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HighlightsThe development of bismuth ferrite as a multiferroic nanomaterial is summarized.The morphology, structures, and properties of bismuth ferrite and its potential applications in multiferroic devices with novel functions are presented and discussed.Some perspectives and issues needed to be solved are described.Multiferroic nanomaterials have attracted great interest due to simultaneous two or more properties such as ferroelectricity, ferromagnetism, and ferroelasticity, which can promise a broad application in multifunctional, low-power consumption, environmentally friendly devices. Bismuth ferrite (BiFeO3, BFO) exhibits both (anti)ferromagnetic and ferroelectric properties at room temperature. Thus, it has played an increasingly important role in multiferroic system. In this review, we systematically discussed the developments of BFO nanomaterials including morphology, structures, properties, and potential applications in multiferroic devices with novel functions. Even the opportunities and challenges were all analyzed and summarized. We hope this review can act as an updating and encourage more researchers to push on the development of BFO nanomaterials in the future.

Transparent electrodes (TEs) made of metallic nanowires, such as Ag, Au, Cu, and Ni, are attracting increasing attention for several reasons: (1) they can act as a substitute for tin oxide-based TEs such as indium-tin oxide (ITO) and fluorine-doped tin oxide (FTO); (2) various methods exist for fabricating such TEs such as filtration, spraying, and Meyer bar coating; (3) greater compatibility with different substrates can be achieved due to the variety of fabrication methods; and (4) extra functions in addition to serving as electrodes, such as catalytic abilities, can be obtained due to the metals of which the TEs are composed. There are a large number of applications for TEs, ranging from electronics and sensors to biomedical devices. This short review is a summary of recent progress, mainly over the past five years, on silver nanowire-based TEs. The focus of the review is on theory development, mechanical, chemical, and thermal stability as well as optical properties. The many applications of TEs are outside the scope of this review.

Triboelectric nanogenerators (TENGs) stand at the forefront of energy harvesting innovation, transforming mechanical energy into electrical power through triboelectrification and electrostatic induction. This groundbreaking technology addresses the urgent need for sustainable and renewable energy solutions, opening new avenues for self-powered systems. Despite their potential, TENGs face challenges such as material optimization for enhanced triboelectric effects, scalability, and improving conversion efficiency under varied conditions. Durability and environmental stability also pose significant hurdles, necessitating further research towards more resilient systems. Nature inspired TENG designs offer promising solutions by emulating biological processes and structures, such as the energy mechanisms of plants and the textured surfaces of animal skins. This biomimetic approach has led to notable improvements in material properties, structural designs, and overall TENG performance, including enhanced energy conversion efficiency and environmental robustness. The exploration into bio-inspired TENGs has unlocked new possibilities in energy harvesting, self-powered sensing, and wearable electronics, emphasizing reduced energy consumption and increased efficiency through innovative design. This review encapsulates the challenges and advancements in nature inspired TENGs, highlighting the integration of biomimetic principles to overcome current limitations. By focusing on augmented electrical properties, biodegradability, and self-healing capabilities, nature inspired TENGs pave the way for more sustainable and versatile energy solutions. Comprehensive and systematic summary of nature inspired TENGs, including materials and structures. Summary of bionic approaches to nature inspired TENGs. Analysis and evaluation of the latest applications of nature inspired TENGs in energy harvesting and self-powered systems. Explanation of current challenges and future development directions of nature inspired TENGs.

Porous gold films have attracted increasing interest over the last ten years due to the unique properties of high specific surface area and electrical conductivity combined with chemical stability and ability to alter the surface chemistry. Several methods have been developed to synthesize porous gold films such as de-alloying, templating, electrochemical, and self-assembling. These porous gold films are used in diverse fields, for example, as electrochemical and Raman sensors or for chemical catalysis. Here, we provide a short review on the progress of porous gold films over the past ten years, including the synthesis and applications of such films.

Triboelectric nanogenerators (TENG:s) are used as efficient energy transducers in energy harvesting converting mechanical energy into electrical energy. Wind is an abundant source of mechanical energy but how should a good triboelectric wind harvester be designed? We have built and studied a TENG driven by air flow in a table-top sized wind tunnel. Our TENG constitutes of a plastic film of size 10 cm × 2 cm which is fluttering between two copper electrodes generating enough power to light up a battery of LED:s. We measured the voltage and frequency of fluttering at different wind speeds from zero up to 8 m/s for three electrode distances 6 mm, 10 mm and 14 mm. We found that the frequency increases linearly with the wind speed with a cutoff at some low speed. Power was generated already at 1.6 m/s. We seem to be able to explain the observed frequency dependence on wind speed by assuming excitation of the film into different harmonics in response to von Kármán vortices. We also find that the voltage increase linearly with frequency. We anticipate that TENG:s of this design could be useful both as generators and speed sensors because they work at low air speeds.

