journal article·2025-04-11

Silsesquioxane-Based Hybrid Semiconductor Polymers for Efficient Antibiotic Photodegradation and Detection Simultaneously

Mengshuang Zhang, Hongzhi Liu

ACS Applied Polymer Materials· Volume 7· Issue 7
Publisher page

Abstract

Recently, photocatalysis technology has become a promising wastewater treatment technology due to its advantages of green, high efficiency, and low cost. In this study, two silsesquioxane-based fluorescent hybrid porous polymers with semiconducting properties, PCS–PSP and PCS–PSSP, were synthesized by the Friedel–Crafts reaction of octavinylsilsesquioxane with 4,4′-thiene-2,5-diyldibenzonitrile (PSP) and 4,4′-(2,2′-bithiophene-5,5′-diyl)dibenzonitrile (PSSP). The study focused on their physicochemical characterization and photocatalytic activity. Compared with PCS–PSSP, PCS–PSP showed higher thermal decomposition temperature ( T 5% = 385 °C), larger specific surface area (1001 m 2 g –1 ), greater pore volume (0.75 cm 3 g –1 ), more substantial light absorption capacity (250–561 nm), and smaller optical band gap ( E g = 2.21 eV). Their photocatalytic ability was carried out to degrade tetracycline (TH) under visible light, and PCS–PSP exhibited a superior performance with 51% of TH adsorption in the dark and 84% removal efficiency after 1 h of light irradiation. Meanwhile, it also has excellent stability and recyclability. Free-radical trapping experiments and electron spin resonance tests revealed that superoxide radicals ( • O 2 – ) played a significant role in the photocatalytic degradation process. Surprisingly, PCS–PSP also can be used as a probe for TH detection with high sensitivity and selectivity. This work provides a strategy for simultaneous antibiotic photodegradation and detection in environmental applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Polydiacetylene-based materials and applications · Dendrimers and Hyperbranched Polymers

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

Affiliations

International Centre for Interdisciplinary Research and Innovation of Silsesquioxane Science, Key Laboratory of Special Functional Aggregated Materials, Ministry of Education, School of Chemistry and Chemical Engineering

Shandong University

Funding

National Key Research and Development Program of China · Shandong University · National Natural Science Foundation of China

References (52)

Show source-provided references
1. 10.1016/j.cej.2023.14753410.1016/j.cej.2023.147534 ↗
2. 10.1016/j.jhazmat.2021.12694410.1016/j.jhazmat.2021.126944 ↗
3. 10.1016/j.cej.2020.12773910.1016/j.cej.2020.127739 ↗
4. 10.1039/D1CE00245G10.1039/D1CE00245G ↗
5. 10.1016/j.chemosphere.2016.03.08310.1016/j.chemosphere.2016.03.083 ↗
6. 10.1016/j.jwpe.2023.10360510.1016/j.jwpe.2023.103605 ↗
7. 10.1007/s10532-023-10018-510.1007/s10532-023-10018-5 ↗
8. 10.1016/j.jhazmat.2020.12446110.1016/j.jhazmat.2020.124461 ↗
9. 10.1016/j.nxmate.2024.10012310.1016/j.nxmate.2024.100123 ↗
10. 10.1016/j.cej.2019.12284210.1016/j.cej.2019.122842 ↗
11. 10.1016/j.jes.2022.06.03210.1016/j.jes.2022.06.032 ↗
12. 10.1016/j.chemosphere.2021.13303210.1016/j.chemosphere.2021.133032 ↗
13. 10.1016/j.apcatb.2020.11917410.1016/j.apcatb.2020.119174 ↗
14. 10.1016/j.apsusc.2018.12.17810.1016/j.apsusc.2018.12.178 ↗
15. 10.1016/j.envres.2022.11333610.1016/j.envres.2022.113336 ↗
16. 10.1039/D0DT00587H10.1039/D0DT00587H ↗
17. 10.1016/j.eurpolymj.2023.11207210.1016/j.eurpolymj.2023.112072 ↗
18. 10.1021/acsapm.2c0170910.1021/acsapm.2c01709 ↗
19. 10.1039/C6TA06656A10.1039/C6TA06656A ↗
20. 10.1016/j.surfcoat.2023.12928510.1016/j.surfcoat.2023.129285 ↗
21. 10.1002/macp.20197000910.1002/macp.201970009 ↗
22. 10.1021/acs.macromol.9b0069910.1021/acs.macromol.9b00699 ↗
23. 10.1021/acs.macromol.9b0070010.1021/acs.macromol.9b00700 ↗
24. 10.1021/acsapm.0c0059110.1021/acsapm.0c00591 ↗
25. 10.1021/ma401423f10.1021/ma401423f ↗
26. 10.1002/cctc.20210123110.1002/cctc.202101231 ↗
27. 10.1002/adfm.20221487510.1002/adfm.202214875 ↗
28. 10.1021/acssuschemeng.2c0093510.1021/acssuschemeng.2c00935 ↗
29. 10.1021/acs.langmuir.4c0080010.1021/acs.langmuir.4c00800 ↗
30. 10.1016/j.cej.2023.14232310.1016/j.cej.2023.142323 ↗
31. 10.1016/j.micromeso.2020.11069510.1016/j.micromeso.2020.110695 ↗
32. 10.1016/j.polymer.2021.12408310.1016/j.polymer.2021.124083 ↗
33. 10.1021/cm101788210.1021/cm1017882 ↗
34. 10.1039/b904665h10.1039/b904665h ↗
35. 10.1021/acsami.0c0134210.1021/acsami.0c01342 ↗
36. 10.1016/j.cej.2021.12861910.1016/j.cej.2021.128619 ↗
37. 10.1016/j.jcis.2018.02.06710.1016/j.jcis.2018.02.067 ↗
38. 10.1021/acsomega.3c0276210.1021/acsomega.3c02762 ↗
39. 10.1007/s11356-011-0736-510.1007/s11356-011-0736-5 ↗
40. 10.1016/j.cej.2023.14213010.1016/j.cej.2023.142130 ↗
41. 10.1016/j.jhazmat.2017.07.00410.1016/j.jhazmat.2017.07.004 ↗
42. 10.1016/j.apcatb.2023.12322610.1016/j.apcatb.2023.123226 ↗
43. 10.1016/j.solidstatesciences.2021.10661110.1016/j.solidstatesciences.2021.106611 ↗
44. 10.1016/j.jcis.2017.06.01810.1016/j.jcis.2017.06.018 ↗
45. 10.1021/acsami.1c0276110.1021/acsami.1c02761 ↗
46. 10.1016/j.cej.2019.03.19610.1016/j.cej.2019.03.196 ↗
47. 10.1016/j.seppur.2022.12153810.1016/j.seppur.2022.121538 ↗
48. 10.1021/jacs.6b0166310.1021/jacs.6b01663 ↗
49. 10.1021/acsapm.2c0153810.1021/acsapm.2c01538 ↗
50. 10.1016/j.polymer.2022.12478810.1016/j.polymer.2022.124788 ↗
51. 10.1002/anie.20120888510.1002/anie.201208885 ↗
52. 10.1002/chem.20210417510.1002/chem.202104175 ↗