Enhancing performance of low-temperature processed CsPbI2Br all-inorganic perovskite solar cells using polyethylene oxide-modified TiO_(2)

CsPbX_(3)-based(X=I,Br,Cl)inorganic perovskite solar cells(PSCs)prepared by low-temperature process have attracted much attention because of their low cost and excellent thermal stability.However,the high trap state density and serious charge recombination between low-temperature processed TiO_(2)film and inorganic perovskite layer interface seriously restrict the performance of all-inorganic PSCs.Here a thin polyethylene oxide(PEO)layer is employed to modify TiO_(2)film to passivate traps and promote carrier collection.The impacts of PEO layer on microstructure and photoelectric characteristics of TiO_(2)film and related devices are systematically studied.Characterization results suggest that PEO modification can reduce the surface roughness of TiO_(2)film,decrease its average surface potential,and passivate trap states.At optimal conditions,the champion efficiency of CsPbI_(2)Br PSCs with PEO-modified TiO_(2)(PEO-PSCs)has been improved to 11.24%from 9.03%of reference PSCs.Moreover,the hysteresis behavior and charge recombination have been suppressed in PEO-PSCs.

Seamlessly Merging the Capacity of P into Sb at Same Voltage with Maintained Superior Cycle Stability and Low-temperature Performance for Li-ion Batteries

Among the alloying-type anodes,elemental Sb possesses the suitable yet safe plateau,simple lithiation pathway,small voltage polarization,high conductivity,and superior cycle stability.However,challenge is that its intrinsic capacity is rather low(660 mAh g^(-1)),<1/6 of silicon.Herein,we propose a seamless integration strategy by merging the voltage and capacity of phosphorus and antimony into a solid solution alloy.Interestingly,the enlistment of P is found greatly enlarge the capacity from 660 to 993 mAh g^(-1) for such Sb_(30)P_(30) solid solution,while maintaining a single and stable discharge plateau(~0.79 V)similar to elemental Sb.Various experimental characterizations including XPS,PDF,Raman,and EDS mapping reveal that in such a material the P and Sb atoms have interacted with each other to form a homogenous solid solution alloy,rather than a simple mixing of the two substances.Thus,the Sb_(30)P_(30) exhibits superior rate performances(807 mAh g^(-1) at 5000 mA g^(-1))and cyclability(821 mAh g^(-1) remained after 300 cycles).Furthermore,such Sb_(60-x)P_(x) alloys can even deliver 621 mAh g^(-1) at
30℃,which can be served as the alternative anode materials for high-energy and low-temperature batteries.This unique seamless integration strategy based on solid solution chemistry can be easily leveraged to manipulate the capacity of other electrode materials at similar voltage.

Structural Engineering of Anode Materials for Low-Temperature Lithium-Ion Batteries:Mechanisms,Strategies,and Prospects

The severe degradation of electrochemical performance for lithium-ion batteries(LIBs)at low temperatures poses a significant challenge to their practical applications.Consequently,extensive efforts have been contributed to explore novel anode materials with high electronic conductivity and rapid Li^(+)diffusion kinetics for achieving favorable low-temperature performance of LIBs.Herein,we try to review the recent reports on the synthesis and characterizations of low-temperature anode materials.First,we summarize the underlying mechanisms responsible for the performance degradation of anode materials at subzero temperatures.Second,detailed discussions concerning the key pathways(boosting electronic conductivity,enhancing Li^(+)diffusion kinetics,and inhibiting lithium dendrite)for improving the low-temperature performance of anode materials are presented.Third,several commonly used low-temperature anode materials are briefly introduced.Fourth,recent progress in the engineering of these low-temperature anode materials is summarized in terms of structural design,morphology control,surface&interface modifications,and multiphase materials.Finally,the challenges that remain to be solved in the field of low-temperature anode materials are discussed.This review was organized to offer valuable insights and guidance for next-generation LIBs with excellent low-temperature electrochemical performance.

