Lithium metal batteries (LMBs) promise high-energy-density storage but face safety issues due to dendrite-induced lithium deposition, irreversible electrolyte consumption, and large volume changes, which hinder their practical applications. To address these issues, tuning lithium deposition by structuring a host for the lithium metal anode has been recognized as an efficient method. Herein, we report a supercritical water molecular scissor-controlled strategy to form a carbon framework derived from biomass wood. Proximate-supercritical water treatment is used to selectively cleave the β-O-4 bonds in lignin, with the extent of degradation controlled by adjusting the treatment environment's acidity. The enhanced thermal power of supercritical water molecules significantly accelerates the etching rate of lignin, increasing the porosity and permeability of the transformed carbon framework. Experimental results and multi-physics simulations show that the interconnected carbon-based pores and inner skeletal multilevel hierarchical structure facilitate rapid electron and ion transfer during battery operation and enhance electrolyte infiltration. Impressively, the as-obtained lithium metal anode exhibits long-term cycling stability for over 2000 hours at 0.5 mA cm-2 with low voltage overpotential. The water-treated Pinus (WTP)-Li//LiCoO2 full cells maintain a high capacity retention rate of 93.3% and a specific capacity of 142 mA h g-1 at 0.5C for 100 cycles.
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