单斜晶系
电化学
塔菲尔方程
化学
过电位
吡啶
晶体结构
金属有机骨架
无机化学
催化作用
结晶学
配体(生物化学)
配位聚合物
电催化剂
热重分析
电极
物理化学
有机化学
吸附
生物化学
受体
作者
Mengyao Ma,Liwen Wang,Jia‐Qian Jiang,Hao Yu,Wenqian Sun,Jinyan Wang,Fengdi Zhou,Xiuling Xu,Yulan Bai
标识
DOI:10.1016/j.jssc.2024.124648
摘要
Metal-organic frameworks (MOFs) have been widely used in filed of electrochemistry. Compared with traditional inorganic porous materials, the polyvalent pyridinecarboxylic acid ligands have many advantages which contains more active sites, flexible coordination mode, adjustable structure. Therefore, it becomes good choice for constructing MOFs materials with excellent performance. In this paper, a novel MOF was synthesized by pyridine polycarboxylic acid ligand and CoCl2·6H2O using solvothermal method. The physicochemical properties were characterized by FT-IR, powder diffraction and thermogravimetry. Single crystal X-ray diffraction reveal that MOF-1 crystallizes in monoclinic system with P21/C space group. The central Co2+ ions have a dual core structure with 5 and 6 coordination, respectively. The carboxyl groups show two kinds of coordination modes μ2: η1: η1 and μ2: η1: η2, and the pyridine N atoms also coordinate to form a three-dimensional network structure. Electrochemical experiments show that MOF-1 has a lower overpotential (339.4 mV) and Tafel slope (65.3 mV·dec−1) with higher ECSA and better OER kinetics. A large number of exposed active sites indicate that the MOF has higher potential as catalyst for oxygen evolution reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI