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Non-Woven rGO Fibers Attached to Non-Woven Aramid Separator for High-Speed Charging and Discharging of Li Metal Anode

机译:连接到非织造芳纶分离器的非织造RGO纤维,用于高速充电和Li金属阳极放电

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Li metal is one of the best candidate anode materials for next-generation Li ion batteries (LIBs) and the most promising anode material that can replace the carbonaceous anode currently in use because of its high theoretical specific capacity and low redox potential (vs. SHE). Nevertheless, in order to apply Li metal to LIBs as an anode, issues such as those related to the cycle characteristics such as the life span and C-rate capability need to be resolved. These issues arise owing to the solid electrolyte interphase (SEI) formed on the surface of the Li metal anode (LMA). Unlike the conventional graphite anode, which exhibits a stable intercalation/de-intercalation mechanism, the Li metal anode, which utilizes a lithiation-delithiation mechanism known as hostless electrochemical plating/stripping to charge/discharge, undergoes repeated formation/collapse of an unstable SEI layer on its surface. Thus, the LMA is continuously exposed to undesirable interfacial reactions with the liquid electrolyte. The continuous occurrence of these side-reactions deteriorates the cycle characteristics of the LMA. In particular, this phenomenon gradually intensifies as the applied current increases, leaving the LMA operative within limited cycles at a high current density. Thus, the surface of the LMA needs to be subjected to additional treatments, based on studies of interfacial phenomena, for introducing it to LIBs, which many research groups attempted. Of the many approaches, studies that stabilization of the LMA surface by the introduction of a conductive interlayer between the LMA and separator or by applying a functional separator provided excellent results and the advantage using Li metal without structural modification. Similarly, a good interlayer or functional separator should be able to control undesirable interfacial reactions by the formation of the stable SEI layer, which prevents accumulation of an inactive layer and liquid electrolyte depletion, maintaining the cycle characteristics of LMA. In particular, when there is a conductive interlayer above the LMA, the conductive interlayer at the top structurally meets the Li~+ ion flux first during the plating step. Therefore, the SEI layer formed is more stable on the conductive interlayer than on the LMA surface and could thus ensure surface stability of the LMA, preventing repeated SEI formation/collapse, dendritic growth, and liquid electrolyte depletion. In consideration of this point, in this work, we proposed non-woven type reduced graphene oxide fibers attached to aramid paper (rGOF-A) as an advanced separator to solve the aforementioned issues presented by an unstable SEI layer. When the rGOF side of rGOF-A contacts the Li metal anode, it functions effectively as a conductive frame, so the electrons can migrate from the underlying the LMA to the rGOF as the current is applied. Thus, the rGOF first meets the Li~+ ion flux rather than the LMA, and the SEI layer, which has different chemical characteristics than those of the LMA surface, forms more stably mainly on rGOF in strong reductive conditions. In other words, rGOF can act a conductive layer and induces formation of the SEI layer in rGOF, not the LMA, helping toward stable operation of the LMA. In addition, this formed stable SEI layer can be effectively confined within the rGOF frame to have a high modulus. Moreover, as the electrolyte is consumed to form the SEI layer on the surface of rGOF, chemically reactive C-F bonds are generated at the surface of rGOF and the partially fluorinated rGOF surface induces the formation of LiF known as the component of the stable SEI during the Li~+ ion plating process. LiF is a key component in a stable SEI layer on the LMA because it has a wide electrochemical stability window and improves the surface diffusion of ions, which can lead to smooth Li plating. Thus, LiF protects the LMA from further repeated SEI layer formation/collapse processes and helps the LMA to operate reliably. T
机译:Li Metal是下一代Li离子电池(Libs)的最佳候选阳极材料之一,以及最有前途的阳极材料,可以代替目前正在使用的碳质阳极,因为其高理论特异性能力和低氧化还原潜力(对她)。然而,为了将Li金属应用于Libs作为阳极,需要解决与循环特性(例如寿命和C速率能力)相关的问题。由于在Li金属阳极(LMA)的表面上形成的固体电解质相互相对(SEI)而出现了这些问题。与常规石墨阳极不同,该石墨阳极具有稳定的插入/去嵌入机制,利用称为无主体电化学电镀/汽提的锂化脱锂机制的LI金属阳极进行充电/放电,经历重复的形成/塌陷的不稳定SEI层面上的层。因此,LMA连续地暴露于与液体电解质的不希望的界面反应。这些副反应的连续发生劣化了LMA的循环特性。特别地,随着施加的电流增加,这种现象逐渐加剧,使LMA在高电流密度下的有限循环内操作。因此,基于对界面现象的研究,LMA的表面需要进行额外的处理,用于将其引入LIBS,其中许多研究组尝试。在许多方法中,通过在LMA和隔膜之间引入导电层间或通过施加功能分离器来稳定LMA表面的研究,使用LI金属提供优异的结果,而没有结构改性。类似地,良好的中间层或功能分离器应该能够通过形成稳定的SEI层来控制不期望的界面反应,这防止了毫无惰性层和液体电解质耗尽的积聚,保持LMA的循环特性。特别地,当LMA上方有导电层间时,顶部的导电层间在电镀步骤期间首先在结构上达到Li +离子磁通。因此,形成的Sei层在导电层间比LMA表面上更稳定,因此可以确保LMA的表面稳定性,防止重复的SEI形成/塌陷,树突生长和液体电解质耗尽。考虑到这一点,在这项工作中,我们提出了附着在芳族纸(RGOF-A)上的非织造型还原的石墨烯氧化物纤维作为先进的分离器,以解决不稳定的SEI层呈现的上述问题。当RGOF-A的RGOF侧接触LI金属阳极时,它有效地作为导电框架起作用,因此当施加电流时,电子可以从下面的LMA迁移到RGOF。因此,RGOF首先符合Li〜+离子磁通而不是LMA,并且SEI层具有与LMA表面不同的化学特性,其形式的强度在强制性条件下的RGOF中更稳定地形成。换句话说,RGOF可以作用导电层并在RGOF中诱导形成SEI层,而不是LMA,有助于LMA的稳定操作。另外,该形成的稳定的SEI层可以有效地限制在RGOF框架内以具有高模量。此外,由于电解质被消耗在RGOF的表面上形成SEI层,因此在RGOF的表面上产生化学反应性CF键,部分氟化的RGOF表面诱导LIF的形成被称为稳定SEI的组分李〜+离子电镀工艺。 LIF是LMA上稳定SEI层中的关键组成部分,因为它具有宽的电化学稳定性窗口,并改善了离子的表面扩散,这可以导致平滑LI电镀。因此,LiF保护LMA从进一步重复的SEI层形成/塌陷过程中保护LMA,并有助于LMA可靠地操作。 T.

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