Many solution processing methods of exfoliation of layered materials have been studied during the last few years; most of them are based on organic solvents or rely on surfactants and other funtionalization agents. Pure water should be an ideal solvent, however, it is generally believed, based on solubility theories that stable dispersions of water could not be achieved and systematic studies are lacking. Here we describe the use of water as a solvent and the stabilization process involved therein. We introduce an exfoliation method of molybdenum disulfide (MoS2) in pure water at high concentration (i.e., 0.14 ± 0.01 g L-1). This was achieved by thinning the bulk MoS2 by mechanical exfoliation between sand papers and dispersing it by liquid exfoliation through probe sonication in water. We observed thin MoS2 nanosheets in water characterized by TEM, AFM and SEM images. The dimensions of the nanosheets were around 200 nm, the same range obtained in organic solvents. Electrophoretic mobility measurements indicated that electrical charges may be responsible for the stabilization of the dispersions. A probability decay equation was proposed to compare the stability of these dispersions with the ones reported in the literature. Water can be used as a solvent to disperse nanosheets and although the stability of the dispersions may not be as high as in organic solvents, the present method could be employed for a number of applications where the dispersions can be produced on site and organic solvents are not desirable.

The rising demand for wireless electronics and sustainable energy solutions drives the search for alternatives to conventional batteries. Triboelectric nanogenerators (TENGs) offer a promising route by converting mechanical energy into electricity via frictional events between two different material surfaces. Here, a simple and scalable surface modification method using conventional laser printing was applied to investigate the effect on triboelectric performance of cellulose-based materials against polytetrafluoroethylene (PTFE). Regenerated cellulose (RC) and cellulose acetate (CA) films were print patterned with black toner in a conventional laser printer at different surface coverages from 0% to 100%. The measured power output for RC films against PTFE showed minimal response from the patterning over the whole range and could be considered as constant with an average of 52 ± 2 W m−2. On the other hand, the CA sample films showed a significant and gradual increase in power output from 45 to 65 W m−2 as the toner print coverage increased from 0% to 100%. These results demonstrate that synergistic interactions between the printed toner and the substrate can strongly influence TENG performance and are highly dependent on the physical and chemical properties of the underlying material. In CA, toner–substrate intermixing enabled by laser printing temperatures exceeding the glass transition temperature provides a proof-of-concept for enhancing triboelectric performance through controlled surface–bulk interactions.

Regenerated cellulose is a promising tribopositive material for sustainable triboelectric nanogenerators (TENGs), although its electrical output remains sensitive to surface and interfacial properties. In this study, regenerated cellulose was modified using atomic layer deposition (ALD) of Al O , TiO , and ZnO to investigate how nanoscale oxide coatings influence triboelectric performance against a tribonegative PTFE counter layer. Two deposition regimes were examined: 7 ALD cycles, representing the early stage of ALD growth, and 200 cycles, representing a more developed coating regime. Triboelectric measurements, dielectric spectroscopy, structural characterization and contact angle analysis, were used to evaluate how ALD modification influences the electrical response of regenerated cellulose. All ALD-modified samples exhibited increased surface charge density and power output compared to unmodified cellulose, while also showing improved retention of triboelectric performance at elevated relative humidity. The 7-cycle samples consistently outperformed the corresponding 200-cycle coatings under low-humidity conditions, whereas the 200-cycle ZnO sample exhibited the highest humidity stability. No direct correlation between wettability and triboelectric output was observed. The results suggest that relatively small interfacial modifications introduced by ALD are sufficient to influence both the triboelectric response and humidity-dependent charge dissipation behavior of regenerated cellulose.

Metal-semiconductor junctions and interfaces have been studied for many years due to their importance in applications such as semiconductor electronics and solar cells. However, semiconductor-metal networks are less studied because there is a lack of effective methods to fabricate such structures. Here, we report a novel Au–ZnO-based metal-semiconductor (M-S)n network in which ZnO nanowires were grown horizontally on gold particles and extended to reach the neighboring particles, forming an (M-S)n network. The (M-S)n network was further used as a gas sensor for sensing ethanol and acetone gases. The results show that the (M-S)n network is sensitive to ethanol (28.1 ppm) and acetone (22.3 ppm) gases and has the capacity to recognize the two gases based on differences in the saturation time. This study provides a method for producing a new type of metal-semiconductor network structure and demonstrates its application in gas sensing.

Hydrogen sulfide (H2S) is a highly toxic and corrosive gas commonly found in industrial emissions and natural gas processing, posing serious risks to human health and environmental safety even at low concentrations. The early detection of H2S is therefore critical for preventing accidents and ensuring compliance with safety regulations. This study presents the development of porous ZnO/SnO2-nanocomposite gas sensors tailored for the ultrasensitive detection of H2S at sub-ppb levels. Utilizing a screen-printing method, we fabricated five different sensor compositions—ranging from pure SnO2 to pure ZnO—and characterized their structural and morphological properties through X-ray diffraction (XRD) and scanning electron microscopy (SEM). Among these, the SnO2/ZnO sensor with a composition-weight ratio of 3:4 demonstrated the highest response at 325 °C, achieving a low detection limit of 0.14 ppb. The sensor was evaluated for detecting H2S concentrations ranging from 5 ppb to 500 ppb under dry, humid air and N2 conditions. The relative concentration error was carefully calculated based on analytical sensitivity, confirming the sensor’s precision in measuring gas concentrations. Our findings underscore the significant advantages of mixture nanocomposites in enhancing gas sensitivity, offering promising applications in environmental monitoring and industrial safety. This research paves the way for the advancement of highly effective gas sensors capable of operating under diverse conditions with high accuracy.