Abstract:Li-metal batteries are the preferred candidates for the next-generation energy storage, due to the lowest electrode potential and high capacity of Li anode. However, the dangerous Li dendrites and serious interface reaction hinder its practical application. In this work, we construct a difunctional protecting layer on the surface of the Li anode (the AgNO
3
-modified Li anode, AMLA) for Li-S batteries. This stable protecting layer can hinder the corrosion reaction with intermediate polys… Show more
“…[ 14 , 21 ] In addition, the high Li ion diffusion coefficient of lithiated carbon and Li‐Ag alloy could facilitate further Li ion reduction within the pores of 3D anode, and thus, Li deposition can occur within the porous 3D Ni anode. [ 22 ] Indeed, the Li‐ion diffusion coefficient of lithiated C and Li‐Ag alloy is considerably higher than those of the bulk Li metal (1 × 10 −8 cm 2 s −1 for LiC 6 and Li‐Ag and 5.6 × 10 −11 cm 2 s −1 for Li). [ 14 , 23 ] SE is the exclusive Li ion pathway within the cell with a bare Ni anode; however, the lithiated C and Li‐Ag alloy in Ni_C_Ag anode could transfer Li‐ion within the porous anode and facilitate the electrochemical reduction of Li‐ion within the anode, which suppresses the separation of the anode/SE interface.…”
Li‐free all‐solid‐state batteries can achieve high energy density and safety. However, separation of the current collector/solid electrolyte interface during Li deposition increases interfacial resistance, which deteriorates safety and reversibility. In this study, a reversible 3D porous anode is designed based on Li deposition behavior that depends on the pore size of the anode. More Li deposits are accommodated within the smaller pores of the Li hosting anode composed of Ni particles with a granular piling structure; this implies the Li movement into the anode is achieved via diffusional Coble creep. Surface modification of Ni with a carbon coating layer and Ag nanoparticles further increases the Li hosting capacity and enables Li deposition without anode/solid electrolyte interface separation. A Li‐free all‐solid‐state full cell with a LiNi0.8Mn0.1Co0.1O2 cathode shows an areal capacity of 2 mAh cm−2 for retaining a Coulombic efficiency of 99.46% for 100 cycles at 30 °C.
“…[ 14 , 21 ] In addition, the high Li ion diffusion coefficient of lithiated carbon and Li‐Ag alloy could facilitate further Li ion reduction within the pores of 3D anode, and thus, Li deposition can occur within the porous 3D Ni anode. [ 22 ] Indeed, the Li‐ion diffusion coefficient of lithiated C and Li‐Ag alloy is considerably higher than those of the bulk Li metal (1 × 10 −8 cm 2 s −1 for LiC 6 and Li‐Ag and 5.6 × 10 −11 cm 2 s −1 for Li). [ 14 , 23 ] SE is the exclusive Li ion pathway within the cell with a bare Ni anode; however, the lithiated C and Li‐Ag alloy in Ni_C_Ag anode could transfer Li‐ion within the porous anode and facilitate the electrochemical reduction of Li‐ion within the anode, which suppresses the separation of the anode/SE interface.…”
Li‐free all‐solid‐state batteries can achieve high energy density and safety. However, separation of the current collector/solid electrolyte interface during Li deposition increases interfacial resistance, which deteriorates safety and reversibility. In this study, a reversible 3D porous anode is designed based on Li deposition behavior that depends on the pore size of the anode. More Li deposits are accommodated within the smaller pores of the Li hosting anode composed of Ni particles with a granular piling structure; this implies the Li movement into the anode is achieved via diffusional Coble creep. Surface modification of Ni with a carbon coating layer and Ag nanoparticles further increases the Li hosting capacity and enables Li deposition without anode/solid electrolyte interface separation. A Li‐free all‐solid‐state full cell with a LiNi0.8Mn0.1Co0.1O2 cathode shows an areal capacity of 2 mAh cm−2 for retaining a Coulombic efficiency of 99.46% for 100 cycles at 30 °C.
“…Thus, the morphological and mechanical advantages of the corresponding freestanding membrane signicantly suppressed the growth kinetics of Li dendrites and improved the interfacial stability with the LMA. 13,36 Furthermore, we evaluated the morphological behavior of the SHSE0, SHSE1, bLi, and mLi symmetric cell parts cycled at 0.2 mA cm −2 , as shown in Fig. 5(a)-(f).…”
Lithium-metal batteries (LMBs) using sandwich-type hybrid solid electrolytes (SHSEs) have been increasingly popular because of their high safety and improved electrochemical performance. However, the inadequate electrodes−SHSE interfacial contact markedly impedes...
“…Ag forms an alloy with Li and is soluble in Li (9 at%@145.5 C). 34,35 The Ag-decorated carbon spheres were synthesized by the carbonization of Agdecorated polymer spheres (for more detail, see the Methods section). TEM images (Fig.…”
Section: Kinetic Factors: LI Deposition Behavior Onto a Composite Ano...mentioning
Factors that determine the Li deposition behavior in Li-free ASSBs with a porous interlayer are systemically identified and Li deposition behavior is interpreted based on both thermodynamics and the kinetics.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.