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Weiwei Yang

Bio: Weiwei Yang is an academic researcher from Harbin Institute of Technology. The author has contributed to research in topics: Materials science & Photocatalysis. The author has an hindex of 27, co-authored 74 publications receiving 1605 citations. Previous affiliations of Weiwei Yang include Jilin Normal University & Brown University.

Papers published on a yearly basis

Papers
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Journal ArticleDOI
TL;DR: The unique oleylamine reduction process makes it possible to prepare MPt NPs with their physical properties and surface chemistry better rationalized for magnetic or catalytic applications.
Abstract: We report a simple, yet general, approach to monodisperse MPt (M = Fe, Co, Ni, Cu, Zn) nanoparticles (NPs) by coreduction of M(acac)2 and Pt(acac)2 (acac = acetylacetonate) with oleylamine at 300 °C. In the current reaction condition, oleylamine serves as the reducing agent, surfactant, and solvent. As an example, we describe in details the synthesis of 9.5 nm CoPt NPs with their compositions controlled from Co37Pt63 to Co69Pt31. These NPs show composition-dependent structural and magnetic properties. The unique oleylamine reduction process makes it possible to prepare MPt NPs with their physical properties and surface chemistry better rationalized for magnetic or catalytic applications.

147 citations

Journal ArticleDOI
TL;DR: In this paper, a PdCu/Ir core/shell nanocrystals were synthesized to achieve the exclusive strain effect, which can significantly boost the oxygen evolution reaction (OER).
Abstract: Core/shell nanocatalysts are a class of promising materials, which achieve the enhanced catalytic activities through the synergy between ligand effect and strain effect. However, it has been challenging to disentangle the contributions from the two effects, which hinders the rational design of superior core/shell nanocatalysts. Herein, we report precise synthesis of PdCu/Ir core/shell nanocrystals, which can significantly boost oxygen evolution reaction (OER) via the exclusive strain effect. The heteroepitaxial coating of four Ir atomic layers onto PdCu nanoparticle gives a relatively thick Ir shell eliminating the ligand effect, but creates a compressive strain of ca. 3.60%. The strained PdCu/Ir catalysts can deliver a low OER overpotential and a high mass activity. Density functional theory (DFT) calculations reveal that the compressive strain in Ir shell downshifts the d-band center and weakens the binding of the intermediates, causing the enhanced OER activity. The compressive strain also boosts hydrogen evolution reaction (HER) activity and the strained nanocrystals can be served as excellent catalysts for both anode and cathode in overall water-splitting electrocatalysis.

121 citations

Journal ArticleDOI
01 Jun 2020-Carbon
TL;DR: In this paper, a 3D double-core double-shell structure and ingenious introduction of tunable ZnO could improve the microwave absorption performances of the (Fe3O4/ZnO)@C nanocomposites, which can be considered as promising absorbing materials.

119 citations

Journal ArticleDOI
TL;DR: Wang et al. as discussed by the authors reported a method to synthesize phosphorus-doped MoS2/g-C3N4 layer-by-layer composite, which could expose more active sites and generate a strong interaction by forming Mo-N bonds for photocatalytic sterilization.

112 citations

Journal ArticleDOI
TL;DR: In this article, the Mott-Schottky effect between PdAg nanowires and graphitic carbon nitride (g-C3N4) was exploited for the photocatalytic dehydrogenation of formic acid.
Abstract: Herein, we report the production of a superior Mott–Schottky heterojunction that is based on PdAg nanowires (NWs) that grow in situ on graphitic carbon nitride (g-C3N4). Due to the strong Mott–Schottky effect between PdAg NWs and g-C3N4, the heterojunction enhances the photocatalytic dehydrogenation of formic acid (FA) (TOF = 420 h−1) without additives and under visible light (λ > 400 nm) at 25 °C, which is the best value among all heterogeneous catalysts reported for the photocatalytic dehydrogenation of FA. The H2 production rate is almost constant under the current reaction conditions. Detailed studies reveal that a favorable charge transfer from g-C3N4 and Ag to Pd makes Pd electron-rich, which enhances the catalytic activity and stability of the heterojunction for the photocatalytic dehydrogenation of FA under visible light. Our studies open up a new route to the design of a metal–semiconductor heterojunction for visible light-driven photocatalytic dehydrogenation of FA.

107 citations


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TL;DR: The most recent advances in the development of Pt-based and Pt-free materials in the field of fuel cell ORR catalysis are reviewed to provide insights into the remaining challenges and directions for future perspectives and research.
Abstract: Developing highly efficient catalysts for the oxygen reduction reaction (ORR) is key to the fabrication of commercially viable fuel cell devices and metal–air batteries for future energy applications. Herein, we review the most recent advances in the development of Pt-based and Pt-free materials in the field of fuel cell ORR catalysis. This review covers catalyst material selection, design, synthesis, and characterization, as well as the theoretical understanding of the catalysis process and mechanisms. The integration of these catalysts into fuel cell operations and the resulting performance/durability are also discussed. Finally, we provide insights into the remaining challenges and directions for future perspectives and research.

