Given the substantial emissions of CO₂ into the atmosphere, there is a critical need for effective CO₂ adsorbents at scale, ideally derived from abundant and sustainable natural resources. In this work, microcrystalline cellulose derived from cotton is used to fabricate cellulose aerogel as porous support via a NaOH/urea-based dissolution and regeneration process, followed by surface modification with a series of amino silane coupling agents to produce aminated cellulose aerogel as CO₂ adsorbent. The as-synthesized optimal adsorbent exhibits a high CO₂ sorption capacity of up to 1.5 and 1.3 mmol g⁻¹ at 0 °C and 25 °C at 1 bar, respectively. Notably, in-depth analysis shows that the adsorbent achieves an impressive capacity of CO₂ uptake of 0.29 mmol g⁻¹ at 25 °C at an exceptionally low CO₂ pressure of 0.4 mbar, i.e., under ambient CO₂ pressure. It implies its potential use as adsorbent both for the traditional point-source capture and the direct air capture as an emerging negative emission technology. This study underscores the environmentally friendly, cost-effective, and biosourced attributes of aminated cellulose aerogel as a compelling alternative for carbon capture, contributing to global initiatives combating CO₂ emissions and stressing the key role of sustainable materials in tackling this global environmental challenge.

Fiber actuators, particularly valuable in soft robotics and environmental sensing, are at the forefront of “smart” materials and materials innovation. In this realm, torsional and tensile biofiber actuators, notable for their cost-effectiveness and biodegradability, mark a critical gap in the development of next-generation functional systems and devices. To address this gap, this study showcased moisture-responsive fiber actuators made from cellulose nanofibrils (CNFs). The initial focus of this contribution was on an innovative torsional actuator, which capitalized on the hydrophilic nature of the CNFs filaments produced through wet-spinning processes. These robust filaments, with a mechanical strength of (237.0 ± 10.7) MPa, were twisted to form the torsional actuator. This actuator demonstrated a rapid rotational response, achieving up to 1180 rpm within merely 10 s of exposure to moisture, and maintained high durability over multiple cycles. Building upon this platform, the study continued and aimed to build up a tensile actuator, which ingeniously integrated a supercoiled nylon fiber core within a moisture-sensitive CNFs sheath. This design enhances the structural support and functionality of the actuator. The pursued transition from torsional to tensile actuator demonstrates an iterative and innovative approach in actuator technology, underscoring the versatility and potential of CNFs in the realm of “smart” actuation materials.

The escalating global energy demand and the imperative to mitigate carbon emissions have intensified the pursuit for sustainable energy solutions, with hydrogen emerging as a pivotal clean energy carrier. Transition metal-based metal-organic frameworks (MOFs) have garnered significant attention for their potential in efficient hydrogen production due to their high surface area, tunable porosity, and versatile catalytic properties. Despite notable advancements in MOF synthesis, critical challenges related to stability, electrical conductivity, and scalability continue to hinder their widespread application. This review provides a comprehensive analysis of recent progress in the design and synthesis of transition metal-based MOFs, emphasizing their role in electrocatalytic and photocatalytic hydrogen production. Key synthetic strategies and their influence on catalytic performance are systematically discussed, alongside the identification of existing limitations and knowledge gaps. By highlighting these critical areas and proposing pathways for future research, this review aims to accelerate the practical integration of MOFs into the emerging hydrogen economy.

A sensitive and simple method for detecting Cu2+ in the water source was proposed by using surface-enhanced Raman scattering spectroscopy (SERS) based on the Ag@SiO2/Au core-shell composite. The Ag@SiO2 SERS tag was synthesized by a simple approach, in which Ag nanoparticles were first embedded with Raman reporter PATP and next coated with a SiO2 shell. The Ag@SiO2 nanoparticles had strong stability even in a high-concentration salty solution, and there were no changes to their properties and appearance within one month. The Ag@SiO2/Au composite was fabricated through a controllable self-assemble process. L-cysteine was decorated on the surface of a functionalized Ag@SiO2/Au composite, as the amino and carboxyl groups of it can form coordinate covalent bond with Cu2+, which shows that the Ag@SiO2/Au composite labelled with L-cysteine has excellent performance for the detection of Cu2+ in aqueous media. In this study, the SERS detection of Cu2+ was carried out using Ag@SiO2 nanoparticles, and the limit of detection (LOD) as low as 0.1 mg/L was achieved.

Given the abundant solar light available on our planet, it is promising to develop an advanced fabric capable of simultaneously providing personal thermal management and facilitating clean water production in an energy-efficient manner. In this study, we present the fabrication of a photothermally active, biodegradable composite cloth composed of titanium carbide MXene and cellulose, achieved through an electrospinning method. This composite cloth exhibits favorable attributes, including chemical stability, mechanical performance, structural flexibility, and wettability. Notably, our 0.1-mm-thick composite cloth (RC/MXene IV) raises the temperature of simulated skin by 5.6 degrees C when compared to a commercially available cotton cloth, which is five times thicker under identical ambient conditions. Remarkably, the composite cloth (RC/MXene V) demonstrates heightened solar light capture efficiency (87.7%) when in a wet state instead of a dry state. Consequently, this cloth functions exceptionally well as a high-performance steam generator, boasting a superior water evaporation rate of 1.34 kg m(-2) h(-1) under one-sun irradiation (equivalent to 1000 W m(-2)). Moreover, it maintains its performance excellence in solar desalination processes. The multifunctionality of these cloths opens doors to a diverse array of outdoor applications, including solar-driven water evaporation and personal heating, thereby enriching the scope of integrated functionalities for textiles.

