纳米线
催化作用
化学
化学工程
乙醇
纳米技术
材料科学
有机化学
工程类
作者
Renqin Yu,Ruiwen Shao,Fanghua Ning,Yaodong Yu,Jing Zhang,Xian‐Yin Ma,Rongying Zhu,Menggang Li,Jianping Lai,Yufeng Zhao,Lingyou Zeng,Jiujun Zhang,Zhonghong Xia
出处
期刊:Small
[Wiley]
日期:2023-10-09
卷期号:20 (7): e2305817-e2305817
被引量:19
标识
DOI:10.1002/smll.202305817
摘要
Abstract Complete ethanol oxidation reaction (EOR) in C1 pathway with 12 transferred electrons is highly desirable yet challenging in direct ethanol fuel cells. Herein, PtRh jagged nanowires synthesized via a simple wet‐chemical approach exhibit exceptional EOR mass activity of 1.63 A mgPt−1 and specific activity of 4.07 mA cm−2, 3.62‐fold and 4.28‐folds increments relative to Pt/C, respectively. High proportions of 69.33% and 73.42% of initial activity are also retained after chronoamperometric test (80 000 s) and 1500 consecutive potential cycles, respectively. More importantly, it is found that PtRh jagged nanowires possess superb anti‐CO poisoning capability. Combining X‐ray absorption spectroscopy, X‐ray photoelectron spectroscopy as well as density functional theory calculations unveil that the remarkable catalytic activity and CO tolerance stem from both the Rh‐induced electronic effect and geometric effect (manifested by shortened Pt─Pt bond length and shrinkage of lattice constants), which facilitates EOR catalysis in C1 pathway and improves reaction kinetics by reducing energy barriers of rate‐determining steps (such as *CO → *COOH). The C1 pathway efficiency of PtRh jagged nanowires is further verified by the high intensity of CO2 relative to CH3COOH/CH3CHO in infrared reflection absorption spectroscopy.
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