Bruno Fontaine

X-ray Characterization, Electronic Band Structure, and Thermoelectric Properties of the Cluster Compound Ag2Tl2Mo9Se11

We report on a detailed investigation of the crystal and electronic band structures and of the transport and thermodynamic properties of the Mo-based cluster compound Ag2Tl2Mo9Se11. This novel structure type crystallizes in the trigonal space group R3̅c and is built of a three-dimensional network of interconnected Mo9Se11 units. Single-crystal X-ray diffraction indicates that the Ag and Tl atoms are distributed in the voids of the cluster framework, both of which show unusually large anisotropic thermal ellipsoids indicative of strong local disorder. First-principles calculations show a weakly dispersive band structure around the Fermi level as well as a semiconducting ground state. The former feature naturally explains the presence of both hole-like and electron-like signals observed in Hall effect. Of particular interest is the very low thermal conductivity that remains quasi-constant between 150 and 800 K at a value of approximately 0.6 W·m(-1)·K(-1). The lattice thermal conductivity is close to its minimum possible value, that is, in a regime where the phonon mean free path nears the mean interatomic distance. Such extremely low values likely originate from the disorder induced by the Ag and Tl atoms giving rise to strong anharmonicity of the lattice vibrations. The strongly limited ability of this compound to transport heat is the key feature that leads to a dimensionless thermoelectric figure of merit ZT of 0.6 at 800 K.

Thermotropic luminescent clustomesogen showing a nematic phase: a combination of experimental and molecular simulation studies.

Octahedral Mo6 nanoclusters are functionalized with two organic ligands containing cyanobiphenyl (CB) units, giving luminescent hybrid liquid crystals (LC). Although the mesogenic density around the bulky inorganic core is constant, the two hybrids show different LC properties. Interestingly, one of them shows a nematic phase, which is particularly rare for this kind of supermolecular system. This surprising result is explained by using large-scale molecular dynamic simulations.

Octahedral niobium cluster-based solid state halides and oxyhalides: effects of the cluster condensation via an oxygen ligand on electronic and magnetic properties

The influences of an oxygen ligand on the structural, magnetic and electronic properties of octahedral niobium cluster-based oxides and oxychlorides are reported. The Nb6 metal cluster is edge-bridged by twelve inner ligands and additionally bonded to six apical ligands to form Nb6Li12La6 units (L = Cl, O) wherein oxygen and chlorine are perfectly ordered. Oxygen favours the interconnection of clusters via double Oi–a/Oa–i bridges in a similar way to the double Si–a/Sa–i bridges found in Chevrel phases based on face capped Mo6Li8La6 units. Periodic density functional theory (DFT) calculations confirm that increasing the number of inner oxygen ligands at the expense of chlorine atoms favours the 14 metal-electron (ME) count per octahedral cluster unit. It is also shown that weak interactions occur between neighbouring clusters. Indeed, magnetic measurements performed on AxNb6Cl12O2 (A = Rb, x = 0.816(8); A = Cs, x = 1) series containing 15-ME species evidence antiferromagnetic interactions at low temperatures. Broken-symmetry DFT calculations of exchange parameters within spin dimer analysis confirm the experimental results.

Prediction of high thermoelectric potential in AMN2 layered nitrides: electronic structure, phonons, and anharmonic effects

Band structures, electronic transport coefficients, harmonic and anharmonic vibrational properties of novel layered nitrides have been studied to evaluate the potential for thermoelectric applications. Using first principles theoretical methods we predict that AMN2 compounds with A = Ca, Sr, and Ba, and M = Ti, Zr, Hf may exhibit Seebeck coefficients in excess of 150 μV K−1 and good electrical conductivities. The phonon dispersions indicate the presence of low lying optic modes that can lead to low thermal conductivity. The analysis of the mode resolved Gruneisen parameter points to large anharmonicity. In addition, we show that the A-site substitution controls the degeneracies at the top of the valence band and the anisotropy of the Seebeck tensors.

