All-vanadium redox flow battery (VRFB) has been considered as a promising candidate for the construction of renewable energy storage system. Expanded graphite possesses immense potential for use as typical bipolar plates in VRFB stacks. Nevertheless, the pure expanded graphite bipolar plates suffer from severe swelling in electrolyte, resulting in the losses of mechanical stability and electrical conductivity, thus leading to the efficiency decay within several cycles. Herein, we present a “nanoglue” strategy for tuning the structure/surface properties of expanded graphite by employing polyvinylidene fluoride (PVDF) polymer as structural sealant. Such PVDF “nanoglue” on expanded graphite results in the fine-repairment toward the surface microcracks and cross-section edges, which is beneficial to suppress the electrolyte permeation and improve the anti-swelling capacity. Moreover, it has been found that the PVDF “nanoglue” can improve the flexibility, allowing for the fabrication of ultrathin bipolar plates (0.67 mm) with low electrical resistivity. Benefiting from these integrated characteristics, the VRFB employing the as-fabricated composite bipolar plates delivers excellent cyclic efficiencies (voltage efficiency, coulombic efficiency, and energy efficiency) and ultralow ohmic voltage loss of less than 1.1 mV (< 0.1% of the VRFB rated voltage of 1.25 V) at a high current density of 200 mA cm− 2.

Developing advanced anode materials is one of the effective strategies to enhance the electrochemical performance of sodiumion batteries (SIBs). Herein, inspired by the biological central nervous system structure, we report a facile and efficient strategy to fabricate the three-dimensional hierarchical neural network-like carbon architectures, where the glucose-derived hard carbon (HC) nanospheres are in situ assembled and embedded in carbon nanotube (CNT) network nanostructure (HC/CNT hybrid networks). The HC nanospheres with large carbon interlayer spacing help to decrease the diffusion length of sodium ions and the interconnected CNT networks enable the rapid electron transfer during charge/discharge process. Benefiting from these structure merits, the as-made HC/CNT hybrid networks can deliver a superior rate capacity of 162 mA h g− 1 at the current density of 5 A g− 1. Additionally, it exhibits excellent cycling performance with a capacity retention rate of 86.3% after 140 cycles. This work offers a promising candidate anode material for SIBs and a new prospect towards carbon-based composites design, simultaneously.