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      Black phosphorus composites with engineered interfaces for high-rate high-capacity lithium storage

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          Abstract

          High-rate lithium (Li) ion batteries that can be charged in minutes and store enough energy for a 350-mile driving range are highly desired for all-electric vehicles. A high charging rate usually leads to sacrifices in capacity and cycling stability. We report use of black phosphorus (BP) as the active anode for high-rate, high-capacity Li storage. The formation of covalent bonds with graphitic carbon restrains edge reconstruction in layered BP particles to ensure open edges for fast Li + entry; the coating of the covalently bonded BP-graphite particles with electrolyte-swollen polyaniline yields a stable solid–electrolyte interphase and inhibits the continuous growth of poorly conducting Li fluorides and carbonates to ensure efficient Li + transport. The resultant composite anode demonstrates an excellent combination of capacity, rate, and cycling endurance.

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          Most cited references43

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          Efficient iterative schemes forab initiototal-energy calculations using a plane-wave basis set

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            Pseudocapacitive Contributions to Electrochemical Energy Storage in TiO2(Anatase) Nanoparticles

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              Ordered mesoporous alpha-MoO3 with iso-oriented nanocrystalline walls for thin-film pseudocapacitors.

              Capacitive energy storage is distinguished from other types of electrochemical energy storage by short charging times and the ability to deliver significantly more power than batteries. A key limitation to this technology is its low energy density and for this reason there is considerable interest in exploring pseudocapacitive materials where faradaic mechanisms offer increased levels of energy storage. Here we show that the capacitive charge-storage properties of mesoporous films of iso-oriented alpha-MoO(3) are superior to those of either mesoporous amorphous material or non-porous crystalline MoO(3). Whereas both crystalline and amorphous mesoporous materials show redox pseudocapacitance, the iso-oriented layered crystalline domains enable lithium ions to be inserted into the van der Waals gaps of the alpha-MoO(3). We propose that this extra contribution arises from an intercalation pseudocapacitance, which occurs on the same timescale as redox pseudocapacitance. The result is increased charge-storage capacity without compromising charge/discharge kinetics in mesoporous crystalline MoO(3).
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                Author and article information

                Contributors
                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                October 08 2020
                October 09 2020
                October 08 2020
                October 09 2020
                : 370
                : 6513
                : 192-197
                Affiliations
                [1 ]Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Materials for Energy Conversion, School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China.
                [2 ]CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, China.
                [3 ]Department of Mechanical Engineering, The University of Texas at Austin, Austin, TX 78712, USA.
                [4 ]Department of Physics, Tamkang University, Tamsui 251, New Taipei City, Taiwan.
                [5 ]State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.
                [6 ]National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029, China.
                [7 ]National Synchrotron Radiation Research Center, 300 Hsinchu, Taiwan.
                [8 ]Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA.
                Article
                10.1126/science.aav5842
                33033214
                1f1ef7a2-6056-41d0-9d29-030e1e12f343
                © 2020

                https://www.sciencemag.org/about/science-licenses-journal-article-reuse

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