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Articles

Emerging applications of nanodiamonds in photocatalysis

, , , ORCID Icon & ORCID Icon
Pages 93-109 | Received 26 Jun 2020, Accepted 04 Jan 2020, Published online: 19 Feb 2021

Figures & data

Figure 1. The optical properties of NDs: (a) UV–vis absorption spectra of Cu2O, NDs, NDs-Cu2O, and physical mixture of NDs and Cu2O [Citation19]. (b) The scattering effect of the NDs in water solution [Citation39]. (c) Fluorescence spectra of NDs suspended in water. Inset: Fluorescence image of NDs suspension excited by 532-nm laser light [Citation2]. (d) Excitation monitored at 450 nm emission (1) and emission at 410 nm excitation (2) spectra of ND-ODA dispersion in dichloromethane; photographs of ND and ND-ODA dispersions in dichloromethane with UV (365 nm, lower row) illumination [Citation3].

Figure 1. The optical properties of NDs: (a) UV–vis absorption spectra of Cu2O, NDs, NDs-Cu2O, and physical mixture of NDs and Cu2O [Citation19]. (b) The scattering effect of the NDs in water solution [Citation39]. (c) Fluorescence spectra of NDs suspended in water. Inset: Fluorescence image of NDs suspension excited by 532-nm laser light [Citation2]. (d) Excitation monitored at 450 nm emission (1) and emission at 410 nm excitation (2) spectra of ND-ODA dispersion in dichloromethane; photographs of ND and ND-ODA dispersions in dichloromethane with UV (365 nm, lower row) illumination [Citation3].

Figure 2. Structure of NDs: (a) Schematic diagram of NDs structure [Citation60]. (b) TEM of NDs [Citation61]. (c) XRD patterns of graphite powders and NDs [Citation19]. (d) FTIR spectra of ND and AND-1000 (ND annealed at 1000 °C under nitrogen atmosphere) [Citation61].

Figure 2. Structure of NDs: (a) Schematic diagram of NDs structure [Citation60]. (b) TEM of NDs [Citation61]. (c) XRD patterns of graphite powders and NDs [Citation19]. (d) FTIR spectra of ND and AND-1000 (ND annealed at 1000 °C under nitrogen atmosphere) [Citation61].

Figure 3. Surface functionalization of NDs [Citation16].

Figure 3. Surface functionalization of NDs [Citation16].

Figure 4. Hydrogen treated NDs exhibited an enhanced photocatalytic hydrogen evolution activity [Citation49]: (a) Time-dependent H2 evolution, by 100 mg of PND, OND, and HND dispersed in 100 mL of water or 30 wt% methanol aqueous solutions under 532 nm Nd-YAG laser pulse irradiation (80 mJ per pulse). (b) Laser power-dependent H2 evolution (3 h) for the HND.

Figure 4. Hydrogen treated NDs exhibited an enhanced photocatalytic hydrogen evolution activity [Citation49]: (a) Time-dependent H2 evolution, by 100 mg of PND, OND, and HND dispersed in 100 mL of water or 30 wt% methanol aqueous solutions under 532 nm Nd-YAG laser pulse irradiation (80 mJ per pulse). (b) Laser power-dependent H2 evolution (3 h) for the HND.

Figure 5. The structure and photocatalytic hydrogen evolution activity of NDs-Cu2O [Citation19]: (a) XRD patterns of graphite powders and NDs. (b, c) TEM and HRTEM images of NDs. (d) XRD patterns of NDs-Cu2O and Cu2O. (e, f) SEM and TEM images of NDs-Cu2O. (g) H2 evolution amounts of NDs-Cu2O nanocrystals with different ND dosages. (h) Typical time course of H2 evolution from water under AM 1.5 and visible light irradiation. (i) Comparison of the quantum efficiencies of NDs-Cu2O under the irradiation with various wavelengths.

Figure 5. The structure and photocatalytic hydrogen evolution activity of NDs-Cu2O [Citation19]: (a) XRD patterns of graphite powders and NDs. (b, c) TEM and HRTEM images of NDs. (d) XRD patterns of NDs-Cu2O and Cu2O. (e, f) SEM and TEM images of NDs-Cu2O. (g) H2 evolution amounts of NDs-Cu2O nanocrystals with different ND dosages. (h) Typical time course of H2 evolution from water under AM 1.5 and visible light irradiation. (i) Comparison of the quantum efficiencies of NDs-Cu2O under the irradiation with various wavelengths.

Figure 6. The SEM images and the photocatalytic hydrogen evolution performance of ND@g-C3N4 [Citation39]: The SEM image of (a) g-C3N4 and (b) ND@g-C3N4 (ND 10 wt%). (c) H2 evolution rate for 5 h over ND@g-C3N4 with different mass ratio of NDs under visible light irradiation. (d) Comparison of H2 evolution activity over g-C3N4, ND/g-C3N4-mix and ND@g-C3N4 (ND 10 wt%) heterostructures under visible light irradiation.

