Stable interfaces constructed by concentrated ether electrolytes to render robust lithium metal batteries

Lithium metal batteries(LMBs)are highly considered as promising candidates for next-generation energy storage systems.However,routine electrolytes cannot tolerate the high potential at cathodes and low potential at anodes simultaneously,leading to severe interfacial reactions.Herein,a highly concentrated electrolyte(HCE)region trapped in porous carbon coating layer is adopted to form a stable and highly conductive solid electrolyte interphase(SEI)on Li metal surface.The protected Li metal anode can potentially match the high-voltage cathode in ester electrolytes.Synergistically,this ingenious design promises high-voltage-resistant interfaces at cathodes and stable SEI with abundance of inorganic components at anodes simultaneously in high-voltage LMBs.The feasibility of this interface-regulation strategy is demonstrated in Li|LiFePO_(4) batteries,realizing a lifespan twice as long as the routine cells,with a huge capacity retention enhancement from 46.4%to 88.7%after 100 cycles.This contribution proof-ofconcepts the emerging principles on the formation and regulation of stable electrode/electrolyte interfaces in the cathode and anode simultaneously towards the next-generation high-energy-density batteries.

MXene-based symmetric supercapacitors with high voltage and high energy density

MXene-based aqueous symmetric supercapacitors(SSCs)are attractive due to their good rate performances and green nature.However,it remains a challenge to reach voltages much over 1.2 V,which significantly diminishes their energy density.Herein,we report on Mo_(1.33)CTz MXene-based SSCs possessing high voltages in a 19.5 M LiCl electrolyte.Benefiting from the vacancy-rich structure and high stable potential window of Mo_(1.33)CTz,the obtained SSCs deliver a maximum energy density of>38.2 mWh cm^(-3) at a power density of 196.6 mW cm^(-3) under an operating voltage of 1.4 V,along with excellent rate performance and impressive cycling stability.This highly concentrated LiCl electrolyte is also applicable to Ti_(3)C_(2)Tz,the most widely studied MXene,achieving a maximum energy density of>41.3 mWh cm^(-3) at a power density of 165.2 mW cm^(-3) with an operating voltage of 1.8 V.The drop in energy density with increasing power in the Ti_(3)C_(2)Tz cells was steeper than for the Mo-based cells.This work provides a roadmap to develop superior SSCs with high voltages and high energy densities.

An all-organic aqueous potassium dual-ion battery

Benefiting from the environmental friendliness of organic electrodes and the high security of aqueous electrolyte,an all-organic aqueous potassium dual-ion full battery(APDIB) was assembled with 21 M potassium bis(fluoroslufonyl)imide(KFSI) water-in-salt as the electrolyte.The APDIB could deliver a reversible capacity of around 50 mAh g^(-1) at 200 mA g^(-1)(based on the weight of total active materials),a long cycle stability over 900 cycles at 500 mA g^(-1) and a high coulombic efficiency of 98.5%.The reaction mechanism of APDIB during the charge/discharge processes is verified:the FSI-could associate/disassociate with the nitrogen atom in the polytriphenylamine(PTPAn) cathode,while the K^(+) could react with C=O bonds in the 3,4,9,10-perylenetetracarboxylic diimide(PTCDI) anode reversibly.Our work contributes toward the understanding the nature of water-into-salt electrolyte and successfully constructed all-organic APDIB.