Xu Mingxia, Zhang Xiuyun, Liu Yaqi, Zhao Xinli, Liu Yongjun, Wu Ruchun, Wang Jinlan
Colleage of Physical Science and Technology, Yangzhou University, Yangzhou, 225009, China.
Qingdao Univ. Sci. & Technol., Shandong Key Lab Biochem. Anal., Coll. Chem. & Mol. Engn., Qingdao, 266042, Peoples R China.
Chemphyschem. 2020 Dec 14;21(24):2651-2659. doi: 10.1002/cphc.202000692. Epub 2020 Nov 18.
Single atom catalysts (SAC) for water splitting hold the promise of producing H in a highly efficient and economical way. As the performance of SACs depends on the interaction between the adsorbate atom and supporting substrate, developing more efficient SACs with suitable substrates is of significance. In this work, inspired by the successful fabrications of borophene in experiments, we systematically study the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) activities of a series of 3d transition metal-based SACs supported by various borophene monolayers (BMs=α_sheet, α _sheet, and β _sheet borophene), TM/BMs, using density functional theory calculations and kinetic simulations. All of the TM/BMs systems exhibit superior HER performance compared to Pt with close to zero thermoneutral Gibbs free energy (ΔG ) of H adsorption. Furthermore, three Ni-deposited systems, namely, Ni/α_BM, Ni/α _BM and Ni/β _BM, were identified to be superior OER catalysts with remarkably reduced overpotentials. Based on these results, Ni/BMs can be expected to serve as stunning bifunctional electrocatalysts for water splitting. This work provides a guideline for developing efficient bifunctional electrocatalysts.
用于水分解的单原子催化剂(SAC)有望以高效且经济的方式产生氢气。由于SAC的性能取决于吸附原子与支撑底物之间的相互作用,因此开发具有合适底物的更高效SAC具有重要意义。在这项工作中,受实验中成功制备硼烯的启发,我们使用密度泛函理论计算和动力学模拟,系统地研究了一系列由各种硼烯单层(BMs = α_片层、α_片层和β_片层硼烯)支撑的3d过渡金属基SAC,即TM/BMs的析氢反应(HER)和析氧反应(OER)活性。与Pt相比,所有TM/BMs体系均表现出优异的HER性能,氢吸附的热中性吉布斯自由能(ΔG)接近零。此外,三种镍沉积体系,即Ni/α_BM、Ni/α _BM和Ni/β _BM,被确定为具有显著降低过电位的优异OER催化剂。基于这些结果,Ni/BMs有望成为用于水分解的出色双功能电催化剂。这项工作为开发高效双功能电催化剂提供了指导。