Multicationic Tetrahedra Networks: Alkaline-Earth-Centered Polyhedra and Non-Condensed AlN6-Octahedra in the Imidonitridophosphates AE2AlP8N15(NH) (AE=Ca, Sr, Ba).

A series of isostructural imidonitridophosphates AE2AlP8N15(NH) (AE=Ca, Sr, Ba) was synthesized at high-pressure/high-temperature conditions (1400 °C and 5-9 GPa) from alkaline-earth metal nitrides or azides Ca3N2/Sr(N3)2/Ba(N3)2 and the binary nitrides AlN and P3N5. NH4F served as a hydrogen source and mineralizing agent. The crystal structures were determined by single-crystal X-ray diffraction and feature a three-dimensional network of vertex-sharing PN4-tetrahedra forming diverse-sized rings that are occupied by aluminum and alkaline earth ions. These structures represent another example of nitridophosphate-based networks that simultaneously incorporate AlN6-octahedra and alkaline-earth-centered polyhedra, with aluminum not participating in the tetrahedra network. They differ from previously reported ones by incorporating non-condensed octahedra instead of strongly condensed octahedra units and contribute to the diversity of multicationic nitridophosphate network structures. The results are supported by atomic resolution EDX mapping, solid-state NMR and FTIR measurements. Eu2+-doped samples show strong luminescence with narrow emissions in the range of green to blue under UV excitation, marking another instance of Eu2+-luminescence within imidonitridophosphates.

Cr5.7Si2.3P8N24-A Chromium(+IV) Nitridosilicate Phosphate with Amphibole-Type Structure.

The first nitridic analog of an amphibole mineral, the quaternary nitridosilicate phosphate Cr5.7Si2.3P8N24 was synthesized under high-pressure high-temperature conditions at 1400 °C and 12 GPa from the binary nitrides Cr2N, Si3N4 and P3N5, using NH4N3 and NH4F as additional nitrogen source and mineralizing agent, respectively. The crystal structure was elucidated by single-crystal X-ray diffraction with microfocused synchrotron radiation (C2/m, a=9.6002(19), b=17.107(3), c=4.8530(10) Å, ß=109.65(3)°). The elemental composition was analyzed by energy dispersive X-ray spectroscopy. The structure consists of vertex-sharing PN4-tetrahedra forming zweier double chains and edge-sharing (Si,Cr)-centered octahedra forming separated ribbons. Atomic resolution scanning transmission electron microscopy shows ordered Si and Cr sites next to a disordered Si/Cr site. Optical spectroscopy indicates a band gap of 2.1 eV. Susceptibility measurements show paramagnetic behavior and support the oxidation state Cr+IV, which is confirmed by EPR. The comprehensive analysis expands the field of Cr-N chemistry and provides access to a nitride analog of one of the most prevalent silicate structures.

Incommensurately Modulated Cu0.9Pb1.2Sb2.9Se6 in the Lillianite Structure Type.

Samples with the nominal composition Cu0.9Pb1.2Sb2.9Se6 mainly contain a phase with incommensurately modulated lillianite-type structure with the respective composition. Single crystal diffraction with synchrotron radiation enabled a detailed refinement using the superspace group Cmcm(α00)00s with lattice parameters a = 4.16537(5), b = 14.0821(2), c = 19.8234(3) Å, and a modulation vector q = 0.6890(2)a* at room temperature. The structure is built up from tilted and distorted NaCl-type slabs that are interconnected by bicapped trigonal prisms, which mainly host Pb atoms, according to a 4L arrangement. Satellites up to the second order reveal positional and occupational modulation that mainly involves a sequence of Sb and Cu atoms and allows the Se substructure to adapt in a way that Sb and Cu feature predominantly octahedral and tetrahedral coordination, respectively. Above 523 K, satellite reflections disappear, and the crystal structure becomes more disordered with average coordination spheres of both Sb and Cu atoms corresponding to distorted octahedra. This phase transition leads to discontinuities in the evolution of lattice parameters and physical properties as functions of temperature. HRTEM investigations corroborate centrosymmetry and highlight atoms that are strongly affected by the modulation. Measurements of transport properties reveal a p-type semiconductor with a thermoelectric figure of merit up to 0.1 at 623 K. In accordance with B factor analysis, a small amount of substitution could increase zT significantly by optimizing the carrier concentration.

