Fundamental Understanding of Electronic Structure in FeN<sub>4</sub> Site on Electrocatalytic Activity via <i>dz</i><sup><i>2</i></sup>‐Orbital‐Driven Charge Tuning for Acidic Oxygen Reduction
Xueli Li, Tengge Chen, Bolong Yang, Zhonghua Xiang
Abstract
Abstract The structural diversity of active sites resulting from traditional pyrolysis hinder our understanding of the local coordination environment (LCE) around the active site, and its effects on performance in the oxygen reduction reaction (ORR). We created a series of FeN 4 active‐site configurations via a pyrolysis‐free approach where LCEs are defined by covalent organic polymers (COPs). Our results suggest a more positive charge on iron atoms in the vicinity of an electron‐withdrawing side‐chain; that is, a high‐valence configuration (Fe H+ N 4 ) that is achieved with a COP BTC @Cl‐CNTs catalyst subject to ‐orbital tuning. A new descriptor ξ, defined as the band center of iron atoms projected on the ‐orbital, was introduced to quantitively explain a volcano‐like regulation mechanism. When ξ is distributed between −1.887 and −1.862 eV, the catalytic performance of the COP BTC @Cl‐CNTs electrocatalyst is optimized.