Melatonin is a pleiotropic signaling molecule that provides physiological protection against diverse environmental stresses in plants. Nonetheless, the mechanisms for melatonin‐mediated ...thermotolerance remain largely unknown. Here, we report that endogenous melatonin levels increased with a rise in ambient temperature and that peaked at 40°C. Foliar pretreatment with an optimal dose of melatonin (10 μmol/L) or the overexpression of N‐acetylserotonin methyltransferase (ASMT) gene effectively ameliorated heat‐induced photoinhibition and electrolyte leakage in tomato plants. Both exogenous melatonin treatment and endogenous melatonin manipulation by overexpression of ASMT decreased the levels of insoluble and ubiquitinated proteins, but enhanced the expression of heat‐shock proteins (HSPs) to refold denatured and unfolded proteins under heat stress. Meanwhile, melatonin also induced expression of several ATG genes and formation of autophagosomes to degrade aggregated proteins under the same stress. Proteomic profile analyses revealed that protein aggregates for a large number of biological processes accumulated in wild‐type plants. However, exogenous melatonin treatment or overexpression of ASMT reduced the accumulation of aggregated proteins. Aggregation responsive proteins such as HSP70 and Rubisco activase were preferentially accumulated and ubiquitinated in wild‐type plants under heat stress, while melatonin mitigated heat stress‐induced accumulation and ubiquitination of aggregated proteins. These results suggest that melatonin promotes cellular protein protection through induction of HSPs and autophagy to refold or degrade denatured proteins under heat stress in tomato plants.
Given increasing environmental issues due to the large usage of non‐biodegradable plastics based on petroleum, new plastic materials, which are economic, environmentally friendly, and recyclable are ...in high demand. One feasible strategy is the bio‐inspired synthesis of mineral‐based hybrid materials. Herein we report a facile route for an amorphous CaCO3 (ACC)‐based hydrogel consisting of very small ACC nanoparticles physically cross‐linked by poly(acrylic acid). The hydrogel is shapeable, stretchable, and self‐healable. Upon drying, the hydrogel forms free‐standing, rigid, and transparent objects with remarkable mechanical performance. By swelling in water, the material can completely recover the initial hydrogel state. As a matrix, thermochromism can also be easily introduced. The present hybrid hydrogel may represent a new class of plastic materials, the “mineral plastics”.
Shapeable, stretchable, recyclable, (thermochromic) amorphous calcium carbonate‐based hybrid supramolecular hydrogels were synthesized, which can reversibly form macroscopic rigid transparent films upon drying. This plastic material may potentially replace conventional plastics in a move towards solving environmental issues.
Carbon aerogels with 3D networks of interconnected nanometer‐sized particles exhibit fascinating physical properties and show great application potential. Efficient and sustainable methods are ...required to produce high‐performance carbon aerogels on a large scale to boost their practical applications. An economical and sustainable method is now developed for the synthesis of ultrathin carbon nanofiber (CNF) aerogels from the wood‐based nanofibrillated cellulose (NFC) aerogels via a catalytic pyrolysis process, which guarantees high carbon residual and well maintenance of the nanofibrous morphology during thermal decomposition of the NFC aerogels. The wood‐derived CNF aerogels exhibit excellent electrical conductivity, a large surface area, and potential as a binder‐free electrode material for supercapacitors. The results suggest great promise in developing new families of carbon aerogels based on the controlled pyrolysis of economical and sustainable nanostructured precursors.
Nano‐woodwork: An economical and sustainable method has now been developed for the synthesis of ultrathin carbon nanofiber (CNF) aerogels by engineering the thermal decomposition chemistry of nanofibrillated wood cellulose. This work suggests great promise in developing new families of carbon aerogels based on the controlled pyrolysis of sustainable nanostructured precursors.