Cu1.5SeyTe1-y (y = 0.2-0.7): A Series of Narrow Band Gap Semiconductors with Low Thermal Conductivity at Ambient Temperature.

Coinage metal chalcogenides offer ideal prerequisites for high thermoelectric performance and sensor applications, with their usually low lattice thermal and high electrical conductivity, as well as small band gaps. In the solid solution Cu1.5SeyTe1-y we synthesized phase pure materials with y = 0.2-0.7 and characterized them concerning selected physical properties. X-ray crystal structure determination was performed for two representatives of the solid solution, Cu1.5Se0.3Te0.7 and Cu1.5Se0.5Te0.5. The entire series crystallizes cubically, in space group Pm3̅n. No structural changes are observed between room temperature and the synthesis temperature of 723 K. The conductivity measurements and Seebeck coefficients of Cu1.5Se0.3Te0.7 and Cu1.5Se0.5Te0.5 indicate that the two representatives are narrow band gap semiconductors (Eg 0.06-0.08 eV). Both compounds show positive Seebeck coefficients and reasonably low thermal conductivities at moderate temperatures. Cu1.5Se0.5Te0.5 is characterized by a bulk modulus of 40.9 GPa.

Tetra-Face-Capped Octahedra in a Tetrahedra Network - Structure Determination and Scanning Transmission Electron Microscopy of SrAl5 P4 N10 O2 F3.

Tetrahedra-based nitridophosphates show a rich structural chemistry, which can be further extended by incorporating cations in higher coordinated positions, for example, in octahedral voids or by substituting the nitrogen atoms in the network with other anions. Following this approach, SrAl5 P4 N10 O2 F3 was synthesized at high-temperature and high-pressure conditions using a multianvil press (1400 °C, 5 GPa) starting from Sr(N3 )2 , c-PON, P3 N5 , AlN, and NH4 F. SrAl5 P4 N10 O2 F3 crystallizes in space group I 4 ‾ m 2 ${I\bar 4m2}$ with a=11.1685(2) and c=7.84850(10) Å. Atomic-resolution EDX mapping with scanning transmission electron microscopy (STEM) indicates atom assignments, which are further corroborated by bond-valence sum (BVS) calculations. Ten Al3+ -centered octahedra form a highly condensed tetra-face-capped octahedra-based unit that is a novel structure motif in network compounds. A network of vertex-sharing PN4 tetrahedra and chains of face-sharing Sr2+ -centered cuboctahedra complement the structure. Eu2+ -doped SrAl5 P4 N10 O2 F3 shows blue emission (λem= 469 nm, fwhm=98 nm; 4504 cm-1 ) when irradiated with UV light.

Combining MN6 Octahedra and PN5 Trigonal Bipyramids in the Mica-like Nitridophosphates MP6 N11 (M=Al, In).

Layered silicates are a very versatile class of materials with high importance to humanity. The new nitridophosphates MP6 N11 (M=Al, In), synthesized from MCl3 , P3 N5 and NH4 N3 in a high-pressure high-temperature reaction at 1100 °C and 8 GPa, show a mica-like layer setup and feature rare nitrogen coordination motifs. The crystal structure of AlP6 N11 was elucidated from synchrotron single-crystal diffraction data (space group Cm (no. 8), a=4.9354(10), b=8.1608(16), c=9.0401(18) Å, ß=98.63(3)°), enabling Rietveld refinement of isotypic InP6 N11 . It is built up from layers of PN4 tetrahedra, PN5 trigonal bipyramids and MN6 octahedra. PN5 trigonal bipyramids have been reported only once and MN6 octahedra are sparsely found in the literature. AlP6 N11 was further characterized by energy-dispersive X-ray (EDX), IR and NMR spectroscopy. Despite the vast amount of known layered silicates, there is no isostructural compound to MP6 N11 as yet.

