Zhang Han, Feng Zhongbao, Wang Lin, Li Dagang, Xing Pengfei
School of Metallurgy, Northeastern University, Shenyang, Liaoning 110819, People's Republic of China.
Nanotechnology. 2020 Sep 4;31(36):365701. doi: 10.1088/1361-6528/ab9396. Epub 2020 May 15.
In the present study, an effective approach is proposed to replace the oxygen evolution reaction with the substituted anodic hydrazine oxidation reaction (HzOR) to assist in hydrogen generation based on a bifunctional porous Ni-Zn electrocatalyst with nanosheet arrays. The Ni-Zn catalyst exhibits an extraordinary HzOR performance with a high current density of 970 mA cm at 0.7 V, and 93.8% of its initial activity after 5000 s, simultaneously delivering an overpotential of 68 mV at 10 mA cm for the hydrogen evolution reaction. Moreover, the electrolytic cell is constructed employing Ni-Zn catalysts as both the anode and cathode, achieving 100 mA cm at an ultralow cell voltage of 0.497 V with an outstanding stability over 10 h. The superior electrocatalytic performance can be ascribed to its porous structure with large active surface area, high electrical conductivity, and most importantly the super-aerophobic nature of the Ni-Zn surface. This work also provides a novel approach to designing and constructing porous structured non-noble metal bifunctional electrocatalysts with super-aerophobic surface to be used for energy-saving hydrogen production.
在本研究中,提出了一种有效的方法,基于具有纳米片阵列的双功能多孔镍锌电催化剂,用取代的阳极肼氧化反应(HzOR)替代析氧反应来辅助制氢。镍锌催化剂在0.7 V时表现出非凡的HzOR性能,电流密度高达970 mA cm,在5000 s后仍保持其初始活性的93.8%,同时在析氢反应中,在10 mA cm时过电位为68 mV。此外,构建了以镍锌催化剂作为阳极和阴极的电解池,在0.497 V的超低电池电压下实现了100 mA cm的电流,并且在超过10小时的时间内具有出色的稳定性。优异的电催化性能可归因于其具有大活性表面积的多孔结构、高电导率,最重要的是镍锌表面的超疏气性。这项工作还提供了一种新颖的方法,用于设计和构建具有超疏气表面的多孔结构非贵金属双功能电催化剂,以用于节能制氢。