Inspired by the ongoing debate about the ion dynamics in the lithium superionic conductor Li10GeP2S12 (LGPS), we present neutron powder diffraction data in combination with analyses of differential ...bond valence and nuclear density maps to elucidate the underlying diffusion pathways in Li10GeP2S12. LGPS exhibits quasi-isotropic three-dimensional lithium diffusion pathways, which is a combination of one-dimensional diffusion channels crossing two diffusion planes. Furthermore, ultrasonic speeds of sound measurements are used to understand the lattice dynamics and obtain the Debye temperature of LGPS. Temperature dependent X-ray diffraction is performed in order to understand the local temperature-dependent behavior of the prevalent structural backbone, as well as the thermal stability of the material. At elevated temperatures, the superionic conducting Li10GeP2S12 phase partially decomposes into Li4P2S6, explaining the deterioration of the ionic conductivity upon heating.
Glassy, glass–ceramic, and crystalline lithium thiophosphates have attracted interest in their use as solid electrolytes in all-solid-state batteries. Despite similar structural motifs, including PS4 ...3–, P2S6 4–, and P2S7 4– polyhedra, these materials exhibit a wide range of possible compositions, crystal structures, and ionic conductivities. Here, we present a combined approach of Bragg diffraction, pair distribution function analysis, Raman spectroscopy, and 31P magic angle spinning nuclear magnetic resonance spectroscopy to study the underlying crystal structure of Li4P2S6. In this work, we show that the material crystallizes in a planar structural arrangement as a glass ceramic composite, explaining the observed relatively low ionic conductivity, depending on the fraction of glass content. Calculations based on density functional theory provide an understanding of occurring diffusion pathways and ionic conductivity of this Li+ ionic conductor.
Superionic chalcopyrites have recently attracted interest in their use as potential thermoelectric materials because of extraordinary low thermal conductivities. To overcome long-term stability ...issues in thermoelectric generators using superionic materials at evaluated temperatures, materials need to be found that show good thermoelectric performance at moderate temperatures. Here, we present the structural and thermoelectric properties of the argyrodite Ag8SiSe6, which exhibits promising thermoelectric performance close to room temperature.
Building on the good thermoelectric performances of binary superionic compounds like Cu2Se, Ag2Se and Cu2S, a better and more detailed understanding of phonon-liquid electron-crystal (PLEC) ...thermoelectric materials is desirable. In this work we present the thermoelectric transport properties of the compound Cu7PSe6 as the first representative of the class of argyrodite-type ion conducting thermoelectrics. With a huge variety of possible compositions and high ionic conductivity even at room temperature, the argyrodites represent a very good model system to study structure–property relationships for PLEC thermoelectric materials. We particularly highlight the extraordinary low thermal conductivity of Cu7PSe6 below the glass limit, which can be associated with the molten copper sublattice leading to a softening of phonon modes.
AgBiSe2 has recently been shown to exhibit promising thermoelectric properties due to the low intrinsic thermal conductivity, stemming from a large degree of lattice anharmonicity. While samples ...synthesized via solid-state routes usually exhibit n-type behavior, p-type transport is seen in samples based on solution synthetic routes possibly due to Ag vacancies. Using a combined approach of synchrotron diffraction, thermoelectric transport measurements and thermal transport modeling, we show the influence of synthetically induced Ag vacancies on the structure of AgBiSe2 and the thermoelectric transport. We identify the degree of anti-site disorder of Ag and Bi due to the occurring phase transformation and the influence of the vacancy content on metal ordering. Additionally, we show that anti-site disorder and vacancies act as scattering centers for phonons, leading to enhanced point defect scattering in this interesting thermoelectric material.
