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首页> 外文期刊>Dyes and Pigments >Synthesis, spectral and electrochemical properties of pyrimidine-containing dyes as photosensitizers for dye-sensitized solar cells
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Synthesis, spectral and electrochemical properties of pyrimidine-containing dyes as photosensitizers for dye-sensitized solar cells

机译:含嘧啶染料作为染料敏化太阳能电池的光敏剂的合成,光谱和电化学性质

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Six novel donor—π—acceptor organic dyes bearing a pyrimidine as the anchoring group have been obtained in good yields by combination of the microwave-assisted Suzuki cross-coupling and nucleophilic aromatic substitution of hydrogen reactions. Their absorption, photoluminescence and electrochemical properties were fully investigated in detail. The infrared spectra of dyes adsorbed on TiO2 indicate the formation of coordinate bonds between the pyrimidine ring of dyes and the Lewis acid sites (exposed Ti~(n+) cations) of the TiO2 surface. This work demonstrates that the pyrimidine rings of dye sensitizers that form a coordinate bond with the Lewis acid site of a TiO2 surface are promising candidates as the electron-withdrawing anchoring group. The data from quantum calculations show that all of the dyes are potentially good photosensitizers for dye-sensitized solar cells.
机译:通过微波辅助的Suzuki交叉偶联和氢反应的亲核芳族取代相结合,以高收率获得了六种带有嘧啶作为锚定基团的新型供体-π-受体有机染料。对它们的吸收,光致发光和电化学性质进行了详细的研究。吸附在TiO2上的染料的红外光谱表明,染料的嘧啶环与TiO2表面的路易斯酸位(暴露的Ti〜(n +)阳离子)之间形成了配位键。这项工作表明,与TiO2表面的路易斯酸位点形成配位键的染料敏化剂的嘧啶环有望作为吸电子的锚定基团。量子计算得出的数据表明,所有染料对于染料敏化太阳能电池都是潜在的良好光敏剂。

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