Development of a 10-litre pilot scale micro-nano bubble (MNB)-enhanced photocatalytic system for wastewater treatment.

A 10-litre pilot scale micro-nano bubble (MNB)-enhanced photocatalytic degradation system was developed using ZnO as the photocatalyst and salicylic acid (SA) as the model pollutant. The effectiveness of the MNB/ZnO/UV system was systematically compared with those of MNB, UV, MNB/UV, MNB/ZnO and ZnO/UV degradation systems. The effects of process parameters, including catalyst dosage, pollutant concentration, air-intake rate, pH and salt content on the degradation of SA, were comprehensively investigated. Optimum performance was obtained at neutral conditions with a catalyst dosage of 0.3 g/L and an air-intake rate of 0.1 L/min. For the degradation of SA, a kinetic constant of 0.04126/min was achieved in the MNB/ZnO/UV system, which is 4.5 times greater than that obtained in the conventional ZnO/UV system. The substantial increase in the degradation rate can be attributed to that the air MNB not only enhanced the gas-liquid mass transfer efficiency but also elevated the concentration of dissolved oxygen. A 10-litre pilot scale MNB/ZnO/UV system was successfully applied to the purification of lake water and river water, demonstrating great application potential for wastewater treatment.

Dimethyl Sulfoxide: An Ideal Electrochemical Probe for Hydroxyl Radical Detection.

In situ and real-time determination of hydroxyl radicals (•OH) in physiological and pathological processes is a great challenge due to their ultrashort lifetime. Herein, an electrochemical method was developed by using dimethyl sulfoxide (DMSO) as a trapping probe for rapid determination of •OH in aqueous solution. When DMSO reacted with •OH, an intermediate product methane sulfinic acid (MSIA) was formed, which can be electrochemically oxidized to methanesulfonic acid (MSA) on the glassy carbon electrode (GCE), resulting in a distinct voltammetric signal that is directly proportional to the concentration of •OH. Other commonly encountered reactive oxygen species (ROS), including hypochlorite anions (ClO-), superoxide anions (O2•-), sulfate radicals (SO4•-), and singlet oxygen (1O2), have showed no interference for •OH determination. Thus, an electrochemical method was developed for the determination of •OH, which exhibits a wide linear range (0.4-5120 µM) and a low limit detection of 0.13 µM (S/N = 3) and was successfully applied for the quantification of •OH in aqueous extracts of cigarette tar (ACT). Alternatively, the same reaction mechanism is also applicable for the determination of DMSO, in which a linear range of 40-320 µM and a detection limit 13.3 µM (S/N = 3) was achieved. The method was used for the evaluation of DMSO content in cell cryopreservation medium. This work demonstrated that DMSO can serve as an electrochemical probe and has valuable application potential in radical study, biological research, and environmental monitoring.

Fabrication of a disposable aptasensing chip for simultaneous label-free detection of four common coexisting mycotoxins.

BACKGROUND: Coexisting multiple mycotoxins in food poses severe health risks on humans due to the augmented toxicity. Current multiplex detection methods for mycotoxins have evolved from instrumental analyses to rapid methods based on the specific recognition of antibody/aptamer using different signal transducers. However, nearly all of the reported aptasensors for multiple mycotoxins detection require external labels and can only simultaneous detection of two mycotoxins due to the limitation of distinguishable labels. The tedious labeling process definitely increases the operation complexity and the detection cost. Therefore, rapid method for simultaneous label-free detection of multiple mycotoxins in cereals is urgently needed. RESULTS: A disposable aptasensing chip was designed for simultaneous label-free detection of fumonisin B1 (FB1), aflatoxin B1 (AFB1), zearalenone (ZEN), and ochratoxin A (OTA) in one sample. Specifically, ITO conductive glass was divided into a rectangle (35 × 25 mm) and then etched by laser to set aside the required four ITO working electrodes (6 mm in diameter) with respective conductive channels. Gold nanoparticles were electrodeposited on the working electrodes to provide abundant anchoring sites for thiolated aptamers immobilization. On this basis, a disposable aptasensing chip for simultaneous label-free detection of four common coexisting mycotoxins has been developed, which used electrochemical impedance spectroscopy as transducer to measure direct biorecognition of the aptamer and corresponding target. This aptasensing chip provided wide linear ranges of 5-1000, 10-250, 10-1250, 10-1500 ng/mL for FB1, AFB1, ZEN, OTA, respectively, with the respective detection limit of 2.47, 3.19, 5.38, 4.87 ng/mL (S/N = 3). SIGNIFICANCE AND NOVELTY: This aptasensing chip shows fantastic characteristics of great simplicity and portability, easy operation, and multiple mycotoxins recognition. They are easy to produce on a large scale at low cost and the design concept can be easily expanded to screen a large panel of coexisting targets. This work provides a new avenue for multi-target detection and represents a substantial advance toward food quality and safety monitoring or other fields.

