Sulfur Heteroatoms Research Articles

Molecular–level insights into the synergistic activation of peracetic acid by ultraviolet and ferrous ions for the degradation of sedimentation sludge water in drinking water treatment plants based on Fourier transform-ion cyclotron resonance mass spectrometry

Sedimentation sludge water (SSW) from sedimentation tanks in drinking water treatment plants contains significant amounts of dissolved organic matter (DOM) and precursors of disinfection byproducts, raising increasing concerns about the safety of finished water following SSW recycling. This study explores the alterations in bulk properties and molecular characteristics of DOM in SSW treated with ultraviolet (UV)/ferrous ions (Fe2+) and peracetic acid (PAA) using fluorescence spectroscopy and Fourier transform ion cyclotron resonance mass spectrometry (FT–ICR MS). The primary reactive species, hydroxyl radicals (·OH) and acylperoxy radicals (CH3C(O)OO·) achieved degradation rates of up to 82.0%, eliminating 84.5% of total fluorescent components and reducing molecular intensity and apparent molecular count by 90.9% and 69.8%, respectively. This treatment significantly reduced the aromaticity of DOM, leading to the formation of more oxidized and stable compounds. Reaction mechanisms indicate that ·OH and CH3C(O)OO· primarily facilitate oxygen addition and dehydrogenation, while CH3C(O)OO· promotes decarboxylation through weak electron transfer processes. The treatment preferentially removes complex DOM containing nitrogen and sulfur heteroatoms, which are key precursors of disinfection byproducts. These findings enhance our understanding of DOM transformations during UV/Fe2+/PAA treatment and provide valuable insights into the safe recycling of SSW.

Synthesis of Some Eco-Friendly Materials for Gold Recovery.

The aim of this study was to develop new materials with adsorbent properties that can be used for the adsorption recovery of Au(III) from aqueous solutions. To achieve this result, it is necessary to obtain inexpensive adsorbent materials in a granular form. Concomitantly, these materials must have a high adsorption capacity and selectivity. Other desired properties of these materials include a higher physical resistance, insolubility in water, and materials that can be regenerated or reused. Among the methods applied for the separation, purification, and preconcentration of platinum-group metal ions, adsorption is recognised as one of the most promising methods because of its simplicity, high efficiency, and wide availability. The studies were carried out using three supports: cellulose (CE), chitosan (Chi), and diatomea earth (Diat). These supports were functionalised by impregnation with extractants, using the ultrasound method. The extractants are environmentally friendly and relatively cheap amino acids, which contain in their structure pendant groups with nitrogen and sulphur heteroatoms (aspartic acid-Asp, l-glutamic acid-Glu, valine-Val, DL-cysteine-Cys, or serine-Ser). After preliminary testing from 75 synthesised materials, CE-Cys was chosen for the further recovery of Au(III) ions from aqueous solutions. To highlight the morphology and the functionalisation of the material, we physicochemically characterised the obtained material. Therefore, the analysis of the specific surface and porosity showed that the CE-Cys material has a specific surface of 4.6 m2/g, with a porosity of about 3 nm. The FT-IR analysis showed the presence, at a wavelength of 3340 cm-1, of the specific NH bond vibration for cysteine. At the same time, pHpZc was determined to be 2.8. The kinetic, thermodynamic, and equilibrium studies showed that the pseudo-second-order kinetic model best describes the adsorption process of Au(III) ions on the CE-Cys material. A maximum adsorption capacity of 12.18 mg per gram of the adsorbent material was achieved. It was established that the CE-Cys material can be reused five times with a good recovery degree.

Processing and Recovery of Heavy Crude Oil Using an HPA-Ni Catalyst and Natural Gas.

