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The surface plasmon can dramatically enhance the absorbance of near-bandgap light, and the enhancement is influenced by the size and material of nanoparticles.
The combination of microwave with multivalent inorganic salt is a viable approach for use to convert the pectin into matrix material of nanoparticles.
Studies of suspensions with the same volume concentration and material of nanoparticles but different sizes [26, 27] showed that the viscosity of suspension increases as the particle size decreases.
Next, we set the diameter of nanoparticles at 60 nm, the D/P of NWAs at 0.3, and the diameter of NWs at 120 nm and study the influence of the material of nanoparticles on the absorptance is displayed in Fig. 4b.
We speculate that the structure, shape, charge and other characteristics of the functionalization groups, the size and core material of nanoparticles might, in different cases and to different extents, participate in the determination of cell fate when confronting autophagy.
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In less than a day, over 40 different catalytic materials of nanoparticles supported on γ-Al2O3, CeO2, TiO2, SiO2 and Y-ZrO2 were prepared and evaluated.
After reduction, a composite material composed of nanoparticles of Pd° (2 9 nm size) evenly distributed in the pores of the silica matrix was obtained.
We suggest that the modulation of surface structure of supporting materials of nanoparticle catalysts can be useful for fabrication of more humidity-resistant heterogeneous catalysts.
Nanoprobes, as a part of nanobiosensors, are able to detect H2O2 using detection principles (chemiluminescence, fluorescence, localized surface plasmon resonance, near-infrared absorption, and electrochemical methods), materials of nanoparticle matrix, and dependence on enzymes [ 73– 76].
In this work, we obtain a hybrid material of FeCo2O4 nanoparticles anchored on hierarchical nitrogen-enriched porous carbon material (denoted as FeCo2O4@NPC-450 °C) and study its activity for oxygen evolution reaction (OER).
DSC was employed to investigate the melting and crystallization behavior of the crystalline material of lipid nanoparticles.
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