Sacrificial agent-free photocatalytic H2O2 evolution via two-electron oxygen reduction using a ternary α-Fe2O3/CQD@g-C3N4 photocatalyst with broad-spectrum response. Issue 36 (1st September 2020)
- Record Type:
- Journal Article
- Title:
- Sacrificial agent-free photocatalytic H2O2 evolution via two-electron oxygen reduction using a ternary α-Fe2O3/CQD@g-C3N4 photocatalyst with broad-spectrum response. Issue 36 (1st September 2020)
- Main Title:
- Sacrificial agent-free photocatalytic H2O2 evolution via two-electron oxygen reduction using a ternary α-Fe2O3/CQD@g-C3N4 photocatalyst with broad-spectrum response
- Authors:
- Chen, Xi
Zhang, Wenwen
Zhang, Lixiang
Feng, Luping
Zhang, Chunxian
Jiang, Jie
Yan, Tingjiang
Wang, Hua - Abstract:
- Abstract : The developed α-Fe2 O3 /CQD@g-C3 N4 can perform a direct one-step two-electron reduction for efficient photocatalytic H2 O2 ; evolution in pure water. Abstract : Ultrathin g-C3 N4 nanosheets have been fabricated via a two-step calcination regulated by melamine precursors at a high heating rate (30 °C min −1 ). The resulting g-C3 N4 nanosheets were further employed as carriers for the growth of carbon quantum dots (CQDs) and (110) exposed α-Fe2 O3 through the PVP-enabled adsorption effects by a solvothermal process. It was discovered that the so fabricated ternary photocatalyst α-Fe2 O3 /CQD@g-C3 N4 presented a broad-spectrum absorption range (up to 800 nm) and particularly enhanced active sites of photogenerated electrons for highly efficient photocatalytic oxygen reduction toward H2 O2 evolution in pure water. A H2 O2 production rate of 1.16 μM min −1 could be expected for the developed photocatalyst under visible light irradiation, which is about 19 times faster than that of pure ultrathin g-C3 N4 . Herein, the loaded Fe2 O3 could transform the H2 O2 evolution from two-step single-electron reduction into one-step two-electron one, as verified by the various active species experiments and rotating ring-disk electrode tests. This work presents a new perspective in designing ultrathin g-C3 N4 through a simple method of precursor-regulated calcination, which features more outstanding advantages than the conventional exfoliation of bulk g-C3 N4 towards ultrathin g-C3Abstract : The developed α-Fe2 O3 /CQD@g-C3 N4 can perform a direct one-step two-electron reduction for efficient photocatalytic H2 O2 ; evolution in pure water. Abstract : Ultrathin g-C3 N4 nanosheets have been fabricated via a two-step calcination regulated by melamine precursors at a high heating rate (30 °C min −1 ). The resulting g-C3 N4 nanosheets were further employed as carriers for the growth of carbon quantum dots (CQDs) and (110) exposed α-Fe2 O3 through the PVP-enabled adsorption effects by a solvothermal process. It was discovered that the so fabricated ternary photocatalyst α-Fe2 O3 /CQD@g-C3 N4 presented a broad-spectrum absorption range (up to 800 nm) and particularly enhanced active sites of photogenerated electrons for highly efficient photocatalytic oxygen reduction toward H2 O2 evolution in pure water. A H2 O2 production rate of 1.16 μM min −1 could be expected for the developed photocatalyst under visible light irradiation, which is about 19 times faster than that of pure ultrathin g-C3 N4 . Herein, the loaded Fe2 O3 could transform the H2 O2 evolution from two-step single-electron reduction into one-step two-electron one, as verified by the various active species experiments and rotating ring-disk electrode tests. This work presents a new perspective in designing ultrathin g-C3 N4 through a simple method of precursor-regulated calcination, which features more outstanding advantages than the conventional exfoliation of bulk g-C3 N4 towards ultrathin g-C3 N4 . More importantly, it provides an optimized photocatalytic reaction route of two-electron oxygen reduction for efficient H2 O2 production in pure water under visible light irradiation, without the need for noble metals or organic sacrificial agents. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 8:Issue 36(2020)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 8:Issue 36(2020)
- Issue Display:
- Volume 8, Issue 36 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 36
- Issue Sort Value:
- 2020-0008-0036-0000
- Page Start:
- 18816
- Page End:
- 18825
- Publication Date:
- 2020-09-01
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0ta05753c ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14312.xml