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One-dimensional (1D)/two-dimensional (2D) heterostructures offer attractive opportunities for developing high-performance gas sensors.

Non-precious metals have been considered as suitable alternatives for high-performance hydrogen evolution reactions (HER). Although the incorporation of carbon substances is shown to improve the number of active sites, electron transfer pathways, and long-term stability, there have been rare reports on their single-step scalable production. Herein, we realize free-standing two-dimensional (2D) carbon sheets heterostructured with nickel (Ni) nanocatalysts by pyrolyzing ultrathin layers of acetate tetrahydrate (i.e. the single precursor for both Ni and C sources) over water-soluble salt crystals. Such a salt-templated methodology is environmentally friendly and readily scalable without the implementation of sophisticated equipment. The resulting 2D carbon sheets exhibit an average small thickness of ∼ 3 nm and lateral dimensions with tens of micrometers, where a large number of nano-sized Ni particles with an average diameter of 14 nm are uniformly dispersed. Such 2D Ni-C sheets demonstrate a small overpotential of 111 mV at 10 mA/cm

Metal-organic frameworks (MOFs) with exceptional features such as high structural diversity and surface area as well as controlled pore size has been considered a promising candidate for developing room temperature highly-sensitive gas sensors. In comparison, the hetero-metallic MOFs with redox-active open-metal sites and mixed metal nodes may create peculiar surface properties and synergetic effects for enhanced gas sensing performances. In this work, the Fe atoms in the Fe3 (Porous coordination network) PCN-250 MOFs are partially replaced by transition metal Co, Mn, and Zn through a facile hydrothermal approach, leading to the formation of hetero-metallic MOFs (Fe2IIIMII, M=Co, Mn, and Zn). While the PCN-250 framework is maintained, the morphological and electronic band structural properties are manipulated upon the partial metal replacement of Fe. More importantly, the room temperature NO2 sensing performances are significantly varied, in which Fe2Mn PCN-250 demonstrates the largest response magnitude for ppb-level NO2 gas compared to those of pure Fe3 PCN-250 and other hetero-metallic MOF structures mainly attributed to the highest binding energy of NO2 gas. This work demonstrates the strong potential of hetero-metallic MOFs with carefully engineered substituted metal clusters for power-saving and high-performance gas sensing applications.

As an emerging semiconductor-based catalyst, g-C3N4 has attracted significant attention for visible light-driven photocatalytic energy conversion, synthesis of chemicals, and environmental remediation.

A comprehensive and critical overview of graphene-based adsorbents in capturing various water contaminants within the recent five years is presented to drive the rational development of high-performance adsorbents with graphene and its derivatives.

Gallium (Ga) and Ga-based liquid metal (LM) alloys offer low toxicity, excellent electrical and thermal conductivities, and fluidity at or near room temperature. Ga-based LM particles (LMPs) synthesized from these LMs exhibit both fluidic and metallic properties and are suitable for versatile functionalization in therapeutics. Functionalized Ga-based LMPs can be actuated using physical or chemical stimuli for drug delivery, cancer treatment, bioimaging, and biosensing. However, many of the fundamentals of their unique characteristics for therapeutics remain underexplored. We present the most recent advances in Ga-based LMPs in therapeutics based on the underlying mechanisms of their design and implementation. We also highlight some future biotechnological opportunities for Ga-based LMPs based on their extraordinary advantages.

Two-dimensional (2D) metal oxides and chalcogenides (MOs & MCs) have been regarded as a new class of promising electro- and photocatalysts for many important chemical reactions such as hydrogen evolution reaction, CO2 reduction reaction and N2 reduction reaction in virtue of their outstanding physicochemical properties. However, pristine 2D MOs & MCs generally show the relatively poor catalytic performances due to the low electrical conductivity, few active sites and fast charge recombination. Therefore, considerable efforts have been devoted to engineering 2D MOs & MCs by rational structural design and chemical modification to further improve the catalytic activities. Herein, we comprehensively review the recent advances for engineering technologies of 2D MOs & MCs, which are mainly focused on the intercalation, doping, defects creation, facet design and compositing with functional materials. Meanwhile, the relationship between morphological, physicochemical, electronic, and optical properties of 2D MOs & MCs and their electro- and photocatalytic performances is also systematically discussed. Finally, we further give the prospect and challenge of the field and possible future research directions, aiming to inspire more research for achieving high-performance 2D MOs & MCs catalysts in energy storage and conversion fields.

