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A series of PtxSny intermetallic nanoparticles including Pt3Sn, PtSn, PtSn2, and PtSn4 were successfully synthesized by an HMDS-assisted method, and the ethanol oxidation reaction tests show that an Sn : Pt molar ratio of 1 : 1 shows the best activity.

We report a facile method to fabricate CuNi nano-octahedra and nanocubes using a colloidal synthesis approach. The CuNi nanocrystals terminated with exclusive crystallographic facets were controlled and achieved by a group of synergetic capping ligands in a hot solution system. Specifically, the growth of {111}-bounded CuNi nano-octahedra is derived by a thermodynamic control, whereas the generation of {100}-terminated CuNi nanocubes is steered by a kinetic capping of chloride. Using a reduction of 4-nitrophenol with sodium borohydride as a model reaction, CuNi nano-octahedra and nanocubes demonstrated a strong facet-dependence due to their different surface energies although both exhibited remarkable catalytic activity with the high rate constant over mass (k/m). A kinetic study indicated that this is a pseudo first-order reaction with an excess of sodium borohydride. CuNi nanocubes as the catalysts showed better catalytic performance (k/m = 385 s-1•g-1) than the CuNi nano-octahedra (k/m = 120 s-1•g-1), indicating that 4-nitrophenol and hydrogen were adsorbed on the 100 facets with their molecules parallel to the surface much easier than those on {111} facets.

Ceria (CeO2) possesses a distinctive redox property due to a reversible conversion to its nonstoichiometric oxide and has been considered as a promising catalyst in the oxidative coupling of methane. Since a heterogeneously catalytic process usually takes place only on the surface of catalysts, it is reasonably expected that the performance of a catalyst, such as CeO2, highly relies on its size- and shape-dependent surface structure. We report our recent progress in achieving exclusive crystal facet-terminated CeO2 nanocrystals using a shape-controlled synthesis protocol in a one-pot colloidal system. We modified a two-phase solvothermal approach to fabricate cubic and truncated octahedral CeO2 nanocrystals with a size-control. During the two-phase solvothermal process, we propose that the Ce-precursors transfer from the aqueous layer to the interface of the organic phase, promoted by the capping ligands (as known as phase-transfer catalysts), for the oxidation and nucleation, and subsequently form CeO2 nanocrystals in the organic layer. As different capping ligands favor binding on diverse crystal facets, tuning the composition of the capping ligand with a precise control could generate nanocrystals that are dominated by a single type of facets with a relatively narrow size distribution.

In this work, we demonstrate a size-controlled synthesis of CuNi octahedral nanocrystals (NCs) using a hot colloidal solution approach. Two different sizes of CuNi nano-octahedra are chosen and investigated. It is determined that the reagent concentration remarkably plays a key role in the formation of the size-defined CuNi octahedral NCs. In terms of the reduction of 4-nitrophenol (4-NP), it uncovers that the obtained CuNi octahedral NCs (in both sizes) exhibit higher catalytic activity than those of CuNi spherical NCs reported previously. It further indicates that the catalytic performance is strongly size-dependent due to their devise specific surface areas of the exposed crystallographic planes.

In the synthesis of metallic nanocrystals (NCs) using a high-temperature colloidal approach, the competition between deposition and diffusion of “free atom (or clusters)” plays an important role as it can direct the morphology of NCs during their evolution. This competition is closely associated with some dynamic conditions such as heat and mass transfer. Stirring speed and ramp rate of heating are two factors that greatly impact the heat and mass transfer processes and consequently determine the morphology of the products but rarely discussed in most synthetic protocols. Herein, we study the syntheses of Pt-M (M = Ni, Fe) NCs as model reactions, showing that a low stirring speed and high ramp rate of heating result in ununiform pod-like NCs, whereas the inverse conditions promote NCs in a uniform shape. This observation can be plausibly explained using a competition mechanism between the deposition and diffusion of the newly reduced atoms during a stage of the NC’s growth.

