Electrodeposition of inorganic compound thin films in the presence of certain organic molecules results in self‐assembly of various hybrid thin films with new properties. Examples of new discoveries by the authors are reviewed, taking cathodic formation of a ZnO/dye hybrid as the leading example. Hybridization of eosinY leads to the formation of highly oriented porous crystalline ZnO as the consequence of dye loading. The hybrid formation is a highly complicated process involving complex chemistry of many molecular and ionic constituents. However, electrochemical analyses of the relevant phenomena indicate the possibility of reaching a comprehensive understanding of the mechanism, giving us the chance to further develop them into industrial technologies. The porous crystals are ideal for photoelectrodes in dye‐sensitized solar cells. As the process also permits the use of non‐heat‐resistant substrates, the technology can be applied for the development of colorful and light‐weight plastic solar cells.
We have developed an efficient, cyan-colored, and novel squaraine-dye-sensitized ZnO solar cell, producing a maximum incident photon-to-electron conversion efficiency (IPCE) of 59% at 630 nm. The solar cell sensitized by Sq 3 having bulky groups to prevent aggregation of dyes has achieved a 1.5% solar-to-electricity conversion efficiency (η) with a short-circuit current density of 4.04 mA cm−2, an open-circuit photovoltage of 0.61 V, and a fill factor of 0.61 under standard AM 1.5 irradiation (100 mW cm−2).
Novel fluorescent dyes, thiazole-boron complexes bearing β-ketoiminate ligands, have been synthesized, and their fluorescence properties were investigated. The BF(2) complexes showed a pronounced aggregation-induced emission enhancement effect because of the restriction of C-Ph intramolecular rotation. The BPh(2) complexes showed higher fluorescence quantum yields than the corresponding BF(2) complexes, both in solution and in the solid state.
A fluorescent dye, the pyridomethene-BF(2) complex, has been synthesized. Although pyridomethenes did not exhibit fluorescence, pyridomethene-BF(2) complexes exhibited fluorescence both in solution and in the solid state. The trifluoromethyl-substituted BF(2) complex formed a J-aggregate and showed the highest fluorescence quantum yield in the solid state among all pyridomethene-BF(2) complexes.
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