Zaman Bilal, Jiao Dongxu, Fan Jinchang, Wang Dewen, Fan Huafeng, Gong Ming, Xu Shan, Liu Yanhua, Faizan Muhammad, Cui Xiaoqiang
School of Materials Science and Engineering, and Key Laboratory of Automobile Materials of MOE, Jilin University, Changchun 130012, China.
School of Materials Science and Engineering, and Key Laboratory of Automobile Materials of MOE, Jilin University, Changchun 130012, China.
J Colloid Interface Sci. 2025 Mar 15;682:548-555. doi: 10.1016/j.jcis.2024.11.246. Epub 2024 Dec 1.
RuO has been recognized as a standard electrocatalyst for acidic oxygen evolution reaction (OER). Nonetheless, its high cost and limited durability are still ongoing challenges. Herein, a RuO/Ni-CoO heterostructure confining a heterointerface (between RuO and Ni-doped CoO) is constructed to realize enhanced OER performance. Specifically, RuO/Ni-CoO containing a low Ru content (2.7 ± 0.3 wt%) achieves an overpotential of 186 mV at a current density of 10 mA cm with a long-run stability (≥1300 h). Also, it exhibits a mass activity of 1202.29 mA mg at an overpotential of 250 mV, exceeding commercial RuO. The results disclose an optimum electron transfer at the heterointerface, wherein Ni doping improves the adsorption energy of oxygen-containing intermediates, thereby facilitating OER. This study presents an effective approach for designing highly active and stable OER electrocatalysts.
RuO已被公认为酸性析氧反应(OER)的标准电催化剂。尽管如此,其高成本和有限的耐久性仍是持续存在的挑战。在此,构建了一种限制异质界面(RuO与镍掺杂的CoO之间)的RuO/Ni-CoO异质结构,以实现增强的OER性能。具体而言,含有低Ru含量(2.7±0.3 wt%)的RuO/Ni-CoO在电流密度为10 mA cm时实现了186 mV的过电位,并具有长期稳定性(≥1300 h)。此外,在250 mV的过电位下,它表现出1202.29 mA mg的质量活性,超过了商业RuO。结果揭示了在异质界面处的最佳电子转移,其中镍掺杂提高了含氧中间体的吸附能,从而促进了OER。本研究提出了一种设计高活性和稳定OER电催化剂的有效方法。