Sun Yuanmiao, Sun Shengnan, Yang Haitao, Xi Shibo, Gracia Jose, Xu Zhichuan J
School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.
Beijing Key Laboratory for Magnetoelectric Materials and Devices (BKLMMD), Beijing Innovation Center of Materials Science and Engineering, College of Engineering, Peking University, Beijing, 100871, China.
Adv Mater. 2020 Oct;32(39):e2003297. doi: 10.1002/adma.202003297. Epub 2020 Aug 9.
Oxygen evolution and reduction reactions play a critical role in determining the efficiency of the water cycling (H O ⇔ H + O ), in which the hydrogen serves as the energy carrier. That calls for a comprehensive understanding of oxygen electrocatalysis for efficient catalyst design. Current opinions on oxygen electrocatalysis have been focused on the thermodynamics of the reactant/intermediate adsorption on the catalysts. Because the oxygen molecule is paramagnetic, its production from or its reduction to diamagnetic hydroxide/water involves spin-related electron transfer. Both electron transfer and orbital interactions between the catalyst and the reactant/intermediate show spin-dependent character, making the reaction kinetics and thermodynamics sensitive to the spin configurations. Herein, a brief introduction on the spintronic explanation of the catalytic phenomena on oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is given. The local spin configurations and orbital interactions in the benchmark transition-metal-based catalysts for OER and ORR are analyzed as examples. To further understand the spintronic oxygen electrocatalysis and to develop more efficient spintronic catalysts, the challenges are summarized and future opportunities proposed. Spin electrocatalysis may emerge as an important topic in the near future and help integrate a comprehensive understanding of oxygen electrocatalysis.
析氧反应和氧还原反应在决定水的循环效率(H₂O ⇔ H₂ + 1/2O₂)中起着关键作用,其中氢作为能量载体。这就需要全面理解氧电催化以进行高效催化剂设计。目前关于氧电催化的观点主要集中在反应物/中间体在催化剂上吸附的热力学。由于氧分子是顺磁性的,其生成或还原为抗磁性的氢氧化物/水涉及与自旋相关的电子转移。催化剂与反应物/中间体之间的电子转移和轨道相互作用均表现出自旋依赖性,使得反应动力学和热力学对自旋构型敏感。在此,对析氧反应(OER)和氧还原反应(ORR)催化现象的自旋电子学解释进行简要介绍。以用于OER和ORR的基准过渡金属基催化剂中的局部自旋构型和轨道相互作用为例进行分析。为了进一步理解自旋电子学氧电催化并开发更高效的自旋电子学催化剂,总结了挑战并提出了未来机遇。自旋电催化可能在不久的将来成为一个重要课题,并有助于形成对氧电催化的全面理解。