Layered double hydroxide-like Mg_3Al_(1–x)Fe_x materials as supports for Ir catalysts: Promotional effects of Fe doping in selective hydrogenation of cinnamaldehyde

Supported Ir catalysts were prepared using layered double hydrotalcite‐like materials,such as Mg3Al1-xFex,containing Fe and Al species in varying amounts as supports.These Ir catalysts were applied for the selective hydrogenation of cinnamaldehyde(CAL).When x was changed from 0(Ir/Mg3Al)to 1(Ir/Mg3Fe),the rate of CAL hydrogenation reached a maximum at approximately x=0.25,while the selectivity to unsaturated alcohol,i.e.,cinnamyl alcohol,monotonously increased from 44.9%to 80.3%.Meanwhile,the size of the supported Ir particles did not change significantly with x,remaining at 1.7-0.2 nm,as determined by transmission electron microscopy.The chemical state of Ir and Fe species in the Ir/Mg3Al1-xFex catalysts was examined by temperature programmed reduction by H2 and X‐ray photoelectron spectroscopy.The surface of the supported Ir particles was also examined through the in‐situ diffuse reflectance infrared Fourier‐transform of a probe molecule of CO.On the basis of these characterization results,the effects of Fe doping to Mg3Al on the structural and catalytic properties of Ir particles in selective CAL hydrogenation were discussed.The significant factors are the electron transfer from Fe2+in the Mg3Al1–xFex support to the dispersed Ir particles and the surface geometry.

Doping Induced Tailoring in the Morphology,Band-Gap and Ferromagnetic Properties of Biocompatible ZnO Nanowires, Nanorods and Nanoparticles

The modification of nanostructured materials is of great interest due to controllable and unusual inherent properties in such materials. Single phase Fe doped Zn O nanostructures have been fabricated through simple, versatile and quick low temperature solution route with reproducible results. The amount of Fe dopant is found to play a significant role for the growth of crystal dimension. The effect of changes in the morphology can be obviously observed in the structural and micro-structural investigations, which may be due to a driving force induced by dipole-dipole interaction. The band gap of Zn O nanostructures is highly shifted towards the visible range with increase of Fe contents, while ferromagnetic properties have been significantly improved.The prepared nanostructures have been found to be nontoxic to SH-SY5 Y Cells. The present study clearly indicates that the Fe doping provides an effective way of tailoring the crystal dimension, optical band-gap and ferromagnetic properties of Zn O nanostructure-materials with nontoxic nature, which make them potential for visible light activated photocatalyst to overcome environmental pollution, fabricate spintronics devices and biosafe drug delivery agent.

Effect of FeS doping on large diamond synthesis in FeNi-C system

The large single-crystal diamond with FeS doping along the （111） face is synthesized from the FeNi-C system by the temperature gradient method （TGM） under high-pressure and high-temperature （HPHT）. the effects of different FeS additive content on the shape, color, and quality of diamond are investigated. It is found that the （111） face of diamond is dominated and the （100） face of diamond disappears gradually with the increase of the FeS content. At the same time, the color of the diamond crystal changes from light yellow to gray-green and even gray-yellow. The stripes and pits corrosion on the diamond surface are observed to turn worse. The effects of FeS doping on the shape and surface morphology of diamond crystal are explained by the number of hang bonds in different surfaces of diamond. It can be shown from the test results of the Fourier transform infrared （FTIR） spectrum that there exists an S element in the obtained diamond. The N element content values in different additive amounts of diamond are calculated. The XPS spectrum results demonstrate that our obtained diamond contains S elements that exist in S-C and S-C-O forms in a diamond lattice. This work contributes to the further understanding and research of FeS-doped large single-crystal diamond characterization.

