Lara Jabbour

Cellulose-based Li-ion batteries: a review

Li-ion batteries (LIBs) are the most employed power source in portable electronics (e.g., cellular phones, laptop computers…) and are accounted as very promising storage/power systems for future electric/hybrid-electric powered transportation. However for their future development, low production costs and environmental friendliness will be key parameters. In this context, the introduction of water processable biosourced polymers such as cellulose and its derivatives is very interesting and is emerging as a viable route toward the development of green materials and processes for LIB manufacturing. The present review briefly introduces the Li-ion technology and gives an overview on cellulose and cellulose derivatives for the elaboration of separators, electrolytes and electrodes.

Aqueous processing of cellulose based paper-anodes for flexible Li-ion batteries

Cellulose fibers were used as novel bio-sourced binder to manufacture flexible cellulose/graphite paper-anodes for Li-ion batteries by means of a simple water-based filtration process easily up-scalable capitalizing conventional papermaking technologies. Paper-anodes showed excellent tensile properties with Young moduli ranging between 60 and 450 MPa, discharge capacity values up to 300/350 mA h g-1 and cycling performances comparable with conventional polymer-bonded graphite anodes.

Flexible cellulose/LiFePO4 paper-cathodes: toward eco-friendly all-paper Li-ion batteries

Today most of commercial Li-ion batteries (LIBs) are manufactured using toxic solvents and synthetic polymer binders. In order to lower the cost and the environmental impact of LIBs an effort must be made to identify low-cost and environmentally friendly materials and processes. In this work, flexible, self-standing and easily recyclable LiFePO4 cathodes are obtained using cellulose fibers as biosourced binder and a quick, aqueous filtration process, easily upscalable capitalizing the well-established papermaking know-how. The obtained paper-cathodes show very good mechanical properties, with Young’s modulus as high as 100 MPa, discharge capacity values up to 110 mAh g−1 and very good cycling performances, comparable with conventional polymer-bonded LiFePO4 cathodes. Moreover, a complete paper-cell, constituted by a paper-cathode, a paper-separator and a paper-anode is presented, showing good cycling performances in terms of specific capacity, efficiency and stability.

UV-Induced Radical Photo-Polymerization: A Smart Tool for Preparing Polymer Electrolyte Membranes for Energy Storage Devices.

In the present work, the preparation and characterization of quasi-solid polymer electrolyte membranes based on methacrylic monomers and oligomers, with the addition of organic plasticizers and lithium salt, are described. Noticeable improvements in the mechanical properties by reinforcement with natural cellulose hand-sheets or nanoscale microfibrillated cellulose fibers are also demonstrated. The ionic conductivity of the various prepared membranes is very high, with average values approaching 10-3 S cm-1 at ambient temperature. The electrochemical stability window is wide (anodic breakdown voltages > 4.5 V vs. Li in all the cases) along with good cyclability in lithium cells at ambient temperature. The galvanostatic cycling tests are conducted by constructing laboratory-scale lithium cells using LiFePO4 as cathode and lithium metal as anode with the selected polymer electrolyte membrane as the electrolyte separator. The results obtained demonstrate that UV induced radical photo-polymerization is a well suited method for an easy and rapid preparation of easy tunable quasi-solid polymer electrolyte membranes for energy storage devices.