Demonstrates enhanced capacity and rate performance in rechargeable Li–Cl2 batteries, suggesting improved energy density for practical applications.
Rechargeable Li─Cl 2 batteries represent a promising high‐energy‐density technology. However, the open‐pore structure of conventional cathode materials poses a fundamental challenge by permitting the uncontrolled diffusion of Cl 2 into the electrolyte, resulting in severe local concentration dilution that plagues rate capability and specific capacity. Herein, a self‐confinement strategy by hollow carbon nanoreactors (HCNRs) is proposed to regulate the local concentration of active Cl 2 species with micropores (≈0.8 nm) on their walls. These micropores act as size‐selective barriers, allowing to block the escape of larger active Cl 2 species (kinetic diameter ≈0.86 nm), and mesopores (30–50 nm) function as nanoreactors that concentrate active Cl 2 species. This design enables the as‐assembled Li─Cl 2 cell to achieve an ultrahigh current density of 100 mA cm −2 during the charge/discharge process and a record‐breaking specific capacity of 8000 mAh g −1 (9 mAh cm −2 ), superior to the reported literature. This hollow nanoreactor design highlights the potential of Li─Cl 2 batteries as high‐power and energy‐dense systems, paving the way for their practical application.
No takes yet. Share an insight, caveat, or question.
Xu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: