Amorphous Selenium Research Articles

Selenium nanoparticles: effect of autoclave treatment on size, shape, phase and antimicrobial properties

Amorphous selenium nanoparticles have been synthesized by pulsed laser ablation in liquids. After undergoing a thermal treatment at 121°C for 60 minutes, the amorphous nanoparticles crystallized into trigonal ones. The antimicrobial properties of both amorphous and trigonal nanoparticles have been compared; and the amorphous ones displayed better antibacterial and antifungal properties compared to the trigonal ones. Specifically, Methicillin-resistant Staphylococcus aureus (MRSA), Ampicillin-resistant Escherichia coli, Pseudomonas aeruginosa, Staphylococcus epidermidis, and Candida albicans were almost completely inhibited in the presence of amorphous selenium nanoparticles at 0.025 microgram/ml concentrations after 24 hours of in vitro culture, compared to controls (no nanoparticles). In summary, such a high sensitivity of these bacterial and fungal strains to low concentrations of amorphous selenium nanoparticles warrants further investigation to develop efficient anti-bacterial and anti-fungal treatments.

Spectroscopic investigation of oxidation in GaSe 2D layered materials

GaSe, a two-dimensional layered metal monochalcogenide, has recently attracted growing interest due to its unique electronic properties and potential technological applications. In this study, we investigate the oxidation mechanisms and properties of GaSe exposed to air for different durations, with the intensive use of Raman spectroscopy, combined with atomic force microscopy (AFM), photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS). Raman analysis reveals the oxidation of GaSe, resulting in the formation of a thin layer comprising Ga2Se3, Ga2O3, and amorphous selenium. Utilizing these signatures, oxidation is then tracked. Raman spectroscopy reveals that GaSe layer becomes oxidized almost immediately after exposure to air. However, the oxidation is a self-limiting process, taking roughly 15 min to construct an 8 Å thick layer of Ga₂O₃. XPS analysis shows a good agreement with Raman analysis. The polarized Raman study suggests that the Ga₂Se₃ and Ga₂O₃ layers tend to reach an oriented structural state over time. In ambient conditions, the intensity of all Raman modes and the luminescence decreases, linked to reduction in GaSe thickness. By using various Raman excitation wavelengths, we highlight the depth-dependent oxidation dynamics in this 2D layered GaSe material.

Angle-Dependent Photoinduced Changes of Near-Infrared Transmission in Amorphous Selenium Films

Angle-Dependent Photoinduced Changes of Near-Infrared Transmission in Amorphous Selenium Films

Retraction: Amorphous selenium nanoparticles improve vascular function in rats with chronic isocarbophos poisoning via inhibiting the apoptosis of vascular endothelial cells.

[This retracts the article DOI: 10.3389/fbioe.2021.673327.].

Ion Beam-Induced modification in the optical properties of the bilayer of nano-structured amorphous selenium and multi-walled carbon Nanotubes: A study by 70 MeV Ni Ions

In this study, we report improved physical properties of selenium with multi-walled carbon nanotubes (MWCNTs) resulting from a homogeneous mixture of CNT-Se bi-layer thin film by using swift heavy ion irradiation. FESEM micrographs clearly showed the inter-diffusion of Se nanoparticles into MWCNTs following swift heavy ion (SHI) irradiation, EDX validates the elemental composition. The existence of different phonon modes (LO mode and D, G, G' bands) has been found in the Raman spectra of the investigated bi-layer thin films. UV–Visible spectroscopic analysis of pristine CNT-Se thin films show two sharp absorption edges at ∼670 nm and ∼340 nm. After swift heavy ion irradiation, the sharp absorption edge at ∼670 nm exhibits a blue shift, whereas the absorption edge at ∼340 nm exhibits a red shift, confirming the homogeneous mixing of two layers. These remarkable shifts found in the optical properties of CNT-Se bi-layer make the investigated material feasible for many optoelectronic device applications.

Evaluating the Effects of Breaking Vacuum During the Fabrication of Amorphous Selenium Detectors.

