question in the
current issue of ACS Nano (4/4). In this work, we reported our observation of two-dimensional
(2D) superlattices consisting of c-In2O3 nanoctahedra and Pd nanospheres, and identified
three types of c-In2O3 skeleton structures in the 2D octahedral c-In2O3-spherical
Pd nanoparticle supercrystal patterns. In collaboration with Dr. Luo at TAMU, we
concluded that (1) the vertices of c-In2O3 nanoctahedra could have higher electrical
charge density than that on edge or plane; (2) most of the Pd nanoparticles locate
on the middle plane of the c-In2O3 nanoctahedra well above the substrate surface
(support film) rather than sitting on it in the 2D supercrystal assembly patterns;
(3) the orientation of c-In2O3 nanoctahedra dominates the structure of a nonspherical
2D supercrystal pattern. On the basis of these investigations in a non-spherical
nanoparticle colloidal system, we confirmed that Coulomb forces resulted from opposite
electrical charges on nanopolyhedra (c-In2O3) and metal nanospheres (Pd) are the
major driving forces to induce such assemblies. Read
more.
Highlight: Shape DOES affect the electrochemical
catalytic activity.
01/06/2010:
We successfully synthesized high-quality Pt3Ni nanopolyhedra (geometric tiny
solids with flat facets and straight edges) using a recently developed wet-chemical
approach, and investigated their shape-dependent oxygen reduction activity which
is a significant reaction in the cathode of proton exchange membrane fuel cells.
Amazingly, we determined that the activity on Pt3Ni nanoctahedra (terminated with
{111} facets) is ~5 folds higher than that of nanocubes (bounded with {100} facets)
with a similar size. This discovery is important for developing new type of electrocatalyst
with a superior oxygen reduction activity used in the real world of fuel cells.
This result will be published in
Nano Letters
soon.
12/1/2009:
For the first time, we found that W(CO)6 can control the morphology of Pt-3d-transition
alloy nanoparticles and we have developed a general approach for preparation {100}-terminated
Pt3M nanocubes (M = Pt or Co, Fe, and Ni). This result was published in
JACS.
11/25/2009:
We released a facile and general synthetic method for preparation of high-quality,
{100}-terminated Pt3M nanocubes (M = Pt or 3d-transition metals Co, Fe, and Ni).
We realize that addition of W(CO)6 is crucial for control of the nucleation process
when the metallic precursors are reduced, whereas an optimized ratio of the solvent
pair, oleylamine and oleic acid, is the key to enabling the lowest total surface
energy on {100} facets in order to develop such cubic nanocrystals in the present
system. This novel method was published in the last issue of
JACS this
year.
04/30/2009:
Shape-controlled catalysis: High-quality Pt-Cu nanocubes with an average
size of about 8 nm were synthesized from a high-temperature organic solution system
in the presence of various capping ligands. These cubic Pt-Cu nanocrystals terminated
with {100} facets demonstrated a superior catalytic activity towards methanol oxidation
compared to similar sized Pt-Cu and Pt nanospheres. This result was published in
Angew. Chem. Int. Ed. on 4/29/2009. This publication was highlighted as "VIP"
(Very Important Paper).
03/5/2009:
We just received an invitation from Chem. Eur. J. that our accepted manuscript,
Soluble InP and GaP Nanowires: Self-Seeded, Solution-Liquid-Solid Synthesis and
Electrical Properties, has been highlighted with a frontispiece in a forthcoming
issue.
02/20/2009:
We have controlled growth parameters and self-assembled various PbSe QD arrays on
flat gold surface for scanning tunneling spectroscopy measurements. The current-voltage
curves of the arrays were analyzed using double-barrier tunnel junction model to
acquire the shunt capacitance between the array and the gold substrate. This article
will be published in J. Phys. Chem. C on 5/7/2009, and the Cover Art will show up
on issue 18, 2009.
