Tuning the p‐Orbital Electron Structure of s‐Block Metal Ca Enables a High‐Performance Electrocatalyst for Oxygen Reduction
Zhiyu Lin, Hao Huang, Ling Cheng, Wei Hu, Pengping Xu, Yang Yang, Jianmin Li, Fei‐Yue Gao, Yang Kang, Shuai Liu, Peng Jiang, Wensheng Yan, Shi Chen, Changlai Wang, Huigang Tong, Minxue Huang, Wei Zheng, Hui Wang, Qianwang Chen
Abstract
Abstract Most previous efforts are devoted to developing transition metals as electrocatalysts guided by the d‐band center model. The metals of the s‐block of the periodic table have so far received little attention in the application of oxygen reduction reactions (ORR). Herein, a carbon catalyst with calcium (Ca) single atom coordinated with N and O is reported, which displays exceptional ORR activities in both acidic condition ( E 1/2 = 0.77 V, 0.1 m HClO 4 ) and alkaline condition ( E 1/2 = 0.90 V, 0.1 m KOH). The CaN, O/C exhibits remarkable performance in zinc–air battery with a maximum power density of 218 mW cm –2 , superior to a series of catalysts reported so far. X‐ray absorption near‐edge structure (XANES) characterization confirms the formation of N‐ and O‐atom‐coordinated Ca in the carbon matrix. Density functional theory (DFT) calculations reveal that the high catalytic activity of main‐group Ca is ascribed to the fact that its p‐orbital electron structure is regulated by N and O coordination so that the highest peak ( E P ) of the projected density of states (PDOS) for the Ca atom is moved close to the Fermi level, thereby facilitating the adsorption of ORR intermediates and electron transfer.