journal article·2022-05Open access

A Dual Functional Diketopyrrolopyrrole‐Based Conjugated Polymer as Single Component Semiconducting Photoresist by Appending Azide Groups in the Side Chains

Chenying Gao, Dandan Shi, Cheng Li, Xiaobo Yu, Xisha Zhang, Zitong Liu, Guanxin Zhang, Deqing Zhang

Advanced Science· Volume 9· Issue 15

Abstract

Abstract Molecular systems that can function as photoresists are essential for the fabrication of flexible electronics through all‐photolithographic processes. Most of the reported molecular systems for photo‐patterning of polymeric semiconductors contain binary or multi‐components. In comparison, single component semiconducting photoresist is advantageous since it will circumvent the optimization of phase separation and ensure the patterned semiconducting thin films to be more uniform. In this paper, a single component semiconducting photoresist (PDPP4T‐N3) by incorporating azide groups into the branching alkyl chains of a diketopyrrolopyrrole‐based conjugated polymer is reported. The results reveal that i) the azide groups make the side chains to be photo‐cross‐linkable; ii) uniform patterns with size as small as 5 µm form under mild UV irradiation (365 nm, 85 mW cm−2) at ambient conditions; iii) such photo‐induced cross‐linking does not affect the inter‐chain packing; iv) benefiting from the single component feature, field‐effect transistors (FETs) with the individual patterned thin films display satisfactorily uniform performances with average charge mobility of 0.61 ± 0.10 cm2 V–1 s–1 and threshold voltage of 3.49 ± 1.43 V. These results offer a simple yet effective design strategy for high‐performance single component semiconducting photoresists, which hold great potentials for flexible electronics processed by all‐photolithography.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Advanced Sensor and Energy Harvesting Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Beijing National Laboratory for Molecular Sciences Organic Solids Laboratory Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China

School of Chemical Sciences University of Chinese Academy of Sciences Beijing 100049 China

State Key Laboratory of Applied Organic Chemistry (SKLAOC) College of Chemistry and Chemical Engineering Lanzhou University Lanzhou 730000 China

Funding

National Natural Science Foundation of China

References (54)

Show source-provided references
1. 10.1038/nature2549410.1038/nature25494 ↗
2. 10.1126/science.aah449610.1126/science.aah4496 ↗
3. 10.1021/acs.chemrev.7b0000310.1021/acs.chemrev.7b00003 ↗
4. 10.1016/j.progpolymsci.2019.10118110.1016/j.progpolymsci.2019.101181 ↗
5. 10.1038/s41563-019-0340-510.1038/s41563-019-0340-5 ↗
6. 10.1039/c3ee00015j10.1039/c3ee00015j ↗
7. 10.1021/acs.accounts.8b0006910.1021/acs.accounts.8b00069 ↗
8. 10.1021/cr100380z10.1021/cr100380z ↗
9. 10.1021/cr050154310.1021/cr0501543 ↗
10. 10.1038/s41563-020-0647-210.1038/s41563-020-0647-2 ↗
11. 10.1002/adma.20190310410.1002/adma.201903104 ↗
12. 10.1021/cr100320w10.1021/cr100320w ↗
13. 10.1126/science.aau075910.1126/science.aau0759 ↗
14. 10.1021/acsami.7b0762410.1021/acsami.7b07624 ↗
15. 10.1021/acs.accounts.0c0089310.1021/acs.accounts.0c00893 ↗
16. 10.1038/417802a10.1038/417802a ↗
17. 10.1002/adma.20190140010.1002/adma.201901400 ↗
18. 10.1002/adma.20160322110.1002/adma.201603221 ↗
19. 10.1002/advs.20200405010.1002/advs.202004050 ↗
20. 10.1039/c0sc00612b10.1039/c0sc00612b ↗
21. 10.1021/acs.chemrev.8b0006310.1021/acs.chemrev.8b00063 ↗
22. 10.1021/acsami.9b1008910.1021/acsami.9b10089 ↗
23. 10.1002/adma.20180018710.1002/adma.201800187 ↗
24. 10.1002/adma.20080220210.1002/adma.200802202 ↗
25. 10.1002/adma.20150420610.1002/adma.201504206 ↗
26. 10.1002/adma.20120015110.1002/adma.201200151 ↗
27. 10.1016/j.cclet.2016.06.02710.1016/j.cclet.2016.06.027 ↗
28. 10.1021/ja210430b10.1021/ja210430b ↗
29. 10.1038/s41467-020-15181-410.1038/s41467-020-15181-4 ↗
30. 10.1021/ja032002010.1021/ja0320020 ↗
31. 10.1126/science.abh355110.1126/science.abh3551 ↗
32. 10.1002/anie.20210842110.1002/anie.202108421 ↗
33. 10.1021/acs.chemmater.8b0431410.1021/acs.chemmater.8b04314 ↗
34. 10.1038/s41467-021-25059-810.1038/s41467-021-25059-8 ↗
35. 10.1039/c1jm12366a10.1039/c1jm12366a ↗
36. Chen R. · Sci. Adv. · 2021 · 7 · 0659
37. 10.1021/ma502289n10.1021/ma502289n ↗
38. 10.1021/ma900026u10.1021/ma900026u ↗
39. 10.1002/pi.471210.1002/pi.4712 ↗
40. 10.1063/1.274917810.1063/1.2749178 ↗
41. 10.1021/cm101818410.1021/cm1018184 ↗
42. 10.1021/ma300172510.1021/ma3001725 ↗
43. 10.1021/cm203058p10.1021/cm203058p ↗
44. 10.1021/ja108599610.1021/ja1085996 ↗
45. 10.1126/sciadv.160007610.1126/sciadv.1600076 ↗
46. 10.1002/advs.20180149710.1002/advs.201801497 ↗
47. 10.1039/b802910e10.1039/b802910e ↗
48. 10.1103/PhysRevB.81.03532710.1103/PhysRevB.81.035327 ↗
49. 10.1038/nmat97810.1038/nmat978 ↗
50. 10.1038/srep0075410.1038/srep00754 ↗
51. 10.1002/adma.20180195110.1002/adma.201801951 ↗
52. 10.1002/adma.20180601010.1002/adma.201806010 ↗
53. 10.1002/adma.20160289310.1002/adma.201602893 ↗
54. 10.1002/adfm.20191023510.1002/adfm.201910235 ↗