Institute of New Materials

Lithium-ion batteries have had a tremendous impact on several sectors of our society; however, the intrinsic limitations of Li-ion chemistry limits their ability to meet the increasing demands of developing more advanced portable electronics, electric vehicles, and grid-scale energy storage systems. Therefore, battery chemistries beyond Li ions are being intensively investigated and need urgent breakthroughs toward commercial applications, wherein the use of metallic Li is one of the most intuitive choices. Despite several decades of oblivion due to safety concerns regarding the growth of Li dendrites, Li-metal anodes are now poised to be revived because of the advances in investigative tools and globally invested efforts. In this review, we first summarize the existing issues with regard to Li anodes and their underlying reasons and then highlight the recent progress made in the development of high-performance Li anodes. Finally, we propose the persisting challenges and opportunities toward the exploration of practical Li-metal anodes.

The chemical structure of donors and acceptors limit the power conversion efficiencies achievable with active layers of binary donor-acceptor mixtures. Here, using quaternary blends, double cascading energy level alignment in bulk heterojunction organic photovoltaic active layers are realized, enabling efficient carrier splitting and transport. Numerous avenues to optimize light absorption, carrier transport, and charge-transfer state energy levels are opened by the chemical constitution of the components. Record-breaking PCEs of 18.07% are achieved where, by electronic structure and morphology optimization, simultaneous improvements of the open-circuit voltage, short-circuit current and fill factor occur. The donor and acceptor chemical structures afford control over electronic structure and charge-transfer state energy levels, enabling manipulation of hole-transfer rates, carrier transport, and non-radiative recombination losses.

With the widespread application of electronic communication technology, the resulting electromagnetic radiation pollution has been significantly increased. Metal matrix electromagnetic interference (EMI) shielding materials have disadvantages such as high density, easy corrosion, difficult processing and high price, etc. Polymer matrix EMI shielding composites possess light weight, corrosion resistance and easy processing. However, the current polymer matrix composites present relatively low electrical conductivity and poor EMI shielding performance. This review firstly discusses the key concept, loss mechanism and test method of EMI shielding. Then the current development status of EMI shielding materials is summarized, and the research progress of polymer matrix EMI shielding composites with different structures is illustrated, especially for their preparation methods and evaluation. Finally, the corresponding key scientific and technical problems are proposed, and their development trend is also prospected.

In modern society, traffic and transportation and the manufacturing industry and construction industries continuously release large amounts of dust and particles into the atmosphere, which can cause heavy air pollution, leading to health hazards. The haze disaster, a serious problem in developing countries such as China and India, has become one of the main issues of global environmental pollution in recent decades. Many air filtration technologies have been developed. Air filtration using electrospun fibers that intercept fine particles/volatile organic gases/bacterium is a relatively new, but highly promising, technique. Due to their interconnected nanoscale pore structures, highly specific surface areas, fine diameters, and porous structure as well as their ability to incorporate active chemistry on a nanoscale surface, electrospun fibers are becoming a promising versatile platform for air filtration. In this review, following a short introduction concerning the need for air filtration and filtration theory and mechanism, electrospun nanofibers membranes for air filtration have been highlighted, including the preparation (electrospinning process) and the parameters relevant to filtration efficacy. Additionally, various types (function) of the electrospun air filtration membranes have been classified in detail. Furthermore, their potential in the filtration of fine particles and chemical pollutants has been discussed. Finally, the challenges of their practical application and the future prospects have been summarized. Given that some advanced electrospun air filtration nanofibrous membranes exist for treating different contaminants from various types of polluted atmosphere, it is believed that they should make a significant contribution in protection against air pollution.

This work provides guidance on controlling anionic redox activity and finding novel high-capacity transition metal oxide cathodes for sodium-ion batteries.

Additive manufacturing is a revolutionary technology that offers a different pathway for material processing and design. However, innovations in either new materials or new processing technologies can seldom be successful without a synergistic combination. We demonstrate an in situ design approach to make alloys spatially modulated in concentration by using laser-powder bed fusion. We show that the partial homogenization of two dissimilar alloy melts—Ti-6Al-4V and a small amount of 316L stainless steel—allows us to produce micrometer-scale concentration modulations of the elements that are contained in 316L in the Ti-6Al-4V matrix. The corresponding phase stability modulation creates a fine scale–modulated β + α′ dual-phase microstructure that exhibits a progressive transformation-induced plasticity effect, which leads to a high tensile strength of ~1.3 gigapascals with a uniform elongation of ~9% and an excellent work-hardening capacity of >300 megapascals. This approach creates a pathway for concentration-modulated heterogeneous alloy design for structural and functional applications.

