α-MnO₂nanotubes-supported Co₃O₄(Co₃O₄/MnO₂) and its carbon nanotubes (CNTs)-hybrids (Co₃O₄/MnO₂-CNTs) have been successfully developed through a facile two-pot precipitation reaction and hydrothermal process, which exhibit the superior bi-functional catalytic activity for both ORR and OER. The high performance is believed to be induced by the hybrid effect among MnO₂nanotubes, hollow Co₃O₄and CNTs, which can produce a synergetic enhancement. When integrated into the practical primary and electrochemically rechargeable Zn-air batteries, such a hybrid catalyst can give a discharge peak power density as high as 450 mW cm⁻². At 1.0 V of cell voltage, a current density of 324 mA cm⁻²is achieved. This performance is superior to all reported non-precious metal catalysts in literature for zinc-air batteries and significantly outperforms the state-of-the-art platinum-based catalyst. Particularly, the rechargeable Zn-air battery can be fabricated into all-solid-state one through a simple solid-state approach, which exhibits an excellent peak power density of 62 mW cm⁻², and the charge and discharge potentials remain virtually unchanged during the overall cycles, which is comparable to the one with liquid electrolyte.

Although lithium (Li) and sodium (Na) metals can be selected as the promising anode materials for next‐generation rechargeable batteries of high energy density, their practical applications are greatly restricted by the uncontrollable dendrite growth. Herein, a platinum (Pt)–copper (Cu) alloy‐coated Cu foam (Pt–Cu foam) is prepared and then used as the substrate for Li and Na metal anodes. Owing to the ultrarough morphology with a three‐dimensional porous structure and the quite large surface area as well as lithiophilicity and sodiophilicity, both Li and Na dendrite growths are significantly suppressed on the substrate. Moreover, during Li plating, the lithiated Pt atoms can dissolve into Li phase, leaving a lot of microsized holes on the substrate. During Na plating, although the sodiated Pt atoms cannot dissolve into Na phase, the sodiation of Pt atoms elevates many microsized blocks above the current collector. Either the holes or the voids on the surface of Pt–Cu foam what can be extra place for deposited alkali metal, what effectively relaxes the internal stress caused by the volume exchange during Li and Na plating/stripping. Therefore, the symmetric batteries of Li@Pt–Cu foam and Na@Pt–Cu foam have both achieved long‐term cycling stability even at ultrahigh areal capacity at 20 mAh cm⁻².

With the increasing power density of electrical and electronic devices, there has been an urgent demand for the development of thermal interface materials (TIMs) with high through-plane thermal conductivity for handling the issue of thermal management. Graphene exhibited significant potential for the development of TIMs, due to its ultra-high intrinsic thermal conductivity. In this perspective, we introduce three state-of-the-art graphene-based TIMs, including dispersed graphene/polymers, graphene framework/polymers and inorganic graphene-based monoliths. The advantages and limitations of them were discussed from an application point of view. In addition, possible strategies and future research directions in the development of high-performance graphene-based TIMs are also discussed.