Unprecedented Electron-Poor Octahedral Ta6 Clusters in a Solid-State Compound: Synthesis, Characterisations and Theoretical Investigations of Cs2BaTa6Br15O3

The crystal structure of Cs2BaTa6Br15O3 has been elucidated by using synchrotron X-ray powder diffraction and absorption experiments. It is built from edge-bridged octahedral [(Ta6Bri9Oi3)Bra6]4− cluster units with a singular poor metallic electron (ME) count equal to thirteen. This leads to a paramagnetic behaviour related to one unpaired electron. The arrangement of the Ta6 clusters is similar to that of Cs2LaTa6Br15O3 exhibiting 14-MEs per [(Ta6Bri9Oi3)Bra6]5− motif. The poorer electron-count cluster presents longer metal–metal distances as foreseen according to the electronic structure of edge-bridged hexanuclear cluster. Density functional theory (DFT) calculations on molecular models were used to rationalise the structural properties of 13- and 14-ME clusters. Periodic DFT calculations demonstrate that the electronic structure of these solid-state compounds is related to those of the discrete octahedral units. Oxygen–barium interactions seem to prevent the geometry of the octahedral cluster to strongly distort, allowing stabilisation of this unprecedented electron-poor Ta6 cluster in the solid state.

Cu Insertion Into the Mo12 Cluster Compound Cs2Mo12Se14: Synthesis, Crystal and Electronic Structures, and Physical Properties.

Mo-based cluster compounds are promising materials for high-temperature thermoelectric applications due to their intrinsic, extremely low thermal conductivity values. In this study, polycrystalline cluster compounds Cs2CuxMo12Se14 were prepared for a wide range of Cu contents (0 ≤ x ≤ 2). All samples crystallize isostructurally in the trigonal space group R3̅. The position of the Cu atoms in the unit cell was determined by X-ray diffraction on a single-crystalline specimen indicating that these atoms fill the empty space between the Mo-Se clusters. Density functional theory calculations predict a metallic ground state for all compositions, in good agreement with the experimental findings. Magnetization measurements indicate a rapid suppression of the superconducting state that develops in the x = 0.0 sample upon Cu insertion. Transport properties measurements, performed in a wide temperature range (2-630 K) on the two end-member compounds x = 0 and x = 2, revealed a multiband electrical conduction as shown by sign reversal of the thermopower as a function of temperature.

Theoretical study on the structural, electronic and physical properties of layered alkaline-earth-group-4 transition-metal nitrides AEMN2

Thermodynamic, structural, and electronic properties of the layered ternary nitrides AEMN2 (AE = alkaline-earth; M = group 4 transition metal) both with the KCoO2 and α-NaFeO2 structure-types are examined within density-functional theory. The AE:M atomic (or ionic) radius ratio seems to be the most important criterion in determining one structural arrangement over the other. We find that the majority of compounds are more stable with the KCoO2 structure-type where M is coordinated to five nitrogen atoms in a distorted square-based pyramidal geometry. Strong interactions occur in both arrangements not only between nitrogen and transition metal atoms, but also between nitrogen and alkaline-earth metal atoms within and between the layers. Calculations show that all the AEMN2 compounds with the tetragonal structure-type KCoO2 are semiconducting with band gaps of approximately 1 eV. However, small band gap conductor and even semi-metallic behavior are computed for compounds with the alternative hexagonal α-NaFeO2 structure-type.

Synthesis, crystal and electronic structures, and physical properties of the novel compounds LaR4Mo36O52 (R = Dy, Er, Yb, and Y) containing infinite chains of trans-edge-shared Mo6 octahedra and Mo2 pairs and rectangular Mo4 clusters with triple Mo-Mo bonds.

