Abstract: Thermoelectricity allows direct conversion between heat and electricity, providing alternatives for green energy technologies. Despite these advantages, for most materials the energy conversion efficiency is limited by the tendency for the electrical and thermal conductivity to be proportional to each other and the Seebeck coefficient to be small. Here we report counter examples, where the heavy fermion compounds Yb TM 2 Zn 20 ( TM = Co, Rh, Ir) exhibit enhanced thermoelectric performance including a large power factor ( PF = 74 μW/cm-K 2 ; TM = Ir) and a high figure of merit ( ZT = 0.07; TM = Ir) at 35 K. The combination of the strongly hybridized electronic state originating from the Yb f -electrons and the novel structural features (large unit cell and possible soft phonon modes) leads to high power factors and small thermal conductivity values. This demonstrates that with further optimization these systems could provide a platform for the next generation of low temperature thermoelectric materials.
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N-Type Bismuth Telluride Nanocomposite Materials Optimization for Thermoelectric Generators in Wearable Applications
Thermoelectric materials could play a crucial role in the future of wearable electronic devices. They can continuously generate electricity from body heat. For efficient operation in wearable systems, in addition to a high thermoelectric figure of merit, zT, the thermoelectric material must have low thermal conductivity and a high Seebeck coefficient. In this study, we successfully synthesized high-performance nanocomposites of n-type Bi2Te2.7Se0.3, optimized especially for body heat harvesting and power generation applications. Different techniques such as dopant optimization, glass inclusion, microwave radiation in a single mode microwave cavity, and sintering conditions were used to optimize the temperature-dependent thermoelectric properties of Bi2Te2.7Se0.3. The effects of these techniques were studied and compared with each other. A room temperature thermal conductivity as low as 0.65 W/mK and high Seebeck coefficient of −297 μV/K were obtained for a wearable application, while maintaining a high thermoelectric figure of merit, zT, of 0.87 and an average zT of 0.82 over the entire temperature range of 25 °C to 225 °C, which makes the material appropriate for a variety of power generation applications.
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- NSF-PAR ID:
- 10106202
- Date Published:
- Journal Name:
- Materials
- Volume:
- 12
- Issue:
- 9
- ISSN:
- 1996-1944
- Page Range / eLocation ID:
- 1529
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Thermoelectric (TE) generators enable the direct and reversible conversion between heat and electricity, providing applications in both refrigeration and power generation. In the last decade, several TE materials with relatively high figures of merit (
zT ) have been reported in the low‐ and high‐temperature regimes. However, there is an urgent demand for high‐performance TE materials working in the mid‐temperature range (400–700 K). Herein, p‐type AgSbTe2materials stabilized with S and Se co‐doping are demonstrated to exhibit an outstanding maximum figure of merit (zT max) of 2.3 at 673 K and an average figure of merit (zT ave) of 1.59 over the wide temperature range of 300–673 K. This exceptional performance arises from an enhanced carrier density resulting from a higher concentration of silver vacancies, a vastly improved Seebeck coefficient enabled by the flattening of the valence band maximum and the inhibited formation of n‐type Ag2Te, and ahighly improved stability beyond 673 K. The optimized material is used to fabricate a single‐leg device with efficiencies up to 13.3% and a unicouple TE device reaching energy conversion efficiencies up to 12.3% at a temperature difference of 370 K. These results highlight an effective strategy to engineer high‐performance TE material in the mid‐temperature range. -
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Abstract Yb10MgSb9is a new Zintl compound (with a composition closer to Yb10.5MgSb9) and a promising thermoelectric material first reported in this work. Undoped Yb10MgSb9has an ultralow thermal conductivity due to crystallographic complexity and exhibits a relatively high peak p‐type Seebeck coefficient and high electrical resistivity. This is consistent with Zintl counting and density functional theory (DFT) calculations that the composition Yb10.5MgSb9should be a semiconductor. Na is found experimentally to be an effective p‐type dopant potentially due to the replacement of Na+for Yb2+, allowing for a significant decrease in electrical resistivity. With doping, a dramatic improvement of electrical conductivity is observed and the glass‐like thermal conductivity remains low, allowing for a significant enhancement of the thermoelectric figure of merit,
zT . Doping increases thezT from 0.23 in undoped Yb10MgSb9to 1.06 in 7 at% Na‐doped Yb10MgSb9at 873K. This high thermoelectric performance found through Na‐doping places this material amongst the leading p‐type Zintl thermoelectrics, making it a promising candidate for future studies and high‐temperature thermoelectric applications. -
Thermoelectric (TE) cement composite is a new type of TE material. Unlike ordinary cement, due to the inclusion of additives, TE cement can mutually transform thermal energy into electrical energy. In extreme weather, the large temperature difference between indoor and outdoor can be harvested by TE cement to generate electricity. In moderate weather, given power input, the same material can provide cooling/heating to adjust room temperature and reduce HAVC load. Therefore, TE cement has energy-saving potential in the application of building enclosures and energy systems. Its ability to convert different forms of energy and use low-grade energy is conducive to the operation of net-zero buildings. In this study, the graphene nanoplatelets and aluminum-doped zinc oxide nanopowder enhanced cement composite, was fabricated. The performance indicator of TE materials includes the dimensionless figure of merit ZT, calculated by Seebeck coefficient, thermal conductivity, and electrical conductivity. These TE properties were measured and calculated by a Physical Property Measurement System at different temperatures. The highest ZT of 15wt.% graphene and 5wt.% AZO enhanced cement composite prepared by the dry method is about 5.93E-5 at 330K.more » « less
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The Mg 3 Sb 2− x Bi x family has emerged as the potential candidates for thermoelectric applications due to their ultra-low lattice thermal conductivity ( κ L ) at room temperature (RT) and structural complexity. Here, using ab initio calculations of the electron-phonon averaged (EPA) approximation coupled with Boltzmann transport equation (BTE), we have studied electronic, phonon and thermoelectric properties of Mg 3 Sb 2− x Bi x (x = 0, 1, and 2) monolayers. In violation of common mass-trend expectations, increasing Bi element content with heavier Zintl phase compounds yields an abnormal change in κ L in two-dimensional Mg 3 Sb 2− x Bi x crystals at RT (∼0.51, 1.86, and 0.25 W/mK for Mg 3 Sb 2 , Mg 3 SbBi, and Mg 3 Bi 2 ). The κ L trend was detailedly analyzed via the phonon heat capacity, group velocity and lifetime parameters. Based on quantitative electronic band structures, the electronic bonding through the crystal orbital Hamilton population (COHP) and electron local function analysis we reveal the underlying mechanism for the semiconductor-semimetallic transition of Mg 3 Sb 2-− x Bi x compounds, and these electronic transport properties (Seebeck coefficient, electrical conductivity, and electronic thermal conductivity) were calculated. We demonstrate that the highest dimensionless figure of merit ZT of Mg 3 Sb 2− x Bi x compounds with increasing Bi content can reach ∼1.6, 0.2, and 0.6 at 700 K, respectively. Our results can indicate that replacing heavier anion element in Zintl phase Mg 3 Sb 2− x Bi x materials go beyond common expectations (a heavier atom always lead to a lower κ L from Slack’s theory), which provide a novel insight for regulating thermoelectric performance without restricting conventional heavy atomic mass approach.more » « less
- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3390/ma12091529