The study of preparing silica/rubber composites used in tires with low rolling resistance in an energy-saving method is fast-growing. In this study, a novel strategy is proposed, in which silica was modified by combing alcohol polyoxyethylene ether (AEO) and 3-mercaptopropyltriethoxysilane (K-MEPTS) for preparing silica/natural rubber (NR) master batches. A thermal gravimetric analyzer and Raman spectroscopy results indicated that both AEO and K-MEPTS could be grafted on to the silica surface, and AEO has a chance to shield the mercaptopropyl group on K-MEPTS. Silica modified by AEO and K-MEPTS together was completely co-coagulated with the rubber in preparing silica/NR composites using the latex compounding method with the help of the interaction between AEO and K-MEPTS. The performance of composites prepared by silica/NR master batches was investigated by a rubber process analyzer (RPA), transmission electron microscopy (TEM) and a tensile tester. These results demonstrate that AEO forms a physical interface between silica and rubber, resulting in good silica dispersion in the matrix. K-MEPTS forms a chemical interface between silica and rubber, enhancing the reinforcing effect of silica and reducing the mutual friction between silica particles. In summary, using a proper combination of AEO and K-MEPTS is a user-friendly approach for preparing silica/NR composites with excellent performance.

Herein, this review article aims to provide a relatively comprehensive summary of research progress in the dissolution and processing of cellulose with ionic liquids.

Abstract Combining the advantages of homogeneous and heterogeneous catalysts, single‐atom catalysts (SACs) are bringing new opportunities to revolutionize ORR catalysis in terms of cost, activity and durability. However, the lack of high‐performance SACs as well as the fundamental understanding of their unique catalytic mechanisms call for serious advances in this field. Herein, for the first time, we develop an Ir‐N‐C single‐atom catalyst (Ir‐SAC) which mimics homogeneous iridium porphyrins for high‐efficiency ORR catalysis. In accordance with theoretical predictions, the as‐developed Ir‐SAC exhibits orders of magnitude higher ORR activity than iridium nanoparticles with a record‐high turnover frequency (TOF) of 24.3 e − site −1 s −1 at 0.85 V vs. RHE) and an impressive mass activity of 12.2 A mg −1 Ir , which far outperforms the previously reported SACs and commercial Pt/C. Atomic structural characterizations and density functional theory calculations reveal that the high activity of Ir‐SAC is attributed to the moderate adsorption energy of reaction intermediates on the mononuclear iridium ion coordinated with four nitrogen atom sites.

Catalytic transformations involving metal carbenes are considered one of the most important aspects of homogeneous transition metal catalysis. Recently, gold-catalyzed generation of gold carbenes from readily available alkynes represents a significant advance in metal carbene chemistry. This Review summarizes the advances in the gold-catalyzed nitrene-transfer reactions of alkynes with nitrogen-transfer reagents, such as azides, nitrogen ylides, isoxazoles, and anthranils, and gold-catalyzed carbene-transfer reactions, involving oxygen atom-transfer reactions of alkynes with nitro compounds, nitrones, sulfoxides, and pyridine N-oxides, through the presumable α-imino gold carbene and α-oxo gold carbene intermediates, respectively. Gold-catalyzed processes are reviewed by highlighting their product diversity, selectivity, and applicability, and the mechanistic rationale is presented where possible.

Ultrahigh–power-density multilayer ceramic capacitors (MLCCs) are critical components in electrical and electronic systems. However, the realization of a high energy density combined with a high efficiency is a major challenge for practical applications. We propose a high-entropy design in barium titanate (BaTiO 3 )–based lead-free MLCCs with polymorphic relaxor phase. This strategy effectively minimizes hysteresis loss by lowering the domain-switching barriers and enhances the breakdown strength by the high atomic disorder with lattice distortion and grain refining. Benefiting from the synergistic effects, we achieved a high energy density of 20.8 joules per cubic centimeter with an ultrahigh efficiency of 97.5% in the MLCCs. This approach should be universally applicable to designing high-performance dielectrics for energy storage and other related functionalities.

