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S. Narayana Jammalamadaka

Publications and source records attributed to S. Narayana Jammalamadaka.

22 records · Page 2Linked to original sources

Stability of geometrically frustrated magnetic state of Ca3CoRhO6 to applications of positive and negative pressure

The influence of negative chemical pressure induced by gradual replacement of Ca by Sr as well as of external pressure (up to 10 kbar) on the magnetism of Ca3CoRhO6 has been investigated by magnetization studies. It is found that the solid solution, Ca(3-x)Sr(x)CoRhO6, exists at least till about x= 1.0 without any change in the crystal structure. Apart from insensitivity of the spin-chain feature to volume expansion, the characteristic features of geometrical frustration interestingly appear at the same temperatures for all compositions, in sharp contrast to the response to Y substitution for Ca (reported previously). Interestingly, huge frequency dependence of ac susceptibility known for the parent compound persists for all compositions. We do not find a change in the properties under external pressure. The stability of the magnetic anomalies of this compound to the volume change (about 4%) is puzzling.

cond-mat.str-el↗

Magnetic behavior of nanocrystalline LaMn2Ge2

The compound, LaMn2Ge2, crystallizing in ThCr2Si2-type tetragonal crystal structure, has been known to undergo ferromagnetic order below (T_C=) 326 K. In this article, we report the magnetic behavior of nanocrystalline form of this compound, obtained by high-energy ball-milling. T_C of this compound is reduced maginally for the nanoform, whereas there is a significant reduction of the magnitude of the saturation magnetic moment with increasing milling time. The coercive field however increases with decreasing particle size. Thus, this work provides a route to tune these parameters by reducing the particle size in this ternary family.

cond-mat.str-el↗

Room temperature soft ferromagnetism in the nanocrystalline form of YCo2 - a well-known bulk Pauli paramagnet

The Laves phase compound, YCo2, is a well-known exchange-enahnced Pauli paramagnet. We report here that, in the nanocrystalline form, this compound interestingly is an itinerant ferromagnet at room temperature with a low coercive-field. The magnitude of the saturation moment (about 1 Bohr-magneton per formula unit) is large enough to infer that the ferromagnetism is not a surface phenomenon in these nanocrystallites. Since these ferromagnetic nanocrystallines are easy to synthesize with a stable form in air, one can explore applications, particularly where hysteresis is a disadvantage.

cond-mat.mtrl-sci↗

Magnetic Anomalies in a New Manganocuprate Gd3Ba2Mn2Cu2O12

The manganocuprate compound Gd3Ba2Mn2Cu2O12 (Gd-3222) has been synthesized by conventional solid state reaction method and its magnetic behavior has been studied by dc and ac magnetization (M) and heat capacity (C) measurements as a function of temperature (T). This compound crystallizes in a tetragonal structure (space group I4/mmm). We find that this compound exhibits three magnetic transitions, around 2.5, 4.8 and 9 K, as inferred from dc and ac magnetic susceptibility (chi) data. However, no evidence for a well-defined lambda-anomaly is found in C(T) above 1.8 K, though there is a gradual upturn below about 10 K. An application of a magnetic field results in a peak around 5K, while ac chi appears to show a very weak frequency dependence below 9 K. Isothermal M curve at 1.8 K exhibits a weak hysteresis without any evidence for saturation even at fields as high as 120 kOe. These results imply that this compound undergoes a spin-glass-like freezing at low temperatures, though the exact nature of the magnetic transition at 10 K is not clear. The magnitude of the magnetocaloric effect, as inferred from M and C data, is quite large over a wide temperature range below 50 K peaking around 4 K.

cond-mat.mtrl-sci↗