4.6 Article

Enhanced light-harvesting of benzodithiophene conjugated porphyrin electron donors in organic solar cells

期刊

JOURNAL OF MATERIALS CHEMISTRY C
卷 7, 期 2, 页码 380-386

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8tc04495c

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资金

  1. Hong Kong Research Grants Council [HKBU 22304115-ECS, C5015-15GF]
  2. Areas of Excellence Scheme [AoE/P-03/08]
  3. Hong Kong Baptist University [FRG2/13-14/083]
  4. National Natural Science Foundation of China [51473139, 91333206, 20974091, 61631166001]
  5. Science, Technology and Innovation of Shenzhen [JCYJ20150630164505504]
  6. Innovation Platform Open Foundation of University of Hunan Province [14K092]
  7. Hunan 2011 Collaborative Innovation Center of Chemical Engineering & Technology with Environmental Benignity and Effective Resource Utilization

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To address the intrinsic issue of conventional porphyrin derivatives with a deficient absorption between Soret and Q bands, we designed and synthesized two porphyrin molecules (BDTP-1 and BDTP-2) bearing a meso-alkyl substituted porphyrin core, benzodithiohene (BDT) ethynylene -bridge and end-capping ethylrhodanine derivatives. Apart from the characteristic Soret and Q bands of porphyrin macrocycle, an extra peak (521 nm for BDTP-1 and 536 nm for BDTP-2) was derived from the BDT units. Using the porphyrin small molecules as electron donors and PC71BM as an electron acceptor, the devices show broad spectral photocurrent generation with a significant contribution from greenlight-harvesting (490-550 nm), resulting in high performances with PCEs up to 7.97%.

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