Visible Light Induced Ag–Polyoxometalate Coassembly into Single‐Cluster Nanowires
Source abstract
Abstract
Abstract 1D superlattices with long‐ranged periodicity present extraordinary application properties due to their unique electronic structures. Here, the visible light driven synthesis of 1D single‐cluster chains constructed by polyoxometalate (POM) and Ag clusters is reported, where two types of clusters align alternatively along the nanowire. Low symmetrical POM clusters of [P2W17O61]10–, [P2W15O56]12–, and [EuW10O36]9– can be used as building blocks. The directly bonding cluster units result in interactive electronic structures of Ag and POM clusters, as well as the greatly promoted electron transfer during the redox reaction. The Ag–P2W17 nanowires perform significantly enhanced activities in both electrochemical sensing and catalytic gasoline desulfurization compared with individual building blocks, demonstrating the extraordinary application properties and promising potentials of cluster‐based heteroconstructions.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Nanocluster Synthesis and Applications · Polyoxometalates: Synthesis and Applications · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Lab of Organic Optoelectronics and Molecular Engineering Department of Chemistry Tsinghua University Beijing 100084 China
Institute for New Energy Materials and Low Carbon Technologies School of Materials Science and Engineering Tianjin University of Technology Tianjin 300387 China
Funding
China Postdoctoral Science Foundation
References (31)
Show source-provided references
1. 10.1126/science.107208610.1126/science.1072086 ↗
2. 10.1038/415617a10.1038/415617a ↗
3. 10.1038/nphoton.2009.18410.1038/nphoton.2009.184 ↗
4. 10.1039/C4CS00180J10.1039/C4CS00180J ↗
5. 10.1007/s12274-019-2560-z10.1007/s12274-019-2560-z ↗
6. 10.1007/s40843-021-1688-710.1007/s40843-021-1688-7 ↗
7. 10.1126/science.aaz257010.1126/science.aaz2570 ↗
8. 10.1002/adma.20080016210.1002/adma.200800162 ↗
9. Lu W. · Sci · 2005 · 102 · 10046
10. 10.1021/nl010099n10.1021/nl010099n ↗
11. 10.1021/nl015688810.1021/nl0156888 ↗
12. 10.1021/jacs.6b0005510.1021/jacs.6b00055 ↗
13. 10.1021/acs.chemrev.6b0019610.1021/acs.chemrev.6b00196 ↗
14. 10.1007/s12274-021-3383-210.1007/s12274-021-3383-2 ↗
15. 10.1039/c2cs35143a10.1039/c2cs35143a ↗
16. 10.1039/c2cs35190k10.1039/c2cs35190k ↗
17. 10.1021/acs.chemrev.6b0076910.1021/acs.chemrev.6b00769 ↗
18. 10.1021/acs.chemrev.5b0070310.1021/acs.chemrev.5b00703 ↗
19. 10.1021/ar500158310.1021/ar5001583 ↗
20. 10.1103/PhysRevB.51.1370510.1103/PhysRevB.51.13705 ↗
21. 10.1039/C6NR01998F10.1039/C6NR01998F ↗
22. 10.1021/acs.accounts.6b0046410.1021/acs.accounts.6b00464 ↗
23. 10.1039/c2cs35176e10.1039/c2cs35176e ↗
24. 10.1021/acs.accounts.7b0005510.1021/acs.accounts.7b00055 ↗
25. 10.1016/j.matt.2020.01.02010.1016/j.matt.2020.01.020 ↗
26. 10.31635/ccschem.020.20200049810.31635/ccschem.020.202000498 ↗
27. 10.1038/s41557-022-00889-110.1038/s41557-022-00889-1 ↗
28. 10.1021/cr500390v10.1021/cr500390v ↗
29. 10.1007/s11426-020-9957-010.1007/s11426-020-9957-0 ↗
30. 10.1016/j.cattod.2008.08.03910.1016/j.cattod.2008.08.039 ↗
31. 10.1126/sciadv.aax108110.1126/sciadv.aax1081 ↗