Distribution Of Ions Research Articles

ASSESSMENT OF POSSIBLE WATER CONTAMINATION IN SHALLOW WELLS OF SULEJA AND ITS ENVIRON NORTH CENTRAL, NIGERIA

This research work aimed at assessing the waste dump impacts on shallow groundwater physico-chemical and biological constituents of Suleja area. Groundwater samples were collected monthly at different locations within the study area. Forty-three (43) samples were collected during the dry season while forty-two (42) samples were collected for the wet season at the same samples locations for standard water quality laboratory analysis. The data sets obtained from the laboratory were subjected to descriptive statistics and Anova test to establish their relationship, including water quality index were calculated. The hydrochemical results revealed mean concentrations of physical parameters in the following order: Conductivity > TH > TDS > Alk > T > pH for the dry season while total dissolve solids range higher to that of total hardness concentrations during the wet season (Conductivity > TDS > TH > Alk > Temp. > pH). The minor ionic distributions revealed higher mean concentration of Sulphate ion followed by chloride, bicarbonate, carbon dioxide, and nitrate ions (SO4 > Cl- > HCO3 > CO2 > NO3) for the both seasons. The major ionic enrichment is in the following order: Ca2+ > Mg2+ > Na+ > K+) for the both seasons. The heavy metals ions revealed high mean concentration of iron followed by zinc, manganese, and copper during the dry season while concentration of manganese preceded that of zinc during the wet season. Both chemical oxygen demand and biological oxygen demand indicated similar concentrations trends through-out the seasons. Hydrochemical result depict average degree of temperature,...

Surface stratification determines the interfacial water structure of simple electrolyte solutions

The distribution of ions at the air/water interface plays a decisive role in many natural processes. Several studies have reported that larger ions tend to be surface-active, implying ions are located on top of the water surface, thereby inducing electric fields that determine the interfacial water structure. Here we challenge this view by combining surface-specific heterodyne-detected vibrational sum-frequency generation with neural network-assisted ab initio molecular dynamics simulations. Our results show that ions in typical electrolyte solutions are, in fact, located in a subsurface region, leading to a stratification of such interfaces into two distinctive water layers. The outermost surface is ion-depleted, and the subsurface layer is ion-enriched. This surface stratification is a key element in explaining the ion-induced water reorganization at the outermost air/water interface.

KxVPO4F (x∼0): A New High‐Voltage and Low‐Stain Cathode Material for Ultrastable Calcium Rechargeable Batteries

AbstractThe utilization of high‐voltage intercalation cathodes in calcium‐ion batteries (CIBs) is impeded by the substantial size and divalent character of Ca2+ ions, which result in pronounced volume alterations and sluggish ion mobility, consequently causing inferior reversibility and low energy/power densities. To tackle these issues, polyanionic K‐vacant KxVPO4F (x∼0, designated as K0VPF) is proposed as high‐voltage and ultra‐stable cathode material in CIBs. The K0VPF demonstrates a decent calcium storage capacity of 75 mAh g−1 at 10 mA g−1 and remarkable capacity retention of 84.2% over 1000 cycles. The average working voltage of the K0VPF is 3.85 V versus Ca2+/Ca, representing the highest value reported for CIB cathodes to date. The combined experimental and theoretical investigations revealed that the low volume changes and hopping diffusion barriers contribute to the extraordinary stability and high‐power capabilities, respectively, of K0VPF. The distribution of Ca ions into polyanionic frameworks with pronounced spatial separation effectively attenuates the Ca2+–Ca2+ repulsive force and thus augmenting the Ca migration kinetics. The high voltage of K0VPF is attributed to the inductive effect from the largely electronegative fluorine. In conjunction with a calcium metal anode and a compatible electrolyte, Ca metal full cells featured a record‐high energy density of ≈300 Wh kg−1.

