The diffraction beamline BM01A at the European Synchrotron Radiation Facility (CRG Swiss-Norwegian beamlines) has been successfully operational for 20 years. Recently, a new multifunctional diffractometer based on the Dectris Pilatus 2M detector has been constructed, commissioned and offered to users. The diffractometer combines a fast and low-noise area detector, which can be tilted and moved horizontally and vertically, together with flexible goniometry for sample positioning and orientation. The diffractometer is controlled by a user-friendly and GUI-based software Pylatus which is also used to control various auxiliary equipment. The latter includes several heating and cooling devices, in situ cells and complimentary spectroscopic tools.

The counterintuitive phenomenon of negative linear compressibility (NLC) is a highly desirable but rare property exploitable in the development of artificial muscles, actuators and next-generation pressure sensors. In all cases, material performance is directly related to the magnitude of intrinsic NLC response. Here we show the molecular framework material zinc(II) dicyanoaurate(I), Zn[Au(CN)(2)](2), exhibits the most extreme and persistent NLC behaviour yet reported: under increasing hydrostatic pressure its crystal structure expands in one direction at a rate that is an order of magnitude greater than both the typical contraction observed for common engineering materials and also the anomalous expansion in established NLC candidates. This extreme behaviour arises from the honeycomb-like structure of Zn[Au(CN)(2)](2) coupling volume reduction to uniaxial expansion, and helical Au…Au 'aurophilic' interactions accommodating abnormally large linear strains by functioning as supramolecular springs.

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A highly porous form of Mg(BH4)2 (see picture; Mg green, BH4 blue, unit cells shown in red) reversibly absorbs H2, N2, and CH2Cl2. At high pressures, this material transforms into an interpenetrated framework that has 79 % higher density than the other polymorphs. Mg(BH4)2 can act as a coordination polymer that has many similarities to metal–organic frameworks

Expansion under compression: The unit‐cell volume of graphite oxide pressurized in water media, continuously increases reaching a sharp maximum at ca. 1.3–1.5 GPa (see picture, squares). Expansion of the lattice to a maximum of about 28–30 % is because of gradual pressure‐induced water insertion into the interlayer space of graphite oxide. The effect is reversible (triangles), resulting in a unique “breathing” of the structure upon pressure variation.

Hoch besetzt: Eine hoch poröse Form von Mg(BH4)2 (siehe Bild; Mg grün, BH4 blau, Elementarzellen rot) adsorbiert H2, N2 und CH2Cl2 reversibel. Bei hohen Drücken wandelt sich das Material in ein verschachteltes Gerüst um, das eine um 79 % höhere Dichte als die anderen Polymorphe aufweist. Mg(BH4)2 kann als ein Koordinationspolymer wirken, das starke Ähnlichkeiten mit Metall‐organischen Gerüsten aufweist.

Our combined theoretical and experimental investigations have led to the discovery of a new polymorph of titanium dioxide, where titanium is seven-coordinated to oxygen in the orthorhombic OI ( Pbca) structure. The zero-pressure bulk modulus of the new phase measured in the pressure range 19 to 36 GPa is 318(3) GPa. We demonstrate that the group IVa dioxides (TiO2, ZrO2, HfO2) on compression at ambient temperature all follow the common path: rutile -->alpha-PbO2-type --> baddeleyite-type (MI) --> orthorhombic OI (Pbca) structure --> cotunnite-type (OII).

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