Chemical Etching Research Articles

Chemical etching of CAD-CAM glass-ceramic-based materials using fluoride solutions for bonding pretreatment.

The surface treatment of glass-ceramic-based materials, namely, lithium disilicate glass (IPS e.max CAD), feldspar porcelain (VITABLOCS Mark II), and a polymer-infiltrated ceramic network (VITA ENAMIC), using aqueous fluoride solutions and their influence on luting agent bonding were investigated. Six experimental aqueous fluoride solutions were applied to these materials, and their effects were assessed by surface topological analysis. The obtained results were compared using non-parametric statistical analyses. Ammonium hydrogen fluoride (AHF) etchant demonstrated the greatest etching effect. Subsequent experiments focused on evaluating different concentrations of the AHF etchant for the bonding pretreatment of glass-ceramic-based materials with a luting agent (PANAVIA V5). AHF, particularly at concentrations above 5 wt%, effectively roughened the surfaces of the materials and improved the bonding performance. Notably, AHF at a concentration of 30 wt% exhibited a more pronounced effect on both etching and bonding capabilities compared to hydrofluoric acid.

Synthesis, physico-chemical characterization, DFT simulation, and field electron behaviour of 2D layered Ti3C2Tx MXene nanosheets

Nanostructures of Ti3C2Tx, one of the members of the MXenes family, have been successfully prepared by chemical etching of Al from Ti3AlC2 (MAX phase) using Hydrofluoric Acid (HF) for various etching durations at room temperature. The phase, morphological, structural, and chemical analysis was performed using XRD, FESEM, TEM, Raman, and x-ray photoelectron spectroscopy. The surface morphology of as-synthesized Ti3C2Tx (MXene) phase is characterized by stacks of layered sheets like structures. Field electron emission (FEE) behaviour was investigated at the base pressure of 1 × 10−8 mbar. The pristine Ti3AlC2 (MAX) and Ti3C2Tx (MXene) nanosheets emitters showed values of turn-on field (defined at current density ∼ 1 μA cm−2) as 4.18 and 1.67 V μm−1, respectively. Furthermore, maximum emission current density of ∼ 825 μA cm−2 was extracted from the MXene nanosheets emitter at an applied field of 3.60 V μm−1, in contrast to ∼71 μA cm−2 drawn at 7.31 V μm−1 from the pristine MAX emitter. The MXene nanosheets emitter exhibited good emission current stabilities at pre-set values ∼ 10 and 100 μA over 3 h duration. Work function values of the MAX and MXene nanosheets emitters were measured using a retarding field analyzer, and found to be 4.4 and 3.6 eV, respectively. Extensive ab-initio simulations have been performed to provide structural and electronic properties, as well as for estimating the work function of Ti3C2 layered material. The estimated electronic density of states revealed its metallic character. The improved FEE performance exhibited by the 2D layered Ti3C2Tx (MXene) nanosheets emitter is attributed to its unique morphology characterized by high aspect ratio, metallic electronic properties and relatively lower work function.

Unveiling the 3D Morphology of Epitaxial GaAs/AlGaAs Quantum Dots.

Strain-free GaAs/AlGaAs semiconductor quantum dots (QDs) grown by droplet etching and nanohole infilling (DENI) are highly promising candidates for the on-demand generation of indistinguishable and entangled photon sources. The spectroscopic fingerprint and quantum optical properties of QDs are significantly influenced by their morphology. The effects of nanohole geometry and infilled material on the exciton binding energies and fine structure splitting are well-understood. However, a comprehensive understanding of GaAs/AlGaAs QD morphology remains elusive. To address this, we employ high-resolution scanning transmission electron microscopy (STEM) and reverse engineering through selective chemical etching and atomic force microscopy (AFM). Cross-sectional STEM of uncapped QDs reveals an inverted conical nanohole with Al-rich sidewalls and defect-free interfaces. Subsequent selective chemical etching and AFM measurements further reveal asymmetries in element distribution. This study enhances the understanding of DENI QD morphology and provides a fundamental three-dimensional structural model for simulating and optimizing their optoelectronic properties.

