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A generalized electrocapillary equation for polarizable and reversible interfaces is derived based on Hansen's method.
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The kinetics for coarsening co-controlled by diffusion and a reversible interface reaction were investigated theoretically.
In particular, the use of a "dynamic reversible hydrophobic interface" between (DODA 40Mo132 and lipophilic silica can render the emerging hybrid mesophases self-adaptive.
There, phosphate species can form reversible and irreversible interfaces with framework aluminium.
Since the Fusion approach is not reversible, our composition interface provides simulation, visualization, and SBML output of models being combined to help the modeler during the composition step.
Reversible complexes involve composite interfaces from modular preformed and unstructured regions that provide strong, specific contacts from the combination of relatively weak, modular interactions.
Electrochemical studies have shown a reversible transfer across the interface controlled by diffusion.
The designed interface exhibited reversible on/off-switching of bio-electrocatalysis on changing the pH between 5 and 8, via phase transition from super hydrophilic to hydrophobic.
The resulting 2D nanocomposite with strong electronic coupling facilitates both electron and Na-ion transfer across the interface and reversible insertion/extraction of Na-ion, enabling fast pseudocapacitive Na-ion storage with reduced voltage hysteresis and excellent durability over 1500 cycles.
However, this method offers only limited selectivity since most chemical interfaces based on reversible chemical interaction are not very selective [9] [13].
It appears that the densification by FS can only be possible if the current collectors, i.e., the electrodes, are specifically designed to enable reversible electrochemical reactions at the interfaces between the electrodes and the ionic compound, insuring the current flow through the powder compact.
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