Landep Ayuningtias, Jae Yeol Ma, Yu-Jin Kim, Yun-Hi Kim
{"title":"有机光伏电池用二酮吡咯吡咯基联苯共轭聚合物的合成与表征","authors":"Landep Ayuningtias, Jae Yeol Ma, Yu-Jin Kim, Yun-Hi Kim","doi":"10.1002/bkcs.70042","DOIUrl":null,"url":null,"abstract":"<p>Designing a moderate band gap is sometimes intentionally chosen. When the donor polymer has a deeper HOMO level, a higher Voc can be gained which boosts total PCE in organic photovoltaics (OPVs) (Liao et al., <i>Joule</i> <b>2020</b>, <i>4</i>(1), 189–206; Mamba et al., <i>J. Phys. Chem. A</i> <b>2021</b>, <i>125</i>(50), 10593–10603; Choi and Jo, <i>Org. Electron.</i> <b>2013</b>, <i>14</i>(6), 1621–1628; Jo et al., <i>Org. Electron.</i> <b>2012</b>, <i>13</i>(10), 2185–2191). This is crucial in DPP-based copolymer frameworks, which frequently have short band gaps and may experience poor Voc. Since DPP is a low bandgap due to strong-acceptor, thus, modifying it with weak donor units can raise the bandgap and lower the HOMO to make it suitable for multi-junctions or higher Voc. We report the synthesis, properties, and photovoltaic applications of a donor-acceptor (D-A) conjugated copolymer based on diketopyrrolopyrrole (DPP) and biphenyl, namely PDDPPhenyl. This polymer exhibits broad absorption ranging from 400 to 900 nm with a band gap of 1.59 eV. As expected, a low HOMO level of −5.29 was gained by introducing biphenyl as a weaker donor. The optimized weight ratio goes to 1:4 for PDPPPhenyl:PC<sub>71</sub>BM with 3.8% PCE.</p>","PeriodicalId":54252,"journal":{"name":"Bulletin of the Korean Chemical Society","volume":"46 7","pages":"754-760"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and characterization of diketopyrrolopyrrole-based conjugated polymer with biphenyl for organic photovoltaic cells\",\"authors\":\"Landep Ayuningtias, Jae Yeol Ma, Yu-Jin Kim, Yun-Hi Kim\",\"doi\":\"10.1002/bkcs.70042\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Designing a moderate band gap is sometimes intentionally chosen. When the donor polymer has a deeper HOMO level, a higher Voc can be gained which boosts total PCE in organic photovoltaics (OPVs) (Liao et al., <i>Joule</i> <b>2020</b>, <i>4</i>(1), 189–206; Mamba et al., <i>J. Phys. Chem. A</i> <b>2021</b>, <i>125</i>(50), 10593–10603; Choi and Jo, <i>Org. Electron.</i> <b>2013</b>, <i>14</i>(6), 1621–1628; Jo et al., <i>Org. Electron.</i> <b>2012</b>, <i>13</i>(10), 2185–2191). This is crucial in DPP-based copolymer frameworks, which frequently have short band gaps and may experience poor Voc. Since DPP is a low bandgap due to strong-acceptor, thus, modifying it with weak donor units can raise the bandgap and lower the HOMO to make it suitable for multi-junctions or higher Voc. We report the synthesis, properties, and photovoltaic applications of a donor-acceptor (D-A) conjugated copolymer based on diketopyrrolopyrrole (DPP) and biphenyl, namely PDDPPhenyl. This polymer exhibits broad absorption ranging from 400 to 900 nm with a band gap of 1.59 eV. As expected, a low HOMO level of −5.29 was gained by introducing biphenyl as a weaker donor. The optimized weight ratio goes to 1:4 for PDPPPhenyl:PC<sub>71</sub>BM with 3.8% PCE.</p>\",\"PeriodicalId\":54252,\"journal\":{\"name\":\"Bulletin of the Korean Chemical Society\",\"volume\":\"46 7\",\"pages\":\"754-760\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of the Korean Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/bkcs.70042\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of the Korean Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bkcs.70042","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis and characterization of diketopyrrolopyrrole-based conjugated polymer with biphenyl for organic photovoltaic cells
Designing a moderate band gap is sometimes intentionally chosen. When the donor polymer has a deeper HOMO level, a higher Voc can be gained which boosts total PCE in organic photovoltaics (OPVs) (Liao et al., Joule2020, 4(1), 189–206; Mamba et al., J. Phys. Chem. A2021, 125(50), 10593–10603; Choi and Jo, Org. Electron.2013, 14(6), 1621–1628; Jo et al., Org. Electron.2012, 13(10), 2185–2191). This is crucial in DPP-based copolymer frameworks, which frequently have short band gaps and may experience poor Voc. Since DPP is a low bandgap due to strong-acceptor, thus, modifying it with weak donor units can raise the bandgap and lower the HOMO to make it suitable for multi-junctions or higher Voc. We report the synthesis, properties, and photovoltaic applications of a donor-acceptor (D-A) conjugated copolymer based on diketopyrrolopyrrole (DPP) and biphenyl, namely PDDPPhenyl. This polymer exhibits broad absorption ranging from 400 to 900 nm with a band gap of 1.59 eV. As expected, a low HOMO level of −5.29 was gained by introducing biphenyl as a weaker donor. The optimized weight ratio goes to 1:4 for PDPPPhenyl:PC71BM with 3.8% PCE.
期刊介绍:
The Bulletin of the Korean Chemical Society is an official research journal of the Korean Chemical Society. It was founded in 1980 and reaches out to the chemical community worldwide. It is strictly peer-reviewed and welcomes Accounts, Communications, Articles, and Notes written in English. The scope of the journal covers all major areas of chemistry: analytical chemistry, electrochemistry, industrial chemistry, inorganic chemistry, life-science chemistry, macromolecular chemistry, organic synthesis, non-synthetic organic chemistry, physical chemistry, and materials chemistry.