2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Interfaces in metal halide perovskites probed by solid-state NMR spectroscopy

      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

          This review outlines the prospects for a range of solid-state NMR spectroscopy techniques to facilitate structural understanding of complex interfaces in metal halide perovskites and transport layers for optoelectronic applications.

          Abstract

          Metal halide perovskites (MHPs) are promising light harvesting and emitting materials that have enabled solar energy conversion efficiencies of over 25% in solution-processed single-junction cells, and found applications in flexible electronics, detectors and other display technologies. Research on MHPs has achieved significant fundamental and technological advancements over the last decade, in large part due to improvements in characterization approaches to understand these materials. It has become clear that engineering the interfaces between device layers, and within the MHP layer itself, is crucially important to develop stable and efficient optoelectronic devices. Interfaces in MHP-based devices exhibit varying degrees of order, which manifest heterogeneities in compositions, structures and optoelectronic properties. This review assesses the overall prospects for a range of solid-state (ss)NMR spectroscopy techniques to facilitate structure-based understanding of complex interfaces in MHPs and contact layers. The role of ssNMR in elucidating local compositions and structures, intermolecular connectivity, phase transitions, degradation products and molecular passivation at MHP interfaces is discussed. In addition, an overview of different dynamic processes in MHPs probed by ssNMR is provided. Finally, we discuss perspectives on the development of ssNMR spectroscopy for investigating interfaces in MHPs for various optoelectronics.

          Related collections

          Most cited references442

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

          Organometal halide perovskites as visible-light sensitizers for photovoltaic cells.

          Two organolead halide perovskite nanocrystals, CH(3)NH(3)PbBr(3) and CH(3)NH(3)PbI(3), were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells. When self-assembled on mesoporous TiO(2) films, the nanocrystalline perovskites exhibit strong band-gap absorptions as semiconductors. The CH(3)NH(3)PbI(3)-based photocell with spectral sensitivity of up to 800 nm yielded a solar energy conversion efficiency of 3.8%. The CH(3)NH(3)PbBr(3)-based cell showed a high photovoltage of 0.96 V with an external quantum conversion efficiency of 65%.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Nanocrystals of Cesium Lead Halide Perovskites (CsPbX3, X = Cl, Br, and I): Novel Optoelectronic Materials Showing Bright Emission with Wide Color Gamut

            Metal halides perovskites, such as hybrid organic–inorganic CH3NH3PbI3, are newcomer optoelectronic materials that have attracted enormous attention as solution-deposited absorbing layers in solar cells with power conversion efficiencies reaching 20%. Herein we demonstrate a new avenue for halide perovskites by designing highly luminescent perovskite-based colloidal quantum dot materials. We have synthesized monodisperse colloidal nanocubes (4–15 nm edge lengths) of fully inorganic cesium lead halide perovskites (CsPbX3, X = Cl, Br, and I or mixed halide systems Cl/Br and Br/I) using inexpensive commercial precursors. Through compositional modulations and quantum size-effects, the bandgap energies and emission spectra are readily tunable over the entire visible spectral region of 410–700 nm. The photoluminescence of CsPbX3 nanocrystals is characterized by narrow emission line-widths of 12–42 nm, wide color gamut covering up to 140% of the NTSC color standard, high quantum yields of up to 90%, and radiative lifetimes in the range of 1–29 ns. The compelling combination of enhanced optical properties and chemical robustness makes CsPbX3 nanocrystals appealing for optoelectronic applications, particularly for blue and green spectral regions (410–530 nm), where typical metal chalcogenide-based quantum dots suffer from photodegradation.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Efficient hybrid solar cells based on meso-superstructured organometal halide perovskites.

              The energy costs associated with separating tightly bound excitons (photoinduced electron-hole pairs) and extracting free charges from highly disordered low-mobility networks represent fundamental losses for many low-cost photovoltaic technologies. We report a low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight. This "meso-superstructured solar cell" exhibits exceptionally few fundamental energy losses; it can generate open-circuit photovoltages of more than 1.1 volts, despite the relatively narrow absorber band gap of 1.55 electron volts. The functionality arises from the use of mesoporous alumina as an inert scaffold that structures the absorber and forces electrons to reside in and be transported through the perovskite.
                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                September 14 2021
                2021
                : 9
                : 35
                : 19206-19244
                Affiliations
                [1 ]Materials Department, University of California, Santa Barbara, California 93106, USA
                [2 ]Cavendish Laboratory, Department of Physics, University of Cambridge, JJ Thomson Avenue, CB3 0HE, Cambridge, UK
                [3 ]Department of Chemistry, University of Cambridge, Lensfield Road, CB2 1EW, Cambridge, UK
                [4 ]Univ. Lille, CNRS, Centrale Lille, Univ. Artois, UMR 8181 – UCCS – Unité de Catalyse et Chimie du Solide, F-59000 Lille, France
                Article
                10.1039/D1TA03572J
                f8fbcedf-8975-4e83-b3f8-ddac1bf4afbf
                © 2021

                http://creativecommons.org/licenses/by-nc/3.0/

                History

                Comments

                Comment on this article