journal article·2026-04-06

CO 2 -Derived Synthesis of Hydrogen-Bonded Organic Framework Films

Siquan Zhang, Yong-Sheng Wei, Ellan K. Berdichevsky, Loris Lombardo, Cheng Luo, Zhichong Yu, Yongqi Ren, Satoshi Horike

ACS Materials Letters· Volume 8· Issue 4
Publisher page

Abstract

We synthesized a hydrogen-bonded organic framework (HOF) built from a CO 2 -derived 4,4′,4″,4‴-(1,4-phenylenebis(methanetriyl))tetrakis(piperazine-1-carbaldehyde). Single-crystal X-ray analysis revealed a two-dimensional network with a sql topology, and the HOF exhibited permanent porosity with a BET surface area of 315 m 2 g –1 and high solution processability. The spin-coating process enabled the fabrication of a homogeneous film with a controllable thickness depending on the concentration of the precursor solutions. The film showed an in-plane proton conductivity of 6.2 × 10 –3 S·cm –1 and an activation energy of 0.13 eV under 30 °C, 95% relative humidity.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Fuel Cells and Related Materials

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

Affiliations

Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan

Institute for Integrated Cell-Material Sciences, Institute for Advanced Study, Kyoto University, Yoshida-Honmachi, Sakyo-ku, Kyoto 606-8501, Japan

Department of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwakecho, Kyoto 606-8502, Japan

Department of Materials Science and Engineering, School of Molecular Science and Engineering

Vidyasirimedhi Institute of Science and Technology

Funding

Ministry of Education, Culture, Sports, Science and Technology · Murata Science and Education Foundation · Asahi Glass Foundation · Foundation for the Promotion of Ion Engineering · Japan Society for the Promotion of Science · Japan Science and Technology Agency · China Scholarship Council · Iketani Science and Technology Foundation · Research Institute for Production Development

References (50)

Show source-provided references
1. 10.1016/j.jes.2021.05.04310.1016/j.jes.2021.05.043 ↗
2. 10.1002/app.4408610.1002/app.44086 ↗
3. 10.1021/jacs.9b1310610.1021/jacs.9b13106 ↗
4. 10.1002/anie.20060376410.1002/anie.200603764 ↗
5. 10.1002/cssc.20150159110.1002/cssc.201501591 ↗
6. 10.1002/cssc.20190140410.1002/cssc.201901404 ↗
7. 10.1038/s41586-019-1760-810.1038/s41586-019-1760-8 ↗
8. 10.1038/s41467-020-17403-110.1038/s41467-020-17403-1 ↗
9. 10.1038/378703a010.1038/378703a0 ↗
10. 10.1002/anie.19971725110.1002/anie.199717251 ↗
11. 10.1126/science.112041110.1126/science.1120411 ↗
12. 10.1021/jacs.1c0822710.1021/jacs.1c08227 ↗
13. 10.1002/anie.20231209510.1002/anie.202312095 ↗
14. 10.1021/jacs.4c0347610.1021/jacs.4c03476 ↗
15. 10.1021/acs.accounts.4c0051910.1021/acs.accounts.4c00519 ↗
16. 10.1021/ja206601610.1021/ja2066016 ↗
17. 10.1002/anie.20190214710.1002/anie.201902147 ↗
18. 10.1038/s41467-025-64715-110.1038/s41467-025-64715-1 ↗
19. 10.1016/j.chempr.2022.07.00910.1016/j.chempr.2022.07.009 ↗
20. 10.1002/adma.20230534410.1002/adma.202305344 ↗
21. 10.1039/D3CS00866E10.1039/D3CS00866E ↗
22. 10.1021/acs.organomet.5b0019010.1021/acs.organomet.5b00190 ↗
23. 10.1016/j.chempr.2022.06.01510.1016/j.chempr.2022.06.015 ↗
24. 10.1039/D4SC02628D10.1039/D4SC02628D ↗
25. 10.1002/anie.20161090110.1002/anie.201610901 ↗
26. 10.1038/s41929-023-00999-010.1038/s41929-023-00999-0 ↗
27. 10.1038/s41929-023-00972-x10.1038/s41929-023-00972-x ↗
28. 10.1002/adma.20230913010.1002/adma.202309130 ↗
29. 10.1038/s41557-025-01744-910.1038/s41557-025-01744-9 ↗
30. 10.1002/anie.20231148010.1002/anie.202311480 ↗
31. 10.1038/s41467-019-10575-510.1038/s41467-019-10575-5 ↗
32. 10.1016/j.chempr.2023.01.01310.1016/j.chempr.2023.01.013 ↗
33. 10.1002/adom.20240232110.1002/adom.202402321 ↗
34. 10.1021/jacs.2c0259810.1021/jacs.2c02598 ↗
35. 10.1016/j.jcou.2017.10.00710.1016/j.jcou.2017.10.007 ↗
36. 10.1002/anie.20210044710.1002/anie.202100447 ↗
37. 10.1021/ja902116f10.1021/ja902116f ↗
38. 10.1021/jacs.9b0801710.1021/jacs.9b08017 ↗
39. 10.1021/acsami.9b1450910.1021/acsami.9b14509 ↗
40. 10.1260/026361705349903210.1260/0263617053499032 ↗
41. 10.1021/acs.chemmater.7b0336110.1021/acs.chemmater.7b03361 ↗
42. 10.1038/s41467-017-01166-310.1038/s41467-017-01166-3 ↗
43. 10.1021/la901476q10.1021/la901476q ↗
44. 10.1038/s42004-019-0225-110.1038/s42004-019-0225-1 ↗
45. 10.1002/adma.20170655110.1002/adma.201706551 ↗
46. 10.1038/s44160-025-00738-210.1038/s44160-025-00738-2 ↗
47. 10.1021/cm950192a10.1021/cm950192a ↗
48. 10.1021/jacs.4c1402910.1021/jacs.4c14029 ↗
49. Staneva M. · J. Chem. Eng. Chem. Res. · 2014 · 1 · 15
50. 10.4028/www.scientific.net/MSF.807.16110.4028/www.scientific.net/MSF.807.161 ↗