Ultraviolet Detection Research Articles

Narrowband Solar-Blind Photodetection of the Plasmonic (In0.3Ga0.7)2O3 Detector via the Synergetic Enhancement of Small-Sized Ag-Nanoparticle Photoabsorbance and Surface Modification.

Currently, research on Ag nanoparticles (AgNPs) predominantly focuses on UV/visible photodetection and UV emission, seemingly overlooking the significance of Ag in enhancing deep ultraviolet photon detection. In this work, (In0.3Ga0.7)2O3 thin films were fabricated by plasma-enhanced chemical vapor deposition. Due to the unique photoabsorbance characteristic and better interaction with photons of small-sized AgNPs, they effectively suppress the UVB absorbance caused by energy band engineering in the (In0.3Ga0.7)2O3 thin film while enhancing photoabsorbance in UVC due to the surface plasmon effect. Therefore, under the synergistic effect of enhanced photon absorbance and hot electron transfer, the performance of the detector is significantly improved, and its responsivity (R), external quantum efficiency, and detectivity (D*) are 193 mA/W, approximately 100%, and 1014 Jones, respectively, at a bias of -6 V. The fast response time and decay time are 634.6 and 194.1 ms, respectively; the rapid decay facilitated by AgNPs is attributed to the increased indirect recombination rate. AgNPs exhibit excellent narrowband response characteristics and absorbance properties in specific wavelength bands for the InGaO photodetector. This research lays the foundation for the practical application of localized surface plasmon resonance-enhanced photon-sensing capabilities.

High-Throughput Drug Stability Assessment via Biomimetic Metalloporphyrin-Catalyzed Reactions Using Laser-Assisted Rapid Evaporative Ionization Mass Spectrometry (LA-REIMS)

Background: Building extensive drug candidate libraries as early in the development pipeline as possible, with high-throughput in vitro absorption, distribution, metabolism, and excretion (ADME) profiling, is crucial for the selection of lead compounds to guide subsequent research and production phases. Traditionally, the analysis of metabolic stability assays heavily relies on high-throughput LC-MS/MS (liquid chromatography tandem mass spectrometry) techniques to meet with the lead profiling demands. Laser-assisted rapid evaporative ionization mass spectrometry (LA-REIMS) is a quick and efficient technique for characterizing complex biological samples without laborious sample preparation. Objective: In this study, using an automated LA-REIMS well plate reader, achieving an 8 s per sample measurement time, the oxidative metabolic stability of active drug agents was assessed using biomimetic metalloporphyrin-based oxidative model reactions. Results: The results obtained using the novel LA-REIMS-based protocol were compared to and corroborated by those obtained using conventional HPLC-UV-MS (high performance liquid chromatography with ultra-violet detection coupled with mass spectrometry) measurements. Conclusions: LA-REIMS emerges as a promising technique, demonstrating potential suitability for semi-quantitative high-throughput metabolic stability in an optimized solvent environment.

Stability-Indicating HPLC Method Development and Validation for the Simultaneous Determination of Vildagliptin and Dapagliflozin in Pharmaceutical Dosage Form.

Vildagliptin (VD) and Dapagliflozin (DP) were determined simultaneously by RP-HPLC using an ultraviolet (UV) detector, a Hypersil Gold C18 (250 × 4.6 mm) column, 5 µm and a mobile phase of acetonitrile: water (adjusted with O-Phosphoric acid to pH 3) in ratio 40: 60% v/v. The estimation wavelength was chosen to be 213 nm. VD and DP were shown to have retention times of 2.9 and 8.3 minutes, respectively. Q2 (R1) ICH guidelines were followed during the validation process. VD and DP correlation coefficient R2 values are 0.9993 and 0.999, respectively. While DP’s linearity range is 1 to 6 µg/mL, VD’s is 10 to 60 µg/mL. The precision and accuracy studies show %relative standard deviation (%RSD) below 2%. Recovery% was assessed to meet the ICH Q2 (R1) guidelines criteria. The presented research on forced degradation showed stability indicating studies. The findings also demonstrated that the suggested method is suitable for determining VD and DP precisely and accurately.

