过电位
电催化剂
纳米线
催化作用
计时安培法
化学工程
材料科学
甲醇燃料
甲醇
电化学
纳米技术
化学
电极
循环伏安法
物理化学
有机化学
工程类
作者
Xiaoyang Fu,Zipeng Zhao,Chengzhang Wan,Yiliu Wang,Fan Zheng,Frank Song,Bocheng Cao,Mufan Li,Xue Wang,Yu Huang,Xiangfeng Duan
出处
期刊:Nano Research
[Springer Nature]
日期:2018-10-01
卷期号:12 (1): 211-215
被引量:73
标识
DOI:10.1007/s12274-018-2204-8
摘要
Direct methanol fuel cells (DMFCs) have received tremendous research interests because of the facile storage of liquid methanol vs. hydrogen. However, the DMFC today is severely plagued by the poor kinetics and rather high overpotential in methanol oxidation reaction (MOR). Here we report the investigation of the ultrathin Rh wavy nanowires as a highly effective MOR electrocatalyst. We show that ultrathin wavy Rh nanowires can be robustly synthesized with 2–3 nm diameters. Electrochemical studies show a current peak at the potential of 0.61 V vs. reversible hydrogen electrode (RHE), considerably lower than that of Pt based catalysts (~ 0.8–0.9 V vs. RHE). Importantly, with ultrathin diameters and favorable charge transport, the Rh nanowires catalysts exhibit an ultrahigh electrochemically active surface area determined from CO-stripping (ECSACO) of 144.2 m2/g, far exceeding that of the commercial Rh black samples (20 m2/g). Together, the Rh nanowire catalysts deliver a mass activity of 722 mA/mg at 0.61 V, considerably higher than many previously reported electrocatalysts at the same potential. The chronoamperometry studies also demonstrate good stability and CO-tolerance compared with the Rh black control sample, making ultrathin Rh wavy nanowires an attractive electrocatalyst for MOR.
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