Synthesizing two dimensional (2D) nanomaterials with controlled sub-nanometer thicknesses from non-layered crystals presents both significant challenges and vast opportunities. However, mechanical exfoliation techniques and physical/wet chemical deposition processes are widely disadvantageous for applicability to non-layered structures. Here we have utilized a simple self-limiting approach to prepare large sheets of 2D zinc oxide (ZnO) at the metal-melt/air interface. These ultra-thin sheets demonstrated highly crystalline hexagonal structures. The specific ZnO hexagonal sheet thickness and its interaction with the substrate were found to have a critical impact on d33. This unusual structure resulted in an exceptionally high out of plane piezoelectricity, yielding a giant value of 80 ± 0.8 pm/V at 2.5 unit-cell thickness for d33, which is 5 Zn-O layers in the wurtzite crystal. This out of plane piezoelectricity value is approximately 8 times larger than that of the value for bulk ZnO. Theoretical studies were carried out to elucidate the impact of the thickness and the substrate’s role on the polarization of the layers. The existence of a large piezoelectricity offered by the synergy of the substrate and specific thickness of ultrathin films offers the opportunity for other groups of potentially piezoelectric materials to be explored.

On-chip optical switches have emerged as a new class of photonic components for high-performance optical communication networks and on-chip interconnects, in which the all-optical configuration without the incorporation of other control-means is highly desired. While two-dimensional (2D) ultrathin materials demonstrate their great potential in developing ultrafast all-optical switches owing to their unique light–matter interaction, such investigations have so far been limited to the fiber optic platform or free space. Here, we realize an all-optical on-chip switch from a silicon waveguide-based asymmetric Mach–Zehnder interferometer (MZI) structure enabled by 2D ultrathin Ga2S3. Upon the visible light excitation at 532 nm, excessive photocarriers in Ga2S3 cause a change of the refractive index and subsequently a phase variation between MZI arms at the 1550 nm operation wavelength, triggering on the optical switch. On the other hand, the switch is off without the visible light stimulation, as the phase variation is recovered due to the ultrafast photo-exciton relaxation behavior of Ga2S3. The Ga2S3-enabled all-optical switch is driven at an extremely small optical power density of 0.12 W cm−2 and exhibits a response and recovery time of 26.3 and 43.5 μs, respectively, which as a combination is superior to those of fiber optic-based all-optical switches enabled by 2D materials. This work may provide a viable approach to develop on-chip all-optical photonic components for practical integrated photonic chips.

In this study, we analyze the influence of the pore structure of an SBA-15 particle on the light emission from its inner adsorbed quantum dots (QDs) and outer light-emitting diode (LED) chips. It is found that the particle features of a high refractive index, comparable feature size of pore structure, and lower amount of QD adsorption help with QD light extraction, demonstrating a mechanism to suppress QD light propagating through pores and thus reducing the reabsorption loss. We consequently developed highly efficient QD white LEDs with wet-mixing QD/SBA-15 nanocomposite particles (NPs) by further optimizing the packaging methods and the introduced NP mass ratio. The LEDs demonstrated a record luminous efficacy (the ratio of luminous flux to electrical power) of 206.8 (entrusted test efficiency of 205.8 lm W-1 certificated by China National Accreditation Service) and 137.6 lm W-1 at 20 mA for white LEDs integrating only green QDs and green-red QD color convertors, respectively, with improved operating stability. These results are comparable to conventional phosphor-based white LEDs, which can be a starting point for white LEDs only using QDs as convertors toward commercialization in the near future.

