Rapid Flame Synthesis of Highly Efficient CuO-CuBi2O4 Heterojunction Photocathode for Improved Charge Separation and Light Capture Efficiency
Source abstract
Abstract
The rapid flame annealing (FA) method has the advantages of convenience and rapidity with an instantaneous temperature rise and fall process. In this work, the influence of flame annealing duration on the front side and back side of CuBi 2 O 4 -based photocathodes was investigated, and photoelectrodes with variable compositions were obtained. A highly efficient CuO@CuO/CuBi 2 O 4 photoelectrode was successfully obtained via a two-step FA method within a few seconds. Excellent hydrogen evolution reaction performance with a photocurrent of 2.3 mA cm –2 @ 0.2 V RHE in 0.1 M Na 2 SO 4 (2.35 mA cm –2 @ 0.6 V RHE in 0.1 M KOH) electrolyte was obtained, which is the highest photocurrent of a CuBi 2 O 4 -based photoelectrode in a neutral electrolyte without a trapping agent so far. The light capture efficiency of the photoelectrode was greatly improved by the introduction of CuO, which formed a heterojunction with CuBi 2 O 4 to promote the charge separation ability. Our work shows the universality of rapid flame annealing in the fabrication of materials, especially for temperature-sensitive compositions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Copper-based nanomaterials and applications · Electronic and Structural Properties of Oxides · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Photonic and Electronic Bandgap Materials, Ministry of Education, School of Physics and Electronic Engineering
Harbin Normal University
College of Chemistry
Jilin University
Funding
Natural Science Foundation of Heilongjiang Province · Graduate Innovation Project of Harbin Normal University
References (33)
Show source-provided references
1. 10.1021/nn100032y10.1021/nn100032y ↗
2. 10.1021/acsaem.9b0133310.1021/acsaem.9b01333 ↗
3. 10.1021/acsami.8b0036710.1021/acsami.8b00367 ↗
4. 10.1021/acsnano.7b0070410.1021/acsnano.7b00704 ↗
5. 10.1021/nn300679d10.1021/nn300679d ↗
6. 10.1038/s41467-019-12977-x10.1038/s41467-019-12977-x ↗
7. 10.1002/aenm.20190298510.1002/aenm.201902985 ↗
8. 10.1016/j.solener.2016.07.02210.1016/j.solener.2016.07.022 ↗
9. 10.1016/j.ijhydene.2021.01.05010.1016/j.ijhydene.2021.01.050 ↗
10. 10.1016/j.apcatb.2019.01.01710.1016/j.apcatb.2019.01.017 ↗
11. 10.1016/j.apcatb.2017.02.01310.1016/j.apcatb.2017.02.013 ↗
12. 10.1021/acs.chemmater.6b0083010.1021/acs.chemmater.6b00830 ↗
13. 10.1021/acs.chemmater.6b0129410.1021/acs.chemmater.6b01294 ↗
14. 10.1039/C4CP03883E10.1039/C4CP03883E ↗
15. 10.1021/acssuschemeng.7b0413310.1021/acssuschemeng.7b04133 ↗
16. 10.1002/smll.20200242910.1002/smll.202002429 ↗
17. 10.1016/S1872-2067(18)63127-410.1016/S1872-2067(18)63127-4 ↗
18. 10.1002/adfm.20191083210.1002/adfm.201910832 ↗
19. 10.1021/nl402690210.1021/nl4026902 ↗
20. 10.1002/smtd.20180008310.1002/smtd.201800083 ↗
21. 10.1021/acsnano.5b0537310.1021/acsnano.5b05373 ↗
22. 10.1002/(SICI)1097-4555(199905)30:5<413::AID-JRS387>3.0.CO;2-N10.1002/(SICI)1097-4555(199905)30:5<413::AID-JRS387>3.0.CO;2-N ↗
23. 10.1016/j.jcat.2020.04.00110.1016/j.jcat.2020.04.001 ↗
24. 10.1016/j.materresbull.2020.11094010.1016/j.materresbull.2020.110940 ↗
25. 10.1155/2009/50243710.1155/2009/502437 ↗
26. 10.1002/cssc.20180140610.1002/cssc.201801406 ↗
27. 10.1002/ange.20181058310.1002/ange.201810583 ↗
28. 10.1016/j.jpowsour.2016.01.07310.1016/j.jpowsour.2016.01.073 ↗
29. 10.1039/C6DT00283H10.1039/C6DT00283H ↗
30. 10.1016/j.susc.2008.06.03410.1016/j.susc.2008.06.034 ↗
31. 10.1002/smtd.20170008010.1002/smtd.201700080 ↗
32. 10.1021/acsami.8b1275310.1021/acsami.8b12753 ↗
33. 10.1016/j.cej.2024.15551410.1016/j.cej.2024.155514 ↗