Modular Principle for Complex Disordered Tetrahedral Frameworks in Quenched High-Pressure Phases of Phosphorus Oxide Nitrides.

Invited for the cover of this issue are the groups of Oliver Oeckler at Leipzig University and Wolfgang Schnick at University of Munich (LMU). The image background depicts a diffraction pattern of an intergrown crystal containing P40 O31 N46 as a night sky. P40 O31 N46 and P74 O59 N84 form complex disordered frameworks, a cutout of which symbolizes the earth's surface (which mainly contains silicates with related building blocks). The structures are built up from chain-like building units, which fall like rain, symbolizing the modular building scheme. Read the full text of the article at 10.1002/chem.202203892.

Comprehensive Investigation of Anion Species in Crystalline Li+ ion Conductor Li27-x [P4 O7+x N9-x ]O3 (x≈1.9(3)).

The Li+ ion conductor Li27-x [P4 O7+x N9-x ]O3 (x≈1.9) has been synthesized from P3 N5 , Li3 N and Li2 O in a Ta ampoule at 800 °C under Ar atmosphere. The cubic compound crystallizes in space group I 4 ‾ 3 d ${I\overline 4 3d}$ with a=12.0106(14) Å and Z=4. It contains both non-condensed [PO2 N2 ]5- and [PO3 N]4- tetrahedra as well as O2- ions, surrounded by Li+ ions. Charge neutrality is achieved by partial occupancy of Li positions, which was refined with neutron powder diffraction data. Measurements of the partial ionic and electronic conductivity show a total ionic conductivity of 6.6×10-8  S cm-1 with an activation energy of 0.46±0.02 eV and a bulk ionic conductivity of 4×10-6  S cm-1 at 25 °C, which is close to the ionic conductivity of amorphous lithium nitridophosphate. This makes Li27-x [P4 O7+x N9-x ]O3 an interesting candidate for investigation of structural factors affecting ionic conductivity in lithium oxonitridophosphates.

Modular Principle for Complex Disordered Tetrahedral Frameworks in Quenched High-Pressure Phases of Phosphorus Oxide Nitrides.

The crystal structures of the new phosphorus oxide nitrides P40 O31 N46 and P74 O59 N84 , which were synthesized from amorphous phosphorus oxide nitride imide, exhibit complex frameworks built up from P(O,N)4 tetrahedra. The latter form various chain-like building units with various degrees of branching. These modular units can be combined and arranged in different ways, which leads to closely related structures and several disordered configurations in each compound. As the material was obtained by high-pressure high-temperature synthesis, the disorder is most likely a consequence of quenching a high-pressure phase with P(O,N)5 trigonal bipyramids. Under ambient conditions, P atoms are expected to relax by moving to the centers of the face-sharing tetrahedra that constitute the bipyramid. Diffraction patterns acquired with microfocused synchrotron radiation reveal that domains of both compounds are intergrown with H3 P8 O8 N9 , whose tetrahedral framework represents a cutout of the structures of both P40 O31 N46 and P74 O59 N84 . Powder diffraction patterns do not indicate any further phases.

Pnictide-Capped Butterfly Cluster in the Crystal Structure of Nb4PnX11 (Pn = N, P; X = Cl, Br, I).

Niobium pnictide halides Nb4PnX11 (Pn = N, P; X = Cl, Br, I) are reported with their average crystal structures. Individual pnictide-capped butterfly cluster cores [Nb4P] in the structure are interconnected into two-dimensional layers, with their electronic and magnetic properties being analyzed.

Temperature-dependent Cu and Ag ion mobility and associated changes of transport properties in pavonite-type Cu1.4Ag0.4Bi5.4Se9.

