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Volumn 15, Issue 7, 2013, Pages 2539-2546

Tuning the photodriven electron transport within the columnar perylenediimide stacks by changing the π-extent of the electron donors

Author keywords

[No Author keywords available]

Indexed keywords

9,10 DIMETHOXYANTHRACENE 2 SULFONATE; 9,10-DIMETHOXYANTHRACENE-2-SULFONATE; ANTHRACENE DERIVATIVE; DRUG DERIVATIVE; IMIDE; PERYLENE; PERYLENEDIIMIDE; WATER;

EID: 84873048601     PISSN: 14639076     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2cp44106c     Document Type: Article
Times cited : (14)

References (36)
  • 10
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    • Although the transportation of the photogenerated charges in the active layers of the BHJ solar cells has so far been achieved by using π-conjugated polymer donors, which are available for extensive charge delocalization along the polymer backbone, they rarely form one dimensional self-organizations at nanoscale without additional synthetic modifications. See
    • R. D. Pensack C. Guo K. Vakhshouri E. D. Gomez J. B. Asbury J. Phys. Chem. C 2012 116 4824
    • (2012) J. Phys. Chem. C , vol.116 , pp. 4824
    • Pensack, R.D.1    Guo, C.2    Vakhshouri, K.3    Gomez, E.D.4    Asbury, J.B.5
  • 22
    • 84918669584 scopus 로고
    • s = 1.52 (1/ε)-0.064 when electron-transfer products are solvent-separated ion pair, where ε is the dielectric constant of the solvent. Because TAIPDI and BSSBP are closely positioned via π-π interactions, the initial products are assumed to be contact ion pair while those of TAIPDI (ref. 14) and the other electron donors (DANS and ANADS) are accepted as solvent separated ion pairs (ref. 27)
    • A. Weller Z. Phys. Chem. 1982 133 93
    • (1982) Z. Phys. Chem. , vol.133 , pp. 93
    • Weller, A.1
  • 24
    • 84055181389 scopus 로고    scopus 로고
    • Because electron donors are not so soluble in MeTHF, the mixture of MeTHF and EtOH has been used. Phosphorescence emissions of DANS and ANADS have been compared to those of 9,10-dimethylanthracene and napthalen-2-amine obtained in MeTHF at 77 K. See Fig. S2 (ESI)
    • M. Supur M. E. El-Khouly J. H. Seok K.-Y. Kay S. Fukuzumi J. Phys. Chem. A 2011 115 14430
    • (2011) J. Phys. Chem. A , vol.115 , pp. 14430
    • Supur, M.1    El-Khouly, M.E.2    Seok, J.H.3    Kay, K.-Y.4    Fukuzumi, S.5
  • 25
    • 56049126474 scopus 로고    scopus 로고
    • - has a broad absorbtion centered at 730 nm (ref. 31). The stilbene radical cation has also broad absorption around 760 nm with a shoulder around 650 nm (ref. 32 and 33). Cis- and trans-isomers of BSSBP may also cause the formation different maxima of radical cation (ref. 32)
    • S. Fukuzumi K. Ohkubo J. Ortiz A. M. Gutierrez F. Fernandez-Lazaro A. Sastre-Santos J. Phys. Chem. A 2008 112 10744
    • (2008) J. Phys. Chem. A , vol.112 , pp. 10744
    • Fukuzumi, S.1    Ohkubo, K.2    Ortiz, J.3    Gutierrez, A.M.4    Fernandez-Lazaro, F.5    Sastre-Santos, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.