Figure 6. The SEM images and the photocatalytic hydrogen evolution performance of ND@g-C3N4 [Citation39]: The SEM image of (a) g-C3N4 and (b) ND@g-C3N4 (ND 10 wt%). (c) H2 evolution rate for 5 h over ND@g-C3N4 with different mass ratio of NDs under visible light irradiation. (d) Comparison of H2 evolution activity over g-C3N4, ND/g-C3N4-mix and ND@g-C3N4 (ND 10 wt%) heterostructures under visible light irradiation.

Figure 7. The TEM images and photocatalytic toluene degradation activity of ZnO was enhanced after coupling with NDs [Citation18]: HRTEM images of (a) ZnO and (b) ZnO/ND. (c) Photocatalytic degradation of gaseous toluene and the CO2 yield of ZnO and ZnO/ND catalysts. (d) Stability after cycles: red lines represented ZnO and green lines represented ZnO/ND.

Figure 7. The TEM images and photocatalytic toluene degradation activity of ZnO was enhanced after coupling with NDs [Citation18]: HRTEM images of (a) ZnO and (b) ZnO/ND. (c) Photocatalytic degradation of gaseous toluene and the CO2 yield of ZnO and ZnO/ND catalysts. (d) Stability after cycles: red lines represented ZnO and green lines represented ZnO/ND.

Figure 8. (a, b) HR-TEM images of ND (8 wt%)/WO3. (c) Magnified HR-TEM image from selected area (red square in panel (b)). (d) SAED pattern of the region depicted in panel (c). (e–h) EELS elemental maps of C (panel (e)), W (panel (f)), O (panel (g)), and C + W + O (panel (h)) in ND (8 wt %)/WO3. (i) Time-dependent profiles of the photocatalytic degradation of CH3CHO. (j) The concurrent production of CO2 on bare WO3, ND (8 wt%)/WO3, and Pt (1 wt%)/WO3 [Citation46].

Figure 8. (a, b) HR-TEM images of ND (8 wt%)/WO3. (c) Magnified HR-TEM image from selected area (red square in panel (b)). (d) SAED pattern of the region depicted in panel (c). (e–h) EELS elemental maps of C (panel (e)), W (panel (f)), O (panel (g)), and C + W + O (panel (h)) in ND (8 wt %)/WO3. (i) Time-dependent profiles of the photocatalytic degradation of CH3CHO. (j) The concurrent production of CO2 on bare WO3, ND (8 wt%)/WO3, and Pt (1 wt%)/WO3 [Citation46].

Figure 9. The enhanced photocatalytic pharmaceuticals (DP and AMX) degradation activity of treated NDs modified TiO2 [Citation81]. Normalized concentration of (a) DP and (b) AMX as a function of time for TiO2 and ND-TiO2 (1.0 g L−1) composites under near-UV/Vis irradiation. (c) Effect of EDTA and t-BuOH on the photocatalytic degradation under near-UV/Vis irradiation of DP using NDDT and NDAT samples. Curves represent the fitting of the pseudo-first order equation to the experimental data. (d) Reusability of the NDDT and NDAT samples for the DP degradation in three consecutive runs.

Figure 9. The enhanced photocatalytic pharmaceuticals (DP and AMX) degradation activity of treated NDs modified TiO2 [Citation81]. Normalized concentration of (a) DP and (b) AMX as a function of time for TiO2 and ND-TiO2 (1.0 g L−1) composites under near-UV/Vis irradiation. (c) Effect of EDTA and t-BuOH on the photocatalytic degradation under near-UV/Vis irradiation of DP using NDDT and NDAT samples. Curves represent the fitting of the pseudo-first order equation to the experimental data. (d) Reusability of the NDDT and NDAT samples for the DP degradation in three consecutive runs.

Figure 10. BDND used to enhance the photocatalytic RhB degradation activity of g-C3N4 [Citation20]. (a) XRD patterns of the as-prepared g-C3N4, BDND@g-C3N4 (BDND 3 wt%), and BDND. (b) UV-vis DRS spectra of g-C3N4 and BDND@g-C3N4 (BDND 3 wt%) heterostructures and (αhν)2 versus curve of g-C3N4 and BDND@g-C3N4 (insert), respectively. (c) Time-dependent absorption spectral pattern of RhB aqueous solution in the presence of BDND@g-C3N4 photocatalyst under visible light irradiation. (d) Photocatalytic degradation of RhB in aqueous solution over g-C3N4, BDND and BDND@g-C3N4 photocatalysts.

Figure 10. BDND used to enhance the photocatalytic RhB degradation activity of g-C3N4 [Citation20]. (a) XRD patterns of the as-prepared g-C3N4, BDND@g-C3N4 (BDND 3 wt%), and BDND. (b) UV-vis DRS spectra of g-C3N4 and BDND@g-C3N4 (BDND 3 wt%) heterostructures and (αhν)2 versus hν curve of g-C3N4 and BDND@g-C3N4 (insert), respectively. (c) Time-dependent absorption spectral pattern of RhB aqueous solution in the presence of BDND@g-C3N4 photocatalyst under visible light irradiation. (d) Photocatalytic degradation of RhB in aqueous solution over g-C3N4, BDND and BDND@g-C3N4 photocatalysts.