Photoluminescent Multicolor Carbon Dots for UV Detection and Dynamic Anticounterfeiting.

Carbon dots (CDs) are an emerging type of fluorescent carbon nanomaterial with broad application prospects. Among them, photochromic CDs have been widely used in the field of optoelectronic devices but rarely in ultraviolet (UV) detection. In this work, we successfully developed photochromic CDs that exhibit reversible emission under light stimulation in an amine solvent system. Notably, the CDs showed ultrafast photochromic behavior in diethylamine solvent, shifting the fluorescence color from cyan-green to orange-red after 2 s of irradiation, with the solution color changing from pale yellow to pale purple. Furthermore, this performance could recover without additional stimuli, simply by standing for several tens of seconds. Structural analysis indicated that rapid photochromism arises from changes in the surface functional group radicals of the CDs, with the reversibility attributed to fluctuation in these radicals. Leveraging the excellent photochromic properties of CDs, we further developed a device for detecting UV indices in sunlight. This opens up broad prospects for developing high-performance UV detection devices based on CDs.

β-Ga2O3 Nanoribbon with Ultra-High Solar-Blind Ultraviolet Polarization Ratio.

Solar-blind ultraviolet (UV) detection plays a critical role in imaging and communication due to its low-noise background, high signal-to-noise ratio, and strong anti-interference capabilities. Detecting the polarization state of UV light can enhance image information and expand the communication dimension. Although polarization detection is explored in visible and infrared light, and applied in fields such as astrophysics and submarine seismic wave detection, solar-blind UV polarization detection remains largely unreported. This is primarily due to the challenge of creating UV polarizers with high transmittance, high extinction ratio, and strong resistance to UV radiation. In this study, it is discovered that the space symmetry breaking of the β-Ga2O3's b-c plane results in a significant optical absorption dichroic ratio. Leveraging β-Ga2O3's high solar-blind UV response, a lensless solar-blind UV polarization-sensitive photodetector, circumventing the challenges associated with solar-blind UV polarizers is designed. This photodetector exhibits an exceptionally high intrinsic polarization ratio under 254nm linearly polarized light, approximately two orders of magnitude higher than other reported nanomaterial-based polarization-sensitive photodetectors. Additionally, it demonstrates significant advantages in solar-blind UV imaging and light communication. This work introduces a novel strategy for solar-blind ultraviolet polarization detection and offers a promising approach for solar-blind light communication.

Syntheses and performance study of three POM-viologen compounds with photo- and electric-stimulation response

In recent years, stimulus responsive materials have received widespread attention. Under solvothermal conditions, three polyoxometalates-viologen organic–inorganic hybrid compounds were successfully constructed by combining a viologen ligand 1-(3-Nitro-benzyl)-[4,4′]bipyridinyl-1-ium bromide (1,3-nibipy·Br) with octamolybdate, namely [Cu2(1,3-nibipy)4(H2O)2(β-Mo8O26)2]·2H2O (1), [Cu2(1,3-nibipy)4(H2O)4(β-Mo8O26)]·(β-Mo8O26) (2) and (1,3-Hnibipy)2·(β-Mo8O26) (3). These three compounds can exhibit color changing properties under both light and electrical stimulation. Through characterizations of PXRD, FT-IR, UV–vis spectra, XPS, EPR, CV, and other tests, the photochromic and electrochromic properties of these three compounds are caused by the generation of viologen radicals. Compounds 1–3 have a rapid photoresponse efficiency and can be made into mixed matrix films for use as ultraviolet detectors. In addition, coated filter paper synthesized from acetonitrile and compounds can serve as an innovative erasable ink-free printing material medium, which is suitable for various erasable ink-free printing and anti-counterfeiting fields. We further investigated the electrochromic devices prepared from compounds 1–3, which achieved color change at a voltage of around −0.2 V and exhibited good stability after 500 cycles.

Effect of Noise Filtering in an Ultraviolet Detector of UHPLC on the Statistical Reliability of Chemometrically Evaluated Repeatability.

