Absolute calibration of the latent heat of transition using differential thermal analysis.

We describe a simple and accurate differential thermal analysis setup to measure the latent heat of solid state materials undergoing abrupt phase transitions in the temperature range from 77 K to above room temperature. We report a numerical technique for the absolute calibration of the latent heat of transition without the need for a reference sample. The technique is applied to three different samples-vanadium sesquioxide undergoing the Mott transition, bismuth barium ruthenate undergoing a magnetoelastic transition, and an intermetallic Heusler compound. In each case, the inferred latent heat value agrees with the literature value within its error margins. To further demonstrate the importance of absolute calibration, we show that the changes in the latent heat of the Mott transition in vanadium sesquioxide (V2O3) remain constant to within 2% even as the depth of supersaturation changes by about 10 K in non-equilibrium dynamic hysteresis measurements. We also apply this technique for the measurement of the temperature-dependent specific heat.

Critical Slowing Down at the Abrupt Mott Transition: When the First-Order Phase Transition Becomes Zeroth Order and Looks Like Second Order.

We report that the thermally induced Mott transition in vanadium sesquioxide shows critical slowing down and enhanced variance ("critical opalescence") of the order parameter fluctuations measured through low-frequency resistance-noise spectroscopy. Coupled with the observed increase of the phase-ordering time, these features suggest that the strong abrupt transition is controlled by a critical-like singularity in the hysteretic metastable phase. The singularity is identified with the spinodal point and is a likely consequence of the strain-induced long-range interaction.

Kinetic Spinodal Instabilities in the Mott Transition in V_{2}O_{3}: Evidence from Hysteresis Scaling and Dissipative Phase Ordering.

We present the first systematic observation of scaling of thermal hysteresis with the temperature scanning rate around an abrupt thermodynamic transition in correlated electron systems. We show that the depth of supercooling and superheating in vanadium sesquioxide (V_{2}O_{3}) shifts with the temperature quench rates. The dynamic scaling exponent is close to the mean field prediction of 2/3. These observations, combined with the purely dissipative continuous ordering seen in "quench-and-hold" experiments, indicate departures from classical nucleation theory toward a barrier-free phase ordering associated with critical dynamics. Observation of critical-like features and scaling in a thermally induced abrupt phase transition suggests that the presence of a spinodal-like instability is not just an artifact of the mean field theories but can also exist in the transformation kinetics of real systems, surviving fluctuations.