Table 1. Comparation of photocatalytic activity based on NDs contained composite photocatalysts toward organic degradation with semiconductor photocatalysts reported recently.

Figure 11. The photochemical reduction performance of diamond analyzed FTIR spectra: FTIR spectra of gaseous headspace demonstrating reduction of CO2 to CO by illuminated diamond, along with control samples [Citation86].

Figure 11. The photochemical reduction performance of diamond analyzed FTIR spectra: FTIR spectra of gaseous headspace demonstrating reduction of CO2 to CO by illuminated diamond, along with control samples [Citation86].

Figure 12. The character of NDs in photocatalytic reduce RGO [Citation49]: (a) Photograph of the GO, HND, and 1:5 ratio of GO:HND (dispersed in water) before and after laser irradiation. (b) TEM image of HND-RGO composites. (c) AFM image and height profile of the photodetector device consisting of 10 nm (avg.) thick HND-RGO. (d) I–V characteristics of the RGO and HND-RGO under 514 nm Ar ion laser irradiation and in the dark, and (e) their DI-t curves under chopped irradiation.

Figure 12. The character of NDs in photocatalytic reduce RGO [Citation49]: (a) Photograph of the GO, HND, and 1:5 ratio of GO:HND (dispersed in water) before and after laser irradiation. (b) TEM image of HND-RGO composites. (c) AFM image and height profile of the photodetector device consisting of 10 nm (avg.) thick HND-RGO. (d) I–V characteristics of the RGO and HND-RGO under 514 nm Ar ion laser irradiation and in the dark, and (e) their DI-t curves under chopped irradiation.

Figure 13. The stability of NDs-based composite photocatalyst: (a) Recycled photocatalytic activity of HND for the H2 evolution [Citation49]. (b) Cycling tests of NDs-Cu2O under AM 1.5 irradiation [Citation19]. (c) Cycling tests of ND@g-C3N4 (ND 10 wt%) under visible light irradiation [Citation39]. (d) XRD patterns of ZnO/ND and ZnO catalysts before and after five reaction cycles [Citation86].

Figure 13. The stability of NDs-based composite photocatalyst: (a) Recycled photocatalytic activity of HND for the H2 evolution [Citation49]. (b) Cycling tests of NDs-Cu2O under AM 1.5 irradiation [Citation19]. (c) Cycling tests of ND@g-C3N4 (ND 10 wt%) under visible light irradiation [Citation39]. (d) XRD patterns of ZnO/ND and ZnO catalysts before and after five reaction cycles [Citation86].

Figure 14. The optical absorption and charge-separation properties of NDs-based composites: UV–vis absorption spectra of Cu2O, NDs, NDs-Cu2O, and physical mixture of NDs and Cu2O (a) and their Tauc plots (b) [Citation19]. (c) Transient photocurrent response curves and (d) electrochemical impedance spectra of ZnO and ZnO/ND catalysts [Citation86].

Figure 14. The optical absorption and charge-separation properties of NDs-based composites: UV–vis absorption spectra of Cu2O, NDs, NDs-Cu2O, and physical mixture of NDs and Cu2O (a) and their Tauc plots (b) [Citation19]. (c) Transient photocurrent response curves and (d) electrochemical impedance spectra of ZnO and ZnO/ND catalysts [Citation86].

Figure 15. Proposed mechanism for photocatalytic degradation of toluene upon ZnO/ND photocatalysts [Citation18].

Figure 15. Proposed mechanism for photocatalytic degradation of toluene upon ZnO/ND photocatalysts [Citation18].

Figure 16. Schematic illustration of proposed for the enhanced photocatalytic RhB degradation upon BDND@g-C3N4 [Citation20].

Figure 16. Schematic illustration of proposed for the enhanced photocatalytic RhB degradation upon BDND@g-C3N4 [Citation20].

Figure 17. Schematic diagram for antifouling and self-cleaning mechanisms of the photocatalytic membrane (PVDF-CND/TiO2) [Citation40].

Figure 17. Schematic diagram for antifouling and self-cleaning mechanisms of the photocatalytic membrane (PVDF-CND/TiO2) [Citation40].

Figure 18. The significant light scattering effect of NDs [Citation39]. (a) UV-vis DRS spectra of g-C3N4 and ND@g-C3N4 (ND 10 wt%) heterostructures and corresponding scattering effect (insert) of the NDs and Pt nanoparticles in water solution. (b) Behavior of light when propagating through g-C3N4 and ND@g-C3N4 (ND 10 wt%) heterostructures.

Figure 18. The significant light scattering effect of NDs [Citation39]. (a) UV-vis DRS spectra of g-C3N4 and ND@g-C3N4 (ND 10 wt%) heterostructures and corresponding scattering effect (insert) of the NDs and Pt nanoparticles in water solution. (b) Behavior of light when propagating through g-C3N4 and ND@g-C3N4 (ND 10 wt%) heterostructures.