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Hierarchical three-dimensional (3D) flower-like n-ZnO/p-NiO heterostructures with various ZnxNiy molar ratios (Zn5Ni1, Zn2Ni1, Zn1Ni1, Zn1Ni2 and Zn1Ni5) were synthesized by a facile hydrothermal method. Their crystal phase, surface morphology, elemental composition and chemical state were comprehensively investigated by XRD, SEM, EDS, TEM and XPS techniques. Gas sensing measurements were conducted on all the as-developed ZnxNiy-based sensors toward ammonia (NH3) detection under various working temperatures from 160 to 340 °C. In particular, the as-prepared Zn1Ni2 sensor exhibited superior NH3 sensing performance under optimum working temperature (280 °C) including high response (25 toward 100 ppm), fast response/recovery time (16 s/7 s), low detection limit (50 ppb), good selectivity and long-term stability. The enhanced NH3 sensing capabilities of Zn1Ni2 sensor could be attributed to both the specific hierarchical structure which facilitates the adsorption of NH3 molecules and produces much more contact sites, and the improved gas response characteristics of p-n heterojunctions. The obtained results clear demonstrated that the optimum n-ZnO/p-NiO heterostructure is indeed very promising sensing material toward NH3 detection for different applications.
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The exhibition of plasmon resonances in two-dimensional (2D) semiconductor compounds is desirable for many applications. Here, by electrochemically intercalating lithium into 2D molybdenum disulfide (MoS2) nanoflakes, plasmon resonances in the visible and near UV wavelength ranges are achieved. These plasmon resonances are controlled by the high doping level of the nanoflakes after the intercalation, producing two distinct resonance peak areas based on the crystal arrangements. The system is also benchmarked for biosensing using bovine serum albumin. This work provides a foundation for developing future 2D MoS2 based biological and optical units.
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Dissulfetos/química , Molibdênio/química , Ressonância de Plasmônio de SuperfícieRESUMO
We report the influence of zinc oxide (ZnO) seed layers on the performance of ZnO-based memristive devices fabricated using an electrodeposition approach. The memristive element is based on a sandwich structure using Ag and Pt electrodes. The ZnO seed layer is employed to tune the morphology of the electrodeposited ZnO films in order to increase the grain boundary density as well as construct highly ordered arrangements of grain boundaries. Additionally, the seed layer also assists in optimizing the concentration of oxygen vacancies in the films. The fabricated devices exhibit memristive switching behaviour with symmetrical and asymmetrical hysteresis loops in the absence and presence of ZnO seed layers, respectively. A modest concentration of oxygen vacancy in electrodeposited ZnO films as well as an increase in the ordered arrangement of grain boundaries leads to higher switching ratios in Ag/ZnO/Pt devices.
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The scientific field of two-dimensional (2D) nanostructures has witnessed tremendous development during the last decade. To date, different synthesis approaches have been developed; therefore, various exceptional properties of this family of advanced materials have been discovered. It has recently been found that the natural surface oxide films of room-temperature liquid metals is an emerging platform for the synthesis of novel types of 2D nanostructures with numerous functional applications. However, most of the developed synthesis techniques for these materials are based on the direct mechanical exfoliation of 2D materials as research targets. This paper reports a facile and functional sonochemical-assisted approach for the synthesis of 2D hybrid and complex multilayered nanostructures with tunable characteristics. In this method, the intense interaction of acoustic waves with microfluidic gallium-based room-temperature liquid galinstan alloy provides the activation energy for synthesis of hybrid 2D nanostructures. The microstructural characterizations reveal the impact of sonochemical synthesis parameters, including the processing time and composition of the ionic synthesis environment, on the growth of GaxOy/Se 2D hybrid structures and InGaxOy/Se multilayered crystalline structures with tunable photonic characteristics. This technique shows promising potential for synthesis of various types of 2D and layered semiconductor nanostructures with tunable photonic characteristics.