Ultrathick electrode design is a promising strategy to enhance the specific energy of Li‐ion batteries (LIBs) without changing the underlying materials chemistry. However, the low Li‐ion conductivity ...caused by ultralong Li‐ion transport pathway in traditional random microstructured electrode heavily deteriorates the rate performance of ultrathick electrodes. Herein, inspired by the vertical microchannels in natural wood as the highway for water transport, the microstructures of wood are successfully duplicated into ultrathick bulk LiCoO2 (LCO) cathode via a sol–gel process to achieve the high areal capacity and excellent rate capability. The X‐ray‐based microtomography demonstrates that the uniform microchannels are built up throughout the whole wood‐templated LCO cathode bringing in 1.5 times lower of tortuosity and ≈2 times higher of Li‐ion conductivity compared to that of random structured LCO cathode. The fabricated wood‐inspired LCO cathode delivers high areal capacity up to 22.7 mAh cm−2 (five times of the existing electrode) and achieves the dynamic stress test at such high areal capacity for the first time. The reported wood‐inspired design will open a new avenue to adopt natural hierarchical structures to improve the performance of LIBs.
Inspired by the vertical microchannels in natural wood as the highway for water transport, an ultra‐thick bulk LiCoO2 (LCO) cathode with vertical channels is fabricated to enhance the transport of Li+. Remarkably, the fabricated LCO cathode shows low tortuosity and high Li‐ion conductivity, and can deliver high areal capacity up to 22.7 mAh cm−2.
Melatonin regulates broad aspects of plant responses to various biotic and abiotic stresses, but the upstream regulation of melatonin biosynthesis by these stresses remains largely unknown. Herein, ...we demonstrate that transcription factor heat‐shock factor A1a (HsfA1a) conferred cadmium (Cd) tolerance to tomato plants, in part through its positive role in inducing melatonin biosynthesis under Cd stress. Analysis of leaf phenotype, chlorophyll content, and photosynthetic efficiency revealed that silencing of the HsfA1a gene decreased Cd tolerance, whereas its overexpression enhanced plant tolerance to Cd. HsfA1a‐silenced plants exhibited reduced melatonin levels, and HsfA1a overexpression stimulated melatonin accumulation and the expression of the melatonin biosynthetic gene caffeic acid O‐methyltransferase 1 (COMT1) under Cd stress. Both an in vitro electrophoretic mobility shift assay and in vivo chromatin immunoprecipitation coupled with qPCR analysis revealed that HsfA1a binds to the COMT1 gene promoter. Meanwhile, Cd stress induced the expression of heat‐shock proteins (HSPs), which was compromised in HsfA1a‐silenced plants and more robustly induced in HsfA1a‐overexpressing plants under Cd stress. COMT1 silencing reduced HsfA1a‐induced Cd tolerance and melatonin accumulation in HsfA1a‐overexpressing plants. Additionally, the HsfA1a‐induced expression of HSPs was partially compromised in COMT1‐silenced wild‐type or HsfA1a‐overexpressing plants under Cd stress. These results demonstrate that HsfA1a confers Cd tolerance by activating transcription of the COMT1 gene and inducing accumulation of melatonin that partially upregulates expression of HSPs.
As an abundant natural resource, wood has gained great attention for thousands of years, spanning from the primitive construction materials to the modern high‐added‐value engineering materials. The ...unique delicate microstructures and the wonderful properties (e.g., low‐density, high strength and stiffness, good toughness, and environmental sustainability) have made wood a natural source of inspiration that guides researchers to invent various wood‐inspired materials. Herein, as an emerging material system, bioinspired artificial wood, with similar cellular structures and comparable mechanical properties, is discussed in the view of the design concept, fabrication strategy, properties, and possible applications. The present challenges and further research opportunities are also presented for artificial woods to thrive. To achieve the final eco‐friendly artificial wood, more endeavors should be made in biomaterials and biodegradable or recyclable engineering of polymers to gain high mechanical properties and environmental sustainability simultaneously.
Artificial woods have emerged as a novel kind of wood‐inspired engineering material with almost exactly the same channel microstructures and similar wall components. The performances of artificial woods depend on both the oriented channel and wall designs. The rational combination of other engineering polymers and channel‐making techniques hold promise to develop more useful artificial woods.
