Fe-lnduced Electronic Transfer and Structural Evolution of Lotus Pod-Like CoNiFeP_(x)@P,N-C Heterostructure for Sustainable Oxygen Evolution

Transition metal phosphides with metallic properties are a promising candidate for electrocatalytic water oxidation,and developing highly active and stable metal phosphide-based oxygen evolution reaction catalysts is still challenging.Herein,we present a facile ion exchange and phosphating processes to transform intestine-like CoNiP_(x)@P,N-C into lotus pod-like CoNiFeP_(x)@P,N-C heterostructure in which numerous P,N-codoped carboncoated CoNiFeP_(x)nanoparticles tightly anchors on the 2D carbon matrix.Meanwhile,the as-prepared CoNiFeP_(x)@P,N-C enables a core-shell structure,high specific surface area,and hierarchical pore structure,which present abundant heterointerfaces and fully exposed active sites.Notably,the incorporation of Fe can also induce electron transfer in CoNiP_(x)@P,IM-C,thereby promoting the oxygen evolution reaction.Consequently,CoNiFeP_(x)@P,IM-C delivers a low overpotential of 278 mV(vs RHE)at a current density of10 mA cm^(-1)and inherits excellent long-term stability with no observable current density decay after 30 h of chronoamperometry test.This work not only highlights heteroatom induction to tune the electronic structure but also provides a facile approach for developing advanced and stable oxygen evolution reaction electrocatalysts with abundant heterointerfaces.

In Situ Coupling of Highly Dispersed Ni/Fe Metal-NC Sites and N-Doped 3D Carbon Fibers Toward Free-Standing Bifunctional Cathode for Flexible Zinc-Air Battery

Designing flexible free-standing air-electrode with efficient OER/ORR performance is of vital importance for the application of Zinc-air batteries in flexible electronics.Herein,a flexible free-standing electrode(Ni/Fe-NC/NCF/CC)is synthesized by in-situ coupling of binary Ni/Fe-NC nanocubes and N-doped carbon nanofibers(NCF)rooted on carbon cloth.The highly dispersed binary Ni/Fe-NC sites ensure excellent ORR activity and create efficient OER active sites relative to Ni-NC and Fe-NC.The in-situ coupling of Ni/Fe-NC and NCF constructs a 3D interconnected network structure that not only provides abundant and stabilized reactive sites but also guarantees fast electron transfer and gas transportation,thus achieving efficient and fast operation of ORR/OER.Therefore,Ni/Fe-NC/NCF/CC displays a much positive potential(0.952 V)at 4.0 mA cm^(-2)for ORR and a low OER overpotential(310 mV)at 50 mA cm^(-2).The Zinc-air battery with Ni/Fe-NC/NCF/CC air-electrode exhibits excellent battery performance with outstanding discharge/charge durability for 2150 cycles.The flexible Zn-air batteries with foldable mechanical properties display a high power density of 105.0 mW cm^(-2).This work widened the way to prepare flexible bifunctional air-electrode by designing composition/structure and in-situ coupling.

Preparation and magnetic hardening of low Ti content(Sm,Zr)(Fe,Co,Ti)_(12) magnets by rapid solidification non-equilibrium method

The Sm–Zr–Fe–Co–Ti quinary-alloys with ThMn12 structure has attracted wide attention for ultra-high intrinsic magnetic properties,showing potentiality to be developed into rare-earth permanent magnets.The Ti element in alloys is crucial for phase stability and magnetic properties,and lower Ti content can increase intrinsic magnetic properties but reduce phase stability.In this study,the 1:12 single-phase melt-spun ribbons with low Ti content was successfully prepared using a rapid solidification non-equilibrium method for the Sm1.1Zr_(0.2)Fe_(9.2)Co_(2.3)Ti_(0.5) quinary-alloy.However,this non-equilibrium ribbon did not achieve good magnetic hardening due to the uneven microstructure and microstrain.Then,annealing was carried out to eliminate micro-strain and homogenize microstructure,therefore,remanence and coercivity were significantly improved even the precipitation of a small amount of a-Fe phase which were not conducive to coercivity.The remanence of 86.1 emu/g and coercivity of 151 kA/m was achieved when annealing at 850℃ for 45 min.After hot pressing,under the action of high temperature and pressure,a small portion of ThMn12 phases in the magnet decompose into Sm-rich phases and a-Fe,while remanence of 4.02 kGs(1 Gs=10^(-4) T),and coercivity of 1.12 kOe(1 Oe=79.5775 A·m^(-1))were still acquired.Our findings can provide reference for exploring practical permanent magnets made of 1:12 type quinary-alloys.

