메뉴 건너뛰기




Volumn 73, Issue 8, 2008, Pages 3189-3196

Tetrafullerene conjugates for all-organic photovoltaics

Author keywords

[No Author keywords available]

Indexed keywords

ELECTRON ENERGY LEVELS; OLIGOMERS; PHOTOVOLTAIC CELLS;

EID: 42149180050     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702740d     Document Type: Article
Times cited : (45)

References (60)
  • 1
    • 8444252980 scopus 로고    scopus 로고
    • Special Issue on Organic Electronics, Chem. Mater. 2004, 16, 4381-4846.
    • (a) Special Issue on Organic Electronics, Chem. Mater. 2004, 16, 4381-4846.
  • 15
    • 21144440701 scopus 로고    scopus 로고
    • For recent reviews on molecular heterojunction, see: a
    • For recent reviews on molecular heterojunction, see: (a) Roncali, J. Chem. Soc. Rev. 2005, 34, 483-495.
    • (2005) Chem. Soc. Rev , vol.34 , pp. 483-495
    • Roncali, J.1
  • 23
    • 0037127186 scopus 로고    scopus 로고
    • 60 dyads, see: Gu, T.; Tsamouras, D.; Melzer, C.; Krasnikov, V.; Gisselbrecht, J.-P.; Gross, M.; Hadziioannou, G.; Nierengarten, J.-F. ChemPhysChem 2002, 3, 124-127.
    • 60 dyads, see: Gu, T.; Tsamouras, D.; Melzer, C.; Krasnikov, V.; Gisselbrecht, J.-P.; Gross, M.; Hadziioannou, G.; Nierengarten, J.-F. ChemPhysChem 2002, 3, 124-127.
  • 24
    • 0037824473 scopus 로고    scopus 로고
    • 60 dyads, see: (a) Negishi, N.; Yamada, K.; Takimiya, K.; Aso, Y.; Otsubo, O.; Tetsuo, Y. Chem. Lett. 2003, 32, 404-405.
    • 60 dyads, see: (a) Negishi, N.; Yamada, K.; Takimiya, K.; Aso, Y.; Otsubo, O.; Tetsuo, Y. Chem. Lett. 2003, 32, 404-405.
  • 27
    • 0037154867 scopus 로고    scopus 로고
    • 60 hybrids, see: (a) Guldi, D. M.; Luo, C.; Swartz, A.; Gómez, R.; Segura, J. L.; Martín, N.; Brabec, C.; Sariciftci, N. S. J. Org. Chem. 2002, 67, 1141-1152.
    • 60 hybrids, see: (a) Guldi, D. M.; Luo, C.; Swartz, A.; Gómez, R.; Segura, J. L.; Martín, N.; Brabec, C.; Sariciftci, N. S. J. Org. Chem. 2002, 67, 1141-1152.
  • 30
    • 3042787888 scopus 로고    scopus 로고
    • 60-porphyrin conjugates, see: Imahori, H.; Fukuzumi, S. Adv. Funct. Mater. 2004, 14, 525-536.
    • 60-porphyrin conjugates, see: Imahori, H.; Fukuzumi, S. Adv. Funct. Mater. 2004, 14, 525-536.
  • 31
    • 18844388701 scopus 로고    scopus 로고
    • 60-tetrathiafulvalene triads, see: (a) Sánchez, L.; Sierra, M.; Martín, N.; Guldi, D. M.; Wienk, M. M.; Janssen, R. A. J. Org. Lett. 2005, 7, 1691-1694.
    • 60-tetrathiafulvalene triads, see: (a) Sánchez, L.; Sierra, M.; Martín, N.; Guldi, D. M.; Wienk, M. M.; Janssen, R. A. J. Org. Lett. 2005, 7, 1691-1694.
  • 33
    • 0029483704 scopus 로고    scopus 로고
    • Yu, G.; Gao, J.; Hummelen, J. C.; Wudl, F.; Heeger, A. J. Science (Washington, DC, U.S.) 1995, 270, 1789-1791.
    • (a) Yu, G.; Gao, J.; Hummelen, J. C.; Wudl, F.; Heeger, A. J. Science (Washington, DC, U.S.) 1995, 270, 1789-1791.
  • 37
    • 33644945010 scopus 로고    scopus 로고
    • Power conversion efficiencies of around 1% were recently reported by Roncali et al. for bulk heterojunction devices prepared from PCBM and different triphenylamine derivatives: (a) Roquet, S.; Cravino, A.; Leriche, P.; Alévêque, O.; Frère, P.; Roncali, J. J. Am. Chem. Soc. 2006, 128, 3459-3466.