Cu1.4Ag0.4Bi5.4Se9, the first quaternary compound in the system Cu/Ag/Bi/Se, was obtained from the elements by melt synthesis after pre-reaction and annealing steps. It exhibits a 4P pavonite-type crystal structure in the spacegroup C2/m, which consists of NaCl-type building blocks extending in two dimensions that are separated by rods of edge-sharing BiSe7 polyhedra and "clusters" of several partially occupied Cu atom sites. Temperature-dependent single crystal X-ray diffraction up to 350 °C helped to explain thermoelectric properties. Cu atoms occupy more and different disordered sites at ≥200 °C. Ag atoms share Bi atom sites and prefer different sites as a function of temperature. Cu1.4Ag0.4Bi5.4Se9 is a metallic n-type thermoelectric material with Seebeck coefficients up to -150 µV K-1. Lattice thermal conductivity significantly decreases from 0.55 W mK-1 to 0.42 W mK-1 with increasing structural disorder. Cu1.4Ag0.4Bi5.4Se9 may thus be described with the phonon-liquid electron-crystal (PLEC) concept and reaches a figure of merit of zTmax = 0.23 at 450 °C. B-factor analysis based on a single parabolic band model shows that the chemical potential of electrons approaches the one corresponding to optimal charge carrier concentration, especially at higher temperatures. With respect to most properties and the easily reproducible synthesis, the compound can well compete with other sulfosalt-like thermoelectric materials and is considerably less toxic than most of them.

Discovery of Two Polymorphs of TiP4 N8 Synthesized from Binary Nitrides.

TiP4 N8 was obtained from the binary nitrides TiN and P3 N5 upon addition of NH4 F as a mineralizer at 8 GPa and 1400 °C. An intricate interplay of disorder and polymorphism was elucidated by in situ temperature-dependent single-crystal X-ray diffraction, STEM-HAADF, and the investigation of annealed samples. This revealed two polymorphs, which consist of dense networks of PN4 tetrahedra (degree of condensation κ=0.5) and either augmented triangular TiN7 prisms or triangular TiN6 prisms for α- and ß-TiP4 N8 , respectively. The structures of TiP4 N8 exhibit body-centered tetragonal (bct) framework topology. DFT calculations confirm the measured band gaps of α- and ß-TiP4 N8 (1.6-1.8 eV) and predict the thermochemistry of the polymorphs in agreement with the experiments.

Nitridic Analogs of Micas AESi3 P4 N10 (NH)2 (AE=Mg, Mg0.94 Ca0.06 , Ca, Sr).

We present the first nitridic analogs of micas, namely AESi3 P4 N10 (NH)2 (AE=Mg, Mg0.94 Ca0.06 , Ca, Sr), which were synthesized under high-pressure high-temperature conditions at 1400 °C and 8 GPa from the refractory nitrides P3 N5 and Si3 N4 , the respective alkaline earth amides, implementing NH4 F as a mineralizer. The crystal structure was elucidated by single-crystal diffraction with microfocused synchrotron radiation, energy-dispersive X-ray spectroscopic (EDX) mapping with atomic resolution, powder X-ray diffraction, and solid-state NMR. The structures consist of typical tetrahedra-octahedra-tetrahedra (T-O-T) layers with P occupying T and Si occupying O layers, realizing the rare motif of sixfold coordinated silicon atoms in nitrides. The presence of H, as an imide group forming the SiN4 (NH)2 octahedra, is confirmed by SCXRD, MAS-NMR, and IR spectroscopy. Eu2+ -doped samples show tunable narrow-band emission from deep blue to cyan (451-492 nm).

High-Pressure Synthesis of Sc5 P12 N23 O3 and Ti5 P12 N24 O2 by Activation of the Binary Nitrides ScN and TiN with NH4 F.

