Lithium (Li) metal anodes have attracted much interest recently for high‐energy battery applications. However, low coulombic efficiency, infinite volume change, and severe dendrite formation limit their reliable implementation over a wide range. Here, an outstanding stability for a Li metal anode is revealed by designing a highly porous and hollow Li foam. This unique structure is capable of tackling many Li metal problems simultaneously: first, it assures uniform electrolyte distribution over the inner and outer electrode's surface; second, it reduces the local current density by providing a larger electroactive surface area; third, it can accommodate volume expansion and dissipate heat efficiently. Moreover, the structure shows superior stability compared to fully Li covered foam with low porosity, and bulky Li foil electrode counterparts. This Li foam exhibits small overpotential (≈25 mV at 4 mA cm⁻²) and high cycling stability for 160 cycles at 4 mA cm⁻². Furthermore, when assembled, the porous Li metal as the anode with LiFePO₄ as the cathode for a full cell, the battery has a high‐rate performance of 138 mAh g⁻¹ at 0.2 C. The beneficial structure of the Li hollow foam is further studied through density functional theory simulations, which confirms that the porous structure has better charge mobility and more uniform Li deposition.

Sapphire has been the most widely used substrate material in LEDs, and the demand for non-C-planes crystal is increasing. In this paper, four crystal planes of the A-, C-, M- and R-plane were selected as the research objects. Nanoindentation technology and chemical mechanical polishing technology were used to study the effect of anisotropy on material properties and processing results. The consequence showed that the C-plane was the easiest crystal plane to process with the material removal rate of 5.93 nm/min, while the R-plane was the most difficult with the material removal rate of 2.47 nm/min. Moreover, the research results have great guiding significance for the processing of sapphire with different crystal orientations.

Nanoindentation technology has been widely adopted to study creep behavior in small regions. However, nanoindentation creep behavior of metallic glass is still not well understood. In the present work, we investigated nanoindentation size effects on creep deformation in a Zr-based bulk metallic glass at room temperature. The total creep strain and strain rate of steady-state creep were gradually decreased with increasing holding depth under a Berkovich indenter, indicating a length-scale-dependent creep resistance. For a spherical indenter, creep deformations were insignificant in elastic regions and then greatly enhanced by increasing holding strain in plastic regions. Strain rate sensitivities (SRS) decreased with increasing holding depth and holding strain at first, and then stabilized as holding depth was beyond about 500 nm for both indenters. SRS values were 0.4–0.5 in elastic regions, in which atomic diffusion and free volume migration could be the creep mechanism. On the other hand, evolution of the shear transformation zone was suggested as a creep mechanism in plastic regions, and the corresponding SRS values were in the range of 0.05 to 0.3.