Supramolecular Modulator Assisted Cryo-Engineered Porous Cu-DNA Nano-Vehicles for Versatile Theranostic Agent Delivery.

DNA nanotechnology combines structural design with therapeutic functions via programmable DNA motifs, but faces challenges in drug loading capacity. Herein a pore-engineering strategy is reported to develop a highly porous, universal DNA nano-vehicle through coordination self-assembly, cryo-engineering, and supramolecular chemistry, adapting to diverse cargo loading with desired theranostic agents. Thus, the complex synthesis and compatibility challenges typically associated with switching between different drug carriers are avoided. To this end, Cu2+ and nucleic acid therapeutic G3139 self-assemble into a prefabricated solid nanostructure, which subsequently undergoes ultrafast freezing and sublimation to introduce porosity, forming highly porous Cu-G3139 nanoparticles (CG NPs). The porous CG NPs efficiently accommodate diverse therapeutic molecules, from chemotherapeutics to non-chemotherapeutic agents, facilitated by positively-charged cyclodextrin. As a proof-of-concept, the photosensitizer indocyanine green (ICG) is loaded and coated with tannic acid (TA) to form CICG@TA, enabling remarkable photothermal and fluorescence imaging-guided synergistic tumor ablation. This work represents the first demonstration of sublimation-induced pore formation in metal-DNA hybrid nanoparticles without chemical etching, offering a scalable "plug-and-play" platform for personalized cancer therapy without redesign. This versatile pore-engineering strategy, merging supramolecular chemistry with cryo-engineered porosity, opens up new avenues for efficient, customized multidrug delivery for diverse tumor theranostic applications.

Electrostatic Force-Assisted Transfer of Flexible Silicon Photodetector Focal Plane Arrays for Image Sensors.

Flexible photodetectors are pivotal in contemporary optoelectronic technology applications, such as data reception and image sensing, yet their performance and yield are often hindered by the challenge of heterogeneous integration between photoactive materials and flexible substrates. Here, we showcase the potential of an electrostatic force-assisted transfer printing technique for integrating Si PIN photodiodes onto flexible substrates. This clean and dry process eliminates the need for chemical etchants, making it a highly desirable method for manufacturing high-performance flexible photodetector arrays, expanding their widespread applications in electronic eyes, robotics, and human-machine interaction. As a demonstration, a 5 × 5 flexible Si photodetector focal plane array is constructed for imaging sensors and shaped into a convex semicylindrical form to achieve a π field of view with long-term mechanical and thermal stability. Such an approach provides a high yield rate and consistent performance, with the single photodetector demonstrating exceptional characteristics, including a responsivity of 0.61 A/W, a response speed of 39.77 MHz, a linear dynamic range of 108.53 dB, and a specific detectivity of 2.75 × 1012 Jones at an applied voltage of -3 V at 940 nm.

Enhanced Capability of Hydrogen Evolution Photocathode by Laminated Interface Engineering of Co/MoS2 QDs/pyramid-black Si.

We present a novel and stable laminated structure to enhance the performance and stability of silicon (Si) photocathode devices for photoelectrochemical (PEC) water splitting. First, by utilizing Cu nanoparticle catalysts to work on a n+p-black Si substrate via the metal-assisted chemical etching, we can achieve the black silicon with a porous pyramid structure. The low depth holes on the surface of the pyramid caused by Cu etching not only help enhance the light capture capability with quite low surface reflectivity (<5%) but also efficiently protect the p-n junction from damage. To improve the charge migration efficiency and mitigate parasitic light absorption from cocatalysts at the same time, we drop casted quantum dots (QDs) MoS2 with the size of nanometer scale as the first layer of catalyst. Hence, we then can safely electrodeposit cocatalyst Co nanoparticles to further enhance interface transfer efficiency. The synergistic effects of cocatalysts and optimized light absorption from the morphology and QDs contributed to the overall enhancement of PEC performance, offering a promising pathway for an efficient, low cost, and stable (over 100 h) hydrogen production photocathode.