Multinary transition metal nitrides and oxonitrides are a versatile and intriguing class of compounds. However, they have been investigated far less than pure oxides. The compounds Sc5 P12 N23 O3 and Ti5 P12 N24 O2 have now been synthesized from the binary nitrides ScN and TiN, respectively, by following a high-pressure high-temperature approach at 8 GPa and 1400 °C. NH4 F acts as a mineralizing agent that supports product formation and crystallization. The starting materials ScN and TiN are seemingly an uncommon choice because of their chemical inertness but, nevertheless, react under these conditions. Sc5 P12 N23 O3 and Ti5 P12 N24 O2 crystallize isotypically with Ti5 B12 O26 , consisting of solely vertex-sharing P(O/N)4 tetrahedra forming two independent interpenetrating diamond-like nets that host TM(O/N)6 (TM=Sc, Ti) octahedra. Ti5 P12 N24 O2 is a mixed-valence compound and shows ordering of Ti3+ and Ti4+ ions.

Structure Elucidation of Complex Endotaxially Intergrown Lanthanum Barium Oxonitridosilicate Oxides by Combination of Microfocused Synchrotron Radiation and Transmission Electron Microscopy.

Single-crystalline domains in intergrown microcrystalline material of the new compounds Ba22.5+x La55-x [Si129 N240-x Ox ]O3 :Ce3+ and Ba25.5+x La77-x [Si170 N312-x O9+x ]O4 :Ce3+ were identified by transmission electron microscopy (TEM). Precise diffraction data from these domains were collected with microfocused synchrotron radiation so that crystal structure elucidation of the complex disordered networks became possible. They are composed of two different interconnected slabs of which one is similar in both compounds, which explains their notorious intergrowth. The distribution of Ba and La is indicated by the analysis of bond-valence sums and by comparison with isostructural Sr28.5+x La75-x [Si170 N312-x O9+x ]O4 . Ce3+ doping leads to yellow luminescence. This is a showcase that highlights the discovery and accurate characterization of new compounds relevant for luminescence applications from heterogeneous microcrystalline samples by exploiting the capability of the combination of TEM and diffraction using the latest focusing techniques for synchrotron radiation.

High-Pressure High-Temperature Synthesis of Mixed Nitridosilicatephosphates and Luminescence of AESiP3 N7 :Eu2+ (AE=Sr, Ba).

Tetrahedra-based nitrides with network structures have emerged as versatile materials with a broad spectrum of properties and applications. Both nitridosilicates and nitridophosphates are well-known examples of such nitrides that upon doping with Eu2+ exhibit intriguing luminescence properties, which makes them attractive for applications. Nitridosilicates and nitridophosphates show manifold structural variability; however, no mixed nitridosilicatephosphates except SiPN3 and SiP2N4NH have been described so far. The compounds AESiP3 N7 (AE=Sr, Ba) were synthesized by a high-pressure high-temperature approach using the multianvil technique (8 GPa, 1400-1700 °C) starting from the respective alkaline earth azides and the binary nitrides P3 N5 and Si3 N4 . The latter were activated by NH4 F, probably acting as a mineralizing agent. SrSiP3 N7 and BaSiP3 N7 were obtained as single crystals. They crystallized in the barylite-1O (M=Sr) and barylite-2O structure types (M=Ba), respectively, with P and Si being occupationally disordered. Cation disorder was further supported by solid-state NMR spectroscopy and energy-dispersive X-ray spectroscopy (EDX) mapping of BaSiP3 N7 with atomic resolution. Upon doping with Eu2+ , both compounds showed blue emission under UV excitation.

Characterization and Decomposition of the Natural van der Waals SnSb2Te4 under Compression.

High pressure X-ray diffraction, Raman scattering, and electrical measurements, together with theoretical calculations, which include the analysis of the topological electron density and electronic localization function, evidence the presence of an isostructural phase transition around 2 GPa, a Fermi resonance around 3.5 GPa, and a pressure-induced decomposition of SnSb2Te4 into the high-pressure phases of its parent binary compounds (α-Sb2Te3 and SnTe) above 7 GPa. The internal polyhedral compressibility, the behavior of the Raman-active modes, the electrical behavior, and the nature of its different bonds under compression have been discussed and compared with their parent binary compounds and with related ternary materials. In this context, the Raman spectrum of SnSb2Te4 exhibits vibrational modes that are associated but forbidden in rocksalt-type SnTe; thus showing a novel way to experimentally observe the forbidden vibrational modes of some compounds. Here, some of the bonds are identified with metavalent bonding, which were already observed in their parent binary compounds. The behavior of SnSb2Te4 is framed within the extended orbital radii map of BA2Te4 compounds, so our results pave the way to understand the pressure behavior and stability ranges of other "natural van der Waals" compounds with similar stoichiometry.

