The platform will undergo maintenance on Sep 14 at about 7:45 AM EST and will be unavailable for approximately 2 hours.
2019
DOI: 10.3389/fchem.2019.00572
|View full text |Cite
|
Sign up to set email alerts
|

Toward High-Performance Li Metal Anode via Difunctional Protecting Layer

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

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
7
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 12 publications
(7 citation statements)
references
References 44 publications
0
7
0
Order By: Relevance
“…[ 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.…”
Section: Resultsmentioning
confidence: 99%
“…[ 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.…”
Section: Resultsmentioning
confidence: 99%
“…Thus, the morphological and mechanical advantages of the corresponding freestanding membrane signicantly 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).…”
Section: Li‖li Symmetric Cell Studymentioning
confidence: 99%
“…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
confidence: 99%