Direct conversion X-ray detectors offer high spatial resolution and improved sensitivity over indirect conversion detectors. As interest increases in their applications, including utilization as the top layer in dual-layer detectors for polyenergetic X-ray detection, additional studies on fabrication techniques are required. Amorphous selenium is a well-studied high-Z semiconductor capable of high-resolution and high-sensitivity imaging in direct architectures. It is already commercially available for mammography, and much work has gone into developing it for higher-energy applications (>20 keV.) To fully attenuate energies required for the low energy (<35 keV) top layer in dual-layer detectors, a-Se thicknesses greater than 200 μm must be fabricated. However, evaporation crucibles have limited capacity and require reloading of crucible material to achieve higher thicknesses, which is performed by opening the chamber and breaking vacuum mid-fabrication. We investigate the effects of splitting the fabrication into two depositions - exposing the sample to air in between - on device performance. We find that there is no significant effect on the transport properties, and a small range of performance parameters can be found - suggesting small fluctuations between devices of ± 5%, independent of fabrication technique and thickness. This implies that as we increase our thicknesses to those required for the low-energy layer of the dual-layer detector, we can expect performance to be maintained.

Elucidating Consequences of Selenium Crystallinity on Its Electrochemical Reduction in Aluminum-Selenium Batteries.

Selenium (Se) is an attractive positive electrode material for rechargeable aluminum (Al) batteries due to its high theoretical capacity of 2037 mA h g-1 and its higher electronic conductivity compared to sulfur. Selenium can undergo a series of electrochemical reactions between Se(-II) and Se(IV), resulting in a six-electron capacity per Se atom. However, existing Al-Se battery literature is inconsistent regarding the different electrochemical reactions possible, while the conditions enabling the electrochemical reduction of Se to Al2Se3 are not well understood. Here, we demonstrate that this electrochemical reduction is achievable using amorphous selenium but is suppressed for crystalline selenium. We further show that the electrochemical oxidation of Se to SeCl4, which occurs at higher potentials, reduces the long-range order of crystalline Se and enables its discharge to Al2Se3. Solid-state 77Se nuclear magnetic resonance (NMR) measurements further establish that the local Se helical structures are maintained upon the loss of crystallinity.

Coupling of Infrared Active Colloidal Quantum Dots and Amorphous Selenium for Fast and Sensitive Photodetection

AbstractColloidal quantum dot (CQD) based infrared (IR) photodetectors offer facile wavelength tunability in the IR and low‐cost fabrication. However, owing to their large surface areas, CQDs intrinsically have significant surface traps critically affecting the speed of CQD photodetectors, typically mediated through tedious surface passivation efforts. In this report, an alternative strategy involving coupling of near‐IR photoactive lead sulfide CQDs with a thermally evaporated amorphous selenium (a‐Se) hole transport layer is proposed. By separating the detector into a photon absorbing CQD region and a charge transport a‐Se region, the study takes advantage of the extremely low noise, predominantly hole‐only transport process in a‐Se. A high 3 dB bandwidth of 2.5 MHz and a competitive specific detectivity of 2.5 × 1011 Jones at room temperature are demonstrated at 980 nm. This report serves as a first demonstration of strong coupling between an IR active CQD absorber and a‐Se, which paves the path to obtain fast and highly photoresponsive IR photodetection in the future.

Advancing room temperature NO2 gas sensing performance through high-energy mechanical milling of Tin-dichalcogenides

Eco-friendly gas sensing devices with simple architecture, reduced cost, and high performance at room temperature are being sought to replace the traditional metallic oxide materials, aiming to address environmental concerns. Lamellae semiconducting materials have shown promising detection properties for this purpose. Here, we investigated the sensing response of SnS2, Sn(S0.5Se0.5)2, and SnSe2 tin-dichalcogenides prepared by high-energy mechanical milling. High RNO2/Rair response signals, from 102 to 106, for 2–100 ppm of NO2 were observed for temperatures between 30 °C and 300 °C. The materials were not sensitive to CO, while H2 detection could only be observed above 200 °C, implying high NO2 selectivity. Additionally, we investigated the influence of samples suspension in water and isopropanol on grain size and morphology. We found that isopropanol crystallizes amorphous selenium phase dispersed in the Sn-Se system and increase the agglomeration in the Sn(S0.5Se0.5)2 system. Deformed and defective particles were observed regardless the preparation methodology. This unique defect-rich morphology might increase surface reactivity for selective NO2 detection by physisorption, owing a high adsorption/desorption rate at room temperature.

