4.6 Article

Coupling of a new porphyrin photosensitizer and cobaloxime cocatalyst for highly efficient photocatalytic H2 evolution

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 36, Pages 20645-20652

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta04517b

Keywords

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Funding

  1. General Research Fund from the Hong Kong Research Grants Council [HKBU 12304320]
  2. Research Committee of Hong Kong Baptist University [(2020/21)-RC-FNRA-IG/20-21/SCI/06]
  3. Science, Technology and Innovation Committee of Shenzhen Municipality [JCYJ20180507183413211]
  4. RGC Senior Research Fellowship Scheme [SRFS2021-5S01]
  5. Hong Kong Polytechnic University [1-ZE1C]
  6. Research Institute for Smart Energy (RISE)
  7. Ms Clarea Au for the Endowed Professorship in Energy [847S]

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ZnDC(p-NI)PP is an efficient and effective photocatalytic hydrogen evolution system with significantly improved performance compared to other common PS. This is achieved through mechanisms of intramolecular energy transfer and electrostatic force promoting rapid electron transfer.
Photocatalytic hydrogen evolution (PHE) is a promising strategy to produce environmentally friendly clean energy with the use of solar power and water. For this, developing an efficient and noble metal free photocatalytic system (PS) comprising high light-harvesting and photostable photosensitizers is an important and challenging task. Herein, a new porphyrin photosensitizer ZnDC(p-NI)PP, containing two naphthalimide (NI) donor chromophores and 4-carboxyphenyl substituents is developed for PHE. Using chloropyridinecobaloxime (CoPyCl) as a cocatalyst in phosphate buffer/THF solution at pH 7.4, the homogeneous PS of ZnDC(p-NI)PP exhibits a very high hydrogen evolution rate (etaH2) of 35.70 mmol g-1 h-1, turnover number (TON) of 5958 and apparent quantum efficiency (AQE) of 10.01%. This performance recorded under the same conditions is significantly higher than that of the PS of ZnDCPP which lacks the NI moieties (etaH2 of 4.64 mmol g-1 h-1, TON of 1397 and AQE of 1.30%), the typical PS of ZnTCPP with four 4-carboxyphenyl substituent groups (etaH2 of 2.43 mmol g-1 h-1, TON of 562 and AQE of 1.00%), and previously reported ZnD(p-NI)PP containing only two NI chromophores (etaH2 of 3.8 mmol g-1 h-1, TON of 590 and AQE of 1.5%). The noticeable performance of ZnDC(p-NI)PP in PHE is attributed to the intramolecular energy transfer from the NI donor chromophore to the porphyrin acceptor that would promote the long-lived photoexcitation states. At the same time, the anionic form (-COO-) of 4-carboxyphenyl substituents at pH 7.4 enables a faster electron transfer from the porphyrin group to the cationic Co(iii) due to electrostatic force. To the best of our knowledge, the PHE results of ZnDC(p-NI)PP represent the best one for porphyrin photosensitizers and cobaloxime PSs reported so far. This work paves a new direction for developing new porphyrin-based materials for efficient PHE through facile molecular structure engineering.

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