Charged Ions Research Articles

Variable-energy cocktail beam technology for investigating synergistic damage in nuclear materials on LEAF platform

This study addresses the critical issue of synergistic radiation damage in structural materials of fusion reactors, focusing on the interaction between the displacement defects and transmutation-produced hydrogen and helium. These effects are simulated and investigated by employing the advanced multi-beam ion implantation capabilities of the LEAF (Low Energy high intensity highly charged ion Accelerator Facility) platform. Firstly, high-intensity cocktail beams, such as “4He+ and 56Fe14+" and “4He+ and 58Ni15+", are generated and characterized successfully. Then, a complex radiation environment is mimicked within the fusion reactors by applying variable-energy irradiation. Secondly, similar penetration depths for different ions, which are crucial for studying synergistic effects, are obtained by precisely controlling the energy of the cocktail beams through the innovative energy modulation system of the LEAF platform. Finally, the post-irradiation analyses, performed by using the transmission electron microscopy (TEM) and nanoindentation, revealed distinct microstructural changes and alterations in material properties, providing insights into the degradation mechanisms under irradiation. This work not only generates diverse and high-intensity “cocktail” ion beams but also achieves rapid energy switching of the beams. Further, the work is expected to pave the way for the implementation of a novel multi-beam irradiation technique in advanced heavy-ion linear accelerators, and also to provide innovative experimental methods and technical support for studying the synergistic effects of nuclear materials.

Anion Selectivities in Zwitterion Grafted Nanopores: Effect of Zwitterion Architecture.

The separation of ions of similar charge is a crucial challenge in many applications, from water treatment to precious metal recovery. Membranes with cross-linked zwitterionic amphiphilic copolymer (ZAC-X) selective layers, which feature self-assembled, zwitterion-lined nanodomains for permeation, offer unique permselectivity between monovalent anions (e.g., Cl-/F-). This has motivated studies on the mechanisms of transport and selectivity in this family of materials. In this study, we conducted molecular dynamics simulations of aqueous salt solutions within zwitterion-functionalized nanopores to elucidate the influence of dipole orientation of the ZI ligands on anion diffusivities, partitioning, and permeabilities. Our model compares systems with contrasting ZI organization: surface-cation-anion (S-ZI+-ZI-, Motif A) and surface-anion-cation (S-ZI--ZI+, Motif B). Our results reveal that Motif A exhibits less pronounced ion pairing due to a spatial separation in the radial profiles of cations and anions. Motif B demonstrates prominent ion pairing for smaller anions owing to their overlap with cation distributions. Further, our potential of mean force profiles reveals that anion partitioning increases with anion size in both ligand motifs, whereas Motif B exhibits significantly higher partitioning selectivity toward larger anions compared to Motif A. Our results for ion diffusivities show that the self-diffusivities of both anions and cations are lower for Motif B compared to Motif A. Such trends in anion partitioning and diffusivities can be explained by differences in the interactions and steric hindrance experienced by the anionic species in Motifs A and B. Finally, our results for anion permselectivity, obtained by combining partitioning and diffusivity, indicate that partitioning trends dominate over diffusivity trends. Consequently, anion permeability increases with anion size, and ligand Motif B yields much higher permselectivity toward larger anions compared to ligand Motif A.

Native Mass Spectrometry of Membrane Protein-Lipid Interactions in Different Detergent Environments.

Native mass spectrometry (MS) reveals the role of specific lipids in modulating membrane protein structure and function. Membrane proteins solubilized in detergents are often introduced into the mass spectrometer. However, detergents commonly used for structural studies, such as dodecylmaltoside, tend to generate highly charged ions, leading to protein unfolding, thereby diminishing their utility in characterizing protein-lipid interactions. Thus, there is a critical need to develop approaches to investigate protein-lipid interactions in different detergents. Here, we demonstrate how charge-reducing molecules, such as spermine and trimethylamine-N-oxide, enable the opportunity to characterize lipid binding to the bacterial water channel (AqpZ) and ammonia channel (AmtB) in complex with regulatory protein GlnK in different detergent environments. We find that protein-lipid interactions not only are protein-dependent but also can be influenced by the detergent and type of charge-reducing molecule. AqpZ-lipid interactions are enhanced in LDAO (n-dodecyl-N,N-dimethylamine-N-oxide), whereas the interaction of AmtB-GlnK with lipids is comparable among different detergents. A fluorescent lipid binding assay also shows detergent dependence for AqpZ-lipid interactions, consistent with results from native MS. Taken together, native MS will play a pivotal role in establishing optimal experimental parameters that will be invaluable for various applications, such as drug discovery as well as biochemical and structural investigations.