Fine-tuning electronic structure of N-doped graphitic carbon-supported Co-and Fe-incorporated Mo_(2)C to achieve ultrahigh electrochemical water oxidation activity

Mo_(2)C is an excellent electrocatalyst for hydrogen evolution reaction(HER).However,Mo_(2)C is a poor electrocatalyst for oxygen evolution reaction(OER).Herein,two different elements,namely Co and Fe,are incorporated in Mo_(2)C that,therefore,has a finely tuned electronic structure,which is not achievable by incorporation of any one of the metals.Consequently,the resulting electrocatalyst Co_(0.8)Fe_(0.2)-Mo_(2)C-80 displayed excellent OER catalytic performance,which is evidenced by a low overpotential of 214.0(and 246.5)mV to attain a current density of 10(and 50)mA cm^(-2),an ultralow Tafel slope of 38.4 mV dec^(-1),and longterm stability in alkaline medium.Theoretical data demonstrates that Co_(0.8)Fe_(0.2)-Mo_(2)C-80 requires the lowest overpotential(1.00 V)for OER and Co centers to be the active sites.The ultrahigh catalytic performance of the electrocatalyst is attributed to the excellent intrinsic catalytic activity due to high Brunauer-Emmett-Teller specific surface area,large electrochemically active surface area,small Tafel slope,and low chargetransfer resistance.

超声波电沉积制备Fe-Ni-Co合金箔

Fe-Ni-Co合金箔是过渡金属合金的一种重要类型,在储氢和磁性材料领域具有巨大的应用前景。本研究在氨基磺酸盐-氯化物电镀液体系中,采用电沉积法在纯钛基底上制备出铁基Fe-Ni-Co合金箔,考察pH值、温度、电流密度、超声波功率对Fe-Ni-Co合金箔的形貌、化学成分、晶体结构的影响。结果表明,当pH=2.0、温度为60℃、电流密度为50 mA/cm^(2)、超声波功率为45 W时,合金箔表面平整且气孔较少,杂质元素含量低,截面成分分布较均匀;合金是以Ni为溶剂、Fe和Co为溶质的置换型固溶体,为面心立方的γ-(Fe, Ni)相,硬度及耐腐蚀性能均较好。

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.

Different El Niño Flavors and Associated Atmospheric Teleconnections as Simulated in a Hybrid Coupled Model

A previously developed hybrid coupled model(HCM)is composed of an intermediate tropical Pacific Ocean model and a global atmospheric general circulation model(AGCM),denoted as HCMAGCM.In this study,different El Niño flavors,namely the Eastern-Pacific(EP)and Central-Pacific(CP)types,and the associated global atmospheric teleconnections are examined in a 1000-yr control simulation of the HCMAGCM.The HCMAGCM indicates profoundly different characteristics among EP and CP El Niño events in terms of related oceanic and atmospheric variables in the tropical Pacific,including the amplitude and spatial patterns of sea surface temperature(SST),zonal wind stress,and precipitation anomalies.An SST budget analysis indicates that the thermocline feedback and zonal advective feedback dominantly contribute to the growth of EP and CP El Niño events,respectively.Corresponding to the shifts in the tropical rainfall and deep convection during EP and CP El Niño events,the model also reproduces the differences in the extratropical atmospheric responses during the boreal winter.In particular,the EP El Niño tends to be dominant in exciting a poleward wave train pattern to the Northern Hemisphere,while the CP El Niño tends to preferably produce a wave train similar to the Pacific North American(PNA)pattern.As a result,different climatic impacts exist in North American regions,with a warm-north and cold-south pattern during an EP El Niño and a warm-northeast and cold-southwest pattern during a CP El Niño,respectively.This modeling result highlights the importance of internal natural processes within the tropical Pacific as they relate to the genesis of ENSO diversity because the active ocean–atmosphere coupling is allowed only in the tropical Pacific within the framework of the HCMAGCM.