The acceleration of very early age cement hydration by C-S-H seeding is getting attention from scholars and field applications because the enhanced early age features do not compromise later age ...performances. This acceleration could be beneficial for several low-CO
cements as a general drawback is usually the low very early age mechanical strengths. However, the mechanistic understanding of this acceleration in commercial cements is not complete. Reported here is a contribution to this understanding from the study of the effects of C-S-H gel seeding in one Portland cement and two belite cements at two widely studied water-cement ratios, 0.50 and 0.40. Two commercially available C-S-H nano-seed-based admixtures, i.e., Master X-Seed 130 and Master X-Seed STE-53, were investigated. A multi-technique approach was adopted by employing calorimetry, thermal analysis, powder diffraction (data analysed by the Rietveld method), mercury intrusion porosimetry, and mechanical strength determination. For instance, the compressive strength at 1 day for the PC (
/
= 0.50) sample increased from 15 MPa for the unseeded mortar to 24 and 22 MPs for the mortars seeded with the XS130 and STE53, respectively. The evolution of the amorphous contents was determined by adding an internal standard before recording the powder patterns. In summary, alite and belite phase hydrations, from the crystalline phase content evolutions, are not significantly accelerated by C-S-H seedings at the studied ages of 1 and 28 d for these cements. Conversely, the hydration rates of tetracalcium alumino-ferrate and tricalcium aluminate were significantly enhanced. It is noted that the degrees of reaction of C
AF for the PC paste (
/
= 0.40) were 10, 30, and 40% at 1, 7, and 28 days. After C-S-H seeding, the values increased to 20, 45, and 60%, respectively. This resulted in larger ettringite contents at very early ages but not at 28 days. At 28 days of hydration, larger amounts of carbonate-containing AFm-type phases were determined. Finally, and importantly, the admixtures yielded larger amounts of amorphous components in the pastes at later hydration ages. This is justified, in part, by the higher content of amorphous iron siliceous hydrogarnet from the enhanced C
AF reactivity.
AgBiSe
has recently been shown to exhibit promising thermoelectric properties due to the low intrinsic thermal conductivity, stemming from a large degree of lattice anharmonicity. While samples ...synthesized via solid-state routes usually exhibit n-type behavior, p-type transport is seen in samples based on solution synthetic routes possibly due to Ag vacancies. Using a combined approach of synchrotron diffraction, thermoelectric transport measurements and thermal transport modeling, we show the influence of synthetically induced Ag vacancies on the structure of AgBiSe
and the thermoelectric transport. We identify the degree of anti-site disorder of Ag and Bi due to the occurring phase transformation and the influence of the vacancy content on metal ordering. Additionally, we show that anti-site disorder and vacancies act as scattering centers for phonons, leading to enhanced point defect scattering in this interesting thermoelectric material.
AgBiSe
2
has recently been shown to exhibit promising thermoelectric properties due to the low intrinsic thermal conductivity, stemming from a large degree of lattice anharmonicity. While samples ...synthesized
via
solid-state routes usually exhibit n-type behavior, p-type transport is seen in samples based on solution synthetic routes possibly due to Ag vacancies. Using a combined approach of synchrotron diffraction, thermoelectric transport measurements and thermal transport modeling, we show the influence of synthetically induced Ag vacancies on the structure of AgBiSe
2
and the thermoelectric transport. We identify the degree of anti-site disorder of Ag and Bi due to the occurring phase transformation and the influence of the vacancy content on metal ordering. Additionally, we show that anti-site disorder and vacancies act as scattering centers for phonons, leading to enhanced point defect scattering in this interesting thermoelectric material.
Ag vacancies in AgBiSe
2
influence Ag-Bi anti-site disorder and provide point defect scattering, reducing the lattice thermal conductivity.
Superionic chalcopyrites have recently attracted interest in their use as potential thermoelectric materials because of extraordinary low thermal conductivities. To overcome long-term stability ...issues in thermoelectric generators using superionic materials at evaluated temperatures, materials need to be found that show good thermoelectric performance at moderate temperatures. Here, we present the structural and thermoelectric properties of the argyrodite Ag8SiSe6, which exhibits promising thermoelectric performance close to room temperature.
Glassy, glass–ceramic, and crystalline lithium thiophosphates have attracted interest in their use as solid electrolytes in all-solid-state batteries. Despite similar structural motifs, including ...PS43–, P2S64–, and P2S74– polyhedra, these materials exhibit a wide range of possible compositions, crystal structures, and ionic conductivities. Here, we present a combined approach of Bragg diffraction, pair distribution function analysis, Raman spectroscopy, and 31P magic angle spinning nuclear magnetic resonance spectroscopy to study the underlying crystal structure of Li4P2S6. In this work, we show that the material crystallizes in a planar structural arrangement as a glass ceramic composite, explaining the observed relatively low ionic conductivity, depending on the fraction of glass content. Calculations based on density functional theory provide an understanding of occurring diffusion pathways and ionic conductivity of this Li+ ionic conductor.