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Acoustic-activated polarization at two-dimensional (2D) domains provide supplementary mechanisms for adjustment of empty and occupied orbitals at material heterointerfaces, activating a wide range of physicochemical applications. The piezoelectric nanodomains grown at 2D liquid-metal heterointerfaces represent a new class of polarization-dependent hybrid nanostructures with a highly challenging fabrication process. Here, the controlled growth of selenium-rich piezoelectric nanodomains on the nonpolar 2D surface of liquid Ga-based nanoparticles (NPs) enabled highly efficient and sustainable CO2 conversion. The Ga-based NPs were engulfed in carbon nanotube (CNT) frameworks. The initial hindrance effects of CNT frameworks suppressed the undesirable Ga-Se amalgamation to guarantee the suitable functions of piezocatalyst. Simultaneously, the CNT-Se mesoporous network enhances the transport and interaction of ionic species at heterointerfaces, providing unique selectivity features for CO2 conversion. Driven by acoustic energy, the multiple contributions of Ga-Se polarized heterointerfaces facilitated the piezoelectric switching and therefore increased the CO2 conversion efficiency to the value of 95.8%. The inherent compositional and functional tunability of the Ga-Se nanojunction reveal superior control over the catalyst heterointerfaces and thereby show promising potential for nanoscale applications.
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Plasmonic nanostructures ensure the reception and harvesting of visible lights for novel photonic applications. In this area, plasmonic crystalline nanodomains decorated on the surface of two-dimensional (2D) semiconductor materials represent a new class of hybrid nanostructures. These plasmonic nanodomains activate supplementary mechanisms at material heterointerfaces, enabling the transfer of photogenerated charge carriers from plasmonic antennae into adjacent 2D semiconductors and therefore activate a wide range of visible-light assisted applications. Here, the controlled growth of crystalline plasmonic nanodomains on 2D Ga2O3 nanosheets was achieved by sonochemical-assisted synthesis. In this technique, Ag and Se nanodomains grew on 2D surface oxide films of gallium-based alloy. The multiple contribution of plasmonic nanodomains enabled the visible-light-assisted hot-electron generation at 2D plasmonic hybrid interfaces, and therefore considerably altered the photonic properties of the 2D Ga2O3 nanosheets. Specifically, the multiple contribution of semiconductor-plasmonic hybrid 2D heterointerfaces enabled efficient CO2 conversion through combined photocatalysis and triboelectric-activated catalysis. The solar-powered acoustic-activated conversion approach of the present study enabled us to achieve the CO2 conversion efficiency of more than 94% in the reaction chambers containing 2D Ga2O3-Ag nanosheets.
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Realizing the neurological information processing by analyzing the complex data transferring behavior of populations and individual neurons is one of the fast-growing fields of neuroscience and bioelectronic technologies. This field is anticipated to cover a wide range of advanced applications, including neural dynamic monitoring, understanding the neurological disorders, human brain-machine communications and even ambitious mind-controlled prosthetic implant systems. To fulfill the requirements of high spatial and temporal resolution recording of neural activities, electrical, optical and biosensing technologies are combined to develop multifunctional bioelectronic and neuro-signal probes. Advanced two-dimensional (2D) layered materials such as graphene, graphene oxide, transition metal dichalcogenides and MXenes with their atomic-layer thickness and multifunctional capabilities show bio-stimulation and multiple sensing properties. These characteristics are beneficial factors for development of ultrathin-film electrodes for flexible neural interfacing with minimum invasive chronic interfaces to the brain cells and cortex. The combination of incredible properties of 2D nanostructure places them in a unique position, as the main materials of choice, for multifunctional reception of neural activities. The current review highlights the recent achievements in 2D-based bioelectronic systems for monitoring of biophysiological indicators and biosignals at neural interfaces.
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The assembly of geometrically complex and dynamically active liquid metal/semiconductor heterointerfaces has drawn extensive attention in multidimensional electronic systems. In this study the chemovoltaic driven reactions have enabled the microfluidity of hydrophobic galinstan into a three-dimensional (3D) semiconductor matrix. A dynamic heterointerface is developed between the atomically thin surface oxide of galinstan and the TiO2-Ni interface. Upon the growth of Ga2O3 film at the Ga2O3-TiO2 heterointerface, the partial reduction of the TiO2 film was confirmed by material characterization techniques. The conductance imaging spectroscopy and electrical measurements are used to investigate the charge transfer at heterointerfaces. Concurrently, the dynamic conductance in artificial synaptic junctions is modulated to mimic the biofunctional communication characteristics of multipolar neurons, including slow and fast inhibitory and excitatory postsynaptic responses. The self-rectifying characteristics, femtojoule energy processing, tunable synaptic events, and notably the coordinated signal recognition are the main characteristics of this multisynaptic device. This novel 3D design of liquid metal-semiconductor structure opens up new opportunities for the development of bioinspired afferent systems. It further facilitates the realization of physical phenomena at liquid metal-semiconductor heterointerfaces.
