2015
DOI: 10.1016/j.cplett.2015.01.011
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A large red-shift in the photoluminescence emission of Mg 1−x Sr x TiO 3

Abstract: a b s t r a c tIn this letter, we report a detailed study of the influence of the synthesis and the optical properties of Sr-doped MgTO 3 powders synthesized via a polymeric precursor method. Our findings explain the shift in PL behavior from blue to near-infrared (NIR) emission, which is caused by different concentrations of deep and shallow defects in the samples and thus enables the design of differently colored materials. Additionally, the present results provide useful insights into designing a new series… Show more

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Cited by 26 publications
(19 citation statements)
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References 27 publications
(60 reference statements)
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“…Moreover, the Raman-active modes located at 397 and 443 cm -1 were caused by the vibrational modes of the oxygen cage [20]. However, it can be seen from Figure 3(a) that the MTO thin film had ten Ramanactive modes (e.g., 5A g + 5E g ), as predicted in the literature [21][22][23][24][25][26][27]. This was attributed to high crystallization at short-range.…”
Section: Introductionsupporting
confidence: 55%
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“…Moreover, the Raman-active modes located at 397 and 443 cm -1 were caused by the vibrational modes of the oxygen cage [20]. However, it can be seen from Figure 3(a) that the MTO thin film had ten Ramanactive modes (e.g., 5A g + 5E g ), as predicted in the literature [21][22][23][24][25][26][27]. This was attributed to high crystallization at short-range.…”
Section: Introductionsupporting
confidence: 55%
“…The other A g modes observed at approximately 390, 500, and 708 cm −1 , respectively, are related to the breathinglike vibrations of the six O atoms. However, by comparing the modes, it can be seen that they had different vibration directions in the octahedral configuration [25,26]. The E g mode typically observed at 275 cm −1 is attributed to the anti-symmetric breathing vibration of the O octahedron [25][26][27].…”
Section: Introductionmentioning
confidence: 99%
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“…In this context, it is well known that the polymeric precursor method is a simple, clean, and efficient approach to fabricate complex functional materials. It also offers excellent chemical homogeneity and precise stoichiometric control during heat treatments at relatively low temperatures [9,15,16]. Hence, this synthetic strategy substantially reduces the presence of segregated phases and does not require long annealing periods compared with other synthetic methods [9,15,16].…”
Section: Introductionmentioning
confidence: 99%