Nitridophosphate-Based Ultra-Narrow-Band Blue-Emitters: Luminescence Properties of AEP8 N14 :Eu2+ (AE=Ca, Sr, Ba).

The nitridophosphates AEP8 N14 (AE=Ca, Sr, Ba) were synthesized at 4-5 GPa and 1050-1150 °C applying a 1000 t press with multianvil apparatus, following the azide route. The crystal structures of CaP8 N14 and SrP8 N14 are isotypic. The space group Cmcm was confirmed by powder X-ray diffraction. The structure of BaP8 N14 (space group Amm2) was elucidated by a combination of transmission electron microscopy and diffraction of microfocused synchrotron radiation. Phase purity was confirmed by Rietveld refinement. IR spectra are consistent with the structure models and the chemical compositions were confirmed by X-ray spectroscopy. Luminescence properties of Eu2+ -doped samples were investigated upon excitation with UV to blue light. CaP8 N14 (λem =470 nm; fwhm=1380 cm-1 ) and SrP8 N14 (λem =440 nm; fwhm=1350 cm-1 ) can be classified as the first ultra-narrow-band blue-emitting Eu2+ -doped nitridophosphates. BaP8 N14 shows a notably broader blue emission (λem =417/457 nm; fwhm=2075/3550 cm-1 ).

A Layered Tin Bismuth Selenide with Three Different Building Blocks that Account for an Extremely Large Lattice Parameter of 283†Å.

The layered compound Sn2.8(4) Bi20.2(4) Se27 exhibits an extraordinarily long-periodic 150R stacking sequence. The crystal structure contains three different building blocks, which form upon the addition of Sn to a Bi-rich bismuth selenide. Sn-doped Bi2 double ("2") layers similar to those in elemental bismuth, Sn0.3 Bi1.7 Se3 quintuple ("5") layers and Sn0.4 Bi2.6 Se4 septuple ("7") layers are arranged in a 7525757525|7525757525|7525757525 sequence, which corresponds to a structure with a=4.1819(4) and c=282.64(6) Šin space group R 3 ‾ m. The structure of a microcrystal was determined using microfocused synchrotron radiation and refined as a formally commensurately modulated structure in (3+1)D superspace (superspace group R 3 ‾ m(00γ)00), with a trivial basic structure that contains just one atom. The stacking sequence as well as the cation distribution are confirmed by aberration-corrected scanning transmission electron microscopy (STEM) in combination with chemical mapping by X-ray spectroscopy with atomic resolution. Stacking faults are not typical but have been observed occasionally.

BaP6 N10 NH:Eu2+ as a Case Study-An Imidonitridophosphate Showing Luminescence.

Barium imidonitridophosphate BaP6 N10 NH was synthesized at 5 GPa and 1000 °C with a high-pressure high-temperature approach using the multianvil technique. Ba(N3 )2 , P3 N5 and NH4 Cl were used as starting materials, applying a combination of azide and mineralizer routes. The structure elucidation of BaP6 N10 NH (P63 , a=7.5633(11), c=8.512(2) Å, Z=2) was performed by a combination of transmission electron microscopy and single-crystal diffraction with microfocused synchrotron radiation. Phase purity was verified by Rietveld refinement. 1 H and 31 P solid-state NMR and FTIR spectroscopy are consistent with the structure model. The chemical composition was confirmed by energy-dispersive X-ray spectroscopy and CHNS analyses. Eu2+ -doped samples of BaP6 N10 NH show blue emission upon excitation with UV to blue light (λem =460 nm, fwhm=2423 cm-1 ) representing unprecedented Eu2+ -luminescence of an imidonitride.