To maintain economic profitability and stabilize fuel prices, refineries actively explore alternatives for efficiently processing (extra) heavy crude oils. These oils are challenging to process due to their complex composition, which includes significant quantities of asphaltenes, resins, and sulfur and nitrogen heteroatoms. A critical initial step in upgrading these oils is the hydrogenation of polyaromatic compounds, requiring substantial hydrogen sources. Methane from natural gas streams is known to act as an effective hydrogen donor. This study investigates the use of a heteropolyacid (HPA) catalyst modified with nickel and methane to enhance the quality of heavy crude oil with an initial 8.0°API (at 15.5 °C) and 2200 cSt viscosity (at 37.5 °C). After treatment in a batch reactor at 380 °C and 4.4 MPa for 2 h, the oil properties markedly improved: API gravity increased from 8.0 to 16.0 (at 15.5 °C), and kinematic viscosity reduced from 2200 to 125 cSt (at 37.5 °C). Additionally, there was a significant decrease in asphaltenes (from 38.7 to 16.4% by weight), sulfur (from 5.9 to 4.0% by weight), and nitrogen (from 971 to 695 ppm). This was accompanied by an increase in the volume of light distillates from 1.3 to 4.9%, and middle distillates from 8.8 to 21.0%. These results suggest that nickel-modified HPA catalysts, combined with methane as a hydrogen donor, are a promising option for upgrading heavy crude oils.

Conformational and Electron Density Analysis of Bicyclo[3.1.0] hexanes: All Roads Lead to Boats

In view of the existence of an optimal conformation for molecular recognition and bearing in mind that nucleosides exhibit a broad range of pharmaceutical properties, whereby their conformation has a key role in molecular recognition, the tendency of the pseudosugar moiety in carbanucleosides to adopt a boat‐like conformation has been studied on the basis of a bicyclo[3.1.0]hexane system, resulting in versatile druglike scaffolds to increase molecular recognition. It is already known that using this system as a pseudosugar can fix the conformation in the northern or southern geometry required for biological activity, according to the relative position of the three‐membered ring. By mapping their energy potential surface, we investigated the preference for boat‐like conformers in bicyclo[3.1.0]hexanes. DFT was utilized alongside NBO analysis to explore the enhanced stability of boat‐like conformers, also considering the influence of oxygen, sulfur, and selenium heteroatoms. Additionally, charge density distribution analysis using QTAIM identified key atoms contributing to stability changes. These findings will help to comprehend this behavior in the drug discovery process when conformationally restricted nucleosides are involved.

Chemical and electrochemical nanofabrication of polyaminothiazole/graphene oxide composites

Poly(2-aminothiazole) is a little-studied conducting polymer with sulfur and nitrogen heteroatoms in the aromatic ring, which reveals prospects for application in various fields. We studied the conditions of chemical synthesis of poly(2-aminothiazole) and its composite with graphene oxide in an aqueous solution, as well as electrochemical deposition on electrode surfaces – Pt and SnO2. The structure of the polymer was investigated by SEM and FT-IR spectroscopy. A quantum-chemical calculation using the semi-empirical PM7 method was carried out. The electrochemical activity of polymer films was examined. Increasing effective parameters of charge transport for poly(2-aminothiazole)/graphene oxide films were detected.

Elevating hydrogen evolution performance with plasma-induced sulfur vacancies and heteroatom doping in hollow-structured MnS–CoS catalysts

Transition-metal sulfides doped with various elements show great promise as highly effective catalysts for the hydrogen evolution reaction (HER), potentially serving as alternatives to Pt-based electrocatalysts. Defect engineering has been identified as a key strategy to enhance the HER activity of such catalysts. This study proposes an effective strategy to generate numerous topological/geometric defects on hollow spherical Mn-doped cobalt sulfide (MnS–CoS) via plasma etching. MnS–CoS catalysts with well-defined cavity structures were successfully prepared using a combination of template-assisted and hydrothermal synthesis methods. Under plasma induction, these catalysts exhibited uniformly formed nanocavity structures with a built-in electric field, which uniformly enhanced their topological/geometric defect levels. The plasma-etched MnS–CoS catalyst demonstrated significantly enhanced HER activity, exhibiting an excellent overpotential of 172 mV at a current density of 10 mA·cm⁻2 in alkaline media and a low Tafel slope of 120 mV·dec⁻¹. These improvements can be attributed to the remarkable conductivity of Co and Mn, along with the unique hollow spherical nanostructure of the material, which contained numerous gaps that promoted electron movement and electrolyte penetration, thereby enhancing the overall catalytic performance. The synergistic effects of heteroatom doping and plasma modulation played a crucial role in achieving outstanding catalytic performance toward the HER. Density-functional theory calculations based on a structural model of MnS–CoS-p confirmed that the introduction of defects and heteroatoms reduced hydrogen adsorption: the Gibbs free energy decreased from 0.72 eV for CoS to 0.23 eV for MnS–CoS-p. The excellent HER activity of the MnS–CoS materials stemmed from the abundance of reactive heterostructured interfaces, which optimized the electronic configuration and, thus, accelerated H2O adsorption and dissociation. This study highlights the potential of combining plasma-assisted defect manipulation and transition-metal-element doping to design high-performance catalysts. The findings also offer valuable insights into the development of environment-friendly energy-conversion technologies.

