Publications by authors named "Zhijie Bi"

Article Synopsis
  • PVDF is a promising material for solid polymer electrolytes because of its good thermal stability and wide electrochemical range, but it faces issues with poor ionic conductivity due to the formation of a harmful alkaline layer on garnet fillers.
  • LiOH on the surface of these fillers contributes to the breakdown of PVDF chains, leading to unwanted chemical bonds; this can be mitigated by treating the fillers with acetic acid to create alkali-free garnets.
  • The modified PVDF electrolyte shows significantly improved ionic conductivity and a wider electrochemical window, resulting in better performance for solid-state lithium batteries, evidenced by higher discharge capacity and cycle stability.
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The polyacrylonitrile (PAN) is an attractive matrix of polymer electrolytes owing to its wide electrochemical window and strong coordination with Li salts. However, the PAN-based electrolytes undergo severe interfacial problems from both cathode and anode sides, including uneven ionic transfer induced by high rigidity of dry PAN-based polymer, as well as inferior stability against Li-metal anode. Herein, the composition regulation of PAN-based electrolytes is proposed by introducing succinonitrile (SN) plastic crystal and LiNO salt for the construction of interfacially stable solid-state lithium batteries.

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An ionic-electronic dual-conductive polymer, fabricated by doping polyethylene glycol into polyaniline, is used to modify LiCoO cathodes for solid lithium batteries. The polymer enables uniform and fast conductive networks in cathodes and stabilizes the generation of cathode interface layers. The cell maintains high cycle stability of 91.

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All-solid Li-O batteries have been constructed with Ag nanowire (AgNW) cathodes coated on Au-buffered garnet ceramic electrolytes and Li anodes on the other sides. Benefiting from the clean contacts of Li, e, and O on the AgNWs, the surface pathway reactions are demonstrated. Upon discharge, two types of LiO morphologies appear.

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Solid-state batteries with alkali metals (Li, Na, etc.) as anodes have the potential to achieve high energy density. However, the Li penetration through the garnet occurs without preindication during electrochemical cycling, leading to sudden short circuit and safety concerns.

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The demand for solid lithium batteries with high energy density and safety boosts the development of solid-state electrolytes in which composite membrane electrolytes consisting of polymers and ceramic fillers are attractive. As the common ceramic filler, perovskite-structured LiLaTiO (LLTO) has great advantage on cost and environmental friendliness by using earth-abundant raw materials in the production. Nevertheless, the chemical instability of LLTO against Li-metal hinders its application.

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To construct a high-performance next-generation carbon-based flexible supercapacitor, high porosity, large mass density, and high flexibility are three significant challenging goals. However, one side always affects another. Herein, high-density tetratomic-doped porous composite carbon derived from sustainable biomaterials is achieved via two-step processes of carbonization and acid-washing treatment.

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Flexible membrane electrolytes consisting of LiLaZrTaO (LLZTO) fillers in poly(propylene carbonate) (PPC) are considered promising for developing solid lithium batteries with high energy density and safety. However, LLZTO particles tend to agglomerate owing to their high surface energy, especially concerning their distribution in PPC that has low surface energy. Moreover, basic LLZTO particles attack PPC, resulting in its decomposition.

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A high-performance electrochromic-energy storage device (EESD) is developed, which successfully realizes the multifunctional combination of electrochromism and energy storage by constructing tungsten trioxide monohydrate (WO·HO) nanosheets and Prussian white (PW) film as asymmetric electrodes. The EESD presents excellent electrochromic properties of broad optical modulation (61.7%), ultrafast response speed (1.

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