journal article·2023-08Open access

Synergistic Effect of Crown Ether and Main‐Chain Engineering for Boosting Hydrogen Evolution of Polymer Photocatalysts in Seawater

Chih‐Li Chang, Tse‐Fu Huang, Wei‐Cheng Lin, Li‐Yu Ting, Chin‐Hsuan Shih, Yan‐Heng Chen, Jia‐Jen Liu, Yu‐Tung Lin, Yuang‐Ting Tseng, Yi‐Hsiang Wu, Yu‐En Sun, Mohamed Hammad Elsayed, Chin‐Wen Chen, Chi‐Hua Yu, Ho‐Hsiu Chou

Advanced Energy Materials· Volume 13· Issue 29

Abstract

Abstract Photocatalytic hydrogen evolution from natural seawater faces the severe challenges of abundant salts, which adsorb on the active sites and result in undesirable side reactions and photocatalyst poisoning. Herein, a series of main‐chain‐engineered discontinuously conjugated polymer (DCP) photocatalysts is presented with bifunctional crown ether (CE) structures for hydrogen evolution from seawater. The hydrophilic CE can significantly inhibit the aggregation of DCPs induced by salts. Meanwhile, cyclic CE can effectively adsorb cations to uncover the active sites to increase their interaction with protons, which can increase the hydrogen evolution rates and significantly reduce the efficiency roll‐off in natural seawater. Through atomistic studies, the formation of hydrogen bonds with bifunctional CE is elucidated and further analysis of the microscale mechanisms is also conducted using molecular dynamics and ab initio techniques. This work suggests that CE‐based polymer has the potential to enhance its ability to produce hydrogen through photocatalysis using seawater.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Covalent Organic Framework Applications · Gas Sensing Nanomaterials and Sensors

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

Affiliations

Department of Chemical Engineering National Tsing Hua University Hsinchu 300044 Taiwan

Research Center for Applied Science Academia Sinica Taipei 11529 Taiwan

Academy of Innovative Semiconductor and Sustainable Manufacturing National Cheng Kung University Tainan 701401 Taiwan

Department of Chemistry Faculty of Science Al‐Azhar University Nasr City Cairo 11884 Egypt

Department of Molecular Science and Engineering National Taipei University of Technology Taipei 106344 Taiwan

Department of Engineering Science National Cheng Kung University Tainan 701401 Taiwan

College of Semiconductor Research National Tsing Hua University Hsinchu 300044 Taiwan

References (60)

Show source-provided references
1. 10.1038/nphoton.2012.17510.1038/nphoton.2012.175 ↗
2. 10.1039/B802262N10.1039/B802262N ↗
3. 10.1002/cctc.20190172510.1002/cctc.201901725 ↗
4. 10.1039/C7SC01747B10.1039/C7SC01747B ↗
5. 10.1038/s41560-019-0456-510.1038/s41560-019-0456-5 ↗
6. 10.1039/B800489G10.1039/B800489G ↗
7. 10.1039/c3985000047410.1039/c39850000474 ↗
8. 10.1038/ncomms950810.1038/ncomms9508 ↗
9. 10.1038/s41557-018-0141-510.1038/s41557-018-0141-5 ↗
10. 10.1002/adma.20200849810.1002/adma.202008498 ↗
11. 10.1002/adfm.20210942310.1002/adfm.202109423 ↗
12. 10.1016/j.apcatb.2022.12114410.1016/j.apcatb.2022.121144 ↗
13. 10.1038/s41467-021-24179-510.1038/s41467-021-24179-5 ↗
14. 10.1038/s41467-021-21527-310.1038/s41467-021-21527-3 ↗
15. 10.1039/D2TA00241H10.1039/D2TA00241H ↗
16. 10.1002/adfm.20221086710.1002/adfm.202210867 ↗
17. 10.1002/smll.20220197410.1002/smll.202201974 ↗
18. 10.1021/acscatal.2c0277010.1021/acscatal.2c02770 ↗
19. 10.1039/C9TA04018H10.1039/C9TA04018H ↗
20. 10.1039/C9TA06219J10.1039/C9TA06219J ↗
21. 10.1016/j.apsusc.2019.14386510.1016/j.apsusc.2019.143865 ↗
22. 10.1039/D0EE01213K10.1039/D0EE01213K ↗
23. 10.1002/adma.20210500710.1002/adma.202105007 ↗
24. 10.1039/C7EE00751E10.1039/C7EE00751E ↗
25. 10.1021/acscatal.8b0167810.1021/acscatal.8b01678 ↗
26. 10.1016/j.apcatb.2019.11843610.1016/j.apcatb.2019.118436 ↗
27. 10.1039/C8TA11383A10.1039/C8TA11383A ↗
28. 10.1021/acssuschemeng.8b0563710.1021/acssuschemeng.8b05637 ↗
29. 10.1038/s41563-019-0591-110.1038/s41563-019-0591-1 ↗
30. 10.1002/anie.20151054210.1002/anie.201510542 ↗
31. 10.1038/s41467-018-07420-610.1038/s41467-018-07420-6 ↗
32. 10.1039/C9TA13514F10.1039/C9TA13514F ↗
33. 10.1038/s41467-022-33211-110.1038/s41467-022-33211-1 ↗
34. 10.1016/j.jphotochem.2007.01.01110.1016/j.jphotochem.2007.01.011 ↗
35. 10.1007/s12274-020-2880-z10.1007/s12274-020-2880-z ↗
36. 10.1039/c1ee01812d10.1039/c1ee01812d ↗
37. 10.1002/chem.20180411910.1002/chem.201804119 ↗
38. 10.1021/acssuschemeng.9b0474910.1021/acssuschemeng.9b04749 ↗
39. 10.1002/adfm.20180815610.1002/adfm.201808156 ↗
40. 10.1016/j.molcata.2011.03.02610.1016/j.molcata.2011.03.026 ↗
41. 10.1016/j.ijhydene.2011.05.16610.1016/j.ijhydene.2011.05.166 ↗
42. 10.1039/C7NR07095K10.1039/C7NR07095K ↗
43. 10.1016/j.apcatb.2018.09.09610.1016/j.apcatb.2018.09.096 ↗
44. 10.1039/C6EE00971A10.1039/C6EE00971A ↗
45. 10.1039/c4cp01043d10.1039/c4cp01043d ↗
46. 10.1039/C1CS15220C10.1039/C1CS15220C ↗
47. 10.1021/acs.chemrev.9b0083910.1021/acs.chemrev.9b00839 ↗
48. 10.1002/aenm.20180218110.1002/aenm.201802181 ↗
49. 10.1016/j.cej.2022.13715810.1016/j.cej.2022.137158 ↗
50. 10.1002/smll.20220207210.1002/smll.202202072 ↗
51. 10.1039/D1SC05784G10.1039/D1SC05784G ↗
52. 10.1021/acsaem.2c0001710.1021/acsaem.2c00017 ↗
53. 10.1021/ja511552k10.1021/ja511552k ↗
54. 10.1016/j.apcatb.2019.01.01010.1016/j.apcatb.2019.01.010 ↗
55. 10.1021/jacs.2c0710310.1021/jacs.2c07103 ↗
56. 10.1021/jacs.0c0610410.1021/jacs.0c06104 ↗
57. 10.1016/j.biortech.2022.12728610.1016/j.biortech.2022.127286 ↗
58. 10.1016/j.dsr.2007.10.00110.1016/j.dsr.2007.10.001 ↗
59. 10.1016/j.cemconcomp.2021.10429810.1016/j.cemconcomp.2021.104298 ↗
60. 10.1002/jcc.2288510.1002/jcc.22885 ↗