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金属-载体相互作用对用于碱性氢氧化反应的碳载镍纳米颗粒催化剂的结构和活性的影响

The Impact of Metal-Support Interaction on the Structure and Activity of Carbon-Supported Ni Nanoparticle Catalysts for Alkaline Hydrogen Oxidation Reaction.

作者信息

Akamine Yoshiki, Nishino Fumiya, Yamashita Takashi, Tsushida Masayuki, Awaya Keisuke, Machida Masato, Zahan Syeda Mushrifa, Dekel Dario R, Ohyama Junya

机构信息

Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan.

Technical Division, Faculty of Engineering, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan.

出版信息

ACS Appl Mater Interfaces. 2024 Dec 18;16(50):69316-69323. doi: 10.1021/acsami.4c15120. Epub 2024 Dec 8.

DOI:10.1021/acsami.4c15120
PMID:39645609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11660032/
Abstract

The effect of the carbon support─Ketjenblack (C) and Vulcan (C)─on the Ni/C catalyst properties toward alkaline hydrogen oxidation reaction (HOR) was investigated. Both Ni/C and Ni/C presented improved catalytic activity with an increase in Ni particle size; however, Ni/C showed activity significantly higher than that of Ni/C at the same particle size. The reason for the difference in the HOR activity due to the types of carbon support was revealed to be the difference in the 3D structure of Ni nanoparticles determined by metal-support interaction, which is changed by the surface structures of carbon supports. These findings bring light to the critical importance of the metal-support interaction in the development of the HOR catalysts.

摘要

研究了碳载体(科琴黑(C)和瓦肯(C))对镍/碳催化剂碱性氢氧化反应(HOR)性能的影响。随着镍粒径的增加,Ni/C和Ni/C的催化活性均有所提高;然而,在相同粒径下,Ni/C的活性明显高于Ni/C。结果表明,由于碳载体类型不同导致HOR活性存在差异的原因是,金属-载体相互作用决定的镍纳米颗粒三维结构存在差异,而这种差异会因碳载体的表面结构而改变。这些发现揭示了金属-载体相互作用在HOR催化剂开发中的至关重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/6e073b674378/am4c15120_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/89d1f4c463c0/am4c15120_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/977bbf1999a7/am4c15120_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/ed53b9bdb2cc/am4c15120_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/ab87867e28eb/am4c15120_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/6e073b674378/am4c15120_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/89d1f4c463c0/am4c15120_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/977bbf1999a7/am4c15120_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/ed53b9bdb2cc/am4c15120_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/ab87867e28eb/am4c15120_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c07f/11660032/6e073b674378/am4c15120_0005.jpg

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本文引用的文献

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Nat Commun. 2024 Jan 2;15(1):76. doi: 10.1038/s41467-023-44320-w.
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Atomic-Scale 3D Structure of a Supported Pd Nanoparticle Revealed by Electron Tomography with Convolution Neural Network-Based Image Inpainting.通过基于卷积神经网络图像修复的电子断层扫描揭示的负载型钯纳米颗粒的原子尺度3D结构
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Three-dimensional nanoimaging of fuel cell catalyst layers.
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Nickel-Based Anode Catalysts for Efficient and Affordable Anion-Exchange Membrane Fuel Cells.用于高效且经济实惠的阴离子交换膜燃料电池的镍基阳极催化剂。
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Controlling the Valence-Electron Arrangement of Nickel Active Centers for Efficient Hydrogen Oxidation Electrocatalysis.控制镍活性中心的价电子排列以实现高效氢氧化电催化
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