Center for Advancing Electronics Dresden (cfaed) and Department of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.
Key Laboratory of Biomass Chemical Engineering of Ministry of Education and College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310027, China.
Adv Mater. 2017 Sep;29(35). doi: 10.1002/adma.201701589. Epub 2017 Jul 17.
Exploring efficient and earth-abundant electrocatalysts is of great importance for electrocatalytic and photoelectrochemical hydrogen production. This study demonstrates a novel ternary electrocatalyst of porous cobalt phosphoselenide nanosheets prepared by a combined hydrogenation and phosphation strategy. Benefiting from the enhanced electric conductivity and large surface area, the ternary nanosheets supported on electrochemically exfoliated graphene electrodes exhibit excellent catalytic activity and durability toward hydrogen evolution in alkali, achieving current densities of 10 and 20 mA cm at overpotentials of 150 and 180 mV, respectively, outperforming those reported for transition metal dichalcogenides and first-row transition metal pyrites catalysts. Theoretical calculations reveal that the synergistic effects of Se vacancies and subsequent P displacements of Se atoms around the vacancies in the resulting cobalt phosphoselenide favorably change the electronic structure of cobalt selenide, assuring a rapid charge transfer and optimal energy barrier of hydrogen desorption, and thus promoting the proton kinetics. The overall-water-splitting with 10 mA cm at a low voltage of 1.64 V is achieved using the ternary electrode as both the anode and cathode, and the performance surpasses that of the Ir/C-Pt/C couple for sufficiently high overpotentials. Moreover, the integration of ternary nanosheets with macroporous silicon enables highly efficient solar-driven photoelectrochemical hydrogen production.
探索高效、丰富的地球资源电催化剂对于电催化和光电化学制氢具有重要意义。本研究通过联合氢化和磷化策略展示了一种新型的多孔钴磷硒化物纳米片三元电催化剂。得益于增强的导电性和大的表面积,三元纳米片负载在电化学剥离石墨烯电极上表现出优异的析氢催化活性和耐久性,在碱性条件下,其过电位为 150 mV 和 180 mV 时,电流密度分别达到 10 mA cm 和 20 mA cm,优于报道的过渡金属二硫属化物和第一过渡金属硫化物催化剂。理论计算表明,所得钴磷硒化物中硒空位的协同作用以及随后硒原子在空位周围的磷取代有利于改变钴硒化物的电子结构,确保快速电荷转移和最佳的氢脱附能垒,从而促进质子动力学。使用三元电极作为阳极和阴极,在 1.64 V 的低电压下实现了 10 mA cm 的全水分解,其性能超过了 Ir/C-Pt/C 对足够高的过电位的性能。此外,三元纳米片与大孔硅的集成实现了高效的太阳能驱动光电化学制氢。