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In order to develop high power lithium ion batteries (LIBs), urgent requirements including adequate safety, higher current density and superior cyclic stability are proposed for separator. Tissue paper, composed of packed cellulose fibers, possesses lower production cost, easier accessibility, superior wettability together with outstanding thermostability, and is thus a candidate to be the substrate for high performance separator. To address the issue of structural failure usually encountered by single polymer as binder during long term cycling, crosslinked binder was constructed on tissue paper to adhere nano-SiO2 through chemical reactions between poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and hyperbranched polyethyleneimine (PEI) in this work. The effects of crosslinking degree on physical properties and electrochemical performance were studied thoroughly. When the feed ratio of PVDF-HFP and PEI is fixed at 10:1, the crosslinked composite separator displays excellent electrolyte uptake and wettability, superior ionic conductivity, better interfacial compatibility as well as higher Li+ transference number (0.56), thus offering battery with prominent rate capabilities. Besides, this crosslinked composite separator exhibits satisfying dimensional stability even treated at 250 °C, better flame retardancy, enhanced mechanical behavior, wider electrochemical window and outstanding cycle stability. Accordingly, tissue paper-based crosslinked composite separators can meet higher requirements put forward by high power LIBs. [ABSTRACT FROM AUTHOR]

A 3-dimensional carbonized multi-walled carbon nanotube (MWCNT) paper was used as the host of nano-tin oxide (SnO2) for lithium-ion batteries (LIBs). The cellulose fibers were fully mixed with MWCNTs in water. Then, the paper was obtained via vacuum filtration. Carbonization was carried out in a vacuum furnace at 1460°C. SnO2 slurry was coated on the carbonized MWCNT paper (CMP). Scanning electron microscopy (SEM) was utilized to observe the anode electrode. The images of SEM indicated that the nano-SnO2 was embedded into the holes of the porous CMP collector. This contributed the increase of contact interface area of the nano-SnO2 and the collector and the significantly reduced interface resistance. Electrochemical tests showed that the initial discharge capacity reached 1745 mAh g−1 with a coulumbic efficiency (CE) of 70.39% at a current density of 50 mA g−1. The composite electrode still maintained a reversible capacity of 753 mAh g−1 with a CE of 98% at a current density of 200 mA g−1 after 100 cycles. These marvelous composite electrodes exhibited a promising future for the next generation of LIBs. [ABSTRACT FROM AUTHOR]

A paper-supported inorganic composite (PIC) separator is prepared by spraying Al 2 O 3 particles onto both surfaces of a commercial paper substrate. The as-prepared PIC separator shows excellent thermal stability without any shrinkage at 130 °C for 30 min, superior wettability towards the electrolyte, with a contact angle of 0°, and high ionic conductivity compared with that of the conventional polyethylene (PE) separator. The graphite|LiCoO 2 full-cells with the PIC separator exhibit good cycling and rate performance. In the nail penetration tests, the pouch cell assembled with the PIC separator shows high safety characteristics. Given the advantages of the PIC separator, it is a good potential replacement for the polyolefin separators used in high-safety lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Conducting polymers have been considered for use as cathode materials in rechargeable lithium-ion batteries (LIBs) since 1981 but problems with poor cycling stability, rapid self-discharge, and low energy and power densities have so far limited their applicability. Herein it is shown that nanostructured freestanding conducting polymer composites [e.g., polypyrrole (PPy) and polyaniline (PANI)] can be used to circumvent these shortcomings. Freestanding and binder-free PPy and cellulose-based composites can straightforwardly be used as versatile organic cathode materials for LIBs. The composite, reinforced with chopped carbon filaments (CCFs), exhibited a large active mass loading of approximately 10 mg cm−2, an areal capacity of 1.0 mAh cm−2 (corresponding to 102 mAh g−1), and stable cycling. With an active mass loading of 4.4 mg cm−2, a capacity of 0.22 mAh cm−2 (corresponding to 58 mAh g−1) was found for current densities of 5 A g−1 yielding discharge times of approximately 40 seconds, and a capacity retention of 91 % over 100 cycles was obtained at 0.2 A g−1. The present method constitutes a straightforward approach for the manufacturing of high-performance freestanding electroactive conducting-polymer-based paper-like electrodes for use in inexpensive and sustainable, high-performance organic LIBs. [ABSTRACT FROM AUTHOR]

Highlights: [•] Processing of Li ion cell electrodes on a pilot paper machine by spray coating. [•] Use of microfibrillated cellulose in the formulation of the electrode slurry. [•] Electrodes displayed excellent mechanical properties and good cycling performances. [•] Pilot scale validation of new/high throughput technology for electrodes processing. [Copyright &y& Elsevier]

Abstract: A commercial rice paper (RP) is used for the first time as a separator membrane in lithium-ion batteries. It consists of interpenetrating cellulose fibers with a diameter of about 5–40μm to form a highly porous structure. The RP is found to be electrochemically stable at a potential below 4.5V vs. Li+/Li. Several kinds of electrode materials including graphite, LiFePO4, LiCoO2 and LiMn2O4 are used to test the compatibility of the RP in Li-ion batteries and to compare with a commercial polypropylene/polyethylene/polypropylene separator membrane. The RP separator with the same thickness gives rise to a lower resistance than the commercial separator. Due to the wonderful flexibility, high porosity, low cost and excellent electrochemical performance of the RP membrane, it is promising to partially replace commercial separators in lithium-ion batteries for low power applications. [Copyright &y& Elsevier]

Paper, invented more than 2,000 years ago and widely used today in our everyday lives, is explored in this study as a platform for energy-storage devices by integration with 1D nanomaterials. Here, we show that commercially available paper can be made highly conductive with a sheet resistance as low as 1 ohm per square (π/sq) by using simple solution processes to achieve conformal coating of single-walled carbon nanotube (CNT) and silver nanowire films. Compared with plastics, paper substrates can dramatically improve film adhesion, greatly simplify the coating process, and significantly lower the cost. Supercapacitors based on CNT-conductive paper show excellent performance. When only CNT mass is considered, a specific capacitance of 200 F/g, a specific energy of 30-47 Watt-hour/kilogram (Wh/kg). a specific power of 200,000 W/kg, and a stable cycling life over 40,000 cycles are achieved. These values are much better than those of devices on other flat substrates, such as plastics. Even in a case in which the weight of all of the dead components is considered, a specific energy of 7.5 Wh/kg is achieved. In addition, this conductive paper can be used as an excellent lightweight current collector in lithium-ion batteries to replace the existing metallic counterparts. This work suggests that our conductive paper can be a highly scalable and low-cost solution for high-performance energy storage devices. [ABSTRACT FROM AUTHOR]