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      Dual modification of Ti 3C 2T x MXene hybridization and cut-off voltage adjustment for MoS 2 to achieve stable sodium storage performance

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          Abstract

          The dual modification of MXene hybridization and cut-off voltage adjustment endows MoS 2/Ti 3C 2T x with enhanced reaction kinetics and satisfactory electrochemical performance.

          Abstract

          Molybdenum disulfide (MoS 2), a typical layered transition metal sulfide with a large interlayer distance, narrow band gap structure, and high theoretical capacity for sodium storage, shows tremendous promise for sodium-ion batteries (SIBs). Unfortunately, the inadequate cycling stability due to the mechanical failure caused by the deep conversion reaction upon cycling at low voltage, combined with its intrinsic poor electical conductivity, results in degraded electrochemical performance. In this work, a novel Ti 3C 2T x MXene was introduced to fabricate a MoS 2/Ti 3C 2T x hybrid through a facile hydrothermal approach, dramatically increasing the reaction kinetics of the hybrid electrode. Additionally, further increasing the discharge cut-off voltage to 0.2 V, the target MoS 2/Ti 3C 2T x exhibits remarkable sodium storage performance in terms of specific capacity, cyclability, and rate capability. Strikingly, the capacity hardly ever decays after 1000 cycles at 1.0 A g −1. Noteworthily, the impressive sodium storage performance of MoS 2/Ti 3C 2T x within 0.2–3.0 V originates from the effective avoidance of deep conversion reations below 0.2 V and improved electronic kinetics from the combination with Ti 3C 2T x flakes. Moreover, ex situ phase characteriztion, kinetic study, and pseudocapacitive effect for charge storage were also investigated to reveal the origin of the improved electrochemical performance. Importantly, the modifications of both electrode structure and cut-off voltage provide an effective way to optimize the electrochemical redox of the target electrode.

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          High areal capacity battery electrodes enabled by segregated nanotube networks

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            Evolution of the electrochemical interface in sodium ion batteries with ether electrolytes

            Ether based electrolytes have surfaced as alternatives to conventional carbonates allowing for enhanced electrochemical performance of sodium-ion batteries; however, the primary source of the improvement remains poorly understood. Here we show that coupling titanium dioxide and other anode materials with diglyme does enable higher efficiency and reversible capacity than those for the combination involving ester electrolytes. Importantly, the electrolyte dependent performance is revealed to be the result of the different structural evolution induced by a varied sodiation depth. A suit of characterizations show that the energy barrier to charge transfer at the interface between electrolyte and electrode is the factor that dominates the interfacial electrochemical characteristics and therefore the energy storage properties. Our study proposes a reliable parameter to assess the intricate sodiation dynamics in sodium-ion batteries and could guide the design of aprotic electrolytes for next generation rechargeable batteries.
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              MXene Titanium Carbide-based Biosensor: Strong Dependence of Exfoliation Method on Performance

              Transition metal carbides, known as MXenes, are generated via the selective etching of "A" layers from their layered, ternary parent compounds, MAX phases, where M corresponds to early d-transition metal, A being a main group sp-element from either Group 13 or 14 and carbon or nitrogen being denoted by X. MXenes are being recognized as a new and uprising class of 2D materials with extraordinary physical and electrochemical properties. The huge specific surface area and outstanding electrical conductivity of MXenes, make them ideal candidates for sensing and energy applications. Herein, we demonstrated the successful incorporation of pristine MXene, Ti3C2 produced via HF etching and subsequent delamination with TBAOH, as a transducer platform toward the development of a second generation electrochemical glucose biosensor. Chronoamperometric studies demonstrate that the proposed biosensing system exhibits high selectivity and excellent electrocatalytic activity toward the detection of glucose, spanning over wide linear ranges of 50-27 750 μM and possess a low limit of detection of 23.0 μM. The findings reported in this study conceptually proves the probable applications of pristine MXenes toward the field of biosensors and pave ways for the future developments of highly selective and sensitive electrochemical biosensors for biomedical and food sampling applications.
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                Author and article information

                Contributors
                Journal
                MCFAC5
                Materials Chemistry Frontiers
                Mater. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1537
                February 27 2023
                2023
                : 7
                : 5
                : 917-928
                Affiliations
                [1 ]School of Chemistry and Chemical Engineering, Yangzhou University, 180-Si-Wang-Ting Road, Yangzhou, Jiangsu 225002, China
                [2 ]Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Electronic Science, East China Normal University, No. 500 Dongchuan Road, Shanghai 200241, China
                Article
                10.1039/D2QM01248K
                538dcfd9-3af8-4733-bbfd-d691f4a97f65
                © 2023

                http://rsc.li/journals-terms-of-use

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