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Hybrid supercapacitors with the composite electrode materials display high energy density at the expense of the reduced cycle stability.
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Meanwhile, it is interesting to note that the photocatalytic hydrogen generation activity has a liner relationship with the hierarchy of materials, which means higher hierarchy materials display higher photocatalytic hydrogen generation activity.
Also these Cu/graphite or Cu/graphene materials displayed high stability even when water is co-fed with ethanol.
In contrast, the use of trisilylated quaternary ammonium precursors yielded materials displaying high porosity combined with moderate structural regularity after surfactant elimination.
In a form of thin-layer electrode on glassy carbon support, in 0.1 M KOH solution, the prepared materials displayed high activity toward oxygen reduction reaction (ORR) in alkaline media, with onset potentials more positive than −0.10 V vs. SCE.
Compared with the electrode made from the nanowire electrode, the hollow composite materials displayed higher discharge capacity and better cycling reversibility, which may be a result of the hollow structure.
The consecutively grafted material displayed high average catalytic activity (27 h−1 TOF) during the first 2 h and high selectivity (>90%).
Y2O3 nanoparticles with an optimized erbium ytterbium composition have been incorporated in a PMMA polymer matrix, resulting in a hybrid amorphous material displaying high gain coefficient values (up to 30 cm−1 as from Amplified Spontaneous Emission experiments) upon moderate 980 nm pumping intensities.
When T2-W STIR sequence was performed (15/36) the compressive material displayed high signal intensity, that was isointense to CSF in all patients (Fig. 2a).
Recrystallized materials display remarkably high activity, stability and selectivity in alkylation of naphthalene with cyclohexene.
The CMO/CHC electrode materials display a high specific capacitance of 779 F g−1 at 1 A g−1 and an excellent rate behavior (77.5% and 63.6% at 20 and 40 A g−1 compared with 1 A g−1, respectively).
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