Temperature inversion enables superior stability for low-temperature Zn-ion batteries

It is challenging for aqueous Zn-ion batteries(ZIBs)to achieve comparable low-temperature(low-T)performance due to the easy-frozen electrolyte and severe Zn dendrites.Herein,an aqueous electrolyte with a low freezing point and high ionic conductivity is proposed.Combined with molecular dynamics simulation and multi-scale interface analysis(time of flight secondary ion mass spectrometry threedimensional mapping and in-situ electrochemical impedance spectroscopy method),the temperature independence of the V_(2)O_(5)cathode and Zn anode is observed to be opposite.Surprisingly,dominated by the solvent structure of the designed electrolyte at low temperatures,vanadium dissolution/shuttle is significantly inhibited,and the zinc dendrites caused by this electrochemical crosstalk are greatly relieved,thus showing an abnormal temperature inversion effect.Through the disclosure and improvement of the above phenomena,the designed Zn||V_(2)O_(5)full cell delivers superior low-T performance,maintaining almost 99%capacity retention after 9500 cycles(working more than 2500 h)at-20°C.This work proposes a kind of electrolyte suitable for low-T ZIBs and reveals the inverse temperature dependence of the Zn anode,which might offer a novel perspective for the investigation of low-T aqueous battery systems.

Perspective on low-temperature electrolytes for LiFePO 4-based lithium-ion batteries

The olivine-type lithium iron phosphate(LiFePO_(4))cathode material is promising and widely used as a high-performance lithium-ion battery cathode material in commercial batteries due to its low cost,environmental friendliness,and high safety.At present,LiFePO_(4)/C sec-ondary batteries are widely used for electronic products,automotive power batteries,and other occasion-related applications with good thermal stability,stable cycle performance,and low room-temperature self-discharge rate.However,LiFePO_(4)-based battery applications are seriously limited when they are operated in a cold climate.This outcome is due to a considerable decrease in Li+transport capabilities within the elec-trode,particularly leading to a dramatic decrease in the electrochemical capacity and power performance of the electrolyte.Therefore,the design of low-temperature electrolytes is important for the further commercial application of LiFePO_(4) batteries.This paper reviews the key factors for the poor low-temperature performance of LiFePO_(4)-based batteries and the research progress of low-temperature electrolytes.Spe-cial attention is paid to electrolyte components,including lithium salts,cosolvents,additives,and the development of new electrolytes.The factors affecting the anode are also analyzed.Finally,according to the current research progress,some viewpoints are summarized to provide suitable modification methods and research suggestions for improving the practicability of LiFePO_(4)/C commercial batteries at low temperat-ures in the future.

A rational preparation strategy of phase tuned MoO_(3) nanostructures for high-performance all-solid asymmetric supercapacitor

In this work,phase and morphology-tuned MoO_(3) nanostructures are synthesized through a novel modified co-precipitation method,and their electrochemical properties are investigated.For the first time,such a simple surfactant-assisted synthesis process aided by minor temperature variations is reported which results in phase transition of the nanoparticles from h-MoO_(3) nano-rods to a-MoO_(3) nano-flakes.The nanostructures thus developed are highly porous and crystalline with significantly large specific surface area as compared to previous literature.The theoretical bandgap energy of the optimized sample calculated using Perdew-Zunger local density approximation(LDA) is in good agreement with the experimental findings.An overall structural,morphological,and surface-behavioural analysis predicts the electrochemical superiority in 2D a-MoO_(3).The cyclic voltammetry and galvano-potentiometry measurements of 2D a-MoO_(3) in the potential window of-0.6 V to +0.2 V present the highest pseudosupercapacitive response with a maximum specific capacitance of 829 F g^(-1)at 2 A g^(-1)as compared to h-MoO_(3) (452 F g^(-1)) and h@a-MoO_(3) (783 F g^(-1)).Thus,the MoO_(3) 2D nanostructures synthesized through our novel synthesis technique display excellent specific capacitance as compared to previous reported data.Additionally,a-MoO_(3) exhibits a galvanostatic charging-discharging cyclic stability of about 91%after 2000 cycles,indicating that it can serve as an excellent electrode material for supercapacitors.A solid-state asymmetric supercapacitor device is successfully constructed using a-MoO_(3) which can light up 4 red LEDs for 10 s.The specific energy density of the device reaches a maximum value of 36.3 W h kg^(-1)at the power density of 50 W kg^(-1).

