journal article·2021-07-21Open access

Near-Infrared-Triggered Nitrogen Fixation over Upconversion Nanoparticles Assembled Carbon Nitride Nanotubes with Nitrogen Vacancies

Yuxiang Zhu, Xianlin Zheng, Wenwen Zhang, Amanj Kheradmand, Shengshen Gu, Marcin Kobielusz, Wojciech Macyk, Haitao Li, Jun Huang, Yijiao Jiang

ACS Applied Materials & Interfaces· Volume 13· Issue 28

Abstract

Photocatalytic artificial fixation of N 2 to NH 3 occurs over NaYF 4:Yb,Tm (NYF) upconversion nanoparticles (NPs) decorated carbon nitride nanotubes with nitrogen vacancies (NYF/NV-CNNTs) in water under near-infrared (NIR) light irradiation. NYF NPs with a particle size of ca. 20 nm were uniformly distributed on the surface of NV-CNNTs. The NYF/NV-CNNTs with 15 wt % NYF exhibited the highest NH 3 production yield of 1.72 mmol L –1 g cat –1, corresponding to an apparent quantum efficiency of 0.50% under NIR light illumination, and about three times higher the activity of the bare CNNTs under UV-filtered solar light. 15 N isotope-labeling NMR results confirm that the N source of ammonia originates from the photochemical N 2 reduction. The spectroelectrochemical measurements reveal that NVs can greatly facilitate the photogenerated electron transfer without energy loss, while the presence of NYF NPs shifts both the deep trap state and the edge of conduction band toward a lower potential. Moreover, NYF NPs endow the photocatalyst with a NIR light absorption via the fluorescence resonance energy transfer process, and NVs have the ability to enhance the active sites for a stronger adsorption of N 2 and decrease the surface quenching effect of NYF NPs, which thus can promote the energy migration within the heterojunctions. This work opens the way toward full solar spectrum photocatalysis for sustainable ammonia synthesis under aqueous system.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Ammonia Synthesis and Nitrogen Reduction · Luminescence Properties of Advanced Materials

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

Affiliations

School of Engineering, Macquarie University, Sydney, New South Wales 2109, Australia

College of Chemical Engineering, Nanjing Forestry University, Nanjing, Jiangsu 210037, P. R. China

Department of Physics and Astronomy, Macquarie University, Sydney, New South Wales 2109, Australia

Faculty of Chemistry, Jagiellonian University, ul. Gronostajowa 2, 30-387 Kraków, Poland

School of Chemical and Biomolecular Engineering, The University of Sydney, Sydney, New South Wales 2006, Australia

Funding

Australian Research Council · China Scholarship Council

References (47)

Show source-provided references
1. 10.1039/C7EE02220D10.1039/C7EE02220D ↗
2. 10.1002/anie.20030155310.1002/anie.200301553 ↗
3. 10.1021/acscatal.7b0043910.1021/acscatal.7b00439 ↗
4. 10.1016/j.apcatb.2019.11827610.1016/j.apcatb.2019.118276 ↗
5. 10.1021/ja00464a01510.1021/ja00464a015 ↗
6. 10.1039/C7MH00557A10.1039/C7MH00557A ↗
7. 10.1021/cr400478f10.1021/cr400478f ↗
8. 10.1021/cr400425h10.1021/cr400425h ↗
9. 10.1021/am404389g10.1021/am404389g ↗
10. 10.1021/nn100457j10.1021/nn100457j ↗
11. 10.1039/c3ce42337a10.1039/c3ce42337a ↗
12. 10.1016/j.apcatb.2010.08.01710.1016/j.apcatb.2010.08.017 ↗
13. 10.1016/j.apsusc.2013.06.06610.1016/j.apsusc.2013.06.066 ↗
14. 10.1039/C6DT02548J10.1039/C6DT02548J ↗
15. 10.1016/j.apcatb.2015.09.02210.1016/j.apcatb.2015.09.022 ↗
16. 10.1016/j.apcatb.2017.11.03710.1016/j.apcatb.2017.11.037 ↗
17. 10.1021/acs.chemrev.6b0007510.1021/acs.chemrev.6b00075 ↗
18. 10.1016/j.apcatb.2020.11916710.1016/j.apcatb.2020.119167 ↗
19. 10.1016/j.jcis.2015.08.06310.1016/j.jcis.2015.08.063 ↗
20. 10.1016/j.matlet.2015.02.01010.1016/j.matlet.2015.02.010 ↗
21. 10.1021/acsami.8b0039310.1021/acsami.8b00393 ↗
22. 10.1016/j.apcatb.2018.12.01510.1016/j.apcatb.2018.12.015 ↗
23. 10.1021/jacs.5b0310510.1021/jacs.5b03105 ↗
24. 10.1039/C6CY00622A10.1039/C6CY00622A ↗
25. 10.1002/adma.20140405710.1002/adma.201404057 ↗
26. 10.1039/C5TA06540B10.1039/C5TA06540B ↗
27. 10.1016/j.jhazmat.2019.12124710.1016/j.jhazmat.2019.121247 ↗
28. 10.1038/nnano.2013.17110.1038/nnano.2013.171 ↗
29. 10.1021/acsami.6b0812910.1021/acsami.6b08129 ↗
30. 10.1039/C4NR00224E10.1039/C4NR00224E ↗
31. 10.1021/jp301026y10.1021/jp301026y ↗
32. 10.1039/c3ta12332d10.1039/c3ta12332d ↗
33. 10.1016/j.apcatb.2017.07.01310.1016/j.apcatb.2017.07.013 ↗
34. 10.1039/c3nr03051b10.1039/c3nr03051b ↗
35. 10.1002/1616-3028(200108)11:4<263::AID-ADFM263>3.0.CO;2-M10.1002/1616-3028(200108)11:4<263::AID-ADFM263>3.0.CO;2-M ↗
36. 10.1016/j.apcatb.2014.10.03910.1016/j.apcatb.2014.10.039 ↗
37. 10.1021/acs.chemmater.5b0234410.1021/acs.chemmater.5b02344 ↗
38. 10.1016/j.apcatb.2017.09.04810.1016/j.apcatb.2017.09.048 ↗
39. 10.3390/ma708564310.3390/ma7085643 ↗
40. 10.1039/c3cp52129j10.1039/c3cp52129j ↗
41. 10.1016/j.cattod.2017.11.01310.1016/j.cattod.2017.11.013 ↗
42. 10.1016/j.apsusc.2015.08.17310.1016/j.apsusc.2015.08.173 ↗
43. 10.1002/smll.20160393810.1002/smll.201603938 ↗
44. 10.1039/c1cc11179e10.1039/c1cc11179e ↗
45. 10.1016/j.apcatb.2013.05.06210.1016/j.apcatb.2013.05.062 ↗
46. 10.1021/cs300808r10.1021/cs300808r ↗
47. 10.1016/j.jpcs.2016.08.00810.1016/j.jpcs.2016.08.008 ↗