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Both composite materials displayed an enhancement of activity and benzaldehyde selectivity with respect to the pure CN.
These materials displayed an initial discharge capacity of 7205 mAh g−1 with a plateau at around 2.66 V at a current density of 100 mA g−1.
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These materials displayed a reversible temperature-induced physical sol gel transition and an irreversible light-activated chemical cross-linking.
These materials displayed a broad range of mechanical and viscoelastic responses ranging from plastic to elastic when examined as hydrated gels and films.
The results indicate that the materials displayed a broad distribution of molecular motions and could be divided into different phases in terms of their mobility above the Tg.
Over more than 60 years these materials displayed a very good combination of properties such as low neutron absorption, creep behavior, stress-corrosion cracking resistance, reduced hydrogen uptake, corrosion, and/or oxidation, especially in the case of Zircaloy-4 [1 3].
Fabricated electrodes from these AC materials displayed a discharge capacity of 50 mAh g−1 at 0.25 A g−1 in a redox-mediated electrolyte of 1 M K3Fe CN 6-1 M HNO3 corresponding to a specific capacitance of 140 F g−1 at the same specific current, with an energy efficiency of 70% after 1000 cycles.
All synthesized hybrid materials display an XRD pattern typical for magnetite or maghemite, with no other impurities being detected.
Furthermore, a two-electrode symmetric supercapacitor based on the carbon material displayed an energy density of 13.3 Wh kg−1 at a high power density of 7125 Wkg 1.
In addition, the strong absorption and suitable energy levels of materials (M6, M7-Br and M7-TFSI) also qualify them as donor materials in organic solar cells (OSCs) and the devices containing M7-TFSI as donor material displayed an efficiency of 6.9%.
At sufficiently high cooling rates, however, most materials display a different behaviour and follow route 2 to the solid state.
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CEO of Professional Science Editing for Scientists @ prosciediting.com