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具有高C1选择性和抗中毒能力的用于乙醇电氧化的高熵PdRhFeCoMo金属烯

High-Entropy PdRhFeCoMo Metallene With High C1 Selectivity and Anti-Poisoning Ability for Ethanol Electrooxidation.

作者信息

Tan Xiaohong, Wang Chenhui, Wang Jiarui, Wang Peng, Xiao Yuhang, Guo Yingying, Chen Jianpo, He Weidong, Li Yan, Cui Hao, Wang Chengxin

机构信息

School of Materials Science and Engineering, Sun Yat-sen University, Guangzhou, 510275, China.

出版信息

Adv Sci (Weinh). 2024 Dec;11(48):e2409109. doi: 10.1002/advs.202409109. Epub 2024 Nov 19.

DOI:10.1002/advs.202409109
PMID:39559911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11672265/
Abstract

The urgent demand for designing highly efficient electrocatalysts for ethanol oxidation reaction (EOR) with elevated C1 selectivity, robust anti-poisoning capability, and high mass activity presents a formidable challenge. Herein, a novel two-dimentional (2D) high-entropy PdRhFeCoMo metallene (PdRhFeCoMo HEM) electrocatalyst is successfully synthesized via a mild one-step solvothermal method. The PdRhFeCoMo HEM, characterized by intentionally designed multi-metallic ensembles and ultra-thin graphene-like structures, delivers an impressive mass activity of 7.47 A mg and specific activity of 25.5 mA cm. Furthermore, it can retain a mass activity of 0.56 A mg after undergoing 20000 s of continuous testing, demonstrating outstanding resistance to poisoning. More significantly, the PdRhFeCoMo HEM demonstrates an elevated capacity for C─C bond cleavage with a superior C1 selectivity of up to 84.12%. In situ spectroscopy analysis, combined with theoretical calculations, reveals that the deliberate design of components and structures effectively regulate the electronic properties of the Pd site, thereby enhancing the adsorption of reactant and reducing the reaction barrier of the C1 pathway. Finally, a flexible solid-state ethanol fuel cell assembled by PdRhFeCoMo HEM presents a maximum power density of 20.1 mW cm and can operate continuously by repeatedly adding ethanol fuel.

摘要

设计高效的乙醇氧化反应(EOR)电催化剂面临着巨大挑战,这类催化剂需要提高C1选择性、具备强大的抗中毒能力和高质量活性。在此,通过温和的一步溶剂热法成功合成了一种新型二维(2D)高熵PdRhFeCoMo金属烯(PdRhFeCoMo HEM)电催化剂。PdRhFeCoMo HEM具有精心设计的多金属组合和超薄类石墨烯结构,展现出令人印象深刻的7.47 A mg的质量活性和25.5 mA cm的比活性。此外,在经过20000 s的连续测试后,它能保持0.56 A mg的质量活性,显示出出色的抗中毒性能。更显著的是,PdRhFeCoMo HEM表现出更高的C─C键裂解能力,C1选择性高达84.12%。原位光谱分析结合理论计算表明,对组分和结构的精心设计有效地调节了Pd位点的电子性质,从而增强了反应物的吸附并降低了C1途径的反应势垒。最后,由PdRhFeCoMo HEM组装的柔性固态乙醇燃料电池呈现出20.1 mW cm的最大功率密度,并且通过反复添加乙醇燃料可以连续运行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/7c46e63ddb7d/ADVS-11-2409109-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/1caad96239b4/ADVS-11-2409109-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/f7b76aff823a/ADVS-11-2409109-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/992d09943225/ADVS-11-2409109-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/494d6b8fea6a/ADVS-11-2409109-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/2ce6cbd6e5ed/ADVS-11-2409109-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/7c46e63ddb7d/ADVS-11-2409109-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/1caad96239b4/ADVS-11-2409109-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/f7b76aff823a/ADVS-11-2409109-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/992d09943225/ADVS-11-2409109-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/494d6b8fea6a/ADVS-11-2409109-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/2ce6cbd6e5ed/ADVS-11-2409109-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c9/11672265/7c46e63ddb7d/ADVS-11-2409109-g001.jpg

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本文引用的文献

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Au/Pt Bimetallic Nanowires with Stepped Pt Sites for Enhanced C-C Cleavage in C2+ Alcohol Electro-oxidation Reactions.具有阶梯状铂位点的金/铂双金属纳米线用于增强C2+醇类电氧化反应中的C-C键裂解
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