Reshaping the concept of bonded magnets——recent progress in the industrialization of anisotropic rare earth-ferro nitrides(SmFeN,NdFeN)

The chemical formula for rare earth-ferro nitrides is R_(x)Fe_(y)N_(z),where R represents a rare earth element.Anisotropic rare earth-ferro nitrides include two types of materials with different chemical compositions and crystal structures:(1) Nd(Fe,M)_(12)N_(x) or Pr(Fe,M)_(12)N_(x),where M=Ti,V,Mo,etc.,having a ThMn_(12)-type tetragonal crystal structure,commonly referred to as Neodymium-Ferro-Nitrogen (NdFeN);(2) Sm_(2)Fe_(17)N_(x), having a Th_(2)Zn_(17)-type rhombohedral crystal structure,abbreviated as Samarium-Ferro-Nitrogen (SmFeN).The academic community refers to these two types of materials collectively as rare earth-ferro nitrides.

Li_(1.125)TM_(0.208)Ni_(0.208)Mn_(0.584)O_(2)(TM=Co或Fe)层状正极材料氧化机理的第一性原理研究

含Co富锂锰基正极材料是一种新型的高能量密度正极材料,它具有较高的容量和良好的循环性能。然而Co是一种稀有元素,价格昂贵,对环境不友好。Fe与Co原子半径和电子排布相似,价格便宜且资源丰富。因此,我们设计了Li_(1.125)TM_(0.208)Ni_(0.208)Mn_(0.584)O_(2)(TM=Co或Fe)富锂层状正极材料体系,采用密度函数理论(DFT)计算方法研究了Fe对氧化过程的影响,探讨了充电过程中的氧化机理及结构稳定性。这个研究将为设计高能量密度富锂正极材料提供了新的视角和概念。

Activated Carbon from Nipa Palm Fronds(Nypa fruticans)with H_(3)PO_(4) and KOH Activators as Fe Adsorbers

Nipa palm is one of the non-wood plants rich in lignocellulosic content.In this study,palm fronds were converted into activated carbon,and their physical,chemical,and morphological properties were characterized.The resulting activated carbon was then applied as an adsorbent of Fe metal in peat water.The carbonization process was carried out for 60 min,followed by sintering at 400℃ for 5 h with a particle size of 200 mesh.KOH and H_(3)PO_(4) were used in the chemical activation process for 24 h.KOH-activated carbon contained 6.13%of moisture,4.55%of ash,17.02%of volatile matter,and 78.84%of fixed carbon,while its Fe reduction efficiency was 28.09%.The H_(3)PO_(4)-activated carbon contained 4.67%of moisture,2.84%of ash,16.41%of volatile matter,and 80.57%of bonded carbon,and the Fe reduction efficiency was 52.25%.KOH-activated carbon and H_(3)PO_(4)-activated carbon contained fixed carbon of 78.84%and 80.57%,respectively,while their average rates of efficiency of Fe reduction were 22.82%and 39.23%,respectively.Overall,the characteristics of activated nipa carbon met the Indonesian standards(SNI No.06-3730-1995).However,H_(3)PO_(4)-activated carbon was found to be better at adsorbing Fe metal from peat water.

Effect of Sc on Al_(3)Fe phase and mechanical properties of as-cast AA5052 aluminum alloy

The AA5052 aluminum alloy is widely used in automobile and aerospace manufacturing,and with the development of light-weight alloys,it is required that these materials exhibit better mechanical properties.Previous studies have demonstrated that the addition of Sc to aluminum alloys can improve both the microstructure and properties of the alloys.In this study,the effect of Sc on the Fe-rich phase and properties of the AA5052 aluminum alloy was studied by adding 0%,0.05%,0.2%,and 0.3%Sc.The results show that with the increase of Sc,the coarse needle-like Fe-rich phase gradually transforms into Chinese-script and then nearly spherical particles,reduce the size of Fe-rich phase,and refine the grain with increase of high angle grain boundaries(HAGBs).These microstructure changes enhance the strength of the AA5052 alloy through Sc addition.The ductility of the alloy is obviously improved because the addition of a lower amount of Sc changes the morphology of Fe-rich phase from needle-like into a Chinese-script,and it is subsequently reduced as a result of significant increase in HAGBs with increasing Sc content.