An upgraded 2D nanosheet-based FRET biosensor: insights into avoiding background and eliminating effects of background fluctuations.

We demonstrated a new class of 2D nanosheet-based FRET biosensor utilizing vertically oriented MoS2 nanosheets on a magnetic nanocarrier. Compared with the non-separated biosensor under identical conditions, this upgraded one can avoid the background signal of the system and eliminate the effects of background fluctuations, which produces more excellent detection methods.

Controlling the ligands of CdZnTe quantum dots to design a super simple ratiometric fluorescence nanosensor for silver ion detection.

A super simple ratiometric fluorescence nanosensor has been fabricated by controlling the ligands of CdZnTe quantum dots (QDs), allowing the sensitive and visual detection of silver ions (Ag+). The green-emitting L-cysteine-protected CdZnTe QDs (Lcys-CdZnTe QDs) had a specific response to Ag+ and were used as the reporting probe, while the red-emitting N-acetyl-L-cysteine-protected CdZnTe QDs (NAC-CdZnTe QDs) showed no obvious response to all tested metal ions and were selected as the reference probe. Simply mixing them without any encapsulated synthesis ultimately produced a time-saving, low-cost detection method, allowing the sensitive and visual detection of Ag+ in samples. The proposed nanosensor exhibited a linear range of 0.5-4.0 µM along with a detection limit of 0.17 µM, and has been successfully applied in real tap water and lake water samples. This nanosensor also showed obvious color changes in the detection process and has potential in visual semi-quantitative detection. Our approach may provide a general and feasible strategy for designing ratiometric fluorescence nanosensors, which will attract a wide range of interest in sensing-related fields.

Gold nanoparticles mediated designing of versatile aptasensor for colorimetric/electrochemical dual-channel detection of aflatoxin B1.

This work is aimed to develop of a new class of versatile aptasensor to specifically detect aflatoxin B1 (AFB1) using dual-channel detection method. To achieve this objective, gold nanoparticles (AuNPs) having peroxidase-like activity and capability of promoting silver deposition were used as the versatile label for both colorimetric and electrochemical techniques. First of all, aptamer (apt) modified Fe3O4@Au magnetic beads (MBs-apt) and cDNA modified AuNPs (cDNA-AuNPs) were prepared to use as capture probes and signal probes, respectively. Taking advantage of hybridization reaction between apt and cDNA, these two probes were coupled with each other to generate MBs-apt/cDNA-AuNPs bioconjugations. The high affinity between apt and AFB1 made cDNA-AuNPs detached from MBs-apt, and the released signal probes were separated and collected using an external magnetic field and used for both colorimetric and electrochemical detection channels. The dual-channel signals were directly proportional to logarithm of AFB1 concentration within the ranges of 5-200 ng mL-1 and 0.05-100 ng mL-1. The detection limit can reach as low as 35 pg mL-1 and 0.43 pg mL-1 for colorimetric and electrochemical channel, respectively. Moreover, the proposed aptasensor has been successfully applied to determine AFB1 in corn samples with satisfactory results. This dual-channel detection method can not only improve the detection precision and diversity significantly, but also can reduce the false-negative and-positive rates in food quality monitoring. We believe we have provided a general strategy with the convincing dual-readout mode which possess great promising in all of the aptamer related fields.

Quantitative Estimation of Oxidative Stress in Cancer Tissue Cells Through Gene Expression Data Analyses.

Quantitative assessment of the intracellular oxidative stress level is a very important problem since it is the basis for elucidation of the fundamental causes of metabolic changes in diseased human cells, particularly cancer. However, the problem proves to be very challenging to solve in vivo because of the complex nature of the problem. Here a computational method is presented for predicting the quantitative level of the intracellular oxidative stress in cancer tissue cells. The basic premise of the predictor is that the genomic mutation level is strongly associated with the intracellular oxidative stress level. Based on this, a statistical analysis is conducted to identify a set of enzyme-encoding genes, whose combined expression levels can well explain the mutation rates in individual cancer tissues in the TCGA database. We have assessed the validity of the predictor by assessing it against genes that are known to have anti-oxidative functions for specific types of oxidative stressors. Then the applications of the predictor are conducted to illustrate its utility.