The amenability of different solvents to electrospray ionization mass spectrometry

Electrospray ionization mass spectrometry is capable of transferring ions from solution to the gas phase across a broad range of solvents. A systematic investigation of the relative performance of different solvents has not been previously conducted, and we sought to remedy this situation. Fourteen solvents across a wide range of polarities were investigated for their ability to provide strong signals for four permanently charged ions. We found the best solvents to be acetone, acetonitrile, dichloromethane, tetrahydrofuran, and the previously unused (in an ESI-MS context) trifluorotoluene.

Generation of multiply charged metal ions in a high current short pulse vacuum arc

We have studied the plasma composition of a high current short pulse vacuum arc discharge with different cathode materials: lanthanum, gadolinium, lead, silver, and tin. We find that for optimal vacuum arc discharge parameters – arc current pulse duration about 2 μs and amplitude about 3 kA – the maximum ion charge state is 11+ and mean ion charge state from 7.8+ for tin to 9.6+ for lanthanum. The mean ion charge state for different materials depends on the discharge voltage and the energy required for ionization to maximum charge state. The cathode surface heats to a temperature of 700 °C–1100 °C in the course of the arc current pulse, depending on the cathode material, and the cathode surface of low melting point metals such as lead and tin melts to a depth of 5 μm and 10 μm, respectively. Surface melting does not lead to change in plasma ion composition, since the ion flux from the cathode considerably exceeds the evaporated atom flux.

Bias disk boost technique for pulsed-operation electron cyclotron resonance ion sources

A simple, effective technique to increase the intensity of multiply charged ions has been developed for pulsed-operation electron cyclotron resonance ion sources (ECRISs). The technique is realized simply by applying an additional boost voltage of about −1 kV to a negative constant voltage on the bias disk. The technique can be applied to general ECRISs by adding electric devices to the bias disk circuit, such as a high-voltage power supply, a fast high-voltage switch, and a diode. The effect of the technique depends on the ion species, and we obtained a maximum ion intensity increase of 66% for O6+ compared with the conventional bias disk method. In particular, the technique can be applied to the existing pulsed-operation ECRISs used at a heavy-ion cancer therapy facility where multi-ion treatment with multiply charged oxygen and neon ions is planned to be introduced.

On the possibility of studying the effect of magnetic reconnection in a laboratory astrophysical experiment using X-ray emission L-spectra of multiply charged ions

The paper considers the application of X-ray spectroscopy with high spatial resolution for investigation of magnetic reconnection in laboratory astrophysical experiments carried out on laser facilities of nano- and pico-second duration at moderate laser intensity on the target 1018 W/cm2. A brief overview of commonly used experimental schemes is given. We present atomic kinetic calculations for the spectra from the L-shells of Ne- and F-like iron ions (Fe, Z = 26), which demonstrate the high sensitivity of the spectra to changes in plasma parameters. An analysis of the range of applicability of various diagnostic approaches to assessing the electron temperature and laser plasma density is carried out. It is shown that transition lines in Ne-like ions are a universal tool for measuring plasma parameters, both in the region of laser interaction with the target and in the reconnection zone.

Transformation Dynamics of Nanosized Bi Films into Semiconductor Films of Bismuth Oxide in the Cold Plasma Device

This work proposes an original method that reveals the transformation dynamics of nanosized Bi films into semiconductor films of bismuth oxide (Bi2O3) and the factors affecting the low‐energy cold plasma on the electro‐optical properties of Bi2O3. In the plasma microreactor with a photosensitive GaAs:Cr electrode, the transformed Bi films 400–1100 nm thick are analyzed by X‐ray diffraction to determine the crystal structure of Bi2O3 and by an electron probe microanalyzer to explore the evolution of the composition. The morphological properties of the Bi films exposed to electron–ion flow are examined by processing the scanning electron microscope images. It is found that as a result of the combined effect of photoactive illumination, charged particles, and active plasma components: 1) an absorption spectrum of a new substance is formed in the range λ = 330–1100 nm; 2) the optical width of the bandgap of the resulting substance is Eg ≈ 3 eV, which satisfactorily coincides with the width of the bandgap of Bi2O3; and 3) to overcome the potential barrier and formation of semiconducting Bi2O3 film energy is required, which is provided by the combined kinetic energy of electrons and negatively charged oxygen ions bombarding on the Bi film.

