He Xuanmeng, Qiao Tong, Zhang Zeqin, Liu Hui, Wang Shaolan, Wang Xinzhen
School of Materials Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, PR China.
School of Materials Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, PR China.
J Colloid Interface Sci. 2023 Nov;649:635-645. doi: 10.1016/j.jcis.2023.06.084. Epub 2023 Jun 17.
Developing transition metal oxide catalysts to replace the noble metal oxide catalysts for efficient oxygen evolution reaction (OER) is essential to promote the practical application of water splitting. Herein, we designed and constructed the carbon cloth (CC) supporting spinel CuMnCoO nanoneedles with regulated electronic structure by multiple metal elements with variable chemical valences in the spinel CuMnCoO. The carbon cloth not only provided good conductivity for the catalytic reaction but also supported the well-standing spinel CuMnCoO nanoneedles arrays with a large special surface area. Meanwhile, the well-standing nanoneedles arrays and mesoporous structure of CuMnCoO nanoneedles enhanced their wettability and facilitated access for electrolyte to electrochemical catalysis. Besides, the regulated electronic structure and generated oxygen vacancies of CuMnCoO/CC by multiple metal elements improved the intrinsic catalytic activity and the durability of OER activity. Profiting from these merits, the CuMnCoO/CC electrode exhibited superior OER activity with an ultralow overpotential of 189 mV at the current density of 10 mA⋅cm and a smaller Tafel slope of 64.1 mV⋅dec, which was competitive with the noble metal oxides electrode. And the CuMnCoO/CC electrode also exhibited long-term durability for OER with 95.3% of current retention after 1000 cycles. Therefore, the competitive OER activity and excellent cycling durability suggested that the CuMnCoO/CC electrode is a potential candidate catalyst for efficient OER.
开发过渡金属氧化物催化剂以取代贵金属氧化物催化剂用于高效析氧反应(OER)对于推动水分解的实际应用至关重要。在此,我们设计并构建了由具有可变化学价态的多种金属元素调控电子结构的碳布(CC)负载尖晶石CuMnCoO纳米针。碳布不仅为催化反应提供了良好的导电性,还支撑了具有大比表面积的直立尖晶石CuMnCoO纳米针阵列。同时,CuMnCoO纳米针的直立纳米针阵列和介孔结构增强了它们的润湿性,并促进电解质进入电化学催化。此外,多种金属元素对CuMnCoO/CC电子结构的调控和产生的氧空位提高了其本征催化活性和OER活性的耐久性。得益于这些优点,CuMnCoO/CC电极在10 mA·cm的电流密度下表现出优异的OER活性,过电位仅为189 mV,塔菲尔斜率为64.1 mV·dec,与贵金属氧化物电极具有竞争力。并且CuMnCoO/CC电极在OER方面也表现出长期耐久性,在1000次循环后电流保留率为95.3%。因此,具有竞争力的OER活性和出色的循环耐久性表明CuMnCoO/CC电极是高效OER的潜在候选催化剂。