Affiliation:
1. Collaborative Innovation Center of Suzhou Nano Science and Technology College of Energy Soochow University Suzhou 215006 China
2. School of Chemistry and Chemical Engineering Nantong University Nantong 226019 China
3. Light Industry Institute of Electrochemical Power Sources Suzhou 215600 China
Abstract
AbstractAs the core of low‐temperature direct ammonia fuel cell (DAFC) technology, electrocatalytic ammonia oxidation reaction (AOR) has proven to be most active on platinum‐based catalysts. However, the AOR is extremely surface sensitive that only the Pt (200) facet exhibits high reaction activity, whereas other facets usually do not make contributions. Herein, the inert (220) surface of PtMo nano‐alloy is successfully awakened as one more active facet in addition to (200) via directional single‐atom Ni‐doping. The introduction of Ni triggers a targeted electron accumulation around Pt sites at the (220) facet that significantly reduces the AOR energy barrier while maintaining the activity of the (200) surface. With a greatly enlarged active surface, the Ni‐decorated PtMo catalyst exhibits a significantly facilitated AOR kinetics with a low onset potential of 0.49 V versus reversible hydrogen electrode and a superior peak current density of 94.96 A g−1 at 5 mV s−1. Notably, the DAFC equipped with such an electrocatalyst reaches a remarkable peak power density of 16.70 mW cm−2 at low temperatures. It is believed that this strategy sheds light on exploiting the intrinsic activity of Pt‐based electrocatalysts, and drives the low‐temperature DAFC technology to a more practical level.
Funder
National Natural Science Foundation of China
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
17 articles.
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