In order to determine the enthalpy change in an irreversible field-induced phase transition, the thermal response to an electric field in 0.87Pb͑Mg 1/3 Nb 2/3 ͒O 3 − 0.13PbTiO 3 was measured and dismantled into characteristic dielectric hysteresis, reversible electrocaloric, and irreversible phase transition responses. Below the depolarization temperature T dp = 18°C, the phase transition enthalpy change increases rapidly to a maximum value of ͉⌬H͉ =77 J/ kg. Above T dp , the field-induced thermal response shows a reversible nature with an increased electrocaloric effect. In addition to earlier enthalpy data presented for temperature-induced transitions, this letter provides information on the enthalpy change in a field-induced phase transition of relaxor ferroelectrics. © 2009 American Institute of Physics. ͓DOI: 10.1063/1.3098067͔ Among other perovskite relaxor ferroelectrics, lead magnesium niobate Pb͑Mg 1/3 Nb 2/3 ͒O 3 ͑PMN͒ characteristics are attributed basically to the existence of lattice disorder and polar nanoregions in a highly polarizable lattice.1,2 As a distinction from traditional ferroelectrics, material exhibits only a short-range macroscopical order in the average cubic relaxor lattice, 3 and a ferroelectric-like long-range macroscopic order can develop through the application of an electric field of sufficient strength at low temperatures. 4,5 In a solidsolution of ͑1−x͒Pb͑Mg 1/3 Nb 2/3 ͒O 3 − xPbTiO 3 ͑PMN-xPT, x in mol %͒, an increasing portion of ferroelectric PbTiO 3 also tends to increase the size of the polar regions and their interaction, leading to the formation of macrodomain states.
6At low x, PMN-xPT behaves like a canonical relaxor PMN and has a mixed phase of an average cubic lattice with confined rhombohedral distortion, 7,8 and on this account, an external stimulus is needed to induce a macroscopic ferroelectric order. The nature of a field-induced transition from nonergodic relaxor to the ferroelectric phase is considered to be irreversible, 9 and the formed polar phase can be relaxed with substantial zero-field heating to above the intrinsic Curie temperature T C0 , which is in principle equivalent to the zero-field thermal depolarization temperature T dp . Additionally, the ferroelectric phase can be induced at temperatures above, but close to, T C0 , which is indicated by the fielddependent Curie temperature T C ͑E͒, and in that case the material shows a behavior similar to that of ordinary ferroelectrics with a first-order phase transition.5,10 However, in contrast to a transition at lower temperatures, the fieldinduced ferroelectric phase appearing above T C0 at temperatures just above the T C ͑E͒ line has a metastable nature, and thus the phase can switch reversibly back to nonpolar in the absence of the inducing field.
5A first-order field-induced transition to the ferroelectric rhombohedral phase is accompanied by an enthalpy change ⌬H, which, under adiabatic conditions, appears as a corresponding temperature change. Due to the irreversibility of the field-induced phase...