journal article·2018-03

Anisotropic Ag2S–Au Triangular Nanoprisms with Desired Configuration for Plasmonic Photocatalytic Hydrogen Generation in Visible/Near‐Infrared Region

Zaizhu Lou, Sooyeon Kim, Mamoru Fujitsuka, Xianguang Yang, Baojun Li, Tetsuro Majima

Advanced Functional Materials· Volume 28· Issue 13
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Abstract

Abstract Anisotropic Ag2S‐edged Au‐triangular nanoprisms (TNPs) are constructed by controlling preferential overgrowth of Ag2S as plasmonic photocatalysts for hydrogen generation. Under visible and near‐infrared light irradiation, Ag2S‐edged Au‐TNPs exhibit almost fourfold higher efficiency (796 µmol h−1 g−1) than those of Ag2S‐covered Au‐TNPs (216 µmol h−1 g−1) and pure Au‐TNPs in hydrogen generation. A single‐particle photoluminescence study demonstrates that the plasmon‐induced hot electrons transfer from Au‐TNPs to Ag2S for hydrogen generation. Finite‐difference‐time‐domain simulations verify that the corners/edges of Au‐TNPs are high‐curvature sites with maximum electric field distributions facilitating hot electron generation and transfer. Therefore, Ag2S‐edged Au‐TNPs are efficient plasmonic photocatalyst with the desired configurations for charge separation boosting hydrogen generation.
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Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Quantum Dots Synthesis And Properties · Copper-based nanomaterials and applications

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

Affiliations

Guangdong Provincial Key Laboratory of Optical Fiber Sensing and Communications Institute of Nanophotonics Jinan University Guangzhou 511443 China

The Institute of Scientific and Industrial Research (SANKEN) Osaka University Mihogaoka 8‐1 Ibaraki Osaka 567‐0047 Japan

Funding

Ministry of Education, Culture, Sports, Science and Technology · National Natural Science Foundation of China · Natural Science Foundation of Guangdong Province

References (35)

Show source-provided references
1. 10.1021/cr300209210.1021/cr3002092 ↗
2. 10.1021/cs300240x10.1021/cs300240x ↗
3. 10.1021/cr068352x10.1021/cr068352x ↗
4. 10.1002/anie.20141120010.1002/anie.201411200 ↗
5. 10.1021/acs.chemrev.7b0016110.1021/acs.chemrev.7b00161 ↗
6. 10.1016/j.apcatb.2017.09.06310.1016/j.apcatb.2017.09.063 ↗
7. 10.1002/anie.20120719910.1002/anie.201207199 ↗
8. 10.1002/anie.20080248310.1002/anie.200802483 ↗
9. 10.1021/acs.jpclett.6b0304510.1021/acs.jpclett.6b03045 ↗
10. 10.1088/0034-4885/76/4/04640110.1088/0034-4885/76/4/046401 ↗
11. 10.1002/anie.20161231510.1002/anie.201612315 ↗
12. 10.1002/anie.20141203010.1002/anie.201412030 ↗
13. 10.1021/acs.langmuir.7b0111710.1021/acs.langmuir.7b01117 ↗
14. 10.1021/acs.jpcc.6b0237010.1021/acs.jpcc.6b02370 ↗
15. 10.1002/anie.20140559810.1002/anie.201405598 ↗
16. 10.1021/acsami.7b0682410.1021/acsami.7b06824 ↗
17. 10.1002/anie.20130023910.1002/anie.201300239 ↗
18. 10.1021/nn404985h10.1021/nn404985h ↗
19. 10.1021/cs400993w10.1021/cs400993w ↗
20. 10.1021/ja076503n10.1021/ja076503n ↗
21. 10.1002/jbio.20091001510.1002/jbio.200910015 ↗
22. 10.1021/jacs.5b1134110.1021/jacs.5b11341 ↗
23. 10.1021/jacs.6b1028810.1021/jacs.6b10288 ↗
24. 10.1021/acsnano.6b0758110.1021/acsnano.6b07581 ↗
25. 10.1021/acsnano.6b0249410.1021/acsnano.6b02494 ↗
26. 10.1021/ja502704n10.1021/ja502704n ↗
27. 10.1021/jp403308k10.1021/jp403308k ↗
28. 10.1002/adom.20150049610.1002/adom.201500496 ↗
29. 10.1016/j.ijhydene.2017.08.14510.1016/j.ijhydene.2017.08.145 ↗
30. 10.1021/acs.langmuir.7b0002910.1021/acs.langmuir.7b00029 ↗
31. 10.1039/c2cc30766a10.1039/c2cc30766a ↗
32. 10.1002/chem.20120141810.1002/chem.201201418 ↗
33. 10.1021/nn500727w10.1021/nn500727w ↗
34. 10.1103/PhysRevB.6.437010.1103/PhysRevB.6.4370 ↗
35. 10.1186/s13065-015-0099-y10.1186/s13065-015-0099-y ↗