TY - JOUR
T1 - Optimised electrochemical energy storage performance of MoS2 anchored to carbon cloth for advanced asymmetric aqueous supercapacitors
AU - Faisal, M.M.
AU - Rigby, Oliver M.
AU - Campbell, Stephen
AU - Hunt, Michael R.C.
PY - 2025/8/20
Y1 - 2025/8/20
N2 - We explore the electrochemical energy storage performance of binder-free molybdenum disulphide decorated carbon cloth electrodes (MoS2@CC) in six aqueous electrolytes, selecting the most suitable combination for the construction of an asymmetric supercapacitor. The MoS2@CC electrodes were synthesised by a single-step hydrothermal method without the use of a binder. Our findings show that the capacitance performance and resilience of the MoS2@CC electrodes are strongly influenced by the electrolyte, particularly the overall conductivity. Optimal performance, balancing capacitance, equivalent series resistance and cycle life was achieved in 1.0 M Na2SO4 in which MoS2@CC delivers a capacitance of 223±2 F g−1, retaining ≈94% capacity after 5000 charge–discharge cycles. In comparison, 0.5 M H2SO4, and 5.0 M LiCl, although initially outperforming 1.0 M Na2SO4, produced rapid electrode degradation. An asymmetric supercapacitor using binder-free MoS2@CC and manganese oxide decorated carbon cloth (MnO2@CC) electrodes in 1.0 M Na2SO4 electrolyte exhibited a capacitance of 55 ± 2 F g−1, a specific energy density of 30.3 ± 0.4 W h kg−1, and a power density of 625 ± 25 W kg−1 over a 2.0 V voltage window comparable with, or superior to, similar devices reported in the literature. The asymmetric cell demonstrated excellent stability, retaining 82% capacitance after 5000 galvanostatic charge–discharge cycles and 80% after 15000 cycles.
AB - We explore the electrochemical energy storage performance of binder-free molybdenum disulphide decorated carbon cloth electrodes (MoS2@CC) in six aqueous electrolytes, selecting the most suitable combination for the construction of an asymmetric supercapacitor. The MoS2@CC electrodes were synthesised by a single-step hydrothermal method without the use of a binder. Our findings show that the capacitance performance and resilience of the MoS2@CC electrodes are strongly influenced by the electrolyte, particularly the overall conductivity. Optimal performance, balancing capacitance, equivalent series resistance and cycle life was achieved in 1.0 M Na2SO4 in which MoS2@CC delivers a capacitance of 223±2 F g−1, retaining ≈94% capacity after 5000 charge–discharge cycles. In comparison, 0.5 M H2SO4, and 5.0 M LiCl, although initially outperforming 1.0 M Na2SO4, produced rapid electrode degradation. An asymmetric supercapacitor using binder-free MoS2@CC and manganese oxide decorated carbon cloth (MnO2@CC) electrodes in 1.0 M Na2SO4 electrolyte exhibited a capacitance of 55 ± 2 F g−1, a specific energy density of 30.3 ± 0.4 W h kg−1, and a power density of 625 ± 25 W kg−1 over a 2.0 V voltage window comparable with, or superior to, similar devices reported in the literature. The asymmetric cell demonstrated excellent stability, retaining 82% capacitance after 5000 galvanostatic charge–discharge cycles and 80% after 15000 cycles.
KW - Aqueous electrolytes
KW - Asymmetric supercapacitors
KW - Carbon cloth
KW - Electrochemical energy storage
KW - Manganese dioxide
KW - Molybdenum disulphide
UR - https://www.scopus.com/pages/publications/105005252217
U2 - 10.1016/j.electacta.2025.146294
DO - 10.1016/j.electacta.2025.146294
M3 - Article
AN - SCOPUS:105005252217
SN - 0013-4686
VL - 532
JO - Electrochimica Acta
JF - Electrochimica Acta
M1 - 146294
ER -