Fe-doping induced Griffiths-like phase in La_(0.7)Ba_(0.3)CoO_3

The effect of Fe-doping on the magnetic properties of the ABO3-type perovskite cobaltites La0.7Ba0.3CoO3（0≤ y≤0.80） is reported. With no apparent structural change in any doped sample, the Curie temperature （Tc） and the magnetization （M） are greatly suppressed for y ≤0.30 samples, while a distinct increase in Tc for the y=0.40 sample is observed. With the further increase of Fe concentration, Tc increases monotonically. Griffiths-like phases in 0.40≤y ≤0.60 samples are confirmed. The formation of the Griffiths-like phase is ascribed to B-site disordering induced isolation of ferromagnetic （FM） clusters above Tc.

Influence of different Fe doping strategies on modulating active sites and oxygen reduction reaction performance of Fe, N-doped carbonaceous catalysts

Fe/N/C catalysts,synthesized through the pyrolysis of Fe-doped metal–organic framework (MOF) precursors,have attracted extensive attention owing to their promising oxygen reduction reaction (ORR) catalytic activity in fuel cells and/or metal-air batteries.However,post-treatments (acid washing,second pyrolysis,and so on) are unavoidable to improve ORR catalytic activity and stability.The method for introducing Fe^(3+) sources (anhydrous Fe Cl_(3)) into the MOF structure,in particular,is a critical step that can avoid time-consuming post-treatments and result in more exposed Fe-N_(x) active sites.Herein,three different Fe doping strategies were systematically investigated to explore their influence on the types of active sites formed and ORR performance.Fe-NC(Zn^(2+)),synthesized by one-step pyrolysis of Fe doped ZIF-8 (Zn^(2+)) precursor which was obtained by adding the anhydrous Fe Cl_(3)source into the Zn(NO_(3))_(2)·6H_(2)O/methanol solution before mixing,possessed the highest Fe-N_(x)active sites due to the high-efficiency substitution of Zn^(2+)ions with Fe^(3+) ions during ZIF-8 growth,the strong interaction between Fe^(3+) ions and N atoms of 2-Methylimidazole (2-MIm),and ZIF-8’s micropore confinement effect.As a result,Fe-NC(Zn^(2+)) presented high ORR activity in the entire p H range (p H=1,7,and 13).At p H=13,Fe-NC(Zn^(2+)) exhibited a half-wave potential (E1/2) of 0.95 V (vs.reversible hydrogen electrode),which was 70 m V higher than that of commercial Pt/C.More importantly,Fe-NC(Zn^(2+)) showed superior ORR stability in neutral media without performance loss after 5,000 cycles.A record-high open-circuit voltage(1.9 V) was obtained when Fe-NC(Zn^(2+)) was used as a cathodic catalyst in assembled Mg-air batteries in neutral media.The assembled liquid and all-solid Mg-air batteries with high performance indicated that Fe-NC(Zn^(2+)) has enormous potential for use in flexible and wearable Mg-air batteries.

Improved water oxidation via Fe doping of CuWO4 photoanodes:Influence of the Fe source and concentration

Iron(Fe)was successfully doped in CuWO4 photoanode films with a combined liquid-phase spin-coating method via the dopant sources of Fe(NO3)3,FeSO4 and FeCl3.The microstructure of the prepared films was characterized by x-ray diffraction,scanning electron microscopy,and atomic force microscopy.The light absorption and photoelectric conversion properties were evaluated by the UV-visible absorption spectra and monochromatic incident photon-to-electron conversion efficiency.The chemical composition and element combination of the samples were examined by x-ray photoelectron spectroscopy.A linear sweep voltammetric and stability test(I-t)were performed with an electrochemical workstation.The results show that the samples are uniform with a thickness of approximately 800 nm and that the photoelectrochemical performance of the doped films is heavily dependent on the Fe source and dopant concentration.Upon optimizing the doping conditions of Fe(NO3)3 and the optimal source,the photocurrent density in the Fe-doped CuWO4 photoanode film is improved by 78%from 0.267 mA/cm2 to 0.476 mA/cm2 at 1.23 V vs reversible hydrogen electrode.The underlying causes are discussed.

