THERMAL-INDUCED DOMAIN PROCESSES IN TRIGLYCINE SULFATE CRYSTALS WITH CHROMIUM IMPURITIES

В работе представлены результаты исследований термоиндуцированных доменных процессов в хромсодержащих кристаллах триглицинсульфата. Показано, что изменение температуры кристаллов ТГС: Cr в отсутствие внешних электрических полей сопровождается перестройкой доменной структуры, которая наиболее интенсивно происходит в области фазового перехода. Деполяризующее поле величиной ~1,4·10 В·м, которое порождается градиентным изменением температуры образца, вызывает процесс переключения его доменной структуры. В неотожженных кристаллах при концентрациях примеси, превышающих 5·10 вес. % процессы переключения затруднены, а интенсивность термоиндуцированных доменных процессов существенно ниже аналогичных для образцов с меньшим содержанием примеси. На интенсивность процессов переключения кристаллов ТГС: Cr существенное влияние оказывает скорость их нагревания. Зависимости интегрального числа скачков переполяризации от скорости нагревания образцов N = f (V) носят экстремальный характер. Экстремумы кривых N = f (V) лежат в интервалах скоростей (0,2-0,8) K·c. Доменная структура кристаллов ТГС:Cr состоит из матрицы основного домена, линзовидных и ламелеобразных доменов. Под воздействием электронного пучка наблюдается эволюция доменной структуры, сопровождающаяся ростом доменов, их слиянием и переключением образца. Высокотемпературный отжиг кристаллов приводит к их полидоменизации. The article presents the results of studies of thermally induced domain processes in chromium-containing crystals of triglycine sulfate (TGS). It is shown that a change in the temperature of TGS: Cr crystals in the absence of external electric fields is accompanied by a rearrangement of the domain structure, that occurs most intensively in the region of the phase transition. A depolarizing field of ~1,4·10 V·m, which is generated by a gradient change in the temperature of the sample, causes the process of switching its domain structure. In unannealed crystals at impurity concentrations exceeding 5·10 wt.%, switching processes are hindered, and the intensity of thermally induced domain processes is significantly lower than that for samples with a lower impurity content. The intensity of the switching processes of TGS: Cr crystals is significantly influenced by the rate of their heating. The dependences of the integral number of polarization-reversal jumps on the heating rate of the samples N = f (V) are extreme. The extrema of the N = f (V) curves lie in the rate intervals (0,2 - 0,8) K·c. The domain structure of TGS: Cr crystals consists of a matrix of the main domain, lenticular and lamellar domains. Evolution of the domain structure is observed under the influence of an electron beam, accompanied by the growth of domains, their coalescence, and sample switching. High-temperature annealing of crystals leads to their polydomenization.

Analyzing Frequency Spectra of Dielectric Loss to Clarify Influence of L,α-alanine Doping on Phase Transition in Triglycine Sulfate

As reported in the literature, the doping of L,α-alanine (LA) led to increasing the phase transition temperature in triglycine sulfate (TGS) – a bio-ferroelectric material that has been widely applied in industry. The nature of this anomaly is commonly investigated by considerably complicated theoretical and experimental techniques. Unlike previous studies, the present work proposes a simple physical method of analyzing frequency spectra for dielectric loss to clarify the relationship between the movement of phase transition positions and the shift of relaxation frequencies observed in the spectra. The experimental results obtained for LA-doped TGS samples synthesized at different LA contents (0, 5, 10, 20, and 30 wt.%) were used for the analysis. It was indicated that the increase in phase transition temperature was accompanied by the decrease in relaxation frequencies due to the enhanced viscosity created by strong hydrogen bonds formed between amino acids of alanine and TGS structure.

RELAXATION FREQUENCY SHIFT IN TRIGLYCINE SULFATE UNDER THE INFLUENCE OF SILICA NANOPARTICLES AT LOW FREQUENCIES

The present work is devoted to clarifying the influence of silica nanoparticles on dielectric relaxation frequencies of a classical ferroelectric – triglycine sulfate at low frequencies (102 – 107 Hz) from 20 ˚C to phase transition point for composite samples prepared at different composition weight ratios. Theresults indicated the reduction of relaxation frequency with increasing the silica content due to the intensified interaction between nanoparticles and tryglycine sulfate inclusion. The nature of this interaction was thoroughly discussed in this study.

Asymmetric autocatalysis triggered by triglycine sulfate with switchable chirality by the direction of electric field

Triglycine sulfate (TGS) acts as a chiral trigger for asymmetric autocatalysis with amplification of enantiomeric excess, i.e., the Soai reaction. Therefore, molecular chirality of highly enantioenriched organic compounds is controlled...