The emergence of piezoelectric properties in two-dimensional (2D) layered transition metal dichalcogenides (TMDs) has triggered the intensive research on using low dimensional materials for conversion of mechanical stimuli into electrical signals or vice versa. While the bulk intrinsically presents no piezoelectric property, the origin of the piezoelectric responses in their 2D thin planes is ascribed to the loss of centrosymmetry. There are also other categories of 2D layered materials such as post-transition metal dichalcogenides (PTMDs) that might be of interests, which have been confirmed theoretically and are yet to be fully explored experimentally. In this work, we investigate the thickness-dependent piezoelectric responses of 2D tin disulfide (SnS2) nanosheets as a representative of layered PTMDs. The results indicate that the 2D SnS2 nanosheets with a thickness of ∼4 nm present an effective out-of-plane piezoelectric response of 2 ± 0.22 pm/V. Furthermore, the thickness dependence of the piezoelectric behavior at a resonant frequency shows that the piezoelectric coefficient decreases with increasing the thickness of 2D SnS2 nanosheets. Additionally, in reference to periodically poled lithium niobate piezoelectric crystal, the measured effective lateral piezoelectric coefficients at different voltages range from 0.61 to 1.55 pm/V with the average value at ∼1 pm/V. This study expands candidates for new piezoelectric materials in the 2D domain with comparable vertical and lateral coefficients, potentially opening a broader horizon for integration into sensors, actuators, and micro- and nanoelectromechanical systems.

The burgeoning research into two-dimensional (2D) materials opens a door to novel photonic and optoelectronic devices utilizing their fascinating electronic and photonic properties in thin-layered architectures. The hybrid integration of 2D materials onto integrated optics platforms thus becomes a potential solution to tackle the bottlenecks of traditional optoelectronic devices. In this paper, we present the recent advances of hybrid integration of a wide range of 2D materials on integrated optics platforms for developing high-performance photodetectors, modulators, lasers, and nonlinear optics. Such hybrid integration enables fully functional on-chip devices to be readily accessible researchers and technology developers, becoming a potential candidate for next-generation photonics and optoelectronics industries.

Nitrogen-doped carbon catalysts prepared from amino-functionalized metal–organic frameworks [amino-MIL-101(Al)] were investigated for the oxygen-reduction reaction (ORR) with special emphasis on el...

The library of true two-dimensional materials is limited since many transition metal compounds are not stratified and can thus not be easily isolated as nanosheets. Here, micron-sized ultrathin rutile TiO2 nanosheets featuring uniform thickness (2 ± 0.5 nm) with dielectric constant (e⊥ = 24) have been synthesized via a liquid metal synthesis strategy.

Metal chalcogenides are important members of the two-dimensional (2D) materials family and have been extensively investigated for high-performance electronic device applications. However, when they are produced on a large-scale, their carrier mobilities are strongly influenced by the surface conditions. Here, we print indium sulphide (In2S3) with the thickness down to the single unit cell limit on wafer-scale out of metallic indium liquid, in which structural indium vacancies are formed in an orderly fashion. First principles investigations reveal that the unique ordered-vacancy structure results in a highly dispersive conduction band with low effective electron mass, forming multiple band-like electronic transport channels sandwiched within the crystal structure which are less influenced by the surface conditions. Back-gated field effect transistors are fabricated, and the measured mobility is up to 58 cm2 V-1 s-1 with a high degree of reproducibility, which is amongst one of the highest reported for wafer-scale-grown ultra-thin metal chalcogenides. This establishes ordered-vacancy-enabled semiconductors in the 2D geometry as suitable alternatives for new generation high-performance electronic devices.

Facile and scalable synthesis of two-dimensional (2D) non-layered materials is highly desirable for novel applications. Iron compounds including hematite (α-Fe2O3) and iron phosphide (FeP) are an important group of semiconductors but their 2D ultrathin morphology has been rarely reported. Here, we develop a water dissolvable template-based synthesis route to produce free-standing ultrathin iron compounds. Such a method also enables the tunability of morphology from mesoporous nanosheet to meso-macroporous hierarchical nanonet utilizing the aging process, while its corresponding surface active area is reduced simultaneously. Ultrathin hematite is relatively inert to electrochemical hydrogen evolution reaction (HER). However, FeP exhibits excellent catalytic performances with a relatively low overpotential of 117 mV and a Tafel slope of 56 mV dec−1, which is as a whole improved over those of reported free-standing binary transition-metal phosphide nanostructures. This work extends the possibility to produce high-quality 2D non-layered materials, which are expected to exhibit unique properties compared to their bulk counterparts.

