the National Key R&D Program(2016YFB0901502,2016YFB0101201)
the National Natural Science Foundation of China(NSFC)
Ministry of Education(B12015)
and Tianjin High-Tech(18JCZDJC31500)
This work was supported by the National Key R&D Program (2016YFB0901502, 2016YFB0101201), the National Natural Science Foundation of China (NSFC) (51771094), Ministry of Education (B12015), and Tianjin High-Tech (18JCZDJC31500).
The authors declare that they have no conflict of interest.
These authors contributed equally to this work.
Supporting information The supporting information is available online at
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Figure 1
(a) Schematic illustration for synthesis of the γ-MnO2@CNT composite. (b) SEM images of γ-MnO2@CNT composite (1:1). (c) HR-TEM image and corresponding SAED pattern of the composite. (d) C 1s and (e) Mn 2p XPS spectra of the composite (color online).
Figure 2
(a) X-ray diffraction patterns of pure γ-MnO2 and γ-MnO2@CNT composite with three different mass ratios. (b) Thermogravimetric analysis of γ-MnO2@CNT composite. (c) Electrochemical impedance spectroscopy (EIS) of SABs with different cathodes and corresponding equivalent electric circuit. (d) Cyclic voltammograms at a constant scan rate of 1 mV s−1. (e) Discharge-charge curves of batteries with different types catalysts. (f) Discharge-charge curves of batteries with different mass ratios of γ-MnO2@CNT (color online).
Figure 3
Electrochemical performances of the SABs with γ-MnO2@CNT (1:1) cathode. (a) Discharge-charge curves at different current density with a voltage window from 1.8 to
Figure 4
Product reversibility. XRD patterns of (a) the γ-MnO2@CNT cathode after discharge and charge. SEM images of (b, c) discharged and (d, e) charged cathodes (color online).