Publication

High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives

Woebkenberg, P. H., Bradley, D. D. C., Kronholm, D., Hummelen, J. C., de Leeuw, D. M., Coelle, M., Anthopoulos, T. D., H. Wobkenberg, P. & Colle, M., Jul-2008, In : Synthetic Metals. 158, 11, p. 468-472 5 p.

Research output: Contribution to journalArticleAcademicpeer-review

APA

Woebkenberg, P. H., Bradley, D. D. C., Kronholm, D., Hummelen, J. C., de Leeuw, D. M., Coelle, M., Anthopoulos, T. D., H. Wobkenberg, P., & Colle, M. (2008). High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives. Synthetic Metals, 158(11), 468-472. https://doi.org/10.1016/j.synthmet.2008.03.016

Author

Woebkenberg, Paul H. ; Bradley, Donal D. C. ; Kronholm, David ; Hummelen, Jan C. ; de Leeuw, Dago M. ; Coelle, Michael ; Anthopoulos, Thomas D. ; H. Wobkenberg, Paul ; Colle, Michael. / High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives. In: Synthetic Metals. 2008 ; Vol. 158, No. 11. pp. 468-472.

Harvard

Woebkenberg, PH, Bradley, DDC, Kronholm, D, Hummelen, JC, de Leeuw, DM, Coelle, M, Anthopoulos, TD, H. Wobkenberg, P & Colle, M 2008, 'High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives', Synthetic Metals, vol. 158, no. 11, pp. 468-472. https://doi.org/10.1016/j.synthmet.2008.03.016

Standard

High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives. / Woebkenberg, Paul H.; Bradley, Donal D. C.; Kronholm, David; Hummelen, Jan C.; de Leeuw, Dago M.; Coelle, Michael; Anthopoulos, Thomas D.; H. Wobkenberg, Paul; Colle, Michael.

In: Synthetic Metals, Vol. 158, No. 11, 07.2008, p. 468-472.

Research output: Contribution to journalArticleAcademicpeer-review

Vancouver

Woebkenberg PH, Bradley DDC, Kronholm D, Hummelen JC, de Leeuw DM, Coelle M et al. High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives. Synthetic Metals. 2008 Jul;158(11):468-472. https://doi.org/10.1016/j.synthmet.2008.03.016


BibTeX

@article{3058452aa1d341c482a6712d280a9fea,
title = "High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives",
abstract = "We report on n-channel organic field-effect transistors (OFETs) based on the solution processable methanofullerenes [6,6]-phenyl-C-61-butyric acid ester ([60]PCBM) and [6,6]-phenyl-C-71-butyric acid methyl ester (170]PCBM). Despite the fact that both derivatives form glassy films when processed from their electron mobilities are high and on the order of 0.21 cm(2/)V s and 0.1 cm(2)/V s, for [60]PCBM solution, and [70]PCBM, respectively. Although the derived mobility of [60]PCBM is comparable to the best values reported in the literature, the electron mobility of [70]PCBM is the highest value reported to date for any C-70 based molecule. We note that this is the only report in which C-60 and Cd-70 methanofullerenes exhibit comparable electron mobilities. The present findings could have significant implications in the area of large-area organic electronics and organic photovoltaics where C-60 derivatives have so far been the most widely used electron acceptor materials. (C) 2008 Elsevier B.V. All rights reserved.",
keywords = "organic transistors, methanofullerenes, fullerene derivatives, n-channel, electron transport, THIN-FILM TRANSISTORS, POLYMER SOLAR-CELLS, COMPLEMENTARY CIRCUITS, SEMICONDUCTORS, METHANOFULLERENE, EFFICIENT, DESIGN",
author = "Woebkenberg, {Paul H.} and Bradley, {Donal D. C.} and David Kronholm and Hummelen, {Jan C.} and {de Leeuw}, {Dago M.} and Michael Coelle and Anthopoulos, {Thomas D.} and {H. Wobkenberg}, Paul and Michael Colle",
year = "2008",
month = jul,
doi = "10.1016/j.synthmet.2008.03.016",
language = "English",
volume = "158",
pages = "468--472",
journal = "Synthetic Metals",
issn = "0379-6779",
publisher = "Elsevier Science",
number = "11",

}

RIS

TY - JOUR

T1 - High mobility n-channel organic field-effect transistors based on soluble C-60 and C-70 fullerene derivatives

AU - Woebkenberg, Paul H.

AU - Bradley, Donal D. C.

AU - Kronholm, David

AU - Hummelen, Jan C.

AU - de Leeuw, Dago M.

AU - Coelle, Michael

AU - Anthopoulos, Thomas D.

AU - H. Wobkenberg, Paul

AU - Colle, Michael

PY - 2008/7

Y1 - 2008/7

N2 - We report on n-channel organic field-effect transistors (OFETs) based on the solution processable methanofullerenes [6,6]-phenyl-C-61-butyric acid ester ([60]PCBM) and [6,6]-phenyl-C-71-butyric acid methyl ester (170]PCBM). Despite the fact that both derivatives form glassy films when processed from their electron mobilities are high and on the order of 0.21 cm(2/)V s and 0.1 cm(2)/V s, for [60]PCBM solution, and [70]PCBM, respectively. Although the derived mobility of [60]PCBM is comparable to the best values reported in the literature, the electron mobility of [70]PCBM is the highest value reported to date for any C-70 based molecule. We note that this is the only report in which C-60 and Cd-70 methanofullerenes exhibit comparable electron mobilities. The present findings could have significant implications in the area of large-area organic electronics and organic photovoltaics where C-60 derivatives have so far been the most widely used electron acceptor materials. (C) 2008 Elsevier B.V. All rights reserved.

AB - We report on n-channel organic field-effect transistors (OFETs) based on the solution processable methanofullerenes [6,6]-phenyl-C-61-butyric acid ester ([60]PCBM) and [6,6]-phenyl-C-71-butyric acid methyl ester (170]PCBM). Despite the fact that both derivatives form glassy films when processed from their electron mobilities are high and on the order of 0.21 cm(2/)V s and 0.1 cm(2)/V s, for [60]PCBM solution, and [70]PCBM, respectively. Although the derived mobility of [60]PCBM is comparable to the best values reported in the literature, the electron mobility of [70]PCBM is the highest value reported to date for any C-70 based molecule. We note that this is the only report in which C-60 and Cd-70 methanofullerenes exhibit comparable electron mobilities. The present findings could have significant implications in the area of large-area organic electronics and organic photovoltaics where C-60 derivatives have so far been the most widely used electron acceptor materials. (C) 2008 Elsevier B.V. All rights reserved.

KW - organic transistors

KW - methanofullerenes

KW - fullerene derivatives

KW - n-channel

KW - electron transport

KW - THIN-FILM TRANSISTORS

KW - POLYMER SOLAR-CELLS

KW - COMPLEMENTARY CIRCUITS

KW - SEMICONDUCTORS

KW - METHANOFULLERENE

KW - EFFICIENT

KW - DESIGN

U2 - 10.1016/j.synthmet.2008.03.016

DO - 10.1016/j.synthmet.2008.03.016

M3 - Article

VL - 158

SP - 468

EP - 472

JO - Synthetic Metals

JF - Synthetic Metals

SN - 0379-6779

IS - 11

ER -

ID: 4757283