Self-supported nickel phosphosulphide nanosheets for highly efficient and stable overall water splitting

被引:76
作者
Luo, Jie [1 ]
Wang, Haiyan [1 ]
Su, Geng [1 ]
Tang, Yulian [1 ]
Liu, Huangqing [2 ]
Tian, Fenyang [1 ]
Li, Deliang [1 ]
机构
[1] Cent South Univ Forestry & Technol, Sch Mat Sci & Engn, Changsha 410004, Hunan, Peoples R China
[2] Hunan Univ, Sch Phys & Elect, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGEN EVOLUTION REACTION; OXYGEN EVOLUTION; HIGH-PERFORMANCE; GRAPHENE OXIDE; BIFUNCTIONAL ELECTROCATALYST; MOLYBDENUM CARBIDE; NANOWIRE ARRAYS; CATALYST; PHOSPHIDE; LAYER;
D O I
10.1039/c7ta02651j
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
Self-supported nickel phosphosulfide (NiP0.62S0.38) nanosheets are fabricated by convenient one-step programming annealing in phosphorus and sulfur gas in series. The as-prepared NiP0.62S0.38 only needs overpotentials of 52 and 240 mV to achieve a current density of 10 mA cm(-2) (j(10)) in alkaline media for HER and OER, respectively. The DFT calculation results reveal that the electronegative phosphosulfide species shift Delta G(H)* to the thermo-neutral position and achieve a balance of hydrogen adsorption and detachment on nickel sites. The excellent OER activity of NiP0.62S0.38 is attributed to the formation of NiP0.62S0.38/NiOOH heterojunctions during water oxidation. Two identical NiP0.62S0.38 electrodes as anode and cathode are utilized to construct an alkaline electrolyzer, which delivers a j(10) at a small potential of 1.52 V, and can stably sustain the j(10) for 200 h, rivalling the integrated state-of-the-art Pt/C and IrO2.
引用
收藏
页码:14865 / 14872
页数:8
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