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The X-ray powder diffraction patterns and the corresponding lattice parameter refinements showed that both samples can be indexed to hexagonal α-NaFeO2 layered structure with space group of R-3m.
Both samples can be therefore considered monodisperse.
This result allows us to conclude that the PL decay for both samples can be described by two exponential functions.
In addition, the crystallite size of both samples can be estimated to be 20 ± 2 nm by Scherrer formula.
All the diffraction peaks of both samples can be indexed to a typical hexagonal α-NaFeO2 layered structure with R3m spacing group.
As it can be seen from Figure 4c,f, for the excitation wavelength of 980 nm, thermal quenching of Er3+-related emission for both samples can be well characterized with only one deactivation energy (EErQ1) equal to approximately 20 meV.
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When comparing both studies samples can be differentiated based on two main axes that correspond to growth condition (iron-replete vs iron limited) and study (current study vs previous study).
The X-ray powder diffraction patterns show that the coating material is pure-phase (NH4 3AlF6 and both pristine and coated samples can be indexed to hexagonal α-NaFeO2 layered structure with space group of R-3 m.
After confirmation of diagnosis, both cytology or histology samples can be used for molecular testing in order to investigate EGFR, ALK, KRAS, ROS1, BRAF and MET mutations.
The diversity of both positive and negative samples can be very restricted in a video surveillance scene recorded by one static camera.
Both milk and blood samples can be used to assess the serological status of cattle [ 22].
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