Platinum-based nanomaterials are well-known to show excellent hydrogen evolution reaction (HER) catalytic performance. The sophisticated structural design facilitates the development of related disciplines such as water splitting devices. Here, a kind of Agcore- Pt atoms-exposedshell structure could be synthesized through ligand exchange between Ag nanoparticles and Pt polysulfide precursor at room temperature (RT). The Ag core maintains its face-centered cubic phase (FCC) crystal phase after the formation of Agcore- Pt atoms-exposedshell structure. While Pt atoms account for only 0.4617 percent of the catalyst mass. With a further electrochemical reduction of Pt (IV) atoms into metallic state Pt (0) atoms from -1.2 V vs. RHE to 0.4 V vs. RHE, the HER catalytic performance of Agcore- Pt atoms-exposedshell would exceed that of commercial 20% Pt/C at low potentials (

Chemically controlling crystal structures in nanoscale is challenging, yet provides an effective way to improve catalytic performances. Pt-based nanoframes are a new class of nanomaterials that have great potential as high-performance catalysts. To date, these nanoframes are formed through acid etching in aqueous solutions, which demands long reaction time and often yields ill-defined surface structures. Herein we demonstrate a robust and unprecedented protocol for facile development of high-performance nanoframe catalysts using size and crystallographic facet-controlled PtNi4 tetrahexahedral nanocrystals prepared through a colloidal synthesis approach as precursors. This new protocol employs the Mond process to preferentially dealloy nickel component in the ⟨100⟩ direction through carbon monoxide etching of carbon-supported PtNi4 tetrahexahedral nanocrystals at an elevated temperature. The resultant Pt3Ni alloy tetrahexahedral nanoframes possess an open, stable, and high-indexed microstructure, containin...

We have prepared nanocomposites of well-defined spherical AgI nanostructures wrapped in reduced graphene oxide nanosheets (AgI@RGO). The as-obtained AgI@RGO nanocomposites exhibit an enhanced photocatalytic activity and stability in the degradation of organic pollutants, namely, Rhodamine B (RhB), in comparison with bare AgI nanospheres. The hybridization of AgI nanospheres with RGO nanosheets affords a good adsorptive capacity for RhB molecules, facilitated charge transfer, and suppressed recombination of electron–hole pairs. These figures of merit lead to an enhanced photocatalytic performance over AgI@RGO. This work opens new possibilities for the development of highly efficient and stable visible-light-driven composite photocatalysts for environmental purification.

Chemically controlling crystal structures in nanoscale is challenging, yet provides an effective way to improve catalytic performances. Pt-based nanoframes are a new class of nanomaterials that have great potential as high-performance catalysts. To date, these nanoframes are formed through acid etching in aqueous solutions, which demands long reaction time and often yields ill-defined surface structures. Herein we demonstrate a robust and unprecedented protocol for facile development of high-performance nanoframe catalysts using size and crystallographic facet-controlled PtNi

The pressure-induced structural evolution of formamidinium-based perovskite FAPbI3 was investigated using in situ synchrotron X-ray diffraction and laser-excited photoluminescence methods. Cubic α-FAPbI3 ( Pm3̅ m) partially and irreversibly transformed to hexagonal δ-FAPbI3 ( P63 mc) at a pressure less than 0.1 GPa. Structural transitions of α-FAPbI3 followed the sequence of Pm3̅ m → P4/ mbm → Im3̅ → partial amorphous during compression to 6.59 GPa, whereas the δ-phase converted to an orthorhombic Cmc21 structure between 1.26 and 1.73 GPa. During decompression, FAPbI3 recovered the P63 mc structure of the δ-phase as a minor component (∼18 wt %) from 2.41-1.40 GPa and the Pm3̅ m structure of the α-phase becomes dominant (∼82 wt %) at 0.10 GPa but with an increased fraction of δ-FAPbI3. The photoluminescence behaviors from both the α- and δ-forms were likely controlled by radiative recombination at the defect levels rather than band-edge emission during pressure cycling. FAPbI3 polymorphism is exquisitely sensitive to pressure. While modest pressures can engineer FAPbI3-based photovoltaic devices, irreversible δ-phase crystallization may be a limiting factor and should be taken into account.