journal article·2020-12-28

Ultrafine Palladium Nanoparticles Stabilized in the Porous Liquid of Covalent Organic Cages for Photocatalytic Hydrogen Evolution

Jian-Hua Zhang, Mei-Juan Wei, Yu-Lin Lu, Zhang-Wen Wei, Hai-Ping Wang, Mei Pan

ACS Applied Energy Materials· Volume 3· Issue 12
Publisher page

Abstract

Soluble covalent organic cages (COCs) were designed to comprise cryptand inner cavities and multiple metal-chelating sites on windows. The porous liquid formed by well-dispersed COCs in solution proves to be an excellent stabilizer for ultrafine palladium nanoparticles with a critical size of 1–3 nm using NaBH4 or methanol as a reductant. When transferring palladium nanoparticles stabilized in the porous liquid of COCs onto carbon nitride (g-C3N4), an efficient heterogeneous photocatalyst could be obtained to possess high catalytic activity for hydrogen evolution from water with long-term durability. This provides prospects for the application of porous liquids in various fields by combining advantages of homogeneous and heterogeneous attributes together.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Advanced Photocatalysis Techniques · Metal-Organic Frameworks: Synthesis and Applications

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

Affiliations

MOE Laboratory of Bioinorganic and Synthetic Chemistry, Lehn Institute of Functional Materials, School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China

School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, China

Funding

Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Guangdong Pearl River Talents Program

References (39)

Show source-provided references
1. 10.1021/acs.chemrev.7b0077610.1021/acs.chemrev.7b00776 ↗
2. 10.1016/j.cej.2020.12548410.1016/j.cej.2020.125484 ↗
3. 10.1021/cs400506q10.1021/cs400506q ↗
4. 10.1021/acsami.0c0341510.1021/acsami.0c03415 ↗
5. 10.1021/acssuschemeng.9b0339210.1021/acssuschemeng.9b03392 ↗
6. 10.1016/j.jcis.2020.05.06410.1016/j.jcis.2020.05.064 ↗
7. 10.1021/acsami.0c0395910.1021/acsami.0c03959 ↗
8. 10.1039/c3cc49331h10.1039/c3cc49331h ↗
9. 10.1016/j.jhazmat.2020.12294510.1016/j.jhazmat.2020.122945 ↗
10. 10.1021/acscatal.8b0465310.1021/acscatal.8b04653 ↗
11. 10.1016/j.apcatb.2020.11905310.1016/j.apcatb.2020.119053 ↗
12. 10.1038/nmat450010.1038/nmat4500 ↗
13. 10.1038/nmat503710.1038/nmat5037 ↗
14. 10.1021/jacs.7b0335710.1021/jacs.7b03357 ↗
15. 10.1039/C6CS00537C10.1039/C6CS00537C ↗
16. 10.1039/c2cs35047e10.1039/c2cs35047e ↗
17. 10.1016/j.ccr.2015.08.00210.1016/j.ccr.2015.08.002 ↗
18. 10.1039/C2CS35320B10.1039/C2CS35320B ↗
19. 10.1039/C4CE01251H10.1039/C4CE01251H ↗
20. 10.1039/C6CS00724D10.1039/C6CS00724D ↗
21. 10.1039/C8CC05369C10.1039/C8CC05369C ↗
22. 10.1021/jacs.6b0618510.1021/jacs.6b06185 ↗
23. 10.1021/jacs.6b1121810.1021/jacs.6b11218 ↗
24. 10.1002/anie.20171237210.1002/anie.201712372 ↗
25. 10.1016/j.chempr.2018.01.00410.1016/j.chempr.2018.01.004 ↗
26. 10.1002/anie.20190016310.1002/anie.201900163 ↗
27. 10.1039/C7CC09918E10.1039/C7CC09918E ↗
28. 10.1021/jacs.5b1330710.1021/jacs.5b13307 ↗
29. 10.1021/jacs.5b0402910.1021/jacs.5b04029 ↗
30. 10.1038/nature1607210.1038/nature16072 ↗
31. 10.1021/jacs.8b0776710.1021/jacs.8b07767 ↗
32. 10.1038/s41929-018-0030-810.1038/s41929-018-0030-8 ↗
33. 10.1021/ja412606t10.1021/ja412606t ↗
34. 10.1002/anie.20190870310.1002/anie.201908703 ↗
35. 10.1039/C6CS00532B10.1039/C6CS00532B ↗
36. 10.1002/adma.20180754010.1002/adma.201807540 ↗
37. 10.1021/acsanm.9b0259010.1021/acsanm.9b02590 ↗
38. 10.1002/anie.20191577410.1002/anie.201915774 ↗
39. 10.1039/C8TA06726K10.1039/C8TA06726K ↗