Compliant Iontronic Triboelectric Gels with Phase-Locked Structure Enabled by Competitive Hydrogen Bonding

Rapid advancements in flexible electronics technology propel soft tactile sensing devices toward high-level biointegration,even attaining tactile perception capabilities surpassing human skin.However,the inherent mechanical mismatch resulting from deficient biomimetic mechanical properties of sensing materials poses a challenge to the application of wearable tactile sensing devices in human-machine interaction.Inspired by the innate biphasic structure of human subcutaneous tissue,this study discloses a skin-compliant wearable iontronic triboelectric gel via phase separation induced by competitive hydrogen bonding.Solvent-nonsolvent interactions are used to construct competitive hydrogen bonding systems to trigger phase separation,and the resulting soft-hard alternating phase-locked structure confers the iontronic triboelectric gel with Young’s modulus(6.8-281.9 kPa)and high tensile properties(880%)compatible with human skin.The abundance of reactive hydroxyl groups gives the gel excellent tribopositive and self-adhesive properties(peel strength>70 N m^(−1)).The self-powered tactile sensing skin based on this gel maintains favorable interface and mechanical stability with the working object,which greatly ensures the high fidelity and reliability of soft tactile sensing signals.This strategy,enabling skin-compliant design and broad dynamic tunability of the mechanical properties of sensing materials,presents a universal platform for broad applications from soft robots to wearable electronics.

Rational Design of Cellulosic Triboelectric Materials for Self‑Powered Wearable Electronics

With the rapid development of the Internet of Things and flexible electronic technologies,there is a growing demand for wireless,sustainable,multifunctional,and independently operating self-powered wearable devices.Nevertheless,structural flexibility,long operating time,and wearing comfort have become key requirements for the widespread adoption of wearable electronics.Triboelectric nanogenerators as a distributed energy harvesting technology have great potential for application development in wearable sensing.Compared with rigid electronics,cellulosic self-powered wearable electronics have significant advantages in terms of flexibility,breathability,and functionality.In this paper,the research progress of advanced cellulosic triboelectric materials for self-powered wearable electronics is reviewed.The interfacial characteristics of cellulose are introduced from the top-down,bottom-up,and interfacial characteristics of the composite material preparation process.Meanwhile,the modulation strategies of triboelectric properties of cellulosic triboelectric materials are presented.Furthermore,the design strategies of triboelectric materials such as surface functionalization,interfacial structure design,and vacuum-assisted self-assembly are systematically discussed.In particular,cellulosic self-powered wearable electronics in the fields of human energy harvesting,tactile sensing,health monitoring,human–machine interaction,and intelligent fire warning are outlined in detail.Finally,the current challenges and future development directions of cellulosic triboelectric materials for self-powered wearable electronics are discussed.

Lignin Interaction with Cellulase during Enzymatic Hydrolysis

The conversion of lignocellulosic biomass into biofuels or biochemicals typically involves a pretreatment process followed by the enzyme-catalyzed hydrolysis of cellulose and hemicellulose components to fermentable sugars.Many factors can contribute to the recalcitrance of biomass,e.g.,the lignin content and structure,crystallinity of cellulose,degree of fiber polymerization,and hemicellulose content,among others.However,nonproductive binding between cellulase and lignin is the factor with the greatest impact on enzymatic hydrolysis.To reduce the nonproductive adsorption of enzymes on lignin and improve the efficiency of enzymatic hydrolysis,this review comprehensively summarized the progress that has been made in understanding the interactions between lignin and enzymes.Firstly,the effects of pretreatment techniques on lignin content and enzymatic hydrolysis were reviewed.The effects of lignin content and functional groups on enzymatic hydrolysis were then summarized.Methods for the preparation and characterization of lignin films were assessed.Finally,the methods applied to characterize the interactions between lignin and cellulase were reviewed,and methods for decreasing the nonproductive binding of enzymes to lignin were discussed.This review provides an overview of the current understanding of how lignin hinders the enzymatic hydrolysis of lignocellulosic biomass,and provides a theoretical basis for the development of more economical and effective methods and additives to reduce the interaction of lignin and enzymes to improve the efficiency of enzymatic hydrolysis.