Effect of Low-Temperature Thermal Oxidation on the Capillary Performance of Sintered Copper Powder Wicks

In this study,a composite powder capillary wick is prepared,manufactured by sintering copper powder and surface treated by low-temperature thermal oxidation.It is used to improve the performance of the capillary wick.The forced flow method and infrared imaging method are used to test the permeability and capillary performance of the samples.The effects of different oxidation temperatures on the performance of capillary wick are investigated.The experimental results show that the wetting performance of the oxidized samples is significantly enhanced.With the increase of oxidation temperature,the permeability decreases.The capillary height and velocity of the thermally oxidized samples are significantly higher than those of the untreated capillary wick.However,the oxidation temperature needs to be adjusted to obtain the best capillary performance.The highest capillary performance is found at oxidation temperature of 300℃,with an increase of 46% compared to the untreated ones.Comparisons with other composite wicks show that the sample with an oxidation temperature of 300℃ has competitive capillary performance,making it a favorable alternative to two-phase heat transfer device.This study shows that combining low-temperature thermal oxidation technology with powder sintering is a convenient and effective method to improve the capillary performance of powder wicks.

Laboratory Study on CR/SBS Modified Asphalt:Preparation and Performance Characterization

Crumble rubber(CR)can be used to prepare CR and styrene-butadiene-styrene(SBS)composite modified asphalt with a good high-and low-temperature performance,meanwhile the addition of CR could work as the substitute for SBS and help reduce the content of SBS.This study contains three main parts:effect of preparation and effect of material composition as well as rheological performance characterization.Factors during the preparation,including shearing temperature,shearing time,mixing time and swelling time,were selected,while base binder,CR content,CR particle size and SBS content in material composition were considered.The effects of these factors were assessed in terms of the conventional performance(penetration,softening point,ductility and storage stability).After identifying these effects,the sample of CR and SBS modified asphalt at the selected preparing condition and material composition(CR/SBSMA)was made,and the corresponding SBS modified and CR modified asphalt(SBSMA and CRMA)were produced for the comparing reason.Subsequently,temperature sweeps from 0℃ to 80℃ were utilized to depict the viscoelasticity of these modified asphalt binders by complex modulus and phase angle.Multiple stress creep recovery tests(MSCR)at 64℃ and bending beam rheometer tests(BBR)at various low temperatures were employed to evaluate the high-and low-temperature performance,respectively.Results highlight that that CR/SBSMA could exhibit an excellent high-temperature performance(better than SBSMA),and a good low-temperature performance(reaching the level of base binder).

Laboratory investigation on effects of organic montmorillonite on performance of crumb rubber modified asphalt

In this paper,organic montmorillonite(OMMT)was added into crumb rubber modified asphalt(CRMA)to improve its high temperature performance,anti-aging performance and storage stability.The effects of different OMMT content on properties of CRMA were studied.The rutting factor obtained by dynamic shear rheological(DSR)test was adopted to evaluate the high-temperature performance.The creep stiffness and m value determined by the bending beam rheometer(BBR)test were employed to evaluate the low-temperature performance.The softening point,ductility,rutting factor before and after rolling thin film ovens test(RTFOT)and pressure aging vessel test(PAV)were compared to characterize the aging properties.Moreover,the segregation test after being reserved for 48 h and 7 d was conducted,and the softening point and rutting factor of upper and lower layers of segregation pipe were adopted to evaluate the storage stability.The results indicated that the high-temperature performance and anti-aging performance were developed with the increasing content of OMMT,while the low-temperature performance deteriorated.The storage stability was improved with the increasing content of OMMT before the content exceeded 4%,after which the storage stability declined.Taking account of all factors,it is suggested that the optimum content of OMMT is 3%−4%.

Low-Temperature Hydrogen Storage Alloy and Its Application in Ni-MH Battery

Rare earth compositions, La, Ce and Pr in Mm(NiCoMnAl)(5) hydrogen storage alloy, were arranged by uniform design method. The discharge performances and kinetics parameters including capacity, exchange current density, symmetry factor and hydrogen diffusion coefficient of the alloy at -40degreesC, were tested in standard tri-electrode cell. And linear regression method was used to analyze the effect of rare earth compositions on the performances of hydrogen storage alloys. The results show that the capacities of the alloys are positively correlative to the square of Ce content at -40degreesC and under both 0.4 and 0.2C rate. The kinetics parameters and hydrogen diffusion coefficient indicate that the low-temperature performances of the alloys are mainly controlled by hydrogen diffusion process, and the surface electrochemical reaction affects the low-temperature performances to a certain extent. The low-temperature discharge capacities of the battery were also tested. The results show excellent low-temperature performances. The battery delivers 69.6% of its room-temperature capacity at -40degreesC and 0.2C rate, 77.7% at -40degreesC and 0.4C rate, 59.1% at -45degreesC and 0.2C rate.

