Browsing by Author "Ji, Xiao"
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Item Fluorinated solid electrolyte interphase enables highly reversible solid-state Li metal battery(AAAS, 2018-12-21) Fan, Xiulin; Ji, Xiao; Han, Fudong; Yue, Jie; Chen, Ji; Chen, Long; Deng, Tao; Jiang, Jianjun; Wang, ChunshengSolid-state electrolytes (SSEs) are receiving great interest because their high mechanical strength and transference number could potentially suppress Li dendrites and their high electrochemical stability allows the use of high-voltage cathodes, which enhances the energy density and safety of batteries. However, the much lower critical current density and easier Li dendrite propagation in SSEs than in nonaqueous liquid electrolytes hindered their possible applications. Herein, we successfully suppressed Li dendrite growth in SSEs by in situ forming an LiF-rich solid electrolyte interphase (SEI) between the SSEs and the Li metal. The LiF-rich SEI successfully suppresses the penetration of Li dendrites into SSEs, while the low electronic conductivity and the intrinsic electrochemical stability of LiF block side reactions between the SSEs and Li. The LiF-rich SEI enhances the room temperature critical current density of Li3PS4 to a record-high value of >2 mA cm−2. Moreover, the Li plating/stripping Coulombic efficiency was escalated from 88% of pristine Li3PS4 to more than 98% for LiF-coated Li3PS4. In situ formation of electronic insulating LiF-rich SEI provides an effective way to prevent Li dendrites in the SSEs, constituting a substantial leap toward the practical applications of next-generation high-energy solid-state Li metal batteries.Item Formation of LiF-rich Cathode-Electrolyte Interphase by Electrolyte Reduction(Wiley, 2022-04-08) Bai, Panxing; Ji, Xiao; Zhang, Jiaxun; Zhang, Weiran; Hou, Singyuk; Su, Hai; Li, Mengjie; Deng, Tao; Cao, Longsheng; Liu, Sufu; He, Xinzi; Xu, Yunhua; Wang, ChunshengThe capacityof transitionmetal oxide cathodefor Li-ionbatteriescan be furtherenhancedby increas-ing the chargingpotential.However,these high voltagecathodessufferfrom fast capacitydecaybecausethelargevolumechangeof cathodebreaksthe activematerialsand cathode-electrolyteinterphase(CEI),resultingin electrolytepenetrationinto brokenactivematerialsand continuousside reactionsbetweencath-ode and electrolytes.Herein,a robustLiF-richCEI wasformedby potentiostaticreductionof fluorinatedelec-trolyteat a low potentialof 1.7 V. By takingLiCoO2asa modelcathode,we demonstratethat the LiF-richCEImaintainsthe structuralintegrityand suppresseselectro-lyte penetrationat a high cut-offpotentialof 4.6 V. TheLiCoO2with LiF-richCEI exhibiteda capacityof198 mAhgItem High-energy and low-cost membrane-free chlorine flow battery(Springer Nature, 2022-03-11) Hou, Singyuk; Chen, Long; Fan, Xiulin; Fan, Xiaotong; Ji, Xiao; Wang, Boyu; Cui, Chunyu; Chen, Ji; Yang, Chongyin; Wang, Wei; Li, Chunzhong; Wang, ChunshengGrid-scale energy storage is essential for reliable electricity transmission and renewable energy integration. Redox flow batteries (RFB) provide affordable and scalable solutions for stationary energy storage. However, most of the current RFB chemistries are based on expensive transition metal ions or synthetic organics. Here, we report a reversible chlorine redox flow battery starting from the electrolysis of aqueous NaCl electrolyte and the as-produced Cl2 is extracted and stored in the carbon tetrachloride (CCl4) or mineral spirit flow. The immiscibility between the CCl4 or mineral spirit and NaCl electrolyte enables a membrane-free design with an energy efficiency of >91% at 10 mA/cm2 and an energy density of 125.7 Wh/L. The chlorine flow battery can meet the stringent price and reliability target for stationary energy storage with the inherently low-cost active materials (~$5/kWh) and the highly reversible Cl2/Cl− redox reaction.