A noise filter, which is usually attached to a detector for chromatography, was applied for the improvement of a signal-to-noise ratio (S/N) on a chromatogram. The objective of this paper is to elucidate the effect of noise filtering in an UV detector of ultra HPLC (UHPLC) on the statistical reliability of chemometrically evaluated repeatability by the function of mutual information (FUMI) theory. To examine the statistical reliability of chemometrically evaluated repeatability in the UHPLC system associated with noise filtering, the standard deviation (SD) values of the area in baseline fluctuations with peak region k (s(k)) were obtained from six chromatograms with noise filtering. Further, the average of s(k) values (σ̂) was calculated from the s(k) values (n = 6) to be alternatively applied as the population SD. All s(k)/σ̂ values were within the 95% confidence intervals (CIs) at the freedom degree of 50, indicating the chemometrically estimated relative SD (RSD) of a peak area and RSD by repeated measurements of at least 50 times had equivalent reliability.

Development and Validation of a Simple UV-HPLC Method to Quantify the Memantine Drug Used in Alzheimer's Treatment.

Memantine, a non-competitive NMDA receptor antagonist, is used to treat Alzheimer's disease. Therefore, loading memantine in nanoparticles (NPs) could be an essential tool to improve the treatment effectiveness while reducing drug toxicity. Even though some approaches have been described to quantify memantine, none reported optimized methods using high-performance liquid chromatography resorting to ultraviolet detection (UV-HPLC) to determine encapsulation in NPs. The present research developed a HPLC method using pre-column derivatization for quantitatively analyzing memantine hydrochloride in NPs. Memantine was derivatized using 9-fluorenylmethyl chloroformate (FMOC). The developed method was fully validated regarding suitability, specificity, linearity, sensitivity, precision, accuracy, and robustness according to the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use guidelines. The retention time of memantine was 11.393 ± 0.003 min, with a mean recovery of 92.9 ± 3.7%. The new chromatographic method was validated and found to respond linearly over 5-140 μg/mL, with a high coefficient of determination. Intraday precision lay between 3.6% and 4.6%, and interday precision between 4.2% and 9.3%. The stability of memantine was also tested at 4 °C and -20 °C, and no signs of decay were found for up to 6 months. The new method was properly validated and proved simple, sensitive, specific, accurate, and precise for determining memantine encapsulation efficiency in lipid NPs. Greenness was evaluated, presenting a final score of 0.45. In the future, this methodology could also be applied to quantify memantine in different nanoformulations.

Effervescence tablets based on magnetic ionic liquids as simple microdevices for the in situ dispersive liquid-liquid microextraction of urinary biomarkers

BackgroundMagnetic ionic liquids (MILs) have been explored in dispersive liquid-liquid microextraction (DLLME). Their usage allows to substitute centrifugation and/or filtration steps by a quick magnetic separation. Besides, effervescence-assisted DLLME is one of the most known options to improve the dispersion of the extractant in the sample, while allowing to avoid the consumption of external energy during dispersion. Despite these interesting features, only one study incorporates MILs containing the tetrachloroferrate anion in effervescence tablets. These MILs are highly viscous and liquid at room temperature, thus compromising the stability of the tablets when used as extraction microdevices in effervescence-assisted DLLME, and only allowing their use in the conventional MIL-DLLME mode. ResultsA new class of effervescence tablets containing a Ni(II)-based MIL, that is solid at room temperature, is here proposed. This type of tablets permits their use, for first time, in the in situ DLLME mode, occurring through the transformation of a water-soluble MIL into a water-insoluble MIL microdroplet. This way, the tablet formulation included: the MIL, the metathesis reagent lithium bis[(trifluoromethyl)sulfonyl]imide, NaH2PO4 and K2CO3 as effervescence precursors salts, and Na2SO4 as salting-out and desiccating agent. The method is combined with high-performance liquid-chromatography and both fluorescence and ultraviolet detection, for the determination of monohydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) and benzophenones (BPs), as biomarkers in urine. The method simply involved the addition of the effervescence tablet to the sample, thus taken place simultaneously the effervescence process and the metathesis reaction, without requiring any external energy consumption. The method presented limits of detection down to 10 ng L−1 for OH-PAHs and to 0.60 μg L−1 for BPs, inter-day relative standard deviations lower than 17 %, and average relative recoveries of 94 % in urine. The determined OH-PAHs contents in urine were between 0.40 and 16 μg L−1, and between 17.8 and 334 μg L−1 for BPs. SignificanceWe have developed the first MIL-based effervescence tablets that are completely solid, thus improving the stability and robustness of these microdevices with respect to previously reported tablets involving MILs, while permitting to perform into the in situ DLLME mode (thus gaining in extraction efficiency). This approach including the MIL-based effervescence tablets constitutes an alternative on-site platform for the analysis of urine, as satisfactory precision, accuracy, and sensitivity are achieved despite not involving any external energy input within the analytical sample preparation setup. This method also constitutes the first application of MIL-based effervescence tablets for bioanalysis.