Self–dual solutions of a field theory model of two linked rings

In this work the connection established in [7,8] between a model of two linked polymers rings with fixed Gaussian linking number forming a 4-plat and the statistical mechanics of non-relativistic anyon particles is explored. The excluded volume interactions have been switched off and only the interactions of entropic origin arising from the topological constraints are considered. An interpretation from the polymer point of view of the field equations that minimize the energy of the model in the limit in which one of the spatial dimensions of the 4-plat becomes very large is provided. It is shown that the self-dual contributions are responsible for the long-range interactions that are necessary for preserving the global topological properties of the system during the thermal fluctuations. The non self-dual part is also related to the topological constraints, and takes into account the local interactions acting on the monomers in order to prevent the breaking of the polymer lines. It turns out that the energy landscape of the two linked rings is quite complex. Assuming as a rough approximation that the monomer densities of half of the 4-plat are constant, at least two points of energy minimum are found. Classes of non-trivial self-dual solutions of the self-dual field equations are derived. One of these classes is characterized by densities of monomers that are the squared modulus of holomorphic functions. The second class is obtained under some assumptions that allow to reduce the self-dual equations to an analog of the Gouy-Chapman equation for the charge distribution of ions in a double layer capacitor. In the present case, the spatial distribution of the electric potential of the ions is replaced by the spatial distribution of the fictitious magnetic fields associated with the presence of the topological constraints. In the limit in which two of the spatial dimensions are large in comparison with the third one, we provide exact formulas for the conformations of the monomer densities of the 4-plat by using the elliptic, hyperbolic and trigonometric solutions of the sinh-Gordon and cosh-Gordon equations which have been used for instance in the construction of classical string solutions in AdS3 and dS3 [9].

Strain-Induced Uphill Hydrogen Distribution in Perovskite Oxide Films.

Incorporating hydrogen into transition-metal oxides (TMOs) provides a facile and powerful way to manipulate the performances of TMOs, and thus numerous efforts have been invested in developing hydrogenation methods and exploring the property modulation via hydrogen doping. However, the distribution of hydrogen ions, which is a key factor in determining the physicochemical properties on a microscopic scale, has not been clearly illustrated. Here, focusing on prototypical perovskite oxide (NdNiO3 and La0.67Sr0.33MnO3) epitaxial films, we find that hydrogen distribution exhibits an anomalous "uphill" feature (against the concentration gradient) under tensile strain, namely, the proton concentration enhances upon getting farther from the hydrogen source. Distinctly, under a compressive strain state, hydrogen shows a normal distribution without uphill features. The epitaxial strain significantly influences the chemical lattice coupling and the energy profile as a function of the hydrogen doping position, thus dominating the hydrogen distribution. Furthermore, the strain-(H+) distribution relationship is maintained in different hydrogenation methods (metal-alkali treatment) which is first applied to perovskite oxides. The discovery of strain-dependent hydrogen distribution in oxides provides insights into tailoring the magnetoelectric and energy-conversion functionalities of TMOs via strain engineering.

Spike desensitisation as a mechanism for high-contrast selectivity in retinal ganglion cells.

In the vertebrate retina, several dozens of parallel channels relay information about the visual world to the brain. These channels are represented by the different types of retinal ganglion cells (RGCs), whose responses are rendered selective for distinct sets of visual features by various mechanisms. These mechanisms can be roughly grouped into synaptic interactions and cell-intrinsic mechanisms, with the latter including dendritic morphology as well as ion channel complement and distribution. Here, we investigate how strongly ion channel complement can shape RGC output by comparing two mouse RGC types, the well-described ON alpha cell and a little-studied ON cell that is EGFP-labelled in the Igfbp5 mouse line and displays an unusual selectivity for stimuli with high contrast. Using patch-clamp recordings and computational modelling, we show that a higher activation threshold and a pronounced slow inactivation of the voltage-gated Na+ channels contribute to the distinct contrast tuning and transient responses in ON Igfbp5 RGCs, respectively. In contrast, such a mechanism could not be observed in ON alpha cells. This study provides an example for the powerful role that the last stage of retinal processing can play in shaping RGC responses.

