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The improved photocatalytic activity of the prepared Ag@PCNS/BiVO4 nanocomposite can be attributed to the synergistic effect among the PCNS, BiVO4 and Ag, which not only improves the visible light response ability and hinders the recombination efficiency of the photogenerated electrons and holes, but also retains the strong the redox ability of the photogenerated charges.
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The photocatalytic mechanism reveals that both Ag and PMo12 can be excited under visible light irradiation, which greatly improves the visible-light absorption of the composites.
The plasmonic effect of the formed Ag nanoparticles improved the visible light absorption performance, which benefits the photocatalytic reaction.
Carbon-doping of TiO2 was performed to improve the visible light response and photocatalytic activity of this catalyst.
Therein, the [BO3] as well as [Ti2BO2] species would redshift the UV visible absorption edge and improve the visible light activity of TiO2.
Remarkably enhanced PEC performance could be obtained by using rGO-BiFeO3 as the photoelectrode material due to its accelerated charge transfer and improved the visible light absorption.
A comprehensive review of the strategies commonly used to improve the visible light absorption of metal oxides by engineering their energy band is then presented.
To improve the visible light photocurrent response, CdS nanoparticles are deposited on the CdWO4 nanowire arrays to form a CdS/CdWO4 heterojunction.
Although it is possible to compensate the color crosstalk to reduce color noise with signal processing, it is better to reduce the color crosstalk as small as possible to improve the visible image qualities.
The extent of band gap narrowing in the case of codoping with (Y, Te) is quite significant (almost 1 eV) to effectively improve the visible light activity of GaS monolayer.
Herein, we report on the fabrication of ZnO NR-rGO nanocomposite via a facile template-free hydrothermal route with an aim to improve the visible photocatalytic efficiency of the ZnO NR based nanocomposites.
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