3d-Orbital Occupancy Regulated Ir-Co Atomic Pair Toward Superior Bifunctional Oxygen Electrocatalysis

• Published in: ACS catalysis 2021-07, Vol.11 (14), p.8837-8846
• Main Authors: Xiao, Meiling, Zhu, Jianbing, Li, Shuang, Li, Gaoran, Liu, Wenwen, Deng, Ya-Ping, Bai, Zhengyu, Ma, Lu, Feng, Ming, Wu, Tianpin, Su, Dong, Lu, Jun, Yu, Aiping, Chen, Zhongwei
• Format: Article
• Language: English
• Subjects: active site; atomic pair; bifunctional oxygen electrocatalysis; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; orbital occupancy; spin polarization
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/acscatal.1c02165

Atomically dispersed metal catalysts are hailed as the most promising catalyst category for oxygen electrocatalysis. However, the challenges in regulating electronic configuration and unveiling the mechanism on the atomic scale are hindering their practical implementation. Herein, we modulate the Co d-orbital electron configuration by constructing the Ir–Co atomic pair toward boosted bifunctional activity. The as-developed dual-atom IrCo–N–C catalyst displays unprecedented activity with a half-wave potential of 0.911 V for oxygen reduction reaction and only 330 mV overpotential at 10 mA cm–2 for oxygen evolution reaction, outperforming the single-atom counterparts as well as the commercial Pt/C and Ir/C benchmarks. The impressive bifunctionality is also verified in a Zn–air battery prototype with an ultra-high cyclability over 450 cycles. Theoretical calculations are performed to shed light on the synergetic effects of the atomic pair site, where the incorporation of Ir atom alters the d-orbital energy level of Co and thus induces the re-arrangement of d-electron toward intensified spin polarization. As a result, the lower occupancy of d z 2 orbital facilitates the electron acceptation from oxygen to form a stronger Co–O σ bond, thereby propelling faster reaction kinetics.