Haq Tanveer Ul, Haik Yousef, Hussain Irshad, Rehman Habib Ur, Al-Ansari Tareq A
Division of Sustainable Development, College of Science and Engineering, Hamad Bin Khalifa University, Qatar Foundation, Doha 34110, Qatar.
Department of Chemistry and Chemical Engineering, SBA School of Science and Engineering, Lahore University of Management and Sciences (LUMS), DHA, Lahore 54792, Pakistan.
ACS Appl Mater Interfaces. 2021 Jan 13;13(1):468-479. doi: 10.1021/acsami.0c17216. Epub 2020 Dec 28.
Oxygen evolution reaction (OER) is a bottleneck process in the water-splitting module for sustainable and clean energy production. Transition metal-based electrocatalysts can be effective as water-splitting catalytic materials because of their appropriate redox properties and natural abundance, but the slow kinetics because of strong adsorption and consequently slow desorption of intermediates on the active sites of catalysts severely hamper the dynamics of the released molecular oxygen and thus remains a formidable challenge. Herein, we report the development of structurally and surface-modified PA-Gd-Ni(OH)Cl (partially alkylated gadolinium-doped nickel oxychloride) nanoclusters (NCs, size ≤ 3 nm) for enhanced and stable OER catalysis at low overpotential and high turnover frequency. The ameliorated catalytic performance was achieved by controlling the surface coverage of these NCs with hydrophobic ligands and through the incorporation of electronegative atoms to facilitate easy adsorption/desorption of intermediates on the catalyst surface, thus improving the liberation of O. Such a surface and structural modification and uniform distribution at the nanoscale length are indeed worth considering to selectively tune the catalytic potential and further modernize the electrode materials for the challenging OER process.
析氧反应(OER)是可持续清洁能源生产的水分解模块中的一个瓶颈过程。基于过渡金属的电催化剂由于其适当的氧化还原特性和天然丰度,可作为有效的水分解催化材料,但由于中间体在催化剂活性位点上的强吸附以及随之而来的缓慢解吸导致的动力学缓慢,严重阻碍了释放的分子氧的动力学,因此仍然是一个巨大的挑战。在此,我们报告了结构和表面改性的PA-Gd-Ni(OH)Cl(部分烷基化的钆掺杂氯氧化镍)纳米团簇(NCs,尺寸≤3nm)的开发,用于在低过电位和高周转频率下增强和稳定的析氧反应催化。通过用疏水配体控制这些纳米团簇的表面覆盖率,并通过引入电负性原子以促进中间体在催化剂表面的轻松吸附/解吸,从而实现了改善的催化性能,进而改善了氧气的释放。这种表面和结构改性以及在纳米尺度长度上的均匀分布确实值得考虑,以选择性地调节催化电位,并进一步使具有挑战性的析氧反应过程的电极材料现代化。