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Silicon-coated molybdenum sulfide nanosheets were prepared in a thin-film shape (Si–MoS 2 TFs) through metal organic chemical vapor deposition (MOCVD) and radio frequency (RF) sputtering. By using MOCVD, the MoS 2 thin films composed of nanosheets were vertically grown on stainless steel substrates. To address the problem of polysulfide dissolution and shuttling effect of MoS 2 during discharge and charge reactions in thin-film Li-ion batteries, the entire surfaces of MoS 2 TFs were covered with silicon layers using RF sputtering. Compared with pristine MoS 2 TFs without protection, the Si–MoS 2 TFs showed excellent reversibility with a high capacity of ∼2000 mAh g−1 for 500 cycles in thin-film Li-ion batteries. Both materials – MoS 2 and Si – were synergistically taken into account to enhance the ability to store Li ions in the host structures and complement each other during repeated conversion and alloying reactions. The underlying reaction principle was elucidated, which provides insight into developing MoS 2 -based thin-film cathodes. [ABSTRACT FROM AUTHOR]

[Display omitted] Electrodeposition and electropolymerization have emerged as versatile tools for the fabrication of chemical and biosensors. The literature in this area, published since 2017, is the main focus of this review. Electropolymerization has played a particularly prominent role in sensor development since its discovery in 1980 by Diaz at IBM. The ability to entrain receptors such as antibodies, engineered virus particles, and metal chelating agents into a conductive polymer sensing element during electropolymerization has proven to be a powerful means of preparing chemiresistors for a variety of analyses. Electrodeposition has also been used to prepare nanostructured metal indicator microelectrodes, enabling of a new modality for transducing biosensors. Electrodeposited metal nanowires have formed the basis for rapid and sensitive sensors for hydrogen gas. Electrodeposition has also been exploited as a powerful means for amplifying weak biosensor signals, extending their dynamic range. Opportunities for the application of electrodeposition and electropolymerization for chemical and biological sensor fabrication and function are discussed. [ABSTRACT FROM AUTHOR]

[Display omitted] van der Waals heterostructures (vdWHs), consisting of more than one type of atomically thin 2D crystal layers are emerging platforms for interesting electrical, optical, and catalytic applications. High yield production of vdWHs with atomic scale precision is crucial prerequisite for practical utilization. Here we present a generalized approach of random solution phase, high yield heteroassembly of semiconducting vdWHs by exploiting inherent surface charge states of 2D materials as well as chemical affinity of specific ligand end-functionalities. Facile removal of noncovalent functionalized ligands via simple pH reversal enables clean interfaces within vdWHs, yielding outstanding optoelectrical and electrochemical properties driven by fluent interfacial charge transfer among the layered 2D structures. The generality of this procedure is demonstrated by the formation of a series of different vdWHs such as WSe 2 -MoS 2 , graphene–MoS 2 - and phospherene–WSe 2 heterostructures. Atomically thin WSe 2 –MoS 2 phototransistor displayed an exceptionally fast response time with high sensitivity. Graphene–MoS 2 overcomes the inherent charge transfer issue of MoS 2 for electrochemical catalyst. Phospherene–WSe 2 successfully addresses poor ambient stability of phospherene together with enhanced surface activity towards chemical sensing. [ABSTRACT FROM AUTHOR]