物理化学学报 >> 2025, Vol. 41 >> Issue (12): 100176.doi: 10.1016/j.actphy.2025.100176
邵毅宏1, 沈荣晨1, 王松2,*(
), 李世杰3,*(
), 张鹏4,*(
), 李鑫1,*(
)
收稿日期:2025-08-08
修回日期:2025-08-28
录用日期:2025-08-28
发布日期:2025-10-23
通讯作者:
Email: Xinli@scau.edu.cn (李鑫)wangsong1984@hbuas.edu.cn (王松)lishijie@zjou.edu.cn (李世杰)zhangp@zzu.edu.cn (张鹏)
基金资助:
Yihong Shao1, Rongchen Shen1, Song Wang2,*(
), Shijie Li3,*(
), Peng Zhang4,*(
), Xin Li1,*(
)
Received:2025-08-08
Revised:2025-08-28
Accepted:2025-08-28
Published:2025-10-23
Contact:
Email: Xinli@scau.edu.cn (Xin Li)wangsong1984@hbuas.edu.cn (Song Wang)lishijie@zjou.edu.cn (Shijie Li)zhangp@zzu.edu.cn (Peng Zhang)
Supported by:摘要:
能源危机与环境恶化的危害日益严峻,亟需发展环境友好型可持续生产技术。将丰富的太阳能直接转化为化学能,被视为一种极具前景的绿色高效技术方案。在此过程中,光催化剂扮演着至关重要的角色。共价有机框架材料(COFs)作为一种通过共价键连接的多孔材料,凭借其高比表面积、优异的结晶性和可调控的结构,展现出卓越的光催化潜力。本综述深入探讨了组分调控对提升COFs光催化性能的作用机制,涵盖调控光吸收、增加活性位点、促进激子解离以及改善载流子分离,并对相关计算模拟与机理表征方法进行了详细论述。更为重要的是,系统总结了组分调控的核心策略,包括杂原子工程、金属单原子工程、离子工程、官能团工程、供体-受体(D-A)分子工程、侧链工程、多组分工程、同分异构工程、共轭桥工程、单分子结工程和层间工程。此外,本文还详细阐述了这些策略在光催化析氢(H2)、过氧化氢(H2O2)合成及二氧化碳(CO2)还原等领域的多样化改性策略与应用。最后,对COF基光催化技术当前面临的挑战及未来发展方向进行了前瞻性展望。
邵毅宏, 沈荣晨, 王松, 李世杰, 张鹏, 李鑫. 共价有机框架中的组分工程用于定制光催化[J]. 物理化学学报, 2025, 41(12), 100176. doi: 10.1016/j.actphy.2025.100176
Yihong Shao, Rongchen Shen, Song Wang, Shijie Li, Peng Zhang, Xin Li. Composition engineering in covalent organic frameworks for tailored photocatalysis[J]. Acta Phys. -Chim. Sin. 2025, 41(12), 100176. doi: 10.1016/j.actphy.2025.100176
表1
"
| COFs | Cocatalyst | Sacrificial reagent | HER (µmol g−1 h−1) | Ref. |
| COF-JLU100 | Pt (3 wt.%) | TEOA | 107380 | [ |
| COF-ST | Pt (3 wt.%) | TEOA | 21.5 | [ |
| SP2c-Py-BT COF | Pt | TEOA | 891.5 | [ |
| Py-ClTP-BT-COF | Pt (5 wt.%) | AA | 8875 | [ |
| BTT-NDA | Pt (3 wt.%) | AA | 5220 | [ |
| TpBpy-Ni2% | Pt | AA | 51300 | [ |
| PyTz-COF | Pt (3 wt.%) | AA | 2072.4 | [ |
| COF-JLU35 | Pt (1 wt.%) | AA | 70800 ± 1900 | [ |
| Tp-2C/BPy2+-COF | Pt (3 wt.%) | AA | 34600 | [ |
| ODA-COF | Pt (9 wt.%) | TEOA | 2615 | [ |
| COF-954 | Pt (5 wt.%) | AA | 137230 | [ |
| PY-DHBD-COF | Pt (1 wt.%) | AA | 42432 | [ |