Transition‐metal phosphides have stimulated great interest as catalysts to drive the hydrogen evolution reaction (HER), but their use as bifunctional catalytic electrodes that enable efficient ...neutral‐pH water splitting has rarely been achieved. Herein, we report the synthesis of ternary Ni0.1Co0.9P porous nanosheets onto conductive carbon fiber paper that can efficiently and robustly catalyze both the HER and water oxidation in 1 m phosphate buffer (PBS; pH 7) electrolyte under ambient conditions. A water electrolysis cell comprising the Ni0.1Co0.9P electrodes demonstrates remarkable activity and stability for the electrochemical splitting of neutral‐pH water. We attribute this performance to the new ternary Ni0.1Co0.9P structure with porous surfaces and favorable electronic states resulting from the synergistic interplay between nickel and cobalt. Ternary metal phosphides hold promise as efficient and low‐cost catalysts for neutral‐pH water splitting devices.
Sheets and paper: Ternary Ni0.1Co0.9P porous nanosheets anchored onto conductive carbon fiber paper, can be used as a bifunctional catalytic material for driving both water reduction and oxidation reactions efficiently in neutral‐pH electrolyte under ambient conditions.
Nanoparticles exist far from the equilibrium state due to their high surface energy. Nanoparticles are therefore extremely unstable and easily change themselves or react with active substances to ...reach a relatively stable state in some cases. This causes desired changes or undesired changes to nanoparticles and thus makes them exhibit a high reactivity and a poor stability. Such dual nature (poor stability and high reactivity) of nanoparticles may result in both negative and positive effects for nanoparticle processing. However, the existing studies mainly focus on the high reactivity of nanoparticles, whereas their poor stability has been neglected or considered inconsequential. In fact, in some cases the unstable process, which is derived from the poor stability of nanoparticles, offers an opportunity to design and fabricate unique nanomaterials, such as by chemically transforming the “captured” intermediate nanostructures during a changing process, assembling destabilized nanoparticles into larger ordered assemblies, or shrinking/processing pristine materials into the desired size or shape via selective etching. In this review, we aim to present the stability and reactivity of nanoparticles on three levels: the foundation, concrete manifestations, and applications. We start with a brief introduction of dangling bonds and the surface chemistry of nanoparticles. Then, concrete manifestations of the poor stability and high reactivity of nanoparticles are presented from four perspectives: dispersion stability, thermal stability, structural stability, and chemical stability/reactivity. Next, we discuss some issues regarding the stability and reactivity of nanomaterials during applications. Finally, conclusions and perspectives on this field are presented.
A wide range of light absorption and rapid electron–hole separation are desired for efficient photocatalysis. Herein, on the basis of a semiconductor‐like metal–organic framework (MOF), a Pt@MOF/Au ...catalyst with two types of metal–MOF interfaces integrates the surface plasmon resonance excitation of Au nanorods with a Pt‐MOF Schottky junction, which not only extends the light absorption of the MOF from the UV to the visible region but also greatly accelerates charge transfer. The spatial separation of Pt and Au particles by the MOF further steers the formation of charge flow and expedites the charge migration. As a result, the Pt@MOF/Au presents an exceptionally high photocatalytic H2 production rate by water splitting under visible light irradiation, far superior to Pt/MOF/Au, MOF/Au and other counterparts with similar Pt or Au contents, highlighting the important role of each component and the Pt location in the catalyst.
Up the junction: A wide‐band‐gap semiconductor‐like metal–organic framework (MOF), MIL‐125, with Pt nanoparticles in its crystal structure and Au nanorods on its outer surface gives Pt@MIL‐125/Au, a catalyst with two metal–MOF interfaces. The integration of surface plasmon resonance (SPR) Au excitation with the Pt–MOF Schottky junction results in high photocatalytic H2 production activity.
Petroleum-based plastics are useful but they pose a great threat to the environment and human health. It is highly desirable yet challenging to develop sustainable structural materials with excellent ...mechanical and thermal properties for plastic replacement. Here, inspired by nacre's multiscale architecture, we report a simple and efficient so called "directional deforming assembly" method to manufacture high-performance structural materials with a unique combination of high strength (281 MPa), high toughness (11.5 MPa m
), high stiffness (20 GPa), low coefficient of thermal expansion (7 × 10
K
) and good thermal stability. Based on all-natural raw materials (cellulose nanofiber and mica microplatelet), the bioinspired structural material possesses better mechanical and thermal properties than petroleum-based plastics, making it a high-performance and eco-friendly alternative structural material to substitute plastics.
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