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To tackle the current crisis of Moore's law, a sophisticated strategy entails the development of multistable memristors, bionic artificial synapses, logic circuits and brain-inspired neuromorphic computing. In comparison with conventional electronic systems, iontronic memristors offer greater potential for the manifestation of artificial intelligence and brain–machine interaction. Organic iontronic memristive materials (OIMs), which possess an organic backbone and exhibit stoichiometric ionic states, have emerged as pivotal contenders for the realization of high-performance bionic iontronic memristors. In this review, a comprehensive analysis of the progress and prospects of OIMs is presented, encompassing their inherent advantages, diverse types, synthesis methodologies, and wide-ranging applications in memristive devices. Predictably, the field of OIMs, as a rapidly developing research subject, presents an exciting opportunity for the development of highly efficient neuro-iontronic systems in areas such as in-sensor computing devices, artificial synapses, and human perception.

Structural health monitoring (SHM) is a critical aspect of ensuring the safety and durability of smart biocomposite materials used as multifunctional materials. Smart biocomposites are composed of renewable or biodegradable materials and have emerged as eco-friendly alternatives of traditional non-biodegradable glass fiber-based composite materials. Although biocomposites exhibit fascinating properties and many desirable traits, real-time and early stage SHM is the most challenging issue to enable their long-term use. Smart biocomposites are integrated with sensors for in situ identification of the progress of damage and composite failure. The sensitivity of such smart biocomposites is a key functionality, which can be tuned by the introduction of an appropriate filler. In particular, nanocarbons hold promising potential to be incorporated in SHM applications of biocomposites. This review focused on the potential applications of nanocarbons in SHM of biocomposites. The aspects related to fabrication techniques and working mechanism of sensors are comprehensively discussed. Furthermore, their unique mechanical and electrical properties and sustainable nature ensure seamless integration into biocomposites, allowing for real-time monitoring without compromising the material's properties. These sensors offer multi-parameter sensing capabilities, such as strain, pressure, humidity, temperature, and chemical exposure, allowing a comprehensive assessment of biocomposite health. Additionally, their durability and longevity in harsh conditions, along with wireless connectivity options, provide cost-effective and sustainable SHM solutions. As research in this field advances, ongoing efforts seek to enhance the sensitivity and selectivity of these sensors, optimizing their performance for real-world applications. This review highlights the significant advances, ongoing efforts to enhance the sensitivity and selectivity, and performance optimization of nanocarbon-based sensors along with their working mechanism in the field of SHM for smart biocomposites. The key challenges and future research perspectives facing the conversion of nanocarbons to smart biocomposites are also displayed.

The formation of aragonite under ambient conditions is typically linked to Mg-rich aqueous environments. The grains that form in such environments show peculiar properties such as aggregate-like appearance and mesocrystalline character. We tested the effect of dissolved Mg2+ ions on the formation of aragonite mesocrystals by synthesizing aragonite with an automatic titrator at constant pH and at different dissolved Mg : Ca ratios, and by studying the properties of the precipitated material with various scanning transmission electron microscopy (STEM) techniques. At all studied Mg : Ca ratios the firstly condensed carbonate phase was Mg-bearing amorphous calcium carbonate (Mg-ACC) that transformed into aragonite during the synthesis experiments. The aragonite grains had typically aggregate-like appearance and spindle shapes, with the external morphologies of the spindles unaffected by variation in solution chemistry. The alignment of the nanocrystals within the aggregates was crystallographically highly coherent, the [001] directions of nanocrystals showing only a small misorientation with respect to one another; however, both parallel and twin assembly of neighbouring crystals occurred. An increase in the dissolved Mg concentration decreased the crystallographic coherence between the aragonite nanocrystals, suggesting an important role of Mg2+ ions in the assembly of aragonite spindles. Whereas the mesoscale-ordered arrangement of nanocrystals implies a particle-mediated assembly, the observed differences in particle size and composition between the amorphous precursor and the crystalline end-product suggest that the crystallization includes at least partial dissolution and re-precipitation. These findings provide insight into the formation of aragonite and could contribute to the understanding of important aspects of the formation of mesocrystals and hierarchically structured biogenic minerals.

