Electronic and Geometric Effects Endow PtRh Jagged Nanowires with Superior Ethanol Oxidation Catalysis
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
Abstract
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 CO 2 relative to CH 3 COOH/CH 3 CHO in infrared reflection absorption spectroscopy.