Facile preparation of a polymer-ZnO composite colloid as an electron transport layer and its effects on inverted polymer solar cells
- Authors
- Yi, Mo-Beom; Ku, Ja Ram; Yoon, Jin Soo; Kal, Jinha; Lee, Wonhee; Oh, Seong-Geun
- Issue Date
- Oct-2020
- Publisher
- Pergamon Press Ltd.
- Keywords
- ZnO; Electron transport layer; Inverted polymer solar cell; Sol-gel synthesis; Organic-inorganic composite
- Citation
- Journal of Physics and Chemistry of Solids, v.145, pp 1 - 9
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Physics and Chemistry of Solids
- Volume
- 145
- Start Page
- 1
- End Page
- 9
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/32738
- DOI
- 10.1016/j.jpcs.2020.109538
- ISSN
- 0022-3697
1879-2553
- Abstract
- A polymer-ZnO colloidal solution was prepared as the organic-inorganic composite electron transport layer of inverted polymer solar cells (i-PSCs) by successive modification of ZnO particles with organic dispersant and polyethyleneimine (PEI), which offers an alternative to previously used complicated processes such as high temperature annealing or multi-layer coatings. The modification of ZnO surfaces with 2-(2-methoxyethoxy) acetic acid (MEA) provides colloidal stability and prevents aggregation of ZnO particles after adding PEI into the ZnO colloidal solution. The amount of incorporated PEI was increased to similar to 10 wt%, and the cell performance parameters of Jsc and fill factor (FF) were enhanced proportional to PEI content because of its contribution in decreasing the work function of ZnO ETL. By fabrication of i-PSCs with the modified ZnO ETL, the power conversion efficiency (PCE) was increased by similar to 40% from 5.10% to 7.51% in the ITO/ETL/PV-D4610:PC60BM/ MoO3/Ag structure. The multi-functionalized ZnO ETL provides a more facile process for preparation of an organic-inorganic composite ETL to improve the performance of i-PSCs.
- Files in This Item
-
Go to Link
- Appears in
Collections - 서울 공과대학 > 서울 화학공학과 > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.