Investigation of charged particles interaction with CeBr3 scintillator by Monte Carlo simulation programs

This work aims to investigate the interaction of charged particles (alpha and proton) with the CeBr3 scintillator by using Monte Carlo simulation. The total mass stopping power (TMSP), projected range, ion distributions, and ion ranges in the CeBr3 at an energy range of 0.01 - 10,000 , were computed by SRIM and FLUKA programs. The simulation results show that the TMSP of CeBr3 obtained by both programs is in good agreement. The alpha particle has a higher TMSP of the CeBr3 than the proton. The projected range of alpha and proton particles increases with increasing energy. The projected range of the proton is higher than that of the alpha particle when compared at the same energy. Finally, the 2D visualization of ion distributions and ion ranges for alpha and proton particles was reported.
 
 

Bionic vine-stems structure for enhancing electrochromic cyclic stability and mechanical stability of multiband spectral regulation fiber

Wearable electrochromic (EC) devices can adjust visible-infrared spectra demonstrate promising potential for applications in display, decoration, personal thermal management, and adaptive thermal camouflage. However, existing flat layer-layer EC devices are hindered by poor air permeability, limited flexibility, and integration difficulties with fabrics, particularly in the realm of intelligent wearables. The creation of highly efficient fiber-shaped infrared (IR) modulation devices with exceptional structural and performance stability represents a significant challenge. We draw inspiration from the arboreous vine-stems structure observed in Chinese wistaria, which effectively minimizes the risk of damage to their vine and stems during harsh weather conditions. We have successfully designed a wearable high efficient multiband spectral regulation fiber (MSRF) with a bioinspired vine-stems structure using carbon fiber and polyaniline (PANI) as the active layer. The planar working electrode (Au) with PANI deposited on its surface was spirally wound around the counter electrode (carbon fiber) and separated by a gel electrolyte (PC/LiClO4), with polyolefin serving as the encapsulation layer. The distribution of electrical potential and lithium ions in the MSRF were analyzed using finite element analysis, demonstrating exceptional electrochromic stability without the length limit of the fiber. Moreover, the MSRF exhibited exceptional IR emissivity (△ε = 0.528) within the 8–14 μm range, fast response time (2.44 s) at low applied potentials (−0.8 V and 0.8 V), robust long-term cycling stability (at least 5000 cycles), and remarkable mechanical stability (at least 5000 bending cycles). The compatibility of the fiber with fabric and potential for patterning using MSRF with high length was also explored, providing new insights into the development of wearable adaptive thermal camouflage and spectral regulation fiber devices.

Quantitative Determination of Metal Ion Adsorption on Cellulose Nanocrystals Surfaces.

Nanocellulose is a bio-based material that holds significant potential in the field of water purification. Of particular interest is their potential use as a key sorbent material for the removal of metal ions from solution. However, the structure of metal ions adsorbed onto cellulose surfaces is not well understood. The focus of this work is to determine quantitatively the three-dimensional distribution of metal ions of different valencies surrounding negatively charged carboxylate functionalized cellulose nanocrystals (CNCs) using anomalous small-angle X-ray scattering (ASAXS). These distributions can affect the water and ionic permeability in these materials. The data show that increasing the carboxylate density on the surface of the CNCs from 740 to 1100 mmol/kg changed the nature of the structure of the adsorbed ions from a monolayer into a multilayer structure. The monolayer was modeled as a Stern layer around the CNC nanoparticles, whereas the multilayer structure was modeled as a diffuse layer on top of the Stern layer around the nanoparticles. Within the Stern layer, the maximum ion density increases from 1680 to 4350 mmol of Rb+/(kg of CNC) with the increase in the carboxylate density on the surface of the nanoparticles. Additionally, the data show that CNCs can leverage multiple mechanisms, such as electrostatic attraction and the chaotropic effect, to adsorb ions of different valencies. By understanding the spatial organization of the adsorbed metal ions, the design of cellulose-based sorbents can be further optimized to improve the uptake capacity and selectivity in separation applications.

