Above 2 W cm−2 direct liquid fuel cells enabled by mitigating cathode polarization†

EES catalysis Pub Date : 2025-03-12 DOI:10.1039/D5EY00005J
Yu Guo, Fukang Gui, Yangkai Han, Yingjian Cao, Zijun Hu, Yongkang Han, Qinggang Tan, Yong Che, Cunman Zhang, Yun Zhao and Qiangfeng Xiao
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Abstract

Among direct liquid fuel cells, the direct borohydride fuel cells (DBFCs) are considered as attractive portable or mobile power sources due to their high theoretical voltage and high energy density. However, the development of DBFCs has been greatly hindered by the borohydride crossover and oxidation at the cathode. Here we have developed DBFCs featuring a borohydride-tolerant Mn–Co–C spinel cathode catalyst and a microscale bipolar interface constituting a poly(arylene piperidinium) anion exchange membrane and Nafion®-based cathode that can achieve breakthroughs in performance and scalability. The areal peak power density surpasses 2 W cm−2 at 80 °C with a platinum loading less than 1 mg cm−2. The three-electrode and crossover studies elucidate that the cathode polarization is significantly mitigated by the suppressed parasitic borohydride oxidation as compared with conventional configurations. The success of transforming the performance from a single cell of 1.5 × 1.5 to 5 × 5 cm2 paves the way for practical applications.

通过减轻阴极极化†实现2w cm−2以上的直接液体燃料电池
在直接液体燃料电池中,直接硼氢化物燃料电池(dbfc)因其理论电压高、能量密度高而被认为是有吸引力的便携式或移动电源。然而,阴极硼氢化物的交叉和氧化极大地阻碍了dbfc的发展。在这里,我们开发了dbfc,具有耐硼氢化物的Mn-Co-C尖晶石阴极催化剂和微尺度双极界面,构成聚(芳烯胡椒鎓)阴离子交换膜和基于Nafion®的阴极,可以在性能和可扩展性方面取得突破。在80°C下,铂负载小于1mg cm - 2,面积峰值功率密度超过2w cm - 2。三电极和交叉研究表明,与传统结构相比,抑制寄生硼氢化物氧化显著减轻了阴极极化。将单个电池的性能从1.5 × 1.5转变为5 × 5 cm2的成功,为实际应用铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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