Wang Tingxia, Zhang Xu, Yu Xiaojiao, Li Junpeng, Wang Kai, Niu Jinfen
School of Science, Xi'an University of Technology, Xi'an 710054, China.
Molecules. 2024 Feb 21;29(5):951. doi: 10.3390/molecules29050951.
A bifunctional electrocatalyst with high efficiency and low costs for overall water splitting is critical to achieving a green hydrogen economy and coping with the energy crisis. However, developing robust electrocatalysts still faces huge challenges, owing to unsatisfactory electron transfer and inherent activity. Herein, NiFe LDH/NiS/VS heterojunctions have been designed as freestanding bifunctional electrocatalysts to split water, exhibiting enhanced electron transfer and abundant catalytic sites. The optimum NiFe LDH/NiS/VS electrocatalyst exhibits a small overpotential of 380 mV at 10 mA cm for overall water splitting and superior electrocatalytic performance in both hydrogen and oxygen evolution reactions (HER/OER). Specifically, the electrocatalyst requires overpotentials of 76 and 286 mV at 10 mA cm for HER and OER, respectively, in alkaline electrolytes, which originate from the synergistic interaction among the facilitated electron transfer and increasingly exposed active sites due to the modulation of interfaces and construction of heterojunctions.
一种用于全水分解的高效低成本双功能电催化剂对于实现绿色氢能经济和应对能源危机至关重要。然而,由于电子转移不令人满意和固有活性,开发稳健的电催化剂仍然面临巨大挑战。在此,NiFe LDH/NiS/VS异质结被设计为独立的双功能电催化剂用于水分解,表现出增强的电子转移和丰富的催化位点。最佳的NiFe LDH/NiS/VS电催化剂在10 mA cm下进行全水分解时表现出380 mV的小过电位,并且在析氢反应和析氧反应(HER/OER)中均具有优异的电催化性能。具体而言,该电催化剂在碱性电解质中进行HER和OER时,在10 mA cm下分别需要76和286 mV的过电位,这源于界面调制和异质结构建导致的促进电子转移和活性位点越来越多地暴露之间的协同相互作用。