Conventional graphitic anodes in lithium-ion batteries cannot provide high-power densities due to slow diffusivity of lithium ions in the bulk electrode material. Here we report photoflash and laser-reduced free-standing graphene paper as high-rate capable anodes for lithium-ion batteries. Photothermal reduction of graphene oxide yields an expanded structure with micrometer-scale pores, cracks, and intersheet voids. This open-pore structure enables access to the underlying sheets of graphene for lithium ions and facilitates efficient intercalation kinetics even at ultrafast charge/discharge rates of >100 C. Importantly, photothermally reduced graphene anodes are structurally robust and display outstanding stability and cycling ability. At charge/discharge rates of ~40 C, photoreduced graphene anodes delivered a steady capacity of ~156 mAh/g(anode) continuously over 1000 charge/discharge cycles, providing a stable power density of ~10 kW/kg(anode). Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization.

Most attempts to emulate the mechanical properties of strong and tough natural composites using helicoidal films of wood-derived cellulose nanocrystals (w-CNCs) fall short in mechanical performance due to the limited shear transfer ability between the w-CNCs. This shortcoming is ascribed to the small w-CNC-w-CNC overlap lengths that lower the shear transfer efficiency. Herein, we present a simple strategy to fabricate superior helicoidal CNC films with mechanical properties that rival those of the best natural materials and are some of the best reported for photonic CNC materials thus far. Assembling the short w-CNCs with a minority fraction of high aspect ratio CNCs derived from tunicates (t-CNCs), we report remarkable simultaneous enhancement of all in-plane mechanical properties and out-of-plane flexibility. The important role of t-CNCs is revealed by coarse grained molecular dynamics simulations where the property enhancement are due to increased interaction lengths and the activation of additional toughening mechanisms. At t-CNC contents greater than 5% by mass the mixed films also display UV reflecting behaviour. These damage tolerant optically active materials hold great promise for application as protective coatings. More broadly, we expect the strategy of using length-bidispersity to be adaptable to mechanically enhancing other matrix-free nanoparticle ensembles.

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