A4 Paper Chemistry: Synthesis of a Versatile and Chemically Modifiable Cellulose Membrane.

Multifunctional cellulose membranes were developed from A4-sized printing paper via chemical modification. A4 paper is a widely used and easily accessible product with high cellulose content. Inspired by cellulose chemistry, we report a simple modification of the A4 paper, converting it from a common office supply to a user-modifiable functionalized cellulose membrane for practical applications. The hydroxyl groups of cellulose enable a facile tuning of its internal structure and polarity via chemical modification. In addition, the functionalized cellulose membrane has more stable mechanical strength compared to commercial cellulose-based filtration membranes. As a proof-of-concept, we demonstrate the separation of a water/oil mixture using the functionalized A4 membrane; we have extended this idea to origami-assisted membrane applications. Finally, this versatile A4 paper chemistry may offer a promising strategy for the development of functional membranes.

Sphere-to-Multipod Transmorphic Change of Nanoconfined Pt Electrocatalyst during Oxygen Reduction Reaction.

An oxygen reduction reaction (ORR) catalyst/support system is designed to have Pt nanoparticles nanoconfined in a nanodimensionally limited space. Holey crumpled reduced graphene oxide plates (hCR-rGO) are used as a carbon support for Pt loading. As expected from interparticular Pt-to-Pt distance of Pt-loaded hCR-rGO longer than that of Pt/C (Pt-loaded carbon black as a practical Pt catalyst), the durability of ORR electroactivity along cycles is improved by replacing the widely used carbon black with hCR-rGO. Unexpected morphological changes of Pt are electrochemically induced during repeated ORR processes. Spherical multifaceted Pt particles are evolved to {110}-dominant dendritic multipods. Nanoconfinement of a limited number of Pt within a nanodimensionally limited space is responsible for the morphological changes. The improved durability observed from Pt-loaded hCR-rGO originates from 1) dendritic pod structure of Pt exposing more active sites to reactants and 2) highly ORR-active Pt {110} planes dominant on the surface.

A Lithium-ion Battery Using Partially Lithiated Graphite Anode and Amphi-redox LiMn2O4 Cathode.

Delithiation followed by lithiation of Li+-occupied (n-type) tetrahedral sites of cubic LiMn2O4 spinel (LMO) at ~4 [Formula: see text] (delivering ~100 mAh gLMO-1) has been used for energy storage by lithium ion batteries (LIBs). In this work, we utilized unoccupied (p-type) octahedral sites of LMO available for lithiation at ~3 [Formula: see text] (delivering additional ~100 mAh gLMO-1) that have never been used for LIBs in full-cell configuration. The whole capacity of amphi-redox LMO, including both oxidizable n-type and reducible p-type redox sites, at ~200 mAh gLMO-1 was realized by using the reactions both at 4 [Formula: see text] and 3 [Formula: see text]. Durable reversibility of the 3 V reaction was achieved by graphene-wrapping LMO nanoparticles (LMO@Gn). Prelithiated graphite (LinC6, n < 1) was used as anodes to lithiate the unoccupied octahedral sites of LMO for the 3 V reaction.

Breathing silicon anodes for durable high-power operations.

Silicon anode materials have been developed to achieve high capacity lithium ion batteries for operating smart phones and driving electric vehicles for longer time. Serious volume expansion induced by lithiation, which is the main drawback of silicon, has been challenged by multi-faceted approaches. Mechanically rigid and stiff polymers (e.g. alginate and carboxymethyl cellulose) were considered as the good choices of binders for silicon because they grab silicon particles in a tight and rigid way so that pulverization and then break-away of the active mass from electric pathways are suppressed. Contrary to the public wisdom, in this work, we demonstrate that electrochemical performances are secured better by letting silicon electrodes breathe in and out lithium ions with volume change rather than by fixing their dimensions. The breathing electrodes were achieved by using a polysaccharide (pullulan), the conformation of which is modulated from chair to boat during elongation. The conformational transition of pullulan was originated from its α glycosidic linkages while the conventional rigid polysaccharide binders have ß linkages.