Computational investigation of electronic, thermoelectric, and optical properties in Cs2Li[formula omitted](X = Br, I) for energy harvesting applications

The remarkable potential of double perovskite materials, characterized by lead-free, non-toxic attributes and robust dynamical stability, positions them as highly promising candidates for both thermoelectric and optoelectronic applications. In light of this, a comprehensive investigation is undertaken through density functional theory to thoroughly explore the optoelectronic and transport characteristics of Cs2LiBiX6 (X = Br, I) double perovskite materials. To ascertain dynamic stability, phonon dispersion band structures are computed, and the structural stability is evaluated through the tolerance factor. The resulting band structures reveal narrow band gaps of 3.45 eV and 1.79 eV for the Br and Indium-based DPs, respectively. These narrow band gaps hold significant importance for applications such as ultraviolet detectors and other optoelectronic devices that function in the visible and UV-light spectrum. Notably, absorption peaks of maximal intensity emerge at 5.1 eV (76 nm) and 4.0 eV (67 nm) for the Br and Indium-based double perovskites, respectively. Furthermore, a comprehensive analysis of thermoelectric behavior is conducted, encompassing the figure of merit, power factor, Seebeck coefficient, and the ratio of electrical to thermal conductivity across a temperature range of 50–800 K. The exceptionally low lattice vibration values, coupled with a substantial enhancement in the thermoelectric figure of merit (ZT), notably underscore their significance for advanced thermoelectric generator applications.

Ultrasound assisted upper critical solution temperature type switchable deep eutectic solvent based liquid-liquid microextraction for the determination of triazole in water

BackgroundThe use of pesticides to protect crops has long been an important measure to provide healthy and safe agricultural products, but excess pesticides flow into fields and rivers, causing environmental pollution. Earlier methods utilizing organic solvent liquid-liquid microextraction for pesticide residue detection were not environmentally friendly. Therefore, it is significant to find a greener and more convenient detection method to determine pesticide residues. ResultsA new method was established to detect three triazole fungicides (TFs), including myclobutanil, epoxiconazole and tebuconazole, in environmental water samples. And the determination was conducted using a high-performance liquid chromatography with the ultraviolet detector (HPLC-UV). The switchable deep eutectic solvent (SDES) can be reversibly switched between hydrophilic and hydrophobic states through temperature modulation. Additionally, the method exhibited excellent linearity for all target analytes within the concentration range of 10–2000 μg L−1, with satisfactory R2 values (≥0.9975). The limits of detection (LODs) ranged from 2.3 to 2.6 μg L−1, and the limits of quantification (LOQs) ranged from 7.8 to 8.7 μg L−1. The accuracy of the method was assessed through intra-day and inter-day precision tests, yielding relative standard deviations (RSDs) in the ranges of 2.8%–6.7% and 2.2%–7.5%, respectively. Density functional theory (DFT) results indicated that hydrogen bonding is a significant factor affecting the binding of DES with triazoles. Three different green assessment tools were used to prove that the SDES-HLLME method had good greenness and broad applicability. SignificanceThis is a homogeneous liquid-liquid microextraction (HLLME) method based on the upper critical solution temperature (UCST) type switchable deep eutectic solvent program, which can complete the extraction within a few minutes without dispersant. In terms of pesticide detection, the analytical method is simple and more conducive to environmental protection.

