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In Mo 3d spectra of the group A (most stoichiometric) sample, both Mo4+ and Mo6+ doublets are observed.
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Though the stoichiometric samples (Mg/B = 1 2) indicated both green and red luminescence, the samples prepared with deficient-MgO and excess-MgO showed only green and red emission, respectively.
Low apparent mobility of the oxygen defects in La1.6+xSr0.4−xAl0.4Mg0.6O4+x/2 caused little improvement in ionic conductivity compared to stoichiometric samples.
Surprisingly, the least stoichiometric samples show up to an order of magnitude higher field-effect mobilities, negligible hysteresis, and threshold voltages close to 0.0 V.
The shape difference of the hydrothermally aged stoichiometric and non-stoichiometric samples probably derives the Ostwald ripening to a different extent due to the different particle size distribution.
The results show that, implanted H+ ions induce defects being different in stoichiometric and non-stoichiometric samples.
Faster hydrogenation kinetics could be obtained in all of the hypo-stoichiometric samples, completing hydrogenation within 300 s at 100 °C.
Thus we could determine their crystallographic structure, their nitrogen content and their optical properties by simulating the reflectance curves with Drude's model for stoichiometric and sub-stoichiometric samples, and an extended Drude model for over-stoichiometric samples.
(The first urine sample of the day tends to be the most concentrated sample).
Among them, the most typical 2D sample should be transition-metal dichalcogenides (TMDs), composed of covalently bonded transition-metal atoms (M) and chalcogen atoms (X = S, Se, Te) in a possible stoichiometric form of MX2 [5], such as MoS2 and WS2, of which each single-layer consists of two S atom layers and a layer of metal atoms sandwiched between the two S layers [6].
Most of the sample available now.
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