Mild polarization electric field in ultra-thin BN-Fe-graphene sandwich structure for efficient nitrogen reduction

The electrocatalytic N_(2)reduction reaction(NRR)is expected to supersede the traditional Haber-Bosch technology for NH3 production under ambient conditions.The activity and selectivity of electrochemical NRR are restricted to a strong polarized electric field induced by the catalyst,correct electron transfer direction,and electron tunneling distance between bare electrode and active sites.By coupling the chemical vapor deposition method with the poly(methyl methacylate)-transfer method,an ultrathin sandwich catalyst,i.e.,Fe atoms(polarized electric field layer)sandwiched between ultrathin(within electron tunneling distance)BN(catalyst layer)and graphene film(conducting layer),is fabricated for electrocatalytic NRR.The sandwich catalyst not only controls the transfer of electrons to the BN surface in the correct direction under applied voltage but also suppresses hydrogen evolution reaction by constructing a neutral polarization electric field without metal exposure.The sandwich electrocatalyst NRR system achieve NH3 yield of 8.9μg h^(−1)cm^(−2)and Faradaic Efficiency of 21.7%.The N_(2)adsorption,activation,and polarization electric field changes of three sandwich catalysts(BN-Fe-G,BN-Fe-BN,and G-Fe-G)during the electrocatalytic NRR are investigated by experiments and density functional theory simulations.Driven by applied voltage,the neutral polarized electric field induced by BN-Fe-G leads to the high activity of electrocatalytic NRR.

Hydrothermal synthesis and enhanced photocatalytic activity of hierarchical flower-like Fe-doped BiVO_4

Fe-doped BiVO4with hierarchical flower-like structure was prepared via a hydrothermal method using sodium dodecylbenzene sulfonate(SDBS)as structure directing agent.X-ray diffraction(XRD),scanning electron microscope(SEM),transmissionelectron microscope(TEM),high resolution transmission electron microscope(HRTEM),X-ray photoelectron spectroscopy(XPS)and UV-Vis were applied for characterization of the as-prepared samples.The formation mechanism of flower-like structure wasproposed based on the evolution of morphology as a function of hydrothermal time.Fe-doped into substitutional sites of BiVO4effectively improved the migration and separation of photogenerated carrier and enhanced the utilization of visible light.Flower-likeFe-doped BiVO4showed much higher visible-light-driven photocatalytic efficiency for degradation of methyl blue compared withthe pristine BiVO4.And the sample with a Fe/Bi mole ratio of2.5%showed the highest photocatalytic efficiency.

The Promoting Effect on the Activities ofFe Doped TiO_2 Photocatalysts

The particles of titanium-iron (Ti/Fe) complex with different Fe contents were prepared by means of the sol-gel method and used as a photocatalyst. The activity of the catalyst was investi- gated as a function of the Fe content during the liquid-phase oxidation of tetracycline, which showed an enhancement at the low Fe content. The XRD, Raman, XPS, and UV-Vis absorp- tion spectra indicated that the crystalline structure of the Ti/Fe complex particles changed from anatase phase to rutile phase when the Fe content increased. The isolated Fe203, Fe304, FeO species were observed and Fe3+ ions were highly dispersed in the TiO2 matrixes, then Ti-O-Fe species were formed. These species increased the surface defects of the Ti/Fe particles. Also, ac- tive hydroxyl radicals could be generated in the catalytic transformation, which led to the higher activity of the catalyst than bare Ti02 for the degradation of tetracycline.

Humidity sensing properties of spray deposited Fe doped TiO_(2)thin film

In the present work,ferrite(Fe)doped TiO_(2)thin films with different volume percentage(vol%)were synthesized using a spray pyrolysis technique.The effect of Fe doping on structural properties such as crystallite size,texture coefficient,microstrain,dislocation densities etc.were evaluated from the X ray diffratometry(XRD)data.XRD data revealed a polycrystalline anatase TiO_(2)phase for sample synthesized up to 2 vol%and mixed anatase and rutile crystalline phase for sample synthesized at 4 vol%Fe doped TiO_(2).The crystalline size was observed to decrease with increase in Fe dopant vol%and also other structural parameters changes with Fe dopant percentage.In the present work,electrical resistance was observed to decrease with a rise in Fe dopant vol%and temperature of the sample.Thermal properties like temperature coefficient of resistance and activation energy also showed strong correlation with Fe dopant vol%.Humidity sensing properties of the synthesized sample altered with a change in Fe dopant vol%.In the present paper,maximum sensitivity of about 88.7%for the sample synthesized with 2 vol%Fe doped TiO_(2)and also the lowest response and recovery time of about 52 and 3 s were reported for the same sample.

