Review on the application of upconversion nanomaterials in heavy metal detection

As a widespread element,heavy metals have a significant impact on human health and threaten human health.It is of great significance to develop analytical technologies that can detect heavy metal ions quickly and accurately.In comparison to conventional fluorescent materials such as organic dyes,quantum dot(QD)labels,and carbon quantum dots(CD),fluorescence detection technology utilizing lanthanide(Ln)ion-doped upconversion nanoparticles(UCNPs)stands out due to its distinctive attributes.These include a notably reduced autofluorescence background,enhanced tissue penetration capabilities,biocompatibility with cellular tissues,and minimal photodamage inflicted on biological samples.The utilization of this technology has garnered considerable attention across multiple fields.In the domain of heavy metal detection,traditional laboratory methods necessitate costly instrumentation and a fully equipped laboratory,involving intricate sample processing procedures and protracted detection periods,as well as a demand for skilled personnel.In contrast,the implementation of this material offers rapid and cost-effective detection,significantly mitigating the technical barriers for operators.Consequently,this represents an exceptional avenue to curtail expenses and broaden the scope of detection within the analytical process.This paper reviews the research progress of UCNPs in the detection of heavy metal ions,encompassing a brief elucidation of the luminescence principle of upconversion nanomaterials and commonly used detection principles.Additionally,it provides a detailed overview of the research status of several common non-metal ions and essential heavy metals.Furthermore,it summarizes the current focal points in UCNP detection and discusses the challenges and prospects associated with it.

Phonon-assisted upconversion photoluminescence of quantum emitters

Quantum emitters are widely used in quantum networks,quantum information processing,and quantum sensing due to their excellent optical properties.Compared with Stokes excitation,quantum emitters under anti-Stokes excitation exhibit better performance.In addition to laser cooling and nanoscale thermometry,anti-Stokes excitation can improve the coherence of single-photon sources for advanced quantum technologies.In this review,we follow the recent advances in phononassisted upconversion photoluminescence of quantum emitters and discuss the upconversion mechanisms,applications,and prospects for quantum emitters with anti-Stokes excitation.

Synthesis and upconversion luminescence of Lu_2O_3:Yb^(3+),Tm^(3+) nanocrystals

Lutetium oxide nanocrystals codoped with Tm3＋ and Yb3＋ were synthesized by the reverse-like co-precipitation method, using ammonium hydrogen carbonate as precipitant. Effects of the Tm3＋, Yb3＋ molar fractions and calcination temperature on the structural and upconversion luminescent properties of the Lu2O3 nanocrystals were investigated. The XRD results show that all the prepared nanocrystals can be readily indexed to pure cubic phase of Lu2O3 and indicate good crystallinity. The experimental results show that concentration quenching occurs when the mole fraction of Tm3＋ is above 0.2%. The optimal Tm3＋ and Yb3＋ doped molar fractions are 0.2% and 2%, respectively. The strong blue （490 nm） and the weak red （653 nm） emissions from the prepared nanocrystals were observed under 980 nm laser excitation, and attributed to the 1G4→3H6 and IG4→3F4 transitions of Tm3＋, respectively. Power-dependent study reveals that the 1G4 levels of Tm3＋ can be populated by three-step energy transfer process. The upconversion emission intensities of 490 nm and 653 nm increase gradually with the increase of calcination temperature. The enhancement of the upconversion luminescence is suggested to be the consequence of reducing number of OH- groups and the enlarged nanoerystal size.

Effect of Er substituting sites on upconversion luminescence of Er^(3+)-doped BaTiO_3 films

Erbium-doped BaTiO3 films on LaNiO3/Si substrates were fabricated by sol-gel method. The crystalline structure, morphologies and upconversion （UC） luminescence properties of films were respectively investigated by X-ray diffraction （XRD）, atomic force microcopy （AFM） and photoluminescence （PL）. The results indicate that both of the microstructure and luminescence are found to be dependent on Er^3＋ substituting sites. The samples with A-site substitution have smaller lattice constants, larger grains and smoother surface than those with B-site substitution. The photoluminescence spectra show that both of the samples have two stronger green emission bands centered at 528 and 548 nm and a weak red emission band centered at 673 nm, which correspond to the relaxation of Er^3＋ from ^2H11/2, ^4S3/2, and ^4F9/2 levels to the ground level ^4I15/2, respectively. Compared with B-site doped films, A-site doped films have a stronger integrated intensity of green emissions and a weaker relative intensity of red emissions. The differences could be explained by the crystalline quality and cross relaxation （CR） process.