| Tz-COF-3 | Pt (3 wt.%) | AA | 43200 | [ |
| PABZ-TP | Pt (0.5 wt.%) | AA | 115000 | [ |
| PTT-COF-FC | Pt (3 wt.%) | AA | 79610 | [ |
| TMT-BO-COF | Pt (5 wt.%) | AA | 23700 | [ |
| TeTpb-COF | Pt (3 wt.%) | AA | 21600 | [ |
| COF-923-AC | Pt | AA | 23400 | [ |
| COF-F NKCOF-113-M | Pt (3 wt.%) Pt (5 wt.%) | AA TEOA | 10580 13100 | [ [ |
表2
"
| COFs | Reaction solution | H2O2 (µmol g−1 h−1) | AQY (%) | Reference |
| TBTN-COF | H2O/O2 | 11013 | 7.59 | [ |
| COF-2CN | H2O/O2 | 1601 | 6.8 | [ |
| TF50-COF | H2O: EtOH/O2 | 1739 | 5.1 | [ |
| TD-COF | H2O/O2 | 4060 | – | [ |
| FS-COF | H2O/O2 | 3904.2 | 6.21 | [ |
| Py-Py-COF | H2O: BA/O2 | 1242 | – | [ |
| TpDz | H2O/O2 | 7327 | 11.9 | [ |
| PD2+-COF | H2O: EtOH/O2 | 11965 | 12.9 | [ |
| PMCR-1 | H2O/O2 | 1445 | – | [ |
| TTF-BT-COF | H2O/O2 | 276000 | 11.19 | [ |
| COF-JLU52 | H2O: BA/O2 | 7624.7 | 18.2 | [ |
| COF-TfpBpy | H2O/air | 694.7 | 8.1 | [ |
| HEP-TAPT-COF | H2O/O2 | 1750 | 15.35 | [ |
| DMCR-1NH | H2O/O2 | 2588 | 10.2 | [ |
| Bpt-CTF | H2O/O2 | 3268.1 | 8.6 | [ |
| DETH-COF | H2O/air | 1665 | 0.063 | [ |
| TPB-DMTP-COF | H2O/O2 | 2882 | 18.4 | [ |
| COF-TpHt | H2O: BnOH/O2 | 11986 | – | [ |
| TAPT-PDA-COF | H2O: IPA/O2 | 706.2 | 1.69 | [ |
| COF-TPT-AZO | H2O/O2(PH=11) | 1498 | – | [ |
表3
"
| COFs | Sacrificial agent | CO2RR (µmol g−1 h−1) | Selectivity (%) | Reference |
| Re-COF | TEOA | 750 (CO) | 98 | [ |
| Re-Bpy-sp2c-COF | TEOA | 1400 (CO) | 86 | [ |
| COOH-COF | TEA | 3700 (CO) | – | [ |
| PI-COF-TT | – | 483.25 (CO) | 93 | [ |
| H-COF-Ni | TEOA | 2847 (CO) | 96 | [ |
| TTCOF-Zn | – | 12.33 (CO) | 100 | [ |
| Ni-TpBpy | TEOA | 811.4 (CO) | 96 | [ |
| Co-2,3-DHTA-COF | TEOA | 18000 (CO) | 95.7 | [ |
| Fe SAS/Tr-COF | TEOA | 980.3 (CO) | 96.4 | [ |
| LaNi-Phen/COF-5 | BIH | 605.8 (CO) | 98.2 | [ |
| N3-COF | – | 13.7 (CH3OH) | – | [ |
| Mo-COF | – | 3.57 (C2H4) | 42.92 | [ |
| CTF | – | 881.3 × 106 (HCOOH) | – | [ |
| TPy-COF-Co | TEOA | 426000 (CO) | – | [ |
| EPCo-COF-AT | MeCN | 17700 (CO) | 97.8 | [ |
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