Chen Guichan, Liu Jiapeng, Chen Dengjie
College of Chemistry and Materials Science, Jinan University, Guangzhou 510632, China.
School of Advanced Energy, Sun Yat-Sen University, Shenzhen 518107, China.
J Colloid Interface Sci. 2025 Jan 15;678(Pt B):506-517. doi: 10.1016/j.jcis.2024.09.002. Epub 2024 Sep 3.
Although decorated nanoparticles offer a great potential to generate extra active sites, their preparation usually requires time- and energy-consuming approaches. We report the remarkable activity and durability augmentation for the oxygen evolution reaction (OER) via effective and facile on-site electrochemical manipulation, using LaNiO as a model catalyst. When compared to the pristine LaNiO, the electrochemically manipulated LaNiO cycled in Fe-containing 0.1 M KOH (i.e., E-LNO+Fe) exhibits an almost three-fold improvement in current density at 1.65 V. It is experimentally and theoretically shown that the electrochemical manipulation leads to the creation of defective LaNiO and NiO on the surfaces, which accelerate phase transformation to (oxy)hydroxides and hence the OER. Furthermore, a Zn-air battery assembled with E-LNO+Fe has demonstrated superior activity by presenting 171 mW cm. Thus, our work demonstrates that substantial performance increases may be achieved by decorating and reconstructing perovskite-oxide electrodes via on-site electrochemical modification.
尽管修饰后的纳米颗粒具有产生额外活性位点的巨大潜力,但其制备通常需要耗时且耗能的方法。我们报道了通过有效且简便的现场电化学操作,以LaNiO为模型催化剂,显著提高了析氧反应(OER)的活性和耐久性。与原始的LaNiO相比,在含Fe的0.1 M KOH中循环的电化学操作后的LaNiO(即E-LNO+Fe)在1.65 V时的电流密度提高了近三倍。实验和理论表明,电化学操作导致表面形成有缺陷的LaNiO和NiO,加速了向(氧)氢氧化物的相变,从而促进了OER。此外,用E-LNO+Fe组装的锌空气电池通过呈现171 mW cm的功率表现出优异的活性。因此,我们的工作表明,通过现场电化学修饰对钙钛矿氧化物电极进行修饰和重构可以实现性能的大幅提升。