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Two-dimensional (2D) semiconductors beyond graphene represent the thinnest stable known nanomaterials. Rapid growth of their family and applications during the last decade of the twenty-first century have brought unprecedented opportunities to the advanced nano- and opto-electronic technologies. In this article, we review the latest progress in findings on the developed 2D nanomaterials. Advanced synthesis techniques of these 2D nanomaterials and heterostructures were summarized and their novel applications were discussed. The fabrication techniques include the state-of-the-art developments of the vapor-phase-based deposition methods and novel van der Waals (vdW) exfoliation approaches for fabrication both amorphous and crystalline 2D nanomaterials with a particular focus on the chemical vapor deposition (CVD), atomic layer deposition (ALD) of 2D semiconductors and their heterostructures as well as on vdW exfoliation of 2D surface oxide films of liquid metals.
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Bio-inspired nano-electronic devices are key instruments for the development of advanced artificial intelligence systems, which will shape the future of humanoid nano-robotics. An emerging demand is realized for an accurate reception of environmental stimuli via visual perception, processing and realization of optical signals. The present study demonstrates the capability of functionalized all-oxide heterostructured two-dimensional (2D) plasmonic devices for the self-adaptive recognition of visual optical pulses. Specifically, the nano-engineering of the metal/semiconductor interface and co-modulation of heterostructured 2D semiconductor hetero-interfaces of Au/WO3 : TiO2 and Au/Ga2O3 : TiO2 facilitated the receptive and nociceptive detection of visible light pulses. A decrease in the dark current of the Au/WO3 : TiO2 unit resulted in the development of sensitive visible light photoreceptors. Furthermore, the modulation of charge transfers at the Au/Ga2O3 : TiO2 hetero-interfaces were the key parameter to determine the optical reception characteristics and nociceptive performance of all-oxide optoelectronic devices. Specifically, the rapid thermal annealing (RTA) of 2D Ga2O3 in N2 atmosphere ensured the modulation of charge transfer at Au/Ga2O3 : TiO2 hetero-interfaces in plasmonic devices. Thus, hetero-interface engineering enabled the effective control of charge transfer at 2D hetero-interfaces for an adaptive perception of visible optical pulses. Consequently, the fabricated sensitive Au/Ga2O3 (N2) : TiO2 bio-inspired unit emulated the optical functionalities of corneal nociceptors.
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Nanoscale Au-ZnO heterostructures were fabricated on 4-in. SiO2/Si wafers by the atomic layer deposition (ALD) technique. Developed Au-ZnO heterostructures after post-deposition annealing at 250 °C were tested for amperometric hydrogen peroxide (H2O2) detection. The surface morphology and nanostructure of Au-ZnO heterostructures were examined by field emission scanning electron microscopy (FE-SEM), Raman spectroscopy, atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), etc. Additionally, the electrochemical behavior of Au-ZnO heterostructures towards H2O2 sensing under various conditions is assessed by chronoamperometry and electrochemical impedance spectroscopy (EIS). The results showed that ALD-fabricated Au-ZnO heterostructures exhibited one of the highest sensitivities of 0.53 µA µM-1 cm-2, the widest linear H2O2 detection range of 1.0 µM-120 mM, a low limit of detection (LOD) of 0.78 µM, excellent selectivity under the normal operation conditions, and great long-term stability. Utilization of the ALD deposition method opens up a unique opportunity for the improvement of the various capabilities of the devices based on Au-ZnO heterostructures for amperometric detection of different chemicals.
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Highly water-soluble cyanocobalamin (also known as vitamin B12) is the most structurally macrocyclic complex comprising cobalt in the center of a corrin ring. Interestingly, it acts as a robust electrocatalyst in water oxidation at â¼0.58 V overpotential with a faradaic efficiency of 97.50% under neutral buffered conditions. The catalyst is impressively stable even after long-term bulk electrolysis, and homogeneous in nature, as established by a series of experiments and characterization techniques.