Copper hexacyanoferrate (CuHCF) nanoparticles with Prussian blue structure present the ability to insert Al ions reversibly in aqueous solution.

China is the largest producer and user of ordinary Portland cement (OPC), and the rapid growth of infrastructure development demands more sustainable building materials for concrete structures. Alkali-activated materials (AAMs) are a new type of energy-saving and environmentally friendly building material with a wide range of potential applications. This paper compares the durability of AAMs and OPC-based materials under sulfate attack, acid corrosion, carbonation, and chloride penetration. Different AAMs have shown distinct durability properties due to different compositions being formed when different raw materials are used. According to the calcium (Ca) concentration of the raw materials, this paper interprets the deterioration mechanisms of three categories of AAMs: calcium-free, low-calcium, and calcium-rich. Conflicts found in the most recent research are highlighted, as they raise concerns regarding the consistence and long-term properties of AAMs. Nevertheless, AAMs show better durability performances than OPC-based materials in general.

Silicon-based materials are considered as strong candidates to next-generation lithium ion battery anodes because of their ultrahigh specific capacities. However, the pulverization and delamination of electrochemical active materials originated from the huge volume expansion (>300%) of silicon during the lithiation process results in rapid capacity fade, especially in high mass loading electrodes. Here we demonstrate that direct chemical vapor deposition (CVD) growth of vertical graphene nanosheets on commercial SiO microparticles can provide a stable conducting network via interconnected vertical graphene encapsulation during lithiation, thus remarkably improving the cycling stability in high mass loading SiO anodes. The vertical graphene encapsulated SiO (d-SiO@vG) anode exhibits a high capacity of 1600 mA h/g and a retention up to 93% after 100 cycles at a high areal mass loading of 1.5 mg/cm2. Furthermore, 5 wt % d-SiO@vG as additives increased the energy density of traditional graphite/NCA 18650 cell by ∼15%. We believe that the results strongly imply the important role of CVD-grown vertical graphene encapsulation in promoting the commercial application of silicon-based anodes.

By means of first-principles computations, we screened a series of transition metal atom anchored C₂N monolayers (TM_x@C₂N) as bifunctional electrocatalysts for both HER and OER.

Abstract Bifunctional hydrogen electrocatalysis (hydrogen‐oxidation and hydrogen‐evolution reactions) in alkaline solution is desirable but challenging. Among all available electrocatalysts, Ni‐based materials are the only non‐precious‐metal‐based candidates for alkaline hydrogen oxidation, but they generally suffer from low activity. Here, we demonstrate that properly alloying Ni with Mo could significantly promote its electrocatalytic performance. Ni 4 Mo alloy nanoparticles are prepared from the reduction of molybdate‐intercalated Ni(OH) 2 nanosheets. The final product exhibits an apparent hydrogen‐oxidation activity exceeding that of the Pt benchmark and a record‐high mass‐specific kinetic current of 79 A g −1 at an overpotential of 50 mV. A superior hydrogen‐evolution performance is also measured in alkaline solution. These experimental data are rationalized by our theoretical simulations, which show that alloying Ni with Mo significantly weakens its hydrogen adsorption, improves the hydroxyl adsorption and decreases the reaction barrier for water formation.

We investigated the reduction of CO₂at the oxygen vacancy on MXene monolayers and Ti₂CO₂exhibited the best catalytic performance. Moreover, we proposed that CO and H₂can introduce sufficient oxygen vacancies on O-terminated MXene.

By first-principles computations, we investigated the electrocatalysis of transition metal atom-anchored C₂N monolayers (TM_x@C₂N, <italic>x</italic> = 1 or 2) for N₂ fixation and proposed that Mo₂@C₂N is a promising electrocatalyst for the reduction of N₂ to NH₃.

A Ti-anchored Ti₂CO₂ monolayer exhibits high activity comparable to many noble metal catalysts for low-temperature CO oxidation.

PO₄³⁻ polyanion-doped Li-rich layered oxides offer excellent energy density retention during long cycling due to the stronger anion bonding of PO₄³⁻ polyanions to transition metal cations.