Yanzheng He, Sisi Liu*, Qiyang Cheng, Yunfei Huan, Lifang Zhang, Wenjun Shi, Weiyi Shen, Fengchun Zhou, Xiaolei Yuan, Mengfan Wang, Chenglin Yan and Tao Qian*,
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引用次数: 0
摘要
低温直接氨燃料电池(DAFC)是大规模、高安全性脱碳发电的关键技术。然而,作为DAFC核心的阳极氨氧化反应(AOR)的活性并不理想,反应机理也不明确。本文受均相催化氨氧化的启发,从理论上预测了一种放松非均相催化中空间和电荷约束的亲核攻击机制,并通过三段式同位素标记实验进行了实验验证。在这一更实用的机制的指导下,在微量钴取代铂的固溶体上实现了高效的AOR工艺,在5 mV s-1下提供了83.96 a g-1的优越电流密度。组装后的DAFC在60°C下的功率密度高达853.75 mW cm-2,可稳定工作300 h,性能保持率为95.14%,将低温DAFC的应用推向了更加实用的时代。
Facilitating Anodic Ammonia Oxidation over Trace Cobalt-Substituted Solid Solution of Platinum to Boost Direct Ammonia Fuel Cell up to 853.75 mW cm–2
Low-temperature direct ammonia fuel cell (DAFC) is a key technology for decarbonized electric generation on a large scale and with high safety. However, as the core of DAFC, the anodic ammonia oxidation reaction (AOR) still suffers from unsatisfactory activity and an ambiguous reaction mechanism. Herein, inspired by homogeneously catalyzed oxidation of ammonia, a nucleophilic attack mechanism that loosens the steric and charge constraints in heterogeneous catalysis is theoretically predicted and experimentally verified by a three-stage isotope-labeling experiment. Guided by this more practical mechanism, a highly efficient AOR process is realized over trace cobalt-substituted solid solution of platinum, delivering a superior current density of 83.96 A g–1 at 5 mV s–1. The assembled DAFC exhibits a remarkable power density of up to 853.75 mW cm–2 at 60 °C and can operate steadily for 300 h with a performance retention rate of 95.14%, propelling the application of low-temperature DAFC to a more practical era.
期刊介绍:
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