Hydrocracking of Low-Temperature Coal Tar over CoMo Catalysts Supported on ZrO2-Al2O3 Composite Oxides

A series of CoMo/ZrO2-Al2O3 catalysts with different contents of ZrO2 were prepared and characterized through XRD,XPS,NH3-TPD,H2-TPR,HR-TEM,and N2 adsorption-desorption technologies.The performance of the catalysts for low-temperature coal tar(LTCT)hydrocracking reaction was investigated.The interaction between active metals and Al2O3 was weakened with the introduction of ZrO2,which increased the MoS2 content and the stack layer number of MoS2 slabs to further promote the catalytic performance.At the same time,the amount of acid sites increased with an increasing ZrO2 content.When the ZrO2 content reached 32%,the pore volume of the catalyst decreased significantly.This phenomenon reduced the content of MoS2 and the stack layer number of MoS2 slabs,which were not conducive to improving the catalytic performance.The catalyst containing 24%of ZrO2 exhibited the best catalytic performance for hydrocracking reaction,with the residue conversion and the total yield of gasoline and diesel fractions reaching 60.64%and 66.54%,respectively,which could fulfill the requirements for hydrocracking LTCT.

Dual single-atom Ce-Ti/MnO_(2)catalyst enhances low-temperature NH_(3)-SCR performance with high H_(2)O and SO_(2)resistance

Mn-based catalysts have exhibited promising performance in low-temperature selective catalytic reduction of NOx with NH_(3)(NH_(3)-SCR).However,challenges such as H_(2)O-or SO_(2)-induced poisoning to these catalysts still remain.Herein,we report an efficient strategy to prepare the dual single-atom Ce-Ti/MnO_(2)catalyst via ball-milling and calcination processes to address these issues.Ce-Ti/MnO_(2)showed better catalytic performance with a higher NO conversion and enhanced H_(2)O-and SO_(2)-resistance at a lowtemperature window(100−150°C)than the MnO_(2),single-atom Ce/MnO_(2),and Ti/MnO_(2)catalysts.The in situ infrared Fourier transform spectroscopy analysis confirmed there is no competitive adsorption between NOx and H_(2)O over the Ce-Ti/MnO_(2)catalyst.The calculation results showed that the synergistic interaction of the neighboring Ce-Ti dual atoms as sacrificial sites weakens the ability of the active Mn sites for binding SO_(2)and H_(2)O but enhances their binding to NH_(3).The insight obtained in this work deepens the understanding of catalysis for NH_(3)-SCR.The synthesis strategy developed in this work is easily scaled up to commercialization and applicable to preparing other MnO_(2)-based single-atom catalysts.

Performance evaluation of a micro turbo-expander for application in low-temperature solar electricity generation

A micro turbo-expander capable of high working speed was specially manufactured for use in an organic Rankine cycle (ORC).A series of tests were executed to examine the performance of the machine.In the experiment,the machine was tested under different inlet pressure conditions (0.2-0.5 MPa).Data such as the compressed air pressure,temperatures of the inlet and the outlet,rotational speed,and electric power generation were analyzed to discover underlying relationships.During the test,the rotational speed of the machine reached as high as 54 000 r/min,the peak value of the temperature drop between the inlet and the outlet reached 42 ℃,the maximum electric power generated by the motor-generator attached to the machine reached 630 W,and the efficiency of the machine reached 0.43.

Anti-Crack Performance of Phosphorus Slag Concrete

Anti-crack performance of concrete with phosphorus slag and fly ash singly and compositely added is investigated in terms of physical performance, hydration heat, dry shrinkage and creep. Index K is introduced to evaluate the crack resistance of phosphorus slag concrete. Results show that the strength of phosphorus slag concrete increases with the increase of fineness, and when surface specific area is greater than 300 m^2/kg, the tendency slows down. Strength decreases with phosphorus slag content increasing and there is an optimal content existing between 30% and 50%. Both phosphorus slag and fly ash have obvious effect on elongating time setting, reducing hydration heat to a large extent and increasing creep value. Crack resistance of phosphorus slag concrete is divided into three stages, namely early hazardous stage, growth stage and later mature stage. With microstructure analysis, mechanism of effect of phosphorus slag on concrete performances and P and F on cement hydration is explored. It is concluded after comprehensive evaluation that the crack resistance of phosphorus slag concrete is approximate to, even to some extent better than that of fly ash concrete.

