TY - JOUR
T1 - Thermal and mechanical cracking in bis(triisopropylsilylethnyl) pentacene thin films
AU - Chen, Jihua
AU - Tee, Chee Keong
AU - Yang, Junyan
AU - Shaw, Charles
AU - Shtein, Max
AU - Anthony, John
AU - Martin, David C.
PY - 2006/12/15
Y1 - 2006/12/15
N2 - Bis(triisopropylsilylethnyl) pentacene (TIPS pentacene) was synthesized to increase its solubility in common liquid solvents and, at the same time, enhance the π-π stacking between neighboring acenes in the crystallized state in comparison with unmodified pentacene. Hot-stage microscopy experiments revealed that during heating voids develop along the long axis of the TIPS pentacene films {along the [210] direction/parallel to the (120) planes) and crystals overlap along the short axis (along the [120] direction/parallel to the (210) planes}. From molecular mechanics simulations, the predominant twin boundaries of (120) and commonly observed cracking planes of (120), (120), and (210) had relatively low surface energies in comparison with planes with similar Miller indices. Organic thin-film transistors with TIPS pentacene as the active layer were fabricated, and the mobility values decreased from 0.4-1.0 cm2/V s before cracking to ∼0.2 cm2/V s after cracking. To maintain the high charge carrier mobility of TIPS pentacene devices, these cracks should be avoided.
AB - Bis(triisopropylsilylethnyl) pentacene (TIPS pentacene) was synthesized to increase its solubility in common liquid solvents and, at the same time, enhance the π-π stacking between neighboring acenes in the crystallized state in comparison with unmodified pentacene. Hot-stage microscopy experiments revealed that during heating voids develop along the long axis of the TIPS pentacene films {along the [210] direction/parallel to the (120) planes) and crystals overlap along the short axis (along the [120] direction/parallel to the (210) planes}. From molecular mechanics simulations, the predominant twin boundaries of (120) and commonly observed cracking planes of (120), (120), and (210) had relatively low surface energies in comparison with planes with similar Miller indices. Organic thin-film transistors with TIPS pentacene as the active layer were fabricated, and the mobility values decreased from 0.4-1.0 cm2/V s before cracking to ∼0.2 cm2/V s after cracking. To maintain the high charge carrier mobility of TIPS pentacene devices, these cracks should be avoided.
KW - Annealing
KW - Charge transport
KW - Functionalized pentacene
KW - Organic semiconductors
KW - Organic thin-film transistors
KW - Structure-property relations
KW - Surface energy
UR - http://www.scopus.com/inward/record.url?scp=33845985301&partnerID=8YFLogxK
U2 - 10.1002/polb.21007
DO - 10.1002/polb.21007
M3 - Article
AN - SCOPUS:33845985301
SN - 0887-6266
VL - 44
SP - 3631
EP - 3641
JO - Journal of Polymer Science, Part B: Polymer Physics
JF - Journal of Polymer Science, Part B: Polymer Physics
IS - 24
ER -