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Vitamina B 12/química , Água/química , Catálise , Cobalto/química , Conformação Molecular , Oxirredução , PotenciometriaRESUMO
Retina nociceptor, as a key sensory receptor, not only enables the transport of warning signals to the human central nervous system upon its exposure to noxious stimuli, but also triggers the motor response that minimizes potential sensitization. In this study, the capability of two-dimensional all-oxide-heterostructured artificial nociceptor as a single device with tunable properties was confirmed. Newly designed nociceptors utilize ultra-thin sub-stoichiometric TiO2-Ga2O3 heterostructures, where the thermally annealed Ga2O3 films play the role of charge transfer controlling component. It is discovered that the phase transformation in Ga2O3 is accompanied by substantial jump in conductivity, induced by thermally assisted internal redox reaction of Ga2O3 nanostructure during annealing. It is also experimentally confirmed that the charge transfer in all-oxide heterostructures can be tuned and controlled by the heterointerfaces manipulation. Results demonstrate that the engineering of heterointerfaces of two-dimensional (2D) films enables the fabrication of either high-sensitive TiO2-Ga2O3 (Ar) or high-threshold TiO2-Ga2O3 (N2) nociceptors. The hypersensitive nociceptor mimics the functionalities of corneal nociceptors of human eye, whereas the delayed reaction of nociceptor is similar to high-threshold nociceptive characteristics of human sensory system. The long-term stability of 2D nociceptors demonstrates the capability of heterointerfaces engineering for effective control of charge transfer at 2D heterostructured devices.
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Atomically thin two-dimensional (2D) semiconductors are the thinnest functional semiconducting materials available today. Among them, both molybdenum trioxide and chalcogenides (MT&Ds) represent key components within the family of different 2D semiconductors for various electronic, optoelectronic and electrochemical applications due to their unique electronic, optical, mechanical and electrochemical properties. However, despite great progress in research dedicated to the development and fabrication of 2D MT&Ds observed within the last decade, there are significant challenges that affected their charge transport behavior and fabrication on a large scale as well as there is high dependence of the carrier mobility on the thickness. In this article, we review the recent progress in the carrier mobility engineering of 2D MT&Ds and elaborate devised strategies dedicated to the optimization of MT&D properties. Specifically, the latest physical and chemical methods towards the surface functionalization and optimization of the major factors influencing the extrinsic transport at the electrode-2D semiconductor interface are discussed.
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Development of the next generation of bio- and nano-electronics is inseparably connected to the innovative concept of emulation and reproduction of biological sensorimotor systems and artificial neurobotics. Here, we report for the first time principally new artificial bioinspired optoelectronic sensorimotor system for the controlable immitation of opto-genetically engineered neurons in the biological motor system. The device is based on inorganic optical synapse (In-doped TiO2 nanofilm) assembled into a liquid metal (galinstan) actuator. The optoelectronic synapse generates polarised excitatory and inhibitory postsynaptic potentials to trigger the liquid metal droplet to vibrate and then mimic the expansion and contraction of biological fibre muscle. The low-energy consumption and precise modulation of electrical and mechanical outputs are the distinguished characteristics of fabricated sensorimotor system. This work is the underlying significant step towards the development of next generation of low-energy the internet of things for bioinspired neurorobotic and bioelectronic system.
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Bioengenharia/métodos , Optogenética/métodos , Robótica/instrumentação , Ligas/química , Sinapses Elétricas/fisiologia , Técnicas Eletroquímicas/métodos , Potenciais Pós-Sinápticos Inibidores/fisiologia , Metais Pesados/química , Músculos/inervação , Músculos/fisiologia , Neurônios/fisiologiaRESUMO
Electrochromic devices, serving as smart glasses, have not yet been intelligent enough to regulate lighting conditions independent of external photosensing devices. On the other hand, their bulky sandwich structures have been suffering setbacks utilized for reflective displays in an effort to compete with mature emissive displays. The key to resolve both problems lies in incorporating the photosensing function into electrochromic devices while simplifying their configuration via replacing ionic electrolytes. However, so far it has not yet been achieved because of the essential operating difference between the optoelectronic devices and the ionic devices. Herein, a concept of a smarter and thinner device: "electrochromic photodetector" is proposed to solve such problems. It is all-solid-state and electrolyte-free and operates with a simple thin metal-semiconductor-metal structure via an electrolytic mechanism. As a proof of concept, a configuration of the electrochromic photodetector is presented in this work based on a tungsten trioxide (WO3) thin film deposited on Au electrodes via facile, low-cost solution processes. The electrochromic photodetector switches between its photosensing and electrochromic functions via voltage modulation within 5 V, which is the result of the semiconductor-metal transition. The transition mechanism is further analyzed to be the voltage-triggered reversible oxygen/water vapor adsorption/intercalation from ambient air.