Experimental and theoretical study on recovered nano amorphous selenium as efficient adsorbents for mercury capture from flue gas

The cost-effective removal of gaseous elemental mercury from coal-fired flue gas is crucial for environmental protection. In this study, nano amorphous selenium (nano-a-Se) adsorbent was recovered from desulfurization wastewater to remove Hg0 in flue gas. The results indicate that nano-a-Se has a high efficiency in the amorphous form with a saturated adsorption capacity of 2034.32 mg g−1. The Se utilization ratio of nano-a-Se reached 80% of the theoretical limit. Meanwhile, nano-a-Se exhibited high resistance to NO and SO2 poisoning. Moreover, the Hg0 removal mechanism of nano-a-Se was analyzed by experimental analysis and density functional theory (DFT) calculations. The results demonstrate that nano-a-Se can convert Hg0 into stable mercury selenide, a high-value by-product with little risk of mercury re-release. Therefore, nano-a-Se is expected to be a novel adsorbent with high efficiency in capturing Hg0, which can help realize the resource utilization of toxic elements from the environment.

Structure of Amorphous Selenium: Small Ring, Big Controversy.

Selenium (Se) discovered in 1817 belongs to the family of chalcogens. Surprisingly, despite the long history of over two centuries and the chemical simplicity of Se, the structure of amorphous Se (a-Se) remains controversial to date regarding the dominance of chains versus rings. Here, we find that vapor-deposited a-Se is composed of disordered rings rather than chains in melt-quenched a-Se. We further reveal that the main origin of this controversy is the facile transition of rings to chains arising from the inherent instability of rings. This transition can be inadvertently triggered by certain characterization techniques themselves containing above-bandgap illumination (above 2.1 eV) or heating (above 50 °C). We finally build a roadmap for obtaining accurate Raman spectra by using above-bandgap excitation lasers with low photon flux (below 1017 phs m-2 s-1) and below-bandgap excitation lasers measured at low temperatures (below -40 °C) to minimize the photoexcitation- and heat-induced ring-to-chain transitions.

Improved temporal performance and optical quantum efficiency of avalanche amorphous selenium for low dose medical imaging.

Active matrix flat panel imagers (AMFPIs) with thin-film transistor arrays experience image quality degradation by electronic noise in low-dose radiography and fluoroscopy. One potential solution is to overcome electronic noise using avalanche gain in an amorphous selenium (a-Se) (HARP) photoconductor in indirect AMFPI. In this work, we aim to improve temporal performance of HARP using a novel composite hole blocking layer (HBL) structure and increase optical quantum efficiency (OQE) to CsI:Tl scintillators by tellurium (Te) doping. Two different HARP structures were fabricated: Composite HBL samples and Te-doped samples. Dark current and optical sensitivity measurements were performed on the composite HBL samples to evaluate avalanche gain and temporal performance. The OQE and temporal performance of the Te-doped samples were characterized by optical sensitivity measurements. A charge transport model was used to investigate the hole mobility and lifetime of the Te-doped samples in combination with time-of-flight measurements. The composite HBL has excellent temporal performance, with ghosting below 3% at 10mR equivalent exposure. Furthermore, the composite HBL samples have dark current and achieved an avalanche gain of 16. Te-doped samples increased OQE from 0.018 to 0.43 for 532nm light. The addition of Te resulted in 2.1% first-frame lag, attributed to hole trapping within the layer. The composite HBL and Te-doping can be utilized to improve upon the limitations of previously developed indirect HARP imagers, showing excellent temporal performance and increased OQE, respectively.

Exploring acylselenourea diselenides: Synthesis, spectroscopy, and structural characterization of phenyl-substituted N,N'-diselanediyl

Acylselenourea diselenides, with the formula [RC(O)NC(Se)NR2]2, are underexplored organoselenated compounds with potential applications in medicinal chemistry, coordination, and organic synthesis. This article presents a comprehensive study on the synthesis, spectroscopy, and structural characterization of the novel diselenide N,N'-diselanediyl-bis-((diphenylamino)methanylylidene)-dibenzamide, i.e., R = Phenyl. The compound was synthesized by a one-pot bimolecular oxidation between the tautomeric forms of the selenourea intermediate PhC(O)NHC(Se)N(Ph)2. The total yield of the reaction was moderate (40 %), with losses attributed to the formation of amorphous red selenium. Spectroscopic analysis, including FT-IR, 1H NMR, and 13C NMR, confirmed the molecular identity of the compound. The crystal structure of diselenide was determined by single-crystal X-ray diffraction analysis, which revealed the formation of a centrosymmetric dimer through a bidirectional hydrogen bond of the C=O···H-Ph type. Hirshfeld surface (HS) analysis and topological study of electron density (ρ) provided detailed information on the strength of the intermolecular and intramolecular interactions in the crystal structure.

Laser fragmentation of amorphous and crystalline selenium of various morphologies and assessment of their antioxidant and protection properties.

