Metrics & MoreArticle Recommendations CONSPECTUS: Over the past few years, the development of new materials has contributed to rapid increases in the power conversion efficiencies (PCEs) of organic photovoltaic (OPV) cells to over 17%, showing great potential for the commercialization of this technology in the near future. At this stage, designing new materials with superior performance and low cost simultaneously is of crucial importance. Chlorinated materials are emerging as new stars with very high PCEs, creating a molecular design trend to replace the most popular fluorinated materials. For example, by using chlorinated non-fullerene acceptors, we recently got a record PCE of 17% for single-junction OPV cells. Firmly based on recent advances, herein we focus on the topic of chlorinated OPV materials, aiming to provide a guideline for further molecular design.In this Account, first, on the basis of most fundamental features of the Cl atom, we highlight the features of chlorinated materials compared with their fluorinated counterparts: (1) Chlorination is more efficient than fluorination in modulating the optical and electrical properties of OPV materials. In many cases, chlorinated materials show lower energy levels and broader absorption spectra than their fluorinated counterparts, which contribute higher output voltages and current densities in the resulting photovoltaic devices. (2) Cl has a large atomic size than F. On one hand, enhanced overlap of π electrons is beneficial for enhancing the intermolecular packing and crystalline property and thus improving the charge transport. On the other hand, if Cl is introduced inappropriately in the backbone or side chain, this feature will cause a more twisted π plane and larger steric hindrance, having negative impacts on the photovoltaic performance of the corresponding materials. (3) Importantly, chlorination is usually chemically cheaper in synthesis, which has the potential to decrease the material cost of OPV cells. Then, we provide a concise review of chlorinated OPV materials, including polymeric and small-molecule donors and non-fullerene acceptors. The photovoltaic performance in various types of OPV cells using chlorinated materials, such as single-junction, tandem, semitransparent, and indoor-light photovoltaic cells is also discussed. For instance, ultranarrow-band-gap chlorinated acceptors can be used to construct highly efficient color-semitransparent OPV cells, and the wide-band-gap chlorinated materials show great potential for fabricating indoor-light photovoltaic devices. Finally, we briefly discuss current questions related to chlorinated OPV materials and highlight the significance of chlorination in future development.
Developing photovoltaic materials with simple chemical structure and easy synthesis still remains a major challenge in the industrialization process of organic solar cells (OSCs). Herein, an ester substituted poly(thiophene vinylene) derivative, PTVT-T, was designed and synthesized in very few steps by adopting commercial available raw-materials. The ester groups on the thiophene units enable PTVT-T with a planar and stable conformation. Moreover, PTVT-T presents wide absorption band and strong aggregation effect in solution, which are the key characteristics to realize high performance in non-fullerene acceptor (NFA) based OSCs. We then prepared OSCs by blending PTVT-T with three representative fullerene- and NF- based acceptors, PC71BM, IT-4F and BTP-eC9. It was found that PTVT-T can work well with all the acceptors, showing great potential to match new emerging NFAs. Particularly, a remarkable PCE of 16.20% is achieved in PTVT-T: BTP-eC9 based device, which is the highest value among the counterparts based on PTV-derivatives. This work demonstrates that PTVT-T shows great potential to the future commercialization of OSCs.
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