Liao Linqing, Gou Wangyan, Zhang Mingkai, Tan Xiaohe, Qi Zening, Xie Min, Ma Yuanyuan, Qu Yongquan
Research & Development Institute of Northwestern Polytechnical University in Shenzhen, Shenzhen, 518057, China.
Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an, 710072, China.
Nanoscale Horiz. 2025 Feb 24;10(3):586-595. doi: 10.1039/d4nh00437j.
Over-oxidation of surface ruthenium active sites of RuO-based electrocatalysts leads to the formation of soluble high-valent Ru species and subsequent structural collapse of electrocatalysts, which results in their low stability for the acidic oxygen evolution reaction (OER). Herein, a binary RuO/NbO electrocatalyst with abundant and intimate interfaces has been rationally designed and synthesized to enhance its OER activity in acidic electrolyte, delivering a low overpotential of 179 mV at 10 mA cm, a small Tafel slope of 73 mV dec, and a stabilized catalytic durability over a period of 750 h. Extensive experiments have demonstrated that the spillover of active oxygen intermediates from RuO to NbO and the subsequent participation of lattice oxygen of NbO instead of RuO for the acidic OER suppressed the over-oxidation of surface ruthenium species and thereby improved the catalytic stability of the binary electrocatalysts.
基于RuO的电催化剂表面钌活性位点的过度氧化会导致可溶性高价钌物种的形成以及电催化剂随后的结构坍塌,这导致其在酸性析氧反应(OER)中稳定性较低。在此,一种具有丰富且紧密界面的二元RuO/NbO电催化剂被合理设计并合成,以增强其在酸性电解质中的OER活性,在10 mA cm时具有179 mV的低过电位、73 mV dec的小塔菲尔斜率以及在750小时内稳定的催化耐久性。大量实验表明,活性氧中间体从RuO溢流到NbO以及随后NbO而非RuO的晶格氧参与酸性OER抑制了表面钌物种的过度氧化,从而提高了二元电催化剂的催化稳定性。