Degradation of dyestuff wastewater using visible light in the presence of a novel nano TiO_2 catalyst doped with upconversion luminescence agent

A new upconversion luminescence agent, 40CdF2·60BaF2·0.8ErO3, was synthesized and its fluorescent spectra were determined. This upconversion luminescence agent can emit five upconversion fluorescent peaks shown in the fluorescent spectra whose wavelengths are all below 387 nm under the excitation of 488 nm visible light. This upconversion luminescence agent was mixed into nano rutile TiO2 powder by ultrasonic and boiling dispersion and the novel doped nano TiO2 photocatalyst utilizing visible light was firstly prepared. The doped TiO2 powder was charactered by XRD and TEM and its photocatalytic activity was tested through the photocatalytic degradation of methyl orange as a model compound under the visible light irradiation emitted by six three basic color lamps. In order to compare the photocatalytic activities, the same experiment was carried out for undoped TiO2 powder. The degradation ratio of methyl orange in the presence of doped nano TiO2 powder reached 32.5% under visible light irradiation at 20 h which was obviously higher than the corresponding 1.64% in the presence of undoped nano TiO2 powder, which indicate the upconversion luminescence agent prepared as dopant can effectively turn visible lights to ultraviolet lights that are absorbed by nano TiO2 particles to produce the electron-cavity pairs. All the results show that the nano rutile TiO2 powder doped with upconversion luminescence agent is a promising photocatalyst using sunlight for treating the industry dye wastewater in great force.

Upconversion Luminescence Properties of Ho^(3+),Tm^(3+),Yb^(3+) Co-Doped Nanocrystal NaYF_4 Synthesized by Hydrothermal Method

Nanocrystal of upconversion （UC） phosphor Ho^3＋, Tm^3＋ , and Yb^3＋ co-doped NaYF4 was prepared by the hydrothermal method in the presence of the complexing agent EDTA. Under 980 nm diode laser excitation, the impact of different concentrations of Ho^3＋ ion on the UC luminescence intensity was discussed. The law of luminescence intensity versus pump power shows that the 474 nm blue emission, 538 nm green emission, and 642 nm red emission are all due to the two-photon process, while the 450 nm blue emission is a three-photon process. The UC mechanism and processes were also analyzed. The sample was characterized by transmission electron microscopy （TEM） and X-ray diffraction （XRD）. The result shows that Ho^3＋ ,Tm^3＋ , and Yb^3＋ co-doped NaYF4 prepared by the hydrothermal method exhibits a hexagonal nanocrystal.

Upconversion luminescence of Y_2O_3:Er^(3+), Yb^(3+) nanoparticles prepared by a homogeneous precipitation method

Y2O3： Er^3＋, Yb^3＋ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm laser excitation. The results of XRD showed that the obtained Y2O3：Er^3＋,Yb^3＋ nanoparticles were of a cubic structure. The average crystallite sizes calculated were in the range of 28-40 nm. Green and red upconversion emission were observed, and attributed to ^2H11/2,^4S3/2→^4I15/2 and ^4F9/2→^4I15/2 transitions of the ion, respectively. The ratio of the intensity of green emission to that of red emission drastically changed with a change in the EDTA 2Na concentration. In the sample synthesized without EDTA, the relative intensity of the green emission was weaker than that of the red emission. The relative intensities of green emission increased with the increased amount of EDTA 2Na used. The possible upconversion luminescence mechanisms were discussed.

Upconversion properties of Y_2O_3:Er films prepared by sol-gel method

Y2O3：Er^3＋ films were prepared by a simple sol-gel process. The structural properties of Y2O3：Er^3＋ films were characterized with X-ray diffraction, Fourier transform infrared spectroscopy and field emission scanning electron microscopy. The results indicated that the Y2O3：Er^3＋ films might have high upconversion efficiency because of their low vibrational energy. Under 785 and 980 nm laser excitation, the samples showed green （^2H11/2→^4I15/2, ^4S3/2→^4I15/2） and red （^4F9/2→^4I15/2） upconversion emissions. The upconversion mechanisms were studied in detail through laser power dependence. Excited state absorption and energy transfer process were discussed as possible upconversion mechanisms. The cross relaxation process in Er^3＋ was also investigated.