In situ growth of Cd0.6Zn0.4S on graphene guided by ion anchoring for boosting hydrogen production

Owing to its large specific surface area and high conductivity, reduced graphene oxide (RGO) serves as an ideal platform for electron transfer. In this study, in situ growth of sulfides on RGO was attributed to metal ion anchoring on graphene oxide nanosheets by electrostatic attraction between negatively charged functional groups and metal ions. Tight binding between sulfides and RGO caused by in situ nucleation and growth can promote direct electron transfer and electron-hole separation, which is a more effective way to enhance hydrogen evolution activity. Cd0.6Zn0.4S/graphene (CZS/RGO) composite photocatalysts with different graphene ratios were prepared and exhibited high photocatalytic activity due to the improved dispersion of CZS and increased electronhole separation. The hydrogen production rate of CZS-0.8/RGO reached 52.50 mmol∙g–1∙h–1, and after nine cycles for 27 h, the hydrogen production efficiency remained at 86.4 %.

Enhancing polypropylene-based separator efficiency in lithium-ion batteries through maleic anhydride addition and corona radiation modification

Polypropylene-grafted-maleic anhydride (PPMA) as a modifier of polypropylene (PP) at different contents and the corona radiation for surface ionization at various modification times were applied to promote the PP-based separator efficiency. The determined microstructural characteristics showed an improvement in the separator's porosity of 6–139 % at the tension amounts of 700–900 %, however, more stretching hurts the mechanical properties. The electrostatic interactions formed between the electrolytes and anhydrides increased the electrolyte sorption capacity in the samples and the surface wettability by 740 % and 25 %, respectively. The electrical test results indicated that the anhydrides led to capturing the electrolytes in the separator and created a resistance against the ion diffusion. This phenomenon reduced the separator resistance from 475 to 165 Ω, and enhanced the charge capacity and ion conductivity from 585 to 871 mAh/g and 0.29 to 0.34 S cm−1, respectively, while the PPMA content increased from 20 to 60 wt.%. The achieved FT-IR illustrated that the ionization caused the creation of more polar groups in the LIB separator, which increased the bulk and surface wettability by 420 % and 21 %, respectively, without any change in the microstructure of the separator. However, raising the exposure time in the radiation process decomposed the sample surface and led to damage in the separator microstructure. This issue reduced the separator porosity as well as the electrolyte absorption amount and ion conductivity.

Groundwater quality assessment for drinking and irrigation purposes and its human health risks in the Sevathur mine region, south India

In this research, 35 samples of groundwater were collected and subjected to analysis with the aim of assessing its appropriateness for both drinking and irrigation purposes in Sevathur mine region, south India. Spatial depiction illustrates the widespread dispersal of primary positively charged ions and negatively charged ions formulated through the Inverse Distance Weighting (IDW) technique within a Geographic Information System (GIS). The Piper and Gibbs plots reveal a variety of water compositions in the surveyed region, encompassing combinations of mixed Ca-Mg-Cl, Ca-Mg-Cl-SO4, Na-K-Cl-SO4, and a few instances falling within the category of Ca-Mg-HCO3. The current features of hydrogeochemical facies result from the interplay between geological formations and water, alongside the occurrence of ion exchange, dissolution and weathering of calcium carbonate, calc-silicate minerals, and halite within subterranean aquifers. The water quality index unveiled that 23% of the samples fall into the poor category, while a substantial 11% are categorized as very poor. Additionally, 3% are undesirable, 17% are unfit for drinking, 23% exhibit a good, and 23% are distinguished by excellent categories. SAR values of subsurface water samples belong to the excellent class. Additionally, the RSC value indicates that 94% of the samples are categorized as suitable class, while 6% are classified as marginal for irrigation purposes. Individuals are advised to avoid drinking groundwater with fluoride levels above the WHO limit (>1.5mg/l), as 26% of samples exceeded this threshold. The region's groundwater chemistry is influenced by natural geological processes, such as mineral dissolution, and ion exchange, as well as human activities, including agricultural practices. Advanced water treatment techniques are being considered to improve water quality and ensure safer drinking water for the community.

