Synergistically coupling ultrasmall PtCu nanoalloys with highly porous CoP nanosheets as an enhanced electrocatalyst for electrochemical hydrogen evolution

被引:17
作者
Gao, Jiaojiao [1 ]
Tang, Xiaowei [2 ]
Du, Peng [1 ]
Li, Huanglong [3 ]
Yuan, Qunhui [1 ]
Xie, Guoqiang [1 ]
Qiu, Hua-Jun [1 ]
机构
[1] Harbin Inst Technol, Sch Mat Sci & Engn, Shenzhen 518055, Peoples R China
[2] Qilu Normal Univ, Math Sch, Jinan 250200, Peoples R China
[3] Tsinghua Univ, Dept Precis Instrument, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
SOLVOTHERMAL SYNTHESIS; OXYGEN REDUCTION; NICKEL PHOSPHIDE; EFFICIENT; PLATINUM; NANOPARTICLES; NANOFRAMES; CATALYST; SURFACE; PERFORMANCE;
D O I
10.1039/c9se01182j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Platinum (Pt) is recognized as one of the most effective catalysts for the hydrogen evolution reaction (HER), but its large-scale application still suffers from high cost and unsatisfactory performance in alkaline solution. Herein, by properly integrating an ultralow amount of Pt with earth-abundant elements, we report a facile dealloying-oxidation-phosphidation method for synthesizing a PtCu nanocluster decorated CoP nanosheet electrocatalyst (PtCu/CoP) with an ultralow Pt loading (2.8 mu g cm(-2)). With only 1/40 Pt loading of commercial 20% Pt/C, the as-prepared PtCu/CoP catalyst outperforms the Pt/C catalyst, requiring an overpotential as low as 20 mV to reach a current density of 10 mA cm(-2), and showing a smaller Tafel slope of 28 mV dec(-1) in 0.5 M H2SO4. In 1.0 M KOH, the PtCu/CoP catalyst also shows a superior performance to that of Pt/C, with an overpotential of 40 mV (10 mA cm(-2)) and a Tafel slope of 49 mV dec(-1). Moreover, the PtCu/CoP catalyst can be continuously operated for 100 h in both acidic and alkaline media, with only insignificant degradation. This work provides an efficient strategy for designing a high performance HER electrocatalyst with ultralow Pt loadings.
引用
收藏
页码:2551 / 2558
页数:8
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