Herein we cover the key concepts in the field of thermoelectric materials research, present the current understanding, and show the latest developments. Current research is aimed at increasing the thermoelectric figure of merit (ZT) by maximizing the power factor and/or minimizing the thermal conductivity. Attempts at maximizing the power factor include the development of new materials, optimization of existing materials by doping, and the exploration of nanoscale materials. The minimization of the thermal conductivity can come through solid-solution alloying, use of materials with intrinsically low thermal conductivity, and nanostructuring. Herein we describe the most promising bulk materials with emphasis on results from the last decade. Single-phase bulk materials are discussed in terms of chemistry, crystal structure, physical properties, and optimization of thermoelectric performance. The new opportunities for enhanced performance bulk nanostructured composite materials are examined and a look into the not so distant future is attempted.
The synthesis, crystal growth, and structural and optoelectronic characterization has been carried out for the perovskite compound CsPbBr 3 . This compound is a direct band gap semiconductor which meets most of the requirements for successful detection of X-and γ-ray radiation, such as high attenuation, high resistivity, and significant photoconductivity response, with detector resolution comparable to that of commercial, state-of-the-art materials. A structural phase transition which occurs during crystal growth at higher temperature does not seem to affect its crystal quality. Its μτ product for both hole and electron carriers is approximately equal. The μτ product for electrons is comparable to cadmium zinc telluride (CZT) and that for holes is 10 times higher than CZT.
The recent observations of superconductivity at temperatures up to 55K in compounds containing layers of iron arsenide [1,2,3,4] have revealed a new class of high temperature superconductors that show striking similarities to the more familiar cuprates. In both series of compounds, the onset of superconductivity is associated with the suppression of magnetic order by doping holes and/or electrons into the band [5] leading to theories in which magnetic fluctuations are either responsible for or strongly coupled to the superconducting order parameter [6]. In the cuprates, theories of magnetic pairing have been invoked to explain the observation of a resonant magnetic excitation that scales in energy with the superconducting energy gap and is suppressed above the superconducting transition temperature, Tc. Such resonant excitations have been shown by inelastic neutron scattering to be a universal feature of the cuprate superconductors [7], and have even been observed in heavy fermion superconductors with much lower transition temperatures [8,9,10]. In this paper, we show neutron scattering evidence of a resonant excitation in Ba0.6K0.4Fe2As2, which is a superconductor below 38 K [4], at the momentum transfer associated with magnetic order in the undoped compound, BaFe2As2, and at an energy transfer that is consistent with scaling in other strongly correlated electron superconductors. As in the cuprates, the peak disappears at Tc providing the first experimental confirmation of a strong coupling of the magnetic fluctuation spectrum to the superconducting order parameter in the new iron arsenide superconductors.Unconventional superconductivity has been the subject of considerable theoretical and experimental interest since the discovery of superconductivity in CeCu 2 Si 2 and other heavy fermion compounds [11], an interest that was only intensified by the discovery of cuprate superconductors with transition temperatures in excess of 100 K [6]. Although significant progress has been made, the origin of unconventional superconductivity is still not understood. The observation of a magnetic resonance in the spin excitation spectrum which appears concurrently with the onset of superconductivity in both the high T c cuprates [12,13,14,15,16] and the heavy fermion superconductors [8,9,10] offers the tantalizing possibility of a unifying theme for unconventional superconductivity that spans a diverse range of superconducting materials. Recently, a new family of superconductors containing layers of Fe 2 As 2 has been discovered with T c s in excess of 50 K stimulating considerable experimental and theoretical activity [1,2,3]. Although there is mounting evidence that the superconductivity in this new family is also unconventional [17], there is as yet no consensus concerning the mechanism giving rise to superconductivity or even the superconducting pairing symmetry. In this letter, we describe neutron scattering data that confirm for the first time the existence of a resonant spin excitation below T c in the iron arsenide ma...
Gamma-ray detection and spectroscopy is the quantitative determination of their energy spectra, and is of critical value and critically important in diverse technological and scientific fields. Here we report an improved melt growth method for cesium lead bromide and a special detector design with asymmetrical metal electrode configuration that leads to a high performance at room temperature. As-grown centimeter-sized crystals possess extremely low impurity levels (below 10 p.p.m. for total 69 elements) and detectors achieve 3.9% energy resolution for 122 keV 57Co gamma-ray and 3.8% for 662 keV 137Cs gamma-ray. Cesium lead bromide is unique among all gamma-ray detection materials in that its hole transport properties are responsible for the high performance. The superior mobility-lifetime product for holes (1.34 × 10−3 cm2 V−1) derives mainly from the record long hole carrier lifetime (over 25 μs). The easily scalable crystal growth and high-energy resolution, highlight cesium lead bromide as an exceptional next generation material for room temperature radiation detection.