Observation of the dynamic evolution process of vacuum arc microscopic particles based on the emission spectrum principle

The distribution of microscopic particles directly affects the recovery of the post arc insulating medium and determines whether the fault current can be interrupted. Based on the principle of vacuum arc emission spectrum, a high-speed spectrum observation platform was built to study the distribution of microscopic particles during the arc burning, and the axial and radial spectral line intensity and density distributions of atoms and ions under different current amplitudes were obtained. The results show that the CuI spectral line intensity has two peaks near the cathode and anode, while in the arc column it is relatively low. The peak of the CuI spectral line intensity near the electrode is caused by electrode evaporation. The peak duration of the CuI spectral line intensity near the cathode is always longer than that near the anode. The CuII spectral line intensity is lower, appears later and disappears earlier, which in the arc column increased obviously, compared with CuI. The CuII density near the cathode is higher than that near the anode, and the CuII density in the arc column is higher than in the two electrodes, which is similar to the axial distribution of electron density. The radial distribution curve of CuI and CuII density is similar to the radial distribution curve of spectral line intensity, and displays the characteristics of a high center and low edge in the radial direction of the arc gap. The difference is that the width of the atomic spectral line is larger than that of the corresponding ionic spectral line, the distribution curve of the ionic spectral line is smooth and symmetrical, and the radial attenuation rate of the CuII density is larger than that of the corresponding CuI. This reflects the ionization of atoms and the effect of magnetic fields. The radial and axial distribution of the particle density is opposite to that of the excitation temperature. Electrode emission will first affect the atom formation.

Magnetic properties of Mn-doped InSb nanowires from first principles

Room-temperature ferromagnetism (RTFM) has been achieved in Mn-doped InSb nanowires (NWs) through experiment. However, the underlying cause of RTFM remains unclear. In this paper, using first-principles calculations, the distribution of Mn ions and magnetic properties of Mn-doped wurtzite and zinc blend InSb NWs have been investigated. Our results indicate that wurtzite (In,Mn)Sb NWs can exhibit superior ferromagnetic behavior compared to zinc blend (In,Mn)Sb NWs. The distribution of Mn ions and magnetic properties in the (In,Mn)Sb NWs is influenced by their size, surface passivation and crystal structure. Furthermore, the ferromagnetic coupling is short-range in passivated (In,Mn)Sb NWs, and as the size of the NW decreases, the Mn-3d level becomes a deep acceptor in the band gap, resulting in an enhancement of ferromagnetism.

Pore‐Scale Modeling of Water and Ion Diffusion in Partially Saturated Clays

AbstractAn accurate mechanistic understanding of solute diffusion in partially saturated clays is critical for assessing the safety of deep geological repositories for radioactive waste. In this study, a pore‐scale numerical framework is developed to simulate water and ion diffusion in partially saturated clays. First, the two‐phase Shan‐Chen Lattice Boltzmann method is employed to establish the liquid‐gas distribution in a reconstructed three‐dimensional pore geometry of a clay. An equivalent solute method is also developed and validated to improve the numerical stability of the solution at the liquid/gas interface corresponding to steep variations of the concentration and diffusion coefficient of the water tracer. By using a mobility‐distance relationship from molecular simulations, Fick's law is numerically solved to simulate water diffusion in nanopores, while the coupled Poisson‐Boltzmann‐Nernst‐Planck equations are solved to simulate ion diffusion under the influence of the electrical double layer (EDL). Our model reveals that the decrease of relative effective diffusion coefficients during the desaturation is more pronounced for ions than for water, due to the additional transport pathway of water tracers in the gas phase. The obtained effective diffusion coefficients of tritiated water and ions agree well with reported data from compacted sedimentary rocks. By comparing the local electric potential and the distribution of ion concentrations in single pores, the simulation results suggest that the EDL in unsaturated clays has a more complex influence on ion distribution than under fully water‐saturated conditions. This study provides critical insights into the coupled transport processes of solutes in partially saturated clays.

