Chinese Journal of Catalysis ›› 2026, Vol. 85: 13-33.DOI: 10.1016/S1872-2067(26)65008-5
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Qing Lana, Su-Juan Jina, Ying-Ying Jiaob,c(
), Zhi-Ming Zhangb(
)
Received:2025-08-21
Accepted:2025-12-09
Online:2026-06-18
Published:2026-05-18
Contact:
*E-mail: yyjiao0210@163.com (Y. Jiao),About author:Ying-Ying Jiao (Tianjin University of Technology, Institute for New Energy Materials and Low Carbon Technologies) obtained her PhD degree from Zheng-zhou University. From 2022 to 2023, she studied at the Polytechnic University of Valencia in Spain as an exchange student. In 2023, she joined the Institute for New Energy Materials and Low Carbon Technologies, Tianjin University of Technology. Her research interests focus on the application of carbon nitride based semiconductor materials in the field of photocatalysis.Supported by:Qing Lan, Su-Juan Jin, Ying-Ying Jiao, Zhi-Ming Zhang. Anchoring single/dual metal centers on carbon nitride: Sustainable routes for greenhouse gas conversion and organic photosynthesis[J]. Chinese Journal of Catalysis, 2026, 85: 13-33.
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URL: https://www.cjcatal.com/EN/10.1016/S1872-2067(26)65008-5
Fig. 1. The development and statistics of g-C?N?-supported SACs and DACs. (a) The number of publications between 2020 and 2025. (b) The number of citations each year.
Fig. 4. (a) Schematic illustration of the preparation of Fe-g-C3N4 SACs. STEM (b), AC-HAADF-STEM (c), and corresponding EDX elemental mapping (d) images of Fe-g-C3N4 SACs. Reprinted with permission from Ref. [43]. Copyright 2022, Elsevier.
Fig. 5. Characterization of SACo/g-C3N4. (a) SEM image of SACo/g-C3N4, and the inset shows the optical image of 1.1 g SACo/g-C3N4. TEM (b) and HAADF-STEM (c) images of SACo/g-C3N4. (d) HAADF and the corresponding EDS mapping images of SACo/g-C3N4, the scale bar is 100 nm. HRTEM (e) and AC-STEM-annular dark field (ADF) (f) images of SACo/g-C3N4. Reprinted with permission from Ref. [55]. Copyright 2021, RSC.
Fig. 6. Physical characterization of Ni-g-C3N4. (a) Schematic illustration of the preparation. SEM (b), HRTEM (c), AC HAADF-STEM (d), and EDS mapping (e) images. Reprinted with permission from Ref. [62]. Copyright 2022, Nature.
Fig. 7. (a) Schematic illustration of the synthesis process of Cu SACs/g-C3N4 photocatalyst. TEM (b), HRTEM (c), and AC STEM (d) images of Cu SACs/g-C3N4. Cu single atoms were marked with red circles. (e) Elemental mapping image of Cu SACs/g-C3N4. Reprinted with permission from Ref. [59]. Copyright 2021, Wiley.
Fig. 8. (a) Schematic diagram of catalyst synthesis processes. (b) Typical time course of CO evolution catalyzed by g-C3N4-CoxNiy and the photocatalytic CO2 reduction mechanism in this system. Reprinted with permission from Ref. [73]. Copyright 2022, Elsvier.
Fig. 9. Two-step strategy for the precise synthesis of heteronuclear DACs. (a) A schematic illustration of the navigation and positioning strategy for fabricating ZnRu-, NiRu-, ZnCu-, CoCu-, NiCu- and BiCu-g-C3N4 heteronuclear DACs. (b) Photocatalytic H2 evolution in H2O in the presence of LA. (c) PA production of ZnRu-g-C3N4 and control samples. (d) A schematic diagram of photocatalysis process (grey, blue, pink and green balls represent C, N, Ru and Zn, respectively). Reprinted with permission from Ref. [75]. Copyright 2024, Nature.
