Rolling up MXene sheets into scrolls to promote their anode performance in lithium-ion batteries

Although Ti3 C2 MXene sheets have attracted extensive attention in lithium-ion storage techniques,their restacking makes against and even hinders the Li ions diffusion within them,thereby decreasing the capacity as well as rate performance of conventional MXene anode.Here,for the first time,we roll up the Ti3 C2 Tx sheets into scrolls with unclosed topological structure and the interlayer galleries to alleviate the restacking problem.Thus,Ti3 C2 Tx scrolls as anode materials in lithium-ion batteries(LIBs)have higher capacity and better rate performance than Ti3 C2 Tx sheets.On the bases of these,high-capacity silicon nanoparticles are added during the rolling process to in-situ produce Ti3 C2 Tx/Si composite scrolls.The addition of 10%silicon nanoparticles shows the best overall improvement among capacity,rate capability and cyclic stability for Ti3 C2 Tx scrolls.

All-climate aqueous supercapacitor enabled by a deep eutectic solvent electrolyte based on salt hydrate

Aqueous supercapacitors(SCs)have received considerable attention owing to the utilization of low-cost,non-flammable,and low-toxicity aqueous electrolytes thus could eliminate the safety and cost concerns,but their wide temperature range applications have generally suffered from frozen of electrolyte and insufficient ionic conductivity at low temperatures.Herein,we demonstrate the feasibility of using an unconventional Deep Eutectic Solvent(DES)based on H2O-Mg(ClO4)2·6 H2O binary system as electrolyte to construct all-climate aqueous carbon-based SC.This unconventional class DES completely base on inorganic substances and achieving simply mix inexpensive salts and water together at the right proportions.Attributed to the attractive feature of extremely low freeze temperature of-69℃,this electrolyte can enable the 1.8 V carbon-based SC to fully work at-40℃with outstanding cycling stability.This DES electrolyte comprising of a single salt and a single solvent without any additive will open up an avenue for developing simple and green electrolytes to construct all-climate SC.

Recovering the electrochemical window by forming a localized solvation nanostructure in ionic liquids with trace water

Motivated by the fascinating merits of wide electrochemical stability window(ESW)and nonflammability,ionic liquids(ILs)have been utilized as advanced electrolytes in various emerging electrochemical energy storage technologies.However,ILs are hygroscopic to the water in the air and the presence of trace water will narrow the ESW of ILs.In this article,we report that a localized solvation nanostructure(LSNS)is formed in ILs,which plays an important role in fully recovering the originally decreased ESW of[EMIM][TFSI]IL owing to the trace water.Such LSNS is consisted of Li^(+)ions with water molecules as the center,TFSI-anions as the secondary periphery and EMIM^(+)cations as the outermost layer after adding the proper amount of LiTFSI.This nanostructure can restrain the possibility of trace water to approach the electrode/electrolyte interfaces and adverse redox reactions,thereby recovering the ESW.Moreover,the effectiveness of this strategy in different kinds of ILs to fully recover ESW decreasing is verified.This article comes up with a feasible method to eliminate the trace water caused ESW drop for ILbased electrolytes and provides a new insight for understanding the molecular-level interaction between different ions in ILs with water molecules.