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- W2947987592 abstract "Graphitic carbon nitride is an ordered two-dimensional stability. However, its bulk structure with low electrical conductivity (less than 1 S cm-1) restricts the applications in electrochemical energy storage. This is because conventional synthesis methods lack effective thickness control, and the excessive nitrogen doping (∼50%) leads to poor electrical conductivity. Here, we report an ultrathin conductive graphitic carbon nitride assembly (thickness of ∼1.0 nm) through graphene-templated van der Waals epitaxial strategy with high electrical conductivity (12.2 S cm-1), narrow pore-size distribution (5.3 nm), large surface area (724.9 m2 g-1), and appropriate nitrogen doping level (18.29%). The ultra-thin structure with nitrogen doping provided numerous channels and active sites for effective ion transportation and storage, while the graphene layers acted as micro current collectors; subsequently, it exhibits high energy storage capability of 936 mF cm-2 at 1 mA cm-2 with excellent stability of over 10 000 cycles. Moreover, the all-solid-state supercapacitors showed an ultra-high energy density of 281.3 μWh cm-2 at 1 mA cm-2 with high rate capability, Coulombic efficiency, and flexibility. This work represents a general framework for the bottom-up synthesis of ultrathin 2D materials, which may promote the application of graphitic carbon nitride in energy storage." @default.
- W2947987592 created "2019-06-07" @default.
- W2947987592 creator A5006897328 @default.
- W2947987592 creator A5052630741 @default.
- W2947987592 creator A5056796852 @default.
- W2947987592 date "2019-05-29" @default.
- W2947987592 modified "2023-10-06" @default.
- W2947987592 title "Ultra-Thin Conductive Graphitic Carbon Nitride Assembly through van der Waals Epitaxy toward High-Energy-Density Flexible Supercapacitors" @default.
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- W2947987592 doi "https://doi.org/10.1021/acs.nanolett.9b01511" @default.
- W2947987592 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31141385" @default.
- W2947987592 hasPublicationYear "2019" @default.
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