A Rapid, Efficient Method for Anodic Aluminum Oxide Membrane Room-Temperature Multi-Detachment from Commercial 1050 Aluminum Alloy.

For commercial processes, through-hole AAO membranes are fabricated from high-purity aluminum by chemical etching. However, this method has the disadvantages of using heavy-metal solutions, creating large amounts of material waste, and leading to an irregular pore structure. Through-hole porous alumina membrane fabrication has been widely investigated due to applications in filters, nanomaterial synthesis, and surface-enhanced Raman scattering. There are several means to obtain freestanding through-hole AAO membranes, but a fast, low-cost, and repetitive process to create complete, high-quality membranes has not yet been established. Here, we propose a rapid and efficient method for the multi-detachment of an AAO membrane at room temperature by integrating the one-time potentiostatic (OTP) method and two-step electrochemical polishing. Economical commercial AA1050 was used instead of traditional high-cost high-purity aluminum for AAO membrane fabrication at 25 °C. The OTP method, which is a single-step process, was applied to achieve a high-quality membrane with unimodal pore distribution and diameters between 35 and 40 nm, maintaining a high consistency over five repetitions. To repeatedly detach the AAO membrane, two-step electrochemical polishing was developed to minimize damage on the AA1050 substrate caused by membrane separation. The mechanism for creating AAO membranes using the OTP method can be divided into three major components, including the Joule heating effect, the dissolution of the barrier layer, and stress effects. The stress is attributed to two factors: bubble formation and the difference in the coefficient of thermal expansion between the AAO membrane and the Al substrate. This highly efficient AAO membrane detachment method will facilitate the rapid production and applications of AAO films.

Effects of adding micro/nano-scale surface roughness on upward flow boiling of R-134a through annular tubes

The enhancement of heat transfer efficiency is crucial for development of high-performance thermal systems in various industrial applications. This study investigates heat transfer and pressure drop during upward saturated flow boiling of R-134a in annular tubes featuring smooth and micro/nano-scale roughened copper surfaces achieved through sandblasting and chemical etching. A high-pressure chamber with a glass side is designed to observe surface wettability and measure contact angles of R-134a on both surfaces. The annular tubes, with inner and outer diameters of 28.6 and 42 mm respectively, and a total heated length of 1000 mm, undergo varying mass flux, vapor quality, and saturation pressure within ranges of 6.73–20.19 kg m−2 s−1, 0.14–0.95, and 530–1000 kPa, alongside heat flux variations from 608 to 2432 W m−2. Results indicate that the application of micro/nano-scale roughness to copper surfaces minimally reduces the contact angle of R-134a which slightly improves its wettability. However, this modification significantly increases the heat transfer coefficient by 256 % compared to the smooth tube, albeit with an associated increase in pressure drop. Additionally, increasing mass flux and vapor quality increases both the heat transfer coefficient and pressure drop. Furthermore, higher heat flux results in a higher heat transfer coefficient with a small increase in pressure drop. Also, the experimental results are compared with some of the available correlations in the literature. The novelty and significance of this work advances our understanding of effect of surface roughness on flow boiling characteristics. Understanding these phenomena is crucial for optimizing the design and performance of heat exchangers and other thermal systems used in various industries, including refrigeration, air conditioning, and power generation.

Tuning surface reflectance and carrier lifetime of cone-shaped macropore structures obtained by platinum-assisted chemical etching of silicon

Tuning surface reflectance and carrier lifetime of cone-shaped macropore structures obtained by platinum-assisted chemical etching of silicon

The Effect of Surface Treatments on the Retentive Strengths of Crowns Fabricated From Polymethylmethacrylate (PMMA) Reinforced With Graphene Nanoparticles After Thermocycling: An In Vitro Study.

