Na-ion batteries (NIBs) have attracted considerable attention in recent years owing to the high abundance and low cost of Na. It is well known that S doping can improve the electrochemical performance of carbon materials for NIBs. However, the current methods for S doping in carbons normally involve toxic precursors or rigorous conditions. In this work, we report a creative and facile strategy for preparing S-doped porous carbons (SCs) via the pyrolysis of conjugated microporous polymers (CMPs). Briefly, thiophene-based CMPs served as the precursors and doping sources simultaneously. Simple direct carbonization of CMPs produced S-doped carbon materials with highly porous structures. When used as an anode for NIBs, the SCs exhibited a high reversible capacity of 440 mAh g at 50 mA g after 100 cycles, superior rate capability, and excellent cycling stability (297 mAh g after 1000 cycles at 500 mA g), outperforming most S-doped carbon materials reported thus far. The excellent performance of the SCs is attributed to the expanded lattice distance after S doping. Furthermore, we employed ex situ X-ray photoelectron spectroscopy to investigate the electrochemical reaction mechanism of the SCs during sodiation-desodiation, which can highlight the role of doped S for Na-ion storage.
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http://dx.doi.org/10.1007/s40820-019-0291-z | DOI Listing |
Chem Commun (Camb)
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Tianjin Key Laboratory of Advanced Functional Porous Materials, Institute for New Energy Materials and Low-Carbon Technologies, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin 300384, China.
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School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093, China.
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