电催化剂
材料科学
吸附
甲醇
电子转移
合金
氧化还原
化学工程
催化作用
无机化学
电化学
物理化学
冶金
化学
电极
有机化学
工程类
作者
Hu Liu,Rongrong Jia,Chuanjian Qin,Qin Yang,Zuobin Tang,Menggang Li,Zhenhui Ma
标识
DOI:10.1002/adfm.202210626
摘要
Abstract Introducing oxophilic metals into Pt‐based alloy catalysts can effectively alleviate the poisoning by CO intermediates (CO*) during methanol oxidation reactions (MOR). However, excessive oxophilic metals on the surface of catalysts tend to form thermodynamically stable carbonyl compound‐like structures, occupying electrocatalytically active sites, which is not conducive to the enhancement of catalytic activity. Herein, a kind of surface segregated FePtRh nanoflowers for effectively eliminating the CO* poisoning during MOR electrocatalysis is presented. The FePtRh nanoflowers are constituted by the Rh‐rich core and Fe‐rich shell. The optimized Fe 21 Pt 66 Rh 13 /C shows a high mass activity of 3.90 A mg Pt −1 and a specific activity of 4.85 mA cm −2 . It is confirmed that the electron transfer from Pt to Rh or Fe atoms is beneficial for the higher anti‐CO poisoning ability, which mainly originate from the alloying of Rh atoms and surface‐segregated structures. Density functional theory calculations reveal the decreased electrons adsorbed by CO* on both Pt–Pt bridge sites and top sites weakens the strong adsorption energy between Pt atoms and CO* intermediates. The optimal nanoflowers also show excellent performance toward ethanol oxidation reaction (EOR) with a high mass activity of 2.76 A mg Pt −1 and the enhanced anti‐CO poisoning ability, as well as the improved stability.
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