Intrinsic ORR Activity Enhancement of Pt Atomic Sites by Engineering the d-Band Center via Local Coordination Tuning
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Authors
Zhu, Xiaofeng
Tan, Xin
Wu, Kuang-Hsu
Haw, S-C
Pao, C-W
Su, Bing-Jian
Jiang, Junjie
Smith, Sean
Chen, J-M
Amal, Rose
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Wiley
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 VRHE and half-wave potential of 0.85 VRHE. It also features a high stability in 15 000-cycle tests and a superior turnover frequency of 6.80 s−1 at 0.9 VRHE. 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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Angewandte Chemie International Edition
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Restricted until
2099-12-31