Electrochemical Self-Assembly of CuSCN/4-Cyano-4’-(N’-methyl)Stilbazolium Hybrid Thin Films
Electrochemical Self-Assembly of CuSCN/4-Cyano-4’-(N’-methyl)Stilbazolium Hybrid Thin Films
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CuSCN/4-Cyano-4-(N-甲基)芪唑杂化薄膜的电化学自组装
DOI:
10.1149/09707.0457ecst
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发表时间:
2020
期刊:
影响因子:
--
通讯作者:
Yoshida Tsukasa
中科院分区:
文献类型:
--
作者:
Tsuda Yuki;Suzuki Toru;Nakamura Tensho;Uda Kyota;Okada Shuji;Yamakado Ryohei;Stadler Philipp;Yoshida Tsukasa
Electrochemical self-assembly (ESA) of CuSCN/4-cyano-4’-(N’-methyl) stilbazolium (CNS+) hybrid thin films has been performed and analyzed in comparison with CuSCN/4-(N, N-dimethylamino)-4’-(N’-methyl) stilbazolium (DAS+) hybrid system. Due to the presence of strongly electron-withdrawing-CN group, CNS+ has a much higher dipole moment than DAS+ to exhibit stronger affinity to CuSCN. CNS+ therefore gave strong impact to the crystal growth of CuSCN with its smaller concentration than DAS+, such as changing crystal orientation, creating unique nanostructure and phase transition from β-to α-CuSCN. CNS+ has been found to obey the same mechanism as DAS+ for its loading into the film. The limit for diffusion limited loading was pushed up to its bulk concentration of 200 mol dm-3, much higher than that for DAS+(60 mol dm-3). Also, the efficiency of dye uptake in the surface reaction limited loading was enhanced about 3 times due to the improved stability of CuSCN/CNS surface complex.