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Lithium tantalate (LiTaO3, or LT) crystal is widely used in optical applications, infrared detection, and acoustic surface wave devices because of its excellent piezoelectric, pyroelectric, and nonlinear optical properties. In this paper, we discuss the defect structure of LT; the preparation method for LT; the influence of doping on LT; and LT’s application in optical, acoustic, and electrical devices. We mainly analyzed the structure and physical properties of LT crystal, the preparation of LT crystal and LT thin films, the periodic polarization of LT crystal, the reduction of LT wafers, and the application potential of LT crystals in lasers and acoustic surface filters according to the most recent research. We also provide an overview of future research directions for LT in the fields of acoustics, optics, and other fields. The applications of LT in 5G, 6G, SAW filters, nonlinear optical devices, and waveguides are expected to provide additional breakthroughs.

Femto-/nanosecond pulse-induced, red and near-infrared absorption is studied in LiNb 1 − x Ta x O 3 ( 0 ⩽ x ⩽ 1 , LNT) solid solutions with the aim of studying transient optical nonlinearities associated with the formation, transport and recombination of optically generated small bound electron polarons with strong coupling to the lattice. As a result, a pronounced, long-lived transient absorption is uncovered for LNT which exceeds lifetimes and starting amplitudes of LiNbO 3 (LN) and LiTaO 3 (LT) by a factor of up to 100 and 10, respectively. The transients reveal a stretched-exponential decay behavior and a thermally activated process which provide strong evidence for an underlying hopping transport mechanism of small bound polarons. All findings are discussed in comparison to the model systems LN and LT within the framework of appropriate band models and optical generation of polarons via two-photon excitation. To explain the significant differences, the simultaneous presence of Nb Li 5 + , Ta Li 5 + antisites, and Ta V 5 + interstitial defects, i.e. a mixture of the intrinsic defects widely established for LN and LT, is assumed for LNT.

Lithium tantalate crystals, as a type of pyroelectric material, stand out from many other pyroelectric materials due to the advantages of high Curie temperature, large pyroelectric coefficient, high figure of merits, and environmental friendliness. Due to the pyroelectric effect caused by their spontaneous polarization, lithium tantalate crystals have broad application prospects in wide spectral bandwidth and uncooled pyroelectric detectors. This article reviews the pyroelectric properties of lithium tantalate crystals and evaluates methods for pyroelectric properties, methods for modulating pyroelectric properties, and pyroelectric detectors and their applications. The prospects of lithium tantalate thin films, doped lithium tantalate crystals, and near stoichiometric lithium tantalate crystals as response components for pyroelectric detectors are also discussed.

Lithium tantalate (LT) exhibits nonlinear optical properties that are comparable to those of lithium niobate (LN), yet the former surpasses the latter in several respects. These include an enhanced optical damage threshold, a wider transparency range, and lower birefringence. Consequently, LT is an excellent material for optical frequency conversion applications. In this study, we have devised a novel device based on thin-film lithium tantalate (TFLT) for the efficient generation of second-harmonic waves. The design employs modal phase-matching (MPM), which circumvents the intricacies of conventional poling techniques, and attains a normalised conversion efficiency of 120% W−1cm−2. In order to address the challenges presented by higher-order modes, a mode converter with an insertion loss of less than 0.1 dB has been developed, thereby ensuring the efficient utilisation of the second harmonic. This study not only demonstrates the potential of TFLT for high-performance SHG, but also promotes the development of integrated nonlinear TFLT platforms.

Near-stoichiometric lithium tantalate (NSLT) wafers with different Li contents were prepared by vapour transfer equilibrium (VTE) method and fabricated into surface acoustic wave filters. The temperature coefficient of frequency, insertion loss, and bandwidth of the surface acoustic wave filters were tested using a special chip test bench and a network analyzer. The results show that the temperature coefficient of frequency shows a trend of first decreasing and then increasing with the increase in Li content, and the temperature stability of the surface acoustic wave filters is best when the Li content is 49.75%. It is also found that the surface acoustic wave filter fabricated from NSLT wafers has 21.18% lower temperature coefficient of frequency, 7.3% lower insertion loss, and 2.8% lower bandwidth than those fabricated from congruent lithium tantalate wafers. Therefore, NSLT crystals are more suitable for applications in acoustic devices, providing a new idea for performance enhancement of 5G communication devices.

