Nanolattices exhibit attractive mechanical properties such as high strength, high specific strength, and high energy absorption. However, at present, such materials cannot achieve effective fusion of the above properties and scalable production, which hinders their applications in energy conversion and other fields. Herein, we report gold and copper quasi-body centered cubic (quasi-BCC) nanolattices with the diameter of the nanobeams as small as 34 nm. We show that the compressive yield strengths of quasi-BCC nanolattices even exceed those of their bulk counterparts, despite their relative densities below 0.5. Simultaneously, these quasi-BCC nanolattices exhibit ultrahigh energy absorption capacities, i.e., 100 ± 6 MJ m⁻³ for gold quasi-BCC nanolattice and 110 ± 10 MJ m⁻³ for copper quasi-BCC nanolattice. Finite element simulations and theoretical calculations reveal that the deformation of quasi-BCC nanolattice is dominated by nanobeam bending. And the anomalous energy absorption capacities substantially stem from the synergy of the naturally high mechanical strength and plasticity of metals, the size reduction-induced mechanical enhancement, and the quasi-BCC nanolattice architecture. Since the sample size can be scaled up to macroscale at high efficiency and affordable cost, the quasi-BCC nanolattices with ultrahigh energy absorption capacity reported in this work may find great potentials in heat transfer, electric conduction, catalysis applications.

In polycrystalline metals, plastic deformation is accompanied by lattice rotations resulting from dislocation glide. Following these rotations in three dimensions requires nondestructive methods that so far have been limited to grain sizes at the micrometer scale. We tracked the rotations of individual grains in nanograined nickel by using three-dimensional orientation mapping in a transmission electron microscope before and after in situ nanomechanical testing. Many of the larger-size grains underwent unexpected lattice rotations, which we attributed to a reversal of rotation during unloading. This inherent reversible rotation originated from a back stress–driven dislocation slip process that was more active for larger grains. These results provide insights into the fundamental deformation mechanisms of nanograined metals and will help to guide strategies for material design and engineering applications.

Ru/B₄C multilayer mirrors are used for hard X-ray monochromators with moderate spectral resolution and high integral flux. To overcome the problem of large compressive stress inherent in Ru/B₄C multilayers, a reactive sputtering technique using a mixture working gas of argon and nitrogen with different partial pressures was tested, and the fabricated multilayers had a period of 3 nm. The intrinsic stress was essentially reduced after nitridation and relaxed to zero value at approximately 15% partial pressure of nitrogen in the working gas. Interface roughness was slightly increased which can be caused by the polycrystalline structure inside the nitridated samples. More importantly, the nitridated multilayers showed an enhanced reflectance (67% at 8.04 keV photon energy) as compared with the one fabricated with pure Ar (54%). The structure analysis with transmission electron microscopy and X-ray photoelectron spectroscopy demonstrated that nitrogen incorporated into a multilayer structure was mostly located in the B₄C layers forming BN compounds, which suppressed the diffusion of boron, stabilized the interfaces and enhanced the reflectance.