Selection of Fe as a barrier for manufacturing low-cost MgB2 multifilament wires-Advanced microscopy study between Fe and B reaction

The high cost of using the niobium(Nb)barrier for manufacturing magnesium diboride(MgB2)mono-and multi-filamentary wires for large-scale applications has become one of the barriers to replacing current commercial niobium-titanium superconductors.The potential of replacing the Nb barrier with a low-cost iron(Fe)barrier for multifilament MgB2 superconducting wires is investigated in this manuscript.Therefore,MgB2 wires with Fe barrier sintered with different temperatures are studied(from 650°C to 900°C for 1 h)to investigate the non-superconducting reaction phase of Fe-B.Their superconducting performance including engineering critical current density(Je)and n-value are tested at 4.2 K in various external magnetic fields.The best sample sintered at 650°C for 1 h has achieved a Je value of 3.64×10^(4) A cm^(−2) and an n-value of 61 in 2 T magnetic field due to the reduced formation of Fe2B,better grain connectivity and homogenous microstructure.For microstructural analysis,the focused ion beam(FIB)is utilised for the first time to acquire three-dimensional microstructures and elemental mappings of the interface between the Fe barrier and MgB2 core of different wires.The results have shown that if the sintering temperature can be controlled properly,the Je and n-value of the wire are still acceptable for magnet applications.The formation of Fe2B is identified along the edge of MgB2,as the temperature increases,the content of Fe2B also increases which causes the degradation in the performance of wires.

Fe、Ni元素微合金化对Al-11Si铝合金微观组织及力学性能的影响

本研究利用扫描电子显微镜(SEM)、能量散射X射线光谱(EDS)和拉伸试验机,研究了Ni(1.2及1.6wt.%)和Fe(0.6及0.8wt.%)含量对Al-11Si铝合金的微观组织及不同温度下的力学性能的影响。实验结果表明,适量的Ni元素对于Al-11Si合金中富含Fe相的类型、形态和分布具有积极作用。在Al-11Si铝合金中添加1.2wt.%Ni和0.6wt.%Fe可以生成一种类似“汉字状”的富Fe强化相。当进一步增加到1.6wt.%Ni和0.8wt.%Fe后,富Fe相变为了长针状,对Al基体产生严重的割裂作用,降低了合金力学性能。由于含有1.2wt.%Ni和0.6wt.%Fe的Al-11Si铝合金中生成了“汉字状”富Fe强化相,合金的高温拉伸性能得到了显著改善。在350℃的测试温度下,Al-11Si铝合金的抗拉强度(UTS)达到了139 MPa。

Elimination, Kinetics and Thermodynamics of Fe(II) Ions by Adsorption in Static and Dynamic Conditions on Activated Carbons in Aqueous Media

This work investigated the removal, kinetics and thermodynamics of iron(II) ions (Fe(II)) by adsorption in static and dynamic conditions in aqueous media on activated carbons (AC-i30min, AC-i1h, and AC-i24h), prepared from palm nut shells collected in the city of Franceville to Gabon, using potassium hydroxide (KOH) as the activating agent. Results on the elimination of Fe(II) in static and dynamic adsorption on prepared activated carbons (ACs) showed that the AC-i24h adsorbent has the best Fe(II) adsorption capacities at saturation (Qsat). The Qsat obtained on AC-i24h in static and dynamic conditions (17.87 and 10.38 mg/g, respectively) were higher than those of AC-i30min (13.89 and 5.54 mg/g respectively) and AC-i1h (14.92 and 8.64 mg/g respectively). Moreover, the static adsorption was more effective in the removal of Fe(II) ions in aqueous media in our experimental conditions. The percentage removal (%E) of Fe(II) obtained on prepared activated carbons in static conditions was better than those obtained in dynamic conditions, especially on AC-i24h, where the %E was 89.27% in static and 61.56% in dynamic. In kinetics, results showed that the pseudo-second-order kinetic model best described the adsorption mechanisms of Fe(II) on prepared activated carbons in static adsorption, with mainly of chemisorption on the solid surfaces. However, in dynamic conditions, the pseudo-first-order kinetic model was more suitable. In addition to the weak interactions between Fe(II) and the activated carbon surfaces, strong interactions (chemisorption) were also observed. Also, thermodynamic data obtained on AC-i24h in static adsorption indicated that the adsorption of Fe(II) was spontaneous and increased with temperature (ΔG˚ H˚ = 503.54 KJ/mol).