The study aimsto assess the effect of surface treatments by chemical agents on the retentive strengths of crowns fabricated from polymethylmethacrylate (PMMA)reinforced with graphene nanoparticles adhesively bonded to abutments after thermocycling. In vitro comparative study. This study is composed of four groups - one control, one treated with 99% pure etchant acetone solution, one treated with 15 wt% potassium hydrogen fluoride solution, and the last group treated with a combination of both solutions. The results showed that the mean load in Group A is 228.46±3.16, Group B is 252.57±7.14, Group C is 184.51±6.61, and Group D is 211.03±2.54. The mean score is highest for Group B followed by Group A and Group D, and it is least for Group C. One-way analysis of variance (ANOVA) detected highly significant differences (p<0.01) among the four groups. It can be concluded that acetone is the best chemical etchant solution forcrowns fabricated from G-CAMdiscs (Graphenano Dental, Graphenano Nanotechnologies, Spain).

Optimization of e-beam lithography parameters for nanofabrication of sub-50 nm gold nanowires and nanogaps based on a bilayer lift-off process

Electron beam lithography (EBL) stands out as a powerful direct-write tool offering nanometer-scale patterning capability and is especially useful in low-volume R&D prototyping when coupled with pattern transfer approaches like etching or lift-off. Among pattern transfer approaches, lift-off is preferred particularly in research settings, as it is cost-effective and safe and does not require tailored wet/dry etch chemistries, fume hoods, and/or complex dry etch tools; all-in-all offering convenient, ‘undercut-free’ pattern transfer rendering it useful, especially for metallic layers and unique alloys with unknown etchant compatibility or low etch selectivity. Despite the widespread use of the lift-off technique and optical/EBL for micron to even sub-micron scales, existing reports in the literature on nanofabrication of metallic structures with critical dimension in the 10–20 nm regime with lift-off-based EBL patterning are either scattered, incomplete, or vary significantly in terms of experimental conditions, which calls for systematic process optimization. To address this issue, beyond what can be found in a typical photoresist datasheet, this paper reports a comprehensive study to calibrate EBL patterning of sub-50 nm metallic nanostructures including gold nanowires and nanogaps based on a lift-off process using bilayer polymethyl-methacrylate as the resist stack. The governing parameters in EBL, including exposure dose, soft-bake temperature, development time, developer solution, substrate type, and proximity effect are experimentally studied through more than 200 EBL runs, and optimal process conditions are determined by field emission scanning electron microscope imaging of the fabricated nanostructures reaching as small as 11 nm feature size.

AFM interlaboratory comparison for nanodimensional metrology on silicon nanowires

Abstract Silicon nanowires (NWs) with a cylindrical form are fabricated by means of nanospheres lithography and metal-assisted chemical etching to obtain high aspect ratio nanostructures (diameter of about 100 nm and length of more than 15 µm) on cm2 area.&amp;#xD;The nanodimensional characterization of individual NWs is performed by using several techniques, because dimensions at the nanoscale strictly relate to functional performances. In this study, we report the results of an interlaboratory comparison between measurements from a metrological atomic force microscope (AFM) and research AFMs located in different national metrology institutes (NMIs) across Europe and in a university.&amp;#xD;The purpose of this study is to characterize two measurands: (i) sidewall roughness (Ra, Rq, Rz, Rsk, Rku parameters), extracted from the top profile measured along the nanowire length, and (ii) diameter of the nanowires measured as top-height. To this goal, the nanowires are spread horizontally on a silicon substrate, which has several areas labelled with a pattern of crosses and letters facilitating the measurement of the same NW, in order to study the reproducibility due to different instruments.&amp;#xD;Measurements show a good agreement between the different NMIs, with a combined standard uncertainty of top-height diameter less than 3%, and with a combined standard uncertainty of roughness parameters well within 5% for Ra and Rq values.

