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An In-Situ Reaction Route to Molecular Level Dispersed Bisimide and ZnO Nanorod Hybrids with Efficient Photo-Induced Charge Transfer

Authors :
Chunzheng Lv
Lirong He
Jiahong Tang
Feng Yang
Chuhong Zhang
Source :
Nanoscale Research Letters, Vol 16, Iss 1, Pp 1-8 (2021)
Publication Year :
2021
Publisher :
SpringerOpen, 2021.

Abstract

Abstract As an important photoconductive hybrid material, perylene/ZnO has attracted tremendous attention for photovoltaic-related applications, but generally faces a great challenge to design molecular level dispersed perylenes/ZnO nanohybrids due to easy phase separation between perylenes and ZnO nanocrystals. In this work, we reported an in-situ reaction method to prepare molecular level dispersed H-aggregates of perylene bisimide/ZnO nanorod hybrids. Surface photovoltage and electric field-induced surface photovoltage spectrum show that the photovoltage intensities of nanorod hybrids increased dramatically for 100 times compared with that of pristine perylene bisimide. The enhancement of photovoltage intensities resulting from two aspects: (1) the photo-generated electrons transfer from perylene bisimide to ZnO nanorod due to the electric field formed on the interface of perylene bisimide/ZnO; (2) the H-aggregates of perylene bisimide in ZnO nanorod composites, which is beneficial for photo-generated charge separation and transportation. The introduction of ordered self-assembly thiol-functionalized perylene-3,4,9,10-tetracarboxylic diimide (T-PTCDI)/ ZnO nanorod composites induces a significant improvement in incident photo-to-electron conversion efficiency. This work provides a novel mentality to boost photo-induced charge transfer efficiency, which brings new inspiration for the preparation of the highly efficient solar cell.

Details

Language :
English
ISSN :
1556276X
Volume :
16
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nanoscale Research Letters
Publication Type :
Academic Journal
Accession number :
edsdoj.02f0456705d440da82269f9a055c42fa
Document Type :
article
Full Text :
https://doi.org/10.1186/s11671-021-03504-3