Broadband Dielectric Spectroscopy: Unraveling Na+diffusion and mixed conduction in Na₂O-modified zinc phosphate glasses for electrode material applications

The fundamental understanding of electric charge (ion + polarons/electrons) transport and relaxation mechanism is essential for applications in solid state ionics. In present work, to study Na+ transport, the electrical conductivity of zinc phosphate glasses modified with Na2O has been investigated in temperature range 313K and 473K and frequency range of 100 mHz to 1 MHz. The experimental data of Nyquist plots is fitted with appropriate equivalent circuits at different temperatures which reveals presence of mixed conduction (polaronic + ionic) and Na+ diffusion (at 50 mol% Na2O) in studied glass samples. The values of frequency exponent (s) obtained from the fitting of experimental data of the real part of electrical conductivity with Almond–West equation (WAE) have been used to determine the conduction mechanism. The electric transport in studied glasses occurred via correlated barrier hopping and non-overlapping small polaron tunnelling conduction models depending on the glass composition and temperature range of investigation. Electric Modulus studies further supports the assertion of composition and temperature dependent conduction mechanisms. The activation energies determined from conductivity, electric modulus, and impedance measurements are found to be consistent, indicating a good correlation in the study.

Metal-modified biochars prepared from blue algae and their ability of adsorbing phosphates from water and utilization as soil amendment

The problem of blue algae accumulation can be alleviated by utilizing blue algae as biomass for resource utilization, which can remove excess phosphates from water to alleviate eutrophication. Herein, Magnesium (Mg) and/or lanthanum (La) were used to modify biochar via high-temperature slow pyrolysis with blue algae as the raw biomass. These modified biochars exhibited abundant carbon (18.0%-50.3%), oxygen content (17.4%-49.1%), along with a high specific surface area (82.26-233.80 m2/g). The surface of metal-modified biochar was enriched with hydroxyl and carboxyl groups and metal elements were efficiently incorporated into biochars. Adsorption kinetic and isotherm experiments were conducted under the optimal pyrolysis temperature of 600 °C, pH of 6.0, and adsorbent dosage of 2.0g/L. The adsorption kinetics studies by metal-modified biochars for phosphate fitted well pseudo-second-order model Redlich-Peterson isotherm model. Biochar modified by Mg and La exhibited the highest removal efficiency (97.8%) for phosphate at adsorption equilibrium. The adsorption mechanism involved the electrostatic interaction between hydroxylated metal oxides and negatively charged phosphate ions and the precipitation of phosphate ions through chemical reactions with metal oxides in the solution. After phosphate adsorption, the pristine and metal-modified biochars derived from blue algae were applied as the soil amendment. Biochar adsorbed phosphate apparently improved the germination rate of seeds facilitated the height, width, weight, and chlorophyll content of vegetable seedlings, and induced oxidative stress, which proved that the biochar recovered after adsorption was a high-quality soil amendment. This study provides a new approach for the treatment of phosphate wastewater and the algae application.

Mn Doped MoO3 with Self-Assembled Nanoflowers Structure and Enhanced Gas Sensing Properties to Triethylamine

Increasing quality of life requires low power consumption and reliable gas sensing technology for real-time monitoring of the environment. Herein, based on the principle of ion compensation and charge compensation, Mn-doped MoO3 self-assembled nanoflowers were designed and prepared, and their gas-sensing performance were studied. Benefiting from abundant defective sites and surface chemical state changes, the sensor exhibits superior characteristics for triethylamine detection, including ultrahigh response (436.9), short response time (7 s), small detection limit (1 ppm), and remarkable selectivity. The gas-sensitive mechanism of M-MoO3 was explained from the points of view of charge compensation and ion compensation, and it was proved that the incorporation of Mn into MoO3 was an effective way to improve its gas sensitivity. This work provides a potential strategy for widespread triethylamine detection and provides new ideas for the design of high-performance sensors.

