中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Advances in Solution-Processed All-Small-Molecule Organic Solar Cells with Non-Fullerene Electron Acceptors

文献类型:期刊论文

作者He Chang; Hou Jianhui
刊名ACTA PHYSICO-CHIMICA SINICA
出版日期2018
卷号34期号:11页码:1202-1210
关键词Organic Photovoltaic Cells Solution-processible Non-fullerene Acceptor Wide Bandgap Small Molecule Bulk-heterojunction
ISSN号1000-6818
DOI10.3866/PKU.WHXB201803271
英文摘要Solution-processed bulk-heterojunction organic solar cells (BHJ-OSCs), with their advantages of light weight, low cost, and easy fabrication, are a photovoltaic technology with practical potentials. In BHJ-OSCs, the exciton dissociation and charge transport are highly sensitive to the molecular packing pattern and phase separation morphology in the active layer. On the other hand, when using photovoltaic small molecules (SMs), the purity can be controlled due to their well-defined chemical structure, and therefore there is better reproducibility in device performance. Especially, the non-fullerene acceptors are easier to tune in their light absorption and energy level. Hence, there has been considerable Year interest in small non-fullerene SM organic solar cells (NF-SM-OSCs). Although these cells have the dual advantages of non-fullerene acceptor materials and SMs, the fabrication of high-efficiency cells still possess great challenges. For example, efficient photovoltaic SMs typically possess an acceptor-donor-acceptor (AD-A) structure that causes intrinsic anisotropy, making it more complicated to modulate and control the morphology of the nanoscale active layer. In this article, we will summarize recent advances in high-performance NF-SM-OSCs, and present an introduction of the specific requirements for SM donors in the small NF-SM-OSCs. We first summarize our works on SM donors with the A-D-A structure. The trialkylthienyl-substituted benzodithiophene (TriBDT-T) unit is employed as the D-core unit, and the A end groups include rhodanine (RN), cyano-rhodanine (RCN), and 1,3-indanone (IDO). The band gap (E-g) of these compounds is about 2.0 eV, with the low-lying highest occupied molecular orbital (HOMO) level of -5.51 eV. First, NF-SM-OSCs with DRTB-T and a non-fullerene acceptor (IDIC) were constructed. The morphology of the active layer was fine-tuned by solvent vapor annealing (SVA), leading to the formation of the desired interconnected nanoscale structure. Our results demonstrate that the molecular design of a wide band gap (WBG) donor to create a well-matched donor-acceptor pair with a low band gap (LBG) non-fullerene SM acceptor, as well as subtle morphological control, provides great potential to realize high-performance NFSM-OSCs. We also studied the molecular orientation optimization from the aspect of molecular design. We designed and synthesized a group of SM compounds having identical pi-conjugated backbones and end groups with different alkyl chain lengths. Since these compounds have identical photoelectric properties, they allow us to focus on the significant influence of the end alkyl chains on the molecular orientation and intermolecular aggregation behavior in solid-state films. Characterization of the DRTB-T-CX films using 2D grazing incidence wide-angle X-ray scattering (GIWAXS) revealed an obvious transition of orientation from edge-on to face-on relative to the substrate when the end alkyl chain is lengthened. This demonstrates that the length of the end alkyl chain can be used to modify the molecular orientation. A DRTB-T-C4/IT-4F-based device achieved a maximum power conversion efficiency (PCE) of up to 11.24%, which is the best performance reported for state-of-the-art NF-SM-OSCs. On this basis, the challenges and prospects of NF-SM-OSCs are discussed.
语种英语
WOS记录号WOS:000431610500006
出版者PEKING UNIV PRESS
源URL[http://ir.iccas.ac.cn/handle/121111/43303]  
专题中国科学院化学研究所
通讯作者He Chang; Hou Jianhui
作者单位Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, State Key Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
He Chang,Hou Jianhui. Advances in Solution-Processed All-Small-Molecule Organic Solar Cells with Non-Fullerene Electron Acceptors[J]. ACTA PHYSICO-CHIMICA SINICA,2018,34(11):1202-1210.
APA He Chang,&Hou Jianhui.(2018).Advances in Solution-Processed All-Small-Molecule Organic Solar Cells with Non-Fullerene Electron Acceptors.ACTA PHYSICO-CHIMICA SINICA,34(11),1202-1210.
MLA He Chang,et al."Advances in Solution-Processed All-Small-Molecule Organic Solar Cells with Non-Fullerene Electron Acceptors".ACTA PHYSICO-CHIMICA SINICA 34.11(2018):1202-1210.

入库方式: OAI收割

来源:化学研究所

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