Investigation of Laser micro-textured triboelectric nanogenerator based self-powered vibration sensor for industry 4.0 application

Self-powered sensors detect a variety of crucial parameters for industrial processes without any external power source for Industry 4.0. It has capabilities to acquire, analyze, and make decisions on real-time data, these sensors are essential for the advancement of automated production systems and smart factories. In this regard, Triboelectric nanogenerators (TENGs) have potential to provide effective solution as self-powered vibration sensor for continuous monitoring of machine tools. Different techniques have been used to enhance the performance of TENG such as material doping, chemical etching, ion injection, etc. However, laser surface texturing is a low-cost, contact less, efficient technique which can be used for improving the response of TENG-based self-powered vibration sensors. In this context, Laser Induced Backside Texturing is a laser micro texturing approach to improve the electrical performance. It induces waviness and surface roughness, which leads to increased surface charge density and triboelectrification capabilities. In this work, laser micro texturing was performed using with 405 nm wavelength semiconductor diode laser to generate line pattern texture on the Fluorinated Ethylene Propylene (FEP). Laser textures TENG (LT-TENG) was developed with laser textured FEP as tribonegative material and pristine Aluminium as tribopositive material, the open-circuit voltage, short-circuit current and power density achieved 23 %, 41 %, and 47 % enhancement respectively, generating 794 V, 44 µA, and 2371.6 µW/cm2. This increase in output leads to an increased sensitivity of the sensor. When mounted on the machines, LT-TENG was able to detect their working state, vibration frequency, and harmonics i.e. 46, 92, 184 Hz for the vacuum pump and 140, 280, 410 Hz for the heat gun. These detected vibration frequencies, and their harmonics were similar to the frequencies detected by the commercial accelerometer (CTC AC115), confirming potential use of LT-TENG as a low-frequency vibration sensor. The developed LT-TENGs was integrated with the Internet of Things (IoT) supported microcontroller, which collects real-time data for continuous monitoring and analysis for machine health monitoring in smart devices.

Dichloro-tin (IV) hexadeca-fluoro-phthalocyanine (F16PcSnCl2) thin film on porous silicon layers by ultrasonic spray pyrolysis, for possible application in optoelectronics devices

Phthalocyanines represent a significant class of organic semiconductors that have garnered attention for their potential applications in conducting polymers and organic electronics. The unique structural characteristics of phthalocyanines, coupled with the intriguing chemical behavior and variations in bandgap associated with different substitution sites, offer exciting prospects for designing novel application devices. In this study, we have successfully fabricated a heterostructure incorporating dichloro tin (IV) hexa deca fluoro phthalocyanine (F16PcSnCl2) on both porous silicon (PS) and crystalline silicon (c-Si). The PS substrate was prepared using metal-assisted chemical etching. To explore the optoelectronic applications, we thoroughly characterized the optical, electrical, and morphological properties of the heterostructure. F16PcSnCl2 exhibits the lowest reflectance within the visible light spectrum, making it highly advantageous for photosensitive applications that necessitate efficient light absorption, diffusion, or scattering. The morphological analysis of the F16PcSnCl2 film reveals the presence of nanosphere-type structures uniformly distributed on both PS and c-Si substrates. The absorbance spectrum exhibits three distinct bands, which serve as typical indicators of the F16PcSnCl2 complex. Several hybrid heterostructures were fabricated for electrical characterization, displaying rectifying ohmic behavior and demonstrating a photocurrent effect in the I-V curves. Notably, when the heterostructures were polarized at 1 V, a pronounced response to pulses of white light was observed in the current–time curves. Overall, the integration of organic and inorganic materials in heterostructures holds great promise for innovative applications in optoelectronics.

