Degradation of NiMo Catalyst Under Intermittent Operation of Anion Exchange Membrane Water Electrolyzer and its Mitigation by Carbon Encapsulation
Sun Seo Jeon, Yunji Choi, Jae Wook Lee, Robert Haaring, Won-Jae Lee, Hyeseong Jeon, Jeonghyun Nam, Eunchong Lee, Seung‐Woo Lee, Minjoon Kim, Yeon Sik Jung, Yousung Jung, Yun Jeong Hwang, Hyunjoo Lee
Abstract
Abstract Developing durable platinum group metal (PGM)‐free catalysts is critical for enabling cost‐effective hydrogen production through anion exchange membrane water electrolyzers (AEMWEs). Here, this study presents NiMo catalysts encapsulated within defective carbon shells. Whereas conventional NiMo catalysts degrade rapidly under intermittent conditions with voltage changes, the carbon‐encapsulated NiMo catalysts exhibit remarkable resistance to degradation with good hydrogen evolution reaction (HER) activity, effectively addressing the challenges associated with renewable energy integration. The carbon shells prevent oxidation‐induced deactivation by inhibiting the structural transformation of metallic Ni into hydroxides accompanying volumetric expansion under open circuit voltage conditions. Using a reference electrode‐integrated AEMWE, overpotential contributions are decoupled and demonstrated that the stability of HER catalyst is decisive for the durable AEMWE operation under intermittent scenarios. This study establishes a strategy for durable PGM‐free catalyst development for sustainable and scalable hydrogen production.