Wu Libo, Zhang Fanghao, Song Shaowei, Ning Minghui, Zhu Qing, Zhou Jianqing, Gao Guanhui, Chen Zhaoyang, Zhou Qiancheng, Xing Xinxin, Tong Tian, Yao Yan, Bao Jiming, Yu Luo, Chen Shuo, Ren Zhifeng
Department of Physics and Texas Center for Superconductivity at the University of Houston (TcSUH), University of Houston, Houston, TX, 77204, USA.
Materials Science and Engineering Program, University of Houston, Houston, TX, 77204, USA.
Adv Mater. 2022 May;34(21):e2201774. doi: 10.1002/adma.202201774. Epub 2022 Apr 24.
Achieving efficient and durable nonprecious hydrogen evolution reaction (HER) catalysts for scaling up alkaline water/seawater electrolysis is desirable but remains a significant challenge. Here, a heterogeneous Ni-MoN catalyst consisting of Ni and MoN nanoparticles on amorphous MoN nanorods that can sustain large-current-density HER with outstanding performance is demonstrated. The hierarchical nanorod-nanoparticle structure, along with a large surface area and multidimensional boundaries/defects endows the catalyst with abundant active sites. The hydrophilic surface helps to achieve accelerated gas-release capabilities and is effective in preventing catalyst degradation during water electrolysis. Theoretical calculations further prove that the combination of Ni and MoN effectively modulates the electron redistribution at their interface and promotes the sluggish water-dissociation kinetics at the Mo sites. Consequently, this Ni-MoN catalyst requires low overpotentials of 61 and 136 mV to drive current densities of 100 and 1000 mA cm , respectively, in 1 m KOH and remains stable during operation for 200 h at a constant current density of 100 or 500 mA cm . This good HER catalyst also works well in alkaline seawater electrolyte and shows outstanding performance toward overall seawater electrolysis with ultralow cell voltages.
开发出高效且耐用的非贵金属析氢反应(HER)催化剂以扩大碱性水/海水电解规模是人们所期望的,但仍然是一项重大挑战。在此,展示了一种由非晶态MoN纳米棒上的Ni和MoN纳米颗粒组成的多相Ni-MoN催化剂,其能够以优异性能维持大电流密度的析氢反应。这种分级纳米棒-纳米颗粒结构,连同大表面积和多维边界/缺陷,赋予了催化剂丰富的活性位点。亲水性表面有助于实现加速的气体释放能力,并有效地防止水电解过程中催化剂的降解。理论计算进一步证明,Ni和MoN的组合有效地调节了它们界面处的电子重新分布,并促进了Mo位点上缓慢的水离解动力学。因此,这种Ni-MoN催化剂在1 m KOH中驱动100和1000 mA cm 的电流密度分别需要61和136 mV的低过电位,并且在100或500 mA cm 的恒定电流密度下运行200小时期间保持稳定。这种良好的析氢反应催化剂在碱性海水电解质中也表现良好,并在超低电池电压下对整体海水电解显示出优异性能。