Advancing quality of laser-based metal powder bed fusion-fabricated filigree sub-millimetre structures: a systematic exploration of a novel hybrid post-processing treatment

Laser-based metal powder bed fusion (PBF-LB/M) offers great potential for producing complex and filigree sub-millimetre parts with customised shapes, such as patient-specific vascular stents. However, stent fabrication via PBF-LB/M encounters fundamental challenges, including dimensional limitations, poor surface quality, difficult support structure handling and geometrical deviations.This study addresses these challenges by investigating the potential and limitations of a novel hybrid post-processing approach. This technique uses the combination of electrochemical polishing and chemical etching and is investigated from process and design perspectives, to emphasise the interactions between the two.With the systematic application of hybrid post-processing, the strut thickness and the surface roughness were substantially reduced. Moreover, it enabled the successful removal of part-internal support structures. Furthermore, angle and orientation-dependent geometrical deviations could be compensated, highlighting the potential of achieving homogenous strut thicknesses within parts containing variable overhang angles.This study demonstrates that the usage of hybrid (electro)chemical post-processing methods with specifically tailored process parameters is a promising approach for overcoming the design- and process-related challenges in PBF-LB/M manufactured sub-millimetre parts.

A label-free immunosensor based on E-SMS optical fiber structure for rapid Ag85B detection of tuberculosis

Tuberculosis, caused by Mycobacterium tuberculosis bacillus, is one of the most prevalent, widespread, infectious, and deadliest diseases in the world. In this work, a compact and sensitive biosensor based on an etched single-mode–multimode–single-mode (E-SMS) optical fiber structure was developed for the rapid detection of Mycobacterium tuberculosis Ag85B protein in phosphate buffered saline solution. This biosensor, based on the multimode interference produced into an E-SMS structure, was fabricated by chemical etching of the cladding region of the multimode fiber, followed by the immobilization of the anti-Ag85B antibody on the surface of the etched region. The functionalized E-SMS biosensor provided high selectivity in the detection of Ag85B protein, with the ability to detect biological interactions in a range of 1.31 µg/mL to 4.36 µg/mL, with a sensitivity of 2.3 nm/(µg/mL); also, signal was even obtained at concentrations as low as 80 ng/mL. This sensitive label-free biosensing technology could contribute significantly improve Mycobacterium tuberculosis detection, management in clinical diagnosis, and medical treatment of infected patients.

A hybrid effective medium description for nanoporous gold films and thickness-mediated control of optical absorption.

With the increasing demand for sensing platforms operating across UV, visible, and near-infrared wavelengths, nanoporous gold has emerged as an ideal substrate for rapid, quantitative detection of analytes with excellent specificity and high sensitivity. This study investigates thickness-mediated compositional changes and their impact on scattering characteristics of thin nanoporous gold films fabricated using selective chemical etching. Specifically, we observe thickness-induced morphological and structural changes across different fabricated samples from 25 to 100 nm in thickness. Upon their optical characterization across UV-VIS-NIR spectral regime, we notice that the constitutional differences among samples manifest distinctively & deterministically in their total optical scattering response. In order to gain insights into these observed scattering responses and to fathom the subtle connections between structural properties of NPG films and their optical response, a hybrid theoretical model comprising Maxwell-Garnett & Bruggeman effective medium approximations has been adopted. Our approach not only allows to appropriately account for the inhomogeneous nature of these films, but also corroborates well with the atomic force microscopy characterizations of the fabricated samples. Furthermore, tracing such a theoretical model is important as it helps in systematically ascertaining additional loss terms emerging in the complex dielectric function of films due to their nanoscale porosity & roughness, permitting a good reproduction of measured optical spectra. We believe, our approach will not only facilitate accurate regulation of losses in NPG thin films but will also aid in deriving customized optical performance from them, thereby advancing their potential applications in sensing and beyond.