Ultraviolet visible spectral water chemical oxygen demand detection method based on two deep neural network model

Water resources are precious resources around the world, but pollution is becoming increasingly severe. While the degree of damage to water caused by organic pollutants is reflected by chemical oxygen demand, which is also an important indicator for hydrological monitoring. Therefore, accurate measurement of chemical oxygen demand is necessary. The rapid development of water quality detection by ultraviolet visible spectrum analysis as an efficient, convenient, and pollution-free new water quality detection method has been achieved. When we were processing ultraviolet visible spectral absorbance data, various environmental factors can affect the chemical oxygen demand light absorption value, thus affecting the accuracy of detection. So there are some goals, such as more comprehensively extracting the feature wavelength and reducing the interference to achieve better detection results. It is expected that the model can be applied to a portable water quality detection device. It is necessary to consider detection time, reduce model training parameters, and improve detection speed. Therefore, this article proposes Competitive Adaptive Weighted Sampling-Convolutional Neural Network-Long Short-Term Memory and Competitive Adaptive Weighted Sampling-Convolutional Long Short-Term Memory models for detecting chemical oxygen demand in water. To verify the effectiveness of the proposed model, the model was trained on the experimental dataset and the detection results of all models involved in the article were compared. It can be confirmed that the application of these two proposed algorithms results in less detection time and higher accuracy in concentration detection.

Open-Source Absorbance Detector with Multiple Deep UV-LEDs for On-Capillary Multiwavelength Detection at a Single Point.

On-capillary ultraviolet photometric detection (UV-PD) in a multiwavelength mode provides comprehensive analytical information. However, achieving single-point multiwavelength UV-PD for capillary-scale instruments typically requires high-cost and complex devices. This study presents the development of a cost-effective, open-source absorbance detector for on-capillary multiwavelength detection. The detector employs three deep UV light-emitting diodes emitting at 235, 255, and 278 nm as light sources, each coupled with its own photodetector for independent detection channels. The components are housed using 3D-printed parts, with an Arduino board used for data acquisition. Three individual optical paths, formed by three slits (60 μm width ×1 mm length), surround the measured capillary and converge at the same detection point. The detector demonstrates simultaneous multiwavelength detection of medicines for both HPLC and CE. This development represents an advancement in portable, low-cost analytical instrumentation, with broad implications for various fields of application.

Highly sensitive full solar-blind ultraviolet spectrum detection and imaging based on PdSe2/Ga2O3 vdW heterojunction.

Solar-blind ultraviolet (UV) photodetectors are in great demand for both military and civilian applications. Here, we have successfully demonstrated the synthesis of the Sn-doped Ga2O3 films with controllable bandgaps to construct PdSe2/Ga2O3 van der Waals (vdW) heterojunctions achieving highly sensitive full solar-blind UV spectrum detection. The assembled device demonstrates a full solar-blind UV spectral self-powered response, with a large responsivity of 123.5 mA/W, a high specific detectivity of 1.63 × 1013 Jones, and a rapid response time of 0.15/2.3 ms. Importantly, an outstanding solar-blind UV imaging application based on an integrated PdSe2/Ga2O3 device array has been demonstrated. Our work paves a feasible path toward achieving highly sensitive solar-blind UV detecting and imaging based on wide-bandgap Ga2O3 films.

All-Inorganic Nanocomposite Enhancing Photomultiplication for Sensitive and Stable Ultraviolet Detection

All-Inorganic Nanocomposite Enhancing Photomultiplication for Sensitive and Stable Ultraviolet Detection

An Aerosol-Assisted Chemical Vapor Deposition Route to Tin-Doped Gallium Oxide Thin Films with Optoelectronic Properties.

