Abstract
In this paper, we report on the use of molecular level interaction between a composite poly(3,4-ethylenedioxythiophene): poly (styrene sulfonate) (PEDOT: PSS) and graphene oxide (GO) hole transport layer (HTL) to improve the long term stability and performance of poly(3-hexylthiophene): poly(3-hexylthiophene): 3′H-cyclopropa [8,25] [5,6] fullerene-C60-D5h(6)-3′-butanoic acid 3′-phenyl methyl ester (P3HT: PCBM)-based bulk heterojunction organic solar cells (OSCs). The device employing this composite HTL demonstrated a maximum power conversion efficiency (PCE) of 4.82% with good reproducibility and retained over 30% of its initial PCE without encapsulation after 15 days under atmospheric conditions. This was a significant improvement compared with devices fabricated with either single GO or PEDOT: PSS HTLs, which retained only 26% and 0% of their initial PCE values of 3.16% and 4.00%, respectively. Hence, we imagine that this air resistant HTL composite will probably contribute significantly to the widespread commercialization of low cost and easily fabricated OSCs.
| Original language | English |
|---|---|
| Pages (from-to) | 24-34 |
| Number of pages | 11 |
| Journal | Solar Energy |
| Volume | 167 |
| DOIs | |
| State | Published - Jun 2018 |
Keywords
- Au
- Bulk heterojunction organic solar cell
- Device fabrication
- GO/PEDOT: PSS
- P3HT-PCBM
- Thin-film deposition
- ZnO