Shaanxi University of Science and Technology

Abstract Construction of Z-scheme heterostructure is of great significance for realizing efficient photocatalytic water splitting. However, the conscious modulation of Z-scheme charge transfer is still a great challenge. Herein, interfacial Mo-S bond and internal electric field modulated Z-scheme heterostructure composed by sulfur vacancies-rich ZnIn 2 S 4 and MoSe 2 was rationally fabricated for efficient photocatalytic hydrogen evolution. Systematic investigations reveal that Mo-S bond and internal electric field induce the Z-scheme charge transfer mechanism as confirmed by the surface photovoltage spectra, DMPO spin-trapping electron paramagnetic resonance spectra and density functional theory calculations. Under the intense synergy among the Mo-S bond, internal electric field and S-vacancies, the optimized photocatalyst exhibits high hydrogen evolution rate of 63.21 mmol∙g −1 ·h −1 with an apparent quantum yield of 76.48% at 420 nm monochromatic light, which is about 18.8-fold of the pristine ZIS. This work affords a useful inspiration on consciously modulating Z-scheme charge transfer by atomic-level interface control and internal electric field to signally promote the photocatalytic performance.

High-performance electromagnetic interference (EMI) shielding materials with ultraflexibility, outstanding mechanical properties, and superior EMI shielding performances are highly desirable for modern integrated electronic and telecommunication systems in areas such as aerospace, military, artificial intelligence, and smart and wearable electronics. Herein, ultraflexible and mechanically strong aramid nanofiber–Ti3C2Tx MXene/silver nanowire (ANF-MXene/AgNW) nanocomposite papers with double-layered structures are fabricated via the facile two-step vacuum-assisted filtration followed by hot-pressing approach. The resultant double-layered nanocomposite papers with a low MXene/AgNW content of 20 wt % exhibit an excellent electrical conductivity of 922.0 S·cm–1, outstanding mechanical properties with a tensile strength of 235.9 MPa and fracture strain of 24.8%, superior EMI shielding effectiveness (EMI SE) of 48.1 dB, and high EMI SE/t of 10 688.9 dB·cm–1, benefiting from the highly efficient double-layered structures, high-performance ANF substrate, and extensive hydrogen-bonding interactions. Particularly, the nanocomposite papers show a maximum electrical conductivity of 3725.6 S·cm–1 and EMI SE of ∼80 dB at a MXene/AgNW content of 80 wt % with an absorption-dominant shielding mechanism owing to the massive ohmic losses in the highly conductive MXene/AgNW layer, multiple internal reflections between Ti3C2Tx MXene nanosheets and polarization relaxation of localized defects, and abundant terminal groups. Compared with the homogeneously blended ones, the double-layered nanocomposite papers possess greater advantages in electrical, mechanical, and EMI shielding performances. Moreover, the multifunctional double-layered nanocomposite papers exhibit excellent thermal management performances such as high Joule heating temperature at low supplied voltages, rapid response time, sufficient heating stability, and reliability. The results indicate that the double-layered nanocomposite papers have excellent potential for high-performance EMI shielding and thermal management applications in aerospace, military, artificial intelligence, and smart and wearable electronics.

Abstract Deep learning has been widely used for medical image segmentation and a large number of papers has been presented recording the success of deep learning in the field. A comprehensive thematic survey on medical image segmentation using deep learning techniques is presented. This paper makes two original contributions. Firstly, compared to traditional surveys that directly divide literatures of deep learning on medical image segmentation into many groups and introduce literatures in detail for each group, we classify currently popular literatures according to a multi‐level structure from coarse to fine. Secondly, this paper focuses on supervised and weakly supervised learning approaches, without including unsupervised approaches since they have been introduced in many old surveys and they are not popular currently. For supervised learning approaches, we analyse literatures in three aspects: the selection of backbone networks, the design of network blocks, and the improvement of loss functions. For weakly supervised learning approaches, we investigate literature according to data augmentation, transfer learning, and interactive segmentation, separately. Compared to existing surveys, this survey classifies the literatures very differently from before and is more convenient for readers to understand the relevant rationale and will guide them to think of appropriate improvements in medical image segmentation based on deep learning approaches.

