已核实 DOI 相关产品: 0

Boosting the electrocatalytic activity on CoN/Ni3N heterojunction by Ce modification for efficient water splitting

Journal 2026 · IF 9.6 · 发表于 2026 年 9 月 18 日
作者: Peihao Ge,Xinping Zhang,Jianmin Yu,Jiao Yang,Lishan Peng
阅读全文 在 PubMed 查看

摘要

Facile electrodeposition-nitridation yields Ce-CoN/Ni 3 N heterostructured catalyst. • Ce tunes electronic structure and generates N vacancies to accelerate HER kinetics. • Ce activates lattice oxygen and drives reconstruction for dual AEM/LOM OER. • Symmetric flow electrolyzer achieves 500 mA cm −2 at 2.04  V over 500 h durability. The design of highly efficient and low-cost bifunctional electrocatalysts for overall water splitting (OWS) is essential to realize a sustainable hydrogen economy. Heterojunction engineering can realize synergistic catalysis by coupling distinct active components, while the low activity at the interfaces needs further improvement by introducing elaborate elements. Herein, we constructed a Ce-modified CoN/Ni 3 N heterojunction catalyst via sequential electrodeposition and nitridation. The introduction of redox-active Ce modulates the interfacial electronic configuration and creates a high density of nitrogen vacancies (N v ), substantially boosting the bifunctional catalytic performance of Ce-CoN/Ni 3 N. The optimal catalyst requires overpotentials of only 27 mV and 267 mV to deliver 10 mA cm −2 for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in 1 M KOH. A two-electrode flow electrolyzer equipped with Ce-CoN/Ni 3 N as bifunctional electrodes achieves a high industrial current density of 500 mA cm −2 at a cell voltage of 2.04 V and maintains stable operation for 500 h. Mechanistic investigations reveal that Ce incorporation elevates the oxidation states of Ni and Co and promotes the generation of N v , which accelerates water dissociation and HER kinetics. Meanwhile, Ce incorporation facilitates surface reconstruction from β -NiOOH to the more active γ -NiOOH phase and activates lattice oxygen, enabling cooperative adsorbate evolution mechanism (AEM) and lattice oxygen mechanism (LOM) pathways that collectively enhance OER kinetics. This study reveals that heterointerface engineering offers an effective and feasible strategy for creating highly active bifunctional electrocatalysts toward practical water electrolysis. Download: Download high-res image (204KB) Download: Download full-size image