材料科学
合金
阳极
纳米线
电催化剂
吸附
氧化还原
直接乙醇燃料电池
冶金
化学工程
纳米技术
电极
电化学
物理化学
化学
工程类
作者
Qi Xue,Zi‐Xin Ge,Zi-Han Yuan,Jiangtao Huang,Bang-Quan He,Yu Chen
标识
DOI:10.1016/j.mtphys.2023.100980
摘要
The highly active, selective and stable anode electrocatalysts for the ethanol oxidation reaction (EOR) are extremely desirable for the application of direct ethanol fuel cells (DEFCs). Herein, one-dimensional Au [email protected]0·20Rh0.08 alloy shell nanowires ([email protected]0·20Rh0.08 CS-NWs) with long aspect ratio and cross-linked network architecture are synthesized. For the EOR, [email protected]0·20Rh0.08 CS-NWs display higher peak current density, better resistance to CO poisoning and more lasting stability compared with [email protected]0.28 CS-NWs and commercial Pt black electrocatalyst, which can be attributed to the trimetallic synergistic effect between the Au, Pt and Rh atoms. Specifically, the Rh can promote the C–C bonds and adsorb OHads while Au can change the electronic structure of Pt, endowing Pt with a high anti-poisoning ability to COads and promoting the complete oxidation of various C1 intermediate to CO2. This work provides an effective strategy for the rational construction of high-performance Pt-based EOR electrocatalysts by optimizing composition, morphology and architecture.
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