| Photo catalyst | Fabricating method | Application | Photocatalyst efficiency | Production | Characteristic | Advantages | Ref. |
|---|---|---|---|---|---|---|---|
| Co-SNC | ball-milling | benzylamine self-coupling reaction | 97.5% conversion with 99% selectivity | N-benzylidene-benzylamine | high-performance dual-site SACs | high selectivity | [ |
| W-SA-PCN | calcining | CH4 Photooxidation | 4956 µmol·gcat∙1 | C1 oxygenates | WN4 coordination mode | high productivity | [ |
| Cu-CCN | molten salts | CO2 photoreduction | 3.086 μmol·h∙1·g∙1 | CO | crystalline g-C3N4 accompanied with Cu ions | highly selectivity | [ |
| Cu/CN | supramolecular preorganization with subsequent condensation, | CO2 photoreduction | 224.2 μmol∙h∙1∙g∙1 | CO | C-Cu-N2 SAC for CO2 activation | high CO-selectivity | [ |
| PCN-RuCu | preassembly-coprecipitation-pyrolysis | CO2 Photoreduction | 19.25 µmol· g-1·h-1 | CH4 | Ru sites account for electron-hole pairs and Cu sites for CO2 hydrogenation | high selectivity of 95% | [ |
| Ag1(x)@PCN | impregnation and pyrolysis | CO2 photoreduction | 160 μmol·h∙1·g∙1 | CO | Ag single atoms anchored on hollow porous polygonal C3N4 tubes | excellent stability | [ |
| M1M2-PCN DACs | photoinduced strategy | Photocatalytic H2 evolution | 345 mmol∙ gRu∙1∙h∙1 | H2 | anchoring heteronuclear dual-metal dimers on a photosensitizing PCN to construct a series of DACs | bimetallic precise identification | [ |
| RuSA-mC3N4 | SBA-15 | CO2 photoreduction | 250 μmol·h∙1·g∙1 | Methanol | Ruthenium single atom over mesoporous C3N4 | high methanol yield | [ |
| CoRu-HCNp | self-seeded process with condensation and carbonization | CO2 photoreduction | 27.3 µmol·g-1·h-1 | CO | Conjugated porous carbon nitride polymer with precise control of Co-Ru atomic configuration | High CO-selectivity | [ |
| Pd1+NPs/ C3N4 | calcining | CO2 photoreduction | 20.3 µmol·g-1·h-1 | CH4 | Pd1 sites activated CO2 and PdNPs sites increased H* coverage | high selectivity of 97.8% | [ |
Table 1 Summary of various applications of g-C3N4-based SACs/DACs.
| Photo catalyst | Fabricating method | Application | Photocatalyst efficiency | Production | Characteristic | Advantages | Ref. |
|---|---|---|---|---|---|---|---|
| Co-SNC | ball-milling | benzylamine self-coupling reaction | 97.5% conversion with 99% selectivity | N-benzylidene-benzylamine | high-performance dual-site SACs | high selectivity | [ |
| W-SA-PCN | calcining | CH4 Photooxidation | 4956 µmol·gcat∙1 | C1 oxygenates | WN4 coordination mode | high productivity | [ |
| Cu-CCN | molten salts | CO2 photoreduction | 3.086 μmol·h∙1·g∙1 | CO | crystalline g-C3N4 accompanied with Cu ions | highly selectivity | [ |
| Cu/CN | supramolecular preorganization with subsequent condensation, | CO2 photoreduction | 224.2 μmol∙h∙1∙g∙1 | CO | C-Cu-N2 SAC for CO2 activation | high CO-selectivity | [ |
| PCN-RuCu | preassembly-coprecipitation-pyrolysis | CO2 Photoreduction | 19.25 µmol· g-1·h-1 | CH4 | Ru sites account for electron-hole pairs and Cu sites for CO2 hydrogenation | high selectivity of 95% | [ |
| Ag1(x)@PCN | impregnation and pyrolysis | CO2 photoreduction | 160 μmol·h∙1·g∙1 | CO | Ag single atoms anchored on hollow porous polygonal C3N4 tubes | excellent stability | [ |
| M1M2-PCN DACs | photoinduced strategy | Photocatalytic H2 evolution | 345 mmol∙ gRu∙1∙h∙1 | H2 | anchoring heteronuclear dual-metal dimers on a photosensitizing PCN to construct a series of DACs | bimetallic precise identification | [ |
| RuSA-mC3N4 | SBA-15 | CO2 photoreduction | 250 μmol·h∙1·g∙1 | Methanol | Ruthenium single atom over mesoporous C3N4 | high methanol yield | [ |
| CoRu-HCNp | self-seeded process with condensation and carbonization | CO2 photoreduction | 27.3 µmol·g-1·h-1 | CO | Conjugated porous carbon nitride polymer with precise control of Co-Ru atomic configuration | High CO-selectivity | [ |
| Pd1+NPs/ C3N4 | calcining | CO2 photoreduction | 20.3 µmol·g-1·h-1 | CH4 | Pd1 sites activated CO2 and PdNPs sites increased H* coverage | high selectivity of 97.8% | [ |
Fig. 10. Calculated PDOS of g-C3N4 (a) and In1/g-C3N4 (b). (c) Calculated Gibbs free energy diagram for CO2 reduction pathways to CO on g-C3N4, In1/g-C3N4 and Co1/g-C3N4. (d) Computed Gibbs free energy for steps in photocatalytic *CO-to-CHO on g-C3N4, In1/g-C3N4 and Co1/g-C3N4. (e) Calculated Gibbs free energy diagram for CO2 reduction pathways to CH4 on Co1In1/g-C3N4. Reprinted with permission from Ref. [61]. Copyright 2025, Elsevier.
