journal article·2020-05

Flexible Porous Organic Polymer Membranes for Protonic Field‐Effect Transistors

Hong Zhong, Guodong Wu, Zhihua Fu, Haowei Lv, Gang Xu, Ruihu Wang

Advanced Materials· Volume 32· Issue 21
Publisher page

Abstract

Abstract Artificial transistors represent an ideal means for meeting the requirements in interfacing with biological systems. It is pivotal to develop new proton‐conductive materials for the transduction between biochemical events and electronic signals. Herein, the first demonstration of a porous organic polymer membrane (POPM) as a proton‐conductive material for protonic field‐effect transistors is presented. The POPM is readily prepared through a thiourea‐formation condensation reaction. Under hydrated conditions and at room temperature, the POPM delivers a proton mobility of 5.7 × 10−3 cm2 V−1 s−1; the charge carrier densities are successfully modulated from 4.3 × 1017 to 14.1 × 1017 cm−3 by the gate voltage. This study provides a type of promising modular proton‐conductive materials for bioelectronics application.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Fuel Cells and Related Materials · Conducting polymers and applications · Covalent Organic Framework Applications

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

Affiliations

State Key Laboratory of Structural Chemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou Fujian 350002 China

University of Chinese Academy of Sciences Beijing 100049 China

Funding

National Basic Research Program of China · National Natural Science Foundation of China · Natural Science Foundation of Fujian Province · Chinese Academy of Sciences · Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences and Peking Union Medical College

References (41)

Show source-provided references
1. 10.1039/b606785a10.1039/b606785a ↗
2. 10.1021/cr200177j10.1021/cr200177j ↗
3. 10.1038/nm.439910.1038/nm.4399 ↗
4. 10.1002/anie.20100124310.1002/anie.201001243 ↗
5. 10.1038/294371a010.1038/294371a0 ↗
6. 10.1002/adma.20140032010.1002/adma.201400320 ↗
7. 10.1038/srep0248110.1038/srep02481 ↗
8. 10.1038/ncomms415810.1038/ncomms4158 ↗
9. 10.1002/advs.20160052710.1002/advs.201600527 ↗
10. 10.1039/C5TC00502G10.1039/C5TC00502G ↗
11. 10.1021/acs.chemmater.6b0033610.1021/acs.chemmater.6b00336 ↗
12. 10.1039/C9TC02452B10.1039/C9TC02452B ↗
13. 10.1002/anie.20180364910.1002/anie.201803649 ↗
14. 10.1002/anie.20120641010.1002/anie.201206410 ↗
15. 10.1039/b902343g10.1039/b902343g ↗
16. 10.1002/anie.20190398010.1002/anie.201903980 ↗
17. 10.1038/nchem.196010.1038/nchem.1960 ↗
18. 10.1038/ncomms148910.1038/ncomms1489 ↗
19. 10.1038/nmat212710.1038/nmat2127 ↗
20. 10.1002/anie.20150836710.1002/anie.201508367 ↗
21. 10.1021/ja502212v10.1021/ja502212v ↗
22. 10.1021/ja511389q10.1021/ja511389q ↗
23. 10.1002/adma.20130125210.1002/adma.201301252 ↗
24. 10.1021/acsami.9b1103210.1021/acsami.9b11032 ↗
25. 10.1039/c3cs35497k10.1039/c3cs35497k ↗
26. 10.1002/adfm.20170146510.1002/adfm.201701465 ↗
27. 10.1021/jacs.8b0959610.1021/jacs.8b09596 ↗
28. 10.1021/acsami.8b2163910.1021/acsami.8b21639 ↗
29. 10.1016/j.bios.2017.07.00110.1016/j.bios.2017.07.001 ↗
30. 10.1016/j.ijbiomac.2019.12.03810.1016/j.ijbiomac.2019.12.038 ↗
31. 10.1016/S0040-4039(01)02295-X10.1016/S0040-4039(01)02295-X ↗
32. 10.1039/C2SC21927A10.1039/C2SC21927A ↗
33. 10.1002/adma.20170515510.1002/adma.201705155 ↗
34. 10.1088/1468-6996/11/3/03300110.1088/1468-6996/11/3/033001 ↗
35. 10.1039/C9SC00131J10.1039/C9SC00131J ↗
36. 10.1039/C8SC04475A10.1039/C8SC04475A ↗
37. 10.1021/acs.chemmater.6b0128610.1021/acs.chemmater.6b01286 ↗
38. 10.1002/chem.20180612610.1002/chem.201806126 ↗
39. 10.1002/adma.20160022210.1002/adma.201600222 ↗
40. 10.1039/dt981000094910.1039/dt9810000949 ↗
41. 10.1088/0953-8984/28/2/02300110.1088/0953-8984/28/2/023001 ↗