Gallium oxide is a wide-bandgap compound semiconductor material renowned for its diverse applications spanning gas sensors, liquid crystal displays, transparent electrodes, and ultraviolet detectors. This paper details the aerosol assisted chemical vapor deposition synthesis of tin doped gallium oxide thin films using gallium acetylacetonate and monobutyltin trichloride dissolved in methanol. It was observed that Sn doping resulted in a reduction in the transmittance of Ga2O3 films within the visible spectrum, while preserving the wide bandgap characteristics of 4.8 eV. Furthermore, Hall effect testing revealed a substantial decrease in the resistivity of Sn-doped Ga2O3 films, reducing it from 4.2 × 106 Ω cm to 2 × 105 Ω cm for the 2.5 at. % Sn:Ga2O3 compared to the nominally undoped Ga2O3.

IMIDAZOLIUM-BASED IONIC LIQUIDS FOR THE SELECTIVE SEPARATION OF TOCOTRIENOL HOMOLOGUES FROM PALM FATTY ACID DISTILLATE VIA LIQUID-LIQUID EXTRACTION

Objective: Tocotrienols have now stepped into the limelight of vitamin E research and have proven to have some exceptional benefits that are not shared by their “older” tocopherol siblings. Unlike tocopherols, tocotrienols are able to inhibit cholesterol biosynthesis, have specific neuroprotective activities stronger antioxidant effects, antihypertensive and anti-cancer. The purpose of this study was to carry out selective separation of tocotrienols homologues from Palm Fatty Acid Distillate (PFAD) by liquid-liquid extraction, using Ionic liquids (ILs) as extractants in the presence of diluent. Methods: Four kinds of imidazolium-based ILs that used are 1-butyl-3-methylimidazolium chloride ([Bmim]Cl), 1-Butyl-3-methylimidazolium acetate ([Bmim]Ac), 1-Hexyl-3-methylimidazolium chloride ([Hmim]Cl) and 1-Ethyl-3-methylimidazolium chloride ([Emim]C]). The extraction is carried out by creating a two-phase system between ILs and PFAD in n-hexane. Quantification of extracted tocotrienols was performed using High-Performance liquid Chromatography (HPLC) with a C18 column, mobile phase methanol: water (97.5:2.5), flow rate 1 ml/min and Ultraviolet (UV) detector at 295 nm. Results: The results showed that the concentration (extraction efficiency) of tocotrienols extracted using ILs in order were [Bmim] Ac 1611.09 mg/Kg (75.41%) and [Hmim][Cl] 1603.39 mg/Kg (75.05%), [Bmim]Cl 1523.60 mg/Kg (71.32%) and [Emim]Cl 1174.24 mg/Kg (54.96%). Conclusion: [Bmim]Ac yielded the highest tocotrienols concentration and extraction efficiency.

Enhancing photo-response performance through ultrathin Al2O3 modification at the p-SnO2:Al/n-GaN heterojunction interface

We report on photoconductive and p-n heterojunction ultraviolet (UV) photodetectors based on p-type Al-doped SnO2 (p-SnO2:Al) thin films. We investigated the structural, optical, and electrical properties of Al-doped SnO2 thin films prepared using sol-gel methods, with our results being strongly supported by first-principles calculations. To achieve a self-powered photodetector device at zero bias, we fabricated p-SnO2:Al thin film on an n-GaN layer to form a p-n heterojunction. The responsivity of the p-n heterojunction UV detector, measured at zero bias, is 0.05 A/W, indicating good rectification properties. In order to improve device performance, a p-n heterojunction with a passivation layer was formed by inserting an ultrathin Al2O3 layer between the n-GaN layer and the p-SnO2:Al layer. With this change, the device's responsivity was 0.44 A/W at 350 nm at zero bias, roughly 10 times better than the detector without the Al2O3 passivation layer. The insertion of an ultrathin Al2O3 layer, which increases the efficiency of carrier separation on the SnO2 side while lowering the rate of carrier recombination at the interface, is responsible for the increased light responsivity performance.