Synergistic effects of adsorption and chemical reduction towards the effective Cr(VI) removal in the presence of the sulfur-doped biochar material.

In this study, the anaerobic sludge withdrawn from thickener in a sewage treatment plant served as the precursor for sludge-based biochar fabrication, which was further modified via sulfur (S) heteroatom doping (i.e., S-BC). The S atom doping resulted in the adjustment of the physicochemical properties towards the carbon material, endowment of abundant functional groups on biochar surface, and increasing the binding sites between biochar and Cr(VI). Compared to the primary biochar (i.e., biochar without heteroatomic doping, named BC), S-BC exhibited a rough surface and possessed remarkable advantages in ash content, specific surface area, and pore volume. The existence of graphene carbon crystal structure for S-BC was confirmed through S-BC by XRD and FTIR analysis. The studies of adsorption kinetics and isotherms showed that pseudo-second-order kinetics and the Langmuir model more fitted the Cr(VI) removal behavior in the presence of S-BC. Therefore, the chemisorption and monolayer adsorption were the primary mechanisms involved in the Cr(VI) removal process. Additionally, XPS analysis results illustrated the aqueous Cr(VI) was efficiently eliminated through the synergistic effect of chemisorption and reduction to Cr(III) in the presence of S-BC. Moreover, S-BC could still achieve the Cr(VI) eliminating efficiency of 85.31% undergoing five cycles with unchanged functional group and crystal structure via FTIR and XRD analysis. Thus, the results of this study may shed light on a new approach for simultaneous economical sludge disposal and the sustainable remediation of the Cr(VI)-contaminated wastewater.

C(sp3)-H cyclizations of 2-(2-vinyl)phenoxy-tert-anilines.

1,5-hydride transfer-triggered cyclization reactions offering a robust method for C(sp3)-C(sp3) coupling and the synthesis of e.g. tetrahydroquinolines have been thoroughly investigated in the literature. Catalysts allowing milder reaction conditions or the development of enantioselective processes were important recent contributions to the field, as well as the studies on subtrates with oxygen or sulfur heteroatoms (besides the originally described nitrogen heterocycles). In a series of studies, we focused on expanded, higher order H-transfers/cyclizations by positioning the interacting substituents on distanced rings. Cyclizations of appropriately functionalized biaryl and fused bicyclic systems led to 7-9 membered rings. In the frame of this research, we set out to study the feasibility of the cyclization and the factors affecting it by in silico methods. The conclusions drawn from computational studies were complemented by cyclization screens on 2-(2-vinyl)phenoxy-tert-anilines and their CH2-expanded analogues, the results of which are presented here. Besides isolating the expected oxazonine products in several cases, we also observed a unique dimer formation, leading to an interesting 5-6-5 ring system.

Heteroatoms chemical tailoring of aluminum nitrite nanotubes as biosensors for 5-hydroxyindole acetic acid (a biomarker for carcinoid tumors): insights from a computational study

This study aims to elucidate the properties of aluminum nitrite nanotubes (AlNNT) encapsulated with phosphorus (P@AlNNT), sulphur (S@AlNNT), and silicon (Si@AlNNT) heteroatoms for use as biosensors for 5-hydroxyindoleacetic acid (5HIAA).

In situ synthesis of europium oxide (Eu2O3) nanoparticles in heteroatom doped carbon nanofibers for boosting the cycling stability of supercapacitors.

Maintaining a high specific energy without losing cycling stability is the focus of the supercapacitor field. In this study, carbon nanofibers including europium oxide nanoparticles (CNF/Eu2O3) have been synthesized in the presence of thiourea via a simple approach and applied for the first time as an electrode for SCs. The CNF/Eu2O3-1 electrode doped with nitrogen and sulfur heteroatoms possessed a favorable specific capacitance of 183.2 F g-1, a specific energy of 9.15 W h kg-1, and an excellent capacitance retention of 94.8% even after 10 000 cycles at 1 A g-1. Such excellent performance is ascribed to the surface functionalities, high surface area, and good interaction of Eu2O3 with CNFs. This strategy will provide guidance for other rare element-based electrodes in the field of energy storage.