Local reaction environment in electrocatalysis.

Beyond conventional electrocatalyst engineering, recent studies have unveiled the effectiveness of manipulating the local reaction environment in enhancing the performance of electrocatalytic reactions. The general principles and strategies of local environmental engineering for different electrocatalytic processes have been extensively investigated. This review provides a critical appraisal of the recent advancements in local reaction environment engineering, aiming to comprehensively assess this emerging field. It presents the interactions among surface structure, ions distribution and local electric field in relation to the local reaction environment. Useful protocols such as the interfacial reactant concentration, mass transport rate, adsorption/desorption behaviors, and binding energy are in-depth discussed toward modifying the local reaction environment. Meanwhile, electrode physical structures and reaction cell configurations are viable optimization methods in engineering local reaction environments. In combination with operando investigation techniques, we conclude that rational modifications of the local reaction environment can significantly enhance various electrocatalytic processes by optimizing the thermodynamic and kinetic properties of the reaction interface. We also outline future research directions to attain a comprehensive understanding and effective modulation of the local reaction environment.

A core-shell model of polymetallic hybrid metal halides.

Most polymetallic hybrid metal halides are assumed to show a homogenous distribution of the metal ions in the bulk. Herein, we demonstrate a core-shell model for the hybrid lead halide [(C6H18N3)2·Pb2Br10] (C6H18N3 = 2-(piperazin-1-yl)ethan-1-aminium) coated with a manganese bromide layer. This model can explain the different photoemission of this composite material, and provides new insights on the investigation of polymetallic low-dimensional organic metal halides.

Prediction of heavy metal ion distribution and Pb and Zn ion concentrations in the tailing pond area.

The pollution caused by tailings ponds has resulted in ecological damage, with soil contamination significantly impacting the daily lives of residents in the vicinity of mining areas and the future development of mining areas. This study assesses the transport status of heavy metal pollution in tailings areas and predicts its impact on future pollution levels. This study focused on lead-zinc tailing ponds, exploring the spatial and chemical distribution characteristics of heavy metals based on the distributions of Pb, Zn, As, Cu, Cr, Cd, Hg, and Ge ions. The concentrations of the major heavy metal ions Pb and Zn in tailings ponds were predicted via the exponential smoothing method. ① The total accumulation of Pb and Zn in the mine tailings ranges from 936.74~1212.61 mg/kg and 1611.85~2191.47 mg/kg, much greater than the total accumulation of the remaining six heavy metals. The total accumulation of associated heavy metal Cu was high, and the lowest total heavy metals were Hg and Ge at only 0.19 mg/kg and 1.05 mg/kg. ② The analyses of soil heavy metal chemical forms reveal that the heavy metals Pb and Zn had the highest exchangeable state content and state ratio and the strongest transport activity in the industrial plaza and village soils. Pb and Zn are the heavy metals with the greatest eco-environmental impacts in the mining area. ③ The predicted results show that the soil concentrations of the heavy metals Pb and Zn around the tailings area in 2026 are 1.335 and 1.191 times the predicted time starting values. The concentrations of the heavy metals Pb and Zn at the starting point of the forecast are already 3.34 and 3.02 times the upper limits of the environmental standard (according to environmental standards for gravelly grey calcium soils). These results have significant implications for heavy metal pollution risk management.

Kinetic energy distributions of atomic ions from disintegration of argon containing nanoclusters in moderately intense nanosecond laser fields: Coulomb explosion or hydrodynamic expansion.

