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      MoS 2@Polyaniline for Aqueous Ammonium‐Ion Supercapacitors

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          Abstract

          Ammonium‐ion aqueous supercapacitors are raising notable attention owing to their cost, safety, and environmental advantages, but the development of optimized electrode materials for ammonium‐ion storage still lacks behind expectations. To overcome current challenges, here, a sulfide‐based composite electrode based on MoS 2 and polyaniline (MoS 2@PANI) is proposed as an ammonium‐ion host. The optimized composite possesses specific capacitances above 450 F g −1 at 1 A g −1, and 86.3% capacitance retention after 5000 cycles in a three‐electrode configuration. PANI not only contributes to the electrochemical performance but also plays a key role in defining the final MoS 2 architecture. Symmetric supercapacitors assembled with such electrodes display energy densities above 60 Wh kg −1 at a power density of 725 W kg −1. Compared with Li + and K + ions, the surface capacitive contribution in NH 4 +‐based devices is lower at every scan rate, which points to an effective generation/breaking of H‐bonds as the mechanism controlling the rate of NH 4 + insertion/de‐insertion. This result is supported by density functional theory calculations, which also show that sulfur vacancies effectively enhance the NH 4 + adsorption energy and improve the electrical conductivity of the whole composite. Overall, this work demonstrates the great potential of composite engineering in optimizing the performance of ammonium‐ion insertion electrodes.

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          Most cited references34

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          Ultra-fast NH4+ Storage: Strong H Bonding between NH4+ and Bi-layered V2O5

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            Initiating Hexagonal MoO 3 for Superb‐Stable and Fast NH 4 + Storage Based on Hydrogen Bond Chemistry

            Nonmetallic ammonium (NH4 + ) ions are applied as charge carriers for aqueous batteries, where hexagonal MoO3 is initially investigated as an anode candidate for NH4 + storage. From experimental and first-principle calculated results, the battery chemistry proceeds with reversible building-breaking behaviors of hydrogen bonds between NH4 + and tunneled MoO3 electrode frameworks, where the ammoniation/deammoniation mechanism is dominated by nondiffusion-controlled pseudocapacitive behavior. Outstanding electrochemical performance of MoO3 for NH4 + storage is delivered with 115 mAh g-1 at 1 C and can retain 32 mAh g-1 at 150 C. Furthermore, it remarkably exhibits ultralong and stable cyclic performance up to 100 000 cycle with 94% capacity retention and high power density of 4170 W kg-1 at 150 C. When coupled with CuFe prussian blue analogous (PBA) cathode, the full ammonium battery can deliver decent energy density 21.3 Wh kg-1 and the resultant flexible ammonium batteries at device level are also pioneeringly developed for potential realistic applications.
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              Ammonium‐Ion Storage Using Electrodeposited Manganese Oxides

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                Author and article information

                Contributors
                Journal
                Advanced Materials
                Advanced Materials
                Wiley
                0935-9648
                1521-4095
                September 2023
                August 07 2023
                September 2023
                : 35
                : 39
                Affiliations
                [1 ] Fujian Provincial Key Laboratory of Fire Retardant Materials College of Materials Xiamen University Xiamen 361005 China
                [2 ] Catalonia Institute for Energy Research (IREC) Sant Adrià de Besòs Barcelona Catalonia 08930 Spain
                [3 ] Institute for Advanced Study Chengdu University Chengdu 610106 China
                [4 ] College of Chemistry and Chemical Engineering Chongqing University of Technology Chongqing 400054 China
                [5 ] ICREA Pg. Lluis Companys 23 Barcelona Catalonia 08010 Spain
                Article
                10.1002/adma.202303732
                1703df51-e0b7-493f-89af-6a63f35eb834
                © 2023

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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