Graphene oxide‐wrapped amorphous copper vanadium oxide is fabricated through a template‐engaged redox reaction followed by vacuum dehydration. This material exhibits high reversible capacity, excellent rate capability, and out standing high‐rate cyclability. The outstanding performance is attributed to the fast capacitive charge storage and the in situ formed copper with enhanced electrical conductivity.

Conversion/alloying reactions, in which more lithium ions are involved, are severely handicapped by the dramatic volume changes. A facile and versatile strategy has been developed for integrating the SnO2 nanorod array in the PPy nanofilm for providing a flexible confinement for anchoring each nanorod and maintaining the entire structural integrity and providing sustainable contact; therefore, exhibiting much more stable cycling stability (701 mA h g(-1) after 300 cycles) and better high-rate capability (512 mA h g(-1) at 3 A g(-1)) when compared with the core-shell SnO2-PPy NA.

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Liquid metals have been widely used as substrates to grow graphene and other 2D materials. On a homogeneous and isotropic liquid surface, a polycrystalline 2D material is formed by coalescence of many randomly nucleated single‐crystal islands, and as a result, the domains in a polycrystal are expected to be randomly aligned. Here, we report the unexpected finding that only 30°‐twinned graphene polycrystals are grown on a liquid Cu surface. Atomic simulations confirm that the unique domain alignment in graphene polycrystals is due to the free rotation of graphene islands on the liquid Cu surface and the highly stable 30°‐grain boundaries in graphene. In‐depth analysis predicts 30 types of possible 30°‐twinned graphene polycrystals and 27 of them are observed. The revealed formation mechanism of graphene polycrystals on a liquid Cu surface deepens our fundamental understanding on polycrystal growth and could serve as a guideline for the controlled synthesis of 2D materials.