1,752 citations

Journal ArticleDOI
TL;DR: Recent progress in the synthesis of intermetallic nanocrystals with controllable sizes and well-defined shapes is highlighted and perspectives on future developments in the context of synthetic control, structure-property relationships, and applications are discussed.
Abstract: At the forefront of nanochemistry, there exists a research endeavor centered around intermetallic nanocrystals, which are unique in terms of long-range atomic ordering, well-defined stoichiometry, and controlled crystal structure. In contrast to alloy nanocrystals with no elemental ordering, it is challenging to synthesize intermetallic nanocrystals with a tight control over their size and shape. Here, recent progress in the synthesis of intermetallic nanocrystals with controllable sizes and well-defined shapes is highlighted. A simple analysis and some insights key to the selection of experimental conditions for generating intermetallic nanocrystals are presented, followed by examples to highlight the viable use of intermetallic nanocrystals as electrocatalysts or catalysts for various reactions, with a focus on the enhanced performance relative to their alloy counterparts that lack elemental ordering. Within the conclusion, perspectives on future developments in the context of synthetic control, structure-property relationships, and applications are discussed.

324 citations

Journal ArticleDOI
TL;DR: In this article, a review summarizes the recent process of heterogeneous supported single atoms, nanoclusters, and nanoparticles catalysts in electrocatalytic reactions, respectively, and figures out the construct strategies and design concepts based on their strengths and weaknesses.
Abstract: Metal-based electrocatalysts with different sizes (single atoms, nanoclusters, and nanoparticles) show different catalytic behaviors for various electrocatalytic reactions. Regulating the coordination environment of active sites with precision to rationally design an efficient electrocatalyst is of great significance for boosting electrocatalytic reactions. This review summarizes the recent process of heterogeneous supported single atoms, nanoclusters, and nanoparticles catalysts in electrocatalytic reactions, respectively, and figures out the construct strategies and design concepts based on their strengths and weaknesses. Specifically, four key factors for enhancing electrocatalytic performance, including electronic structure, coordination environment, support property, and interfacial interactions are proposed to provide an overall comprehension to readers in this field. Finally, some insights into the current challenges and future opportunities of the heterogeneous supported electrocatalysts are provided.

311 citations

Journal ArticleDOI
TL;DR: In this class of synthesis precursors are heated within a reaction medium to induce a chemical reaction that yields monomer for nucleation and growth as discussed by the authors, which is a reliable means to achieve high quality nanomaterials on large scales with little or no batch-to-batch variation.
Abstract: The successful transition of any nanocrystal-based product from the research phase to the commercial arena hinges on the ability to produce the required nanomaterial on large scales. The synthesis of colloidal nanocrystals using a heat-up (non-injection) method is a reliable means to achieve high quality nanomaterials on large scales with little or no batch-to-batch variation. In this class of synthesis precursors are heated within a reaction medium to induce a chemical reaction that yields monomer for nucleation and growth. Use of the heat-up technique circumvents the pitfalls of mixing time and poor heat management inherent to classical “hot-injection” methods. In heat-up syntheses monomer is produced in a more continuous fashion during the heating stage, making it more difficult to separate the nucleation and growth stages of the reaction, a factor that is conventionally considered detrimental toward achieving homogeneous colloidal dispersions. However, through the judicious selection of precursors, st...

303 citations

Journal ArticleDOI
TL;DR: A comprehensive review of recent advances in metal oxide-based electrocatalysts for hydrogen evolution reaction (HER) can be found in this paper, with special emphasis on designed strategies for promoting performance and property-activity correlation.
Abstract: Hydrogen production from electrochemical water splitting represents a highly promising technology for sustainable energy storage, but its widespread implementation heavily relies on the development of high-performance and cost-effective hydrogen evolution reaction (HER) electrocatalysts. Metal oxides, an important family of functional materials with diverse compositions and structures, were traditionally believed inactive towards HER. Encouragingly, the continuous breakthroughs and significant progress in recent years (mainly from 2015 onwards) make engineered metal oxides emerge as promising candidates for HER electrocatalysis. In this article, we present a comprehensive review of recent advances in metal oxide-based electrocatalysts for HER. We start with a brief description of some key fundamental concepts of HER, such as mechanisms, computational activity descriptors, and experimental parameters used to evaluate catalytic performance. This is followed by a overview of various types of metal oxide-based HER electrocatalysts reported so far, including single transition metal oxides, spinel oxides, perovskite oxides, metal (oxy)hydroxides, specially-structured metal oxides and oxide-containing hybrids, with special emphasis on designed strategies for promoting performance and property–activity correlation. Finally, some concluding remarks and perspectives about future opportunities of this exciting field are provided.

294 citations