Issue 11, 2015

Carbon-encapsulated CdSe quantum dot inorganic hybrid nanobelts for high performance photoelectronic devices based on the efficient separation and transfer of photoinduced holes

Abstract

We developed a facile method of combustion synthesis followed by a selenylation process to synthesize carbon-encapsulated CdSe hybrid nanobelts. In the nanohybrids, hexagonal-wurtzite-structured CdSe quantum dots (QDs) are formed in situ and embedded uniformly in the carbon nanobelt (CNB) matrix, resulting in the formation of an analogous p–i–n junction along the radius of the QDs due to the appearance of an inversion layer on the QD surfaces, which favors the separation of photoexcited electron–hole pairs by built-in electric field. Electrons accumulate in the QD core, while holes migrate to the QD surface and then quickly transfer to the CNB matrix. Additionally, the nanohybrids can enhance significantly the absorption of the whole energy range of visible light. The nanohybrids can show p-type conductivity with hole mobility as high as 1.4 × 104 cm2 V−1 s−1, and, furthermore, the single nanohybrid-based devices not only show excellent photodetection performance at a certain bias, but also show photovoltaic-based self-powered photodetection performance at zero bias upon illuminating one end electrode of the devices, pointing a way to the development of novel photoelectronic materials and devices for energy applications.

Graphical abstract: Carbon-encapsulated CdSe quantum dot inorganic hybrid nanobelts for high performance photoelectronic devices based on the efficient separation and transfer of photoinduced holes

Article information

Article type
Paper
Submitted
03 Dec 2014
Accepted
14 Jan 2015
First published
16 Jan 2015

J. Mater. Chem. C, 2015,3, 2471-2478

Author version available

Carbon-encapsulated CdSe quantum dot inorganic hybrid nanobelts for high performance photoelectronic devices based on the efficient separation and transfer of photoinduced holes

J. Zhao, M. Cao, B. Cheng, G. Wu, H. Guo, Y. Ai, X. Su, Y. Xiao and S. Lei, J. Mater. Chem. C, 2015, 3, 2471 DOI: 10.1039/C4TC02776K

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