乙二醇
材料科学
纳米线
催化作用
法拉第效率
选择性
乙烯
化学工程
合金
纳米技术
电极
电催化剂
乙醇酸
键裂
分解
单层
膜
电化学
多相催化
串联
无机化学
纳米颗粒
能量转换
组合化学
纳米复合材料
作者
Yaming Liu,Zhenle Hu,Xinrui Zhu,Xin Li,Tong Zuo,Yutian Zhao,Guoqiang Liu,Yanting Cheng,Chao Zhi,Jiaguang Meng,Xiang Li,Jingnan Wang,Mingshang Jin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-03-09
卷期号:20 (11): 9428-9439
被引量:1
标识
DOI:10.1021/acsnano.5c21597
摘要
While traditional Pt-based catalysts suffer from inadequate selectivity and stability in electrocatalytic ethylene glycol oxidation reactions, we present a general and scalable synthesis strategy, fabricating a broad multimetallic Pt-based alloy nanowires (NWs) library from binary to quinary. Among these, the PtAgCuRhRu NWs exhibit exceptional performance, with a mass activity ∼8 times higher than that of Pt/C and a Faradaic efficiency for glycolic acid (GA) reaching 93.49%. In the membrane electrode assembly electrolyzer, the catalyst maintained its activity over 140 h with 99% GA selectivity. In situ experimental and theoretical calculations reveal oxygenophilic Rh and Ru promote *OH adsorption, facilitating the conversion of *COCH2OH to GA and the oxidative removal of COads, enhancing activity and stability. Additionally, the high energy barrier for C–C bond cleavage suppresses undesired decomposition due to the introduction of Ag and Cu, leading to superior GA selectivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI