Department of Chemistry, William Mong Institute of Nano Science and Technology, The Hong Kong University of Science and Technology , Clear Water Bay, Kowloon, Hong Kong.
College of Science, China University of Petroleum , Qingdao 266555, PR China.
J Am Chem Soc. 2015 Sep 23;137(37):11900-3. doi: 10.1021/jacs.5b07728. Epub 2015 Sep 14.
We report on the synthesis of iron-nickel sulfide (INS) ultrathin nanosheets by topotactic conversion from a hydroxide precursor. The INS nanosheets exhibit excellent activity and stability in strong acidic solutions as a hydrogen evolution reaction (HER) catalyst, lending an attractive alternative to the Pt catalyst. The metallic α-INS nanosheets show an even lower overpotential of 105 mV at 10 mA/cm(2) and a smaller Tafel slope of 40 mV/dec. With the help of DFT calculations, the high specific surface area, facile ion transport and charge transfer, abundant electrochemical active sites, suitable H(+) adsorption, and H2 formation kinetics and energetics are proposed to contribute to the high activity of the INS ultrathin nanosheets toward HER.
我们报告了通过从氢氧化物前体的拓扑转化合成铁镍硫化物(INS)超薄纳米片。作为析氢反应(HER)催化剂,INS 纳米片在强酸溶液中表现出优异的活性和稳定性,为 Pt 催化剂提供了一种有吸引力的替代品。金属α-INS 纳米片在 10 mA/cm(2)时的过电位更低,仅为 105 mV,Tafel 斜率更小,为 40 mV/dec。借助 DFT 计算,提出了高比表面积、易于离子传输和电荷转移、丰富的电化学活性位点、合适的 H(+)吸附以及 H2 形成动力学和能学,这些都有助于 INS 超薄纳米片在 HER 中具有高活性。