The fabrication of stable, tailored domain patterns in ferroelectric crystals has wide applications in optical and electronic industries. All-optical ferroelectric poling by pulse laser irradiation has been developed recently. In this work, we studied the creation of the domain structures in MgO-doped lithium tantalate by focused irradiation with a femtosecond near-infrared laser. Cherenkov-type second harmonic generation microscopy was used for domain imaging of the bulk. We have revealed the creation of enveloped domains around the induced microtracks under the action of the depolarization field. The domain growth is due to a pyroelectric field caused by a nonuniform temperature change. The domains in the bulk were revealed to have a three-ray star-shaped cross-section. It was shown that an increase in the field excess above the threshold leads to consequential changes in domain shape from a three-ray star to a triangular and a circular shape. The appearance of comb-like domains as a result of linear scanning was demonstrated. All effects were considered in terms of a kinetic approach, taking into account the domain wall motion by step generation and kink motion driven by excess of the local field over the threshold. The obtained knowledge is useful for the all-optical methods of domain engineering in ferroelectrics.

Femto-/nanosecond pulse-induced, red and near-infrared absorption is studied in LiNb1−xTaxO3 (0⩽x⩽1, LNT) solid solutions with the aim of studying transient optical nonlinearities associated with the formation, transport and recombination of optically generated small bound electron polarons with strong coupling to the lattice. As a result, a pronounced, long-lived transient absorption is uncovered for LNT which exceeds lifetimes and starting amplitudes of LiNbO3 (LN) and LiTaO3 (LT) by a factor of up to 100 and 10, respectively. The transients reveal a stretched-exponential decay behavior and a thermally activated process which provide strong evidence for an underlying hopping transport mechanism of small bound polarons. All findings are discussed in comparison to the model systems LN and LT within the framework of appropriate band models and optical generation of polarons via two-photon excitation. To explain the significant differences, the simultaneous presence of NbLi5+, TaLi5+ antisites, and TaV5+ interstitial defects, i.e. a mixture of the intrinsic defects widely established for LN and LT, is assumed for LNT.

The Raman spectra of a lithium tantalate crystal doubly doped with chromium and neodymium LiTaO3:Cr(0.2):Nd(0.45 wt%) have been studied in this paper. Raman spectra of the first and second orders have been found to be located against the background of a luminescent halo with a maximum at ≈1250 cm−1. Several Raman bands have been detected in the frequency range of 900–2000 cm−1. Their frequencies were 940, 1034, 1113, 1171, 1250, 1343, 1428, 1491, 1582, 1735, 1838, and 1925 cm−1. These bands correspond to overtone processes. We have determined that the frequencies of 1838 and 1925 cm−1 bands are significantly higher than the exact value of the overtone frequency corresponding to the fundamental mode 4A1(z)LO (864 cm−1).

Recently, it was established that the X-ray generation intensity increases in a certain range of temperature variation rates (6–8°C/min) of lithium tantalate single crystal (LiTaO 3 ). In this work, the pyroelectric current generation is studied as a function of the temperature variation rate. Four stages of the pyroelectric current generation dynamics are determined. In the same rate range (6–8°C/min), an anomalously long stage of current saturation is observed, which is most likely the cause of the observed effect of an increase in the X-ray intensity. The observed anomaly is described, as well as systematic features in the pyroelectric current dynamics with varying the pyroelectric material temperature with a constant rate.

In this paper, a gas detection system with an environmental compensation algorithm based on nondispersive infrared (NDIR) technology was designed. The prepared infrared pyroelectric detector was a dual-channel type based on the lithium tantalate (LiTaO3) wafer. The design of the optical gas chamber adopted a combination of two ellipsoids and a spherical top surface, which not only enhanced the coupling efficiency of the light propagation but also facilitated the miniaturization of the sensor module. In addition to this, a temperature and humidity compensation algorithm based on the least square method was proposed to make the measurement accuracy up to ±0.9% full scale (FS).