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The use of nano-sized SnO and SiO1.1 powders as anode materials for lithium ion batteries can give high cycle capacities.
In the range 2.5 4.5 V, the third cycle capacities are 175 ± 5 mAh g−1 for the bare and 3% NiO-coated compounds, but capacity-fading starts from fifth cycle onwards.
SirT1-null mitochondria produced higher levels of H2O2 when using pyruvate+malate or palmitoylcarnitine (Figure 6E), suggesting that SirT1-null mitochondria have higher than normal beta-oxidation and TCA cycle capacities.
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The polymer is rechargeable and returns to its initial charge-discharge cycle capacity.
FePO4 coated samples exhibited both improved rate and cycle capacity compared with the pristine LiNi1/3Co1/3Mn1/3O2.
Does walk training improve peak walking capacity, cycle capacity, and quality of life compared to cycle training?
The SEM images (Fig. 4 and Supplementary Figs. 3 8) reveal the top-view morphology of the interfacial-layer-coated Li foils after extended stripping/plating at 1 mA cm 2 with a cycle capacity of 1 mAh cm 2.
A Li/CPE/FeS1+x cells ran at id = ich = 50 μA/cm2 (c/1 rate) and 125 °C for over 650 charge/discharge cycles with 0.06% per cycle capacity loss and 100% Faradaic efficiency.
The effect on cycle capacity is reported of cathode material (metal oxide, carbon, and current collector) in lithium/metal oxide cells cycled with fumed silica-based composite electrolytes.
Secondly, a new cycle degradation mechanism is demonstrated that NaAlH4 would decompose above 1.42 V during the charge process, which leads to a rapid degradation of cycle capacity.
Compared with La0.8Sr0.2FeO3, La0.6Sr0.4FeO3 electrode is a more promising candidate for electrochemical hydrogen storage because of its higher cycle capacity at various temperatures.
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