The mechanical properties of metallic materials often degrade under harsh cryogenic conditions, posing challenges for low-temperature infrastructures¹. Here we introduce a dual-scale atomic-ordering nanostructure, characterized by an exceptionally high number density of co-existing subnanoscale short-range ordering (approximately 2.4 × 10²⁶ m⁻³) and nanoscale long-range ordering (approximately 4.5 × 10²⁵ m⁻³) domains, within a metallic solid-solution matrix in a CoNiV-based alloy to improve the synergy of strength and ductility at low temperatures. We observe an ordering-induced increase in dislocation shear stress as well as a more rapid dislocation multiplication owing to the dislocation blocking effect of nanoscale long-range ordering and the associated generation of new dislocations. The latter effect also releases stress concentrations at nanoscale long-range-ordered obstacles that otherwise would promote damage initiation and failure. Consequently, the alloy shows a strength–elongation product of 76 GPa % with a yield strength of approximately 1.2 GPa at 87 K, outperforming materials devoid of such ordering hierarchy, containing only short-range ordered or coherent precipitates of a few tens of nanometres. Our results highlight the impact of dual co-existing chemical ordering on the mechanical properties of complex alloys and offer guidelines to control these ordering states to enhance their mechanical performance for cryogenic applications.

In the past decades, the families of negative thermal expansion (NTE) materials have been in the uninterrupted growth with more new NTE materials reported; in particular, metal fluorides as the new members begin to draw attention. Herein, recent progress on the NTE properties of metal fluorides is reviewed, including compounds, mechanisms and the control of thermal expansion. Although some achievements have been made, there are still great development prospects. More in-depth investigations on metal fluorides with NTE behavior are expected

The near-zero temperature coefficient of resistivity (NZ-TCR) behavior is reported in the antiperovskite compounds Mn_3+xNi_1−xN (0 ≤ x ≤ 0.333). Our results indicate that the broad temperature range (above 275 K extending to above 220 K) of NZ-TCR is obtained by Mn doping at the Ni site. The short-range magnetic ordering is revealed by both neutron powder diffraction and inverse magnetic susceptibility. Further, we find a strong correlation between the anomalous resistivity change of Mn_3+xNi_1−xN from the metal-like to the NZ-TCR behavior and the lack of the long-range magnetic ordering. The possible mechanism of NZ-TCR behavior is discussed using the spin-disorder scattering model.

Resistivity measurements are widely exploited to uncover electronic excitations and phase transitions in metallic solids. While single crystals are preferably studied to explore crystalline anisotropies, these usually cancel out in polycrystalline materials. Here we show that in polycrystalline Mn₃Zn_0.5Ge_0.5N with non-collinear antiferromagnetic order, changes in the diagonal and, rather unexpected, off-diagonal components of the resistivity tensor occur at low temperatures indicating subtle transitions between magnetic phases of different symmetry. This is supported by neutron scattering and explained within a phenomenological model which suggests that the phase transitions in magnetic field are associated with field induced topological orbital momenta. The fact that we observe transitions between spin phases in a polycrystal, where effects of crystalline anisotropy are cancelled suggests that they are only controlled by exchange interactions. The observation of an off-diagonal resistivity extends the possibilities for realising antiferromagnetic spintronics with polycrystalline materials.