[PDF][PDF] Ternary organic solar cells offer 14% power conversion efficiency

Z Xiao, X Jia, L Ding - Sci. Bull, 2017 - researchgate.net
The ZnO precursor solution was prepared according to literature.[1] It was spin-coated onto
ITO glass (4000 rpm for 30 s). The films were annealed at 200 C in air for 20 min. ZnO film …

A–D–A small molecule acceptors with ladder-type arenes for organic solar cells

D He, F Zhao, L Jiang, C Wang - Journal of Materials Chemistry A, 2018 - pubs.rsc.org
A–D–A small molecule acceptors (SMAs) have attracted much attention due to their merits of
strong absorption, low bandgap, relatively high electron mobility and suitable miscibility with …

Fullerene based acceptors for efficient bulk heterojunction organic solar cell applications

R Ganesamoorthy, G Sathiyan, P Sakthivel - Solar Energy Materials and …, 2017 - Elsevier
Bulk hetro-junction organic solar cells (BHJ-OSCs) which made by coating the blend of
highly electron rich, poly-3-hexylthiophene (P3HT) as a donor and extremely electron …

Assessing intra-and inter-molecular charge transfer excitations in non-fullerene acceptors using electroabsorption spectroscopy

S Mahadevan, T Liu, SM Pratik, Y Li, HY Ho… - Nature …, 2024 - nature.com
Organic photovoltaic cells using Y6 non-fullerene acceptors have recently achieved high
efficiency, and it was suggested to be attributed to the charge-transfer (CT) nature of the …

Computational analysis to understand the performance difference between two small-molecule acceptors differing in their terminal electron-deficient group

A Mahmood, A Irfan - Journal of Computational Electronics, 2020 - Springer
The end groups of small-molecule acceptors strongly affect their properties and
performance. In this study, theoretical analysis is performed to determine the reason why two …

Molecular electron acceptors for efficient fullerene-free organic solar cells

S Li, Z Zhang, M Shi, CZ Li, H Chen - Physical Chemistry Chemical …, 2017 - pubs.rsc.org
Nowadays, organic solar cells (OSCs) with efficiencies over 10% have been achieved
through the elaborate design of electron donors and fullerene acceptors. However, the …

A novel thiazole based acceptor for fullerene-free organic solar cells

A Mahmood, J Hu, A Tang, F Chen, X Wang, E Zhou - Dyes and Pigments, 2018 - Elsevier
In this work, an electron-withdrawing thiazole ring is used as a bridged unit in the design of
the small molecular electron acceptor. The new electron acceptor, namely DC-IDT2Tz, was …

Supramolecular purification and regioselective functionalization of fullerenes and endohedral metallofullerenes

C Fuertes-Espinosa, M Pujals, X Ribas - Chem, 2020 - cell.com
Fullerenes and endohedral metallofullerenes (EMFs) are exceptional compounds of
outstanding interest in many fields for their physicochemical properties, including material …

Development of isomer-free fullerene bisadducts for efficient polymer solar cells

Z Xiao, X Geng, D He, X Jia, L Ding - Energy & Environmental Science, 2016 - pubs.rsc.org
Isomer-free fullerene bisadducts have been predicted to be high-performance acceptors for
bulk-heterojunction (BHJ) solar cells. They can afford a higher open-circuit voltage …

Influence of thiophene and furan π–bridge on the properties of poly (benzodithiophene-alt-bis (π–bridge) pyrrolopyrrole-1, 3-dione) for organic solar cell applications

R Agneeswari, D Kim, SW Park, S Jang, HS Yang… - Polymer, 2021 - Elsevier
Abstract A new polymer, P (BDT-fPPD), which incorporates 4, 8-bis (2-ethylhexyloxy) benzo
[1, 2-b: 4, 5-bʹ] dithiophene (BDT) and 4, 6-bis (furan-2-yl)-2, 5-dioctylpyrrolo [3],[4] 3, 4-c] …