SMILES string
O=C1N(C(CCCCCC)CCCCCC)C(C2=C(C1=CC=C3C4=C(C(C=C5)=CC6=C5C(C=CC(C7=CC8=C9C%10=C7C%11=C%12C(C%13=CC=C%12C%10=CC=C9C(N(C(CCCCCC)CCCCCC)C8=O)=O)=C(C(N(C(CCCCCC)CCCCCC)C%13=O)=O)C=C%11)=C%14)=C%14C6%15C%16=CC=CC=C%16C%17=C%15C=CC=C%17)C=C(C(N(C(CCCCCC)CCCCCC)C
description
Band gap: 2.1 eV
assay
99%
form
solid
solubility
chlorobenzene: soluble, chloroform: soluble, dichlorobenzene: soluble
orbital energy
HOMO -5.9 eV , LUMO -3.8 eV
flash_point_f
Not applicable
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_c
Not applicable
High-efficiency non-fullerene organic solar cells enabled by a difluorobenzothiadiazole-based donor polymer combined with a properly matched small molecule acceptor.
Zhao J, et al.
Energy & Environmental Science, 8(2), 520-525 (2015)
Towards rational design of organic electron acceptors for photovoltaics: a study based on perylenediimide derivatives.
Yan Q, et al.
Chemical Science, 4(12), 4389-4394 (2013)
The influence of spacer units on molecular properties and solar cell performance of non-fullerene acceptors.
Zhao J, et al.
Journal of Material Chemistry A, 3(40), 20108-20112 (2015)
商品
Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.
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