Acta Phys. -Chim. Sin. ›› 2025, Vol. 41 ›› Issue (5): 100039.doi: 10.1016/j.actphy.2024.100039
Special Issue: S-scheme heterojunction in photocatalysis
• REVIEW • Previous Articles Next Articles
Hui Wang1, Abdelkader Labidi1, Menghan Ren1, Feroz Shaik2, Chuanyi Wang1,*(
)
Received:2024-11-06
Revised:2024-12-03
Accepted:2024-12-06
Published:2025-04-18
Contact:
Email: wangchuanyi@sust.edu.cn; Tel.: +86-29-86131724 (Chuanyi Wang)
Supported by:Hui Wang, Abdelkader Labidi, Menghan Ren, Feroz Shaik, Chuanyi Wang. Recent Progress of Microstructure-Regulated g-C3N4 in Photocatalytic NO Conversion: The Pivotal Roles of Adsorption/Activation Sites[J]. Acta Phys. -Chim. Sin. 2025, 41(5), 100039. doi: 10.1016/j.actphy.2024.100039
Table 1
Compare the photocatalytic NO conversion efficiency reported by different g-C3N4-based materials in this work."
| No. | Microstructure control method | Type | Photocatalyst amount (g) | Light source | Initial Conc. | Conv. (%) | NO2 Conc. | Ref. |
| 1 | Vacancy engineering | N2C vacancy | 0.1 | 150 W commercial tungsten halogen lamp equipped with a 420 nm cut-off filter | 600 ppb | 41.84 | 77.8 ppb | [ |
| 2 | N3C vacancy | 0.1 | 150 W tungsten halogen lamp | – | 57.1 | 82.15 ppb | [ | |
| 3 | N3C vacancy | 0.2 | 30 W LED (Visible region) | 600 ppb | 66.7 | 26.8 ppb | [ | |
| 4 | N3C vacancy | 0.2 | LED lamp | 600 ppb | 40.3 | 87.7 ppb | [ | |
| 5 | C vacancy | 0.2 | LED lamp (λ ≥ 448 nm) | 600 ppb | 47.0 | 30 ppb | [ | |
| 6 | non-intrinsic O vacancies | 0.1 | 300 W xenon lamp equipped with a cut-off filter (λ>420 nm) | 500 ppb | 47.7 | 25 ppb | [ | |
| 7 | Doping | Sulfur doping | 0.2 | 150 W visible light LED lamp (λ > 400 nm) | 600 ppb | 53 | 58.86 ppb | [ |
| 8 | Boron doping | 0.1 | 500 W Xe lamp | 600 ppb | 54 | – | [ | |
| 9 | Sulfur doping | 0.025 | LED array (450 nm centre wavelength) | 1 ppm | 50 | 200 ppb | [ | |
| 10 | C self doping | 0.2 | 150 W commercial tungsten halogen lamp | 550 ppb | 56.77 | – | [ | |
| 11 | Sulfur doping | 0.2 | Xe lamp | 500 ppb | 78.0 | – | [ | |
| 12 | Na+, Li+ interlayer doping | 0.2 | 30 W visible LED lamp | 600 ppb | 82 | 3.7 ppb | [ | |
| 13 | Zn interlayer doping | 0.1 | 150 W metal halide lamp (λ greater than 420 nm) | 600 ppb | 49 | 5.88 ppb | [ | |
| 14 | Ca interlayer doping | 0.2 | 150 W commercial tungsten halogen lamp | 500 ppb | 54.78 | – | [ | |
| 15 | Sr cavity filling | 0.05 | xenon lamp with a 420 nm filter | 600 ppb | 55 | 66 ppb | [ | |
| 16 | Functional group modification | Oxygenated functional group | 0.2 | 150 W commercial tungsten halogen lamp equipped with a UV light cutoff filter (420 nm) | 500 ppb | 45.5 | – | [ |
| 17 | Cyano and hydroxyl groups | 0.05 | 300 W xenon lamp equipped with a cut-off filter (λ > 420 nm) | 600 ppb | 46.2 | 77.61 ppb | [ | |
| 18 | hydroxyl groups | 0.2 | Visible light LED lamp (λ ≥ 420 nm) | 600 ppb | 65.0 | 117 ppb | [ | |
| 19 | Oxygenated functional group | 0.1 | 150 W commercial tungsten halogen lamp | 500 ppb | 50.4 | – | [ | |
| 20 | Cocatalyst loading | SrSO4 loading | 0.05 | 30 W LED lamp | 600 ppb | 67.5 | 85.05 ppb | [ |
