Zhang Lijie, Jang Haeseong, Liu Huihui, Kim Min Gyu, Yang Dongjiang, Liu Shangguo, Liu Xien, Cho Jaephil
State Key Laboratory Based of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, 266042, P. R. China.
Department of Energy Engineering, Department of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, South Korea.
Angew Chem Int Ed Engl. 2021 Aug 16;60(34):18821-18829. doi: 10.1002/anie.202106631. Epub 2021 Jul 12.
The oxygen evolution reaction (OER) is a key reaction for many electrochemical devices. To date, many OER electrocatalysts function well in alkaline media, but exhibit poor performances in neutral and acidic media, especially the acidic stability. Herein, sodium-decorated amorphous/crystalline RuO with rich oxygen vacancies (a/c-RuO ) was developed as a pH-universal OER electrocatalyst. The a/c-RuO shows remarkable resistance to acid corrosion and oxidation during OER, which leads to an extremely high catalytic stability, as confirmed by a negligible overpotential increase after continuously catalyzing OER for 60 h at pH=1. Besides, a/c-RuO also exhibits superior OER activities to commercial RuO and most reported OER catalysts under all pH conditions. Theoretical calculations indicated that the introduction of Na dopant and oxygen vacancy in RuO weakens the adsorption strength of the OER intermediates by engineering the d-band center, thereby lowering the energy barrier for OER.
析氧反应(OER)是许多电化学装置中的关键反应。迄今为止,许多OER电催化剂在碱性介质中表现良好,但在中性和酸性介质中表现不佳,尤其是酸性稳定性。在此,开发了具有丰富氧空位的钠修饰非晶态/晶态RuO(a/c-RuO)作为一种pH通用的OER电催化剂。a/c-RuO在OER过程中表现出对酸腐蚀和氧化的显著抗性,这导致了极高的催化稳定性,在pH = 1下连续催化OER 60小时后过电位增加可忽略不计,这证实了这一点。此外,在所有pH条件下,a/c-RuO对商业RuO和大多数报道的OER催化剂也表现出优异的OER活性。理论计算表明,在RuO中引入Na掺杂剂和氧空位通过设计d带中心减弱了OER中间体的吸附强度,从而降低了OER的能垒。