Upconversion luminescence and temperature sensing performance of Er^(3+) ions doped self-activated KYb(MoO_(4))_(2) phosphors

In this work,a series of self-activated KYb(MoO_(4))_(2) phosphors with various x at% Er^(3+) doping concentrations(x=0.5,1,3,5,8,10,15) was synthesized by the solid-state reaction method.The phase structure of the as-prepared samples was analyzed by X-ray diffraction(XRD),XRD Rietveld refinement and Fourier transform infrared(FT-IR) spectroscopy.The as-prepared samples retain the orthorhombic structure with space group of Pbcn even Er^(3+) doping concentration up to 15 at%.High-purity upconversion(UC) green emission with green to red intensity ratio of 55 is observed from the as-prepared samples upon the excitation of 980 nm semiconductor laser and the optimum doping concentration of Er^(3+) ions in the self-activated KYb(MoO_(4))_(2) host is revealed as 3 at%.The strong green UC emission is confirmed as a two-photon process based on the power-dependent UC spectra.In addition,the fluorescence intensity ratios(FIRs) of the two thermally-coupled energy levels,namely ^(2)H_(11/2) and ^(4)S_(3/2).of Er^(3+) ions were investigated in the temperature region 300-570 K to evaluate the optical temperature sensor behavior of the sample.The maximum relative sensitivity(S_(R)) is determined to be 0.0069 K^(-1) at300 K and the absolute sensitivity(S_(A)) is determined to be 0.0126 K^(-1) at 300 K.The S_(A) of self-activated KYb(MoO_(4))2:Er^(3+)is almost twice that of traditional KY(MoO_(4))2:Er^(3+)/Yb^(3+)codoping phosphor.The results demonstrate that Er^(3+) ions doped self-activated KYb(MoO_(4))2 phosphor has promising application in visible display,trademark security and optical temperature sensors.

Theoretic and Experimental Studies on Titania Nanotube Doped with Ag Metal Ions

The electronic state density and energy bands of Ag-doped anatase TiO2 are studied by WIEN2k software package based on DFT. The calculation results show that the band-gap of anatase titania became bigger after doping with Ag metal ions. The band-gap transfers from 2.04 to 2.5 eV, but a new energy band appears among the forbidden band after the Ag atom substitution. The interband width of Ag-TiO2 is 0.17 eV, which is located at –0.07 eV; more excitation and jump routes are opened for the electrons. The lowest excitation energy can achieve 1.2 eV, which may allow the photons with lower energy （at longer wavelength, such as visible light） to be absorbed. Ag ions are implanted into the titania nanotube sample by MEVVA （Metal Vapor Vacuum Arc） implanter. The photo-electrochemical response and photo-degradation experiment of titania nanotube samples implanted with Ag ions are tested under UV and visible light; the results indicated that the performance of implanted titania naotubes is enhanced both under UV and visible light; it is worth mentioning that the photocurrent density can reach 0.145 mA/cm2 under visible light, which is 181 times higher than those of pure TiNT, and the k value of degradation methyl orange can obtain 0.30 h-1, which is 71 times higher than that of pure TiNT. All the experimental results are consistent well with the theoretic ones.

Optical properties and dynamic process in metal ions doped on CdSe quantum dots sensitized solar cells

In recent years, the nanostructure for solar cells have attracted considerable attention from scientists as a result of a promising candidate for low cost devices. In this work, quantum dots sensitized solar cells with effective performance based on a co-sensitized Cd S∕Cd Se：Mn2＋（or Cu2＋） nanocrystal, which was made by successive ionic layer absorption and reaction, are discussed. The optical, physical, chemical, and photovoltaic properties of quantum dots sensitized solar cells were sensitized to Mn2＋and Cu2＋dopants. Therefore, the short current（JSC）of the quantum dot sensitized solar cells is boosted dramatically from 12.351 mA∕cm2 for pure Cd Se nanoparticles to 18.990 mA∕cm2 for Mn2＋ions and 19.915 mA∕cm2 for Cu2＋ions. Actually, metal dopant extended the band gap of pure Cd Se nanoparticles, reduced recombination, enhanced the efficiency of devices, and improved the charge transfer and collection. In addition, Mn2＋and Cu2＋dopants rose to the level of the conduction band of pure Cd Se nanoparticles, which leads to the reduction of the charge recombination, enhances the lightharvesting efficiency, and improves the charge diffusion and collection. The results also were confirmed by the obtained experimental data of photoluminescence decay and electrochemical impedance spectroscopy.

