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A maximum specific electrode capacitance of ∼20 F/g and a maximum specific power of ∼80 W/kg were achieved by manufactured SnO2 with 1.5 wt.% RuO2.
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The resulting VO2@PCNFs electrode displays a wide operation voltage (−1.0 to 1.1 V in three electrode systems), maximum specific capacitance of 778 F g−1 (at 1 A g 1), and excellent rate capability.
The maximum specific capacitance of this composite electrode was 100 F g−1 at 5 mV s−1 scan rate.
The Co(OH 2/GF electrode reveals maximum specific capacitance about 1139 F g−1 at 10 A g−1 charge-discharge current density in 1 M KOH aqueous solution.
The maximum specific capacitance of the prepared electrode materials are 2000 F g−1 at current density of 1 A g−1, which is evidently higher than that of the sample prepared without copper incorporation.
The VS2 electrode exhibits a maximum specific capacitance of 349 F g−1 with a super stable behavior in three-electrode liquid-state configuration.
Thus, when used as supercapacitor electrodes, a maximum specific capacitance of 604 F/g at a current density of 1.81 A/g was reached for PPy nanofibers.
Electrochemical characterizations indicate that the maximum specific capacitance of the MoS2/NG electrodes reaches up to 245F/g at 0.25A/g (and 146F/g at 20A/g).
Electrochemical measurements reveal that the maximum specific capacitance of the MoS2 graphene electrodes reaches up to 243 F g−1 at a discharge current density 1 A g−1.
By optimizing the charge density applied during electrodeposition, the electrodes delivered maximum specific capacity of 228 C g−1 (507 F g−1) at 1 A g−1 for the sample electrodeposited at −0.3 C cm−2.
Specifically, under the same test conditions, CoAl LDH@Ni(OH 2 electrode exhibits the maximum specific capacitance of 1528 F g−1 (by galvanostatic discharge at the current density of 5 mA cm−2 in 2 M KOH, based on the total mass; that for CoAl LDH NSAs is only 738 F g−1) and excellent cycling performance (retaining 92% of its original capacitance after 1300 times of cycling).
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