The novel quaternary reduced molybdenum oxides LaR(4)Mo(36)O(52) (R = Dy, Er, Yb, and Y) have been synthesized with solid-state reactions at 1400 degrees C for 48 h in sealed molybdenum crucibles. The crystal structure was determined on a single crystal of LaEr(4)Mo(36)O(52) by X-ray diffraction. LaEr(4)Mo(36)O(52) crystallizes in the tetragonal space group I4 with two formula units per cell and the following lattice parameters: a = 19.8348(2) and c = 5.6594(1) A. The Mo network is dominated by infinite chains of trans-edge-shared Mo(6) octahedra, which coexist with Mo(2) pairs and rectangular Mo(4) clusters. The Mo-Mo distances within the infinite chains range from 2.5967(7) to 2.8529(8) A and from 2.239(3) to 2.667(2) A in the Mo(2) pairs and rectangular Mo(4) clusters, respectively. The Mo-O distances are comprised between 1.993(7) and 2.149(7) A, as usually observed in these types of compound. The La(3+) and Er(3+) ions are in a square-prismatic [LaO(8)] and a tricapped trigonal-prismatic [ErO(9)] environment of oxygen atoms, respectively. The La-O distances range from 2.555(6) to 2.719(6) A and the Er-O ones from 2.260(6) to 2.469(5) A. Theoretical calculations allow the determination of the optimal electron count of both motifs in the title compound. Weak interactions occur between neighboring dimetallic and tetrametallic clusters and between trans-edge-sharing infinite chains and dimers and tetramers. The presence of rectangular clusters is favored on the basis of theoretical considerations. Single-crystal resistivity measurements show that LaEr(4)Mo(36)O(52) is metallic between 4.2 and 300 K, in agreement with the band structure calculations. Magnetic susceptibility measurements indicate that the oxidation state of the magnetic rare earths is +3, and there is an absence of localized moments on the Mo network.

Enhancement of the Thermoelectric Properties of FeGa3-type Structures with Group 6 Transition Metals: A Computational Exploration

The possible existence of group 6 TM3 compounds with T = Cr, Mo, W and M = Ga, In is investigated with the aid of density functional theory calculations. Their most probable crystal structure is expected to be of the FeGa3 type tetragonal space group P42/mnm. All compounds are computed to be semiconductors with a band gap ranging from 0.08 to 0.43 eV, at the modified Becke-Johnson level of theory. The thermoelectric properties are analyzed via calculations based on Boltzmann transport equation under a constant relaxation time approximation. Promising power factors are computed for both n- and p-type WGa3 because of a band degeneracy around the Fermi level similar to that of heavily doped PbTe and SnTe materials. If the optimal chemical potential can be reached, a thermoelectric figure of merit up to 0.6 at 800 K for both n- and p-type may be expected for WGa3.

Realizing a Stable High Thermoelectric zT ~ 2 over a Broad Temperature Range in Ge1-x-yGaxSbyTe via Band Engineering and Hybrid Flash-SPS Processing

We report a remarkably high and stable thermoelectric figure of merit zT close to 2 by manipulating the electronic bands in Ga–Sb codoped GeTe, which has been processed by hybrid flash-spark plasma sintering. According to the experimental results and first-principles calculations, the vast enhancement achieved in the thermopower due to codoping of Ga (2 mol%) and Sb (8 mol%) in GeTe is attributed to a concoction of reasons: (i) suppression of hole concentration; (ii) improved band convergence by decreasing the energy separation between the two valence band maxima to 0.026 eV; (iii) Ga predominantly contributing to the top of the valence band in Ga–Sb codoped GeTe, despite the Ga-induced resonance state not being located at a favorable position near the Fermi level; (iv) active participation of several bands increasing the hole carrier effective mass; (v) facilitating band degeneracy by reducing the R3m → Fmm structural transition temperature from 700 K to 580 K. The synergy between these complementary and beneficial effects, in addition to the reduced thermal conductivity, enabled the flash sintered Ge0.90Ga0.02Sb0.08Te composition to not only exhibit a peak of zT of ∼1.95 at 723 K, but also to maintain/stabilize its high performance over a broad temperature range (600–775 K), thus making it a serious candidate for mid-temperature range energy harvesting devices.