Modulating nanograin size and oxygen vacancy of porous ZnO nanosheets by highly concentrated Fe-doping effect for durable visible photocatalytic disinfection

Visible light-driven environmentally friendly ZnO semiconductor for durable photocatalytic disinfection and purification of drinking water is very promising.However,the high requirement in ultraviolet absorption and rapid recombination velocity of the photogenerated electron-hole severely hamper the sustainable implementation of ZnO in photocatalysis.Herein,by one"two birds with one stone"strategy,Fe-doping ZnO porous nanosheets(Fe-ZnOPN)composed of ultrafine nanoparticles can be constructed by hydrothermal synthesis of basic zinc carbonate and controlled low-temperature pyrolytic methods.By highly concentrated Fe-doping effect(>7 wt%),the tailoring ZnO nanograin size(~10 nm)and rich oxygen vacancy of catalyst were accessed by ion/vacancy diffusion and nanocrystal rearrangement,superior to the ZnO porous nanosheets(~37 nm).The obtained Fe-ZnOPN were endowed with a larger specific surface area,improved visible light harvesting ability,light response and separation of charge carriers.Such characters allowed the resulting catalyst to afford a 100%bactericidal efficiency against Pseudomonas aeruginosa and Staphylococcus aureus under visible light irradiation(>420 nm).Impressively,the Fe-ZnOPN could show practical disinfection ability in different water resources and multiple reuse ability.The mechanism study revealed that excellent photocatalytic disinfection performance of Fe-ZnOPN correlated with the in situ generated active oxidative substances,destruction of bacterial biofilm and resulting nucleic acids leakage,thereby causing irreversible physical damage.This study provided a new reference for designing environmentally friendly photocatalytic sterilization materials and disinfectants,which can be used in the practical disinfection of drinking water.

Fe,N,S-doped porous carbon as oxygen reduction reaction catalyst in acidic medium with high activity and durability synthesized using CaCl_2 as template

Proton exchange membrane fuel cells suffer from the sluggish kinetics of the oxygen reduction reaction(ORR)and the high cost of Pt catalysts.In the present work,a high‐performance ORR catalystbased on Fe,N,S‐doped porous carbon(FeNS‐PC)was synthesized using melamine formaldehyderesin as C and N precursors,Fe(SCN)3as Fe and S precursors,and CaCl2as a template via a two‐stepheat treatment without a harsh template removal step.The results show that the catalyst treated at900℃(FeNS‐PC‐900)had a high surface area of775m2/g,a high mass activity of10.2A/g in anacidic medium,and excellent durability;the half‐wave potential decreased by only20mV after10000potential cycles.The FeNS‐PC‐900catalyst was used as the cathode in a proton exchangemembrane fuel cell and delivered a peak power density of0.49W/cm2.FeNS‐PC‐900therefore hasgood potential for use in practical applications.

Synthesis and Performance of Li Fe_xMn_(1-x)PO_4/C as Cathode Material for Lithium Ion Batteries

LiFe Mn1-xPO4/C composites were synthesized by a solid-state reaction route using phenolic resin as both reducing agent and carbon source. The effect of Fe doping on the crystallinity and electrochemical performance of LiFexMnt xPOJC was investigated. The experimental results show that the Fe2＋ substitution for Mn2＋ will lead to crystal lattice shrinkage of LiFe Mn1-xPO4/C particles due to the smaller ionic radii of Fe2＋ In the investigated Fe doping range （x = 0 to 0.7）, LiFe Mn1-xPO4/C （x = 0.4） composites exhibited a maximum discharge capacity of 148.8 mAh/g at 0.1 C while LiF%MnI_xPO4/C （x = 0.7） composite showed the best cycle capability with a capacity retention ratio of 99.0% after 30 cycles at 0.2 C. On the contrary, the LiFe Mnl-xPO4/ C （x = 0.5） composite performed better trade-off on discharge capacity and capacity retention ratio, 127.2 mAh/ g and 94.7% after the first 30 cycles at 0.2 C, respectively, which is more preferred for practical applications.