Covalent organic frameworks (COFs) have historically been of interest to researchers in different areas due to their distinctive characteristics, including well-ordered pores, large specific surface area, and structural tunability. In the past few years, as COF synthesis techniques developed, COF-based composites fabricated by integrating COFs and other functional materials including various kinds of metal or metal oxide nanoparticles, ionic liquids, metal–organic frameworks, silica, polymers, enzymes and carbon nanomaterials have emerged as a novel kind of porous hybrid material. Herein, we first provide a thorough summary of advanced strategies for preparing COF-based composites; then, the emerging applications of COF-based composites in diverse fields due to their synergistic effects are systematically highlighted, including analytical chemistry (sensing, extraction, membrane separation, and chromatographic separation) and catalysis. Finally, the current challenges associated with future perspectives of COF-based composites are also briefly discussed to inspire the advancement of more COF-based composites with excellent properties.

The complex atomic scale structure of high entropy alloys presents new opportunities to expand the deformation theories of mechanical metallurgy. In this regard, solute-defect interactions have emerged as critical piece in elucidating the operation of deformation mechanisms. While notable progress has been made in understanding solute-defect interactions for random solute arrangements, recent interest in high entropy alloys with short-range order adds a new layer of structural complexity for which a cohesive picture has yet to emerge. To this end, this minireview synthesizes the current understanding of short-range order effects on defect behavior through an examination of the key recent literature. This analysis centers on the nanoscale metallurgy of deformation mechanisms, with the order-induced changes to the relevant defect energy landscapes serving as a touchstone for discussion. The topics reviewed include dislocation-mediated strengthening, twinning and phase transformation-based mechanisms, and vacancy-mediated processes. This minireview concludes with remarks on current challenges and opportunities for future efforts.

Both at the academic and the industrial level, material scientists are exploring routes for mass production and functionalization of graphene, carbon nanotubes (CNT), carbon dots, 2D materials, and heterostructures of these. Proper application of the novel materials requires fast and thorough characterization of the samples. Raman spectroscopy stands out as a standard non-invasive technique capable of giving key information on the structure and electronic properties of nanomaterials, including the presence of defects, degree of functionalization, diameter (in the case of CNT), different polytypes, doping, etc. Here, we present a computational tool to automatically analyze the Raman spectral features of nanomaterials, which we illustrate with the example of CNT and graphene. The algorithm manages hundreds of spectra simultaneously and provides statistical information (distribution of Raman shifts, average values of shifts and relative intensities, standard deviations, correlation between different peaks, etc.) of the main spectral features defining the structure and electronic properties of the samples, as well as publication-ready graphical material.

An introduction to the Nanoscale themed collection organised in celebration of the 25th anniversary of the Key Laboratory for Special Functional Materials at Henan University in China, featuring research in all aspects of nanoscience and nanotechnology.

The upconversion phenomenon allows for the emission of nanoparticles (NPs) under excitation with near-infrared (NIR) light. Such property is demanded in biology and medicine to detect or treat diseases such as tumours. The transparency of biological systems for NIR light is limited to three spectral ranges, called biological windows. However, the most frequently used excitation laser to obtain upconversion is out of these ranges, with a wavelength of around 975 nm. In this article, we show an alternative – Tm3+/Er3+-doped NPs that can convert 1208 nm excitation radiation, which is in the range of the 2nd biological window, to visible light within the 1st biological window. The spectroscopic properties of the core@shell NaYF4:Tm3+@NaYF4 and NaYF4:Er3+,Tm3+@NaYF4 NPs revealed a complex mechanism responsible for the observed upconversion. To explain emission in the studied NPs, we propose an energy looping mechanism: a sequence of ground state absorption, energy transfers and cross-relaxation (CR) processes between Tm3+ ions. Next, the excited Tm3+ ions transfer the absorbed energy to Er3+ ions, which results in green, red and NIR emission at 526, 546, 660, 698, 802 and 982 nm. The ratio between these bands is temperature-dependent and can be used in remote optical thermometers with high relative temperature sensitivity, up to 2.37%/°C at 57 °C. The excitation and emission properties of the studied NPs fall within 1st and 2nd biological windows, making them promising candidates for studies in biological systems.