Thermoelectric (Peltier) heat pumps are capable of refrigerating solid or fluid objects, and unlike conventional vapor compressor systems, they can be miniaturized without loss of efficiency. More efficient thermoelectric materials need to be identified, especially for low-temperature applications in electronics and devices. The material CsBi(4)Te(6) has been synthesized and its properties have been studied. When doped appropriately, it exhibits a high thermoelectric figure of merit below room temperature (ZT(max) approximately 0.8 at 225 kelvin). At cryogenic temperatures, the thermoelectric properties of CsBi(4)Te(6) appear to match or exceed those of Bi(2-x)Sb(x)Te(3-y)Se(y) alloys.
Lead sulfide, a compound consisting of elements with high natural abundance, can be converted into an excellent thermoelectric material. We report extensive doping studies, which show that the power factor maximum for pure n-type PbS can be raised substantially to ~12 μW cm(-1) K(-2) at >723 K using 1.0 mol % PbCl(2) as the electron donor dopant. We also report that the lattice thermal conductivity of PbS can be greatly reduced by adding selected metal sulfide phases. The thermal conductivity at 723 K can be reduced by ~50%, 52%, 30%, and 42% through introduction of up to 5.0 mol % Bi(2)S(3), Sb(2)S(3), SrS, and CaS, respectively. These phases form as nanoscale precipitates in the PbS matrix, as confirmed by transmission electron microscopy (TEM), and the experimental results show that they cause huge phonon scattering. As a consequence of this nanostructuring, ZT values as high as 0.8 and 0.78 at 723 K can be obtained for nominal bulk PbS material. When processed with spark plasma sintering, PbS samples with 1.0 mol % Bi(2)S(3) dispersion phase and doped with 1.0 mol % PbCl(2) show even lower levels of lattice thermal conductivity and further enhanced ZT values of 1.1 at 923 K. The promising thermoelectric properties promote PbS as a robust alternative to PbTe and other thermoelectric materials.
A theory of superconductivity in the iron-based materials requires an understanding of the phase diagram of the normal state. In these compounds, superconductivity emerges when stripe spin density wave (SDW) order is suppressed by doping, pressure or atomic disorder. This magnetic order is often pre-empted by nematic order, whose origin is yet to be resolved. One scenario is that nematic order is driven by orbital ordering of the iron 3d electrons that triggers stripe SDW order. Another is that magnetic interactions produce a spin-nematic phase, which then induces orbital order. Here we report the observation by neutron powder diffraction of an additional fourfold-symmetric phase in Ba 1 À x Na x Fe 2 As 2 close to the suppression of SDW order, which is consistent with the predictions of magnetically driven models of nematic order.
We report the results of a systematic investigation of the phase diagram of the iron-based superconductor, Ba 1-x K x Fe 2 As 2 , from x = 0 to x = 1.0 using high resolution neutron and x-ray diffraction and magnetization measurements. The polycrystalline samples were prepared with an estimated compositional variation of ∆x ≲ 0.01, allowing a more precise estimate of the phase boundaries than reported so far. At room temperature, Ba 1-x K x Fe 2 As 2 crystallizes in a tetragonal structure with the space group symmetry of I4/mmm, but at low doping, the samples undergo a coincident first-order structural and magnetic phase transition to an orthorhombic (O) structure with space group Fmmm and a striped antiferromagnet (AF) with space group F c mm'm'. The transition temperature falls from a maximum of 139 K in the undoped compound to 0 K at x = 0.252, with a critical exponent as a function of doping of 0.25(2) and 0.12(1) for the structural and magnetic order parameters, respectively. The onset of superconductivity occurs at a critical concentration of x = 0.130(3) and the superconducting transition temperature grows linearly with x until it crosses the AF/O phase boundary. Below this concentration, there is microscopic phase coexistence of the AF/O and superconducting order parameters, although a slight suppression of the AF/O order is evidence that the phases are competing. At higher doping, superconductivity has a maximum T c of 38 K at x = 0.4 falling to 3 K at x = 1.0. We discuss reasons for the suppression of the spin-density-wave order and the electron-hole asymmetry in the phase diagram.2
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