Liu Huan, Xu Cheng-Yan, Du Yue, Ma Fei-Xiang, Li Yue, Yu Jing, Zhen Liang
MIIT Key Laboratory of Advanced Structural-Functional Integration Materials & Green Manufacturing Technology, School of Materials Science and Engineering, Harbin Institute of Technology, Harbin, 150001, China.
MOE Key Laboratory of Micro-Systems and Micro-Structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Sci Rep. 2019 Feb 13;9(1):1951. doi: 10.1038/s41598-018-35831-4.
Development of hydrogen as clean and efficient energy carrier for future is imperative. Water electrolysis, is considered as one of the most promising ways to realize large-scaled hydrogen production. However, a big obstacle of it is to reduce the electric energy consumption for water oxidation in the anode. Engineering of hierarchical architectures on the electrocatalysts could provide abundant active sites and thus boost the sluggish reaction kinetics of water oxidation. Herein, a sequential synthesis method is developed for in-situ growth of ultrathin CoS nanosheets vertically aligned on N and S co-doped reduced graphene oxide (CoS/N,S-rGO) as novel and efficient electrocatalysts for water splitting. This architecture with vertically aligned ultrathin CoS nanosheets on N,S/rGO is adopted to facilitate the electron transport and exposure of active sites. Benefiting from the synergetic catalysis between CoS nanosheets and N,S/rGO, CoS/N,S-rGO presents remarkable electrocatalytic activity towards oxygen evolution with a low overpotential (266 mV to achieve current density of 10 mA cm), small Tafel slope of 75.5 mV dec, and good durability in alkaline medium. This remarkable OER electrocatalytic activity is outperforms most of the known noble-metal-free electrocatalysts.
开发氢气作为未来清洁高效的能量载体势在必行。水电解被认为是实现大规模制氢最有前景的方法之一。然而,其一个重大障碍是降低阳极水氧化的电能消耗。在电催化剂上构建分级结构可以提供丰富的活性位点,从而加速缓慢的水氧化反应动力学。在此,开发了一种顺序合成方法,用于原位生长垂直排列在氮和硫共掺杂还原氧化石墨烯(CoS/N,S-rGO)上的超薄CoS纳米片,作为用于水分解的新型高效电催化剂。这种在N,S/rGO上具有垂直排列超薄CoS纳米片的结构有助于电子传输和活性位点的暴露。受益于CoS纳米片与N,S/rGO之间的协同催化作用,CoS/N,S-rGO对析氧表现出显著的电催化活性,过电位低(达到10 mA cm电流密度时为266 mV),塔菲尔斜率小,为75.5 mV dec,并且在碱性介质中具有良好的耐久性。这种显著的析氧反应电催化活性优于大多数已知的无贵金属电催化剂。