Effects of （LiCe） co-substitution on the structural and electrical properties of CaBi2Nb209 ceramics

The piezoelectric, dielectric, and ferroelectric properties of the （LiCe） co-substituted calcium bismuth niobate （CaBi2Nb209, CBNO） are investigated. The piezoelectric properties of CBNO ceramics are significantly enhanced and the dielectric loss tan 5 decreased. This makes poling using （LiCe） co-substitution easier. The ceramics （where represents A-site Ca2＋ vacancies, possess a pure layered structure phase and no other phases can be found. The Cao.ss（LiCe）0.04[]0.04Bi2Nb209 ceramics possess optimal piezoelectric properties, with piezoelectric coefficient （d33） and Curie temperature （Tc） found to be 13.3 pC/N and 960 ℃ respectively. The dielectric and piezoelectric properties of the （LiCe） co-substituted CBNO ceramics exhibit very stable temperature behaviours. This demonstrates that the CBNO ceramics are a promising candidate for ultrahigh temperature applications.

Effects of (LiCe) co-substitution on the structural and electrical properties of CaBi_(2)Nb_(2)O_(9) ceramics

The piezoelectric,dielectric,and ferroelectric properties of the(LiCe) co-substituted calcium bismuth niobate(CaBi2Nb2O9,CBNO) are investigated.The piezoelectric properties of CBNO ceramics are significantly enhanced and the dielectric loss tan δ decreased.This makes poling using(LiCe) co-substitution easier.The ceramics(where represents A-site Ca2+ vacancies,possess a pure layered structure phase and no other phases can be found.The Ca0.88(LiCe)0.04 0.04Bi2Nb2O9 ceramics possess optimal piezoelectric properties,with piezoelectric coefficient(d 33) and Curie temperature(TC) found to be 13.3 pC/N and 960 C,respectively.The dielectric and piezoelectric properties of the(LiCe) co-substituted CBNO ceramics exhibit very stable temperature behaviours.This demonstrates that the CBNO ceramics are a promising candidate for ultrahigh temperature applications.

Alkali and alkaline ions co-substitution of P2 sodium layered oxides for sodium ion batteries

Alkali and alkaline ion substitutions enhance the electrochemical properties of P2 sodium layered oxide,while the effect on electrochemical property enhancement of alkali and alkaline ions co-substitution is still unclear.In this work,the structural and electrochemical properties of the Li alkali and Mg alkaline ions co-substituted P2 layered oxide Na_(0.67)(Li_(0.5)Mg_(0.5))_(0.1)(Ni_(0.33)Mn_(0.67))_(0.9)O_(2)are investigated in detail.Compared to the pristine and single-ion substituted materials,the co-substituted material shows an enhanced cycling performance with a reversible ca-pacity of 127 mAh/g and a capacity retention of 75%over 100 cycles at 0.5C.Galvanostatic intermittent titration technique(GITT)and cyclic voltammetry(CV)results show that the Li and Mg synergistically improve the ion diffusion.Moreover,the structure stability is also improved by the Li and Mg co-substitution that is clarified by operando X-ray diffraction(XRD)measurements.These results explain the origin of the enhanced electrochemical properties of the Li/Mg co-substituted P2 layered oxides for sodium ion batteries.

Co-substitution of carbonate and fluoride in hydroxyapatite： Effect on substitution type and content

The nanosized hydroxyapatite substituted by fluoride and carbonate ions （CFHA） had been synthesized by aqueous precipitation method. CFHA had been considered as potential bone graft material for orthopedic and dental applications. The objective of this study was to determine the effects of simultaneously incorporated CO2/3- and F- on the substitution type and content. The morphologies of CFHAs were observed by TEM. The carbonate substitution type and content were characterized by FTIR. The fluoride contents were determined by F-selective electrode. The phase compositions and crystallinity of the samples were investigated by XRD. The fluoride and carbonate contents of CFHA increase with the dopant concentrations nonlinearly, The carbonate substitution has much more obvious effect on morphology compared with the fluoride substitution. The co-existence of CO2/3-and F- ions can influence the corresponding substitution fraction. The isomorphic substitution of sodium for calcium in the substitution process of CO2/3-can improve crystal degree and favor the B-type substitutions. Due to the closeness of the ion radii and equivalent substitution of F- and OH-, F- will occupy the OH- sites of HA crystals more easily, compelling most of the CO2/3- to be located in the B sites.