Effects of Filler-Asphalt Ratio on the Properties of Lignin and Polyester Fiber Reinforced SMPU/SBS Modified Asphalt Mortar

To understand the effects offiller-asphalt ratio on different properties of lignin and polyesterfiber reinforced shape memory polyurethane(SMPU)/styrene butadiene styrene(SBS)composite modified asphalt mortar(PSAM),as well as to reveal the reinforcing and toughening mechanisms of lignin and polyesterfibers on PSAM,SMPU,SBS and mineral powder werefirst utilized to prepare PSAM.Then the conventional,rheological and anti-cracking properties of ligninfiber reinforced PSAM(LFAM)and polyesterfiber reinforced PSAM(PFAM)at dif-ferentfiller-asphalt ratios were characterized.Test results indicate that the shear strength,deformation resistance and viscosity are increased after adding 0.8wt%ligninfiber or polyesterfiber and increasing thefiller-asphalt ratio from 0.8 to 1.2.The optimalfiller-asphalt ratio of 1.0 is proposed after comprehensive performance assessments of PSAM.Polyesterfiber shows a better reinforcing effect than ligninfiber,but its improvement in the thermal stability of PSAM is not significant at high temperatures.Additionally,the complex modulus,storage modulus,loss modulus and rutting resistance factor of PSAM are improved after adding ligninfiber and polyesterfiber,as well as show an increasing trend as thefiller-asphalt ratio is raised,but the phase angle is gradually decreased.Further,the increase of elastic components in PSAM effectively enhances the anti-deformation ability of PSAM at high temperatures,and polyesterfiber more obviously improves the high-temperature deformation resistance of PSAM than ligninfiber.Finally,the anti-cracking performance of PFAM and LFAM at low temperatures is reduced by 74.2%and 46.7%,respectively,as thefiller-asphalt ratio is raised from 0.8 to 1.2.The low-temperature anti-cracking performance of LFAM is lower than that of PFAM at the samefiller-asphalt ratio,even lower than that of PSA.Compared with ligninfiber,the anti-cracking performance and deformation resistance of PSAM at low temperature is more greatly enhanced by polyester fiber.

Fatigue Property of Basalt Fiber-Modified Asphalt Mixture under Complicated Environment

The fatigue property of asphalt mixtures under complicated environment （low-temperature bending performance, chloride penetration, freezing-thawing cycle and their coupling effect） and the improvement effect for relevant property of basalt fiber-reinforcing asphalt mixture under complicated environment are studied. Two grading types of asphalt mixtures, AC-16I and AC-13I, are chosen, whose optimum asphalt-aggregate ratio and optimum dosage of basalt fiber are determined by the Marshall test. The standard specimens are made firstly, and then the low temperature bending tests of asphalt mixture and basalt fiber-reinforced asphalt mixture under the coupling effect of the chloride erosion and freezing-thawing cycle have been carried out. Finally, the fatigue property tests of asphalt mixture and basalt fiber-reinforced asphalt mixture under complex environment are performed on MTS material testing system. The results indicate that the tensile strength, the maximum curving tensile stress, the curving stiffness modulus, and fatigue properties of asphalt mixture are influenced by the coupling effect of the chloride erosion and freezing-thawing cycle. The low-temperature bending performance and fatigue property of asphalt mixtures under complicated environment can be greatly improved by adding moderate basalt fiber. The dense gradation asphalt mixture possesses stronger ability to resist adverse environmental effects under the same condition.