Identification of an Individualized Prognostic Signature Based on the RWSR Model in Early-Stage Bladder Carcinoma.

Bladder cancer (BLCA) is the fourth common cancer among males in the United States, which is also the fourth leading cause of cancer-related death in old males. BLCA has a high recurrence rate, with over 50% of patients which has at least one recurrence within five years. Due to the complexity of the molecular mechanisms and heterogeneous cancer feature, BLCA clinicians find it hard to make an efficient management decision as they lack reliable assessment of mortality risk. Meanwhile, there is currently no screening suitable prognostic signature or method recommended for early detection, which is significantly important to early-stage detection and prognosis. In this study, a novel model, named the risk-weighted sparse regression (RWSR) model, is constructed to identify a robust signature for patients of early-stage BLCA. The 17-gene signature is generated and then validated as an independent prognostic factor in BLCA cohorts from GSE13507 and TCGA_BLCA datasets. Meanwhile, a risk score model is developed and validated among the 17-gene signature. The risk score is also considered an independent factor for prognosis prediction, which is confirmed through prognosis analysis. The Kaplan-Meier with the log-rank test is used to assess survival difference. Furthermore, the predictive capacity of the signature is proved through stratification analysis. Finally, an effective patient classification is completed by a combination of the 17-gene signature and stage information, which is for better survival prediction and treatment decisions. Besides, 11 genes in the signature, such as coiled-coil domain containing 73 (CCDC73) and protein kinase, DNA-activated, and catalytic subunit (PRKDC), are proved to be prognosis marker genes or strongly associated with prognosis and progress of other types of cancer in published literature already. As a result, this paper would more accurately predict a patient's prognosis and improve surveillance in the clinical setting, which may provide a quantitative and reliable decision-making basis for the treatment plan.

Pressure-dependent distinct luminescent evolutions of pyrene and TPA-Py single crystals.

The effects of the high pressure on two single crystals, pyrene and N,N-diphenyl-4-(pyren-1-yl)aniline (TPA-Py), were studied by in situ fluorescent and Raman spectroscopies. During the compression, the pyrene with one structureless excimer emission band showed a continuous bathochromic-shift. In contrast, with the pressure increasing to 10.36 GPa, TPA-Py previously dominated with the hybridized local and charge transfer (HLCT) excited state gradually exhibited a new band at longer wavelengths, which is assigned to a new excited state species with the intramolecular charge transfer (ICT) state, caused by the pressure-induced changes on its molecular configuration. Accompanied by the spectral changes, a sequential color variation from blue to cyan was observed, giving a change to yellow and then red. The significant broadening of the full-width half-maximum (FWHM) of the TPA-Py is observed due to the enhanced dipole-dipole interaction and the existence of pressure gradient. Both pyrene and TPA-Py showed the delayed recovery of the luminescence in the compression-decompression cycle, which results from the poor reversibility of electronic structure caused by the compression-induced piezochromic effect. Furthermore, the evolutions of the Raman spectra of pyrene and TPA-Py indicated that the pressure-induced reversible transformation is caused by the molecular conformational change. This study is a deeper understanding of the structure-property relation of the HLCT species and will be a helpful reference for the regulation of photoluminescence in these intramolecular electron donor-acceptor crystal materials.

High brightness blue light-emitting diodes based on CsPb(Cl/Br)3 perovskite QDs with phenethylammonium chloride passivation.

