Exploring the Different Roles of Particle Size in Photoelectrochemical and Photocatalytic Water Oxidation on BiVO4
Source abstract
Abstract
Water oxidation on visible-light-active bismuth vanadate (BiVO 4 ) has commonly been demonstrated to be viable in powder suspension (PS) and particulate photoelectrochemical (PEC) systems. Here, we demonstrate that particle size reduction, which is known to be efficacious in promoting charge carrier extraction and boosting surface active sites, has an opposite effect on BiVO 4 ’s photoactivity in the two systems. With three BiVO 4 samples of distinctive particle sizes, smaller BiVO 4 particle size is shown to be beneficial for enhancing PEC photocurrent generation, but deleterious for photocatalytic O 2 evolution on suspended BiVO 4 . Such contrary effect of particle size in the PEC and PS systems is revealed to be due to the different governing factors of the systems: charge transport in the former and charge separation in the latter. Smaller particle size was found to enrich the interparticle and the particle/FTO substrate contacts which improve charge transport and charge collection efficiency in BiVO 4 particulate electrode. On the contrary, larger particle size is necessary for improved photocatalytic O 2 evolution because of increased crystallinity and greater band bending, which are essential for charge separation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Gas Sensing Nanomaterials and Sensors · Copper-based nanomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Particles and Catalysis Research Group, School of Chemical Engineering, The University of New South Wales, Sydney, New South Wales 2052, Australia
Funding
Australian Research Council
References (43)
Show source-provided references
1. 10.1016/S1010-6030(02)00070-910.1016/S1010-6030(02)00070-9 ↗
2. 10.1246/cl.2004.134810.1246/cl.2004.1348 ↗
3. 10.1021/ja203296z10.1021/ja203296z ↗
4. 10.1021/cs400208910.1021/cs4002089 ↗
5. 10.1021/ja992541y10.1021/ja992541y ↗
6. 10.1021/jp057539+10.1021/jp057539+ ↗
7. 10.1023/A:101903472881610.1023/A:1019034728816 ↗
8. 10.1021/cm010339010.1021/cm0103390 ↗
9. 10.1039/b310428a10.1039/b310428a ↗
10. 10.1021/jp203004v10.1021/jp203004v ↗
11. 10.1002/cctc.20120047210.1002/cctc.201200472 ↗
12. 10.1126/science.124691310.1126/science.1246913 ↗
13. 10.1039/c1ee01812d10.1039/c1ee01812d ↗
14. 10.1039/c2ee22608a10.1039/c2ee22608a ↗
15. 10.1039/C3CP54356K10.1039/C3CP54356K ↗
16. 10.1021/jp300755210.1021/jp3007552 ↗
17. 10.1021/jp210584b10.1021/jp210584b ↗
18. 10.1021/ja207348x10.1021/ja207348x ↗
19. 10.1039/c1ee02444b10.1039/c1ee02444b ↗
20. 10.1021/ja209001d10.1021/ja209001d ↗
21. 10.1039/b713338c10.1039/b713338c ↗
22. 10.1021/jp210207q10.1021/jp210207q ↗
23. 10.1038/ncomms319510.1038/ncomms3195 ↗
24. 10.1021/jz401325710.1021/jz4013257 ↗
25. 10.1021/nl500022z10.1021/nl500022z ↗
26. Osterloh F. E. · 2015 · 10510.1007/128_2015_633 ↗
27. 10.1007/s11244-016-0549-310.1007/s11244-016-0549-3 ↗
28. 10.1016/j.ijhydene.2009.02.00610.1016/j.ijhydene.2009.02.006 ↗
29. 10.1021/am200247y10.1021/am200247y ↗
30. 10.1039/c0jm00961j10.1039/c0jm00961j ↗
31. 10.1115/1.400117210.1115/1.4001172 ↗
32. 10.1021/jz100978u10.1021/jz100978u ↗
33. 10.1021/jp200274k10.1021/jp200274k ↗
34. 10.1016/j.ijhydene.2015.01.08510.1016/j.ijhydene.2015.01.085 ↗
35. 10.1103/PhysRevLett.41.142510.1103/PhysRevLett.41.1425 ↗
36. 10.1002/(SICI)1096-9918(199807)26:8<549::AID-SIA396>3.0.CO;2-Q10.1002/(SICI)1096-9918(199807)26:8<549::AID-SIA396>3.0.CO;2-Q ↗
37. 10.1039/c2cp40807d10.1039/c2cp40807d ↗
38. 10.1021/nl201766h10.1021/nl201766h ↗
39. 10.1021/jz300179k10.1021/jz300179k ↗
40. 10.1021/jp002232q10.1021/jp002232q ↗
41. 10.1021/cr300062610.1021/cr3000626 ↗
42. 10.1016/S1010-6030(00)00204-510.1016/S1010-6030(00)00204-5 ↗
43. 10.1039/b202140d10.1039/b202140d ↗