Effect of surface pretreatment on the polypyrrole coating of acrylonitrile butadiene styrene. Part A: Synthesis and characterization

This paper investigates the synergistic effects of a two-step surface modification approach on acrylonitrile butadiene styrene (ABS) plastics. The first step involves a mechanical grinding pretreatment followed by chemical etching in sulfuric acid and hydrogen peroxide, which increases surface roughness and enhances the wettability of the ABS surface. The second step focuses on the chemical synthesis of polypyrrole (PPy) on the pretreated ABS, demonstrating improvements in PPy surface roughness and adhesion after grinding and chemical etching. Adhesion tests reveal a significant increase from 0 % (PPy on untreated ABS) to 66 % (PPy on the grounded ABS) and ultimately to 100 % (PPy on the grounded ABS after chemical etching). This research is dedicated to a comprehensive exploration of the fundamental mechanisms, substantiated by a rigorous analysis involving X-ray photoelectron spectroscopy (XPS) examination, scanning electron microscopy (SEM) and contact angle measurements. Furthermore, the electric conductivity of PPy coatings is enhanced through electrochemical doping of PPy using dodecyl sulfate anions (DS/PPy/ABS) and the incorporation of silver particles (Ag/PPy/ABS). Raman spectroscopy demonstrates the Surface-Enhanced Raman Scattering (SERS) effect of silver particles on PPy coatings, showcasing their interaction. X-ray diffraction (XRD) confirms the enhanced crystallinity of DS/PPy/ABS, aligning with increased conductivity after electrochemical doping with DS anions.

Optimizing Ni–Cr patterned boron-doped diamond band electrodes: Doping effects on electrochemical efficiency and posaconazole sensing performance

There is growing interest in developing diamond electrodes with defined geometries such as, for example, micrometer-sized electrode arrays to acquire signals for electroanalysis. For electroanalytical sensing applications, it is essential to achieve precise conductive patterns on the insulating surface. This work provides a novel approach to boron-doped diamond patterning using nichrome masking for selective seeding on an oxidized silicon substrate. The optimized process involves nichrome deposition, sonication, chemical etching, seeding, and tailored chemical vapor deposition of boron-doped diamond with an intrinsic layer to suppress boron diffusion. Through a systematic investigation, it was determined that isolated boron-doped diamond band electrodes can be efficiently produced on non-conductive silica. Additionally, the influence of boron doping on electrochemical performance was studied, with higher doping enhancing the electrochemical response of band electrodes. To demonstrate sensing capabilities, boron-doped diamond bands were used to detect posaconazole, an antifungal drug, exploiting its electroactive behaviour. A linear correlation between posaconazole concentration and oxidation peak current was observed over 1.43 × 10−8 – 5.71 × 10−6 M with a 1.4 × 10−8 M detection limit. The developed boron-doped diamond microbands could significantly impact the field of electroanalysis, facilitating detection of diverse biologically relevant molecules. Overall, this diamond patterning approach overcomes major challenges towards all-diamond electrochemical sensor chips.

Solvent-Assisted Structural Modifications of Sulfur Dots Followed by Time-Dependent Emergence of a New Emissive State and Long-Lived Afterglow.

Sulfur dots are a new class of recently developed nonmetallic luminescent nanomaterials with various potential applications. Herein, we synthesized sulfur dots using a mild chemical etching method and then modified the structural features of the as-synthesized sulfur dots using a slow and defined solvent-assisted aggregation process. This increases the particle size and overall crystallinity along with the modifications of the surface functional groups, which eventually show a new emission band at longer wavelengths. Detailed photophysical and temperature-dependent luminescence studies confirmed that the new emissive state evolves due to interparticle interactions in the excited state. Furthermore, the occurrence of a new emissive state in a longer-wavelength region helped reduce the energy gap between the lowest excited singlet state and the lowest excited triplet state in modified sulfur dots, resulting in an aqueous stable room-temperature phosphorescence/afterglow emission through efficient intersystem crossing. This typical efficacious afterglow emission directly shows the potential applicability of structurally modified sulfur dots in encryption devices and can also be potentially effective in light emitting diodes (LED) and sensing devices.