| 21 | CaCO3 loading | 0.2 | LED lamp (λ > 420 nm) | 550 ppb | 51.18 | 107.5 ppb | [ | |
| 22 | ZIF-67/CoOOH loading | 0.2 | 150 W metal halide lamp with a 420 nm cutoff | 500 ppb | 52.5 | 0 | [ | |
| 23 | Au loading | 0.2 | 150 W commercial halogen tungsten lamp | 500 ppb | 41.0 | 10.25 ppb | [ | |
| 24 | Construction of and heterojunctions | (BiO)2CO3@ g-C3N4 heterojunction | – | 150 W commercial tungsten halogen lamp | – | 53.28 | – | [ |
| 25 | g-C3N4/BO0.2N0.8 heterojunction | 0.2 | Metal halide lamp (150 W) was used as the light source with a visible light filter (λ > 420 nm). | 500 ppb | 30.2 | 4.53 ppb | [ | |
| 26 | Pd1/g-C3N4-UiO-66-NH2 heterojunction | 10–40 | 300 W Xenon lamp | 40–70 ppm | 93.91 | 1.02 ppm | [ | |
| 27 | Graphene quantum dots/g-C3N4 | 0.08 | 300 W Xe lamp | 600 ppb | 90.0 | 140.4 ppb | [ | |
| 28 | UiO-67/g-C3N4 S- scheme heterojunction | 0.2 | Tungsten halogen lamp (150 W) | 500 ppb | 60.4 | – | [ | |
| 29 | CeO2/g-C3N4 S- scheme heterojunction | 0.05 | 300 W Xe lamp | 600 ppb | 73.8 | 96 ppb | [ |
Fig 3
NO oxidation and NO2 fabrication over g-C3N4 and Nd-CN (a); Types of N defects in g-C3N4 structure (b); Carried electrons for pristine g-C3N4 and Nd-CN (c); Optimized structures of O2 adsorption on g-C3N4 and Nd-CN (d); Spin-trapping ESR spectra for •O− and •OH over g-C3N4 and Nd-CN (e); Optimized structure of NO adsorption on g-C3N4 and Nd-CN (f). Reproduced with permission [67]. Copyright 2020, Elsevier."
Fig 4
NO oxidation and NO2 fabrication over g-C3N4 and Nd-CN (a); Optimized structure of NO adsorption on g-C3N4 and ACN (b); In situ C 1s XPS spectra of ACN and ACN after 30 minutes of illumination time (c); Optimized structures of O2 adsorption on g-C3N4 and ACN (d); Spin-trapping ESR spectra for •O2− and 1O2 over g-C3N4 and ACN (e); Adsorption configuration of O2 and NO2 molecules on g-C3N4 and ACN (f); Calculation of reaction pathways for NO2 oxidation on g-C3N4 and ACN (g). Reproduced with permission [68]. Copyright 2021, Wiley."
Fig 5
Carbon vacancy modified g-C3N4 nanotubes for selective oxidation of NO to NO2− (a); Photocatalytic NO oxidation over T 500 and TNx (b); Electron localization function (ELF) of T500 and TN500 (c); Optimized structure of NO adsorption on T500 and TN500 (d); Optimized structure of O2 adsorption on T500 and TN500 (e); Photocatalytic NO oxidation (f) and the concentration of NO2 (g) over TN 500 in the presence of different scavengers. Reproduced with permission [71]. Copyright 2020, Elsevier."
Fig 6
NO oxidation (a) and NO2 fabrication (b) over CN, OCN and VO-CN; Optimized structure of NO adsorption on CN, OCN and VO-CN (c); Optimized structures of O2 adsorption on CN and VO-CN (d); Spin-trapping ESR spectra for •OH and •O2− over CN and VO-CN (e). Reproduced with permission [72]. Copyright 2024, Elsevier."
Fig 7
Photocatalytic NO oxidation (a) and selectivity of products (b) over CN and CN-S; Optimized structure of O2 adsorption on CN and CN-S (c); Spin-trapping ESR spectra for •O2− (d) and •OH (e) over CN and CN-S; Optimized structure of NO adsorption on CN and CN-S (f). Reproduced with permission [73]. Copyright 2023, Elsevier."