This letter demonstrates that a novel, highly efficient enzyme electrode can be directly obtained using covalent attachment between carboxyl acid groups of graphene oxide sheets and amines of glucose oxidase. The resulting biosensor exhibits a broad linear range up to 28 mM x mm(-2) glucose with a sensitivity of 8.045 mA x cm(-2) x M(-1). The glucose oxidase-immobilized graphene oxide electrode also shows a reproducibility and a good storage stability, suggesting potentials for a wide range of practical applications. The biocompatibility of as-synthesized graphene oxide nanosheets with human cells, especially retinal pigment epithelium (RPE) cells, was investigated for the first time in the present work. Microporous graphene oxide exhibits good biocompatibility and has potential advantages with respect to cell attachment and proliferation, leading to opportunities for using graphene-based biosensors for the clinical diagnosis.

Electrically conductive polymer composite-based smart strain sensors with different conductive fillers, phase morphology, and imperative features were reviewed.

Abstract The utilization of antiferroelectric (AFE) materials is thought to be an effective approach to enhance the energy density of dielectric capacitors. However, the high energy dissipation and inferior reliability that are associated with the antiferroelectric–ferroelectric phase transition are the main issues that restrict the applications of antiferroelectric ceramics. Here, simultaneously achieving high energy density and efficiency in a dielectric ceramic is proposed by combining antiferroelectric and relaxor features. Based on this concept, a lead‐free dielectric (Na 0.5 Bi 0.5 )TiO 3 ‐ x (Sr 0.7 Bi 0.2 )TiO 3 (NBT‐ x SBT) system is investigated and the corresponding multilayer ceramic capacitors (MLCCs) are fabricated. A record‐high energy density of 9.5 J cm −3 , together with a high energy efficiency of 92%, is achieved in NBT‐0.45SBT multilayer ceramic capacitors, which consist of ten dielectric layers with the single‐layer thickness of 20 µm and the internal electrode area of 6.25 mm 2 . Furthermore, the newly developed capacitor exhibits a wide temperature usage range of ‐60 to 120 °C, with an energy‐density variation of less than 10%, and satisfactory cycling reliability, with degradation of less than 8% over 10 6 cycles. These characteristics demonstrate that the NBT‐0.45SBT multilayer ceramic is a promising candidate for high‐power energy storage applications.

Luminescent carbon quantum dots (CQDs) are a new form of nanocarbon materials that have gained widespread attention in recent years, especially in chemical sensing, biosensing, bioimaging, nanomedicine, photocatalysis and electrocatalysis. CQDs can be prepared simply and inexpensively by multiple techniques, such as the arc-discharge method, microwave pyrolysis, hydrothermal method and electrochemical synthesis. CQDs show excellent physical and chemical properties like high crystallization, good dispersibility, photoluminescence properties. In particular, the small size, superconductivity and rapid electron transfer of CQDs endow the CQDs-based composite with improved electrical conductivity and catalytic activity. Besides, CQDs have abundant functional groups on the surface which could facilitate the preparation of multi-component electrical active catalysts. The interactions inside these multi-component catalysts may further enhance the catalytic performance by promoting charge transfer and intermolecular electron transfer which plays an important role in electrochemistry. Most recent researches on CQDs have focused on their fluorescence characteristics and photocatalytic properties. This review will summarize the primary advances of CQDs in the synthetic methods, excellent physical and electronic properties, and application in electrocatalysis, including oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reduction (HER) and CO2 reduction reaction (CO2RR).

Abstract Searching for advanced microwave absorption (MA) nanomaterials is one of the most feasible ways to address the increasing electromagnetic pollution in both military and civil fields. To this end, graphene and MXene have won the widespread attention as the main representatives due to their remarkable structures and properties. The common features such as the large aspect ratio, active chemical surface, and varieties of synthesis processes endow graphene and MXene with unique superiorities for developing high‐efficiency MA structures, in particular lightweight assemblies and various hybrids. Meanwhile, the structural and performance differences (such as different conductivities) between them result in distinctive techniques in the design, fabrication, and application of their MA materials. Herein, the research progress in graphene‐ and MXene‐based MA materials is reviewed, with a special focus on advances in general strategies. Moreover, through the comparison between graphene‐ and MXene‐based MA materials, their respective advantages in achieving high‐performance MA are presented. Furthermore, the future challenge, research orientation, and prospect for these MA materials are also highlighted and discussed.