We report kinetic energies (KE) of multiply charged atomic ions (MCAI) from interactions of moderately intense nanosecond lasers at 532 nm with argon containing clusters, including neat and doped clusters with a trace amount of trichlorobenzene. We develop a mathematical method to retrieve speed and thereby kinetic energy information from analyzing the time-of-flight profiles of the MCAI. This method should be generally applicable in detections of energetic charged particles with high velocities, a realm where velocity map imaging is inadequate. From this analysis, we discover that the KE of MCAI from doped clusters demonstrates a quadratic dependence on the charge of the atomic ions, while for neat clusters, the dependence is cubic. This result confirms the nature of the cluster disintegration process to be dominated by Coulomb explosion. This result bears more similarity to reports from extreme vacuum ultraviolet (EUV) fields with similar intensities, than to reports from near infrared (NIR) intense laser fields. However, the charge state distribution from our experiment is the opposite: we observe more higher charge state ions than reported in EUV fields, and our charge state distribution is actually similar to those reported in NIR fields. We also report a significant effect of the external electric field on the charge state distribution of the atomic ions: the presence of an electric field can significantly increase the charge from the atomic ions, as shown by a three-fold reduction in the average kinetic energy per charge. Although molecular dynamics simulations have been implemented for experiments in the EUV and NIR, our results allude to the need of a concerted effort in this regime of moderately intense nanosecond laser fields. The significant decrease in charge state distribution and the significant increase in KE from doped clusters, compared with neat clusters, is a telltale sign that the true interaction time between the laser field and the cluster may be substantially shorter than the duration of the laser, a welcome relief for molecular dynamics simulations.

Optimizing ionic transport in argyrodites: a unified view on the role of sulfur/halide distribution and local environments.

Understanding diffusion mechanisms in solid electrolytes is crucial for advancing solid-state battery technologies. This study investigates the role of structural disorder in Li7-x PS6-x Br x argyrodites using ab initio molecular dynamics, focusing on the correlation between key structural descriptors and Li-ion conductivity. Commonly suggested parameters, such as configurational entropy, bromide site occupancy, and bromine content, correlate with Li-ion diffusivity but do not consistently explain conductivity trends. We find that a uniform distribution of bromine and sulfur ions across the 4a and 4d sublattices is critical for achieving high conductivity by facilitating optimal lithium jump activation energies, anion-lithium distances, and charge distribution. Additionally, we introduce the ionic potential as a simple descriptor that predicts argyrodite conductivity by assessing the interaction strength between cations and anions. By analyzing the correlation between ionic potential and conductivity for a range of argyrodite compositions published over the past decade, we demonstrate its broad applicability. Minimizing and equalizing ionic potentials across both sublattices enhances conductivity by reducing the strength of anion-lithium interactions. Our analysis of local environments coordinating Li jumps reveals that balancing high and low-energy pathways is crucial for enabling macroscopic diffusion, supported by investigating percolating pathways. This study highlights the significance of the anionic framework in lithium mobility and informs the design of solid electrolytes for improved energy storage systems.

Electrohydrodynamics of diffuse porous colloids.

The present article deals with the electrohydrodynamic motion of diffuse porous particles governed by an applied DC electric field. The spatial distribution of monomers as well as the charge distribution across the particle are considered to follow sigmoidal distribution involving decay length. Such a parameter measures the degree of inhomogeneity of the monomer distribution across the particle. The diffuse porous particles resemble several colloidal entities which are often seen in the environment as well as in biological and pharmaceutical industries. Considering the impact of bulk pH and ion steric effects, we modelled the electrohydrodynamics of such porous particulates based on the modified Boltzmann distribution for the spatial distribution of electrolyte ions and the Poisson equation for electric potential as well as the conservation of mass and momentum principles. We adopt regular perturbation analysis with weak field assumption and the perturbed equations are solved numerically to calculate the electrophoretic mobility and neutralization fraction of the particle charge during its motion as well as fluid collection efficiency. We further deduced the closed form relation between the drag force experienced by the charged porous particle and the fluid collection efficiency. In addition to the numerical results, we further derived the closed form analytical results for all the intrinsic parameters indicated above derived within the Debye-Hückel electrostatic framework and homogeneous distribution of monomers within the particle for which the decay length vanishes. The deduced mathematical results as indicated above will be useful to analyze several electrostatic and hydrodynamic features of a wide class of porous particulate and environmental entities.