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Please be advised that the name of one of the coauthors in the original article [1] has been incorrectly spelled: 'Ranish M. Ramachandran' should be 'Ranjith K. Ramachandran'.
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Wafer-scale, conformal, two-dimensional (2D) TiO2-Ga2O3 n-p heterostructures with a thickness of less than 10 nm were fabricated on the Si/SiO2 substrates by the atomic layer deposition (ALD) technique for the first time with subsequent post-deposition annealing at a temperature of 250 °C. The best deposition parameters were established. The structure and morphology of 2D TiO2-Ga2O3 n-p heterostructures were characterized by the scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), etc. 2D TiO2-Ga2O3 n-p heterostructures demonstrated efficient photocatalytic activity towards methyl orange (MO) degradation at the UV light (λ = 254 nm) irradiation. The improvement of TiO2-Ga2O3 n-p heterostructure capabilities is due to the development of the defects on Ga2O3-TiO2 interface, which were able to trap electrons faster.
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Electrically responsive plasmonic devices, which benefit from the privilege of surface plasmon excited hot carries, have supported fascinating applications in the visible-light-assisted technologies. The properties of plasmonic devices can be tuned by controlling charge transfer. It can be attained by intentional architecturing of the metal-semiconductor (MS) interfaces. In this study, the wafer-scaled fabrication of two-dimensional (2D) TiO2 semiconductors on the granular Au metal substrate is achieved using the atomic layer deposition (ALD) technique. The ALD-developed 2D MS heterojunctions exhibited substantial enhancement of the photoresponsivity and demonstrated the improvement of response time for 2D Au-TiO2-based plasmonic devices under visible light illumination. To circumvent the undesired dark current in the plasmonic devices, a 2D WO3 nanofilm (â¼0.7 nm) was employed as the intermediate layer on the MS interface to develop the metal-insulator-semiconductor (MIS) 2D heterostructure. As a result, 13.4% improvement of the external quantum efficiency was obtained for fabricated 2D Au-WO3-TiO2 heterojunctions. The impedancometry measurements confirmed the modulation of charge transfer at the 2D MS interface using MIS architectonics. Broadband photoresponsivity from the UV to the visible light region was observed for Au-TiO2 and Au-WO3-TiO2 heterostructures, whereas near-infrared responsivity was not observed. Consequently, considering the versatile nature of the ALD technique, this approach can facilitate the architecturing and design of novel 2D MS and MIS heterojunctions for efficient plasmonic devices.
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The positively charged azolium moieties make imidazolium linker an ideal linker for the construction of cationic metal-organic frameworks because the ligand induces cationic environments in the frameworks. Therefore, we employed two imidazolium ligands, 1,3-bis(4-carboxyphenyl)imidazolium chloride (H2L+Cl¯) and 1,3-bis(3,5-dicarboxyphenyl)imidazolium chloride (H4L+Cl¯), to synthesize two nickel azolium-based MOFs, 1 and 2. The as-synthesis MOFs were characterized by PXRD, TGA, FE-SEM, HR-TEM, FTIR and BET measurements. By applying 1 and 2 in liquid phase adsorption of charged molecules of dyes, they successfully exhibit remarkable efficiency for adsorptive removal of anionic dyes, Methyl orange (MO), Congo red (CR), and Orange II sodium salt (OS), from aqueous solution. The framework proves efficient in photocatalytic degradation of anionic dye. Furthermore, in the gaseous phase adsorption, 1 and 2 selectively adsorb CO2 over CH4 due to the higher quadrupole moment of CO2. Overall, the results show that azolium-based MOFs have potential applications for adsorptive removal of charged organic contaminants from both aqueous and gaseous environment.