Publications by authors named "Shuaiming He"

Multifunctional fibers with high mechanical strength enable advanced applications of smart textiles, robotics, and biomedicine. Herein, we reported a one-step degumming method to fabricate strong, stiff, and humidity-responsive smart cellulosic fibers from abundant natural grass. The facile process involves partially removing lignin and hemicellulose functioning as glue in grass, which leads to the separation of vessels, parenchymal cells, and cellulosic fibers, where cellulosic fibers are manufactured at kilogram scale.

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One possible solution against the accumulation of petrochemical plastics in natural environments is to develop biodegradable plastic substitutes using natural components. However, discovering all-natural alternatives that meet specific properties, such as optical transparency, fire retardancy and mechanical resilience, which have made petrochemical plastics successful, remains challenging. Current approaches still rely on iterative optimization experiments.

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The issue of mercury pollution in environmental remediation has garnered significant attention due to its severe health hazards to humans. Various strategies have been devised to mitigate the impact of toxic mercury ions, including coagulation, ion exchange, adsorption, membrane technology, and electrochemical treatment. Among these approaches, adsorption has emerged as an efficient and widely employed method for the uptake of low concentrations of mercury ions.

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Supramolecular frameworks have been widely synthesized for ion transport applications. However, conventional approaches of constructing ion transport pathways in supramolecular frameworks typically require complex processes and display poor scalability, high cost, and limited sustainability. Here, we report the scalable and cost-effective synthesis of an ion-conducting (e.

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The development of green materials, especially the preparation of high-performance conductive hydrogels from biodegradable biomass materials, is of great importance and has received worldwide attention. As an aromatic polymer found in many natural biomass resources, lignin has the advantage of being renewable, biodegradable, non-toxic, widely available, and inexpensive. The unique physicochemical properties of lignin, such as the presence of hydroxyl, carboxyl, and sulfonate groups, make it promising for use in composite conductive hydrogels.

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Conventional plastic foams are usually produced by fossil-fuel-derived polymers, which are difficult to degrade in nature. As an alternative, cellulose is a promising biodegradable polymer that can be used to fabricate greener foams, yet such a process typically relies on methods (e.g.

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Silica glasses have wide applications in industrial fields due to their extraordinary properties, such as high transparency, low thermal expansion coefficient, and high hardness. However, current methods of fabricating silica glass generally require long thermal treatment time (up to hours) and complex setups, leading to high cost and slow manufacturing speed. Herein, to obtain high-quality glasses using a facile and rapid method, an ultrafast high-temperature sintering (UHS) technique is reported that requires no additional pressure.

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Wood-based hydrogel with a unique anisotropic structure is an attractive soft material, but the presence of rigid crystalline cellulose in natural wood makes the hydrogel less flexible. In this study, an all-wood hydrogel was constructed by cross-linking cellulose fibers, polyvinyl alcohol (PVA) chains, and lignin molecules through the Hofmeister effect. The all-wood hydrogel shows a high tensile strength of 36.

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The global demand for plastic foam materials is enormous (annual worth of ≈$341.3 billion) and still surging with an annual growth rate of 4.8%, driven by increasing modern societal needs.

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Recently, great efforts have been devoted to developing conductive adhesive hydrogels to meet the needs of various applications. However, grand challenges remain in achieving anisotropic hydrogels simultaneously featuring multiple properties using natural polymers and renewable resources. Here, a cellulose-based conductive hydrogel with strong, ultrastretchable, and adhesive properties is prepared via a simple magnetic field-induced strategy.

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Although solid-state lithium (Li)-metal batteries promise both high energy density and safety, existing solid ion conductors fail to satisfy the rigorous requirements of battery operations. Inorganic ion conductors allow fast ion transport, but their rigid and brittle nature prevents good interfacial contact with electrodes. Conversely, polymer ion conductors that are Li-metal-stable usually provide better interfacial compatibility and mechanical tolerance, but typically suffer from inferior ionic conductivity owing to the coupling of the ion transport with the motion of the polymer chains.

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Solid-state batteries (SSBs) promise better safety and potentially higher energy density than the conventional liquid- or gel-based ones. In practice, the implementation of SSBs often necessitates 3D porous scaffolds made by ceramic solid-state electrolytes (SSEs). Herein, a general and facile method to sinter 3D porous scaffolds with a range of ceramic SSEs on various substrates at high temperature in seconds is reported.