Introduction: The process of laser-induced breakdown of amorphous and crystalline selenium nanoparticles (Se NPs) of various shapes during nanosecond laser fragmentation of aqueous colloidal solutions of nanoparticles with different concentrations has been studied. Methods: The methods of studying the characteristics of plasma and acoustic oscillations induced by optical breakdown are applied. The methods of assessing the concentration of hydrogen peroxide and hydroxyl radicals, the amount of long-lived reactive species of protein and 8-oxoguanine are applied. Results: It has been established that in the process of laser fragmentation of selenium nanoparticles at a wavelength of 532nm, corresponding to the maximum absorption of selenium, the highest probability of breakdown, the number of plasma flashes, their luminosity and the amplitude of acoustic signals are achieved at concentrations of the order of 109NPs/mL. It has been shown that the use of selenium nanoparticles of various shapes and structures leads to a change in the photoacoustic signal during laser-induced breakdown. When crystalline selenium nanoparticles are irradiated, the intensity of the photoacoustic response during breakdown turns out to be greater (1.5 times for flash luminosity and 3 times for acoustics) than when amorphous particles are irradiated at the same concentration. It has been shown that selenium nanoparticles exhibit significant antioxidant properties. Selenium nanoparticles effectively prevent the formation of reactive oxygen species (ROS) during water radiolysis, eliminate radiation-induced long-lived reactive species of protein, and reduce the radiation-chemical yield of a key marker of oxidative DNA damage - 8-oxoguanine. Discussion: In general, the intensity of processes occurring during laser fragmentation of amorphous and crystalline selenium nanoparticles differs significantly. The antioxidant properties are more pronounced in amorphous selenium nanoparticles compared to crystalline selenium nanoparticles.

Evaluation of a Large Area, 83 μm Pixel Pitch Amorphous Selenium Indirect Flat Panel Detector.

Dual-layer detectors provide a low-cost solution to improved material decomposition and lesion differentiation in X-ray imaging, while eliminating motion artifacts from multiple exposures. Most designs utilize two indirect detectors with scintillators designed for low-energy and higher-energy detection and separated by a copper filter to harden the beam for high energy detection. To improve the performance of the bottom detector and lower dose requirements, we have previously proposed an alloyed amorphous selenium photodetector to achieve improved resolution and absorption at green wavelengths, better suited to high-performance scintillators such as CsI:Tl. In this work, we demonstrate a baseline prototype for the bottom layer-a continuous, large area 83 μm pixel pitch flat panel indirect detector with well-established amorphous selenium as the photodetector-and verify the architecture's performance and detector design. We characterize lag, noise-power spectrum, detective quantum efficiency, and modular transfer function of the detector, and show resolution up to 6 lp/mm when operated at an applied bias of 150 V. This provides a starting point for evaluating the alloyed selenium materials, and shows promise for this detector in the future dual-layer design.

Perovskite materials in X-ray detection and imaging: recent progress, challenges, and future prospects.

Perovskite materials have attracted significant attention as innovative and efficient X-ray detectors owing to their unique properties compared to traditional X-ray detectors. Herein, chronologically, we present an in-depth analysis of X-ray detection technologies employing organic-inorganic hybrids (OIHs), all-inorganic and lead-free perovskite material-based single crystals (SCs), thin/thick films and wafers. Particularly, this review systematically scrutinizes the advancement of the diverse synthesis methods, structural modifications, and device architectures exploited to enhance the radiation sensing performance. In addition, a critical analysis of the crucial factors affecting the performance of the devices is also provided. Our findings revealed that the improvement from single crystallization techniques dominated the film and wafer growth techniques. The probable reason for this is that SC-based devices display a lower trap density, higher resistivity, large carrier mobility and lifetime compared to film- and wafer-based devices. Ultimately, devices with SCs showed outstanding sensitivity and the lowest detectable dose rate (LDDR). These results are superior to some traditional X-ray detectors such as amorphous selenium and CZT. In addition, the limited performance of film-based devices is attributed to the defect formation in the bulk film, surfaces, and grain boundaries. However, wafer-based devices showed the worst performance because of the formation of voids, which impede the movement of charge carriers. We also observed that by performing structural modification, various research groups achieved high-performance devices together with stability. Finally, by fusing the findings from diverse research works, we provide a valuable resource for researchers in the field of X-ray detection, imaging and materials science. Ultimately, this review will serve as a roadmap for directing the difficulties associated with perovskite materials in X-ray detection and imaging, proposing insights into the recent status, challenges, and promising directions for future research.

