X射线吸收精细结构
锰
催化作用
氧烷
化学
无机化学
电催化剂
析氧
吸收(声学)
扩展X射线吸收精细结构
八面体
氧化态
X射线吸收光谱法
吸收光谱法
氧化物
光谱学
材料科学
结晶学
物理化学
电极
晶体结构
电化学
生物化学
复合材料
有机化学
量子力学
物理
作者
Shun Tsunekawa,Futaba Yamamoto,Ke‐Hsuan Wang,Masanari Nagasaka,Hayato Yuzawa,Satoru Takakusagi,Hiroshi Kondoh,Kiyotaka Asakura,Takeshi Kawai,Masaaki Yoshida
标识
DOI:10.1021/acs.jpcc.0c05571
摘要
A layered manganese oxide catalyst containing K+ cations [K/MnOx catalyst] was developed, and its ability to efficiently decompose water was demonstrated. Operando hard/tender/soft X-ray absorption fine structure (XAFS) techniques were used to investigate the function of the K/MnOx catalyst under working conditions. The Mn valency depended on the potential and the amount of K+ cation adsorption. Mn K-edge (hard X-ray) XAFS measurements for the K/MnOx catalyst suggested that the Mn in the catalyst was an Mn3+ species with an octahedral δ-MnO2 structure at a lower electrode potential, which changed reversibly to an Mn4+ species with a δ-MnO2 structure at higher potential during oxygen evolution. A similar result was obtained from operando O K-edge (soft X-ray) XAFS. The chemical state of K species was analyzed using operando K K-edge (tender X-ray) XAFS, which indicated that K+ cations were intercalated with hydrated states in the δ-MnO2 layers. These operando XAFS results demonstrated that the layered δ-MnO2 containing hydrated K+ cations functioned as efficient oxygen evolution electrocatalysts because of the presence of Mn3+ reaction sites.
科研通智能强力驱动
Strongly Powered by AbleSci AI