Electron transfer at single CdSe/ZnS quantum dot/adsorbate interface

Abey Issac*, Shengye Jin, Tianquan Lian

*المؤلف المقابل لهذا العمل

نتاج البحث: Conference contribution


Electron transfer at quantum dot/molecule interface has become a subject of intense recent interest because of the application of quantum dots (QDs) in novel solar cells and because of its ability to generate multiple excitons with one absorbed photon. Ensemble averaged ultrafast spectroscopic studies show that photoinduced interfacial electron transfer (IFET) between CdS or CdSe QDs and Rhodamine B molecules exhibit multi-exponential kinetics. Fluctuation in emission intensity (blinking) and exciton lifetimes have also been observed on single QDs. To understand how the dynamic and static heterogeneity contribute to the interfacial electron transfer from and to QDs, we have studied these dynamics in single CdSe/ZnS quantum dots attached with Rhodamine B molecules. Our results showed that the fluorescence lifetime of individual QD-dye nanoassembly is shorter than that of QDs, suggesting the quenching of excitons by interfacial electron transfer. The rate of electron transfer was shown to increase with number of dyes per QD. We will discuss the static and dynamic distributions of ET rates at the single quantum dot/adsorbate interface.

اللغة الأصليةEnglish
عنوان منشور المضيفAmerican Chemical Society - 235th National Meeting, Abstracts of Scientific Papers
حالة النشرPublished - 2008
منشور خارجيًانعم
الحدث235th National Meeting of the American Chemical Society, ACS 2008 - New Orleans, LA, United States
المدة: أبريل ٦ ٢٠٠٨أبريل ١٠ ٢٠٠٨

سلسلة المنشورات

الاسمACS National Meeting Book of Abstracts
رقم المعيار الدولي للدوريات (المطبوع)0065-7727


Other235th National Meeting of the American Chemical Society, ACS 2008
الدولة/الإقليمUnited States
المدينةNew Orleans, LA

ASJC Scopus subject areas

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