Publications by authors named "Zhenming Cao"

Nanoparticle sintering has long been a major challenge in developing catalytic systems for use at elevated temperatures. Here we report an electron microscopy study of the extraordinary sinter resistance of a catalytic system comprised of sub-2 nm Pt nanoparticles on a Se-decorated carbon support. When heated to 700 °C, the average size of the Pt nanoparticles only increased from 1.

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Ligand exchange is fundamentally related to the surface chemistry of nanoparticles in solution and is also an essential procedure for their synthesis and solution processing. The solution of ligand-bearing nanoparticles can be regarded as a dynamic equilibrium of bound and free ligands depending on the concentration and temperature. The direct experimental calibration of the ligand exchange dynamics relies on the in situ and real-time quantification of bound and free ligands.

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Implementing fast-charging lithium-ion batteries (LIBs) is severely hindered by the issues of Li plating and poor rate capability for conventional graphite anode. Wadsley-Roth phase TiNb O is regarded as a promising anode candidate to satisfy the requirements of fast-charging LIBs. However, the unsatisfactory electrochemical kinetics resulting from sluggish ion and electron transfer still limit its wide applications.

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Despite extensive efforts devoted to the synthesis of Pt-Co bimetallic nanocrystals for fuel cell and related applications, it remains a challenge to simultaneously control atomic arrangements in the bulk and on the surface. Here we report a synthesis of Pt-Co@Pt octahedral nanocrystals that feature an intermetallic, face-centered tetragonal Pt-Co core and an ultrathin Pt shell, together with the dominance of {111} facets on the surface. When evaluated as a catalyst toward the oxygen reduction reaction (ORR), the nanocrystals delivered a mass activity of 2.

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Platinum (Pt)-based catalysts have shown excellent catalytic performance in many fields, particularly for the oxygen reduction reaction (ORR) and direct oxidation of small fuel molecules. Further development of Pt-based electrocatalysts relies on the morphology design of Pt-based alloy nanocrystals (NCs) with highly accessible and active surface sites to optimize Pt atomic utilization. In this work, we reported PtCo-excavated rhombic dodecahedral (ERD) NCs consisting of the self-assembly of 24 ultrathin nanosheets synthesized by a simple wet chemical method.

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Article Synopsis
  • PCV2 is a tiny virus that causes diseases in pigs and is the smallest DNA virus known.
  • Scientists found a way to make virus-like particles (VLPs) using a special protein (Cap) that comes from this virus, which works better when made in silkworms than in bacteria.
  • They used a special test to show that these VLPs can help create a vaccine against PCV2, making it a promising and inexpensive option for pig health.
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We report a robust method for effectively removing the chemisorbed Br ions, a capping agent, from the surface of Pd nanocubes to maximize their catalytic activity. The Br ions can be removed by simply heating the sample in water, but the desorption of Br ions will expose the underneath Pd atoms to the O from air for the formation of a relatively thick oxide layer. During potential cycling, the oxide layer evolves into detrimental features such as steps and terraces.

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Type III interferon (IFN-λ) has recently been shown to exert a significant antiviral impact against viruses in vertebrates. Avian leukosis virus subgroup J (ALV-J), which causes tumor disease and immunosuppression in infected chicken, is a retrovirus that is difficult to prevent and control because of a lack of vaccines and drugs. Here, we obtained chicken IFN-λ (chIFN-λ) using a silkworm bioreactor and demonstrated that chIFN-λ has antiviral activity against ALV-J infection of both chicken embryo fibroblast cell line (DF1) and epithelial cell line (LMH).

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Carbon-supported Pt nanoparticles are used as catalysts for a variety of reactions including the oxygen reduction reaction (ORR) key to proton-exchange membrane fuel cells, but their catalytic performance has long been plagued by detachment and sintering. Here we report the growth of sub-2 nm Pt particles on a commercial carbon support via the galvanic reaction between a Pt(II) precursor and a uniform film of amorphous Se predeposited on the support. The residual Se could serve as a linker to strongly anchor the Pt nanoparticles to the carbon surface, leading to a catalytic system with extraordinary activity and durability toward ORR.

