Wednesday, 3 October 2018
Universal Ballroom (Expo Center)
Electronic devices have been advanced rapidly over the last few decades with improved performance through high-level integration. Lithium ion batteries (LIB), which is representative rechargeable energy storage system, is increasingly demanding to high-energy-density storage system for the stable operation of high performance devices like mobile, laptop, etc. In addition, a recent quantum leap in electronic vehicles (EVs) require to energy storage system with long cycling stability incomparable to previous electronic devices. To achieve high performances and long lifetime, the use of lithium metal is one of attractive anode for as LIBs, because Li metal has high theoretical specific capacity of 3860 mAh/g, low redox potential of -3.04V (verse the standard hydrogen electrode) and low gravimetric density of 0.59 g/cm3. Nevertheless, since Li metal anode has the lithiation-delithiation mechanism of the ‘hostless’ electrochemical plating/stripping unlike the conventional graphite anode, it is confronted with serious problems occurred from uncontrollable interfacial reaction between surface of lithium metal anode and electrolyte applying to traditional LIB system; that is (1) the uncontrollable formation of solid electrolyte interphase (SEI) layer limitless volume expansion of Li metal anode (2) the dendritic growth and isolation of Li interface derived from inhomogeneous deposition of Li+ ion flux (3) the Li surface fracture induced by heterogeneously plated Li+ ion. Through these process, repetitive formation of undesirable SEI layer at surface of Li anode make fresh electrolyte dissipation and concurrently the anode surface becomes more distorted. These side-phenomena strongly correlate with low coulombic efficiency and decreasing lifetime of lithium metal battery (LMB) system where lithium metal is used as anode. In this works, in a dimensional aspect, to solve such problem mentioned above through stabilizing of surface of lithium metal anode, we introduce Janus-faced protective layer (JPL) as gel polymer electrolyte. JPL was composed with dual layer of Ni (3~7μm) embedded poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) and bare PVdF-HFP through simple casting method. The process of preparing JPL membrane is so simple to instantly bring in existing roll-to-roll process, and it is also possible to make a low cost process considered relatively low nickel price. In terms of mechanical property, it is based on flexible polymer and shows the merit of being foldable enough to able origami. In addition, JPL play a role of protection of Li metal anode. JPL has two functionalities. The metal part of JPL directly contacted with anode, and this layer was frameworks for preventing irregular SEI layer formation through inward plating of Li ion, the polymer part is stable state enough to be used as a gel polymer electrolyte. When lithium metal anode is subjected to cycle-test while keeping in contact with the nickel side of JPL membrane, Scanning electron microscope (SEM) image showed that the surface of lithium metal anode was very clean without any fluctuation compared to the case where only polypropylene (PP) separator was used. (Figure. 1) Moreover, as shown in Figure 2., the LMB system applied JPL show high stability of tolerable overvoltage within 5mV, 15mV even at high-current of 10mA/cm2, 20mA/cm2, respectively, in Li//JPL/JPL//Li symmetric cell. These results are attributable to effective function of each layer as mentioned earlier. JPL consists of two layer, the tough and adhesive nature of PVdF-HFP prevents the polymer part from being damaged or torn by dendritic growth and simultaneously ensure that metal part functions as robust framework for SEI layer formation without escaped particle from the membrane. This frameworks induce the SEI layer, which can act as a resistive element, to grown in the metal part while surface of Li metal anode become get out of main subject from the SEI layer formation. By virtue of that property, JPL has not allow forming resistive elements on the surface of Li metal anode, preventing the voltage rising up due to the formation of resistive elements at surface, so tolerability of overvoltage with clean surface of anode is maintained. In conclusion, the model study of nickel micro-particle/PVdF-HFP composite suggests the straightforward direction of protective layer to apply lithium metal as anode in LIB system with alleviating the problem caused by the ‘hostless’ property of lithium metal anode. Thus, when JPL is introduced to a LIB system, it shows a fairly positive possibility for high performance Lithium metal battery.