Phase Evolution and Magnetic Studies of La and Refractory Metals Co-substituted α-Fe/R_2Fe_(14)B-type Nanocomposites

Phase evolution and magnetic properties of (Nd_o.95La_0.05)9.5-11Febal.M_2B10.5. where M=Cr, Ti, Nb, V, Mo, Zr, Hf, Ta, Mn or W, melt spun ribbons have been investigated. Almost all the alloy ribbons. except for(Nd_0.95La_0.05)_9.5Fe_78M_2B_10.5(M=Mo and Mn),consist merely two magnetic phases, namely α-Fe and R_2Fe_14B, which display a better combination of _iH_c and magnetic energy product. Remanence (Br) and coercivity (i_H_c) values in the range of 8.0 to 9.1 kG and 9.5 to 18.9 kOe. respectively, can be achieved. Among compositions studied, the Ti and W-substitutions were found to be most effective in increasing the Br and i_H_c, respectively. For a fixed refractory metal substitution, namely, M=C_r, Ti or Nb, an increase in the total rare earth concentration resulted in nanocomposites of small grain sizes and a high volume fraction of the R_2Fe_14B phase, leading to an increase in the magnetic properties.

Electromagnetic and Microwave Absorbing Properties of Co-Substituted Nickel-Zinc Ferrite

Co-substituted Ni-Zn ferrite was prepared by a chemical codeposition. The electromagnetic properties, zero reflection conditions and simulated reflection losses of the samples were investigated. As a result, it is found that with Co contents rising, the saturation magnetization (Ms) shows a tendency of decrease, while coercivity (Hc) varies clearly. In addition, Ni-Zn ferrite with different cobalt content can meet zero reflection conditions. And the reflection loss calculation indicates that with the increase of cobalt contents, the reflection loss peak moves to high frequenc; moreover, to increase Co content more than 0.15, and the absorption intensity as well as the absorbing band of microwave absorber are enhanced obviously.

Improved microwave dielectric properties of MgAl_(2)O_(4)spinel ceramics through(Li_(1/3)Ti_(2/3))^(3+)doping

A series of nominal compositions MgAl_(2-x)(Li_(1/3)Ti_(2/3))_(x)O_(4)(x=0,0.04,0.08,0.12,0.16,and 0.20)ceramics were successfully prepared via the conventional solid-state reaction route.The phase compositions,microstructures,and microwave dielectric properties were investigated.The results of x-ray diffraction(XRD)and scanning electron microscopy(SEM)showed that a single phase of MgAl_(2-x)(Li_(1/3)Ti_(2/3))_(x)O_(4)ceramics with a spinel structure was obtained at x≤0.12,whereas the second phase of MgTi_(2)O_(5)appeared when x>0.12.The cell parameters were obtained by XRD refinement.As the x values increased,the unit cell volume kept expanding.This phenomenon could be attributed to the partial substitution of(Li_(1/3)Ti_(2/3))^(3+)for Al^(3+).Results showed that(Li_(1/3)Ti_(2/3))^(3+)doping into MgAl_(2)O_(4)spinel ceramics effectively reduced the sintering temperature and improved the quality factor(Q_f)values.Good microwave dielectric properties were achieved for a sample at x=0.20 sintering at 1500℃in air for 4 h:dielectric constantε_(r)=8.78,temperature coefficient of resonant frequencyτ_(f)=-85 ppm/℃,and Q_(f)=62300 GHz.The Q_(f)value of the x=0.20 sample was about 2 times higher than that of pure MgAl_(2)O_(4)ceramics(31600 GHz).Thus,MgAl_(2-x)(Li_(1/3)Ti_(2/3))_(x)O_(4)ceramics with excellent microwave dielectric properties can be applied to 5G communications.

Synthesis and electrochemical properties of LiNi_(0.87)Co_(0.10)Mg_(0.03)O_2 cathode materials

A Co-Mg co-substituted LiNi0.87Co0.10Mg0.03O2 cathode material was prepared by a co-precipitation method. The prepared LiNi0.87Co0.10Mg0.03O2 exhibits excellent electrochemical properties, such as initial discharge capacities of 202.6 mA.h/g and 190.5 mA.h/g at 0.2C and 1C rate, respectively, in operating voltage range of 3.0-4.3 V （versus Li^＋/Li）. The capacity retentions are 96.1% and 93.4% at 0.2C and 1C, respectively, after 50 cycles. Moreover, the cycle performance of the sample was investigated in a 053048-type square Li ion battery. This type of battery can keep 81.7% of initial capacity after 500 charge-discharge cycles at 1C rate, which is close to that of commercial LiCoO2 battery. Therefore, the as-prepared material is capable of such high energy applications as portable product power.

