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To promote silver nanowire (AgNW) as a viable commercial alternative for transparent electrodes, it is necessary to further develop industrially scalable, high‐performance yielding and cost‐efficient methods of purifying large quantities of as‐prepared AgNW suspensions. In this work, a facile, effective, and mass scalable purification method that employs a novel dynamic agitation‐induced centrifugal filtration concept to obtain highly purified and printable AgNW solutions. This unique dynamic filtration system, which amalgamates the advantages of membrane filtration, centrifugal filtration and "cross‐flow" filtration, is effective at (1) removing nanoparticles, short nanorods and organic additives from as‐prepared AgNW suspensions without producing aggregation; (2) concentrating purified AgNW suspensions to a desirable concentration; and (3) formulating printable AgNW suspensions with suitable solvents. The resulting purified, polyol‐method synthesized AgNW with a modest aspect ratio of ≈1000 and narrowed length distribution, can be coated into flexible transparent electrodes to yield a transmittance of 99.2% and 95.2% at 230 and 29.6 ohm sq‐1 respectively. These performance metrics are comparable or exceed that of most transparent electrodes made from AgNW with larger aspect ratio (>2000) but purified through conventional purification methods. To maximize the dynamic purification efficiency, a model is also developed to describe and predict this dynamic filtration process. A facile, effective, and mass scalable purification method that employs a novel dynamic agitation‐induced centrifugal filtration concept to obtain highly purified and printable silver nanowire solutions, which can be directly coated into flexible transparent electrodes to yield a transmittance of 99.2% and 95.2% at 230 and 29.6 ohm sq−1, respectively, is introduced. [ABSTRACT FROM AUTHOR]

Abstract: The development of strain sensors with both large strain range (>50%) and high gauge factor (>100) is a grand challenge. High sensitivity requires material to perform considerable structural deformation under tiny strain, whereas high stretchability demands structural connection or morphological integrity for materials upon large deformation, yet both features are hard to be achieved in one thin film. A new 0D–1D–2D ternary nanocomposite–based strain sensor is developed that possesses high sensitivity in broad working strain range (gauge factor 2392.9 at 62%), low hysteresis, good linearity, and long‐term durability. The skin‐mountable strain sensor, fabricated through one‐step screen‐printing process, is made of 1D silver nanowire offering high electrical conductivity, 2D graphene oxide offering brittle layered structure, and 0D fullerene offering lubricity. The fullerene constitutes a critical component that lowers the friction between graphene oxide–based layers and facilitates the sliding between adjacent layers without hurting the brittle nature of the nanocomposite film. When stretching, layer slippage induced by fullerene can accommodate partial applied stress and boost the strain, while cracks originating and propagating in the brittle nanocomposite film ensure large resistance change over the whole working strain range. Such high comprehensive performance renders the strain sensor applicable to full‐spectrum human motion detection. [ABSTRACT FROM AUTHOR]

• 3D porous and highly conductive thick electrodes were designed by 3D printing. • 3D-printed thick electrodes were constructed by using nanocomponents-based hybrid ink. • 3D-printed electrodes show both high areal capacity and rate performance. • This strategy represents a simple process for the preparation of thick electrodes. The development of robust performing lithium-ion batteries (LIBs) with high areal capacity is a challenge that persists to date. One commonly used strategy to increase areal capacity is increasing the thickness of the battery electrodes. However, the practical application of these thick electrodes is hindered thanks to the fundamental issues of incomplete electrolyte infiltration, poor mechanical properties, and slow charge and ion transport. Herein, a new method is presented wherein a thick electrode is constructed by 3D printing a highly-conductive and hierarchical network of silver nanowires (AgNWs), graphene and Li 4 Ti 5 O 12 together as a mixed functional ink. The amalgamation of highly conductive AgNW network, interconnected 3D graphene scaffold, and hierarchical porous structure can allow the 3D-printed electrode to demonstrate much improved charge and ion transport, and to alleviate internal stresses during the charging and discharging process even under ultrahigh thickness state. As a result, the LIBs utilizing these thick electrodes have a rate capability of 121 mAh g−1 at 10C, high areal capacities up to 4.74 mAh cm−2, and stable cycling performance (capacity retention of ~95.5% after 100 cycles). These performance metrics provide a route for a new design strategy using thick electrodes for high-performance energy storage devices. [ABSTRACT FROM AUTHOR]