Pickering multiphase systems stabilized by solid particles have recently attracted increasing attention due to their excellent stability. Among various solid stabilizers, natural and renewable cellulosic micro/nanoparticles that are derived from agricultural and forestry sources have become promising candidates for Pickering stabilization due to their unique morphological features and tunable surface properties. In this review, recent progress on forming and stabilizing Pickering multiphase systems using cellulosic colloidal particles is summarized, including the physicochemical factors affecting their assembly at the interfaces and the preparation methods suitable for producing Pickering emulsions. In addition, relevant application prospects of corresponding Pickering multiphase materials are outlined. Finally, current challenges and future perspectives of such renewable Pickering multiphase systems are presented. This review aims to encourage the utilization of cellulosic micro/nanoparticles as key components in the development of Pickering systems, leading to enhanced performance and unique functionalities. image

Chiral architectures, one of the key structural features of natural systems ranging from the nanoscale to macroscale, are an infinite source of inspiration for functional materials. Researchers have been, and still are, strongly pursuing the goal of constructing such structures with renewable and sustainable building blocks via simple and efficient strategies. With the merits of high sustainability, renewability, and the ability to self-assemble into chiral nematic structures in aqueous suspensions that can be preserved in the solid state, polysaccharide nanocrystals (PNs) including cellulose nanocrystals (CNCs) and chitin nanocrystals (ChNCs) offer opportunities to reach the target. We herein provide a comprehensive review that focuses on the development of CNCs and ChNCs for the use in advanced functional materials. First, the introduction of CNCs and ChNCs, and cellulose- and chitin-formed chiral nematic organizations in the natural world, are given. Then, the self-assembly process of such PNs and the factors influencing this process are comprehensively discussed. After that, we showcased the emerging applications of the self-assembled chiral nematic structures of CNCs and ChNCs. Finally, this review concludes with perspectives on the challenges and opportunities in this field.

Understanding the reconstruction of surface sites is crucial for gaining insights into the true active sites and catalytic mechanisms. While extensive research has been conducted on reconstruction behaviors of atomically dispersed metallic catalytic sites, limited attention has been paid to non-metallic ones despite their potential catalytic activity comparable or even superior to their noble-metal counterpart. Herein, we report a carbonaceous, atomically dispersed non-metallic selenium catalyst that displayed exceptional catalytic activity in the hydrazine oxidation reaction (HzOR) in alkaline media, outperforming the noble-metal Pt catalysts. In situ X-ray absorption spectroscopy (XAS) and Fourier transform infrared spectroscopy revealed that the pristine SeC₄ site pre-adsorbs an ∗OH ligand, followed by HzOR occurring on the other side of the OH–SeC₄. Theoretical calculations proposed that the pre-adsorbed ∗OH group pulls electrons from the Se site, resulting in a more positively charged Se and a higher polarity of Se–C bonds, thereby enhancing surface reactivity toward HzO/R.

Passive daytime radiative cooling (PDRC) as a zero-energy-consumption cooling technique offers rich opportunities in reducing global energy consumption and mitigating CO2 emissions. Developing high-performance PDRC coolers with practical applicability based on sustainable materials is of great significance, but remains a big challenge. Herein, polyvinyl alcohol (PVA) and esterified cellulose (EC) extracted from sawdust were used as raw materials to construct foams by using a dual-crosslinking assisted-unidirectional freeze-drying strategy followed by hydrophobic surface modification. The resultant PVA/EC (PEC) foams with ideal hierarchical macropore structure displayed various excellent features, such as low thermal conductivity (26.2 mW·m−1·K−1), high solar reflectance (95 %) and infrared emissivity (0.97), superhydrophobicity as well as high mechanical properties. The features allowed the PEC foams to be used as radiative coolers with excellent PDRC performance and thermal insulating materials. A maximum sub-ambient temperature drops of 10.2 °C could be achieved for optimal PEC foams. Building simulations indicated that PEC foams could save 55.8 % of the energy consumption for Xi'an. Our work would give inspiration for designing various types of PDRC coolers, including but certainly not limited to foams-based radiative coolers. 

Colloidal lignin particles (CLPs) have sparked various intriguing insights toward bio-polymeric materials and triggered many lignin-featured innovative applications. Here, we report a multi-solvent sequential fractionation methodology integrating green solvents of acetone, 1-butanol, and ethanol to fractionate industrial lignin for CLPs fabrication. Through a rationally designed fractionation strategy, multigrade lignin fractions with variable hydroxyl group contents, molecular weights, and high purity were obtained without altering their original chemical structures. CLPs with well-defined morphology, narrow size distribution, excellent thermal stability, and long-term colloidal stability can be obtained by rational selection of lignin fractions. We further elucidated that trace elements (S, N) were reorganized onto the near-surface area of CLPs from lignin fractions during the formation process in the form of -SO₄²⁻ and -NH₂. This work provides a sustainable and efficient strategy for refining industrial lignin into high-quality fractions and an in-depth insight into the CLPs formation process, holding great promise for enriching the existing libraries of colloidal materials.