Abstract To meet the practical demand of overall water splitting and regenerative metal–air batteries, highly efficient, low‐cost, and durable electrocatalysts for the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER) are required to displace noble metal catalysts. In this work, a facile solid‐state synthesis strategy is developed to construct the interfacial engineering of W 2 N/WC heterostructures, in which abundant interfaces are formed. Under high temperature (800 °C), volatile CN x species from dicyanodiamide are trapped by WO 3 nanorods, followed by simultaneous nitridation and carbonization, to form W 2 N/WC heterostructure catalysts. The resultant W 2 N/WC heterostructure catalysts exhibit an efficient and stable electrocatalytic performance toward the ORR, OER, and HER, including a half‐wave potential of 0.81 V (ORR) and a low overpotential at 10 mA cm −2 for the OER (320 mV) and HER (148.5 mV). Furthermore, a W 2 N/WC‐based Zn–air battery shows outstanding high power density (172 mW cm −2 ). Density functional theory and X‐ray absorption fine structure analysis computations reveal that W 2 N/WC interfaces synergistically facilitate transport and separation of charge, thus accelerating the electrochemical ORR, OER, and HER. This work paves a novel avenue for constructing efficient and low‐cost electrocatalysts for electrochemical energy devices.

Multifunctional wearable electronic devices based on natural materials are highly desirable for versatile applications of energy conversion, electronic skin and artificial intelligence. Herein, multifunctional wearable silver nanowire decorated leather (AgNW/leather) nanocomposites with hierarchical structures for integrated visual Joule heating, electromagnetic interference (EMI) shielding and piezoresistive sensing are fabricated via the facile vacuum-assisted filtration process. The AgNWs penetrate the micro-nanoporous structures in the corium side of leather constructing highly-efficient conductive networks. The resultant flexible and mechanically strong AgNW/leather nanocomposites exhibit extremely low sheet resistance of 0.8 Ω/sq, superior visual Joule heating temperatures up to 108 °C at low supplied voltage of 2.0 V due to efficient energy conversion, excellent EMI shielding effectiveness (EMI SE) of ≈55 dB and outstanding piezoresistive sensing ability in human motion detection. This work demonstrates the fabrication of multifunctional AgNW/leather nanocomposites for next-generation wearable electronic devices in energy conversion, electronic skin and artificial intelligence, etc.

Abstract Aramid nanofibers (ANFs) are of great interest in various applications due to its 1D nanoscale, high aspect ratio, high specific surface area, excellent strength, and modulus as well as impressive chemical and thermal stabilities. It is considered as one of the most promising nano‐sized building blocks with excellent properties and has therefore drawn increasing attention since 2011. However, no review has summarized the research progress and the prospective challenges of ANF. Herein, the methods of ANF fabrication and their relative merits are comprehensively discussed together with the challenges and progress in the deprotonation method for preparing ANF. The fabrication methods and development of ANF‐based advanced materials with different macroscopic morphologies, including the 1D ANF aerogel fiber, 2D ANF film/nanopaper/coating, and 3D ANF gel and particle are also described. Furthermore, the applications of ANF in nanocomposite reinforcement, battery separators, electrical insulation nanopaper, flexible electronics, and adsorption and filtration media are presented. Additionally, the possible challenges and outlooks toward the future development of ANF are highlighted. This review indicates that the ANF and ANF‐based materials mentioned herein will boost the development of next‐generation advanced functional materials.

Abstract Ionic conductive hydrogels (ICHs) integrate the conductive performance and soft nature of tissue‐like materials to imitate the features of human skin with mechanical and sensory traits; thus, they are considered promising substitutes for conventional rigid metallic conductors when fabricating human‐motion sensors. However, the simultaneous incorporation of excellent stretchability, toughness, ionic conductivity, self‐healing, and adhesion via a simple method remains a grand challenge. Herein, a novel ICH platform is proposed by designing a phenylboronic acid‐ionic liquid (PBA‐IL) with multiple roles that simultaneously realize the highly mechanical, electrical, and versatile properties. This elaborately designed semi‐interpenetrating network ICH is fabricated via a facile one‐step approach by introducing cellulose nanofibrils (CNFs) into the PBA‐IL/acrylamide cross‐linked network. Ingeniously, the dynamic boronic ester bonds and physical interactions (hydrogen bonds and electrostatic interactions) of the cross‐linked network endow these hydrogels with remarkable stretchability (1810 ± 38%), toughness (2.65 ± 0.03 MJ m −3 ), self‐healing property (92 ± 2% efficiency), adhesiveness, and transparency. Moreover, the construction of this material shows that CNFs can synergistically enhance mechanical performance and conductivity. The wide working strain range (≈1000%) and high sensitivity (GF = 8.36) make this ICH a promising candidate for constructing the next generation of gel‐based strain sensor platforms.