Magnetism Regulation of (In_(1-x)Fe_x)_2O_3 Semiconductors Prepared by Sol-gel Method

Fe doped In2O3 samples （In1-xFex）2O3 （x=0, 0.05, 0.1, 0.2 and 0.3） on glass substrate were prepared by sol-gel method. The XRD results demonstrate that the solubility of Fe ions in In2O3 matrix is around 20%, above which impurity phase can be observed. The transmittance of the samples with x=0, 0.05, 0.1 and 0.2 are above 80% in the visible region while the transimittance of the glass is 90%. The transmittance curves slightly red-shifts as x increasing. All of the samples except x=0 are ferromagnetic at room temperature. The highest saturation magnetization moment is reached in the sample x=0.2 with 330 emu/cm3, and the coercive force is 169 Oe which is also the largest in our samples. The results indicate that the addition of Fe ions could tune the structure, the ferromagnetism and optical property in the In2O3 matrix.

Transport Properties of Rare Earth Manganese Oxide La_(0.67)Ca_(0.33)Mn_(1-x)Fe_xO_3

The transport properties were studied for rare earth manganese oxide La_(0.67)Ca_(0.33)Mn_(1-x)Fe_xO_3 (x=0～0.3) systems. It is found that with increasing Fe^(3+)-doping content x, the resistance increases and the insulator-metal transition temperature (T_(IM)) shifts to lower temperature. If the doping content is small, the transport properties manifest metallic characteristics in the temperature range of T<T_(IM), while they will obey a thermal activation model in the temperature range of T>T_(IM). Such a behavior may be attributed to the Fe^(3+)-doping and possible Mn ions scattering to electrons. The Fe^(3+) doping may lead to the formation of Fe^(3+)-O^(2-)-Mn^(4+) channels, which could terminate the double exchange Mn^(3+)-O^(2-)-Mn^(4+) channels. The antiferromagnetic clusters of Fe ions may induce the Mn ions to scetter to the electrons.

EFFECT OF Fe ON SURFACE REACTION OF Co_(3)Ti WITH WATER VAPOR

The surface reaction of Co 3Ti alloys (with and without Fe) with water vapor was investigated by using Auger electron spectroscopy (AES). The results showed that the rate of the surface reaction is much lower in Co 21 5Ti 3Fe alloy as compared with Co 3Ti (Co 23Ti) alloy. The surface reaction of Co 21 5Ti 3Fe alloy with water vapor saturates at exposure of 2×10 -3 Pa·s, but it does not saturate even at 0 1 Pa·s exposure for Co 3Ti alloy without Fe. The results also indicated that the kinetic of the surface reaction of Co 21 5Ti 3Fe with water vapor is much smaller than that of Co 3Ti at the same exposure. All the above results illustrate that the suppression of environmental embrittlement by addition of Fe to Co 3Ti alloy is attributed to its reduction of the surface reaction kinetics with water vapor.

