Recent improvements in flexible electronics have increased the need to develop flexible and lightweight power sources. However, current flexible electrodes are limited by low capacitance, poor mechanical properties, and lack of cycling stability. In this article, we describe an ionic liquid-processed supramolecular assembly of cellulose and 3,4-ethylenedioxythiophene for the formation of a flexible and conductive cellulose/poly(3,4-ethylenedioxythiophene) PEDOT:poly(styrene sulfonate) (PSS) composite matrix. On this base, multiwalled carbon nanotubes (MWCNTs) were incorporated into the matrix to fabricate an MWCNT-reinforced cellulose/PEDOT:PSS film (MCPP), which exhibited favorable flexibility and conductivity. The MCPP-based electrode displayed comprehensively excellent electrochemical properties, such as a low resistance of 0.45 Ω, a high specific capacitance of 485 F g at 1 A g, and good cycling stability, with a capacity retention of 95% after 2000 cycles at 2 A g. An MCPP-based symmetric solid-state supercapacitor with Ni foam as the current collector and PVA/KOH gel as the electrolyte exhibited a specific capacitance of 380 F g at 0.25 A g and achieved a maximum energy density of 13.2 Wh kg (0.25 A g) with a power density of 0.126 kW kg or an energy density of 4.86 Wh kg at 10 A g, corresponding to a high power density of 4.99 kW kg. Another kind of MCPP-based solid-state supercapacitor without the Ni foam showed excellent flexibility and a high volumetric capacitance of 50.4 F cm at 0.05 A cm. Both the electrodes and the supercapacitors were environmentally stable and could be operated under remarkable deformation or high temperature without damage to their structural integrity or a significant decrease in capacitive performance. Overall, this work provides a strategy for the fabrication of flexible and conductive energy-storage films with ionic liquid-processed cellulose as a medium.

A flexible, transparent, and renewable mesoporous cellulose membrane (mCel‐membrane) featuring uniform mesopores of ≈24.7 nm and high porosity of 71.78% is prepared via a facile and scalable solution‐phase inversion process. KOH‐saturated mCel‐membrane as a polymer electrolyte demonstrates a high electrolyte retention of 451.2 wt%, a high ionic conductivity of 0.325 S cm−1, and excellent mechanical flexibility and robustness. A solid‐state electric double layer capacitor (EDLC) using activated carbon as electrodes, the KOH‐saturated mCel‐membrane as a polymer electrolyte exhibits a high capacitance of 110 F g−1 at 1.0 A g−1, and long cycling life of 10 000 cycles with 84.7% capacitance retention. Moreover, a highly integrated planar‐type micro‐supercapacitor (MSC) can be facilely fabricated by directly depositing the electrode materials on the mCel‐membrane‐based polymer electrolyte without using complicated devices. The resulting MSC exhibits a high areal capacitance of 153.34 mF cm−2 and volumetric capacitance of 191.66 F cm−3 at 10 mV s−1, representing one of the highest values among all carbon‐based MSC devices. These findings suggest that the developed renewable, flexible, mesoporous cellulose membrane holds great promise in the practical applications of flexible, solid‐state, portable energy storage devices that are not limited to supercapacitors.

Improving the flame retardancy of wood is an imperative yet highly challenging step in the application of wood in densely populated spaces. In this study, Mg-Al-layered double-hydroxide (LDH) coating was successfully fabricated on a wood substrate to confer flame-retardant and smoke-suppression properties. The chemical compositions and bonding states characterized by energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy confirmed the coating constituents of Mg-Al LDH. The coating evenly covered the sample wood surfaces and provided both mechanical enhancement and flame-retardancy effects. The limiting oxygen index of the Mg-Al LDH-coated wood increased to 39.1% from 18.9% in the untreated wood. CONE calorimetry testing revealed a 58% reduction in total smoke production and a 41% reduction in maximum smoke production ratio in the Mg-Al LDH-coated wood compared to the untreated wood; the peak heat release rate and total heat release were also reduced by 49% and 40%, respectively. The Mg-Al LDH coating is essentially hydrophilic, but simple surface modification by fluoroalkyl silane could make it superhydrophobic, with a water contact angle of 152° and a sliding angle of 8.6°. The results of this study altogether suggest that Mg-Al LDH coating is a feasible and highly effective approach to nanoconstructing wood materials with favorable flame-retardant and smoke-suppression properties.

Nanocellulose has been used as a sustainable nanomaterial for constructing advanced electrochemical energy-storage systems with renewability, lightweight, flexibility, high performance, and satisfying safety. Here, we demonstrate a high-performance all-nanofiber asymmetric supercapacitor (ASC) assembled using a forest-based, nanocellulose-derived hierarchical porous carbon (nanocellulose carbon, HPC) anode, a mesoporous nanocellulose membrane separator (nanocellulose separator), and a NiCo2O4 cathode with nanocellulose carbon as the support matrix (nanocellulose cathode, HPC/NiCo2O4). HPC has a three-dimensional porous structure comprising interconnected nanofibers with an ultrahigh surface area of 2046 m2 g–1. When integrated with the mesoporous feature of the nanocellulose membrane separator, these properties facilitate the quick delivery of both ions and electrons even with a thick (up to several hundreds of micrometers) and highly loaded (5.8 mg cm–2) ASC design. Consequently, the all-nanofiber ASC demonstrates a high electrochemical performance (64.83 F g–1 (10.84 F cm–3) at 0.25 A g–1 and 32.78 F g–1 or 5.48 F cm–3 at 4 A g–1) that surpasses most cellulose-based ASCs ever reported. Moreover, the nanocellulose components promise renewability, low cost, and biodegradability, thereby presenting a promising direction toward high-power, environmentally friendly, and renewable energy-storage devices.

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