Anomalous scaling law of strength and toughness of cellulose nanopaper.

The quest for both strength and toughness is perpetual in advanced material design; unfortunately, these two mechanical properties are generally mutually exclusive. So far there exists only limited success of attaining both strength and toughness, which often needs material-specific, complicated, or expensive synthesis processes and thus can hardly be applicable to other materials. A general mechanism to address the conflict between strength and toughness still remains elusive. Here we report a first-of-its-kind study of the dependence of strength and toughness of cellulose nanopaper on the size of the constituent cellulose fibers. Surprisingly, we find that both the strength and toughness of cellulose nanopaper increase simultaneously (40 and 130 times, respectively) as the size of the constituent cellulose fibers decreases (from a mean diameter of 27 µm to 11 nm), revealing an anomalous but highly desirable scaling law of the mechanical properties of cellulose nanopaper: the smaller, the stronger and the tougher. Further fundamental mechanistic studies reveal that reduced intrinsic defect size and facile (re)formation of strong hydrogen bonding among cellulose molecular chains is the underlying key to this new scaling law of mechanical properties. These mechanistic findings are generally applicable to other material building blocks, and therefore open up abundant opportunities to use the fundamental bottom-up strategy to design a new class of functional materials that are both strong and tough.

Tin anode for sodium-ion batteries using natural wood fiber as a mechanical buffer and electrolyte reservoir.

Sodium (Na)-ion batteries offer an attractive option for low cost grid scale storage due to the abundance of Na. Tin (Sn) is touted as a high capacity anode for Na-ion batteries with a high theoretical capacity of 847 mAh/g, but it has several limitations such as large volume expansion with cycling, slow kinetics, and unstable solid electrolyte interphase (SEI) formation. In this article, we demonstrate that an anode consisting of a Sn thin film deposited on a hierarchical wood fiber substrate simultaneously addresses all the challenges associated with Sn anodes. The soft nature of wood fibers effectively releases the mechanical stresses associated with the sodiation process, and the mesoporous structure functions as an electrolyte reservoir that allows for ion transport through the outer and inner surface of the fiber. These properties are confirmed experimentally and computationally. A stable cycling performance of 400 cycles with an initial capacity of 339 mAh/g is demonstrated; a significant improvement over other reported Sn nanostructures. The soft and mesoporous wood fiber substrate can be utilized as a new platform for low cost Na-ion batteries.

Transparent nanopaper with tailored optical properties.

Nanopaper is a flexible, transparent, and renewable substrate that is emerging as a replacement for plastic in printed "green" electronics. The underlying science of transparency of nanopaper is that the diameter of these fibers is much smaller than the light wavelength, which significantly decreases the light scattering as compared to regular fibers. Cellulose fibers have a hierarchical structure, which consists of numerous smaller fibers. In this manuscript, we demonstrate a nanopaper design with different fiber diameters, and conclude that the light transmittance and scattering depend on the fiber diameter and packing density. The optical properties of the nanopaper and their dependence on the cellulose fiber diameter are thoroughly explained through Chandrasekhar's radiative-transfer theory and multiple scattering method simulations. The controllable optical properties of highly transparent nanopaper present an unprecedented opportunity for growth of next-generation optoelectronics.

Porous amorphous FePO4 nanoparticles connected by single-wall carbon nanotubes for sodium ion battery cathodes.

Sodium ion batteries (SIBs) are promising candidates for the applications of large-scale energy storage due to their cost-effective and environmental-friendly characteristics. Nevertheless, it remains a practical challenge to find a cathode material of SIBs showing ideal performance (capacity, reversibility, etc.). We report here a nanocomposite material of amorphous, porous FePO(4) nanoparticles electrically wired by single-wall carbon nanotubes as a potential cathode material for SIBs. The hydrothermally synthesized nanocomposite shows excellent cell performance with unprecedented cycling stability and reversibility. The discharge capacity of as high as 120 mAh/g is delivered at a 0.1 C rate (10 mA/g). The capacity retentions are about 70 mAh/g, 60 mAh/g, and 55 mAh/g at higher currents of 20 mA/g, 40 mA/g, and 60 mA/g, respectively. Even at a 1 C rate (100 mA/g), a capacity of about 50 mAh/g is still retained after 300 cycles. With a simple synthetic procedure, cost-effective chemicals, and desirable cell performance, this method offers a highly promising candidate for commercialized cathode materials of SIBs.