Abstract
A study is made demonstrating that in deuterated triglycine sulfate crystals the maximum pyrocoefficient value measured simultaneously by quasistatic and dynamic methods decreases with the increase of the heat flux power. For dynamic measurements the position and magnitude of the pyrocurrent maximum depend on the heat flux density. This behaviour of the pyroresponse is explained by the instability of the monodomain state and depolarization of the crystal surface layer.
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