John C. Douglin, Hideo Notsu, Shinsuke Nagata, Sapir Willdorf-Cohen, Jinliu Zhong, Junya Ohyama, Jiawei Hu, Syeda M. Zahan, Andres O. Godoy, Changlai Wang, Oluwafemi Sanumi, Masayuki Tsushida, Karam Yassin, Jasna Jankovic, Charles E. Diesendruck, Yuta Nabae, Dario R. Dekel
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Upon purification, the resulting catalyst demonstrates outstanding performance as cathodes in anion-exchange membrane fuel cells (AEMFCs) owing to sufficiently stabilized Fe single-atoms at the FeN<sub>4</sub> sites yielding a peak power density (<i>P</i><sub>max</sub>) as high as ∼1.8 W cm<sup>−2</sup> and specific power values up to 11.3 W <span></span><math>\n <semantics>\n <msubsup>\n <mi>mg</mi>\n <mi>PGM</mi>\n <mrow>\n <mo>−</mo>\n <mn>1</mn>\n </mrow>\n </msubsup>\n <annotation>${\\mathrm{mg}}_{{\\mathrm{PGM}}}^{ - 1}$</annotation>\n </semantics></math>; the latter being the greatest reported among CRM-free cathode AEMFCs. The SAC also shows remarkable in situ durability under a very high current density of 1000 mA cm<sup>−2</sup>, a first introduced here, with only a 2 mV h<sup>−1</sup> decay. 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引用次数: 0
摘要
单原子催化剂(SACs)具有明确的单一金属原子活性位点,由于其可调谐以提高活性和稳定性,在电催化领域中得到了突出的应用。在本研究中,在不使用牺牲模板的情况下,通过热解聚酰亚胺纳米颗粒和铁,合成了一种无关键原料(CRM)的SAC,用于碱性介质中的氧还原反应(ORR)。纯化后的催化剂在阴离子交换膜燃料电池(aemfc)中表现出优异的阴极性能,因为FeN4位点上的Fe单原子足够稳定,峰值功率密度(Pmax)高达约1.8 W cm-2,比功率值高达11.3 W mg PGM - 1 ${\ mathm {mg}}_{\ mathm {PGM}}}}^{- 1}$;后者是无crm阴极aemfc中报道最多的。在1000 mA cm-2的高电流密度下,SAC也显示出显著的原位耐久性,只有2 mV的h-1衰减。最令人印象深刻的是,当SAC与NiMo阳极结合在118°C下测试完全无cr的高温(HT)-AEMFC时,Pmax为372 mW cm-2,极限电流密度为~ 1.14 a cm-2。这项工作代表了下一代无crm aemfc的耐用SAC阴极催化剂发展的一个重要里程碑。
Template-Free Fabrication of Single Atom Fe-Based Cathodes Unlock High-Performing Anion-Exchange Membrane Fuel Cells
Single-atom catalysts (SACs) possessing well-defined active sites of singular metal atoms have gained prominence in the field of electrocatalysis as they can be tuned to enhance activity and stability. In this study, a critical-raw-material (CRM)-free SAC is synthesized for the oxygen reduction reaction (ORR) in alkaline media by pyrolyzing polyimide nanoparticles and Fe without using a sacrificial template. Upon purification, the resulting catalyst demonstrates outstanding performance as cathodes in anion-exchange membrane fuel cells (AEMFCs) owing to sufficiently stabilized Fe single-atoms at the FeN4 sites yielding a peak power density (Pmax) as high as ∼1.8 W cm−2 and specific power values up to 11.3 W ; the latter being the greatest reported among CRM-free cathode AEMFCs. The SAC also shows remarkable in situ durability under a very high current density of 1000 mA cm−2, a first introduced here, with only a 2 mV h−1 decay. Most impressively, when the SAC is combined with a NiMo anode to test a completely CRM-free high-temperature (HT)-AEMFC at 118 °C, a Pmax of 372 mW cm−2 and limiting current density of ∼1.14 A cm−2 are achieved. This work represents a significant milestone in the development of durable SAC cathode catalysts for the next generation of CRM-free AEMFCs.
期刊介绍:
Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.