All inorganic perovskite quantum dots (QDs) (CsPbX3, X = Cl, Br, I) have been applied on light-emitting devices (LEDs) in recent years due to their excellent optical and optoelectronic properties. However, blue-light emitting perovskite QD LEDs (PQD-LEDs) exhibit poor performances compared with their green- and red-light emitting counterparts. Herein, we fabricated high performing blue-light emitting PQD-LEDs based on phenethylammonium chloride (PEACl) modified CsPb(Cl/Br)3 QDs. Firstly, the PEA-CsPbCl3 QDs were synthesized by introducing certain amounts of PEACl in the conventional hot-injection synthesis process. The merit of our synthesis lies in the fact that not only the Cl vacancies of CsPbCl3 QDs are efficiently modified by introducing the PEACl precursor, but also the partial long-chain organic ligands (OLA) capping on the surface of CsPbCl3 QDs are simultaneously replaced by shorter PEACl chains. Consequently, the PEA-CsPbCl3 QDs emitting at 410 nm with a PLQY of 62.3% were achieved. Furthermore, to meet the requirement of display applications, we exchanged Cl- with Br- ions at room temperature to precisely control the blue emission in the 460-470 nm spectral region and with a maximum PLQY of 80.2% at 470 nm. Finally, the PQD-LEDs based on PEA-CsPb(Cl/Br)3 perovskite QDs emitting at 462, 465, 468 and 470 nm were fabricated. The PQD-LEDs exhibit a maximal EQE of 2.15% and luminance of 620 cd m-2, which provides the highest value of luminance for the PQD-LEDs in the blue spectral range that satisfies the requirement of practical display applications.

White light-emitting devices based on ZnCdS/ZnS and perovskite nanocrystal heterojunction.

Perovskite white light-emitting devices (WLEDs) without intercalation layers have not been achieved due to the ion exchange. Although the intercalation layers prevent ion exchange between perovskite nanocrystals (NCs), it also creates a new problem of charge imbalance and the structure becomes more complex. In this study, blue emitting ZnCdS/ZnS NCs with high quantum yield and stability are introduced to work with the yellow emission from CsPb(Br/I)3 perovskite NCs for WLEDs. The WLEDs are constituted of ITO/ZnO/PEI/ZnCdS/ZnS NCs/CsPb(Br/I)3 NCs/TCTA/MoO3/Au. This design avoids ion exchange between different perovskites NCs, and realizes white light emission by simple fabrication. As a result, we achieved the white light coordinates of (0.34, 0.34) and a correlated color temperature of 5153 K.

Remarkable pressure-induced emission enhancement based on intermolecular charge transfer in halogen bond-driven dual-component co-crystals.

A series of two-component co-crystals driven by IN interactions based on the bipyridine (BIPY) chromophore with one among three different co-former building blocks, iodopentafluorobenzene (IPFB), 1,4-diiodotetrafluorobenzene (DITFB) and 1,3,5-trifluoro-2,4,6-triiodobenzene (IFB), were prepared and analysed via infared spectroscopy and single-crystal X-ray diffraction. By comparing the IN distances in the co-crystal structures, we found that the higher the -F ratio in the building blocks the closer the contact of the IN bond, enhancing the intermolecular interactions in these co-crystals as well. That is, the positive electrostatic potential on the iodine atom(s) in the co-formers was enhanced by the presence of strong electron-withdrawing groups. The distinct spectroscopic behaviours (fluorescence and Raman spectra) among the two-component BIPY co-crystal systems in response to hydrostatic pressure were also investigated. Interestingly, the fluorescence of BIPY-DITFB presented intriguing abnormal evolution from dark to bright, suggesting a new charge transfer state due to the decreased intermolecular distance and the enhanced IN interactions. Theoretical simulations by Materials Studio also showed the shortened IN distance and the increased angle of C-IN, evidencing the enhanced IN interactions. In contrast, BIPY-IFB showed only slightly enhanced fluorescence intensity at 550 nm consistent with BIPY-DITFB. Once the pressure was relieved, both the Raman and fluorescence spectra for BIPY co-crystal systems entirely self-recovered. Remarkable emission enhancement in a solid-state co-crystal has been rarely reported in previous publications and in fact, this study paves a unique way for designing and developing novel stimuli-responsive photo-functional materials.

Considerably enhanced exciton emission of CsPbCl3 perovskite quantum dots by the introduction of potassium and lanthanide ions.

The photoluminescence quantum yield (PLQY) of blue-violet emission of CsPbCl3 quantum dots (QDs) is still low, which has limited their application in multi-colour displays. It is important to search for efficient perovskite phosphors within this wavelength range. In this work, we first considerably enhanced the photoluminescence quantum yield (PLQY) of the CsPbCl3 QDs from 3.2 to 10.3% by the introduction of potassium ions (K+). Then, various lanthanide elements (La, Y, Eu, Lu) were further doped into KxCs1-xPbCl3 QDs. The lanthanide doped KxCs1-xPbCl3 QDs still demonstrated emissions around 408 nm and the PLQY was further improved to 31%. Finally, we carried out anion exchange by gradually substituting chlorine with bromine. Efficient and tunable emissions ranging from 408-495 nm were obtained, with a maximum PLQY of 90%. This work provides a new approach to improve the efficiency of the blue-violet light of perovskite QDs.

