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用于氧还原反应的纳米金属间化合物 AuCu₃ 催化剂:性能与机理。

Nano-intermetallic AuCu₃ catalyst for oxygen reduction reaction: performance and mechanism.

机构信息

College of Engineering, Peking University, Beijing, 100871, China.

出版信息

Small. 2014 Jul 9;10(13):2662-9. doi: 10.1002/smll.201400068. Epub 2014 Mar 27.

Abstract

This paper introduces a new approach for catalyst design using the non-precious metal Cu as one of the catalytic active centers. This differs from previous studies that considered precious metals to be responsible for the catalytic reaction in precious alloys. Intermetallic AuCu3/C nanoparticles with a diameter of 3 nm were developed for the first time, with uniform dispersion and a narrow size distribution. The ca. 3 nm as-synthesised AuCu3/C showed superior catalytic performance for oxygen reduction reactions (ORR) in alkaline solutions, with comparable half-wave potential and 1.5 times mass current density of commercial Pt/C at 0.80 V (vs. reversible hydrogen electrode (RHE)). The advanced catalytic activities are mainly attributed to the synergetic effects of electro-active atomic Au and Cu on the particle surface, in which Cu helps to activate the O2 molecule and Au benefits OH(-) desorption. The excellent durability and methanol tolerance exhibited in alkaline solutions provide another advantage for AuCu3/C to be considered as a potential alternative cathode catalyst in alkaline fuel cells.

摘要

本文提出了一种使用非贵金属 Cu 作为催化活性中心之一的新型催化剂设计方法。这与之前的研究不同,之前的研究认为贵金属是贵金属合金中催化反应的原因。首次开发出直径为 3nm 的均一分散、窄粒径分布的纳米级金铜间充化合物 AuCu3/C。所制备的约 3nm AuCu3/C 在碱性溶液中对氧还原反应(ORR)表现出优异的催化性能,在 0.80V(相对于可逆氢电极(RHE))时具有可比的半波电位和 1.5 倍的质量电流密度的商业 Pt/C。先进的催化活性主要归因于颗粒表面上电活性原子 Au 和 Cu 的协同作用,其中 Cu 有助于激活 O2 分子,Au 有利于 OH(-)脱附。在碱性溶液中表现出的优异耐久性和甲醇耐受性为 AuCu3/C 作为碱性燃料电池中潜在的替代阴极催化剂提供了另一个优势。

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