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Gold (Au) typically crystallizes in a cubic close-packed ( ccp) structure to present a face-centered cubic ( fcc) lattice or crystal phase. Herein, we demonstrate that Au nanoscale hexagonal stars featuring a hexagonal close-packed ( hcp) structure can be synthesized in an aqueous system in the presence of fcc-Au nanospheres as the seeds. The success of this synthesis critically relies on the use of ethylenediaminetetraacetic acid to complex with Au ions (the precursor) and the introduction of 2-phospho-l-ascorbic acid trisodium salt (Asc-2P) as a novel reducing agent to maneuver the reduction kinetics.

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Bombyx mori Nucleopolyhedrovirus (BmNPV), which is a member of the Baculoviridae family, is a significant pathogen of the silkworm. The infection of BmNPV is often lethal and causes about 20% loss of cocoon in the silk industry annually. To explore the effects of different gene inhibition strategies on the replication cycle of baculovirus, we constructed the mutant virus to infect BmN cells directly and further identified ie0, ie1, and gp64 as the essential viral genes of BmNPV.

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Developing active and durable electro-catalysts toward ethanol oxidation reaction (EOR) with high selectivity toward the C-C bond cleavage is an important issue for the commercialization of direct ethanol fuel cell. Unfortunately, current ethanol oxidation electro-catalysts (e.g.

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Seed-mediated growth is the most general way to controllably synthesize bimetal nano-heterostructures. Despite successful instances through trial and error were reported, the way for second metal depositing on the seed, namely whether the symmetry of resulted nano-heterostructure follows the original crystal symmetry of seed metal, remains an unpredictable issue to date. In this work, we propose that the thermodynamic factor, i.

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Catalyst sintering, a main cause of the loss of catalytic activity and/or selectivity at high reaction temperatures, is a major concern and grand challenge in the general area of heterogeneous catalysis. Although all heterogeneous catalysts are inevitably subjected to sintering during their operation, the immediate and drastic consequences can be mitigated by carefully engineering the catalytic particles and their interactions with the supports. In this tutorial review, we highlight recent progress in understanding the physical chemistry and materials science involved in sintering, including the discussion of advanced techniques, such as in situ microscopy and spectroscopy, for investigating the sintering process and its rate.

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Owing to high specific capacity of ∼250 mA h g, lithium-rich layered oxide cathode materials (LiNi Co MnO) have been considered as one of the most promising candidates for the next-generation cathode materials of lithium ion batteries. However, the commercialization of this kind of cathode materials seriously restricted by voltage decay upon cycling though Li-rich materials with high cobalt content have been widely studied and show good capacity. This research successfully suppresses voltage decay upon cycling while maintaining high specific capacity with low Co/Ni ratio in Li-rich cathode materials.

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Single crystalline noble metal nanocages are the most promising candidates for heterogeneous catalysis due to their large specific surface area, well-defined structure and enhanced structural stability. Herein, based on the observation of an unexpected phenomenon that the alloying of Pt and transition metals by co-reduction is more preferential than the formation of pure Pt NCs, we propose a feasible one-pot strategy to synthesize a uniformly epitaxial core-shell Pt-Ni structure with a Ni-rich alloy as the core and a Pt-rich alloy as the shell. The as-prepared Pt-Ni core-shell structures are subsequently etched into monocrystalline Pt-Ni branched nanocages with the wall thickness being 2.

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Due to their distinctive structure, inherently anisotropic properties and broad applications, Janus colloidal particles have attracted tremendous attention and it is significant to synthesize high yield Janus colloidal particles in a cost-effective and reliable way. On the other hand, due to the expanded electromagnetic interference problems, it is highly desired to develop excellent electromagnetic wave absorbing materials with an ultra-wide absorption bandwidth for practical application. Herein, a confined liquid-solid redox reaction strategy has been developed to fabricate a series of Fe(CoNi) ternary alloy particles.