Tunability of triplet excited states and photophysical behaviour of bis-cyclometalated iridium(III) complexes with imidazo[4,5-f][1,10]phenanthroline.

This is a comprehensive study of the photophysical behaviour of heteroleptic iridium(III) complexes with imidazo[4,5-f][1,10]phenanthroline (imphen) as an ancillary ligand, represented by the general formula [Ir(N∩C)2(imphen)]PF6. As cyclometalating ligands, 2-phenylpyridine (Hppy), 2-phenylquinoline (Hpquin), 2-phenylbenzothiazole (Hpbztz), and 2-(2-pyridyl)benzothiophene (pybzthH) were used. The impact of structural modifications of cyclometalating ligands was widely explored by a combination of steady-state and time-resolved optical techniques accompanied by theoretical calculations. We evidenced that the cyclometalating ligands induce essential changes in the nature of the emissive excited state and the emission characteristics of [Ir(N∩C)2(imphen)]PF6. While the complex [Ir(ppy)2(imphen)]PF6 (1) is a typical 3MLLCT emitter, the lowest triplet states of [Ir(pquin)2(imphen)]PF6 (2), [Ir(pbztz)2(imphen)]PF6 (3) and [Ir(pybzth)2(imphen)]PF6 (4) have a predominant 3LCN∩C character. The phosphorescence colour of the investigated Ir(III) complexes changes from greenish-yellow to red, their quantum yields vary from 56 to 2%, and their triplet excited-state lifetimes fall in the 743-3840 ns range. The highest photoluminescence quantum yield was revealed for 2 in CH2Cl2, while complex 3 in MeCN shows the most pronounced increase in the lifetime. Both complexes 2 and 3 show an increased efficiency of singlet oxygen generation. The herein discussed structure-property relationships are of high significance for controlling photoinduced processes in heteroleptic iridium(III) complexes with the imphen-based ancillary ligand, and making further progress in effectively tuning the emission energies, quantum yields and excited-state lifetimes of these systems by structural modifications of cyclometalating ligands, especially the π-conjugation, the position of the N-donor and the presence of sulfur heteroatoms.

Preparation and properties of heteroatom-doped bacterial cellulose-derived carbonaceous materials

In this study, nitrogen and sulfur heteroatom-doped bacterial cellulose (BC) derived carbon materials have been prepared by a simple, feasible, and environmentally friendly approach that can be easily scaled up for various applications.In the first step, BC was successfully fabricated with chitosan and carrageenan compounds by a layer-by-layer assembly technique without using any template. The resulting composites were then subjected to carbonization to enrich carbon content of the material while incorporation of nitrogen and sulfur heteroatoms into the carbon structure without applying a chemical treatment.A wide variety of BC-derived N- and S-doped carbons were prepared using chitosan and different types of carrageenan precursors. The results showed that the dominant heteroatom on the BC composites was dependent on the last heteroatom precursor used in the layer-by-layer assembly process. The skeleton of the BC composites did not collapse after carbonization and the resulting materials were highly dense and porous having ribbon-like carbon structures. The use of iota-carrageenan as a sulfur precursor with combination of chitosan as a nitrogen precursor resulted in better heteroatom-doped carbons as compared to other carrageenan compounds studied.Synthesized carbons showed great potential as catalyst for hydrothermal conversion of glucose to hydrogen as tested in this study.

Microcrystalline Nanofiber Electrode with Adaptive Intrinsic Structure and Microscopic Interface.

