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从中性和三重激发态的卟啉分子到胶体 TiO2 和 AuTiO2 纳米粒子的电子转移动力学。

Electron transfer dynamics from the singlet and triplet excited states of meso-tetrakis(p-carboxyphenyl)porphyrin into colloidal TiO2 and AuTiO2 nanoparticles.

机构信息

School of Chemistry, Bharathidasan University, Tiruchirappalli 620 024, Tamil Nadu, India.

出版信息

J Colloid Interface Sci. 2010 Aug 15;348(2):642-8. doi: 10.1016/j.jcis.2010.05.002. Epub 2010 May 7.

Abstract

Electron transfer dynamics of meso-tetrakis(p-carboxyphenyl)porphyrin [TCPP] adsorbed on colloidal TiO(2) and AuTiO(2) nanoparticles have been investigated by time resolved absorption and fluorescence spectroscopy. Optical absorption studies reveal that the TCPP form complex with TiO(2) and AuTiO(2) nanoparticles. Excitation of TCPP adsorbed on the TiO(2) nanoparticle surface leads to electron injection on the conduction band of TiO(2). Electron injection has been confirmed by direct detection of cation radical of the adsorbed dye (TCPP*(+)). The rate constant for the electron injection process is determined from both the singlet and triplet state respectively. The rate of electron injection for TCPP-AuTiO(2) is much faster than TCPP-TiO(2). The injected electrons are quickly transferred to Au and it escorts to ignore the back electron transfer (recombination) process.

摘要

通过时间分辨吸收和荧光光谱法研究了吸附在胶体 TiO(2)和 AuTiO(2)纳米粒子上的间四(对羧基苯基)卟啉[TCPP]的电子转移动力学。光学吸收研究表明,TCPP 与 TiO(2)和 AuTiO(2)纳米粒子形成配合物。在 TiO(2)纳米粒子表面吸附的 TCPP 的激发导致电子注入 TiO(2)的导带。通过直接检测吸附染料(TCPP*(+))的阳离子自由基,证实了电子注入。电子注入过程的速率常数分别从单重态和三重态确定。TCPP-AuTiO(2)的电子注入速率比 TCPP-TiO(2)快得多。注入的电子很快转移到 Au 上,并忽略了反向电子转移(复合)过程。

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