Wan Lei, Lin Dongcheng, Liu Jing, Xu Ziang, Xu Qin, Zhen Yihan, Pang Maobin, Wang Baoguo
Department of Chemical Engineering, Tsinghua University, Beijing, China, 100084.
ACS Nano. 2024 Aug 27;18(34):22901-22916. doi: 10.1021/acsnano.4c03668. Epub 2024 Aug 13.
Developing a high-efficiency and stable anode catalyst layer (CL) is crucial for promoting the practical applications of anion exchange membrane (AEM) water electrolyzers. Herein, a hierarchical nanosheet array composed of oxygen vacancy-enriched CoCrO nanosheets and dispersed FeNi layered double hydroxide (LDH) is proposed to regulate the electronic structure and increase the electrical conductivity for improving the intrinsic activity of the oxygen evolution reaction (OER). The CoCrO/NiFe LDH electrodes require an overpotential of 205 mV to achieve a current density of 100 mA cm, and they exhibit long-term stability at 1000 mA cm over 7000 h. Notably, a breakthrough strategy is introduced in membrane electrode assembly (MEA) fabrication by transferring CoCrO/NiFe LDH to the surface of an AEM, forming a 3D-interlocked anode CL, significantly reducing the overall cell resistance and enhancing the liquid/gas mass transfer. In AEM water electrolysis, it exhibits an ultralow cell voltage of 1.55 V to achieve a current density of 1.0 A cm in 1 M KOH, outperforming the state-of-the-art Pt/C//IrO. This work provides a valuable approach to designing high-efficiency electrocatalysts at the single-cell level for advanced alkaline water electrolysis technologies.
开发高效稳定的阳极催化剂层(CL)对于推动阴离子交换膜(AEM)水电解槽的实际应用至关重要。在此,提出了一种由富含氧空位的CoCrO纳米片和分散的FeNi层状双氢氧化物(LDH)组成的分级纳米片阵列,以调节电子结构并提高电导率,从而改善析氧反应(OER)的本征活性。CoCrO/NiFe LDH电极在电流密度为100 mA cm时需要205 mV的过电位,并且在1000 mA cm下表现出超过7000 h的长期稳定性。值得注意的是,在膜电极组件(MEA)制造中引入了一种突破性策略,即将CoCrO/NiFe LDH转移到AEM表面,形成三维互锁的阳极CL,显著降低了整体电池电阻并增强了液/气传质。在AEM水电解中,它在1 M KOH中实现1.0 A cm电流密度时表现出1.55 V的超低电池电压,优于目前最先进的Pt/C//IrO。这项工作为在单电池水平上设计用于先进碱性水电解技术的高效电催化剂提供了一种有价值的方法。