Cobalt-Based MOF-on-MOF Two-Dimensional Heterojunction Nanostructures for Enhanced Oxygen Evolution Reaction Electrocatalytic Activity

异质结 化学 析氧 电化学 金属有机骨架 纳米结构 化学工程 电极 无机化学 纳米技术 材料科学 物理化学 吸附 光电子学 物理 工程类
作者
Qingqing Zha,Feifei Yuan,Guoxu Qin,Yonghong Ni
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:59 (2): 1295-1305 被引量:173
标识
DOI:10.1021/acs.inorgchem.9b03011
摘要

Two-dimensional (2D) Co-based MOF-on-MOF heterojunction nanostructures with improved electrocatalytic activity were successfully constructed via a mild two-step solution route, employing Co2+ ions as the center atoms, and 1,4-benzenedicarboxylate (BDC) and 4,4'-biphenyldicarboxylate (BPDC) as ligands. The as-obtained heterojunction nanostructures were characterized by field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Brunauer-Emmett-Teller (BET) surface area analysis, thermogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS) technologies. Electrochemical measurements showed that as-prepared Co-BPDC/Co-BDC heterojunction nanostructures presented markedly enhanced OER electrocatalytic activity, compared with single Co-BPDC, Co-BDC, and/or their physical mixture. Also, the Co-BPDC/Co-BDC-3 heterojunction prepared after treatment for 3 h exhibited the strongest catalytic activity. To reach the current density jgeo = 10 mA cm-2, the Co-BPDC/Co-BDC-3 heterojunction-modified glassy carbon electrode required an overpotential of 335 mV in 1 M KOH, which was reduced by 57 and 93 mV, compared to the electrodes modified by Co-BDC and Co-BPDC, respectively. Simultaneously, the heterojunction catalyst also displayed better long-term stability. The improvement of the above performances should be attributed to the increased structure stability, BET surface area, ECSA, and electron transfer ability of the heterojunction.
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