The development of high-performing cathode materials for aqueous zinc-ion batteries (ZIBs) is highly important for the future large-scale energy storage. Owing to the distinctive framework structure, diversity of valences, and high electrochemical activity, spinel materials have been widely investigated and used for aqueous ZIBs. However, the stubborn issues of low electrical conductivity and sluggish kinetics plague their smooth applications in aqueous ZIBs, which stimulates the development of effective strategies to address these issues. This review highlights the recent advances of spinel-based cathode materials that include the configuration of aqueous ZIBs and corresponding reaction mechanisms. Subsequently, the classifications of spinel materials and their properties are also discussed. Then, the review mainly summarizes the effective strategies for elevating their electrochemical performance, including their morphology and structure design, defect engineering, heteroatom doping, and coupling with a conductive support. In the final section, several sound prospects in this fervent field are also proposed for future research and applications.

Two-step photoexcitation overall water splitting based on particulate photocatalysts represents a promising approach for low-cost solar hydrogen production. The performance of an O2-evolution photocatalyst and electron mediator between two photocatalysts crucially influences the construction of an efficient two-step excitation water-splitting system. Bismuth–tantalum oxyhalides are emerging photocatalysts for O2 evolution reactions and can be applied in two-step water-splitting systems. In this study, a highly crystalline Bi4TaO8Cl0.9Br0.1 solid solution with microplatelet morphology was synthesized by the dual flux method. The light absorption intensity and charge transfer efficiency of the Bi4TaO8Cl0.9Br0.1 solid solution were higher than those of Bi4TaO8Cl and Bi4TaO8Br; thus, the sacrificial O2 evolution activity of Bi4TaO8Cl0.9Br0.1 photocatalyst was obviously enhanced. The two-step excitation water splitting with a solid-state electron mediator was successfully constructed using Bi4TaO8Cl0.9Br0.1 as the O2-evolution photocatalyst and Ru/SrTiO3:Rh as the H2-evolution photocatalyst. The CoOx cocatalyst and reduced graphene oxide decorations on the surface of Bi4TaO8Cl0.9Br0.1 promoted the catalytic O2 generation process on Bi4TaO8Cl0.9Br0.1 and electron transfer between CoOx/Bi4TaO8Cl0.9Br0.1 and Ru/SrTiO3:Rh photocatalysts, respectively. As a result, the apparent quantum yield for this overall water-splitting system was 1.26% at 420 nm, which surpassed the present performance of the two-step excitation water-splitting systems consisting of metal oxyhalide photocatalysts. This study demonstrates the validity of high-quality solid-solution photocatalysts with suitable surface modification for efficient solar hydrogen production from water splitting.

Transforming CO2 into renewable fuels or valuable carbon compounds could be a practical means to tackle the issues of global warming and energy crisis. Photocatalytic CO2 reduction is more energy-efficient and environmentally friendly, and offers a broader range of potential applications than other CO2 conversion techniques. Ferroelectric materials, which belong to a class of materials with switchable polarization, are attractive candidates as catalysts due to their distinctive and substantial impact on surface physical and chemical characteristics. This review provides a concise overview of the fundamental principles underlying photocatalysis and the mechanism involved in CO2 reduction. Additionally, the composition and properties of ferroelectric materials are introduced. This review expands on the research progress in using ferroelectric materials for photocatalytic reduction of CO2 from three perspectives: directly as a catalyst, by modification, and construction of heterojunctions. Finally, the future potential of ferroelectric materials for photocatalytic CO2 reduction is presented. This review may be a valuable guide for creating reasonable and more effective photocatalysts based on ferroelectric materials.

Emerging resistive switching devices hold the potential to realize densely packed passive nanocrossbar arrays, suitable for deployment as random access memory devices (ReRAMs) in both embedded and high-capacity storage applications. In this study, we have engineered ReRAMs comprising ITO/(UVO-treated) amorphous ZnO (a-ZnO)/MAPbI3/Ag which effectively mitigate cross-talk currents without additional components. Significantly, we successfully executed a comprehensive set of 12 distinct 2-input sequential logic functions in a single halide perovskite ReRAM unit for the first time. Furthermore, these logic functions are devoid of any dependency on external light sources, entail merely 1 or 2 logic steps, and showcase symmetrical operability. A superior resistive switching behavior was achieved by harmonizing the charge transport within the bulk MAPbI3 and the tunneling barriers at the interfaces. The outcomes indicate progress in mitigating cross-talk and executing multiple logic functions within a single halide perovskite ReRAM unit, offering a new perspective for the advancement of halide perovskite ReRAMs.

