Department of Chemistry, Missouri University of Science and Technology, Rolla, MO, 65409, USA.
Materials Research Center, Missouri University of Science and Technology, Rolla, MO, 65409, USA.
Sci Rep. 2017 May 25;7(1):2401. doi: 10.1038/s41598-017-02285-z.
Herein we have shown that electrodeposited NiSe can be used as a bifunctional electrocatalyst under alkaline conditions to split water at very low potential by catalyzing both oxygen evolution and hydrogen evolution reactions at anode and cathode, respectively, achieving a very high electrolysis energy efficiency exceeding 80% at considerably high current densities (100 mA cm). The OER catalytic activity as well as electrolysis energy efficiency surpasses any previously reported OER electrocatalyst in alkaline medium and energy efficiency of an electrolyzer using state-of-the-art Pt and RuO as the HER and OER catalyst, respectively. Through detailed electrochemical and structural characterization, we have shown that the enhanced catalytic activity is attributed to directional growth of the electrodeposited film that exposes a Ni-rich lattice plane as the terminating plane, as well as increased covalency of the selenide lattice which decreases the Ni(II) to Ni(III) oxidation potential. Thereby, the high efficiency along with extended stability makes NiSe as the most efficient water electrolyzer known to-date.
在此,我们展示了电沉积的 NiSe 可以在碱性条件下用作双功能电催化剂,通过分别在阳极和阴极催化氧气析出反应和氢气析出反应来实现水的低电位分解,在相当高的电流密度(100 mA cm)下实现了非常高的电解能效,超过 80%。OER 催化活性和电解能效超过了碱性介质中以前报道的任何 OER 电催化剂,以及使用最先进的 Pt 和 RuO 作为 HER 和 OER 催化剂的电解槽的能效。通过详细的电化学和结构表征,我们表明增强的催化活性归因于电沉积膜的定向生长,其暴露富 Ni 的晶格平面作为终止平面,以及硒化物晶格的共价键增加,从而降低了 Ni(II)到 Ni(III)的氧化电位。因此,高效率和延长的稳定性使得 NiSe 成为迄今为止已知的最有效的水电解槽。