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      Transparent MoS 2/PEDOT Composite Counter Electrodes for Bifacial Dye-Sensitized Solar Cells

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          Abstract

          Dye-sensitized solar cells (DSSCs) are solar energy conversion devices with high efficiency and simple fabrication procedures. Developing transparent counter electrode (CE) materials for bifacial DSSCs can address the needs of window-type building-integrated photovoltaics (BIPVs). Herein, transparent organic–inorganic hybrid composite films of molybdenum disulfide and poly(3,4-ethylenedioxythiophene) (MoS 2/PEDOT) are prepared to take full advantage of the conductivity and electrocatalytic ability of the two components. MoS 2 is synthesized by hydrothermal method and spin-coated to form the MoS 2 layer, and then PEDOT films are electrochemically polymerized on top of the MoS 2 film to form the composite CEs. The DSSC with the optimized MoS 2/PEDOT composite CE shows power conversion efficiency (PCE) of 7% under front illumination and 4.82% under back illumination. Compared with the DSSC made by the PEDOT CE and the Pt CE, the DSSC fabricated by the MoS 2/PEDOT composite CE improves the PCE by 10.6% and 6.4% for front illumination, respectively. It proves that the transparent MoS 2/PEDOT CE owes superior conductivity and catalytic properties, and it is an excellent candidate for bifacial DSSC in the application of BIPVs.

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          All-Polymer Solar Cells: Recent Progress, Challenges, and Prospects

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            Interlayer-expanded molybdenum disulfide nanocomposites for electrochemical magnesium storage.

            Mg rechargeable batteries (MgRBs) represent a safe and high-energy battery technology but suffer from the lack of suitable cathode materials due to the slow solid-state diffusion of the highly polarizing divalent Mg ion. Previous methods improve performance at the cost of incompatibility with anode/electrolyte and drastic decrease in volumetric energy density. Herein we report interlayer expansion as a general and effective atomic-level lattice engineering approach to transform inactive intercalation hosts into efficient Mg storage materials without introducing adverse side effects. As a proof-of-concept we have combined theory, synthesis, electrochemical measurement, and kinetic analysis to improve Mg diffusion behavior in MoS2, which is a poor Mg transporting material in its pristine form. First-principles simulations suggest that expanded interlayer spacing allows for fast Mg diffusion because of weakened Mg-host interactions. Experimentally, the expansion was realized by inserting a controlled amount of poly(ethylene oxide) into the lattice of MoS2 to increase the interlayer distance from 0.62 nm to up to 1.45 nm. The expansion boosts Mg diffusivity by 2 orders of magnitude, effectively enabling the otherwise barely active MoS2 to approach its theoretical storage capacity as well as to achieve one of the highest rate capabilities among Mg-intercalation materials. The interlayer expansion approach can be leveraged to a wide range of host materials for the storage of various ions, leading to novel intercalation chemistry and opening up new opportunities for the development of advanced materials for next-generation energy storage.
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              Opening Two-Dimensional Materials for Energy Conversion and Storage: A Concept

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                09 April 2020
                21 April 2020
                : 5
                : 15
                : 8687-8696
                Affiliations
                []School of Chemistry and Chemical Engineering, Northwestern Polytechnical University , Xi’an, Shaanxi 710129, China
                []Shaanxi Institute of Flexible Electronics (SIFE), Northwestern Polytechnical University , Xi’an, Shaanxi 710072, China
                [§ ]School of Materials Science and Engineering, Northwestern Polytechnical University , Xi’an, Shaanxi 710072, China
                []Department of Electrical Engineering and Computer Sciences, College of Engineering, South Dakota State University , Brookings, South Dakota 57007, United States
                Author notes
                Article
                10.1021/acsomega.0c00175
                7178793
                32337431
                a219eab2-a902-45bf-aac2-aeac84809be0
                Copyright © 2020 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 14 January 2020
                : 27 March 2020
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