35
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Enhancing the performance of pure organic room-temperature phosphorescent luminophores

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Once considered the exclusive property of metal complexes, the phenomenon of room-temperature phosphorescence (RTP) has been increasingly realized in pure organic luminophores recently. Using precise molecular design and synthetic approaches to modulate their weak spin–orbit coupling, highly active triplet excitons, and ultrafast deactivation, organic luminophores can be endowed with long-lived and bright RTP characteristics. This has sparked intense explorations into organic luminophores with enhanced RTP features for different applications. This Review discusses the fundamental mechanism of RTP in pure organic luminophores, followed by design principles, enhancement strategies, and formulation methods to achieve highly phosphorescent and long-lived organic RTP luminophores even in aqueous media. The current challenges and future directions of this field are also discussed in the summary and outlook.

          Abstract

          Pure organic molecules displaying room-temperature phosphorescence (RTP) are a rapidly emerging class of luminophores. In this Review, the authors discuss the principles for their rational design and development, from the underlying photophysical mechanisms of organic RTP, to enhancement and processing strategies for their practical application.

          Related collections

          Most cited references54

          • Record: found
          • Abstract: found
          • Article: not found

          Organic Optoelectronic Materials: Mechanisms and Applications.

          Organic (opto)electronic materials have received considerable attention due to their applications in thin-film-transistors, light-emitting diodes, solar cells, sensors, photorefractive devices, and many others. The technological promises include low cost of these materials and the possibility of their room-temperature deposition from solution on large-area and/or flexible substrates. The article reviews the current understanding of the physical mechanisms that determine the (opto)electronic properties of high-performance organic materials. The focus of the review is on photoinduced processes and on electronic properties important for optoelectronic applications relying on charge carrier photogeneration. Additionally, it highlights the capabilities of various experimental techniques for characterization of these materials, summarizes top-of-the-line device performance, and outlines recent trends in the further development of the field. The properties of materials based both on small molecules and on conjugated polymers are considered, and their applications in organic solar cells, photodetectors, and photorefractive devices are discussed.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Spin—Orbit Coupling and the Radiationless Processes in Nitrogen Heterocyclics

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Efficient charge generation by relaxed charge-transfer states at organic interfaces.

              Interfaces between organic electron-donating (D) and electron-accepting (A) materials have the ability to generate charge carriers on illumination. Efficient organic solar cells require a high yield for this process, combined with a minimum of energy losses. Here, we investigate the role of the lowest energy emissive interfacial charge-transfer state (CT1) in the charge generation process. We measure the quantum yield and the electric field dependence of charge generation on excitation of the charge-transfer (CT) state manifold via weakly allowed, low-energy optical transitions. For a wide range of photovoltaic devices based on polymer:fullerene, small-molecule:C60 and polymer:polymer blends, our study reveals that the internal quantum efficiency (IQE) is essentially independent of whether or not D, A or CT states with an energy higher than that of CT1 are excited. The best materials systems show an IQE higher than 90% without the need for excess electronic or vibrational energy.
                Bookmark

                Author and article information

                Contributors
                cheliub@nus.edu.sg
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                8 May 2019
                8 May 2019
                2019
                : 10
                : 2111
                Affiliations
                ISNI 0000 0001 2180 6431, GRID grid.4280.e, Department of Chemical and Biomolecular Engineering, , National University of Singapore, ; 4 Engineering Drive 4, Singapore, 117585 Singapore
                Author information
                http://orcid.org/0000-0003-0405-1369
                Article
                10033
                10.1038/s41467-019-10033-2
                6506551
                31068598
                ae6b16b3-ddc5-495f-91f5-2d909798e0cd
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 17 July 2018
                : 22 March 2019
                Categories
                Review Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                optical materials,nanoscience and technology,optical materials and structures

                Comments

                Comment on this article