Regulating local chemical environment in O_(3)-type layered sodium oxides by dual-site Mg^(2+)/B^(3+)substitution achieves durable and high-rate cathode

The O_(3)-Na_(0.85)Ni_(0.2)Fe_(0.4)Mn_(0.4)O_(2)layered oxide cathode material possesses the advantages of high specific capacity,low cost,and simple synthesis.However,sluggish kinetics and complicated phase transition caused by the large size difference between Na+and tetrahedral gaps lead to poor rate and cycling performance.Therefore,a scalable and feasible strategy was proposed to modulate local chemical environment by introducing Mg^(2+)and B^(3+)into O_(3)-Na_(0.85)Ni_(0.2)Fe_(0.4)Mn0.4O_(2),which can distinctly improve kinetic transport rate as well as electrochemical performance.The capacity retention of O_(3)-(Na_(0.82)Mg_(0.04))(Ni_(0.2)Fe_(0.4)Mn_(0.4))B_(0.02)O_(2)(NFMB)increases from 43.3%and 12.4%to 89.5%and 89.0%at 1 C and 3 C after 200 cycles,respectively.Moreover,the electrode still delivers high rate capacity of 93.9 mAh/g when current density increases to 10 C.Mg^(2+)ions riveted on Na layer act as a“pillar”to stabilize crystal structure and inhibit structural change during the desodiumization process.B^(3+)ions entering tetrahedral interstice of the TM layer strengthen the TM-O bond,lower Na+diffusion energy barrier and inhibits the slip of TM layer.Furthermore,the assembled full batteries with the modified cathode material deliver a high energy density of 278.2Wh/kg with commercial hard carbon as anode.This work provides a strategy for the modification of high-performance SIB layered oxide materials to develop the next-generation cost-effective energy storage grid systems.

Optical and magnetic properties of perovskite materials:Ba_(0.3)La_(0.7)Ti_(0.3)Fe_(0.7)O_(3) and Ba_(0.1)La_(0.9)Ti_(0.1)Fe_(0.9)O_(3)

Structural,optical and magnetic properties are reported for new synthesized perovskite materials.Ba_(0.3)La_(0.7)Ti_(0.3)Fe_(0.7)O_(3) and Ba_(0.1)La_(0.9)Ti_(0.1)Fe_(0.9)O_(3) compositions were prepared via solid state reaction.X-ray analysis confirms that both compositions show feature of perovskite structure.Rietveld refinement method was used to confirm the phase formation and investigate the structure and space group.The study demonstrates the formation of orthorhombic structure with Pnma space group for Ba_(0.3)La_(0.7)Ti_(0.3)Fe_(0.7)O_(3) while the composition Ba_(0.1)La_(0.9)Ti_(0.1)Fe_(0.9)O_(3) structure adopts Pbnm symmetry.UV–vis spectroscopy measurements show very broad and intense UV–visible light absorption,the estimated band gap ranges between 2.07 and 2.15 eV.Magnetic measurements were carried out for the compositions Ba_(0.3)La_(0.7)Ti_(0.3)Fe_(0.7)O_(3) and Ba_(0.1)La_(0.9)Ti_(0.1)Fe_(0.9)O_(3).The hysteresis loops of both samples at 300 and 10 K show a strong ferromagnetic behavior.The temperature dependent magnetization at 0.05 T under field-cooled(FC)and zero field cooled(ZFC)modes shows magnetic frustration or spin glass-like behavior.

Microstructure and Ferroelectric Properties of (Bi_(0.9)Ho_(0.1))_(3.999)Ti_(2.997)V_(0.003)O_(12) Thin Films Prepared by Sol-gel Method for Nonvolatile Memory

The （Bi0.9Ho0.1）3.999Ti2.997V0.003012 （BHTV） films have been prepared on Pt/Ti/SiO2/Si substrates by solgel method. The microstructure and ferroelectric properties of the BHTV films were investigated. The BHTV films show a single phase of Bi-layered Aurivillius structure and dense microstructure. The Ho3＋/V5＋ cosubstitution can effectively improve the ferroelectric properties. The BHTV film exhibits good ferroelectric properties with 2Pr of 47.6℃/cm2, 2Ec of 265 kV/cm （at applied field of 420 kV/cm）, dielectric constant of 305, dielectric loss of 0.031 （at 1 MHz）, good insulting behavior, as well as the fatigue-free behavior.