Flexible thermoelectric CMTs/KCl/gelatin composite for a wearable pressure and temperature sensor.

Flexible sensors have promising applications in the fields of health monitoring and artificial intelligence, which have attracted much attention from researchers. However, the design and manufacture of sensors with multiple sensing functions (like simultaneously having both temperature and pressure sensing capabilities) still present a significant challenge. Here, an ionic thermoelectric sensor for synchronous temperature and pressure sensing was developed on the basis of a carbon microtubes (CMTs)/potassium chloride (KCl)/gelatin composite consisting of gelatin as the polymer matrix, CMTs as the conductive material and KCl as the ion source. The designed CMTs/KCl/gelatin composite with the good ductility (830%) and flexibility can achieve a Seebeck coefficient of 4 mV K-1 and a dual stimulus responsiveness to pressure and temperature. In addition, not only the movement of the human body (e.g., fingers, arms), but also the temperature difference between the human body and the environment, were able to be monitored by the designed CMTs/KCl/gelatin sensors. This study provides a novel strategy for the design and preparation of high-performance flexible sensors by utilizing ion-gel thermoelectric materials and promotes the research of temperature and pressure sensing technologies.

3D-Printed Carbon-Based Conformal Electromagnetic Interference Shielding Module for Integrated Electronics.

Electromagnetic interference shielding (EMI SE) modules are the core component of modern electronics. However, the traditional metal-based SE modules always take up indispensable three-dimensional space inside electronics, posing a major obstacle to the integration of electronics. The innovation of integrating 3D-printed conformal shielding (c-SE) modules with packaging materials onto core electronics offers infinite possibilities to satisfy ideal SE function without occupying additional space. Herein, the 3D printable carbon-based inks with various proportions of graphene and carbon nanotube nanoparticles are well-formulated by manipulating their rheological peculiarity. Accordingly, the free-constructed architectures with arbitrarily-customized structure and multifunctionality are created via 3D printing. In particular, the SE performance of 3D-printed frame is up to 61.4 dB, simultaneously accompanied with an ultralight architecture of 0.076 g cm-3 and a superhigh specific shielding of 802.4 dB cm3 g-1. Moreover, as a proof-of-concept, the 3D-printed c-SE module is in situ integrated into core electronics, successfully replacing the traditional metal-based module to afford multiple functions for electromagnetic compatibility and thermal dissipation. Thus, this scientific innovation completely makes up the blank for assembling carbon-based c-SE modules and sheds a brilliant light on developing the next generation of high-performance shielding materials with arbitrarily-customized structure for integrated electronics.

Assembling all-wood-derived carbon/carbon dots-assisted phase change materials for high-efficiency thermal-energy harvesters.

The collection and storage of renewable, sustainable and clean energy including wind, solar, and tidal energy has attracted considerable attention because of its promising potential to replace fossil energy sources. Advanced energy-storage materials are the core component for energy harvesters, affording the high-efficiency conversion of these new-style energy sources. Herein, originated from nature, a series of all-wood-derived carbon-assisted phase change materials (PCMs) were purposed by incorporating carbon dots-modified polyethylene glycol matrix into carbon skeletons via a vacuum-impregnation strategy. The resultant PCMs possessed desired anti-leakage capability and superior thermophysical behaviors. In particular, the optimum sample posed high latent heat (131.5 J/g) and well thermal stability, where the corresponding enthalpy still reserved 90 % over 100 heating/cooling cycles. More importantly, the as-fabricated thermal-energy harvester presented prominent capability to strorage and release multiple forms of thermal energy, as well as high-efficiency solar-energy utilization, corresponding to a photothermal conversion efficiency of 88 % in simulated sunlight irradiation, far exceeding some reported PCMs. Overall, with the introduction of wood-derived carbon dots and carbon skeletons, the assembled all-wood-derived carbon-assisted PCMs afforded trinity advantages on thermal performance, cycling stability, and energy conversion efficiency, which provide a promising potential for the practical application in thermal-energy harvesters.

Bleaching-free, lignin-tolerant, high-yield production of nanocrystalline cellulose from lignocellulosic biomass.

Nanocrystalline cellulose (NCC) preparation in an integrated fractionation manner is expected to solve the problems of low yield and environmental impact in the traditional process. An integrated fractionation strategy for NCC production from wood was developed through catalytic biomass fractionation, the partial dissolution of cellulose-rich materials (CRMs) in aqueous tetrabutylphosphonium hydroxide, and short-term ultrasonication. The presented process could tolerate a high CRM lignin content of 21.2 wt % and provide a high NCC yield of 76.6 wt % (34.3 wt % of the original biomass). The increase in the CRM lignin content decreased the NCC yield, facilitated the crystal transition of NCC from cellulose I to cellulose II, and showed no apparent effects on the NCC morphology. A partial/selective dissolution mechanism is proposed for the presented strategy. This study provided a promising efficient fractionation-based method toward comprehensive and high-value utilization of lignocellulosic biomass through effective delignification and high-yield NCC production.