Fig 8
NO oxidation (a) and NO2 fabrication (b) over g-C3N4 and CN-NaLi; Optimized geometric structure of NO molecules adsorption on g-C3N4 and CN-NaLi (c); Photocatalytic NO oxidation over CN-NaLi in the presence of different scavengers (d); Spin-trapping ESR spectrum for •O2− over g-C3N4 and CN-NaLi (e). Reproduced with permission [77]. Copyright 2022, Elsevier."
Fig 10
NO oxidation and NO2 fabrication over g-C3N4 and MCN (a); 1H solid-state nuclear magnetic resonance (NMR) spectra of g-C3N4 and MCN (b); The model of H atom existence in g-C3N4 (c); NO-TPD spectra of g-C3N4 and MCN (d); The model for covalent bonding between O2 substituted H atoms and amide or imine groups (e); The model for hydrogen bonding between O2 and amide or imine groups (f); O2-TPD spectra of g-C3N4 and MCN (g); O2 forms covalent bonds with two amidogen groups or imino groups (h); O2-TPD before and after deamination of g-C3N4 (i); Spin-trapping ESR spectra for •O2− and •OH over g-C3N4 and MCN (j). Reproduced with permission [80]. Copyright 2024, American Chemical Society."
Fig 11
Photocatalytic NO oxidation over g-C3N4 and OCN (a); Optimization of geometric structure of g-C3N4 modified by heteroatom O at C1 and C2 sites (b); Differential charge density between oxygen atoms and g-C3N4 and Electron localization function (ELF) of OCN (c); Optimized geometric structure of O2 molecules adsorption on g-C3N4 and OCN (d); Spin-trapping ESR spectrum for •O2− over g-C3N4 and and OCN (e); Optimized geometric structure of NO molecules adsorption on g-C3N4 and OCN (f). Reproduced with permission [81]. Copyright 2019, Elsevier."
Fig 12
NO oxidation and NO2 fabrication over CN and DCN-O-R (a); DMPO spin-trapping ESR for •O2− detection (b); In situ DRIFTS spectroscopy of CN and DCN-O-R photocatalytic NO conversion (c); The capture experiments for photocatalytic NO conversion over DCN-O-R (d); Mechanism diagram of CN and DCN-O-R photocatalytic conversion of NO (e); Reproduced with permission [82]. Copyright 2023, MDPI."
Fig 14
Photocatalytic NO oxidation over g-C3N4 and xCa-CN (a); selectivity of products over g-C3N4 (b) and xCa-CN (c); Spin-trapping ESR spectra for •O2− (d), •OH (e) and 1O2 (f) over g-C3N4 and xCa-CN; Optimized geometric structure of NO molecules adsorption on g-C3N4 and xCa-CN (g); Optimized geometric structure of NO2 molecules adsorption on g-C3N4, CN-cyano group and xCa-CN (h). Reproduced with permission [86]. Copyright 2023, Elsevier."
Fig 15
Mechanism diagram of CN-BOC heterojunction photocatalytic removal of NO (a); Photocatalytic NO oxidation over g-C3N4 and CN-BOC (b); UV-Vis DRS (c); Optimized geometric structure of NO (d) and O2 (e) molecules adsorption on g-C3N4 and CN-BOC; Spin-trapping ESR spectra for •O2− (f), •OH (g) and 1O2 (h) over g-C3N4 and CN-BOC. Reproduced with permission [89]. Copyright 2020, Elsevier."
Fig 16
NO oxidation and NO2 fabrication over g-C3N4, g-C3N4/BN and g-C3N4/BO0.2N0.8 (a); Differential charge density of g-C3N4/BN and g-C3N4/BO0.2N0.8 (b); O2 adsorption on the surfaces of g-C3N4/BN and g-C3N4/BO0.2N0.8 (c); Spin-trapping ESR spectrum for •O2− over g-C3N4, g-C3N4/BN and g-C3N4/BO0.2N0.8 (d); The stepwise NO oxidation process on different sides of g-C3N4/BN (e) and g-C3N4/BO0.2N0.8 (f); The entire NO oxidation process on different sides of g-C3N4/BN (g) and g-C3N4/BO0.2N0.8 (h). Reproduced with permission [90]. Copyright 2020, American Chemical Society."
Fig 17
NO oxidation and NO2 fabrication over CN, UiO-67 and CNU (a); The capture experiments for photocatalytic NO conversion over CNU (b); Spin-trapping ESR spectra for •O2− over CN, UiO-67 and CNU (c); In situ DRIFTS spectra of NO absorption (d, e) and photocatalytic reaction (f, g) processes on CN and CNU. Reproduced with permission [93]. Copyright 2024, Elsevier."
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