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Ruthenium(ii)-polypyridyl zirconium(iv) metal–organic frameworks as a new class of sensitized solar cells

机译:钌(II)-polypyridyl锆(IV)金属有机框架作为新的敏化太阳能电池

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A series of Ru( II )L _(2) L′ (L = 2,2′-bipyridyl, L′ = 2,2′-bipyridine-5,5′-dicarboxylic acid), RuDCBPY, -containing zirconium( IV ) coordination polymer thin films have been prepared as sensitizing materials for solar cell applications. These metal–organic framework (MOF) sensitized solar cells, MOFSCs, each are shown to generate photocurrent in response to simulated 1 sun illumination. Emission lifetime measurements indicate the excited state quenching of RuDCBPY at the MOF–TiO _(2) interface is extremely efficient (>90%), presumably due to electron injection into TiO _(2) . A mechanism is proposed in which RuDCBPY-centers photo-excited within the MOF-bulk undergo isotropic energy migration up to 25 nm from the point of origin. This work represents the first example in which a MOFSC is directly compared to the constituent dye adsorbed on TiO _(2) (DSC). Importantly, the MOFSCs outperformed their RuDCBPY–TiO _(2) DSC counterpart under the conditions used here and, thus, are solidified as promising solar cell platforms.
机译:一系列ru(ii)l _(2)l'(l = 2,2'-bibyridyl,l'= 2,2'-bijyridine-5,5,5'-二羧酸),rudcbpy,锆(IV )配位聚合物薄膜已被制备为太阳能电池应用的敏化材料。这些金属有机框架(MOF)敏化太阳能电池MOFSCs,每个MOFSCs都被示出为响应于模拟的1阳光照明而产生光电流。发射寿命测量表明MOF-TiO _(2)界面在MOF-TiO _(2)界面的激发态猝灭是非常有效的(> 90%),可能是由于电子注入到TiO _(2)中。提出了一种机制,其中在MOF-BULK内的鲁德比中心的照片激发,从原产点达到25nm的各向同性能量迁移。该工作代表了第一例,其中将MOFSC直接与吸附在TiO _(2)(DSC)上的组成染料进行比较。重要的是,MOFSCS在这里使用的条件下优于其RudcBpy-TiO_(2)DSC对应物,因此,作为有前途的太阳能电池平台固化。

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