A strategy of microcrystalline aggregation is proposed to fabricate energy storage electrode with outstanding capacity and stability. Carbon-rich electrode (BDTG) functionalized with benzo[1,2-b:4,5-b']dithiophene units and butadiyne segments are prepared. The linear conjugate chains pack as microcrystalline nanofibers on nanoscale, which further aggregates to form a porous interpenetrating network. The microcrystalline aggregation feature of BDTG exhibit stable structure during long cycling test, revealing the following advantage in structure and property. The stretchable butadiyne linker facilitates reversible adsorption and desorption of Li with the aid of adjacent sulfur heteroatom. The alkyne-alkene transition exhibits intrinsic structural stability of microcrystalline region in BDTG electrodes. Meanwhile, alkynyl groups and sulfur heteroatoms on the surface of BDTG nanofibers participate in the formation of microscopic interface, providing a stable interfacial contact between BDTG electrodes and adjacent electrolyte. As a proof-of-concept, BDTG-based electrode shows high capacity (1430 mAh g-1 at 50mA g-1) and excellent cycle performance (8000 cycles under 5 A g-1) in half-cell of lithium-ion batteries, and a reversible capacity of 120 mAh g-1 is obtained under the current density of 2 C in full-cell. This work shows microcrystalline aggregation is beneficial to realize adaptive intrinsic structure and interface contact during the charge-discharge process.

RETRACTED ARTICLE: Single-atoms (N, P, S) encapsulation of Ni-doped graphene/PEDOT hybrid materials as sensors for H2S gas applications: intuition from computational study

This comprehensive study was dedicated to augmenting the sensing capabilities of Ni@GP_PEDOT@H2S through the strategic functionalization with nitrogen, phosphorus, and sulfur heteroatoms. Governed by density functional theory (DFT) computations at the gd3bj-B3LYP/def2svp level of theory, the investigation meticulously assessed the performance efficacy of electronically tailored nanocomposites in detecting H2S gas—a corrosive byproduct generated by sulfate reducing bacteria (SRB), bearing latent threats to infrastructure integrity especially in the oil and gas industry. Impressively, the analysed systems, comprising Ni@GP_PEDOT@H2S, N_Ni@GP_PEDOT@H2S, P_Ni@GP_PEDOT@H2S, and S_Ni@GP_PEDOT@H2S, unveiled both structural and electronic properties of noteworthy distinction, thereby substantiating their heightened reactivity. Results of adsorption studies revealed distinct adsorption energies (− 13.0887, − 10.1771, − 16.8166, and − 14.0955 eV) associated respectively with N_Ni@GP_PEDOT@H2S, P_Ni@GP_PEDOT@H2S, S_Ni@GP_PEDOT@H2S, and Ni@GP_PEDOT systems. These disparities vividly underscored the diverse strengths of the adsorbed H2S on the surfaces, significantly accentuating the robustness of S_Ni@GP_PEDOT@H2S as a premier adsorbent, fuelled by the notably strong sulfur-surface interactions. Fascinatingly, the sensor descriptor findings unveiled multifaceted facets pivotal for H2S detection. Ultimately, molecular dynamic simulations corroborated the cumulative findings, collectively underscoring the pivotal significance of this study in propelling the domain of H2S gas detection and sensor device innovation.

Synthesis of multicolour luminescent graphitic carbon nitride quantum dots through controlled graphitization and surface states

Carbon nitride quantum dots are important metal free semiconductors due to their controlled optoelectronics and low toxicity. Here the sulphur heteroatom doping of these nanomaterials is achieved by the low cost hydrothermal process leading to a multicolour photoluminescence. A simple change in water/dimethyl sulfoxide ratio as a solvent helps to achieve a wide tunability in photoluminescence, almost from blue, green, yellow to red with a high quantum yield. This change has been accounted for the particle size, bond conjugation, and heteroatom doping of carbon nitride nanoparticles. Due to multicolour emission, benignity and low cost these materials can be the promising candidates for various optoelectronic applications.

A Decenary Update on Metal Oxide Nanoparticles as a Heterogeneous Greener Catalyst for the Synthesis of Bioactive Heterocycles

Abstract: In recent years, heterocycle derivatives have emerged as promising molecules, and have exhibited remarkable pharmacological applications. The statistical data analysis of the presently available drug molecules in the market has revealed that more than 70% of the drug candidates are derived from the heterocycles. Various synthetic protocols have been established employing a wide range of catalysts and reaction conditions; among them, one of the catalytic areas includes nanomaterials of metals and metal oxides. Nanocatalysts play an important role in the organic transformation under green chemistry protocol, due to their recycling nature and provision of the required catalytic amount. In this review, we have provided a comprehensive summary of the re-cent progress made in the catalytic heterogeneous metal oxide NPs application, exclusively for the synthesis of heterocyclic compounds reported in the period from 2012 to 2021. Also, this review provides an inherent framework for the reader to select a suitable catalytic system of interest to synthesize desired oxygen, nitrogen, and sulphur heteroatoms containing heterocyclic scaffold with potential pharmacological activities.

