Hu Lei, Xiong Tuzhi, Liu Ran, Hu Yuwen, Mao Yanchao, Balogun M-Sadeeq Jie Tang, Tong Yexiang
MOE of the Key Laboratory of Bioinorganic and Synthetic Chemistry, The Key Lab of Low-Carbon Chemistry & Energy Conservation of, Guangdong Province, School of Chemistry, Sun Yat-sen University, Guangzhou, 510275, P. R. China.
College of Materials Science and Engineering, Hunan University, Changsha, 410082, Hunan, P. R. China.
Chemistry. 2019 May 7;25(26):6575-6583. doi: 10.1002/chem.201900045. Epub 2019 Apr 12.
In the work reported herein, the electrocatalytic properties of Co O in hydrogen and oxygen evolution reactions have been significantly enhanced by coating a shell layer of a copper-based metal-organic framework on Co O porous nanowire arrays and using the products as high-performance bifunctional electrocatalysts for overall water splitting. The coating of the copper-based metal-organic framework resulted in the hybridization of the copper-embedded protective carbon shell layer with Co O to create a strong Cu-O-Co bonding interaction for efficient hydrogen adsorption. The hybridization also led to electronically induced oxygen defects and nitrogen doping to effectively enhance the electrical conductivity of Co O . The optimal as-prepared core-shell hybrid material displayed excellent overall-water-splitting catalytic activity that required overall voltages of 1.45 and 1.57 V to reach onset and a current density of 10 mA cm , respectively. This is the first report to highlight the relevance of hybridizing MOF-based co-catalysts to boost the electrocatalytic performance of nonprecious transition-metal oxides.
在本文报道的工作中,通过在CoO多孔纳米线阵列上包覆一层铜基金属有机框架,并将所得产物用作高效双功能电催化剂用于全水分解,CoO在析氢和析氧反应中的电催化性能得到了显著增强。铜基金属有机框架的包覆导致嵌入铜的保护碳壳层与CoO发生杂化,形成强大的Cu-O-Co键相互作用以实现高效氢吸附。这种杂化还导致电子诱导的氧缺陷和氮掺杂,从而有效提高CoO的电导率。所制备的最佳核壳杂化材料表现出优异的全水分解催化活性,分别需要1.45 V和1.57 V的全电压才能达到起始点和10 mA cm的电流密度。这是首篇强调基于金属有机框架的助催化剂杂化对提高非贵金属过渡金属氧化物电催化性能的相关性的报告。