Self-Assembly Monolayer Inspired Stable Artificial Solid Electrolyte Interphase Design for Next-Generation Lithium Metal Batteries.

Lithium metal is widely regarded as the "ultimate" anode for energy-dense Li batteries, but its high reactivity and delicate interface make it prone to dendrite formation, limiting its practical use. Inspired by self-assembled monolayers on metal surfaces, we propose a facile yet effective strategy to stabilize Li metal anodes by creating an artificial solid electrolyte interphase (SEI). Our method involves dip-coating Li metal in MPDMS to create an SEI layer that is rich in inorganic components, allowing uniform Li plating/stripping under a low overpotential over 500 cycles in carbonate electrolytes. In comparison, pristine Li metal shows a rapid increase in overpotential after merely 300 cycles, leading to failure soon after. Molecular dynamics simulations demonstrate that this uniform artificial SEI suppresses Li dendrite formation. We further demonstrated its enhanced stability pairing with LiFePO4 and LiNi1-x-yCoxMnyO2 cathodes, highlighting the proposed strategy as a promising solution for practical Li metal batteries.

High-pressure carbon dioxide-hydrothermal enhance yield and methylene blue adsorption performance of banana pseudo-stem activated carbon.

In order to reduce environmental risks and fungus disease spread of banana waste, the high-pressure CO2-hydrothermal treatment was developed to produce hydrochar as a precursor of activated carbon from banana pseudo-stem(BP). SEM, BET, XRD, Raman and FTIR was used to investigate the influence mechanism of the high-pressure CO2-hydrothermal pretreatment on the yield and methylene blue(MB) adsorption capacities of the activated carbon. The results show that although the adsorption capacities of BP after high-pressure CO2-hydrothermal pretreatment(BPx) is decrease due to decrease of oxygen-containing functional group and flatter spatial structure, that of BPx after KOH activation(BPx-A) significantly increase and is higher than that of BP by direct KOH activation(BP-A). Because BP-A presents honeycomb porous microstructures and has a higher mesoporous structure(138-472 m2/g), plentiful active sites and rich the abundant influential adsorption group of MB adsorption. In addition, compared to BP-A(0.68%), the total yield of BPx-A(2.42-9.11%) is 356-1340%.