Heteroatom Functionalization of H-Terminated Diamond Surfaces.

Diamond surface functionalization has received significant research interest recently. Specifically, H-termination has been widely adopted because it endows the diamond surface with negative electron affinity and the hole carrier is injected in the presence of surface transfer dopants. Exploring different functional groups' attachment on diamond surfaces and their impact on the electronic structure, using wet and dry chemical approaches, would hence be of interest in engineering diamond as a semiconductor. Here, we report the functionalization of the H-terminated diamond surface with nitrogen and sulfur heteroatoms. Surface characterization of functionalized diamond surfaces shows that these groups are well-distributed and covalently bonded to diamonds. Four chemical functional groups (-SH, -S-S-, -S-O, and -S=O) were found on the sulfurized diamond surface, and two groups (-NH2 and =NH) upon amination. We also report co-functionalization of surface with N and S (N-S), where sulfurization promotes sequential amination efficiency with reduced exposure time. Electrical measurement shows that heteroatom-modified diamond surfaces possess higher conductivity than H-terminated diamonds. Density functional theory (DFT) shows that upon functionalization with various N/S ratios, the conduction band minimum and valence band maximum downshift, which lowers the bandgap in comparison to an H-terminated diamond. These observations suggest the possibility of heteroatom functionalizations with enhanced surface electrical conductivity on the diamond that are useful for various electronic applications.

Lead-sulfur interaction induced damp and water stability in pure formamidinium lead triiodide

Research efforts in various multitudes have been demonstrated to stabilize methylammonium (MA)- and bromide (Br)-free formamidinium lead triiodide (FAPI) perovskite thin films. Despite these commendable efforts, pure FAPI perovskite thin film is prone to critical phase-transition issues due to its thermodynamically stable non-perovskite phase (2H). Here, in this work, we propose a rational additivization strategy to overcome this challenge. Our multifunctional ammonium salt containing a sulfur heteroatom shifts the thermodynamic stability from the 2H phase to an intermediate phase closer to the cubic phase. Along with the high crystallinity, micron-sized grains with preferred (00h) facet orientation stem the Pb…S interaction to offer exceptional stability against high relative humidity, direct water incursion, and shelf-life aging. Our findings through experimental and theoretical studies substantiate the role of Pb…S interaction in stabilizing the perovskite cubic phase and the stoichiometric distribution of elemental components.

Enhanced Electron Mobility and Interfacial Properties by Introducing Nitrogen and Sulfur Heteroatoms into Naphthalene Diimide-Based Electron Transport Materials for Inverted Perovskite Solar Cells: A Theoretical Study

Enhanced Electron Mobility and Interfacial Properties by Introducing Nitrogen and Sulfur Heteroatoms into Naphthalene Diimide-Based Electron Transport Materials for Inverted Perovskite Solar Cells: A Theoretical Study

Solid-State Phosphors from Coal-Derived Carbon Quantum Dots.

With unique optical and chemical properties, carbon quantum dots (CQDs) find tremendous applications in chemistry, biology, and materials science to medicine. To expand the applicability of coal-derived CQDs from the liquid to solid state, we herein report the sustainable synthesis of solid phosphors from coal-derived CQDs using poly(vinyl alcohol) (PVA) and silica (SiO2) as an organic and inorganic matrix. Two coal-derived CQDs were obtained using an eco-friendly ultrasonic-assisted wet oxidation method. The structural and chemical properties of the CQDs were extensively investigated and compared with commercial CQDs. The coal-derived CQDs exhibited blue fluorescence with 8.9 and 14.9% quantum yields. The CQDs were found to be self-co-doped with nitrogen and sulfur heteroatoms through surface and edge functional groups. Solid-state fluorescence of PVA/CQD composite films confirmed that the CQDs retained their excellent blue emission in a dry solid matrix. A facile one-pot sol-gel method was employed to fabricate SiO2/CQD phosphors with the unique fluorescence emission. Due to their special structural features, coal-derived CQDs favored the heterogeneous nucleation and rapid formation of SiO2/CQD phosphors. Further, coal-derived CQDs caused high-intensity white light emission with CIE coordinates of (0.312, 0.339) by endowing a suitable band gap structure in a SiO2/CQD solid phosphor for potential optical applications.