Metal-organic frameworks (MOFs) with exceptional features such as high structural diversity and surface area as well as controlled pore size has been considered a promising candidate for developing room temperature highly-sensitive gas sensors. In comparison, the hetero-metallic MOFs with redox-active open-metal sites and mixed metal nodes may create peculiar surface properties and synergetic effects for enhanced gas sensing performances. In this work, the Fe atoms in the Fe

Fiber-optic gas sensors have been considered a low-cost, effective, and robust approach for monitoring nitrogen dioxide (NO

Excitation wavelength-dependent photoluminescence (PL) in two-dimensional (2D) transition-metal chalcogenides enables a strong excitonic interaction for high-performance chemical and biological sensing applications. In this work, we explore the possible candidates in the domain of post-transition-metal chalcogenides. Few-layered 2D p-type tin monosulfide (SnS) nanoflakes with submicrometer lateral dimensions are synthesized from the liquid phase exfoliation of bulk crystals. Excitation wavelength-dependent PL is found, and the excitonic radiative lifetime is more than one order enhanced compared to that of the bulk counterpart because of the quantum confinement effect. Paramagnetic NO2 gas is selected as a representative to investigate the exciton-driven chemical-sensing properties of 2D SnS. Physisorption of NO2 results in the formation of dipoles on the surface of 2D SnS, causing the redistribution of photoexcited charges in the body and therefore modifying PL properties. For practical sensing applications, 2D SnS is integrated into a resistive transducing platform. Under light irradiation, the sensor exhibits excellent sensitivity and selectivity to NO2 at a relatively low operating temperature of 60 °C. The limit of detection is 17 parts per billion (ppb), which is significantly improved over other previously reported 2D p-type semiconductor-based NO2 sensors.

Microperoxidase-11 (MP-11) has been widely used in enzymatic reactions. Further improvement of its performance requires a better charge transfer and more exposure of its active site in the enzymatic conversions, which can be achieved by immobilisation of MP-11 into functional materials. However, conventional immobilisation techniques always suffer from non-specific and uncontrolled weak interactions and energy level of two entities in the hybrid is not perfectly matched, thus resulting in limited improvement of the system. In this work, a hybrid material of layered MoO3 and MP-11 was synthesised by a self-assembly technique through a covalent interaction. Physicochemical characterisation indicated that there is a charge transfer from MP-11 to MoO3 and a covalent bond is formed in the hybrid. A notable enhancement of biocatalysis and photocurrent conversion were observed in the studies, which are due to a synergistic effect and band alignment of the two entities in the hybrid. The superior combined properties provide a great opportunity for developing high performance enzymatic conversion systems.

Intriguing physical and chemical properties of atomically thin semiconductors provide avenues for the development of the next-generation electronics, optoelectronics, and sensing applications. Howe...

The structurally colored surface of anodic aluminum oxide (AAO) is highly useful for decoration and anti-counterfeiting applications, which are of significance for both scientific and industrial communities. This study presents the first demonstration of the fabrication of an iridescent film of porous AAO on an industrial aluminum alloy substrate, with alternatingly electrodeposited Cu and SiO2 nanoparticles (NPs). A rainbow effect was effectively obtained for the optimized sample with appropriate alternating electrodeposition times. The structure and optical properties of a series of the electrodeposited AAO-based thin film were investigated. The Cu and SiO2 NPs were found to be uniformly deposited into the porous structure of the AAO film, and the alternating electrodeposition repeating twice led to the formation of the optimal AAO-based thin film that exhibited a rainbow effect and superior anti-corrosion performance.

Molybdenum based compounds are an emerging class of non-metallic catalytic materials for the hydrogen evolution reaction (HER) in acidic media. However, most of them lose considerable catalytic performance and exhibit poor long-term stability in alkaline media. Here, planar molybdenum oxide, with high alkaline stability and ordered intracrystalline pores, is developed as the HER candidate. The pores with diameters in the order of ∼5–7 A are HER-active, and appear after an NH4+ doping-driven phase transition from the orthorhombic to hexagonal phase. Such a unique structure facilitates the diffusion of ionic entities and water molecules to the HER sites and helps in the removal of gaseous products, therefore improving the surface active area and reaction kinetics. These intracrystalline pores also reduce the long term stress on electrodes. The corresponding HER activity is extremely stable for >40 h in an alkaline medium at an overpotential of 138 mV with a Tafel slope of 50 mV dec−1. Such properties offer a superior combination compared to those of other reported molybdenum based nanostructures, hence providing a great opportunity for developing high-performance alkaline non-metal HER catalysts.