Investigation of supramolecular interaction in 4, 4'-bipyridine crystal by hydrostatic pressure spectroscopies.

The luminescence and structural changes of 4, 4'-bipyridine in the crystal and powder forms under the effect of high pressure applied by a diamond anvil cell has been investigated through the fluorescence and Raman spectroscopies. In its single crystal structure, the 4, 4'-bipyridine molecules are paralleled arranged with the identifiable CH⋯N and π⋯π interactions among molecules. However, in the powder form, these intermolecular interactions nearly diminish. The 4, 4'-bipyridine crystal shows the obvious bathochromic-shifting of the emission band, which is different from the powder sample that displays a fixed luminescent band during compression. Additionally, the Raman bands of them both show shifts to higher wavenumbers as different degrees. The detailed peak assignments are performed based on the theoretical calculation through B3LYP method. Comparisons in spectral behaviors between the crystal and powder under compression show the crystal form exhibits a superior mechanochromic performance relative to the powder one, because the intermolecular interactions in the crystal form play dominating roles and they can be easily tuned along with pressure in such a highly ordered structure compared to the powder form. The relation investigation between property and supramolecular interactions not only makes deeper understanding in the mechanochromic mechanisms of 4, 4'-bipyridine, but also gives a helpful reference for the molecular designs of coordination polymers and co-crystals with 4, 4'-bipyridine involved.

Highly efficient and stable blue-emitting CsPbBr3@SiO2 nanospheres through low temperature synthesis for nanoprinting and WLED.

Inorganic perovskite quantum dots (QDs) have attracted wide attention in display and solid-state lighting because of their easily tunable band-gaps and high photoluminescence quantum yields (PLQY) of green light emission. However, some drawbacks limit their practical applications, including the low PLQY of blue light emission and the instability in the moisture environment. In this work, efficient blue-light emitting CsPbBr3 perovskite QDs with PLQY of 72% were developed through a bandgap engineering approach. The achieved blue-light emitting PLQY is much higher than the values acquired in the inorganic perovskite QDs in the literature. And the emission color of the as-prepared QDs can be facially tuned by only adjusting the reaction temperature. Further, the mono-dispersed perovskite QDs@SiO2 composites were constructed benefiting from the low temperature synthesis. The optical performance of the QDs could be well persisted even in the moisture environment. Finally, the as-prepared QDs@SiO2 composite was fabricated as the QD ink on the anti-counterfeit printing technology, from which the obtained pattern would emit varied color under UV lamp. And the as-prepared composites was also applied for fabricating WLED, with Commission Internationale de l'Eclairage (CIE) color coordinates of (0.33, 0.38) and power efficiency of 32.5 lm W-1, demonstrating their promising potentials in solid-state lighting.

White light emission in Bi3+/Mn2+ ion co-doped CsPbCl3 perovskite nanocrystals.

Colloidal perovskite nanocrystals (NCs), especially the fully inorganic cesium lead halide (CsPbX3, X = Cl, Br, I) NCs, have been considered as promising candidates for lighting and display applications due to their narrow band emission, tunable band gap and high photoluminescence quantum yields (QYs). However, owing to the anion exchange in the CsPbX3 NCs, stable multi-color and white light emissions are difficult to achieve, thus limiting their practical optoelectronic applications. In this work, dual ion Bi3+/Mn2+ codoped CsPbCl3 perovskite NCs were prepared through the hot injection method for the first time to the best of our knowledge. Through simply adjusting the doping ion concentrations, the codoped NCs exhibited tunable emissions spanning the wide range of correlated color temperature (CCT) from 19 000 K to 4250 K under UV excitation. This interesting spectroscopic behaviour benefits from efficient energy transfer from the perovskite NC host to the intrinsic energy levels of Bi3+ or Mn2+ doping ions. Finally, taking advantage of the cooperation between the excitonic transition of the CsPbCl3 perovskite NC host and the intrinsic emissions from Bi3+ and Mn2+ ions, white light emission with the Commission Internationale de l'Eclairage (CIE) color coordinates of (0.33, 0.29) was developed in the codoped CsPbCl3 NCs.

