| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 5460993 | 1516201 | 2017 | 6 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Structural evolution of MnTi0·8Ru0·2O3
												
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																																												کلمات کلیدی
												
											موضوعات مرتبط
												
													مهندسی و علوم پایه
													مهندسی مواد
													فلزات و آلیاژها
												
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												چکیده انگلیسی
												Here, we present the structural studies on MnTi1-xRuxO3(x = 0, 0.2) compounds. The role of Ti ions in the magnetism of MnTiO3 was unclear so here this issue has been tried to address. The magnetic susceptibility (Ï) data shows that the 3-dimensional magnetic character has been improved in the doped MnTiO3. The x = 0 compound goes paramagnetic to antiferromagnetic phase at a temperature â¼64 K followed by a broad peak at a temperature â¼100 K. But in x = 0.2 compound, the antiferromagnetic transition temperature has been shifted towards the lower temperature to â¼47.5 K with a broad peak at temperature â¼79 K. On the doping of Ru at Ti site a sharp anomaly in the temperature dependent magnetic susceptibility (Ï) measurement is observed â¼47.5 K in the case of x = 0.2 compound. This sharp anomaly is attributed to the improved 3D character of magnetism which arises because of the direct exchange interaction between Mn-Ti/Ru ions in addition to the inter-layer super superexchange interaction between Mn-Mn ions via two intervening oxygen ions. It is interesting to note that even though the TN and T2D are at low temperatures compared to the x = 0 compound, the onset temperature of these two temperatures occurs at much higher temperature than as observed in x = 0 compound.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Alloys and Compounds - Volume 693, 5 February 2017, Pages 164-169
											Journal: Journal of Alloys and Compounds - Volume 693, 5 February 2017, Pages 164-169
نویسندگان
												R.K. Maurya, R. Bindu,