Fig. 11. (a) EXAFS spectra of Co K-edge for Co foil, Co3O4 and Co1In1/g-C3N4. (b) Co K-edge FT-EXAFS spectra. (c) EXAFS spectra of In K-edge for In foil, In2O3 and Co1In1/g-C3N4. (d) In K-edge FT-EXAFS spectra. In-situ DRIFTS spectra at different irradiation times on g-C3N4 (e) and Co1In1/g-C3N4 (f). Reprinted with permission from Ref. [61]. Copyright 2025, Elsevier.
Fig. 12. (a) HAADF-STEM image of W-SA-g-C3N4-7.5 showing the W-single-atom distribution on g-C3N4, (b) CH3OH yield of SAP and control samples, (c) Time-course plots of CH3OH yield, and (d) DFT calculations results for CH4 oxidation with W-SA-g-C3N4-7.5 as the photocatalyst. Reprinted with permission from Ref. [79]. Copyright 2022, Wiley.
Fig. 13. TEM images and synchrotron radiation analysis of g-C3N4 and Cu/g-C3N4 samples. TEM (a), (b) HADDF-STEM, and (c) EDS elemental mapping images of Cu/g-C3N4-3. (d) FT-EXAFS and (e) XANES spectra of Cu K-edge for the Cu/g-C3N4 samples with Cu foil, Cu2O and CuO as the references. (f) CO2 photoreduction performance of g-C3N4 and Cu/g-C3N4 at the first hour of irradiation. (g) Time courses of photocatalytic activities of Cu/g-C3N4-0.25 and (h) GC-MS analysis of reaction products with 12C and 13C as carbon source, respectively. Reprinted with permission from Ref. [84]. Copyright 2020, American Chemical Society.
Fig. 14. (a) Schematic illustration of synthetic procedure for PtCu-g-C3N4. (b) AC-HAADF-STEM images of PtCu-g-C3N4 (the right shows partially zoomed-in images of the selected region 2, and corresponding intensity pro?le along the labeled line 1; scale bar: 0.1 nm). (c) The Cu and Pt contents measured by ICP-MS test. (d) Comparable photocatalytic yield for CO of PtCu-g-C3N4, Cu-g-C3N4, Pt-g-C3N4, and g-C3N4 under simulated solar illumination. Reprinted with permission from Ref. [93]. Copyright 2022, Elsevier.
Fig. 15. (a) Schematic illustration of the developed ball-milling approach. (b) HAADF-STEM/EDX-mapping images of Co-SNC and Co-NC. (c-f) Catalytic performance of Co-SNC in benzylamine self-coupling reaction. Reprinted with permission from Ref. [18]. Copyright 2021, Wiley-VCH.
Fig. 16. (a) Diagrammatic illustration of the preparation of Ni-SA/g-C3N4. (b) Representative HAADF-STEM image. (c) The intensity pro?les obtained in regions 1 and 2 in (b). (d) TEM and matching EDS elemental mapping images of Ni-SA/g-C3N4, (e) Oxidative imine formation catalyzed by a Ni SAC. Reprinted with permission from Ref. [99]. Copyright 2022, American Chemical Society.
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