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The interface contributes, but the volumetric capacitance/resistance dominates.
As we know, the trapped charges are responsible for the ΔV FB (hysteresis width) [15], and we assume that the two-dimensional distribution of traps near the interface contributes to the film capacitance.
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The incorporation of CsI between ITO and ZnO was found to favorably modify the energy-level alignment at the interface, contributing to the charge collection efficiency as well as protecting the adjacent light absorbing polymer layers from degradation.
Both the solidification micro-voids and steep stress gradient appearing in the interface contributed to the propagation of interfacial crack that will critically affect the mechanical properties of laser deposited material.
Assuming the two-dimensional distribution of traps in the vicinity of the interface contributing to the film capacitance, we investigated the charge trapping behavior through the C-V hysteresis characteristics.
The crystal formation at the interface contributed to the improved adhesion of the particles to the matrix.
Figure 7 exemplifies the low-energy binding pose achieved and the probable hydrophobic interactions and electrostatic contacts brought about by residues at the interface contributing to the stabilization of the host parasite modeled complex.
This theory is very different from previously popular switching mechanism for HfO2 based devices, in which only O anions at the electrode/oxide interface contributes to the switching while the electrodes (e.g., Ta, Ti, and Hf) only serve as the oxygen gettering layer23.
In contrast to previous reports emphasizing the role of the interfacial redox reaction, we have found that charge trapping at the interface is responsible for 78 87% of the hysteresis and that the interfacial redox reaction at the graphene/SiO2 interface contributes only 13 22%.
It was shown that the potential drop across the electrical double layer of oriented ionic dipoles at the metal/polymer interface contributes a major part of the measured Volta potentials.
The His-104 mutants allowed us to ask if and how the dimer interface contributes to holdase function without the confounding complications of comparing aggregation of model denatured client proteins at differing pHs.
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