Krivina Raina A, Lindquist Grace A, Beaudoin Sarah R, Stovall Timothy Nathan, Thompson Willow L, Twight Liam P, Marsh Douglas, Grzyb Joseph, Fabrizio Kevin, Hutchison James E, Boettcher Shannon W
Department of Chemistry and Biochemistry and the Oregon Center for Electrochemistry, University of Oregon, Eugene, OR, 97403, USA.
Department of Chemistry and Biochemistry, University of Oregon, Eugene, OR, 97403, USA.
Adv Mater. 2022 Sep;34(35):e2203033. doi: 10.1002/adma.202203033. Epub 2022 Jul 30.
Anion-exchange-membrane water electrolyzers (AEMWEs) in principle operate without soluble electrolyte using earth-abundant catalysts and cell materials and thus lower the cost of green H . Current systems lack competitive performance and the durability needed for commercialization. One critical issue is a poor understanding of catalyst-specific degradation processes in the electrolyzer. While non-platinum-group-metal (non-PGM) oxygen-evolution catalysts show excellent performance and durability in strongly alkaline electrolyte, this has not transferred directly to pure-water AEMWEs. Here, AEMWEs with five non-PGM anode catalysts are built and the catalysts' structural stability and interactions with the alkaline ionomer are characterized during electrolyzer operation and post-mortem. The results show catalyst electrical conductivity is one key to obtaining high-performing systems and that many non-PGM catalysts restructure during operation. Dynamic Fe sites correlate with enhanced degradation rates, as does the addition of soluble Fe impurities. In contrast, electronically conductive Co O nanoparticles (without Fe in the crystal structure) yield AEMWEs from simple, standard preparation methods, with performance and stability comparable to IrO . These results reveal the fundamental dynamic catalytic processes resulting in AEMWE device failure under relevant conditions, demonstrate a viable non-PGM catalyst for AEMWE operation, and illustrate underlying design rules for engineering anode catalyst/ionomer layers with higher performance and durability.
阴离子交换膜水电解槽(AEMWEs)原则上在不使用可溶性电解质的情况下运行,使用储量丰富的催化剂和电池材料,从而降低绿色氢气的成本。目前的系统缺乏具有竞争力的性能和商业化所需的耐久性。一个关键问题是对电解槽中特定催化剂的降解过程了解不足。虽然非铂族金属(non-PGM)析氧催化剂在强碱性电解质中表现出优异的性能和耐久性,但这并未直接转化为纯水AEMWEs。在此,构建了具有五种非铂族金属阳极催化剂的AEMWEs,并在电解槽运行期间和事后对催化剂的结构稳定性以及与碱性离聚物的相互作用进行了表征。结果表明,催化剂的电导率是获得高性能系统的关键之一,并且许多非铂族金属催化剂在运行过程中会发生结构重组。动态铁位点与降解速率的提高相关,可溶性铁杂质的添加也是如此。相比之下,具有电子导电性的CoO纳米颗粒(晶体结构中不含铁)通过简单的标准制备方法就能制备出AEMWEs,其性能和稳定性与IrO相当。这些结果揭示了在相关条件下导致AEMWE装置失效的基本动态催化过程,展示了一种用于AEMWE运行的可行的非铂族金属催化剂,并阐明了设计具有更高性能和耐久性的阳极催化剂/离聚物层的潜在规则。