化学
催化作用
金属
Atom(片上系统)
合理设计
鉴定(生物学)
纳米技术
可靠性(半导体)
组合化学
吸收(声学)
吸收光谱法
碳纤维
钥匙(锁)
电子结构
活动站点
扩展X射线吸收精细结构
协调数
协议(科学)
化学物理
表征(材料科学)
作者
Guolei Cai,Haifeng Lv,Yifan Li,Guikai Zhang,Jing Zhang,Xianghua Kong,Xiaojun Wu,Song Wan Jin,Hengxing Ji
摘要
Atomically dispersed catalysts (ADCs) embedded within carbon substrates are gaining considerable attention for their high metal atom utilization and exceptional catalytic activity. The coordination structure of the active catalytic center is crucial to catalytic performance; however, accurately characterizing these structures remains challenging due to the inherent structural diversity in real-world ADCs and the difficulty of identifying the light elements (e.g., C and N) surrounding central metal atoms. Herein, we propose a protocol to interpret the X-ray absorption spectroscopy, thereby identifying the most probable representative structures of ADCs. Our method integrates average coordination numbers, oxidation states of central metal atoms, and the specific light elements bonded to these metal atoms. This protocol is applicable to single-, dual-, and trimetal atom catalysts, offering a more rational method for structural assignment. By addressing key methodological limitations in current structural assignments for ADCs, our approach improves the reliability of active site identification and provides a foundation for more accurate structure-activity relationship studies in catalytic systems.
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