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磁场下的自旋极化析氧反应

Spin-polarized oxygen evolution reaction under magnetic field.

作者信息

Ren Xiao, Wu Tianze, Sun Yuanmiao, Li Yan, Xian Guoyu, Liu Xianhu, Shen Chengmin, Gracia Jose, Gao Hong-Jun, Yang Haitao, Xu Zhichuan J

机构信息

Beijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of Science, Beijing, China.

School of Material Science and Engineering, Nanyang Technological University, Singapore, Singapore.

出版信息

Nat Commun. 2021 May 10;12(1):2608. doi: 10.1038/s41467-021-22865-y.

Abstract

The oxygen evolution reaction (OER) is the bottleneck that limits the energy efficiency of water-splitting. The process involves four electrons' transfer and the generation of triplet state O from singlet state species (OH or HO). Recently, explicit spin selection was described as a possible way to promote OER in alkaline conditions, but the specific spin-polarized kinetics remains unclear. Here, we report that by using ferromagnetic ordered catalysts as the spin polarizer for spin selection under a constant magnetic field, the OER can be enhanced. However, it does not applicable to non-ferromagnetic catalysts. We found that the spin polarization occurs at the first electron transfer step in OER, where coherent spin exchange happens between the ferromagnetic catalyst and the adsorbed oxygen species with fast kinetics, under the principle of spin angular momentum conservation. In the next three electron transfer steps, as the adsorbed O species adopt fixed spin direction, the OER electrons need to follow the Hund rule and Pauling exclusion principle, thus to carry out spin polarization spontaneously and finally lead to the generation of triplet state O. Here, we showcase spin-polarized kinetics of oxygen evolution reaction, which gives references in the understanding and design of spin-dependent catalysts.

摘要

析氧反应(OER)是限制水分解能量效率的瓶颈。该过程涉及四个电子的转移以及从单重态物种(OH或HO)生成三重态O。最近,明确的自旋选择被描述为在碱性条件下促进OER的一种可能方式,但具体的自旋极化动力学仍不清楚。在此,我们报告通过使用铁磁有序催化剂作为恒定磁场下自旋选择的自旋极化器,可以增强OER。然而,它不适用于非铁磁催化剂。我们发现自旋极化发生在OER的第一个电子转移步骤,在自旋角动量守恒的原理下,铁磁催化剂与吸附的氧物种之间以快速动力学发生相干自旋交换。在接下来的三个电子转移步骤中,由于吸附的O物种采用固定的自旋方向,OER电子需要遵循洪德规则和泡利不相容原理,从而自发地进行自旋极化并最终导致三重态O的生成。在此,我们展示了析氧反应的自旋极化动力学,这为理解和设计自旋依赖催化剂提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eab/8110536/7f41f97cfa0d/41467_2021_22865_Fig1_HTML.jpg

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