Synthesis and upconversion luminescence properties of NaYF_4:Yb^(3+)/Er^(3+) microspheres

Cubic NaYF4：Yb^3＋（20%）/Er^3＋（1%） microspheres were synthesized by EDTA-assisted hydrothermal method. Under 980 nm excitation, ultraviolet （^4G11/2→^4I15/2）, violet （^2H9/2→^4I15/2）, green （^4F7/2→^4I15/2, 2H11/2→^4I15/2, and ^4S3/2→^4I15/2）, and red （^4F9/2→^4I15/2） upconversion fluorescence were observed. The number of laser photons absorbed in one upconversion excitation process, n, was determined to be 3.89, 1.61, 2.55, and 1.09 for the ultraviolet, violet, green, and red emissions, respectively. Obviously, n=3.89 indicated that a four-photon process was involved in populating the ^4G11/2 state, and n=2.55 indicated that a three-photon process was involved in populating the ^4F7/2/^2H11/2/^4S3/2 levels. For the violet and red emissions, the population of the states ^2H9/2 and ^4F9/2 separately came from three-photon and two-photon processes. The decrease of n was well explained by the mechanism of competition between linear decay and upconversion processes for the depletion of the intermediate excited states.

Effect of Yb^(3+) concentration on the structures and upconversion luminescence properties of Y_2O_3:Er^(3+) ultrafine phosphors

Y2O3：Er^3＋ ultrafine phosphors with a varying Yb^3＋ ion concentration were prepared by a urea homogeneous precipitation method. The results of XRD show that all the samples are of a pure cubic structure and the average crystallite sizes can be calculated as 45, 34, and 28 nm for Y2O3：Er^3＋ ultrafine phosphors with Yb^3＋ ion concentrations of 0, 10%, and 20%, respectively. The lattice constant and cell volume of the ultrafine phosphors decrease with enhancing Yb^3＋ ion concentration. The upconversion luminescence spectra of all the samples were studied under 980 nm laser excitation. The strong green and red upconversion emission were observed, and attributed to the ^2H11/2→^4I15/2, ^4S3/2 → ^4I15/2 and ^4F9/2 →^4I15/2 transitions of Er^3＋, respectively. The intensity of red emission increases with increasing Yb^3＋ ion concentration. The effect of Yb^3＋ ion concentration on the structures and upconversion luminescence mechanism were discussed.

Molecularly imprinted polymer based on upconversion nanoparticles for highly selective and sensitive determination of Ochratoxin A

A novel molecularly imprinted polymer (MIP) based on upconversion nanoparticles (UCNPs) was successfully synthesized for determination of Ochratoxin A (OTA). The MIP was developed on the silica-coated UCNPs using N-(1-hydroxy-2-naphthoyl amido)-(L)-phenylalanine (HNA-Phe) as the alternative template. The final composite combined the advantages of the high selectivity of MIP with the high fluorescence intensity of UCNPs which was selective and sensitive to OTA. Under the optimal condition, the fluorescence intensity of UCNPs@SiO2@MIP decreases linearly when the concentration of OTA increases from 0.05 to 1.0 mg/L. The detection limit of OTA with the method was 0.031 mg/L. At three spiked concentration levels (50, 100 and 200 μg/kg), the recovery ranges of OTA in corn, rice and feed are 88.0%–91.6%, 80.2%–91.6% and 89.2%–90.4%, respectively.

Upconversion Nanoparticles-Encoded Hydrogel Microbeads-Based Multiplexed Protein Detection

