Ge Shi

Abstract Graphene oxide is extensively compounded with polymers toward a wide variety of applications. Less studied are few‐layer or multi‐layer highly crystalline graphene, both of which are herein named as graphene platelets. This article aims to provide the most recent advancements of graphene platelets and their polymer composites. A first focus lies on cost‐effective fabrication strategies of graphene platelets – intercalation and exfoliation – which work in a relative mass scale, e.g., 5.3 g h −1 . As no heavy oxidization is involved, the platelets have high crystalline integrity, e.g., C:O ratio over 8.0, with thicknesses 2–4 nm and lateral dimension up to a few micrometers. Through carefully selecting the solvent for dispersion and the molecules for surface modification, graphene platelets can be liquid‐processable, enabling them to be printed, coated, or compounded with various polymers. A purpose‐designed experiment is undertaken to unravel the effect of reasonable ultrasonication time on the platelet thickness. Typical polymer/graphene platelet composites are critically examined for their preparation, structure, and applications such as thermal management and flexible/stretchable electronic devices. Perspectives on the limitations, current challenges, and future prospects for graphene platelets and their polymer composites are provided.

Low-cost and efficient oxygen reduction reaction (ORR)/oxygen evolution reaction (OER) bifunctional electrocatalysts are vital for the applications of rechargeable Zn–air batteries (ZABs). Given the high catalytic activity of single-atom catalysts (SACs), preparing SACs on a large scale for ZABs is desirable but remains challenging. Herein, in situ formation of single-atom Fe–N–C catalysts on plate wood-based porous carbon is achieved via a facile Lewis acid pretreatment and carbonization process. Lewis acid FeCl3 pretreatment on the cell wall of wood not only produces abundant microchannels but also successfully introduces atomically dispersed Fe–N active species into the hierarchical structure. Such uniformly dispersive SACs on the hierarchical structure enhance the ORR/OER performance and durability. A ZAB using the catalyst in the cathode shows a high power density (70.2 mW cm–2, at quasi solid state) and long-term stability. This work provides a new path for the large-scale preparation of high-performance SACs.

Abstract With the increase of environmental pollution and depletion of fossil fuel resources, the utilization of renewable biomass resources for developing functional materials or fine chemicals is of great value and has attracted considerable attention. Nanocellulose, as a well‐known renewable nanomaterial, is regarded as a promising nano building block for advanced functional materials owing to its unique structure and properties, as well as natural abundance. Typically, its high mechanical strength, structural flexibility, reinforcing capabilities, and tunable self‐assembly behavior makes it highly attractive to fabricate flexible materials for various applications. Herein, the recent progress in the design, properties, and applications of advanced flexible materials from nanocellulose is comprehensively summarized. The preparation and properties of nanocellulose are first briefly introduced and discuss its merits in fabricating flexible materials. Then, various advanced flexible materials from nanocellulose are introduced, and the critical role of nanocellulose in constructing flexible materials is highlighted based on its intrinsic properties. After that, their applications in energy storage, electronics, sensor, biomedical, thermally insulating, photonic devices, etc., are presented. At last, the outlook of the current challenges and future perspectives for developing nanocellulose‐derived flexible materials are discussed.