An organic visible-photocatalytic-adsorbence mechanism to high-efficient removal of heavy metal antimony ions

Purification of emerging heavy metal antimony contaminated water based on advanced ingenious strategies.An activated modified coconut shell charcoal(CSC)was synthesized and evaluated as a substrate-supported loaded organic photovoltaic material,PM6:PYIT:PM6-b-PYIT,to prepare a surprisingly highly efficient,stable,environmentally friendly,and recyclable organic photocatalyst(CSC–N–P.P.P),which showed excellent effects on the simultaneous removal of Sb(Ⅲ)and Sb(Ⅴ).The removal efficiency of CSC-N-P.P.P on Sb(Ⅲ)and Sb(Ⅴ)reached an amazing 99.9%in quite a short duration of 15 min.At the same time,under ppb level and indoor visible light(~1 W m^(2)),it can be treated to meet the drinking water standards set by the European Union and the U.S.National Environmental Protection Agency in 5 min,and even after 25 cycles of recycling,the efficiency is still maintained at about 80%,in addition to the removal of As(Ⅲ),Cd(Ⅱ),Cr(Ⅵ),and Pb(Ⅱ)can also be realized.The catalyst not only solves the problems of low reuse rate,difficult structure adjustment and high energy consumption of traditional photocatalysts but also has strong applicability and practical significance.The pioneering approach provides a much-needed solution strategy for removing highly toxic heavy metal antimony pollution from the environment.

Biofilm response and removal via the coupling of visible-light-driven photocatalysis and biodegradation in an environment of sulfamethoxazole and Cr(Ⅵ)

The widespread contamination of water systems with antibiotics and heavy metals has gained much attention.Intimately coupled visible-light-responsive photocatalysis and biodegradation(ICPB)provides a novel approach for removing such mixed pollutants.In ICPB,the photocatalysis products are biodegraded by a protected biofilm,leading to the mineralization of refractory organics.In the present study,the ICPB approach exhibited excellent photocatalytic activity and biodegradation,providing up to~1.27 times the degradation rate of sulfamethoxazole(SMX)and 1.16 times the Cr(Ⅵ)reduction rate of visiblelight-induced photocatalysis.Three-dimensional fluorescence analysis demonstrated the synergistic ICPB effects of photocatalysis and biodegradation for removing SMX and reducing Cr(Ⅵ).In addition,the toxicity of the SMX intermediates and Cr(Ⅵ)in the ICPB process significantly decreased.The use of MoS_(2)/CoS_(2)photocatalyst accelerated the separation of electrons and holes,with·O_(2)^(–)and h+attacking SMX and ereducing Cr(Ⅵ),providing an effective means for enhancing the removal and mineralization of these mixed pollutants via the ICPB technique.The microbial community results demonstrate that bacteria that are conducive to pollutant removal are were enriched by the acclimation and ICPB operation processes,thus significantly improving the performance of the ICPB system.

Fabrication of highly water-repelling paper by surface coating with stearic acid modified calcium carbonate particles and reactive biopolymers

Cellulose paper is the most attractive green packaging material due to its recyclability, renewability, sustainability and biodegradability. In some applications, paper with a high level of water resistance is desirable to meet specific requirements in modern packaging fields. This research aimed to develop a water-repelling paper with cost-effective and nontoxic materials. Commercial precipitated calcium carbonate (PCC) particles were modified by stearic acid (SA) and incorporated with soybean oil-based binder as a water repelling coating agent. The water-repelling efficiency of the coated paper was highly dependent on the ratio of SA / PCC as well as the binder content in the coating formula. PCC particles modified with 12wt% SA were efficient in increasing the water contact angle (WCA) of the coated paper to 146° at a coating weight of 5 g/m2. The binder for the coating was synthesized with acrylated epoxidized soybean oil (AESO) through Michael addition reaction. The triglyceride structure in the polymer chain imparted good bio-degradability to the binder polymer. It was found that surface modification of PCC with stearic acid played an important role in improving the WCA of paper. A super hydrophobic paper with a WCA of 162° was fabricated with a coating formula of 60% SA-modified PCC and 40 wt% AESO-binder.

Bio-modification of eucalyptus chemithermomechanical pulp

Eucalyptus chemithermomechanical pulp(CTMP)was modified with the white-rot fungus 19-6 in a stationary culture condition.Different factors that influence the effect of white-rot fungus treatment,including additional nutrition,pH value,temperature,treatment time and oxygen input were investigated.The results show that the energy consumption of post refining of CTMP treated by white-rot fungus 19-6 was lower than that of untreated pulp and the strength properties also obviously improved.At a freeness level of about 330 mL,compared to the untreated pulp,the tensile index,tear index and internal bonding strength increased by 21.3%,27.4% and 33.1%,respectively.Unfortunately,the treatment with white-rot fungus substantially decreased all optical properties except for opacity,which was essentially unchanged.Brightness and light scatter-ing coefficient were reduced to as much as 25%and 21%compared to the untreated pulps.However,after a tow-stage“Na_(2)S_(2)O_(4)-H_(2)O_(2)”bleaching,the final brightness can reach 70.3%ISO,which is similar to that of the untreated CTMP.