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

被引:140
作者
Zha, Qingqing [1 ]
Yuan, Feifei [1 ]
Qin, Guoxu [1 ]
Ni, Yonghong [1 ]
机构
[1] Anhui Normal Univ, Wuhu, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; PERFORMANCE; NANOSHEETS; NANOPARTICLES; EFFICIENCY; SURFACE; ARRAY; OER;
D O I
10.1021/acs.inorgchem.9b03011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
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'-biphenyldicar-boxylate (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 j(geo) = 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.
引用
收藏
页码:1295 / 1305
页数:11
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