Key role of e g band broadening in nickel-based oxyhydroxides on coupled oxygen evolution mechanism

• Published in: Nature communications Vol. 14; no. 1; pp. 1 - 10
• Main Authors: Haoyin Zhong, Qi Zhang, Junchen Yu, Xin Zhang, Chao Wu, Hang An, Yifan Ma, Hao Wang, Jun Zhang, Yong-Wei Zhang, Caozheng Diao, Zhi Gen Yu, Shibo Xi, Xiaopeng Wang, Junmin Xue
• Format: Journal Article
• Language: English
• Published: Nature Portfolio 01.12.2023
• ISSN: 2041-1723
• DOI: 10.1038/s41467-023-43302-2

Abstract A coupled oxygen evolution mechanism (COM) during oxygen evolution reaction (OER) has been reported in nickel oxyhydroxides (NiOOH)-based materials by realizing e g * band (3d electron states with e g symmetry) broadening and light irradiation. However, the link between the e g * band broadening extent and COM-based OER activities remains unclear. Here, Ni1-xFexOOH (x = 0, 0.05, 0,2) are prepared to investigate the underlying mechanism governing COM-based activities. It is revealed that in low potential region, realizing stronger e g * band broadening could facilitate the *OH deprotonation. Meanwhile, in high potential region where the photon utilization is the rate-determining step, a stronger e g * band broadening would widen the non-overlapping region between d z 2 and a 1g * orbitals, thereby enhancing photon utilization efficiency. Consequently, a stronger e g * band broadening could effectuate more efficient OER activities. Moreover, we demonstrate the universality of this concept by extending it to reconstruction-derived X-NiOOH (X = NiS2, NiSe2, Ni4P5) with varying extent of e g * band broadening. Such an understanding of the COM would provide valuable guidance for the future development of highly efficient OER electrocatalysts.