Nanofluidic-enhanced high-mass-loading electrodes for energy-dense and high-rate lithium–sulfur batteries†
Abstract
High-mass-loading sulfur cathodes with high areal capacity are critical for developing energy-dense lithium–sulfur (Li–S) batteries. However, facilitating efficient Li+ ion and electron transport in high-mass-loading sulfur electrodes remains a great challenge due to the extended pathways and inferior ion-electron transfer, especially at a high charge/discharge rate. To address the issue, we develop an ion-gated coating layer inspired by the nanofluidic effects in organisms (IGCL-NFE), which enhances the Li+ diffusion coefficient (D) and transference number (μ+) to enable ultrafast and selective Li+ transport in thick sulfur electrodes. The IGCL-NFE exhibits a characteristic biomimetic nanofluidic ion transport behavior, yielding a high μ+ (∼2.1 times higher than that in the bulk solution) and a high D (∼1012 times higher than that in the bulk solution) at a low Li salt concentration of 10−6 mol L−1. With selective and fast Li+ conduction, coupled with the high electrical conductivity of the IGCL-NFE, the IGCL-NFE-enhanced sulfur cathode demonstrates exceptional rate performance (757.8 mAh g−1 after 300 cycles) at a high rate of 10.0 C. As a proof of concept, Li–S batteries utilizing the dry electrode with an ultrahigh sulfur loading of 18.7 mg cm−2 achieve an impressive energy density of 430.6 Wh kg−1. Furthermore, the Li–S full cell exhibits stable cycling performance over 100 cycles, retaining a high capacity of 1313.9 mAh g−1 even at −20 °C. The nature-inspired, nanofluidic-enhanced electrode design presents a promising strategy for developing ultrahigh-mass-loading and high-rate Li–S batteries.