TY - JOUR
T1 - Poly(alkoxyphenylene-thienylene) Langmuir-Schäfer thin-films for advanced performance transistors
AU - Pignataro, Bruno Giuseppe
AU - Giotta, Livia
AU - Zamhonin, Pier Giorgio
AU - Sabbatini, Luigia
AU - Lang, Philippe
AU - Tanese, Maria C.
AU - Colangiuli, Donate
AU - Conoci, Sabrina
AU - Farinola, Gianluca M.
AU - Babudri, Francesco
AU - Valli, Ludovico
AU - Torsi, Luisa
AU - Naso, Francesco
PY - 2006
Y1 - 2006
N2 - Solution processed Langmuir-Scha ̈fer and cast thin films of regioregular poly(2,5-dioctyloxy-1,4- phenylene-alt-2,5-thienylene) are investigated as transistor active layers. The study of their field-effect properties evidences that no transistor behavior can be seen with a cast film channel material. This was not surprising considering the twisted conformation of the polymer backbone predicted by various theoretical studies. Strikingly, the Langmuir-Scha ̈fer (LS) thin films exhibit a field-effect mobility of 5 × 10-4 cm2/V‚s, the highest attained so far with an alkoxy-substituted conjugated polymer. Extensive optical, morphological, and structural thin-film characterization supports the attribution of the effect to the longer conjugation length achieved in the Langmuir-Scha ̈fer deposited film, likely due to an improved backbone planarity. This study shows that a technologically appealing deposition procedure, such as the LS one, can be exploited to significantly improve the inherently poor field-effect properties of twisted conjugated backbones. This achievement could promote the exploitation for electronic, and possibly sensing, applications of the wealth of opportunities offered by the alkoxy substitution on the phenylene units for convenient tailoring of the phenylene-thienylene backbone with molecules of chemical and biological interest.
AB - Solution processed Langmuir-Scha ̈fer and cast thin films of regioregular poly(2,5-dioctyloxy-1,4- phenylene-alt-2,5-thienylene) are investigated as transistor active layers. The study of their field-effect properties evidences that no transistor behavior can be seen with a cast film channel material. This was not surprising considering the twisted conformation of the polymer backbone predicted by various theoretical studies. Strikingly, the Langmuir-Scha ̈fer (LS) thin films exhibit a field-effect mobility of 5 × 10-4 cm2/V‚s, the highest attained so far with an alkoxy-substituted conjugated polymer. Extensive optical, morphological, and structural thin-film characterization supports the attribution of the effect to the longer conjugation length achieved in the Langmuir-Scha ̈fer deposited film, likely due to an improved backbone planarity. This study shows that a technologically appealing deposition procedure, such as the LS one, can be exploited to significantly improve the inherently poor field-effect properties of twisted conjugated backbones. This achievement could promote the exploitation for electronic, and possibly sensing, applications of the wealth of opportunities offered by the alkoxy substitution on the phenylene units for convenient tailoring of the phenylene-thienylene backbone with molecules of chemical and biological interest.
KW - BLODGETT-FILMS
KW - CONDUCTING POLYMERS
KW - CONJUGATED POLYMERS
KW - FIELD-EFFECT TRANSISTORS
KW - OPTICAL-PROPERTIES
KW - PHENYLENE
KW - POLYTHIOPHENES
KW - REGIOREGULAR POLY(3-HEXYLTHIOPHENE)
KW - REPEAT UNITS
KW - STILLE COUPLING REACTION
KW - BLODGETT-FILMS
KW - CONDUCTING POLYMERS
KW - CONJUGATED POLYMERS
KW - FIELD-EFFECT TRANSISTORS
KW - OPTICAL-PROPERTIES
KW - PHENYLENE
KW - POLYTHIOPHENES
KW - REGIOREGULAR POLY(3-HEXYLTHIOPHENE)
KW - REPEAT UNITS
KW - STILLE COUPLING REACTION
UR - http://hdl.handle.net/10447/34458
M3 - Article
VL - 18
SP - 778
EP - 784
JO - Chemistry of Materials
JF - Chemistry of Materials
SN - 0897-4756
ER -