Effect of Doped Alkali Metal Ions on the SO_(2) Capture Performance of MnO_(2) Desulfurization Materials at Low Temperature

Sulfur dioxide(SO_(2))emissions from diesel exhaust pose a serious threat to the environment and human health.Thus,desulfurization technology and the performance of desulfurization materials must be improved.In this study,MnO_(2) was modified with various alkali metal ions using the impregnation method to enhance its SO_(2) capture performance.The composites were characterized intensively by scanning electron microscopy,energydispersive X-ray spectroscopy,X-ray diffraction spectroscopy,and Brunauer-Emmett-Teller theory.The SO_(2) capture performance of these composites were measured via thermogravimetry,and the effect of doping with alkali metal ions on the SO_(2) capture performance of MnO_(2) was investigated.Results showed that the SO_(2) capture performance of MnO_(2) could be enhanced by doping with alkali metal ions,and the MnO_(2) composite doped with LiOH(2.0 mol/L)had the best SO_(2) capture capacity(124 mgSO_(2)/gMaterial),which was 18%higher than that of pure MnO_(2).Moreover,the type and concentration of alkali metal ions had varying effects on the SO_(2) capture performance of MnO_(2).In our experiment,the SO_(2) capture performance of the MnO_(2) doped with NaOH,LiCl,Na2CO3,K2CO3,and Li2CO3 composites were worse than that of pure MnO_(2).Therefore,the influences of the type and concentration of alkali metal ions to be doped into desulfurization materials must be considered comprehensively.

Rare earth doped CaCu_3Ti_4O_(12) electronic ceramics for high frequency applications

Ca1-xRxCu3Ti4O12(R=La,Y,Gd;x=0,0.1,0.2,0.3) electronic ceramics were fabricated by conventional solid-state reaction method.The microstructure and dielectric properties as well as impedance behavior were carefully investigated.XRD results showed that the secondary phases with the general formula R2Ti2O7 existed at grain boundaries of rare earth doped ceramics,which inhibited abnormal grain growth.The dielectric constant decreased from 4×105 in pure CaCu3Ti4O12(CCTO) ceramics to 2×103 with rare earth doping....

Urchin-like Na-doped zinc oxide nanoneedles for low-concentration and exclusive VOC detections

In the early-stage diagnosis of lung cancer,the low-concentration(<5 ppm)volatile organic compounds(VOCs)are extensively identified to be the biomarkers for breath analysis.Herein,the urchin-like sodium(Na)-doped zinc oxide(ZnO)nanoneedles were synthesized through a hydrothermal strategy with the addition of different contents of citric acid.The Na-doped ZnO gas sensor with a 3:1 molar ratio of Na^(+)and citric acid showed outstanding sensing properties with an optimal selectivity to various VOCs(formaldehyde(HCOH),isopropanol,acetone,and ammonia)based on working temperature regulation.Specifically,significantly enhanced sensitivity(21.3@5 ppm)compared with pristine ZnO(~7-fold),low limit of detection(LOD)(298 ppb),robust humidity resistance,and long-term stability of formaldehyde sensing performances were obtained,which can be attributed to the formation of a higher concentration of oxygen vacancies(20.98%)and the active electron transitions.Furthermore,the improved sensing mechanism was demonstrated by the exquisite band structure and introduction of the additional acceptor level,which resulted in the narrowed bandgap of ZnO.

Photocatalytic Inhibition of Cyanobacterial Growth Using Silver-doped TiO_2 under UV-C Light

Capacity of the silver-doped TiO2 under UV-C light to restrain cyanobacterial growth was explored with Anabaena sp. PCC 7120 and Microcystis aeruginosa as test species. The survival, chlorophyll bleaching, photosynthetic activity, DNA breakages, antioxidant enzyme activities, lipid peroxidation, and cellular morphologic structure of test cyanobacteria were analyzed. The results indicate that the test cyanobacteria with UV-C photocatalysis by silver-doped TiO2 sufferd from effects of reactive oxygen species, which promote the damage of the cell wall and the peroxidation of cell membranes, and subsequently, aggravate the losses of cell organelle and viability. The results suggest that UV-C photocatalysis by the silver ions doped TiO2 could be a promising method to prevent fast and excessive growth of cyanobacteria in eutrophic water sources.

