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Perovskite-Like Metal-Organic Framework of Cobalt Formate as High-Performance Electrocatalyst for Dye-Sensitized
Yu-Chien Lee1,2,3, Chun-Ting Li1
1Department of Chemistry, National Taiwan Normal University, Taipei, 11677, Taiwan.
Abstract:
Perovskite-like metal-organic framework of cobalt formate, that is, [(CH3)2NH2][Co(HCOO)3]n (denoted as Co(HCOO)3), has successfully grown on a conductive carbon cloth (CC) with or without surfactant. The insertion of various thiolate surfactants, for example, 2-mercaptobenzoxazole (MBO), 2-mercaptobenzimidazole (MBI), and 2-mercaptobenzothiazole (MBT), effectively confined the particle size to microcubes owing to the core@shell structure of H2O@dimethylformamide (DMF) reverse micelles. The insertion of benzeneselenolate (PhSe-) caused the formation of both microcubes and nanotubes. When some H2O@DMF reverse micelles were intensively surrounded by benzeneselenious anions (R-SeO3 - or R-SeO2 -), the strong π-π stacking among benzenes would induce the crystal growth through 1D direction, leading to the formation of Co(HCOO)3 nanotubes uniformly covered on CC. Among all the CC/Co(HCOO)3 electrodes, the CC/PhSe-doped Co(HCOO)3 electrodes reached the optimal electrocatalytic performance toward triiodide reduction, and thereby functioned as the outstanding counter electrode in dye-sensitized solar cell (DSSC). Good DSSCs' efficiencies of 9.73% (1 sun) and 24% (at 6 klux) can be obtained by using CC/PhSe-doped Co(HCOO)3, which surpassed the cells with CC/bare Co(HCOO)3 (5.25% at 1 sun) and the benchmark CC/Pt (9.85% at 1 sun), owing to numerous electro-donating R-SeO3 -/R-SeO2 - dopants as active sites and facile 1D charge-transfer pathways.
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