LAPSE:2023.27234
Published Article
LAPSE:2023.27234
Application of Metal-Organic Frameworks and Covalent Organic Frameworks as (Photo)Active Material in Hybrid Photovoltaic Technologies
April 4, 2023
Abstract
Metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) are two innovative classes of porous coordination polymers. MOFs are three-dimensional materials made up of secondary building blocks comprised of metal ions/clusters and organic ligands whereas COFs are 2D or 3D highly porous organic solids made up by light elements (i.e., H, B, C, N, O). Both MOFs and COFs, being highly conjugated scaffolds, are very promising as photoactive materials for applications in photocatalysis and artificial photosynthesis because of their tunable electronic properties, high surface area, remarkable light and thermal stability, easy and relative low-cost synthesis, and structural versatility. These properties make them perfectly suitable for photovoltaic application: throughout this review, we summarize recent advances in the employment of both MOFs and COFs in emerging photovoltaics, namely dye-sensitized solar cells (DSSCs) organic photovoltaic (OPV) and perovskite solar cells (PSCs). MOFs are successfully implemented in DSSCs as photoanodic material or solid-state sensitizers and in PSCs mainly as hole or electron transporting materials. An innovative paradigm, in which the porous conductive polymer acts as standing-alone sensitized photoanode, is exploited too. Conversely, COFs are mostly implemented as photoactive material or as hole transporting material in PSCs.
Keywords
covalent organic frameworks, dye-sensitized solar cells, emerging photovoltaics, metal organic frameworks, perovskite solar cells
Subject
Suggested Citation
Yildirim O, Bonomo M, Barbero N, Atzori C, Civalleri B, Bonino F, Viscardi G, Barolo C. Application of Metal-Organic Frameworks and Covalent Organic Frameworks as (Photo)Active Material in Hybrid Photovoltaic Technologies. (2023). LAPSE:2023.27234
Author Affiliations
Yildirim O: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy [ORCID]
Bonomo M: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy [ORCID]
Barbero N: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy [ORCID]
Atzori C: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy; European Synchrotron Radiation Facility, 71 Avenue des Martyrs, CS 40220, CEDEX 9, 38043 Grenoble, France [ORCID]
Civalleri B: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy [ORCID]
Bonino F: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy [ORCID]
Viscardi G: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy [ORCID]
Barolo C: Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, via G. Quarello 15a, 10135 Turin, Italy; ICxT Interdepartmental Centre, Università degli Studi di Torino, Via Lungo Dora, Siena 100, 10153 Turin, Italy [ORCID]
Journal Name
Energies
Volume
13
Issue
21
Article Number
E5602
Year
2020
Publication Date
2020-10-26
ISSN
1996-1073
Version Comments
Original Submission
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PII: en13215602, Publication Type: Review
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LAPSE:2023.27234
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https://doi.org/10.3390/en13215602
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