Size limits and fission channels of doubly charged noble gas clusters.

Small, highly charged liquid droplets are unstable with respect to spontaneous charge separation when their size drops below the Rayleigh limit or, in other words, their fissility parameter X exceeds the value 1. The absence of small doubly charged atomic cluster ions in mass spectra below an element-specific appearance size na has sometimes been attributed to the onset of barrierless fission at X = 1. However, more realistic models suggest that na marks the size below which the rate of fission surpasses that of competing dissociative channels, and the Rayleigh limit of doubly charged van der Waals clusters has remained unchartered. Here we explore a novel approach to form small dicationic clusters, namely by Penning ionization of singly charged noble gas (Ng) clusters that are embedded in helium nanodroplets; the dications are then gently extracted from the nanodroplets by low-energy collisions with helium gas. We observe Ngn2+ ions that are about 40% smaller than previously reported for xenon and krypton and about 20% for argon. These findings suggest that fission barriers have been underestimated in previous theoretical work. Furthermore, we measure the size distributions of fragment ions that are produced by collisional excitation of mass-selected dications. At lowest collision gas pressure, dicationic Kr and Xe clusters that are smaller than previously observed are found to evaporate an atom before they undergo highly symmetric fission. The distribution of fragments resulting from fission of small dicationic Ar clusters is bimodal.

Constructing micro/nano-photonics barcodes based on micro-region upconversion emission spectrum of single core-shell microcrystal

The construction of core-shell structures with different structural properties based on the epitaxial growth technique has become an effective technique for regulating the luminescence properties of micro/nanocrystals. In order to obtain richer spectral information, NaYF<sub>4</sub>:50%Yb<sup>3+</sup>/2%Tm<sup>3+</sup>@NaYF<sub>4</sub>@NaYF<sub>4</sub>:20%Yb<sup>3+</sup>/2%Er<sup>3+</sup>@NaYF<sub>4</sub>@NaYbF<sub>4</sub>:2%Er<sup>3+</sup> multilayered core-shell microcrystals are prepared by using multiple epitaxial growth through introducing surface modifiers and controlling their reaction conditions. The XRD and SEM results clearly show that the core-shell microcrystals possess a pure hexagonal crystal structure in the form of a disk. The microdesk has a thickness of about 2.32 μm and a diameter of about 28.31 μm. The upconversion luminescence characteristics of different single microcrystal structures are investigated by a confocal microspectroscopy system. In order to realize the selective excitation and emission of a single microcrystal, the spatial distribution of luminescent ions can be controlled through introducing an intermediate isolation layer. Under 980 nm laser excitation, different excitation sites of the single microdisk exhibit different upconversion emission characteristics. The significant blue (450 and 475 nm), red (648 nm) and green (524 and 540 nm) emissions are observed, which mainly originat from Tm<sup>3+</sup> and Er<sup>3+</sup> radiative transitions. Meanwhile, the red and blue upconversion emission intensities of the microcrystals are improved by using various shell layers. In addition, the luminescence and energy-transfer features of single microcrystals are explored by changing the excitation position. The experimental results demonstrate that the incorporation of NaYF<sub>4</sub> inert shells between luminescent layers can regulate luminescence and prevent ions from interacting. By utilizing the spectral fingerprint data of dopant ions in various shell layers, we create customizable micro-nano photonic barcodes and employ them for optical anti-counterfeiting detection. This study explores the use of constructed core-shell structures with luminescent tunable micron core-shell structures to acquire diverse spectral information and maintain stability through their structural properties. Thus, this core-shell structure provides a novel method for using upconversion luminescent microcrystals into micro- and nanophotonics to achieve anti-counterfeiting and display purposes.