We report a post-synthetic treatment method based on perfluorobutanesulfonic acid (PFBA) to ameliorate the photophysical performance of perovskite nanocrystals. By virtue of the PFBA treatment, both the photoluminescence efficiency and stability of perovskite quantum dot-based colloidal solutions and the electrical conductivity of their close-packed films are simultaneously improved.

Soft polymeric microrobots that can be loaded with nanocargoes and driven via external field stimuli can provide innovative solutions in various fields, including precise microscale assembly, targeted therapeutics, microsurgery, and the capture and degradation of unwanted wastewater fragments. However, in aquatic environments, it remains challenging to operate with microrobotic devices due to the predominant viscous resistances and the robots’ limited actuation and sensing capabilities attributed to their miniaturization. The miniature size prevents the incorporation of onboard batteries that can provide sufficient power for propulsion and navigation, necessitating a wireless power supply. Current research examines untethered microrobot manipulation using external magnetic, electric, thermodynamic, or acoustic field-guided technologies: all strategies capable of wireless energy transmission towards sensitive and hard-to-reach locations. Nonetheless, developing a manipulation strategy that harnesses simple-to-induce strong propulsive forces in a stable manner over extended periods of time remains a significant endeavor. This study presents the fabrication and manipulation of a microrobot consisting of a magnetized soft polymeric composite material that enables a combination of stable acoustic propulsion through starfish-inspired artificial cilia and magnetic field-guided navigation. The acousto-magnetic manipulation strategy leverages the unique benefits of each applied field in the viscous-dominated microscale, namely precise magnetic orientation and strong acoustic thrust.

Carbon slurries have been used as “flowable electrodes” in various electrochemical systems, and the slurry flow characteristics play an important role in the system electrochemical performance. For example, in an electrochemical flow capacitor (EFC), activated carbon particles must pass electrical charge from a stationary electrode to surrounding particles via particle-electrode and particle–particle interactions to store energy in the electric double layer. So far, particle behaviors under a continuous flow condition have not been observed due to the slurry's opacity, and studies of the device's performance thus have been mainly on a bulk level. To understand the relation between the hydrodynamic behavior and the electrochemical performance of carbon slurries, we have constructed a microfluidic EFC (μ-EFC) using transparent materials. The μ-EFC allows for direct observation of particle interactions in flowing carbon slurries using high-speed camera recording, and concurrent measurements of the electrochemical performance via chronoamperometry. The results indicate an interesting dependence of the particle cluster interaction on the flowrate, and its effect on the slurry charging/discharging behavior. It is found that an optimal flowrate could exist for better electrochemical performance.

The design of three-dimensional ceramic nanofibrous materials with high-temperature insulation and flame-retardant characteristics is of significant interest due to the effectively improved mechanical properties. However, achieving a pure ceramic monolith with ultra-low density, high elasticity and toughness remains a great challenge. Herein, a low-cost, scalable strategy to fabricate ultralight and mechanically robust N-doped TiO2 ceramic nanofibrous sponges with a continuous stratified structure by conjugate electrospinning is reported. Remarkably, the introduction of dopamine into the precursor nanofibers is engineered, which realizes the nitrogen doping to inhibit the TiO2 grain growth, endowing single nanofibers with a smoother, less defective surface. Besides, the self-polymerization process of dopamine allows the construction of bonding points between nanofibers and optimizes the distribution of inorganic micelles on polymer templates. Moreover, a rotating disk receiving device under different rotating speeds is designed to obtain N-doped TiO2 sponges with various interlamellar spacings, further affecting the maximum compressive deformation capacity. The resulting ceramic sponges, consisting of fluffy crosslinked nanofiber layers, possess low densities of 12–45 mg cm−3, which can quickly recover under a large strain of 80% and have only 9.2% plastic deformation after 100 compression cycles. In addition, the sponge also exhibits a temperature-invariant superelasticity at 25–800 °C and a low heat conductivity of 0.0285 W m−1 K−1, with an outstanding thermal insulation property, making it an ideal insulation material for high-temperature or harsh conditions.

