The dimensionless thermoelectric figure of merit (ZT) in bismuth antimony telluride (BiSbTe) bulk alloys has remained around 1 for more than 50 years. We show that a peak ZT of 1.4 at 100 degrees C can be achieved in a p-type nanocrystalline BiSbTe bulk alloy. These nanocrystalline bulk materials were made by hot pressing nanopowders that were ball-milled from crystalline ingots under inert conditions. Electrical transport measurements, coupled with microstructure studies and modeling, show that the ZT improvement is the result of low thermal conductivity caused by the increased phonon scattering by grain boundaries and defects. More importantly, ZT is about 1.2 at room temperature and 0.8 at 250 degrees C, which makes these materials useful for cooling and power generation. Cooling devices that use these materials have produced high-temperature differences of 86 degrees , 106 degrees , and 119 degrees C with hot-side temperatures set at 50 degrees, 100 degrees, and 150 degrees C, respectively. This discovery sets the stage for use of a new nanocomposite approach in developing high-performance low-cost bulk thermoelectric materials.
The conversion of sunlight into electricity has been dominated by photovoltaic and solar thermal power generation. Photovoltaic cells are deployed widely, mostly as flat panels, whereas solar thermal electricity generation relying on optical concentrators and mechanical heat engines is only seen in large-scale power plants. Here we demonstrate a promising flat-panel solar thermal to electric power conversion technology based on the Seebeck effect and high thermal concentration, thus enabling wider applications. The developed solar thermoelectric generators (STEGs) achieved a peak efficiency of 4.6% under AM1.5G (1 kW m(-2)) conditions. The efficiency is 7-8 times higher than the previously reported best value for a flat-panel STEG, and is enabled by the use of high-performance nanostructured thermoelectric materials and spectrally-selective solar absorbers in an innovative design that exploits high thermal concentration in an evacuated environment. Our work opens up a promising new approach which has the potential to achieve cost-effective conversion of solar energy into electricity.
The peak dimensionless thermoelectric figure-of-merit (ZT) of Bi(2)Te(3)-based n-type single crystals is about 0.85 in the ab plane at room temperature, which has not been improved over the last 50 years due to the high thermal conductivity of 1.65 W m(-1) K(-1) even though the power factor is 47 x 10(-4) W m(-1) K(-2). In samples with random grain orientations, we found that the thermal conductivity can be decreased by making grain size smaller through ball milling and hot pressing, but the power factor decreased with a similar percentage, resulting in no gain in ZT. Reorienting the ab planes of the small crystals by repressing the as-pressed samples enhanced the peak ZT from 0.85 to 1.04 at about 125 degrees C, a 22% improvement, mainly due to the more increase on power factor than on thermal conductivity. Further improvement is expected when the ab plane of most of the small crystals is reoriented to the direction perpendicular to the press direction and grains are made even smaller.
By ball milling alloyed bulk crystalline ingots into nanopowders and hot pressing them, we had demonstrated high figure-of-merit in nanostructured bulk bismuth antimony telluride. In this study, we use the same ball milling and hot press technique, but start with elemental chunks of bismuth, antimony, and tellurium to avoid the ingot formation step. We show that a peak ZT of about 1.3 in the temperature range of 75 and 100 degrees C has been achieved. This process is more economical and environmentally friendly than starting from alloyed bulk crystalline ingots. The ZT improvement is caused mostly by the lower thermal conductivity, similar as the case using ingot. Transmission electron microscopy observations of the microstructures suggest that the lower thermal conductivity is mainly due to the increased phonon scattering from the increased grain boundaries of the nanograins, precipitates, nanodots, and defects. Our material also exhibits a ZT of 0.7 at 250 degrees C, similar to the value obtained when ingot was used. This study demonstrates that high ZT values can be achieved in nanostructured bulk materials with ball milling elemental chunks, suggesting that the approach can be applied to other materials that are hard to be made into ingot, in addition to its advantage of lower manufacturing cost.
One-dimensional (1D) semiconducting nanoscale materials have attracted considerable attention because of their importance in understanding the fundamental properties of low dimensionality in materials as well as in nanodevice applications. Many methods, including vapor-liquid-solid (VLS), [1] vapor-solid (VS), [2] and solution-based, have been developed to synthesize 1D semiconducting nanoscale materials such as nanoscale wires, [3][4][5][6][7][8][9][10][11] belts, [12][13][14][15][16] rods, [17,18] tubes, [19][20][21][22] and needles. [23,24] Usually, these methods require templates/catalysts and tedious operational procedures.Here, we demonstrate a new strategy for the growth of aligned ultralong ZnO nanobelts, yielding an average length of 3.3 mm and widths up to 6 lm, on metal substrates in a one-step process via molten-salt-assisted template-free thermal evaporation. These ultralong nanobelts show enhanced field emission. The electric field for an emission current density of 1 mA cm -2 is 2.9 V lm -1 , the lowest value ever reported for pure 1D ZnO nanostructures grown on flat surfaces, corresponding to a field-enhancement factor of about 1.4 × 10 4 . This approach is simple, efficient, and inexpensive, which significantly facilitates device fabrication.By combining a general molten-salt process, [25] which is usually used to prepare micrometer-scale ceramic powders (although it was also used for the synthesis of ZnO nanorods [26] in a thermal evaporation process [16] ), we have designed a new approach, molten-salt-assisted thermal evaporation, and we demonstrate that this approach can produce aligned ultralong ZnO nanobelts over a large area. The key point of this new approach is the evaporation of Zn metal powder in a liquid environment of molten sodium chloride (NaCl) salt.
The microstructures of bulk nanograined p-type bismuth antimony telluride with a thermoelectric dimensionless figure-of-merit ZT = 1.4 are investigated using transmission electron microscopy. It is found that the bulk material contains both nano- and microsized grains. Between the nanograins, bismuth-rich interface regions with a 4 nm thickness were detected. In addition, nanoprecipitates as well as other defects are also found to be embedded in the nanograins. The high ZT is attributed to the slight increase in the electrical conductivity, and to the large decrease of the thermal conductivity.
We report a high-yield synthesis of single-crystal hexagonal Sb2Te3 nanoplates using a solvothermal approach. The experimental results show that the concentration of capping agent CTAB played a key role in the formation of nanoplates. This new nanostructure may provide opportunity for the exploration of novel thermoelectric properties and have potential applications in thermoelectric nanodevices.
This study investigates the thermal conductivity and viscosity of copper nanoparticles in ethylene glycol. The nanofluid was prepared by synthesizing copper nanoparticles using a chemical reduction method, with water as the solvent, and then dispersing them in ethylene glycol using a sonicator. Volume loadings of up to 2% were prepared. The measured increase in thermal conductivity was twice the value predicted by the Maxwell effective medium theory. The increase in viscosity was about four times of that predicted by the Einstein law of viscosity. Analytical calculations suggest that this nanofluid would not be beneficial as a coolant in heat exchangers without changing the tube diameter. However, increasing the tube diameter to exploit the increased thermal conductivity of the nanofluid can lead to better thermal performance.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
334 Leonard St
Brooklyn, NY 11211
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.