We report on the magnetoresistance (MR) effect in a unipolar p-channel field-effect transistor based on amorphous thin film of low molecular weight 2,2 0 ,7,7 0-tetrakis(diphenylamino)-9,9 0-spirobifluorene (Spiro-TAD). To scrutinize the origin of this effect two themes have been studied: (i) the influence of gate dielectric SiO 2 surface treatment and (ii) the importance of organic molecular p-dopant 1,3,4,5,7,8hexafluorotetracyanonaphthoquinodimethane (F6-TNAP) thin films sandwiched between SiO 2 and Spiro-TAD. A device fabricated on bare SiO 2 shows larger MR than one fabricated on hexamethyldisilazanetreated SiO 2 , suggesting the bipolaron species as the origin of this effect. This could be understood through two aspects. (i) The stabilization of bipolaron, i.e. trapped charge-stabilized bipolaron. Due to large energy cost for bipolaron formation, the stabilization of bipolaron by a trap with opposite sign is favored. Additionally, interface doping of Spiro-TAD with F6-TNAP reveals a significant enhancement in MR caused by an increase in trap density and charge carriers, boosting the effectiveness of bipolaron stabilization. (ii) Larger energetic disorder that might compensate the energy cost for bipolaron formation is expected to be obtained for a device fabricated on bare SiO 2 caused by dipolar disorder at the corresponding interface. Adding a thin layer of F6-TNAP is expected to increase the energetic disorder as well.

Drying under solvent atmosphere (DUSA) was investigated as an experimental technique to generate self-assembled nanowires and needles from solutions of organic molecules under controlled conditions.

We present unique properties of self‐assembled spirobi‐fluorene‐substituted perylenetetraccarboxylic diimide wires. The wires have shown an unusual molecular packing motif beyond the typical π‐π stacking. We are also able to estimate the corresponding electron mobility. Finally, the self‐healing effect of such wires, including the reversible color change, is presented and described

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