Graphene, a single layer, hexagonally packed two-dimensional carbon sheet is an attractive candidate for diverse applications including antibacterial potential and drug delivery. One of the knowledge gaps in biomedical application of graphene is the interaction of these materials with the cells. To address this, we investigated the interaction between graphene materials (graphene and graphene oxide) and plasma membranes of cells (bacterial and mammalian cells). The interactions of four of the most abundant phospholipids in bacteria and mammalian plasma membranes with graphene materials were studied using density functional theory (DFT) at the atomic level. The calculations showed that the mammalian phospholipids have stronger bonding to each other compared to bacterial phospholipids. When the graphene/graphene oxide sheet is approaching the phospholipid pairs, the bacterial pairs exhibit less repulsive interactions, thereby a more stable system with the sheets was found. We also assembled bacterial and mammalian phospholipids into liposomes. We further observed that the bacterial liposomes and cells let the graphene flakes penetrate the membrane. The differential scanning calorimetry measurements of liposomes revealed that the bacterial liposomes have the lowest heat capacity; this strengthens the theoretical predictions of weaker interaction between the bacterial phospholipids compared to the mammalian phospholipids. We further demonstrated that graphene oxide could be internalized into the mammalian liposomes without disrupting the membrane integrity. The results suggest that the weak bonding among bacteria phospholipids and less repulsive force when graphene materials approach, result in graphene materials interacting differently with the bacteria compared to mammalian cells.

Trifunctional ORR/OER/HER catalysts are emerging for various sustainable energy storage and conversion technologies. For this function, employing materials with 1D structures leads to catalysts having limited surface area and structural robustness. Instead of 1D catalysts, heterostructured catalysts (i.e., catalysts consisting of interfaces created by combining diverse structural components) have attracted much attention due to their high efficiency. We have fabricated a directly grown 1D–1D heterostructured bimetallic N-doped carbon trifunctional catalyst based on Fe/Co bimetallic–organic frameworks, forming nanobrushes (FeCoNC-NB) with improved resistance to collapsing and substantial numbers of exposed active sites. The secondary 1D structure of this design contributes to creating interparticle conductive networks. By combining the brush-like heterostructure, FeCo alloy active sites, and N-doped carbon as support and for encapsulation of the metal, the catalyst features a high ORR Eonset value (1.046 V), low OER overpotential (363 mV), and comparable HER overpotential (254 mV) in alkaline electrolyte. Zn–air batteries with FeCoNC-NB demonstrate a power density of 195 mW cm−2 and a superior battery life of up to 350 h. Self-powered FeCoNC-NB-based water electrolyzers as energy conversion devices are also demonstrated. This work drives the progress of trifunctional catalysts based on heterostructured nonprecious metal N-doped carbon for energy storage and conversion developments.

Systematic interface and defect engineering strategies have been demonstrated to be an effective way to modulate the electron transfer and nonlinear absorption properties in semiconductor heterojunctions. However, the role played by defects and interfacial strain in electron transfer at the interface of the MoX2 (X = Se, S, Te)@ZnO heterojunction remains poorly understood. Herein, using the MoX2@ZnO heterojunction, we reveal that vacancies play a critical role in the interfacial electron transfer of heterojunctions. Specifically, we present the defect and interface engineering of the MoX2@ZnO heterojunction for controlled charge transfer and electron excitation-relaxation. The experimental characterization combined with first-principles calculations showed that the presence of defects promoted the transport of photogenerated carriers at the heterojunction interface, thereby inhibiting their rapid recombination. The DFT calculation confirmed that the electron band structure, density of states and charge density distribution in the system changed after the formation of Mo–O bonds. On the basis of defects and interfacial stress and the effective charge transfer, the MoX2@ZnO heterojunction exhibited excellent excitation and emission behaviors. The nonlinear optical regulation behavior of TMDs is expected to be realized with the help of the defects and interface/surface synergistically modulated effect of ZnO nanoparticles. The local strain generation on the MoX2@ZnO heterojunction boundary provides a new method for the design of new heterogeneous materials and will be of great significance to investigate the contact physical behavior and application of metals and two-dimensional (2D) semiconductors. This work provides some inspiration for the construction of heterojunctions with rich defects and surface/interface charge transfer channels to promote tunable electron transfer dynamics, thereby achieving a good nonlinear optical conversion efficiency and efficient charge separation in optoelectronic functional materials.