Integrating energy donor and acceptor chromophores as ligands within one MOF for advanced artificial photosynthesis is of great interest but appears to be a major challenge. Herein, via a simple one-pot synthetic strategy, an energy acceptor porphyrin ligand 5,15-di(p-benzoato)porphyrin (HDPBP) was successfully integrated into an energy donor 1,4-naphthalenedicarboxylic acid (HNDC)-based MOF (UiO-66-NDC) to construct a mixed-ligand MOF, donated as UiO-66-NDC-HDPBP. Benefiting from the ample overlap between the emission spectrum of HNDC and the absorption spectrum of HDPBP, an efficient energy transfer (EnT) process from the donor HNDC to the acceptor HDPBP within UiO-66-NDC-HDPBP can occur and be captured by time-resolved spectroscopy. Furthermore, the singlet oxygen (O) generation efficiency of UiO-66-NDC-HDPBP mediated by this EnT process as well as the EnT process from the triplet state (T) of the photosensitizer HDPBP ligand to the ground state of molecular oxygen (O) upon light irradiation can be maximized via simply regulating the loading amount of HDPBP, leading to boosted photocatalytic activities toward important aerobic oxidation reactions of amines and sulfides, even under sunlight and ambient air. This work explores an avenue to construct high-efficiency energy donor and acceptor-based light-harvesting systems by utilizing mixed-ligand MOFs as platforms to advanced artificial photosynthesis.
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http://dx.doi.org/10.1016/j.jcis.2025.03.020 | DOI Listing |
Angew Chem Int Ed Engl
March 2025
South China University of Technology, State Key Laboratory of Luminescent Materials and Devices, Wushan Road 381, 510640, Guangzhou, CHINA.
Energy loss (Eloss) between optical energy gap (Eg) and open-circuit voltage (eVoc) sets efficiency upper limits for organic solar cells (OSCs). Nevertheless, further breaking the limit of Eloss in OSCs is challenging, especially via structurally simple materials in binary OSCs. Herein, a structurally simple non-halogenated polymer donor, namely PBDCT, is developed for realizing high-efficiency OSCs with record-breaking Eloss.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Department of Chemistry, and the Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, PR China.
Research on room temperature phosphorescence (RTP) of metal-organic frameworks (MOFs) has been rapidly developed in recent years. However, it is still challenging to realize long-wavelength RTP (>580 nm). In this article, a new strategy is proposed to achieve the red-shifted RTP through constructing dual-ligand MOFs.
View Article and Find Full Text PDFAnal Chim Acta
May 2025
State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, Guangxi University, Nanning, Guangxi, 530004, PR China; College of Life Science and Technology, Guangxi University, Nanning, Guangxi, 530004, PR China; Medical College of Guangxi University, Guangxi University, Nanning, Guangxi, 530004, PR China; Center for Instrumental Analysis, Guangxi University, Nanning, Guangxi, 530004, PR China. Electronic address:
Tryptophan (Trp) is an essential amino acid obtained from human diet. It is involved not only in de novo biosynthesis of proteins but also in complex metabolic pathways. Redox transformation of tryptophan is under-explored in comparison with kynurenine, serotonin and indole pyruvate pathways.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
School of Materials Science and Engineering, Changsha University of Science & Technology, Changsha 410114, China.
Integrating energy donor and acceptor chromophores as ligands within one MOF for advanced artificial photosynthesis is of great interest but appears to be a major challenge. Herein, via a simple one-pot synthetic strategy, an energy acceptor porphyrin ligand 5,15-di(p-benzoato)porphyrin (HDPBP) was successfully integrated into an energy donor 1,4-naphthalenedicarboxylic acid (HNDC)-based MOF (UiO-66-NDC) to construct a mixed-ligand MOF, donated as UiO-66-NDC-HDPBP. Benefiting from the ample overlap between the emission spectrum of HNDC and the absorption spectrum of HDPBP, an efficient energy transfer (EnT) process from the donor HNDC to the acceptor HDPBP within UiO-66-NDC-HDPBP can occur and be captured by time-resolved spectroscopy.
View Article and Find Full Text PDFChem Rec
March 2025
University of Leuven, KU Leuven), LOMAC Celestijnenlaan 200F, B-3001, Leuven, Belgium.
Photosynthesis in plants has inspired photochemical reactions in organic chemistry. Synthetic organic chemists always seek cost-effective, operationally simple, averting the use of toxic and difficult-to-remove metallic catalysts, atom economical, and high product purity in organic reactions. In the last few decades, the use of light as a catalyst in organic reactions has increased exponentially as literature has exploded with examples, particularly by using toxic and expensive metal complexes, photosensitizers like organic dyes, hypervalent iodine, or by using inorganic semiconductors.
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