Coal-based Si self-doped disordered porous carbon for supercapacitor electrodes

In preparing activated carbon for coal-based supercapacitors, silicon in coal usually requires removal with hydrofluoric acid, which is neither economical nor environmentally friendly. However, silicon can be used as the anode in lithium batteries due to its high theoretical capacity. So silicon was retained to study its effect on supercapacitors. By retaining silicon without hydrofluoric acid treatment and activating at lower temperature, the prepared Si-doped activated carbon achieved a high specific capacitance of 318.3F/g at 0.5 A/g in the three-electrode test system. Omitting hydrofluoric acid treatment increased the specific capacitance by 49 %. Experimental results show that this 4.92 % silicon doping, mainly CSiO3, is the main reason for the enhancement. Density functional theory (DFT) simulations confirmed that CSiO3 improves double-layer capacitance by localizing surface charge and enhancing electrolyte ion adsorption, while also boosting quantum capacitance. High activation temperatures increase coal-activator reactions but also decrease disorder of the carbon, reducing specific capacitance. Temperature experiments show that the specific capacitance increases and then decreases in the range of 600 ∼ 950 °C, and reaches a peak at 650 °C. This study presents a simple, effective method to enhance supercapacitor performance with silicon-carbon precursors and provides detailed explanation on the capacitance enhancement mechanism for the first time.

3D Z-Scheme Conjugated Polymer/Cu2O for Organic Photoelectrochemical Transistor Bioassay

Organic photoelectrochemical transistor (OPECT) is an emerging technology studying photo-electric-biological recognition events. Here, this work reports the three-dimensional (3D) Z-scheme poly(1,4-diethynylbenzene) (pDEB)@Cu2O heterojunction as a high-efficacy photogating module and its application for OPECT bioassay. Specifically, 3D Z-scheme pDEB@Cu2O heterojunction enabled fast charge transport and ion diffusion in the system, achieving remarkable amplification capability with a current gain as high as ca. 9.6×103. By linking with GOx-labeled sandwich immunorecognition, the impact of GOx-generated H2O2 on the OPECT made possible the sensitive bioassay. Exemplified by carcinoembryonic antigen (CEA) as the model target, the OPECT device achieved a linear detection range spanning from 100 fg/mL to 100 ng/mL and coupled with a detection limit as low as 72 fg/mL. This work provided a generic and extensible platform for the designation of novel bioassay systems.

Polyzwitterionic hydrogel using waste biomass as solar absorbent for efficient evaporation in high salinity brine

Solar-driven interfacial vapor generation (SVG) is a promising strategy for brine purification. However, the effective combination of functional evaporator backbones and solar absorbers for SVG enhancement remains challenging in high-salinity brines (≥10 wt%). Herein, a biomass-based polyzwitterionic hydrogel (PZH) was developed to improve the SVG performances in 10 wt% brine. Zwitterions with specific anti-polyelectrolyte effects served as backbones for accelerating H2O transportation, with fewer salt deposits and macropore channels. The biomass of straw prepared at a pyrolysis temperature at 600 ℃ was the most effective solar absorber. The synthesis of So600-PZH-8mm yielded the optimal solar evaporator with a low evaporation enthalpy of 877.79 J·g−1, a remarkable solar-to-vapor energy efficiency of 87.1 %, and a high evaporation rate of 3.57 kg·m−2·h−1 under 1 sun irradiation and a relative humidity of 30 %. Multi-cycle evaporation tests further verified the high quality of the steam water, high salt resistance, reliability, and durability of So600-PZH-8mm in practical applications. Furthermore, density functional theory calculations of the binding energies of charged groups and ions verified the anti-polyelectrolyte effect and swelling behavior of the PZHs. Overall, this study demonstrated the effectiveness of waste biomass as solar absorber for high-efficiency solar adsorption and water activation, which opens a new perspective to inspire the up-conversion of waste biomass in more valuable and meaningful ways.

Experimental overview of nanoferrites: synthesis, characterization and performance evaluation in wastewater treatment

