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二硫化镍的电子调制用于高效水电解

Electronic Modulation of Nickel Disulfide toward Efficient Water Electrolysis.

作者信息

Dinh Khang Ngoc, Sun Yongxiu, Pei Zengxia, Yuan Ziwen, Suwardi Ady, Huang Qianwei, Liao Xiaozhou, Wang Zhiguo, Chen Yuan, Yan Qingyu

机构信息

Energy Research Institute@NTU (ERI@N), Interdisciplinary Graduate School, Nanyang Technological University, Singapore, 637553, Singapore.

School of Materials Science and Engineering Nanyang Technological University, Singapore, 639798, Singapore.

出版信息

Small. 2020 Apr;16(17):e1905885. doi: 10.1002/smll.201905885. Epub 2020 Apr 3.

DOI:10.1002/smll.201905885
PMID:32243082
Abstract

Developing highly efficient earth-abundant nickel-based compounds is an important step to realize hydrogen generation from water. Herein, the electronic modulation of the semiconducting NiS by cation doping for advanced water electrolysis is reported. Both theoretical calculations and temperature-dependent resistivity measurements indicate the semiconductor-to-conductor transition of NiS after Cu incorporation. Further calculations also suggest the advantages of Cu dopant to cathodic water electrolysis by bringing Gibbs free energy of H adsorption at both Ni sites and S sites much closer to zero. It is noteworthy that water dissociation on Cu-doped NiS (Cu-NiS ) surface is even more favorable than those on NiS and Pt(111). Thus, the prepared Cu-NiS shows noticeably improved performance toward alkaline hydrogen and oxygen evolution reactions (HER and OER). Specifically, it requires merely 232 mV OER overpotential to drive 10 mA cm ; in parallel with Tafel slopes of 46 mV dec . Regarding HER, an onset overpotential of only 68 mV is achieved. When integrated as both electrodes for water electrolysis, Cu-NiS needs only 1.64 V to drive 10 mA cm , surpassing the state-of-the-art Ir/C-Pt/C couple (1.71 V). This work opens up an avenue to engineer low-cost and earth-abundant catalysts performing on par with the noble-metal-based one for water splitting.

摘要

开发高效的、地球上储量丰富的镍基化合物是实现水制氢的重要一步。在此,报道了通过阳离子掺杂对半导体硫化镍(NiS)进行电子调制以实现先进的水电解。理论计算和与温度相关的电阻率测量均表明,掺入铜后NiS发生了从半导体到导体的转变。进一步的计算还表明,铜掺杂剂通过使镍位点和硫位点上氢吸附的吉布斯自由能更接近零,对阴极水电解具有优势。值得注意的是,铜掺杂的NiS(Cu-NiS)表面的水离解甚至比NiS和Pt(111)表面更有利。因此,制备的Cu-NiS在碱性析氢反应和析氧反应(HER和OER)中表现出显著改善的性能。具体而言,驱动10 mA cm只需232 mV的OER过电位;同时塔菲尔斜率为46 mV dec。关于HER,仅实现了68 mV的起始过电位。当作为水电解的两个电极集成时,Cu-NiS驱动10 mA cm仅需1.64 V,超过了目前最先进的Ir/C-Pt/C电极对(1.71 V)。这项工作开辟了一条途径,可设计出与基于贵金属的催化剂性能相当的低成本、地球上储量丰富的水分解催化剂。

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