过电位
金红石
氧气
催化作用
格子(音乐)
焊剂(冶金)
固溶体
电解
材料科学
化学工程
锡
析氧
无机化学
化学物理
化学计量学
微晶
离子交换
电解水
分解水
化学
碱性水电解
纳米颗粒
离子
锐钛矿
作者
Fan Wang,Weitian Wang,Tao Wang,Xin Wang,Kevin M. Siniard,Juntian Fan,Beenish Bashir,Alexander S. Ivanov,Xiangyu Li,Jun Li,Guoxiang Hu,Feng‐Yuan Zhang,Gangli Wang,Sheng Dai
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-07
卷期号:64 (49): e202514922-e202514922
被引量:2
标识
DOI:10.1002/anie.202514922
摘要
Developing efficient and stable electrocatalysts for the acidic oxygen evolution reaction (OER) is vital for advancing proton exchange membrane water electrolysis (PEMWE) technologies. Here, we report a flux synthesis of nitrogen-doped Ti-Ru rutile-type solid-solution oxides (M-TiRu4) using molten NaNO3 as the flux medium. The flux medium promotes the low-temperature conversion of TiN to rutile TiO2, while in situ-formed RuO2 nanoparticles facilitate lattice templating and couple with interfacial ion migration, enabling the formation of homogeneous solid solutions with abundant lattice heterogeneity. Simultaneously, nitrogen atoms are stably incorporated into the lattice of solid solutions, inducing bandgap narrowing, which enhances electronic conductivity. The developed M-TiRu4 catalyst exhibits exceptional acidic OER performance, delivering a low overpotential of 194 mV at 10 mA cm-2, superior durability over 600 h, and a Ru mass activity 7.8 times that of commercial RuO2. At the device level, M-TiRu4 enables PEMWE operation at 1.64 V @ 2 A cm-2 and maintains stable performance at 500 mA cm-2 for 200 h with a minimal degradation rate of 20 µV h-1. This work demonstrates a robust approach for designing high-performance, durable acidic OER catalysts via synergistic lattice and electronic structure engineering, paving the way for next-generation water-splitting technologies.
科研通智能强力驱动
Strongly Powered by AbleSci AI