Pseudocapacitive sodium storage of Fe1-xS@N-doped carbon for low-temperature operation

Constructing potential anodes for sodium-ion batteries(SIBs)with a wide temperature property has captured enormous interests in recent years.Fe1-xS,a zero-band gap material confirmed by density states calculation,is an ideal electrode for fast energy storage on account of its low cost and high theoretical capacity.Herein,Fe1-xS nanosheet wrapped by nitrogen-doped carbon(Fe1-xS@NC)is engineered through a post-sulfidation strategy using Fe-based metal-organic framework(Fe-MOF)as the precursor.The obtained Fe1-xS@NC agaric-like structure can well shorten the charge diffusion pathway,and significantly enhance the ionic/electronic conductivities and the reaction kinetics.As expected,the Fe1-xS@NC electrode,as a prospective SIB anode,delivers a desirable capacity up to 510.2 mA h g^-1 at a high rate of8000 mA g^-1.Additionally,even operated at low temperatures of 0 and-25°C,high reversible capacities of 387.1 and 223.4 mA h g^-1 can still be obtained at 2000 mA g^-1,respectively,indicating its huge potential use at harsh temperatures.More noticeably,the full battery made by the Fe1-xS@NC anode and Na3 V2(PO4)2 O2 F cathode achieves a remarkable rate capacity(186.8 mA h g^-1 at 2000 m A g^-1)and an impressive cycle performance(183.6 m A h g^-1 after 100 cycles at700 mA g^-1)between 0.3 and 3.8 V.Such excellent electrochemical performance is mainly contributed by its pseudocapacitive-dominated behavior,which brings fast electrode kinetics and robust structural stability to the whole electrode.

The Properties of Road Base Course Materials of Granular Soils Stabilized by AGS Granular Soil Stabilizing Cement

The properties of road base course materials of granular soils stabilized by AGS granular soil stabilizing cement were studied.The AGS cement has an expansibility to a certain degree,so the dry shrinkage of AGS cement paste and AGS stabilized granular is much lower than that of Portland slag cement.AGS has a good suitability to granular soils.Granular soils stabilized by AGS have a much higher strength than that of soils stabilized by P S cement.The same strength can be reached with 20% reduction of cement dosage for AGS cement.And their elastic and resilient modulus are similar,but the former has a much higher tensile splitting strength,so the AGS stabilized granular has a much better anti-cracking performance than that of the P S stabilized granular.The reduced value of the strength and the density with the retard time for the granular soils stabilized by AGS is lower than that for P S cement.

Extraordinary Compatibility to Mass Loading and Rate Capability of Hierarchically Porous Carbon Nanorods Electrode Derived from the Waste Tire Pyrolysis Oil

The conversion of waste tire pyrolysis oil(WTPO)into S-doped porous carbon nanorods(labeled as WPCNs)with hierarchical pore structure is realized by a simple template-directed approach.The specific surface area of as-obtained porous carbon nanorods can reach up to 1448 m^(2) g^(−1) without the addition of any activating agent.As the capacitive electrode,WPCNs possess the extraordinary compatibility to capacitance,different electrolyte systems as well as long-term cycle life even at a commercial-level areal mass loading(10 mg cm^(−2)).Besides,only an extremely small capacitance fluctuation is observed under the extreme circumstance(−40 to 80℃),reflecting the excellent high-and low-temperature performance.The relationship between the pore structure and capacitive behavior is analyzed by comparing WPCNs with mesopores-dominated asphalt-derived porous carbon nanorods(APCNs)and micropores-dominated activated carbon.The molecular dynamics simulation further reveals the ion diffusion and transfer ability of the as-prepared carbon materials under different pore size distribution.The total ion flow(NT)of WPCNs calculated by the simulation is obviously larger than APCNs and the N_(T) ratio between them is similar with the experimental average capacitance ratio.Furthermore,this work also provides a valuable strategy to prepare the electrode material with high capacitive energy storage ability through the high value-added utilization of WTPO.

INFLUENCE OF CaF_(2)-4LiF ADDITIVE ON SINTERING AND ENERGY STORAGE PERFORMANCE OF SrTiO_(3)CERAMICS

The CaF_(2)-4LiF additive was added into SrTiO_(3)ceramics in order to decrease the sintering temperature for compact pulse power application.The crystalline structure,microstructure and energy storage performance of sintered ceramics were studied.Incorporating CaF_(2)-4LiF additive to SrTiO_(3)ceramics contributes to a notably enhancement of the energy storage density.The great enhancement in energy storage density occurred due to the notable increase in breakdown strength and the refinement of microstructure.With 2 at%additive,the samples exhibited an average breakdown strength of 31.8kV/mm,and an energy storage density of 1.212 J/cm^(3)which is about 1.4 times higher than pure SrTiO_(3).