Prolonging charge-separation states by doping lanthanide-ions into {001}/{101} facets-coexposed TiO_(2) nanosheets for enhancing photocatalytic H_(2) evolution

Ultrathin TiO_(2)nanosheets with coexposed{001}/{101}facets have attracted considerable attention because of their high photocatalytic activity.However,the charge-separated states in the TiO_(2)nanosheets must be extended to further enhance their photocatalytic activity for H_(2)evolution.Herein,we present a successful attempt to selectively dope lanthanide ions into the{101}facets of ultrathin TiO_(2)nanosheets with coexposed{001}/{101}facets through a facile one-step solvothermal method.The lanthanide doping slightly extended the light-harvesting region and markedly improved the charge-separated states of the TiO_(2)nanosheets as evidenced by UV-vis absorption and steady-state/transient photoluminescence spectra.Upon simulated sunlight irradiation,we observed a 4.2-fold enhancement in the photocatalytic H_(2)evolution activity of optimal Yb^(3+)-doped TiO_(2)nanosheets compared to that of their undoped counterparts.Furthermore,when Pt nanoparticles were used as cocatalysts to reduce the H_(2)overpotential in this system,the photocatalytic activity enhancement factor increased to 8.5.By combining these results with those of control experiments,we confirmed that the extended charge-separated states play the main role in the enhancement of the photocatalytic H_(2)evolution activity of lanthanide-doped TiO_(2)nanosheets with coexposed{001}/{101}facets.

Characterization of metal doped-titanium dioxide and behaviors on photocatalytic oxidation of nitrogen oxides

A series of nanosized ion-doped TiO2 catalysts with different ion content （between 0.1 at.% and 1.0 at.%） have been prepared by wet impregnation method and investigated with respect to their behavior for UV photocatalytic oxidation of nitric oxide. The catalytic activity was correlated with structural, electronic and surface examinations of the catalysts using X-ray diffraction analysis （XRD）, ultraviolet-visible （UV-Vis） absorption spectroscopy, transmission electron microscopy （TEM）, energy disperse spectrometer （EDS） and high resolution-transmission electron microscopy （HR-TEM） techniques. An enhancement of the photocatalytic activity was observed for Zn2＋ doping catalyst ranged from 0.1 at.% to 1.0 at.% which was attributed to the lengthened lifetime of electrons and holes. The improvement in photocatalytic activity could be also observed with the low doping concentration of Cr^3＋ （0.1 at.%）. However, the doping of Fe^3＋, Mo^6＋, Mn^2＋ and the high doping concentration of Cr^3＋ had no contribution to photocatalytic activity of nitric oxide.

Relationship between Crystal Structure and Luminescence Properties of (Y_(0.96-x)Ln_xCe_(0.04))_3Al_5O_(12) (Ln=Gd, La, Lu) Phosphors

The doping effects of La^3＋, Gd^3＋ and Lu^3＋ on the crystal structure and luminescence properties of （Yo96-x LnxCe0.04）3Al5O12（Ln = Gd, La, Lu） phosphors were studied. The X-ray diffraction patterns presented that with the inerease of the doping concentrations of La^3＋ and Gd^3＋ ions, the d-value of （Y0.96-xLnxCe0.04）3Al5O12 （Ln = Gd, La） inereased and the larger the doping ion, the stronger the effect would be. The doping amount causing phase transition in （Y0.96-xLnxCe0.04）3Al5O12 decreased with the inerease of the ionic radii of the doping lanthanide ions （La^3＋： 0.106 nm, Gd^3＋： 0. 094 nm, Lu^3＋ ： 0.083 nm）. The bigger doping ion of Gd^3＋ made the emission of （Y0.96-xGdxCe0.04）3Al5O12 move to red spectral region, but the smaller one of Lu^3＋ made it blue.

Photocatalytic degradation of Rhodamine B under visible light with Nd-doped titanium dioxide films

Microporous titanium dioxide films were prepared by the sol-gel methods on glass substrates, using tetrabutyl titanate as source material. In order to absorb the visible light and increase the photocatalytic activities, different concentrations of neodymium ions (Nd/Ti molar ratio was 0.5%, 0.7%, 0.9%, and 1.1% respectively) were added into the sol. X-ray diffraction (XRD), X-ray photoelectron spectros-copy (XPS), and atom force microscopy (AFM) were applied to characterize the modified films. A kind of typical textile industry pollutant (Rhodamine B) was used to evaluate the photocatalytic activities of the films under visible light. The results showed that the activities of the films were improved by doping Nd ions into the sol.