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Many efforts have been dedicated to exploring nanofluidic systems for various applications including water purification and energy generation. However, creating robust nanofluidic materials with tunable channel orientations and numerous nanochannels or nanopores on a large scale remains challenging. Here, we demonstrate a scalable and cost-effective method to fabricate a robust and highly conductive nanofluidic wood hydrogel membrane in which ions can transport across the membrane.

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Transparent wood is considered a promising structural and light management material for energy-efficient engineering applications. However, the solution-based delignification process that is used to fabricate transparent wood generally consumes large amounts of chemicals and energy. Here, we report a method to produce optically transparent wood by modifying the wood's lignin structure using a solar-assisted chemical brushing approach.

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Lignin serves as a binder that forms strong matrices of the cell walls of wood. However, it has many photolabile chromophore groups that create a monotonic brownish color and make wood susceptible to photodegradation. Herein, a new strategy is reported for modifying lignin using an in situ, rapid, and scalable process that involves the photocatalytic oxidation of native lignin in wood by H O and UV light.

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Lignocellulose nanofibrils (LCNF) were used to prepare oil-in-water Pickering emulsions and to assess the role residual lignin in interfacial stabilization. Two LCNF fractions of similar morphology (length ∼700 nm and width ∼8 nm) and structure (polymorphism and crystallinity) were obtained by microfluidization of fibers obtained by hydrothermal treatment of wood with a recyclable organic acid. The LCNF with higher residual lignin was less hydrophilic and, correspondingly, performed better as Pickering stabilizer, producing emulsions of smaller droplet size and higher resistance to creaming.

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Nowadays, energy-saving building materials are important for reducing indoor energy consumption by enabling better thermal insulation, promoting effective sunlight harvesting and offering comfortable indoor lighting. Here, we demonstrate a novel scalable aesthetic transparent wood (called aesthetic wood hereafter) with combined aesthetic features (e.g.

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Wood materials are being reinvented to carry superior properties for a variety of new applications. Cutting-edge nanomanufacturing transforms traditional bulky and low-value woods into advanced materials that have desired structures, durability, and functions to replace nonrenewable plastics, polymers, and metals. Here, a first prospect report on how novel nanowood materials have been developed and applied in water and associated industries is provided, wherein their unique features and promises are discussed.

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Thin films of several microns in thickness are ubiquitously used in packaging, electronics, and acoustic sensors. Here we demonstrate that natural wood can be directly converted into an ultrathin film with a record-small thickness of less than 10 μm through partial delignification followed by densification. Benefiting from this aligned and laminated structure, the ultrathin wood film exhibits excellent mechanical properties with a high tensile strength of 342 MPa and a Young's modulus of 43.

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Graphene-based nanocomposites have attracted tremendous attention in recent years. In this study, a facile yet effective approach was developed to synthesize reduced graphene oxide and an Ag-graphene nanocomposite. The basic strategy involved in the preparation of reduced graphene oxide includes reducing graphene oxide with dopamine, followed by in situ syntheses of the Ag-PDA-reducing graphene oxide (RGO) nanocomposite through adding AgNO solution and a small amount of dopamine.

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Developing advanced building materials with both excellent thermal insulating and optical properties to replace common glass (thermal conductivity of ∼1 W m K) is highly desirable for energy-efficient applications. The recent development of transparent wood suggests a promising building material with many advantages, including high optical transmittance, tunable optical haze, and excellent thermal insulation. However, previous transparent wood materials generally have a high haze (typically greater than 40%), which is a major obstacle for their practical application in the replacement of glass.

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Current membrane distillation (MD) is challenged by the inefficiency of water thermal separation from dissolved solutes, controlled by membrane porosity and thermal conductivity. Existing petroleum-derived polymeric membranes face major development barriers. Here, we demonstrate a first robust MD membrane directly fabricated from sustainable wood material.

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Reducing human reliance on energy-inefficient cooling methods such as air conditioning would have a large impact on the global energy landscape. By a process of complete delignification and densification of wood, we developed a structural material with a mechanical strength of 404.3 megapascals, more than eight times that of natural wood.

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Emerging solar desalination by interfacial evaporation shows great potential in response to global water scarcity because of its high solar-to-vapor efficiency, low environmental impact, and off-grid capability. However, solute accumulation at the heating interface has severely impacted the performance and long-term stability of current solar evaporation systems. Here, a self-regenerating solar evaporator featuring excellent antifouling properties using a rationally designed artificial channel-array in a natural wood substrate is reported.

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