An asymmetric supercapacitor (ASC) with high energy density is designed using flower-like MoS 2 and MnO 2 grown on graphene nanosheets (GNS) as negative and positive electrodes, respectively. In this paper, flowerlike MoS 2 /GNS and MnO 2 /GNS were controllably synthesized through a hydrothermal approach. The prepared MoS 2 /GNS hybrid displays a typical crinkly and rippled structure with ultrathin MoS 2 nanosheets uniformly grown on the surface of graphene. Additionally, the MoS 2 /GNS electrode exhibits superior electrochemical performance, such as high specific capacitance (320 F g -1 at 2 A g -1 ). The MoS 2 /GNS holds great promise as a negative electrode for an ASC due to its high specific capacitance and wide operation window in negative potential. The assembled all-solid-state ASC delivers a remarkable energy density of 78.9 Wh kg -1 at a power density of 284.1 W kg -1 . Thus the MoS 2 /GNS hybrid is a promising electrode material for next-generation storage systems.Subsequently, 5 mL of L-cysteine solution (160 mg mL -1 ) was dropwised into the above solution. Finally, it was transferred into a 50 mL Teflon-lined stainless steel autoclave, which was sealed and heated in an oven at 180 °C for 12 h. During the hydrothermal approach, L-cysteine will decompose and release S 2ions, acting as the sulfur source. Additionally, L-cysteine is the reducing agent for the formation of MoS 2 , because that the Mo (VI) will be reduced to Mo(IV) by L-cysteine. The product were collected by centrifugation, washed with deionized water and ethanol for several times and vacuum dried at 60 °C for 24 h. The final product was loaded into the tube furnace and calcined in N 2 atmosphere at 550 °C for 2 h. For comparison, bare MoS 2 and the samples with various ratio of MoS 2 to GNS were also prepared under the same condition.
Preparation of MnO 2 /GNS hybrid170 mL of KMnO 4 aqueous solution (0.34 mg mL -1 ) was added into 32 mL of GNS dispersion (1.6 mg mL -1 ) and the above solution was maintained at 65 °C for 24 h under stirring. After it was cooled to room temperature, the precipitate was collected by centrifuge, washed with ethanol and deionized water and dried in vacuum oven at 100 °C for 12 h. Bare MnO 2 samples were also prepared for comparison. MnO 2 -1 was obtained by thermal treatment of MnO 2 /GNS at 400 °C in air to remove the GNS.Another bare MnO 2 sample (MnO 2 -2) was prepared through the oxidation-reduction reaction between KMnO 4 and ethyl alcohol according to our previously work. 40
Characterization methodsX-ray diffraction (XRD) equipped with Cu Kα radiation (λ = 0.15406 nm) was used to characterize the crystallographic structures of the materials. X-ray photoelectron spectrometer (XPS) analysis was performed using nonmonochromatic,