Ribbon-like Cu doped V6O13 as Cathode Material for High-performance Lithium Ion Batteries

Ribbon-like Cu doped V6O（13） was synthesized via a simple solvothermal approach followed by heat treatment in air.As an cathode material for lithium ion battery,the ribbon-like Cu doped V6O（13 ）electrode exhibited good capacity retention with a reversible capacity of over 313 m Ah·g^-1 for up to 50 cycles at 0.1C,as well as a high charge capacity of 306 m Ah·g^-1 at a high current rate of 1 C,in comparison to undoped V6O（13 ）electrode（267 m Ah·g^-1 at 0.1C and 273 m Ah·g^-1 at 1 C）.The high rate capability and better cycleability of the doped electrode can be attributed to the influence of the Cu ions on the mophology and the electronic conductivity of V6O（13） during the lithiation and delithiation process.

Surface modification and characterization of F-Co doped spinel LiMn_2O_4

Spinel LiCo0.09Mn1.91O3.92F0.08 as cathode material was modified with LiCoO2 by the sol-gel method, and the crystal structure, morphology and electrochemical performance were characterized with XRD, SEM, EDS, AAS and charge-discharge test in this paper. The results show that a good clad coated on parent material can be synthesized by the sol-gel method, and the materials with modification have perfect spinel structure. LiCo0.09Mn1.91O3.92F0.08 materials coated by LiCoO2 improve the stability of crystal structure and decrease the dissolution of Mn into electrolyte. With the LiCoO2 content increasing, the specific capacity and cycle performance of samples are improved. The capacity loss is also suppressed distinctly even at 55 ℃.

Preparation and Properties of Lanthanum Trivalent Ion Doped TiO_2 Nanopowders by Liquid Plasma Spray

The lanthanum trivalent ion doped TiO2 nanopowders were prepared by liquid plasma spray with solution of titanium tetra-tert-butoxide and alcohol as feedstock and La(NO3)3·6H2O as doping component. The photocatalytic activity of samples at different doping concentrations in photocatalytic degradation of methyl orange was discussed. The powders were characterized by Transmission Electron Microscopy (TEM) and X-Ray Diffraction (XRD), and the effect of doped ion on the pattern, phase composition and crystallite sizes were analyzed. The results indicated that lanthanum trivalent ion doped TiO2 nanopowders could be prepared by liquid plasma spray. Lanthanum trivalent ion doping increased the photocatalytic activity of TiO2 greatly, the optimal doping concentration was 0.5%. The doped powders were the mixture of anatase phase and rutile phase. The contents of anatase phase decreased firstly and then increased with an increase in the contents of lanthanum trivalent ion. Doping lanthanum trivalent ion could make the TiO2 nanopowders uniform and reduced its particle size.

Photocatalytic Activity of Nanosized TiO_2 Enhanced by co-doping with Fe^(3+) and Nd^(3+) Ions

In this study, nanosized TiO2 co-doped with Fe3+ and Nd3+ ions was synthesized via a sol-gel method. The metallic ion doped TiO2 was thoroughly characterized with XRD and UV-vis, and the photocatalytic activity was evaluated by degrading methylene blue (MB) solution. The results indicated that TiO2 crystalline size was reduced and phase transformation of anatase to rutile was suppressed as the content of doped Nd3+ ion increased in the co-doped TiO2. The UV-vis spectra of co-doped TiO2 seemed to simply overlay two spectra of single metal doped TiO2, and had significantly increased absorbance in the ranges of 400～500 nm, 565～600 nm and 730～765 nm as compared to pure TiO2. The photocatalytic activity of co-doped TiO2 was obviously enhanced, and raised about 30% compared to that of pure TiO2 as doped Nd3+ content was 0.15% and Fe3+ content was 0.05%, respectively. The enhanced catalytic activity was attributed to a synergistic effect of two doped ions, where doped Fe3+ ion inhibited the recombination of photogenerated electron and hole, and Nd3+ ion brought more surface carboxyl to promote the degradation reaction.

Spectral properties of Ce^(3+) doped yttrium lanthanum oxide transparent ceramics

Ce3＋-doped yttrium lanthanum oxide （Y0.9La0.1）2O3 transparent ceramics is fabricated with nanopowders and sintered in H2 atmosphere. The spectral properties of Ce：（Y0.9La0.1）2O3 transparent ceramics are investigated. There appear two characteristic absorption peaks of Ce3＋ ions at 230~nm and 400~nm, separately. It is found that Ce3＋ ions can efficiently produce emission at 384~nm from （Y0.9La0.1）2O3 transparent ceramic host, while the emission is completely quenched in Re2O3 （Re=Y, Lu, La） host materials.