    • Power conversion efficiencies of around 1% were recently reported by Roncali et al. for bulk heterojunction devices prepared from PCBM and different triphenylamine derivatives: (a) Roquet, S.; Cravino, A.; Leriche, P.; Alévêque, O.; Frère, P.; Roncali, J. J. Am. Chem. Soc. 2006, 128, 3459-3466.
  • 41
    • 14744273171 scopus 로고    scopus 로고
    • The substitution pattern, conjugation, and electronic structure of functionalized phenylacetylene and phenylvinylene structures are known to exhibit remarkable optical and electronic properties because of their multiple conjugated pathways. For recent examples, see: a
    • The substitution pattern, conjugation, and electronic structure of functionalized phenylacetylene and phenylvinylene structures are known to exhibit remarkable optical and electronic properties because of their multiple conjugated pathways. For recent examples, see: (a) Marsden, J. A.; Miller, J. J.; Shirtcliff, L. D.; Haley, M. M. J Am. Chem. Soc. 2005, 128, 2464-2476.
    • (2005) J Am. Chem. Soc , vol.128 , pp. 2464-2476
    • Marsden, J.A.1    Miller, J.J.2    Shirtcliff, L.D.3    Haley, M.M.4
  • 45
    • 0000389904 scopus 로고    scopus 로고
    • It is well-established that functionalization of the fullerene cage causes a rise of the LUMO energy level of the organofullerenes produced: Echegoyen, L, Echegoyen, L. E. Acc. Chem. Res. 1998, 31, 593-601
    • It is well-established that functionalization of the fullerene cage causes a rise of the LUMO energy level of the organofullerenes produced: Echegoyen, L.; Echegoyen, L. E. Acc. Chem. Res. 1998, 31, 593-601.
  • 47
    • 42149093692 scopus 로고    scopus 로고
    • Unambiguous assignment of these weak waves to oxidative processes corresponding to the central π-conjugated oligomer was achieved using DPV measurements
    • Unambiguous assignment of these weak waves to oxidative processes corresponding to the central π-conjugated oligomer was achieved using DPV measurements.
  • 48
    • 33645449951 scopus 로고    scopus 로고
    • Oxidation waves of π-conjugated oligomers sometimes appear as broad and difficult to assign waves in CV. For recent examples, see: (a) Zen, A, Bilge, A, Galbrecht, F, Alle, R, Meerholz, K, Grenzer, J, Neher, D, Scherf, U, Farrell, T. J. Am. Chem. Soc. 2006, 128, 3914-3915
    • Oxidation waves of π-conjugated oligomers sometimes appear as broad and difficult to assign waves in CV. For recent examples, see: (a) Zen, A.; Bilge, A.; Galbrecht, F.; Alle, R.; Meerholz, K.; Grenzer, J.; Neher, D.; Scherf, U.; Farrell, T. J. Am. Chem. Soc. 2006, 128, 3914-3915.
  • 53
    • 42149150342 scopus 로고    scopus 로고
    • We note that, especially for 5b, the lifetime of the singlet excited state inferred from transient absorption and fluorescence spectroscopy is different. Since the fluorescence can be measured very sensitively over several orders of magnitude and over a longer time period, these values are likely more accurate
    • We note that, especially for 5b, the lifetime of the singlet excited state inferred from transient absorption and fluorescence spectroscopy is different. Since the fluorescence can be measured very sensitively over several orders of magnitude and over a longer time period, these values are likely more accurate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.