journal article·2022-12-21

Piezotronic Effect Induced Schottky Barrier Decrease to Boost the Plasmonic Charge Separation of BaTiO3-Au Heterojunction for the Photocatalytic Selective Oxidation of Aminobenzyl Alcohol

Hong Liu, Ren Zhu, Nannan Shi, Long Zhang, Shun Li, Jianming Zhang

ACS Applied Materials & Interfaces· Volume 14· Issue 50
Publisher page

Abstract

-Au (BTO-Au) for the efficient selective oxidization of benzyl alcohol to benzaldehyde upon piezotronic effect boosted plasmonic photocharge carrier transfer. With the aid of ultrasonic mechanical vibration, the reaction rate of the photocatalytic organic conversion would be considerably accelerated, which is about 4.2 and 6.2 times higher than those driven by sole visible light irradiation and sole ultrasonication, respectively. Photoelectrochemical tests under ultrasonic stimuli reveal the BTO-Au catalytic system is independent of the light intensity, showing a consistent photocurrent density, over a wide range of incident light brightness. The largely enhanced photocatalytic activity can be ascribed to the synergetic effect of surface plasmonic resonance (SPR)-piezotronic coupling by which a built-in electric field induced by the piezotronic effect significantly favors the oriented mobilization of energetic charge carriers generated by the SPR effect at the heterojunction. Notably, a decrease of the Schottky barrier height of ∼0.3 eV at the BTO-Au interface is verified experimentally, due to the band bending of BTO induced by the piezotronic effect, which can greatly augment the hot electron transfer efficiency. This work highlights the coupling of the piezotronic effect with SPR within the BTO-Au nanostructure as a versatile and promising route for efficient charge transfer in photocatalytic organic conversion.
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Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications · TiO2 Photocatalysis and Solar Cells

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

Affiliations

Institute of Quantum and Sustainable Technology (IQST), School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, Jiangsu212013, China

Oxford Instruments Asylum Research, 461 Hongcao Road, Shanghai200233, China

China Nanoport, Thermo Fisher Scientific, 2517 Jinke Road, Shanghai201203, China

Foshan (Southern China) Institute for New Materials, Foshan, Guangdong528200, China

Funding

Ministry of Science and Technology of the People's Republic of China · Natural Science Foundation of Jiangsu Province · National Natural Science Foundation of China · Guangdong Basic and Applied Basic Research Foundation

References (54)

Show source-provided references
1. 10.1039/C6CS00185H10.1039/C6CS00185H ↗
2. 10.1016/j.apcatb.2019.02.07110.1016/j.apcatb.2019.02.071 ↗
3. Appelbaum, A. I.Process of Manufacturing Benzaldehyde. US Patent 1302273A, 1918.
4. Kantem, M. L.; Choudary, B. M.; Sreekanth, P.; Rao, K. K.Process for the Production of Benzaldehyde by the Catalytic Liquid Phase Air Oxidation of Toluene. US Patent 6495726, 2002.
5. Chaudhari, R. V.; Rajurkar, K. B.; Tonde, S. S.; Rane, V. H.Process for the Liquid Phase Oxidation of Toluene to Benzaldehyde. US Patent 7411099, 2006.
6. 10.1002/adma.20220018010.1002/adma.202200180 ↗
7. 10.1002/adfm.20200192210.1002/adfm.202001922 ↗
8. 10.1039/C8TA03680B10.1039/C8TA03680B ↗
9. 10.1021/jacs.6b1285010.1021/jacs.6b12850 ↗
10. 10.1039/c1cc13801d10.1039/c1cc13801d ↗
11. 10.1016/j.apcatb.2016.01.03810.1016/j.apcatb.2016.01.038 ↗
12. 10.1016/j.apcatb.2017.08.03310.1016/j.apcatb.2017.08.033 ↗
13. 10.1021/ja305225s10.1021/ja305225s ↗
14. 10.1021/ja212064710.1021/ja2120647 ↗
15. 10.1007/s12274-021-3604-810.1007/s12274-021-3604-8 ↗
16. 10.1038/nmat315110.1038/nmat3151 ↗
17. 10.1038/nphoton.2015.14210.1038/nphoton.2015.142 ↗
18. 10.1038/nmat286610.1038/nmat2866 ↗
19. 10.1039/C7NR08487K10.1039/C7NR08487K ↗
20. 10.1016/j.nanoen.2019.05.06710.1016/j.nanoen.2019.05.067 ↗
21. 10.1088/1361-6463/ab197810.1088/1361-6463/ab1978 ↗
22. 10.1021/acsanm.0c0003910.1021/acsanm.0c00039 ↗
23. 10.1016/j.nanoen.2022.10703110.1016/j.nanoen.2022.107031 ↗
24. 10.1002/adfm.20200515810.1002/adfm.202005158 ↗
25. 10.1002/aenm.20200021410.1002/aenm.202000214 ↗
26. 10.1021/acs.chemrev.8b0059910.1021/acs.chemrev.8b00599 ↗
27. 10.1002/smll.20220250710.1002/smll.202202507 ↗
28. 10.1039/D1TC02559G10.1039/D1TC02559G ↗
29. 10.1016/j.jallcom.2019.06.11510.1016/j.jallcom.2019.06.115 ↗
30. 10.1016/j.apcatb.2022.12136910.1016/j.apcatb.2022.121369 ↗
31. 10.1002/adma.20200197610.1002/adma.202001976 ↗
32. 10.1021/nl504630j10.1021/nl504630j ↗
33. 10.1016/j.apsusc.2021.15180710.1016/j.apsusc.2021.151807 ↗
34. 10.1016/j.elspec.2018.03.00810.1016/j.elspec.2018.03.008 ↗
35. Junger M. C. · 1986
36. 10.1021/jp805799310.1021/jp8057993 ↗
37. 10.35848/1347-4065/ac7d9610.35848/1347-4065/ac7d96 ↗
38. 10.1016/j.apcatb.2012.05.03610.1016/j.apcatb.2012.05.036 ↗
39. 10.1021/acsami.7b0015810.1021/acsami.7b00158 ↗
40. 10.1039/C9NH00026G10.1039/C9NH00026G ↗
41. 10.1002/ange.20220351910.1002/ange.202203519 ↗
42. 10.1002/adfm.20210254010.1002/adfm.202102540 ↗
43. 10.1021/acsnano.0c0627810.1021/acsnano.0c06278 ↗
44. 10.1021/acsnano.6b0026310.1021/acsnano.6b00263 ↗
45. 10.1038/nphoton.2013.23810.1038/nphoton.2013.238 ↗
46. 10.1021/acsami.1c0741010.1021/acsami.1c07410 ↗
47. 10.1038/srep1137410.1038/srep11374 ↗
48. 10.1039/C4CY01545B10.1039/C4CY01545B ↗
49. 10.1039/C7TC02633A10.1039/C7TC02633A ↗
50. 10.1016/j.cattod.2019.10.01410.1016/j.cattod.2019.10.014 ↗
51. 10.1016/j.jcat.2016.12.02510.1016/j.jcat.2016.12.025 ↗
52. 10.1021/acsami.6b1518410.1021/acsami.6b15184 ↗
53. 10.1021/acssuschemeng.8b0322210.1021/acssuschemeng.8b03222 ↗
54. 10.1021/nn502303h10.1021/nn502303h ↗