Tian Liang, Wang Qiangqiang, Li Yuyang, Ren Xiang, Wei Qin, Wu Dan
Collaborative Innovation Centre for Green Chemical Manufacturing and Accurate Detection School of Chemistry and Chemical Engineering, University of Jinan, Jinan, 250022, Shandong, China.
Key Laboratory of Interfacial Reaction & Sensing Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan, 250022, Shandong, China.
Dalton Trans. 2022 Jul 12;51(27):10552-10557. doi: 10.1039/d2dt01257j.
The oxygen evolution reaction (OER) has become the main barrier to electrochemical water splitting, owing to sluggish kinetics. To accelerate the OER process, a nature-abundant non-noble metal catalyst with outstanding catalytic activity is required. Here, a hierarchical CoMoO@CoFe layered double hydroxide (LDH, denoted by CoMoO@CoFe/NF) heterostructure supported on three-dimensional (3D) nickel foam (NF) was synthesised by electrodepositing CoFe-LDH nanosheets on the surface of CoMoO nanoplates to boost the electrocatalytic performance for the OER. The coupling between CoMoO and CoFe-LDH established abundant boundaries, which exposed abundant active sites. Furthermore, the electron transfer in the hierarchical heterostructure effectively promoted the adsorption and dissociation of HO molecules. Harnessing the aforementioned synergistic effect significantly improved the intrinsic reaction kinetics of the OER. At 10 mA cm, CoMoO@CoFe/NF reached a small overpotential of 245 mV at room temperature and exhibited outstanding stability for at least 47 h. Furthermore, the Tafel slope for CoMoO@CoFe/NF was only 46 mV dec. This study provides new ideas for the rational design of hierarchical structures and the use of interface interactions.
由于动力学缓慢,析氧反应(OER)已成为电化学水分解的主要障碍。为了加速OER过程,需要一种具有出色催化活性的天然丰富的非贵金属催化剂。在此,通过在CoMoO纳米片表面电沉积CoFe-LDH纳米片,合成了一种负载在三维(3D)泡沫镍(NF)上的分级CoMoO@CoFe层状双氢氧化物(LDH,记为CoMoO@CoFe/NF)异质结构,以提高对OER的电催化性能。CoMoO与CoFe-LDH之间的耦合建立了丰富的边界,从而暴露出丰富的活性位点。此外,分级异质结构中的电子转移有效地促进了HO分子的吸附和解离。利用上述协同效应显著改善了OER的本征反应动力学。在10 mA cm时,CoMoO@CoFe/NF在室温下达到了245 mV的小过电位,并表现出至少47 h的出色稳定性。此外,CoMoO@CoFe/NF的塔菲尔斜率仅为46 mV dec。该研究为分级结构的合理设计和界面相互作用的利用提供了新思路。