Fluorescently encoded microbeads are in demand for multiplexed applications in different fields.Compared to organic dye-based commercially available Luminex's x MAP technology, upconversion nanoparticles(UCNPs) are better alternatives due to their large antiStokes shift, photostability, nil background, and single wavelength excitation. Here, we developed a new multiplexed detection system using UCNPs for encoding poly(ethylene glycol) diacrylate(PEGDA) microbeads as well as for labeling reporter antibody. However, to prepare UCNPs-encoded microbeads, currently used swellingbased encapsulation leads to non-uniformity, which is undesirable for fluorescence-based multiplexing. Hence,we utilized droplet microfluidics to obtain encoded microbeads of uniform size, shape, and UCNPs distribution inside. Additionally, PEGDA microbeads lack functionality for probe antibodies conjugation on their surface.Methods to functionalize the surface of PEGDA microbeads(acrylic acid incorporation, polydopamine coating)reported thus far quench the fluorescence of UCNPs. Here,PEGDA microbeads surface was coated with silica followed by carboxyl modification without compromising the fluorescence intensity of UCNPs. In this study, droplet microfluidics-assisted UCNPs-encoded microbeads of uniform shape, size, and fluorescence were prepared.Multiple color codes were generated by mixing UCNPs emitting red and green colors at different ratios prior to encapsulation. UCNPs emitting blue color were used to label the reporter antibody. Probe antibodies were covalently immobilized on red UCNPs-encoded microbeads for specific capture of human serum albumin(HSA) as a model protein. The system was also demonstrated for multiplexed detection of both human C-reactive protein(hCRP) and HSA protein by immobilizing anti-h CRP antibodies on green UCNPs.

Upconversion Luminescence of Ce^(3+) Doped BK7 Glass by Femtosecond Laser Irradiation

Near-infrared to visible upconversion luminescence was observed in a multicomponent silicate （BK7） glass containing Ce^3 ＋ ions under focused infrared femtosecond laser irradiation. The emission spectra show that the upconversion luminescence comes from the 4f-5d transition of the Ce^3 ＋ ions. The relationship between the intensity of the Ce^3 ＋ emission and the pump power reveals that a three-photon absorption predominates in the conversion process from the near-infrared into the blue luminescence. The analysis of the upconversion mechanism suggests that the upconversion luminescence may come from a three-photon simultaneous absorption that leads to a population of the 5d level in which the characteristic luminescence occurs.

TiO_2 composite nanotubes embedded with CdS and upconversion nanoparticles for near infrared light driven photocatalysis

We report a colloidal process to coat a layer of TiO2onto SiO2composite nanofibers containing embedded CdS and upconversion nanoparticles(UCNPs).The SiO2composite nanofibers were fabricated by electrospinning.To improve the energy transfer efficiency,UCNPs and CdS nanoparticles were bound in close proximity to each other within the SiO2matrix.β‐NaYF4:Yb(30%),Tm(0.5%)@NaYF4:Yb(20%),Er(2%)core–shell nanoparticles were used as nanotransducers for near infrared light.These nanoparticles exhibited enhanced upconversion fluorescence compared withβ‐NaYF4:Yb(30%),Tm(0.5%)orβ–NaYF4:Yb(30%),Tm(0.5%)@NaYF4nanoparticles.The morphologies,size and chemical compositions have been extensively investigated using field emission scanning electron microscopy(FESEM),transmission electron microscopy(TEM),X‐ray diffraction(XRD)and X‐ray photoelectron spectra(XPS),respectively.The TEM images showed that the TiO2composite nanotubes were embedded with a large amount of UCNPs and CdS nanoparticles.The composite TiO2nanotubes degraded more than90%of rhodamine B(RhB)dye during20min of irradiation by simulated solar light.In particular,more than50%of RhB was decomposed in70min,under irradiation of near infrared light(NIR).This high degradation was attributed to the full spectrum absorption of solar light,and the enhanced transfer efficiency for near infrared light.The as‐prepared nanostructures can harness solar energy,and provide an alternative to overcome energy shortages and environmental protection.

Recent progress in the green synthesis of rare-earth doped upconversion nanophosphors for optical bioimaging from cells to animals

Rare-earth doped upconversion nanophosphors(UCNPs), which convert low energy near-infrared(NIR) photons into high energy photons such as ultraviolet, visible light and NIR light, have found various applications in optical bioimaging. In this review article, we summarize recent advances in the synthesis and applications of UCNPs achieved by us and other groups in the past few years. The approaches for the synthesis of UCNPs are presented,with an emphasis on the role of green chemistry in the advancement of this field, followed by a focused overview on their latest applications in optical bioimaging from subcellular structures through cells to living animals. Challenges and opportunities for the use of UCNPs in biomedical diagnosis and therapy are discussed.

