Lee Jooyoung, Jung Hyeonjung, Park Yoo Sei, Woo Seongwon, Yang Juchan, Jang Myeong Je, Jeong Jaehoon, Kwon Nayoung, Lim Byungkwon, Han Jeong Woo, Choi Sung Mook
Materials Center for Energy Convergence, Surface Technology Division, Korea Institute of Materials Science (KIMS), Changwon, 51508, Republic of Korea.
Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Gyeongbuk, 37673, Republic of Korea.
Small. 2021 Jul;17(28):e2100639. doi: 10.1002/smll.202100639. Epub 2021 Jun 3.
Developing high-efficiency and low-cost oxygen-evolving electrodes in anion exchange membrane (AEM) water electrolysis technology is one of the major challenges. Herein, it is demonstrated that the surface corrosion of a conventional Ni foam electrode in the presence of Fe and V cations can transform it into an electrode with a high catalytic performance for oxygen evolution reaction (OER). The corroded electrode consists of a ternary NiFeV layered double hydroxide (LDH) nanosheet array supported on the Ni foam surface. This NiFeV LDH electrode achieves an OER current density of 100 mA cm at an overpotential of 272 mV in 1 m KOH, outperforming the IrO catalyst by 180 mV. Density functional theory calculations reveal that the unique structure and the presence of vanadium in NiFeV LDH play a key role in achieving improved OER activity. When coupled with a commercial Pt/C cathode catalyst, the resulting AEM water electrolyzer achieves a cell current density as high as 2.1 A cm at a voltage of only 1.8 V in 1 m KOH, which is similar to the performance of the proton exchange membrane water electrolyzer obtained from the IrO and Pt/C catalysts pair.
在阴离子交换膜(AEM)水电解技术中开发高效低成本的析氧电极是主要挑战之一。在此,证明了在铁和钒阳离子存在下传统泡沫镍电极的表面腐蚀可将其转变为对析氧反应(OER)具有高催化性能的电极。腐蚀后的电极由负载在泡沫镍表面的三元镍铁钒层状双氢氧化物(LDH)纳米片阵列组成。该镍铁钒LDH电极在1 m KOH中过电位为272 mV时实现了100 mA cm的OER电流密度,比IrO催化剂性能优180 mV。密度泛函理论计算表明,镍铁钒LDH中独特的结构和钒的存在对提高OER活性起关键作用。当与商业Pt/C阴极催化剂耦合时,所得的AEM水电解槽在1 m KOH中仅1.8 V的电压下实现了高达2.1 A cm的电池电流密度,这与由IrO和Pt/C催化剂对获得的质子交换膜水电解槽的性能相似。