Huang Jin, Li Yun, Huang Rui-Kang, He Chun-Ting, Gong Li, Hu Qiong, Wang Lishi, Xu Yan-Tong, Tian Xiao-Yun, Liu Si-Yang, Ye Zi-Ming, Wang Fuxin, Zhou Dong-Dong, Zhang Wei-Xiong, Zhang Jie-Peng
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, China.
Instrumental Analysis and Research Center, Sun Yat-Sen University, Guangzhou, 510275, China.
Angew Chem Int Ed Engl. 2018 Apr 16;57(17):4632-4636. doi: 10.1002/anie.201801029. Epub 2018 Mar 13.
Two-dimensional (2D) materials and ultrathin nanosheets are advantageous for elevating the catalysis performance and elucidating the catalysis mechanism of heterogeneous catalysts, but they are mostly restricted to inorganic or organic materials based on covalent bonds. We report an electrochemical/chemical exfoliation strategy for synthesizing metal-organic 2D materials based on coordination bonds. A catechol functionalized ligand is used as the redox active pillar to construct a pillared-layer framework. When the 3D pillared-layer MOF serves as an electrocatalyst for water oxidation (pH 13), the pillar ligands can be oxidized in situ and removed. The remaining ultrathin (2 nm) nanosheets of the metal-organic layers are an efficient catalyst with overpotentials as low as 211 mV at 10 mA cm and a turnover frequency as high as 30 s at an overpotential of 300 mV.
二维(2D)材料和超薄纳米片有利于提高多相催化剂的催化性能并阐明其催化机理,但它们大多局限于基于共价键的无机或有机材料。我们报道了一种基于配位键合成金属有机二维材料的电化学/化学剥离策略。一种儿茶酚官能化配体用作氧化还原活性支柱以构建柱状层框架。当三维柱状层金属有机框架用作水氧化(pH = 13)的电催化剂时,支柱配体可原位氧化并去除。剩余的金属有机层超薄(2纳米)纳米片是一种高效催化剂,在10 mA cm时过电位低至211 mV,在300 mV过电位下周转频率高达30 s。