Boosting Lithium Storage in Free-Standing Black Phosphorus Anode via Multifunction of Nanocellulose.

Layer-structured black phosphorus (BP) demonstrating high specific capacity has been viewed as a very promising anode material for future high-energy-density Li-ion batteries (LIBs). However, its practical application is hindered by large volume change of BP and poor mechanical stability of BP anodes by traditional slurry casting technology. Here, a free-standing flexible anode composed of BP nanosheets and nanocellulose (NC) nanowires is fabricated via a facile vacuum-assisted filtration approach. The constructed free-standing BP@NC composite anode offers three-dimensional (3D) mixed-conducting network for Li/e transports. The substrate of NC film has a certain flexibility up to 10.2% elongation that can restrain the volume change of BP and electrode during operation. In addition, molecular dynamic (MD) simulation and density function theory (DFT) show the greatly enhanced Li diffusion in BP@NC composite where the Li ions receive less repulsive force at the interface of BP interlayer and nanocellulose. Benefiting from above multifunction of nanocellulose, the BP@NC composite exhibits high capacities of 1020.1 mAh g at 0.1 A g after 230 cycles and 994.4 mAh g at 0.2 A g after 400 cycles, corresponding to high capacity retentions of 87.1% and 84.9%, respectively. Our results provide a low-cost and effective strategy to develop advanced electrodes for next-generation rechargeable batteries.