Perspectives of dielectric and A.C. conductivity behavior of MWCNT and graphene-doped amorphous Selenium thin films

Perspectives of dielectric and A.C. conductivity behavior of MWCNT and graphene-doped amorphous Selenium thin films

Microbial-Based Biotechnology: Production and Evaluation of Selenium-Tellurium Nanoalloys

Using seleno-compounds and telluric compounds is a practical approach for developing solutions against drug-resistant bacterial infections and malignancies. It will accelerate the search for novel treatments or adjuvants for existing therapies. Selenium and tellurium nanospheres can be produced by lactic acid bacteria. The bacteria can differentiate the selenium and tellurium when the medium contains both selenite and tellurite. Therefore, our question in this study was the following: are they making alloys from the selenium and tellurium and what will be the composition, color, and shape of the nanoparticles? We used a simple microbial synthesis to produce nanoselenium, nanotellurium, and their alloys from sodium selenite and sodium tellurite using Lactobacillus casei. This bacterium produced red spherical amorphous elemental selenium nanospheres with a diameter of 206 ± 33 nm from selenite and amorphous black nanorods with a length of 176 ± 32 nm and a cross-section of 62 ± 13 nm from tellurite. If the initial medium contains a mixture of selenite and tellurite, the resulting nanoparticles will contain selenium and tellurium in the same ratios in the alloy as in the medium. This proves that Lactobacillus casei cannot distinguish between selenite and tellurite. The shape of the nanoparticles varies from spherical to rod-shaped, depending on the ratio of selenium and tellurium. The color of nanomaterials ranges from red to black, depending on the percentage of selenium and tellurium. These nanomaterials could be good candidates in the pharmaceutical industry due to their antipathogenic and anticarcinogenic properties.

Interfacial Modification of a Zn Anode by Amorphous Se toward Long-Life and Hydrogen Evolution-Free Aqueous Rechargeable Batteries.

The Zn anode in rechargeable aqueous Zn-ion batteries suffers from hydrogen gas evolution and dendrite growth, which are critical issues that make the battery impractical. Here, the Zn anode performance is greatly improved by coating an amorphous selenium overlayer with a simple chemical bath reaction process. The reduction of SeO32- ions by the Zn metal leads to the formation of an amorphous Se layer, and the optimal reaction time that determines the thickness of the Se coating as well as the Zn anode performance is found to be 2 h. The symmetric cell using Zn@Se exhibits improved rate performance and an ultralong cycle life of 4500 h after being tested at 1 mA cm-2 and 1 mAh cm-2, respectively. Compared to the bare Zn anode, the Zn@Se anode leads to a larger Zn2+ transference number and reduced charge transfer resistance. The button-type MnO2∥Zn@Se full cell exhibits higher capacity and a much longer cycle life compared to the counterpart using a bare Zn anode. Also, pouch-type MnO2∥Zn@Se full cells with a high capacity of 9.7 mAh cm-2 are made to demonstrate the inhibition of hydrogen evolution and practical applications. It is found that the in situ formation of an amorphous ZnO nanosheet network induced by the amorphous Se overlayer plays a key role in enhancing the Zn anode performance.

Synthesis and Characterization of Amorphous Selenium, Cadmium and Silver Selenide Thin Films on Polyamide-6

Increasing photon absorption by capturing light is an important way to increase the efficiency of photovoltaic devices. In this regard, the small optical band gap (Eg) and high absorption coefficient of Se-containing thin nanofilms make them ideal for next generation photovoltaic devices based on selenides. Amorphous selenium was introduced into polyamide-6 (PA 6) via a chemical synthesis in a bath and the influence of the products of its reaction with Cd2+ and Ag+ ions on the film phase composition, topographic and optical properties were evaluated. AFM data have revealed that the surface roughness of the a-Se/PA 6 composite noticeably increases compared to that of unreacted PA 6. However, at later stages of film deposition, the roughness decreases, and the thin film becomes smoother and uniform. The incorporation of solid inorganic nanoparticles into flexible polyamide network causes chain stretching, which has been confirmed by ATR-FTIR spectroscopy data. The data of X-ray diffraction analysis, depending on the stage of synthesis, showed the crystalline composition of the film with peaks of Se8, CdSe, Ag2Se and Ag, which may explain the observed optical properties. The optical properties of the composites indicate a shift in the band gap from 4.46 eV for PA 6 to 2.23–1.64 eV upon the stepwise deposition of amorphous Se, CdSe and Ag2Se. Eg is conveniently located in the visible region of solar energy, making the obtained nanofilms ideal for solar energy harvesting.