Robust versatile nanocellulose/polyvinyl alcohol/carbon dot hydrogels for biomechanical sensing.

A new type of nanocellulose/poly(vinyl alcohol)/carbon dot (NPC) multifunctional hydrogel was successfully fabricated by an one-step in-situ hydrothermal method. The one-pot strategy led to the formation of a complex hydrogen bonding/dynamic boric acid ester/nitrogen-doped carbon dots network, and endowed the hydrogel with multifunctionality. The hydrogel underwent self-healing at room temperature (25 °C) and exhibited double-emission fluorescence and high mechanical strength (tensile strength of up to 2.98 MPa). An NPC hydrogel-based capacitive sensor exhibited remarkable linear capacitance responsiveness toward pressure, strain, and glucose concentration, and enabled real-time synchronous quantitative pressure/glucose sensing with multiple linear correlations, which was a key performance criteria for biomechanical sensors. The versatility and multiple advantages of the as-prepared hydrogel demonstrate the potential of biological-mechanical sensing materials using natural cellulosic biomass.

Flexible Conductive Cellulose Network-Based Composite Hydrogel for Multifunctional Supercapacitors.

With the continuous development of energy storage devices towards sustainability and versatility, the development of biomass-based multi-functional energy storage devices has become one of the important directions. In this study, a symmetric dual-function supercapacitor was constructed based on a cellulose network/polyacrylamide/polyaniline (CPP) composite hydrogel. The presented supercapacitor, with excellent electrochemical performance and an areal capacitance of 1.73 mF/cm2 at 5 mV/s, an energy density of 0.62 µW h/cm2 at a power density of 7.03 µW/cm2, a wide electrochemical window of 1.6 V and a promising cycling stability, can be achieved. The transmittance of the supercapacitor at 500 nm decreased by 9.6% after the electrification at 3 V, and the device can exhibit periodic transmittance change under the square potential input between 0.0 V and 3.0 V at regular intervals of 10 s. The present construction strategy provides a basis for the preparation of multifunctional devices with natural renewable materials and structures.

Lignocellulosic biomass delignification using aqueous alcohol solutions with the catalysis of acidic ionic liquids: A comparison study of solvents.

The exploration of effective deconstruction of biomass complex structures and mild fractionation into individual components is a profound challenge for the development of biorefinery. Herein, a biomass fractionation process, via treating biomass in various aqueous alcohol solutions with the catalysis of acidic ionic liquids 1-butyl-3-methylimidazolium hydrogen sulfate, was demonstrated to fractionate coir and poplar into cellulose materials with a lignin content as low as 0.95% and lignin with a delignification rate of up to 98%. The participation of acidic ionic liquids into the solvent system greatly multiplied the biomass fractionation efficiency. The analysis on effects of the chemical structure and solubility parameter of alcohols on the delignification efficiency provided a rational and meaningful way to predict and screen solvent for the biomass fractionation process. Lignin in the present study exhibited similar structure with milled wood lignin, and comparable molecular and thermal properties with the conventional organosolv lignin.

Facile pulping of lignocellulosic biomass using choline acetate.

Treating ground bagasse or Southern yellow pine in the biodegradable ionic liquid (IL), choline acetate ([Cho][OAc]), at 100°C for 24h led to dissolution of hemicellulose and lignin, while leaving the cellulose pulp undissolved, with a 54.3% (bagasse) or 34.3% (pine) reduction in lignin content. The IL solution of the dissolved biopolymers can be separated from the undissolved particles either by addition of water (20 wt% of IL) followed by filtration or by centrifugation. Hemicellulose (19.0 wt% of original bagasse, 10.2 wt% of original pine, containing 14-18 wt% lignin) and lignin (5.0 wt% of original bagasse, 6.0 wt% of original pine) could be subsequently precipitated. The pulp obtained from [Cho][OAc] treatment can be rapidly dissolved in 1-ethyl-3-methylimidazolium acetate (e.g., 17 h for raw bagasse vs. 7h for pulp), and precipitated as cellulose-rich material (CRM) with a lower lignin content (e.g., 23.6% for raw bagasse vs. 10.6% for CRM).