No abstract

The separator is of great importance for regulating ion transmission, maintaining electrode stability, and device safety in lithium‐ion batteries. Despite their many advantages, glass microfiber separators have shortcomings that often give rise to poor cycle performance and fatal short‐circuit risk when used in flexible batteries. Here, we propose the use of a scalable non‐Newtonian fluidic cellulose permeation‐diffusion strategy to develop a cellulose/glass microfiber composite film with an hourglass‐gradient structure. Due to the unique gradient morphology resulting from the presence of cellulose macromolecules, the as‐prepared composite film showed an improved surface mass density, adjustable pore structure, controllable ion transport, ideal mechanical flexibility, and robustness. When used as the separator in an assembled lithium‐ion battery, the composite film exhibited rapid ion diffusion and Li dendrite inhibition, which endowed the battery with excellent cycle stability (specific capacity of 108.5 mAh g−1 after 1000 cycles) and good rate performance. This composite film shows great potential application in flexible lithium‐ion batteries including but not limited to pouch cells.

An in‐depth understanding of the electronic structures of catalytically active centers and their surrounding vicinity is key to clarifying the structure–activity relationship, and thus enabling the design and development of novel metal‐free carbon‐based materials with desired catalytic performance. In this study, boron atoms are introduced into phosphorus‐doped nanoporous carbon via an efficient strategy, so that the resulting material delivers better catalytic performance. The doped B atoms alter the electronic structures of active sites and cause the adjacent C atoms to act as additional active sites that catalyze the reaction. The B/P co‐doped nanoporous carbon shows remarkable catalytic performance for benzyl alcohol oxidation, achieving high yield (over 91% within 2 h) and selectivity (95%), as well as low activation energy (32.2 kJ mol−1). Moreover, both the conversion and selectivity remain above 90% after five reaction cycles. Density functional theory calculations indicate that the introduction of B to P‐doped nanoporous carbon significantly increases the electron density at the Fermi level and that the oxidation of benzyl alcohol occurs via a different reaction pathway with a very low energy barrier. These findings provide important insights into the relationship between catalytic performance and electronic structure for the design of dual‐doped metal‐free carbon catalysts.

Cellulose with numerous hydroxyl groups and electronegative atoms can form extensive hydrogen bonds, which are nonnegligible recalcitrants to dissolution and to further utilizations. Herein, an indepth understanding of the interactions...

Hydrogen bonds (HBs) are vital construction fundamentals of natural biopolymers. Investigating the hydrogen bonding interactions of biopolymers is crucial for the conformation, transformation, and construction of their functional materials. In...