02/04/2009:
Zhaoping's article, "Soluble InP and GaP Nanowires: Self-Seeded, Solution-Liquid-Solid
Synthesis and Electrical Properties" was accepted by Chem. Eur. J. In recent years,
a solution-based approach supported by a solution-liquid-solid (SLS) mechanism has
been developed to enable the quality-control in addition to previous physical processing
methods. Nevertheless, there still has a large room to improve the wet-chemical
synthesis of III-V nanowires. Our modified strategy presented in this publication
avoids some issues that exist in the SLS method, such as heterogeneous phase of
catalyst and potential metallic contamination in nanowires. We also demonstrate
excellent quality of the as-prepared InP and GaP nanowires, including low native
point defects for carrier concentrations and few structural defects (especially
for InP). The scientific impacts of this work lie in the fact that in this relatively
facile solution-based approach developed in our group the catalyst seeds can be
in-situ generated by the decomposition of the metalorganic precursor, In(CH3)3 or
Ga(C2H5)3, at an appropriately high temperature without using any special surfactant.
Moreover, this synthetic approach may be promising in readily extending to a preparation
strategy of other high-quality III-V nanowires including GaAs, GaSb, InAs, InSb,
and their (Ga/In)(P/As/Sb) alloys.
09/22/2008:
Jun's research article, "
Simple Cubic Super Crystals Containing PbTe Nanocubes and Their Core-Shell Building
Blocks", was published in JACS. In this full paper, we report a preparation
of high-quality cubic PbTe nanocrystals, their square-array assemblies in two-dimensional
patterns, as well as simple cubic super crystals. The influence of oleylamine in
nanocrystal synthesis and core-shell formation through an anion-exchange mechanism
was also studied. The simple cubic super crystals together with two-dimensional
assembly patterns containing PbTe nanocubes and their core-shell building blocks
were fully characterized. Such super crystals consisting of structural building
blocks may allow engineering of more complex materials from which novel properties
may emerge.
09/09/2008:
Jun's research communication, entitled "p-Type Field-Effect Transistors of Single-Crystal
ZnTe Nanobelts", was published in Angewandte Chemie Int. Ed. In this work, we have
been succeeded, for the first time, in preparation of straight ZnTe nanobelts with
extremely low thickness (< 6 nm). We further determined a crystal growth direction
of < (-2)0 0 > in the growth of the belts, which has never been reported previously.
We also demonstrated these single-crystal ZnTe nanobelts as p-type field-effect
transistors, revealing a bright future of applications in nanodevice engineering.
03/19/2008:
Our self-assembly paper, entitled "Super-Crystal Structures of Octahedral c-In2O3
Nanocrystals", was published in JACS. Three-dimensional (3D) self-assembly of nanocrystal
(NC) superlattice, i.e. super crystal (SC), has attracted increasing attention.
The small building blocks for assemblies are usually spherical nanocrystals. Recent
progress indicates that it is possible to achieve a super crystal using non-spherical
NCs, such as cubic NCs.
In this article, we describe and analyze 2D and some 3D assemblies of uniform cubic-phase
In2O3 NCs with octohedral shapes. We demonstrate our amazing observations on this
kind of super crystals (or superlattices) as a model system, exposing largeness
at least in tens of microns scale and other unique features such as steps, terraces,
kinks and vacancies which are similar to those from a single crystal. Based on the
EM observations, three types of well-defined octahedral NC packing structures in
such super crystal system are also identified.
02/13/2008:
Zhaoping's III-V QD paper was published in Angewandte Chemie and highlighted as
VIP very important paper on Feb. 13, 2007.
III-V semiconductors are very important materials and are of great interest for
new generation of microelectronics. Colloidal III-V semiconductor nanocrystals have
also been a subject of intensive studies because of their rich phenomena associated
with quantum-confinement effects. However, studies of III-V nanocrystals are largely
restrained due to the difficulty of their synthetic chemistry. The scientific impacts
of this work lie on that we have introduced a new concept, co-reduction, to understand
the formation of InP. We believe that this report may provide the following breakthroughs:
(1) We demonstrate an great improvement of the synthetic conditions using a novel
approach, e,g, shortening the period of reaction time and reducing the cost of precursor;
(2) This novel method has skipped expensive or more hazardous P-sources, such as
tris(trimethylsilyl)phosphine in the process of InP nanocrystal synthesis, making
this synthetic strategy noticeably "greener" and more economical. (3) The present
work may benefit the further scale-up of such III-V chemical synthesis as well,
creating a new direction in extending this achievement to the preparations of InAs
and InSb nanocrystals using AsCl3 and SbCl3 as the pnicogen sources, respectively.