4.6 Article

Donor-Substituted β-Functionalized Porphyrin Dyes on Hierarchically Structured Mesoporous TiO2 Spheres. Highly Efficient Dye-Sensitized Solar Cells

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 115, 期 39, 页码 19343-19354

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jp202307b

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资金

  1. World Class University from the Ministry of Education, Science, and Technology (MEST) [R32-2010-000-10217]
  2. Ministry of Knowledge Economy of Korea [2010-A011-0033]
  3. KIST [2E21833]
  4. National Sciences Foundation
  5. Robert A. Welch Foundation [CHE-1057904, F-1018]
  6. Korea Evaluation Institute of Industrial Technology (KEIT) [K0006001] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Council of Science & Technology (NST), Republic of Korea [2E2215] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  8. National Research Foundation of Korea [2005-0093839, R32-2011-000-10217-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Novel zinc porphyrin dyes for use in dye-sensitized solar cells (DSSCs) have been synthesized. These dyes are based on a molecular design that relies on donor-pi-acceptor interactions, a concept implemented by introducing a bis(4-tert-butylphenyl)amino group at the meso position of the porphyrin opposite to what are 2-propenoic or 2,4-pentadienoic acid anchoring groups at the beta-pyrrolic positions. Incorporating an electron-donating group (i.e., the diarylamine) on the porphyrin core serves as the considerable electronic coupling between the donor site and porphyrin core, and hence, the HOMO-LUMO energy gap is decreased. This change is reflected in the remarkable red shift and broadening of the absorption spectra relative to an unfunctionalized parent system. This substitution, in conjunction with functionalization with carboxylic acid moieties on the beta-pyrrolic positions, also provides what is an effectively aligned donor-pi-acceptor dipolar architecture. This, in turn, gives rise to advantageous charge-transfer properties, including what are significant improvements of the electron injection efficiency on titanium oxide (TiO2) compared to our previous models without a donor substituent. The DSSCs of this study were composed of zero-dimensional hierarchical structured TiO2 spheres with a diameter of 600-800 nm prepared from P-25 and anatase TiO2 nanoparticles, which functioned as the photoelectrodes. With the anatase TiO2-based DSSCs, the power conversion efficiencies (eta) as well as the photocurrent action spectra were relatively enhanced, an effect ascribed to the characteristic mesoporous effect and associated electrophysical properties of the anatase TiO2 spheres. Among the dyes prepared in the context of the present study, the doubly functionalized carboxylic acid derivative, tda-2b-bd-Zn, gave rise to the highest power conversion. The eta value was 7.47%, and the maximum incident photon-to-current efficiency was 77.3% at the Soret band. The overall eta value of tda-2b-bd-Zn is comparable to the performance of typical ruthenium-based dyes, such as N3 (eta = 7.68%), under the same conditions.

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