异质结
电解质
无定形固体
电催化剂
材料科学
催化作用
兴奋剂
化学工程
无机化学
电极
纳米技术
电化学
化学
物理化学
结晶学
光电子学
生物化学
工程类
作者
Meng Zhang,Weizhe Chen,Zhiliang Liu,Jinlu He,Yanqin Wang
标识
DOI:10.1016/j.electacta.2022.141269
摘要
• P-doped P-MoS 2 /Co x S y @C/CFP heterojunction electrocatalyst is firstly constructed. • The catalyst shows excellent HER performances both in alkaline and acidic mediums. • The optimized electronic structure of the catalyst is the intrinsic reason for the excellent HER performances. • DFT calculations confirms the decrease the d-band center and the rate-degerming step. It is still challenging for the development of highly efficient non-noble metal electrocatalysts toward hydrogen evolution reaction (HER). Herein, an unreported material constructing strategy of combining crystalline-amorphous hetero-interface and heteroatomic doping towards electrocatalytic HER is firstly presented. The authors fabricate a self-supported P-MoS 2 /Co x S y @C/CFP electrode consisting of P-doped crystalline-amorphous MoS 2 /Co x S y heterojunction in-situ grown on carbon fiber paper (CFP). Benefitting from the strong electronic interaction at the interface of crystalline MoS 2 and amorphous Co x S y , the electronic structure of MoS 2 /Co x S y @C/CFP is optimized. Moreover, the P doping can further optimize the electronic structure and enhance water adsorption of the catalyst and lower the kinetic energy barrier of HER. The heterojunction P-MoS 2 /Co x S y @C/CFP can not only exhibit excellent HER activity in alkaline electrolyte but also in acidic electrolyte, with the relatively lower overpotentials of 59 mV and 135 mV at the current density of 10 mA•cm −2 in 1 M KOH and 0.5 M H 2 SO 4 ; 140 mV and 205 mV at the current density of 100 mA•cm −2 in 1 M KOH and 0.5 M H 2 SO 4 , respectively, which the HER performance is among the best for non-precious metal-based electrocatalysts usable in both acidic and alkaline mediums. Theoretical calculations also confirm that the construction of crystalline-amorphous heterointerface between MoS 2 and Co x S y and P doping can effectively accelerate the electron transport and promote the HER reaction kinetics, thus enhancing the HER performance. This construction strategy for HER electrocatalyst provides a new avenue on electrocatalytic research. A novel P-doped coral-like MoS 2 /Co x S y /C heterojuntion with abundant hetero-interfaces is successfully constructed, which exhibits excellent hydrogen evolution reaction (HER) performance both in alkaline and acidic mediums, with the relatively lower overpotentials of 59 mV and 135 mV at the current density of 10 mA•cm −2 in 1 M KOH and 0.5 M H 2 SO 4 ; 140 mV and 205 mV at the current density of 100 mA•cm −2 in 1 M KOH and 0.5 M H 2 SO 4 , respectively. The HER performance is among the best for non-precious metal-based electrocatalysts usable in both acidic and alkaline mediums.
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