journal article·2013-06-24

Electrochemical Synthesis of Transparent, Amorphous, C60‐Rich, Photoactive, and Low‐Doped Film with an Interconnected Structure

Mao Li, Shinsuke Ishihara, Kei Ohkubo, Meiyong Liao, Qingmin Ji, Cheng Gu, Yuyu Pan, Xiangfen Jiang, Misaho Akada, Jonathan P. Hill, Takashi Nakanishi, Yuguang Ma, Yusuke Yamauchi, Shunichi Fukuzumi, Katsuhiko Ariga

Small· Volume 9· Issue 12
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Abstract

An electrochemical synthesis is developed through quantitative electrochemical reaction of N-alkylcarbazole leading to a novel class of structurally interconnected high-C60 content (60 wt%) polymer films with negligible doping and intrinsic physicochemical properties of pure C60. This strategy allows preparation of previously unavailable low-doped fullerene-containing non-conjugated polymers and broadens the potential applications of electrochemical synthesis for controlled polymer film structures. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Fullerene Chemistry and Applications · Conducting polymers and applications

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References (42)

Show source-provided references
1. 10.1002/anie.20070250610.1002/anie.200702506 ↗
2. 10.1021/cr068421810.1021/cr0684218 ↗
3. 10.1039/b900402p10.1039/b900402p ↗
4. 10.1002/anie.20090174610.1002/anie.200901746 ↗
5. 10.1002/adma.20090369710.1002/adma.200903697 ↗
6. 10.1039/c000680g10.1039/c000680g ↗
7. 10.1039/c0cs00225a10.1039/c0cs00225a ↗
8. 10.1039/C0CP01178A10.1039/C0CP01178A ↗
9. 10.1021/cr068389h10.1021/cr068389h ↗
10. 10.1038/350600a010.1038/350600a0 ↗
11. 10.1038/3509514910.1038/35095149 ↗
12. 10.1126/science.106571110.1126/science.1065711 ↗
13. 10.1021/ar970138v10.1021/ar970138v ↗
14. 10.1021/ja047768u10.1021/ja047768u ↗
15. 10.1039/C1CS15201G10.1039/C1CS15201G ↗
16. 10.1002/anie.20046117410.1002/anie.200461174 ↗
17. 10.1021/nn200269510.1021/nn2002695 ↗
18. 10.1021/ja907414z10.1021/ja907414z ↗
19. 10.1103/PhysRevB.55.476610.1103/PhysRevB.55.4766 ↗
20. 10.1023/A:101436841878410.1023/A:1014368418784 ↗
21. 10.1021/ja052408810.1021/ja0524088 ↗
22. 10.1002/anie.20090010610.1002/anie.200900106 ↗
23. 10.1002/anie.19941628110.1002/anie.199416281 ↗
24. 10.1002/anie.19950194110.1002/anie.199501941 ↗
25. 10.1021/ja980552610.1021/ja9805526 ↗
26. 10.1021/cm990733m10.1021/cm990733m ↗
27. 10.1021/cm034364c10.1021/cm034364c ↗
28. 10.1021/jp912033q10.1021/jp912033q ↗
29. 10.1021/ol048081h10.1021/ol048081h ↗
30. 10.1021/ja202768k10.1021/ja202768k ↗
31. 10.1021/jp063123010.1021/jp0631230 ↗
32. 10.1039/b607242a10.1039/b607242a ↗
33. 10.1002/adma.20030037610.1002/adma.200300376 ↗
34. 10.1016/S0379-6779(97)81214-310.1016/S0379-6779(97)81214-3 ↗
35. 10.1063/1.35419910.1063/1.354199 ↗
36. 10.1021/jp980410y10.1021/jp980410y ↗
37. Sze S. M. · 1981
38. 10.1016/j.jelechem.2005.10.02010.1016/j.jelechem.2005.10.020 ↗
39. 10.2217/nnm.11.10710.2217/nnm.11.107 ↗
40. 10.1021/ja037624010.1021/ja0376240 ↗
41. 10.1038/356225a010.1038/356225a0 ↗
42. 10.1002/smll.20110159410.1002/smll.201101594 ↗