Piezoelectric nanogenerators with large output, high sensitivity, and good flexibility have attracted extensive interest in wearable electronics and personal healthcare. In this paper, the authors propose a high‐performance flexible piezoelectric nanogenerator based on piezoelectrically enhanced nanocomposite micropillar array of polyvinylidene fluoride‐trifluoroethylene (P(VDF‐TrFE))/barium titanate (BaTiO 3 ) for energy harvesting and highly sensitive self‐powered sensing. By a reliable and scalable nanoimprinting process, the piezoelectrically enhanced vertically aligned P(VDF‐TrFE)/BaTiO 3 nanocomposite micropillar arrays are fabricated. The piezoelectric device exhibits enhanced voltage of 13.2 V and a current density of 0.33 µA cm −2 , which an enhancement by a factor of 7.3 relatives to the pristine P(VDF‐TrFE) bulk film. The mechanisms of high performance are mainly attributed to the enhanced piezoelectricity of the P(VDF‐TrFE)/BaTiO 3 nanocomposite materials and the improved mechanical flexibility of the micropillar array. Under mechanical impact, stable electricity is stably generated from the nanogenerator and used to drive various electronic devices to work continuously, implying its significance in the field of consumer electronic devices. Furthermore, it can be applied as self‐powered flexible sensor work in a noncontact mode for detecting air pressure and wearable sensors for detecting some human vital signs including different modes of breath and heartbeat pulse, which shows its potential applications in flexible electronics and medical sciences.

F positron emission tomography and ultrasound discussed as illustrative examples. The presence of C-F bonds can also be used to tailor membrane permeability and pharmacokinetic properties of drugs and delivery agents for enhanced cell uptake and therapeutics. A key message of this review is that while the promise of C-F containing materials is significant, a subset of highly fluorinated compounds such as per- and polyfluoroalkyl substances (PFAS), have been identified as posing a potential risk to human health. The unique properties of the C-F bond and the significant potential for fluorine-fluorine interactions in PFAS structures necessitate the development of new strategies for facile and efficient environmental removal and remediation. Recent progress in the development of fluorine-containing compounds as molecular imaging and therapeutic agents will be reviewed and their design features contrasted with environmental and health risks for PFAS systems. Finally, present challenges and future directions in the exploitation of the biological aspects of fluorinated systems will be described.

In recent years, there have been rapid advances in the synthesis of lead halide perovskite nanocrystals (NCs) for use in solar cells, light emitting diodes, lasers, and photodetectors. These compounds have a set of intriguing optical, excitonic, and charge transport properties, including outstanding photoluminescence quantum yield (PLQY) and tunable optical band gap. However, the necessary inclusion of lead, a toxic element, raises a critical concern for future commercial development. To address the toxicity issue, intense recent research effort has been devoted to developing lead-free halide perovskite (LFHP) NCs. In this Review, we present a comprehensive overview of currently explored LFHP NCs with an emphasis on their crystal structures, synthesis, optical properties, and environmental stabilities (e.g., UV, heat, and moisture resistance). In addition, strategies for enhancing optical properties and stabilities of LFHP NCs as well as the state-of-the-art applications are discussed. With the perspective of their properties and current challenges, we provide an outlook for future directions in this rapidly evolving field to achieve high-quality LFHP NCs for a broader range of fundamental research and practical applications.

This article addresses the connected-component labeling problem which consists in assigning a unique label to all pixels of each connected component (i.e., each object) in a binary image. Connected-component labeling is indispensable for distinguishing different objects in a binary image, and prerequisite for image analysis and object recognition in the image. Therefore, connected-component labeling is one of the most important processes for image analysis, image understanding, pattern recognition, and computer vision. In this article, we review state-of-the-art connected-component labeling algorithms presented in the last decade, explain the main strategies and algorithms, present their pseudo codes, and give experimental results in order to bring order of the algorithms. Moreover, we will also discuss parallel implementation and hardware implementation of connected-component labeling algorithms, extension for n-D images, and try to indicate future work on the connected component labeling problem.