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Predictable synthesis of bimetallic nanocrystals with spatially controlled metal distributions offers a versatile route to the development of highly efficient nanocatalysts. Here we report a one-pot synthesis of super branched Rh-on-Cu nanoscale sea urchins (Rh-Cu NSUrs) with a high density of Cu-Rh interfaces by manipulating the ligand coordination chemistry. Structural analysis and UV-vis spectra reveal that ascorbic acid can serve as a Rh-selective coordination ligand in the nonaqueous synthesis to reverse the reduction potentials of Rh and Cu cations.

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The Kirkendall effect has been recently used to produce hollow nanostructures by taking advantage of the different diffusion rates of species involved in the chemical transformations of nanoscale objects. Here we demonstrate a nanoscale Kirkendall cavitation process that can transform solid palladium nanocrystals into hollow palladium nanocrystals through insertion and extraction of phosphorus. The key to success in producing monometallic hollow nanocrystals is the effective extraction of phosphorus through an oxidation reaction, which promotes the outward diffusion of phosphorus from the compound nanocrystals of palladium phosphide and consequently the inward diffusion of vacancies and their coalescence into larger voids.

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In wet chemical syntheses of noble metal nanocrystals, surfactants play crucial roles in regulating their morphology. To date, more attention has been paid to the effect of the surfactant on the surface energy of crystal facets, while less attention has been paid to its effect on the growth kinetics. In this paper, using the growth of Au-Pd alloy nanocrystals as an example, we demonstrate that different concentration of surfactant hexadecyltrimethyl ammonium chloride (CTAC) may cause the different packing density of CTA bilayers on different sites (face, edge or vertex) of crystallite surface, which would change the crystal growth kinetics and result in preferential crystal growth along the edge or vertex of crystallites.

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Crystal phase regulations may endow materials with enhanced or new functionalities. However, syntheses of noble metal-based allomorphic nanomaterials are extremely difficult, and only a few successful examples have been found. Herein, we report the discovery of hexagonal close-packed Pt-Ni alloy, despite the fact that Pt-Ni alloys are typically crystallized in face-centred cubic structures.

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For new composite materials with functional nanoparticles (NPs) embedded in metal organic frameworks (MOFs), rational design and precise control over their architectures are imperative for achieving enhanced performance and novel functions. Especially in catalysis, the activity and selectivity of such composite materials are strongly determined by the encapsulation state and thickness of the MOF shell, which greatly influences the diffusion and adsorption of substance molecules onto the NP surface. In this study, MOF-74(Ni)-encapsulated Rh-Ni hierarchical heterostructures (Rh-Ni@MOF-74(Ni)) were successfully constructed using magnetic Rh-Ni-alloyed nanoflowers (NFs) as a self-sacrificial template.

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Excavated polyhedral noble-metal materials that were built by the orderly assembly of ultrathin nanosheets have both large surface areas and well-defined facets, and therefore could be promising candidates for diverse important applications. In this work, excavated cubic Pt-Sn alloy nanocrystals (NCs) with {110} facets were constructed from twelve nanosheets by a simple co-reduction method with the assistance of the surface regulator polyvinylpyrrolidone. The specific surface area of the excavated cubic Pt-Sn NCs is comparable to that of commercial Pt black despite their larger particle size.

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Downsizing large Au particles into small particles with controllable size remains challenging. In this study, we redispersed large sintered Au particles on activated carbon (Au/C) to highly dispersed nanoparticles with uniform distribution and controllable size after treatment with iodohydrocarbons. The Au/C catalyst was conducted for a number of deactivation/regeneration cycles with negligible deterioration in catalytic performance for acetylene hydrochlorination.

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