Yu Tian , Qi Lu , Qian Wang , Xudong Lv , Yuyan Tao , Chenglong Wang , Yangjun Xia
{"title":"Terpolymer analogous D18 enables balanced charge mobility and mitigating non-radiative energy loss of the organic solar cells","authors":"Yu Tian , Qi Lu , Qian Wang , Xudong Lv , Yuyan Tao , Chenglong Wang , Yangjun Xia","doi":"10.1016/j.dyepig.2025.113002","DOIUrl":null,"url":null,"abstract":"<div><div>Fluorine side chain engineering has been widely used to optimize the organic photovoltaic materials <em>via</em> the regulation of the energy levels, crystallinity, and mitigation of the non-radiative energy loss (<em>ΔE</em><sub>nr</sub>) of the devices from them as well. Herein, the notable wide bandgap conjugated polymeric donor materials of D18 were optimized by the introduction of the third component of 4,8-di(3,4-difluoro-5-(2-ethylhexyl)thiophene-2-yl)benzo[1,2-<em>b</em>:4,5-<em>b</em>']dithiophene (BDT-4F) to generate the polymers with the name of D18-4F-5, D18-4F-10, D18-4F-20, D18-4F-30, and D18-4F-100 as well. As compared with the D18, the absorption spectra of analogous polymers of the D18 were almost not changed in the solid state, but the highest occupied molecular orbital (HOMO) energy levels were successively deepened, alongside the gradually increasing <em>π-π</em> stacking distance and decreasing the <em>d</em>-interlayer spacing distance in the solid state. In parallel, the open circuit voltage (<em>V</em><sub>OC</sub>) of the non-fullerene-based organic solar cells (NFAs–OSCs) from the blends of the polymers paired with Y6 were increased from 0.860 V to ∼0.876 V−0.874 V, and then up to 0.892 V, alongside the decrease of the short current density (<em>J</em><sub>SC</sub>) from 27.61 mA/cm<sup>2</sup> to 20.59 mA/cm<sup>2</sup>, fill factors (<em>FF</em>) from 76.29 % to 53.11 %. The particular interest NFAs–OSCs with the higher power conversion efficiency (PCE) of 18.11 % relative to that of 16.89 % for the counterpart devices from the blends of D18:Y6, is achieved from the D18-4F-10:Y6 blends. Beyond that, the more balanced charge transporting, efficiently suppressed charge bimolecular recombination, and lower <em>ΔE</em><sub>nr</sub> etc. of the devices of the D18-4F-10:Y6 as compared with D18:Y6, were observed and supported by a range of physical measurements.</div></div>","PeriodicalId":302,"journal":{"name":"Dyes and Pigments","volume":"242 ","pages":"Article 113002"},"PeriodicalIF":4.1000,"publicationDate":"2025-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dyes and Pigments","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0143720825003729","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
Fluorine side chain engineering has been widely used to optimize the organic photovoltaic materials via the regulation of the energy levels, crystallinity, and mitigation of the non-radiative energy loss (ΔEnr) of the devices from them as well. Herein, the notable wide bandgap conjugated polymeric donor materials of D18 were optimized by the introduction of the third component of 4,8-di(3,4-difluoro-5-(2-ethylhexyl)thiophene-2-yl)benzo[1,2-b:4,5-b']dithiophene (BDT-4F) to generate the polymers with the name of D18-4F-5, D18-4F-10, D18-4F-20, D18-4F-30, and D18-4F-100 as well. As compared with the D18, the absorption spectra of analogous polymers of the D18 were almost not changed in the solid state, but the highest occupied molecular orbital (HOMO) energy levels were successively deepened, alongside the gradually increasing π-π stacking distance and decreasing the d-interlayer spacing distance in the solid state. In parallel, the open circuit voltage (VOC) of the non-fullerene-based organic solar cells (NFAs–OSCs) from the blends of the polymers paired with Y6 were increased from 0.860 V to ∼0.876 V−0.874 V, and then up to 0.892 V, alongside the decrease of the short current density (JSC) from 27.61 mA/cm2 to 20.59 mA/cm2, fill factors (FF) from 76.29 % to 53.11 %. The particular interest NFAs–OSCs with the higher power conversion efficiency (PCE) of 18.11 % relative to that of 16.89 % for the counterpart devices from the blends of D18:Y6, is achieved from the D18-4F-10:Y6 blends. Beyond that, the more balanced charge transporting, efficiently suppressed charge bimolecular recombination, and lower ΔEnr etc. of the devices of the D18-4F-10:Y6 as compared with D18:Y6, were observed and supported by a range of physical measurements.
期刊介绍:
Dyes and Pigments covers the scientific and technical aspects of the chemistry and physics of dyes, pigments and their intermediates. Emphasis is placed on the properties of the colouring matters themselves rather than on their applications or the system in which they may be applied.
Thus the journal accepts research and review papers on the synthesis of dyes, pigments and intermediates, their physical or chemical properties, e.g. spectroscopic, surface, solution or solid state characteristics, the physical aspects of their preparation, e.g. precipitation, nucleation and growth, crystal formation, liquid crystalline characteristics, their photochemical, ecological or biological properties and the relationship between colour and chemical constitution. However, papers are considered which deal with the more fundamental aspects of colourant application and of the interactions of colourants with substrates or media.
The journal will interest a wide variety of workers in a range of disciplines whose work involves dyes, pigments and their intermediates, and provides a platform for investigators with common interests but diverse fields of activity such as cosmetics, reprographics, dye and pigment synthesis, medical research, polymers, etc.