High-performance and rapid response electrical heaters with ultraflexibility, superior heat resistance, and mechanical properties are highly desirable for the development of wearable devices, artificial intelligence, and high-performance heating systems in areas such as aerospace and the military. Herein, a facile and efficient two-step vacuum-assisted filtration followed by hot-pressing approach is presented to fabricate versatile electrical heaters based on the high-performance aramid nanofibers (ANFs) and highly conductive Ag nanowires (AgNWs). The resultant ANF/AgNW nanocomposite papers present ultraflexibility, extremely low sheet resistance (minimum Rs of 0.12 Ω/sq), and outstanding heat resistance (thermal degradation temperature above 500 °C) and mechanical properties (tensile strength of 285.7 MPa, tensile modulus of 6.51 GPa with a AgNW area fraction of 0.4 g/m2), benefiting from the partial embedding of AgNWs into the ANF substrate and the extensive hydrogen-bonding interactions. Moreover, the ANF/AgNW nanocomposite paper-based electrical heaters exhibit satisfyingly high heating temperatures (up to ∼200 °C) with rapid response time (10–30 s) at low AgNW area fractions and supplied voltages (0.5–5 V) and possess sufficient heating reliability, stability, and repeatability during the long-term and repeated heating and cooling cycles. Fully functional applications of the ANF/AgNW nanocomposite paper-based electrical heaters are demonstrated, indicating their excellent potential for emerging electronic applications such as wearable devices, artificial intelligence, and high-performance heating systems.

In this work, we report a facile, clean, controllable and scalable phase engineering technique for monolayer MoS2. We found that weak Ar-plasma bombardment can locally induce 2H→1T phase transition in monolayer MoS2 to form mosaic structures. These 2H→1T phase transitions are stabilized by point defects (single S-vacancies) and the sizes of induced 1T domains are typically a few nanometers, as revealed by scanning tunneling microscopy measurements. On the basis of a selected-area phase patterning process, we fabricated MoS2 FETs inducing 1T phase transition within the metal contact areas, which exhibit substantially improved device performances. Our results open up a new route for phase engineering in monolayer MoS2 and other transition metal dichalcogenide (TMD) materials.

Aramid nanofibers (ANFs) have become promising nanoscale building blocks due to their extraordinary performance. However, there are numerous challenges related to the preparation of ANFs, such as the lengthy preparation cycle (7-10 days), low preparation concentration (0.2 wt %), and high difficulty in quantitatively judging the end point of the deprotonation reaction. Herein, we report three time-saving and high-efficiency strategies (fibrillation, ultrasonication, and proton donor-assisted deprotonation) to prepare ANFs with excellent performance. The fiber micromorphology during the deprotonation and protonation recovery processes was first investigated. Then the end point of the deprotonation reaction was detected by Raman spectra and the cationic demand of the ANF/DMSO system. Finally, the size, preparation cycle, and performance of the corresponding ANFs and ANF films fabricated by different approaches were investigated in detail. The results showed that proton donor-assisted deprotonation significantly shortened the traditional preparation cycle from 7 days to 4 h, and is the most efficient method reported thus far. It is noteworthy that a high concentration of ANFs (4.0 wt %) could also be achieved within 12 h. Interestingly, the fabricated ANFs exhibit rigid morphology and a small diameter with a narrow size distribution (10.7 ± 1.0 nm). The resultant ANF film displays desired characteristics of high strength and toughness. The work offers a timesaving, feasible and effective strategy to realize the large-scale production for ANFs, which will facilitate the application of ANFs in the production of advanced nanomaterials.

Abstract Hydrogen production is the key step for the future hydrogen economy. As a promising H 2 production route, electrolysis of water suffers from high overpotentials and high energy consumption. This study proposes an N‐doped CoP as the novel and effective electrocatalyst for hydrogen evolution reaction (HER) and constructs a coupled system for simultaneous hydrogen and sulfur production. Nitrogen doping lowers the d‐band of CoP and weakens the H adsorption on the surface of CoP because of the strong electronegativity of nitrogen as compared to phosphorus. The H adsorption that is close to thermos‐neutral states enables the effective electrolysis of the HER. Only −42 mV is required to drive a current density of −10 mA cm −2 for the HER. The oxygen evolution reaction in the anode is replaced by the oxidation reaction of Fe 2+ , which is regenerated by a coupled H 2 S absorption reaction. The coupled system can significantly reduce the energy consumption of the HER and recover useful sulfur sources.