纳米线
阴极
氢氧化物
燃料电池
化学工程
材料科学
电子转移
传质
膜
纳米技术
化学
光化学
物理化学
色谱法
生物化学
工程类
作者
Zhongbin Zhuang,Dongyue Xin,Xuerui Liu,Chengjin Chen,Haiyong Wang,Bowen Chen,Shuxin Zhang,Jinjie Fang,Deng Chen,Wei Zhu
标识
DOI:10.1002/cctc.202401628
摘要
Hydroxide exchange membrane fuel cells (HEMFCs) are promising due to the potential use of non‐precious metal catalysts. However, the performance of HEMFCs based on non‐precious catalysts is still unsatisfactory, and one reason for this is hindered mass transfer in the catalyst layer. Here, we employ a hydrothermal method to grow in situ a MnO2 nanowire thin mesh (NTM) catalytic layer on the gas diffusion electrode. The HEMFC prepared with MnO2 NTM cathode achieves a peak power density of 425 mW cm−2, surpassing the performance of an HEMFC prepared using the traditional powder catalyst spraying method by 4 times. High‐frequency resistance and limiting current tests indicate that the MnO2 NTM reduces ohmic resistance and improves mass transfer, thereby enhancing the HEMFC performance. Furthermore, the peak power density of the HEMFC is increased to 626 mW cm−2 by depositing additional active Co3O4 nanoparticles on the MnO2 NTM. These findings demonstrate that an interconnected and porous catalyst layer structure is beneficial for improving mass transfer properties, which in turn enhances HEMFC performance.
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