Water as a green solvent for sustainable sample preparation: single drop microextraction of N-nitrosamines from losartan tablets.

Water, renowned for its sustainability and minimal toxicity, is an ideal candidate for environmentally friendly solvent-based microextraction. However, its potential as an extractant solvent in miniaturized sample preparation remains largely unexplored. This paper pioneers using water as the extraction solvent in headspace single-drop microextraction (HS-SDME) for N-nitrosamines from losartan tablets. Autonomous HS-SDME is executed by an Arduino-controlled, lab-made Cartesian robot, using water for the online preconcentration of enriched extracts through direct injection into a column-switching system. Critical experimental parameters influencing HS-SDME performance are systematically explored through univariate and multivariate experiments. While most previously reported methods for determining N-nitrosamines in pharmaceutical formulations rely on highly selective mass spectrometry detection techniques to handle the strong matrix effects typical of pharmaceutical samples, the water-based HS-SDME method efficiently eliminates the interfering effects of a large amount of the pharmaceutical active ingredient and tablet excipients, allowing straightforward analysis using high-performance liquid chromatography with ultraviolet detection (HPLC-UV-Vis). Under optimized conditions, the developed method exhibits linear responses from 100 to 2400ngg-1, demonstrating appropriate detectability, precision, and accuracy for the proposed application. Additionally, the environmental sustainability of the method is assessed using the AGREEprep methodology, positioning it as an outstanding green alternative for determining hazardous contaminants in pharmaceutical products.

Spatial Nonuniformity of Photoresponse in SiC UV Avalanche Photodiodes Operating in Linear and Geiger Mode

Silicon Carbide's intrinsic material properties, along with the availability of low-defect density, 6" substrates, make it an attractive material system for visible-blind ultraviolet (UV) detectors. Avalanche photodiodes (APDs) made from SiC have been shown to operate both as linear mode detectors with high gain (>10⁷) and as single-photon avalanche detectors (SPADs) with competitive photon detection efficiency. However, reported spatial non-uniformities in photoresponse of these devices will reduce sensitivity [1,2].In this paper, we examine the impact of device geometry, epitaxial variations, and crystal anisotropy on the spatial uniformity of photoresponse in SiC APDs. Photoresponse maps are generated using a fast 285 nm pulsed LED source that is tightly focused to a ~10 µm spot. Response maps are measured for devices with different geometries fabricated on the same chip in both linear-mode and Geiger-mode. Measurements on standard pin diodes will be presented, along with separate absorption, charge, and multiplication (SACM) structures.Experimental results indicate that all devices exhibit localized regions of high photoresponse at gain > 1000 and that the spreading of the photoresponse is highly directional. Finger diodes with 120 μm x 30 μm mesas exhibit good response uniformity with a variation < 30% across the device. In contrast, diodes with 60 and 90 μm square-shaped mesas exhibit similar uniform response spreading along one edge that is bounded by the size of the mesa, but a >10x drop in relative response over ~30-40 μm in the orthogonal direction which is much shorter than the extent of the mesa. Devices with 100 μm circular mesas exhibit somewhat similar results to the square diodes, but with the presence of multiple hot spots in response.Experimental results are analyzed through 3D numerical modeling of devices which accounts for the effects of doping and thickness variations across the substrate as well as the anisotropy of impact ionization. Modeling indicates that small variations in the thickness in the drift regions of a diode can yield meaningful variations in avalanche gain across the mesa. The impact of anisotropic impact ionization will be considered using full-band 3D Monte Carlo calculations. X. Bai, H.-D. Liu, D. C. McIntosh and J. C. Campbell, "High-Detectivity and High-Single-Photon-Detection-Efficiency 4H-SiC Avalanche Photodiodes," IEEE J. Quantum Electron. 45 300-303 (2009). DOI: 10.1109/JQE.2009.2013093.L. Su et al, "Recent progress of SiC UV single photon counting avalanche photodiodes," J. Semicond. 40 121802 (2019). DOI: 10.1088/1674-4926/40/12/121802. Figure 1