White light emission in 0D halide perovskite[(CH_(3))_(3)S]_(2)SnCl_(6)·H_(2)O crystals through variation of doping ns^(2) ions

With the rapid development of white LEDs,the research of new and efficient white light emitting materials has attracted increasing attention.Zero dimensional(0D)organic–inorganic hybrid metal halide perovskites with superior luminescent property are promising candidates for LED application,due to their abundant and tailorable structure.Herein,[(CH_(3))_(3)S]_(2)SnCl_(6)・H_(2)O is synthesized as a host for dopant ions Bi^(3+)and Sb^(3+).The Sb^(3+)doped,or Bi^(3+)/Sb^(3+)co-doped,[(CH_(3))3S]_(2)SnCl_(6)・H_(2)O has a tunable optical emission spectrum by means of varying dopant ratio and excitation wavelength.As a result,we can achieve single-phase materials suitable for emission ranging from cold white light to warm white light.The intrinsic mechanism is examined in this work,to clarify the dopant effect on the optical properties.The high stability of title crystalline material,against water,oxygen and heat,makes it promising for further application.

Synthesis,structure and luminescence properties of KEu_(0.01)Gd_(0.19)Yb_(0.8)(WO_4)_2 powder

The synthesis of co-doped KEu0.01Gd0.19Yb0.8（WO4）2 was achieved by a modified Pechini method at 750℃. The structure of obtained compound was confirmed using X-ray diffraction measurement and Raman spectroscopy. The Scherrer＇s formula was used to confirm the grain sizes visualized by TEM technique. The grain sizes of about 100 nm of monoclinic KGW were successfully obtained by this meth- odology. In order to study spectroscopic properties of the prepared system the emission spectra were measured. The effective down- and up-conversion processes in non-resonant system were investigated.

Cubic multi-ions-doped Na_(2)TiO_(3) nanorod-like coatings:Structure-stable,highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition

The dissolution-derived release of bioactive ions from ceramic coatings on metallic implants,despite improving osseointegration,renders a concern on the interfacial breakdown of the metal/coating/bone system during longterm service.Consequently,persistent efforts to seek alternative strategies instead of dissolution-derived activation are pressingly carrying out.Inspired by bone mineral containing ions as Ca2+,Mg2+,Sr2+and Zn2+,here we hydrothermally grew the quadruple ions co-doped Na2TiO3 nanorod-like coatings.The co-doped ions partially substitute Na+in Na2TiO3,and can be efficiently released from cubic lattice via exchange with Na+in fluid rather than dissolution,endowing the coatings superior long-term stability of structure and bond strength.Regulated by the coatings-conditioned extracellular ions,TLR4-NFκB signalling is enhanced to act primarily in macrophages(MΦs)at 6 h while CaSR-PI3K-Akt1 signalling is potentiated to act predominately since 24 h,triggering MΦs in a M1 response early and then in a M2 response to sequentially secrete diverse cytokines.Acting on endothelial and mesenchymal stem cells with the released ions and cytokines,the immunomodulatory coatings greatly promote Type-H(CD31hiEmcnhi)angiogenesis and osteogenesis in vitro and in vivo,providing new insights into orchestrating insoluble ceramics-coated implants for early vascularized osseointegration in combination with long-term fixation to bone.

Recovery of lithium using H_(4)Mn_(3.5)Ti_(1.5)O_(12)/reduced graphene oxide/polyacrylamide composite hydrogel from brine by Ads-ESIX process

Powdery Li^(+)-imprinted manganese oxides adsorbent was widely used to the recovery of Li^(+),but there are some difficulties,such as poor stability in acid solution,inconvenience of operation and separation.In this work,a useful hydrogel composite based H_(4)Mn_(3.5)Ti_(1.5)O_(12)/reduced graphene oxide/polyacrylamide(HMTO-rGO/PAM)was fabricated by thermal initiation method with promising stable,conductive and selective properties.The resulting materials were characterized by field emission scanning electron microscope,infrared absorption spectrum,X-ray diffraction,X-ray photoelectron spectroscopy and electrochemical techniques.The recovery of Li^(+)was investigated using HMTO-rGO/PAM from brine by a separated two-stage sorption statically and electrically switched ion exchange desorption process.The adsorption capacity of 51.5 mg·g^(-1)could be achieved with an initial Li^(+)concentration of 200 mg·L^(-1)in pH 10,at 45℃ for 12 h.Li^(+)ions could be quickly desorbed by cyclic voltammetry(CV)in pH 3,0.1 mol·L^(-1)HCl/NH;Cl accompanying the exchange of Li^(+)and H+(NH;)and the transfer of LMTO-rGO/PAM to HMTO-rGO/PAM.