催化作用
氧还原反应
动力学
铂金
水准点(测量)
氧还原
氮气
化学
金属
物理化学
电极
物理
电化学
有机化学
地理
量子力学
生物化学
大地测量学
作者
Xiaofeng Zhu,Xin Tan,Kuang‐Hsu Wu,Shu‐Chih Haw,Chih‐Wen Pao,Bing‐Jian Su,Junjie Jiang,Sean C. Smith,Jin‐Ming Chen,Rose Amal,Xunyu Lu
标识
DOI:10.1002/anie.202107790
摘要
Abstract A considerable amount of platinum (Pt) is required to ensure an adequate rate for the oxygen reduction reaction (ORR) in fuel cells and metal‐air batteries. Thus, the implementation of atomic Pt catalysts holds promise for minimizing the Pt content. In this contribution, atomic Pt sites with nitrogen (N) and phosphorus (P) co‐coordination on a carbon matrix (PtNPC) are conceptually predicted and experimentally developed to alter the d‐band center of Pt, thereby promoting the intrinsic ORR activity. PtNPC with a record‐low Pt content (≈0.026 wt %) consequently shows a benchmark‐comparable activity for ORR with an onset of 1.0 V RHE and half‐wave potential of 0.85 V RHE . It also features a high stability in 15 000‐cycle tests and a superior turnover frequency of 6.80 s −1 at 0.9 V RHE . Damjanovic kinetics analysis reveals a tuned ORR kinetics of PtNPC from a mixed 2/4‐electron to a predominately 4‐electron route. It is discovered that coordinated P species significantly shifts d‐band center of Pt atoms, accounting for the exceptional performance of PtNPC.
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