Abstract This study investigates the potential of ferrite nanoparticles (BaFe12O19, MnFe2O4, NiFe2O4, and Co1–0.5Ni0.5Fe2O4) as eco-friendly adsorbents for the removal of heavy metals (Zn2+, Ni2+, Co2+, and Mn2+) from wastewater. Moreover, the adsorption experiments were conducted under varying contact times (30 min, 1 h, 2 h, and 4 h) and pH levels (2, 7, and 12) for five cycles to evaluate their significant dynamic effects on the removal efficiency. All ferrite nanoparticles were synthesized by the co-precipitation method and characterized (XRD, FT-IR, and SEM) to ascertain their crystal structure, morphology, size distribution, and crystallographic structures before wastewater treatments. The results demonstrated that BaFe12O19 had a particle size of 8.65 nm and achieved maximum adsorption ability of 93%, 91%, 94%, and 91% for Zn2+, Ni2+, Co2+, and Mn2+, respectively, at a pH of 7 after 4 h of treatment. Since the neutral pH value affects the binding of heavy metal ions, therefore governing the adsorption efficiency and selectivity. In contrast, NiFe2O4 (1.41 nm) revealed maximum removal of Zn2+, Ni2+, Co2+, and Mn2+ were 78%, 71%, 88%, and 83%, respectively, at a pH of 12 after 4 h. This was attributed to the negatively charged surface leading to stronger electrostatic attractions between the positively charged metal ions and the adsorbent surface, resulting in higher adsorption uptake. Notably, the higher removal rate of ions was observed during initially 1 h, suggesting a decline in efficiency rate with extended treatment time. Additionally, the experimental study over five cycles concluded that the adsorbent could be effectively regenerated and reused.

Cyclic Ether Derived Stable Solid Electrolyte Interphase on Bismuth Anodes for Ultrahigh-Rate Sodium-Ion Storage.

The bismuth anode has garnered significant attention due to its high theoretical Na-storage capacity (386mAh g-1). There have been numerous research reports on the stable solid electrolyte interphase (SEI) facilitated by electrolytes utilizing ether solvents. In this contribution, cyclic tetrahydrofuran (THF) and 2-methyltetrahydrofuran (MeTHF) ethers are employed as solvents to investigate the sodium-ion storage properties of bismuth anodes. A series of detailed characterizations are utilized to analyze the impact of electrolyte solvation structure and SEI chemical composition on the kinetics of sodium-ion storage. The findings reveal that bismuth anodes in both THF and MeTHF-based electrolytes exhibit exceptional rate performance at low current densities, but in THF-based electrolytes, the reversible capacity is higher at high current densities (316.7mAh g-1 in THF compared to 9.7mAh g-1 in MeTHF at 50A g-1). This stark difference is attributed to the formation of an inorganic-rich, thin, and uniform SEI derived from THF-based electrolyte. Although the SEI derived from MeTHF-based electrolyte also consists predominantly of inorganic components, it is thicker and contains more organic species compared to the THF-derived SEI, impeding charge transfer and ion diffusion. This study offers valuable insights into the utilization of cyclic ether electrolytes for Na-ion batteries.

Tailoring optical and electrical properties of PVP-I2 complexes through gamma irradiation-induced structural defect Engineering for optoelectronic applications

This study investigates the complexation of iodine with polyvinylpyrrolidone (PVP) subjected to gamma irradiation at doses of 0, 10, 20, and 30 kGy. The complex formation involves I2 acting as a Lewis acid with electron-rich PVP as a Lewis base through a charge transfer mechanism. UV–visible spectroscopy revealed a red shift of the absorption peak at 337 nm for irradiated PVP-I2 samples, indicating stronger interactions between the triiodide ion (I3¯) and irradiated PVP. FTIR analysis confirmed the formation of new C≡N moieties arising from PVP-I2 complexation. The FT-Raman analysis revealed a new C≡N peak at 2360 cm−1 in irradiated PVP-I2 samples, with increasing intensity correlating to higher irradiation doses, indicating enhanced electron delocalization due to complex formation. XRD analysis showed that PVP-I2 samples irradiated at 0 and 10 kGy exhibited higher crystallinity than those irradiated at 20 and 30 kGy, suggesting that high-dose irradiation causes PVP radiolysis and ring opening. Dielectric measurements demonstrated enhanced polarizability and ionic conductivity of irradiated PVP-I2 films, related to structural disorder promoting charge dissociation and ion mobility. The direct bandgap decreased from 2.75 eV for unirradiated samples to 2.55 eV for samples irradiated at 30 kGy, indicating the creation of new optically active defect states. Urbach energy increased from 0.85 eV to 1.55 eV with increasing irradiation dose, confirming increased disorder in the PVP structure. These findings reveal that gamma irradiation significantly alters the optical and electrical properties of PVP-I2 films by creating defects and disrupting structure, offering new insights for tailoring these materials for optoelectronic applications.