Study on the green upconversion saturation in Er^(3+) doped oxyfluoride tellurite glass

The upconversion emission spectra of Er^3＋ doped oxyfluoride tellurite glasses excited by 808 nm laser diode （LD） were measured. The dependence of 550 nm upconversion emission on the excitation intensity was analyzed. Quadratic intensity dependence was only observed at weak excitation intensity. With increasing the excitation intensity, saturation was turned out. The experimental results were fitted to a model based on the rate equations.

Preparation and upconversion luminescence of YAG(Y_3Al_5O_(12)):Yb^(3+),Ho^(3+) nanocrystals

Cubic YAG：Yb3＋, Ho3＋ pure phase nanocrystals were synthesized by using coprecipition nitrate and ammonium hydrogen carbonate as raw materials.After calcining the precipitates at 800 °C, the resultant YAG：Yb3＋, Ho3＋ nanocrystals were nearly spheric and the particle size was about 40 nm.Intense upconversion spectra were observed on the powder compact pumped by a 980 nm continuous wave diode laser, and green emission centered at 549 nm, red emission centered at 667 nm, and NIR centered at 760 nm were all due to two photons process, which originated from 5S2（5F4）→5I8, 5F5→5I8, and 5S2（5F4）→5I7 transitions, respectively.

Infrared to ultraviolet upconversion luminescence in Nd^(3+) doped nano-glass-ceramic

Nd^3＋ doped transparent oxyfiuoride glass ceramic containing β-YF3 nanocrystals was prepared and the upconversion luminescence behaviors of Nd^3＋ in the precursor glass and glass ceramic were investigated. Under 796 nm laser excitation, ultraviolet upconversion emissions of Nd^3＋ ions at 354 nm （^4D3/2→^4I11/2） and 382 nm （^4D3/2→^4I11/2） were observed at room temperature. Power dependence analysis demonstrated that three-photon upconversion processes populated the ^4D3/2 excited state. In comparison with those of the precursor glass, the ultraviolet emissions were enhanced by a factor of 500 in the glass ceramic, which was attributed to the change in the ligand field of Nd^3＋ ions and the decrease in phonon energy because of the partition of Nd^3＋ ions into the β-YF3 nanocrystals after crystallization.

Three-color upconversion luminescence of rare earth codoped oxyhalide tellurite glasses

The red, green, and blue upconversion properties of Er^3＋/Tm^3＋/Yb^3＋-codoped oxyhalide tellurite glasses were studied under 980 nm LD excitation. The intense red （657 nm）, green （530 and 545 nm）, and blue （476 nm） emissions were simultaneously observed at room temperature. The results showed that the mixed halide modified tellurite glass （TZFCB） had strong upconversion emissions. The effect of halide on upconversion intensity was observed and discussed, and possible upconversion mechanisms were evaluated. The intense red, green, and blue upconversion luminescence of Er^3＋/Tm^3＋/Yb^3＋-codoped oxyhalide tellurite glasses might be a potentially useful material for developing three-dimensional displays applications.

Synthesis and Upconversion Luminescence of LaF_3:Yb^(3+),Er^(3+)/SiO_2 Core/Shell Microcrystals

LaF3：Yb^3＋ , Er^＋ microcrystals were synthesized by a hydrothermal method, and then, the LaF3： Yb^3＋ , Er^＋ microcrystals were coated with silica. Phase identification of LaF3： Yb^3＋ , Er^＋ and LaF3： Yb^3＋ , Er^＋/SiO2 was performed via XRD. The TEM image showed that the size of LaF3： Yb^3＋ , Er^＋ was 150 nm and LaF3： Yb^3＋ , Er^＋/SiO2 presented clearly a core/shell structure with 20 nm shell thickness. The upconversion spectra of LaF3： Yb^3＋ , Er^＋ and LaF3： Yb^3＋ , Er^＋/SiO2 in solid state and in ethanol were studied with a 980 nm diode laser as the excitation source. The upconversion spectra showed that the silica shell had little effect on the properties of fluorescence of the LaF3：Yb^3＋ , Er^＋ microcrystals. At the same time, the green luminescence photo of LaF3： Yb3＋, Er3＋/SiO2 in the PBS buffer was obtained, which indicated that the LaF3： Yb^3＋ , Er^＋/SiO2 could be used in biological applications.