Carbon dot/polyvinylpyrrolidone hybrid nanofibers with efficient solid-state photoluminescence constructed using an electrospinning technique.

Carbon dots (CDs) are the promising candidates for application in optoelectronic and biological areas due to their excellent photostability, unique photoluminescence, good biocompatibility, low toxicity and chemical inertness. However, the self-quenching of photoluminescence as they are dried into the solid state dramatically limits their further application. Therefore, realizing efficient photoluminescence and large-scale production of CDs in the solid state is an urgent challenge. Herein, solid-state hybrid nanofibers based on CDs and polyvinylpyrrolidone (PVP) are constructed through an electrospinning process. The resulting solid-state hybrid PVP/CD nanofibers present much enhanced photoluminescence performance compared to the corresponding pristine colloidal CDs due to the decrease in non-radiative recombination of electron-holes. Owing to the suppressed self-quenching of CDs, the photoluminescence quantum yield is considerably improved from 42.9% of pristine CDs to 83.5% of nanofibers under the excitation wavelength of 360 nm. This has great application potential in optical or optoelectronic devices.

A facile and universal strategy for preparation of long wavelength emission carbon dots.

Carbon dots (CDs) have emerged as a promising new type of fluorescent nanomaterial, although one of their main problems is the tuning of the emission wavelength toward the long wavelength region. In this work, the influence of reaction solvents to emission of CDs was systematically studied using four groups of classical precursors (citric acid individually mixed with four nitrogenous organic compounds). Water and toluene were selected to represent the hydrophobic and hydrophilic reaction medium, respectively. It is interesting to observe that in toluene solvent, all the CD products yield two emission bands of blue and yellow light, and the relative intensity of the yellow to blue can be finely tuned by the precursors. In contrast, the CDs formed in water only demonstrate blue emission. Systematic studies indicate that the spectral change results from the content control of carbogenic/defect states to surface states and the energy transfer from the carbogenic/defect states to the surface states. Moreover, solid-state luminescent CD-polymers were fabricated that also demonstrated continuously tunable emission properties. This work provides a new strategy for recognizing the generation of long wavelength-emitting CDs.

Remarkable Enhancement of Upconversion Luminescence on Cap-Ag/PMMA Ordered Platform and Trademark Anticounterfeiting.

High brightness of upconversion luminescence (UCL) for a thinner layer of UC nanoparticles is significant for routine applications of effective trademark anticounterfeiting technology. In this work, efficient UCL of NaYF4:Yb3+,Er3+/Tm3+ was realized by combining a Ta2O5 dielectric layer on the cyclical island silver films supported by poly(methyl methacrylate) opal photonic crystals (PCs). The synergistic modulation of localized surface plasmon resonance and PC effect results in a significant improvement of the local electromagnetic field and an optimum UC enhancement of 145 folds. Furthermore, colorful pattern nanoprinting has been applied to this composite and used for trademark anticounterfeiting. The combination of angle-dependent PC effect and infrared-to-visible UCL represents a more advanced anticounterfeiting technique.

Synthesis and Luminescence Properties of Water Soluble α-NaGdF4/ß-NaYF4:Yb,Er Core-Shell Nanoparticles.

Hexagonal phase (ß) sodium rare earth tetrafluorides (NaREF4, RE = Y, Gd, Lu, et al.) are considered the ideal matrices for lanthanide (Ln) ions doped upconversion (UC) luminescence materials, because they can provide favorable crystal lattice structures for the doped luminescent Ln ions to make intensive emissions. However, the cubic phase (α) NaREF4 always preferentially forms at low reaction temperature in short time as it is dynamically stable. Therefore, it is hard to obtain small sized ß-NaREF4 via the traditional solvothermal method. In this paper, small sized ß-NaYF4:Yb,Er nanoparticles were synthesized by a heterogeneous-core-induced method via the solvothermal reaction. The heterogeneous α-NaGdF4/ß-NaYF4: Yb, Er core-shell structure was confirmed by the local elemental mapping. The formation mechanism of ß-NaYF4:Yb,Er shell on the surface of α-NaGdF4 core was explained in detail. We reasoned that a hetero interface with a lower lattice symmetric structure was produced by cation exchanges between the core and shell, which caused the preferential growth of anisotropic hexagonal phase shell. The existence of this hetero interface has also been proven by observation of Gd3+ UC emission.