反键分子轨道
离子
碱金属
催化作用
无机化学
电子
材料科学
光化学
化学
掺杂剂
氧气
水溶液中的金属离子
反应机理
类金属
金属
析氧
多相催化
氧化还原
化学工程
铷
作者
Jin Wang,Zhenghui Zhang,Zhenghui Zhang,Rong Wang,Ying Xin,Yexin Zhang,Zhaoliang Zhang,Zhaoliang Zhang,Zhaoliang Zhang
标识
DOI:10.1002/advs.202514470
摘要
Abstract Alkali ions, widely employed as promoters, play crucial roles in heterogeneous catalysis. However, their electron donation mechanism remains poorly understood because alkali ions do not have transferable electrons as metallic alkalis do. Here, a new mechanistic pathway is identified for potassium (K) ions to act as electron donors by constructing single chains of K ions confined within hexagonal WO 3 tunnels with theoretical limit‐breakthrough K concentrations. The as‐produced high‐electron‐density K δ+ (0<δ<1) ions not only facilitate the formation of oxygen vacancies that behave classical electronic effect but, more importantly, also directly donate electrons to [WO 6 ] motif antibonding orbitals, thereby triggering the lattice oxygen activation. As a proof of concept, the resultant catalyst containing K δ+ ions predominantly promotes soot oxidation with O 2 , a challenging solid‐solid‐gas reaction in automotive catalysis, achieving a reaction rate 3.1‐fold greater than the conventional K⁺‐ion confined counterpart. The electron donation effect of metalloid K δ+ ions would be heuristic for enhancing other important heterogeneous catalytic reactions.
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