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Attachment of protoporphyrin dyes to nanostructured Zno surfaces: Characterization by near edge X-ray absorption fine structure spectroscopy

机译:原卟啉染料附着到纳米结构的Zno表面上:通过近边缘X射线吸收精细结构光谱表征

摘要

The attachment of H2- and metal (Co- and Zn-) protoporphyrin IX molecules to ZnO nanorods and single-crystal surfaces is investigated by Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy. The carboxyl groups of the protoporphyrin are found to be essential for anchoring the molecules to ZnO surfaces. The crystallographic orientation of the exposed ZnO face has an influence on the dye immobilization, with the highest uptake observed for the oxygen-terminated ZnO (000-1) surface. The preparation conditions are crucial for the dye immobilization. Under certain preparation conditions, there is a Zn atom exchange between the H2-protoporphyrin and the ZnO surface, i.e., a metalation of H2-protoporphyrin IX to form Zn-protoporphyrin. Moreover, in the presence of chenodeoxycholic acid as coabsorber, the ZnO single-crystal surfaces are etched, as indicated by the loss of the orientation-dependent spectral features. These results help to pinpoint the chemical reactions that are responsible for the poor efficiency of ZnO-based dye-sensitized solar cells, especially those built from ZnO nanorod arrays. © 2011 American Chemical Society.
机译:通过近边缘X射线吸收精细结构(NEXAFS)光谱研究了H2-和金属(钴和Zn-)原卟啉IX分子对ZnO纳米棒和单晶表面的附着。发现原卟啉的羧基对于将分子锚定至ZnO表面是必不可少的。暴露的ZnO面的晶体学取向会影响染料的固定化,对于氧封端的ZnO(000-1)表面,其吸收率最高。制备条件对于染料固定至关重要。在某些制备条件下,H2-原卟啉与ZnO表面之间存在Zn原子交换,即H2-原卟啉IX的金属化以形成Zn-原卟啉。而且,在鹅去氧胆酸作为共吸收剂的存在下,如取向依赖性光谱特征的丧失所表明的,ZnO单晶表面被蚀刻。这些结果有助于查明导致ZnO基染料敏化太阳能电池(尤其是由ZnO纳米棒阵列构建的太阳能电池)效率低下的化学反应。 ©2011美国化学学会。

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