Bio-inspired design of an in-situ multifunctional polymeric solid-electrolyte interphase for Zn metal anode cycling at 30 mA cm-2 and 30 mA h cm-2

Author(s):  
Xiaohui Zeng ◽  
Kaixuan Xie ◽  
Sailin Liu ◽  
Shilin Zhang ◽  
Junnan Hao ◽  
...  

Solid-electrolyte interphase (SEI) is highly designable to restrain Zn dendrite growth and side reactions between Zn anode and water in rechargeable aqueous zinc-ion batteries (RAZBs), but it remains a challenge....

Author(s):  
Yuzhu Chu ◽  
Shu Zhang ◽  
Shuang Wu ◽  
Zhenglin Hu ◽  
Guanglei Cui ◽  
...  

In-situ constructing multifunctional solid electrolyte interphase (SEI) for Zn anode is promising to address the dendrite growth and side reactions (corrosion and hydrogen evolution) in aqueous Zn-ion batteries. However, there...


2021 ◽  
Author(s):  
Xianzhong Yang ◽  
Chao Li ◽  
Zhongti Sun ◽  
Shuai Yang ◽  
Zixiong Shi ◽  
...  

Abstract Zn metal anode has garnered growing scientific and industrial interest owing to its appropriate redox potential, low cost and good safety. Nevertheless, the instability of Zn metal, caused by dendrite formation, hydrogen evolution and side reactions, gives rise to poor electrochemical stability and unsatisfactory cycling life, greatly hampering large-scale utilization. Herein, an in-situ grown ZnSe layer with controllable thickness is crafted over one side of commercial Zn foil via chemical vapor deposition, aiming to achieve optimized interfacial manipulation between aqueous electrolyte/Zn anode. Thus-derived ZnSe overlayer not only prevents water penetration and restricts Zn2+ two-dimensional diffusion, but also homogenizes the electric field at the interface and facilitates favorable (002) plane growth of Zn. As a result, dendrite-free and homogeneous Zn deposition is obtained; side reactions are concurrently inhibited. In consequence, a high Coulombic efficiency of 99.2% and high cyclic stability for 860 cycles at 1.0 mA cm–2 in symmetrical cells is harvested. Meanwhile, when paired with V2O5 cathode, assembled full cell achieves an outstanding initial capacity (200 mAh g–1) and elongated lifespan (a capacity retention of 84% after 1000 cycles) at 5.0 A g–1. Our highly reversible Zn anode enabled by the interfacial manipulation strategy is anticipated to satisfy the demand of industrial and commercial use.


2020 ◽  
Author(s):  
Tingting Yang ◽  
Hui Li ◽  
Yongfu Tang ◽  
Jingzhao Chen ◽  
Hongjun Ye ◽  
...  

Abstract The growth of lithium (Li) whiskers is detrimental to Li batteries. However, it remains a challenge to directly track Li whisker growth. Here we report in situ observations of electrochemically induced Li deposition under a CO2 atmosphere inside an environmental transmission electron microscope. We find that the morphology of individual Li deposits is strongly influenced by the competing processes of cracking and self-healing of the solid electrolyte interphase (SEI). When cracking overwhelms self-healing, the directional growth of Li whiskers predominates. In contrast, when self-healing dominates over cracking, the isotropic growth of round Li particles prevails. The Li deposition rate and SEI constituent can be tuned to control the Li morphologies. We reveal a new “weak-spot” mode of Li dendrite growth, which is attributed to the operation of the Bardeen-Herring growth mechanism in the whisker’s cross section. This work has implications for the control of Li dendrite growth in Li batteries.


2016 ◽  
Vol 163 (3) ◽  
pp. A592-A598 ◽  
Author(s):  
Z. Liu ◽  
Y. Qi ◽  
Y. X. Lin ◽  
L. Chen ◽  
P. Lu ◽  
...  

2018 ◽  
Vol 4 (12) ◽  
pp. eaau9245 ◽  
Author(s):  
Xiulin Fan ◽  
Xiao Ji ◽  
Fudong Han ◽  
Jie Yue ◽  
Ji Chen ◽  
...  

Solid-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 Li3PS4to a record-high value of >2 mA cm−2. Moreover, the Li plating/stripping Coulombic efficiency was escalated from 88% of pristine Li3PS4to 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.


Author(s):  
Jun Pu ◽  
Chenglin Zhong ◽  
Jiahao Liu ◽  
Zhenghua Wang ◽  
Dongliang Chao

Li/Na metal anodes, based on their high theoretical capacity and low electrochemical potential, provide promising alternatives for next-generation high energy batteries. However, their unstable solid-electrolyte interphase and dendrite growth remain...


Author(s):  
G. Ramos-Sanchez ◽  
F. A. Soto ◽  
J. M. Martinez de la Hoz ◽  
Z. Liu ◽  
P. P. Mukherjee ◽  
...  

Understanding interfacial phenomena such as ion and electron transport at dynamic interfaces is crucial for revolutionizing the development of materials and devices for energy-related applications. Moreover, advances in this field would enhance the progress of related electrochemical interfacial problems in biology, medicine, electronics, and photonics, among others. Although significant progress is taking place through in situ experimentation, modeling has emerged as the ideal complement to investigate details at the electronic and atomistic levels, which are more difficult or impossible to be captured with current experimental techniques. Among the most important interfacial phenomena, side reactions occurring at the surface of the negative electrodes of Li-ion batteries, due to the electrochemical instability of the electrolyte, result in the formation of a solid-electrolyte interphase layer (SEI). In this work, we briefly review the main mechanisms associated with SEI reduction reactions of aprotic organic solvents studied by quantum mechanical methods. We then report the results of a Kinetic Monte Carlo method to understand the initial stages of SEI growth.


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