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Besides, the non-Laves ZrxNiy secondary phases are found to play importance roles in the reversibility of hydrogen storage in the gas phase and battery performance in activation, rate capability, charge retention, and cycle life.
The significant improvement in specific capacitance with excellent sustainability to higher current, superior rate capability, charge storage capacity and cycling stability can be attributed to the synergistic effect of electrical double-layer capacitance and pseudocapacitance resulting from Gr and PANi respectively and excellent catalytic ability of Pt NPs.
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Beyond the achieved high capacitance value, the rate capability (charge-discharge capacitance at high current density) is also outstanding.
Such a structure could have capability of high capacity charge storage.
The performance of a supercapattery depends on its energy density, rate capability of charge and discharge and stability of electrode.
The study shows that the capability of charge accumulation in electric double layer is controlled primarily by electrolyte properties.
Nowadays, the fabrication of photoanodes with high light-harvesting capability and charge transfer efficiency is a key challenge for photoelectrochemical (PEC) water splitting.
Due to the inclusion of hierarchically-connected micropores and mesopores, aMP carbon has considerable capability for charge storage and the delivery of energy at high rates.
When tested in an electrochemical Na half-cell, the NCO-NNA electrode exhibits excellent Na storage capability: a charge capacity as high as 400 mAh g−1 is achieved at a current density of 50 mA g−1.
It has been reported in previous photocatalytic studies on TiO2 that besides the light absorption capability and charge transportation, the adsorption of reactant is also a critical factor [7].
The electrochemical performance including cyclability, the rate capability and charge transfer kinetics of SnO2@amorphous Tis2 is further enhanced by calcining at a higher temperature because the adsorbed water and hydroxyl groups (H2O/OH−) was removed from the surface of amorphous TiO2.
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