Fe-doped epitaxial YBCO films prepared by chemical solution deposition

YBa2Cu3O7-d （YBCO）-coated conductors havewide-ranging potential in large-scale applications such assuperconducting maglev trains and superconducting electriccables, but low current carrying capability restrains thepractical application of YBCO-coated conductors at hightemperatures and high magnetic fields. It is crucial todevelop YBCO-coated conductors with high critical currentdensity. In this paper, epitaxial, dense, smooth, andcrack-free Fe-doped YBCO films were prepared on aLaAlO3 single crystal substrate via a fluorine-free polymerassistedmetal organic deposition method. The effects ofthe dilute Fe doping on microstructure and superconductingcharacter of YBCO films were investigated. The criticaltemperature for superconducting of the Fe-dopedYBCO films decreases slightly. However, the in-fieldcritical current density of YBCO films improves with diluteFe doping of amounts less than x = 0.005, compared to thepure YBCO film. Therefore, the current carrying capabilityof YBCO film can improve by doping with appropriateamounts of Fe. This means that dilute Fe doping in YBCOfilms may be a feasible way to prepare high-performancecoated conductors.

Fe doping promoted electrocatalytic N2 reduction reaction of 2H MoS2

Electrocatalytic N2 reduction to ammonia is a fascinating alternative to Haber-Bosch process and also considered as an energy sto rage method.This work,Fe doped MoS2/carbon cloth(CC) has been studied on the electro-catalysis fix nitrogen indicating the doped Fe can indeed enhance the MoS2 material ability.Compared with MoS2/CC,Fe-Mo-S-3/CC not only increases 10 times in the rate of production ammonia,but also 5 times in Faraday efficiency.

Microwave-assisted molybdenum-nickel alloy for efficient water electrolysis under large current density through spillover and Fe doping

The development of high-efficiency electrocatalysts for overall water splitting under large current density is significant and challenging.Herein,a high-performing Fe-doped MoNi alloy catalyst(M-H-MoNiFe-50)abundant with flower-like nanorods assemblies has been prepared by high-pressure microwave reaction and hydrogen reduction.Firstly,Fe doped NiMoO_(4) precursor(M-MoNiFe-50)was synthesized by microwave fast heating,ensuring the robustness of nanorods,which owns larger area and improved catalytic activity than that by conventional hydrothermal method.Secondly,M-MoNiFe-50 was reduced in H_(2)/Ar to fabricate Fe-incorporated MoNi_(4) alloys(M-H-MoNiFe-50),greatly enhancing the conductivity and facilitating hydrogen/oxygen spillover.The final M-H-MoNiFe-50 exhibits remarkable activity for alkaline/acidic hydrogen evolution reaction and oxygen evolution reaction with low overpotential of 208(alkaline),254(acid)and 347 mV at 1,000 mA·cm^(−2).Moreover,an alkaline water electrolyzer is established using M-H-MoNiFe-50 as anode and cathode,generating a current density of 100 mA·cm^(−2) at 1.58 V with encouraging durability of 50 h at 1,000 mA·cm^(−2).The extraordinary water splitting performance can be chalked up to the large surface area,favorable charge transfer,modified electron distribution,intrinsic robustness as well as an efficient gas spillover of M-H-MoNiFe-50.The final electrocatalyst has great prospects for practical application and confirms the significance of Fe doping,microwave method and spillover effect for catalytic performance improvement.

Surface-mediated iron on porous cobalt oxide with high energy state for efficient water oxidation electrocatalysis

Surface engineering of active materials to generate desired energy state is critical to fabricate high-performance heterogeneous catalysts.However, its realization in a controllable level remains challenging. Using oxygen evolution reaction(OER) as a model reaction, we report a surface-mediated Fe deposition strategy to electronically tailor surface energy states of porous Co_(3)O_(4)(Fe-pCo_(3)O_(4)) for enhanced activity towards OER. The Fe-pCo_(3)O_(4) exhibits a low overpotential of 280 mV to reach an OER current density of 100 mA cm^(-2), and a fast-kinetic behavior with a low Tafel slop of 58.2 mV dec^(-1), outperforming Co_(3)O_(4)-based OER catalysts recently reported and also the noble IrO_(2). The engineered material retains 100% of its original activity after operating at an overpotential of 350 m V for 100 h. A combination of theoretical calculations and experimental results finds out that the surface doped Fe promotes a high energy state and desired coordination environment in the near surface region, which enables optimized OER intermediates binding and favorably changes the rate-determining step.