Influence of thermomechanical treatment on recrystallization and softening resistance of Cu-6.5Fe-0.3Mg alloy

The recrystallization and softening resistance of a Cu-6.5Fe-0.3Mg(mass fraction,%)alloy prepared by Process 1(cold rolling heat treatment)and Process 2(hot/cold rolling heat treatment)were studied using Vickers hardness tests,tensile tests,scanning electron microscopy and transmission electron microscopy.The softening temperature,hardness and tensile strength of the alloy prepared by Process 2 were 110°C,HV 15 and 114 MPa higher,respectively,than those of the alloy prepared by Process 1 after aging at 300°C.The recrystallization activation energy of the alloys prepared by Process 1 and Process 2 were 72.83 and 98.11 kJ/mol,respectively.The pinning effects of the precipitates of the two alloys on grain boundaries and dislocations were basically the same.The softening mechanism was mainly attributed to the loss of dislocation strengthening.The higher Fe fiber density inhibited the average free migration path of dislocations and grain boundary migration in the alloy,which was the main reason for higher softening temperature of the alloy prepared by Process 2.

Effect of Ni content on the weldability of middle-chromium hyperpure ferritic stainless steels 00Cr21Ti

Excellent weldability substantially contributes to the intrinsic quality of steels,while appropriate chemical composition plays a primary role in the essential weldability of steels.The poor weldability of ferritic stainless steels could be improved through modification with minor alloy elements while minimally increasing the cost.Therefore,studying the effect of minor alloy elements on the weldability of steels is of considerable importance.In this study,several steels of middle-chromium hyperpure ferritic stainless 00Cr21Ti with different Ni content(0.3%,0.5%,0.8%,and 1.0%)were developed,and their weldabilities of butt joint samples welded using the metal inert gas welding process,including the influence of welded joints on the microstructure,tensile performance,corrosion resistance,and fatigue property,were investigated.Results show that the steels with w(Ni)≥0.8%exhibit excellent mechanical properties compared with those with low-Ni content steels,further,their impact toughness at normal atmospheric temperature meets the industrial application standard and the fatigue property is similar to that of 304 austenitic stainless steel.Moreover,results show that the corrosion resistance of all the samples is almost at the same level.The results acquired in this study are supposed to be useful for the optimization of the chemical composition of stainless steels aiming to improve weldability.

Electrochemical characterization of Ni-Co and Ni-Co-Fe for oxidation of methyl alcohol fuel with high energetic catalytic surface

Non Pt based metals and alloys as electrode materials for methyl alcohol fuel cells have been investigated w ith an aim of finding high electrocatalytic surface property for the faster electrode reactions.Electrodes w ere fabricated by electrodeposition on pure Al foil,from an electrolyte of Ni,Co,Fe salts.The optimum condition of electrodeposition w ere found out by a series of experiments,varying the chemistry of the electrolyte,pH valve,temperature,current and cell potential.Polarization study of the coated Ni-Co or Ni-CoFe alloy on pure Al w as found to exhibit high exchange current density,indicating an improved electro catalytic surface w ith faster charge-discharge reactions at anode and cathode and low overvoltage.Electrochemical impedance studies on coated and uncoated surface clearly show ed that the polarization resistance and impedance w ere decreased by Ni-Co or Ni-Co-Fe coating.X-ray diffraction(XRD),energy dispersive X-ray spectroscopy(EDX)and atomic absorption spectroscopy(AAS)studies confirmed the presence of alloying elements and constituents of the alloy.The morphology of the deposits from scanning electron microscope(SEM)images indicated that the electrode surface w as a three dimensional space w hich increased the effective surface area for the electrode reactions to take place.

Are Ni/and Ni5Fe1/biochar catalysts suitable for synthetic natural gas production?A comparison with g-Al2O3 supported catalysts

Among challenges implicit in the transition to the post-fossil fuel energetic model,the finite amount of resources available for the technological implementation of CO_(2) revalorizing processes arises as a central issue.The development of fully renewable catalytic systems with easier metal recovery strategies would promote the viability and sustainability of synthetic natural gas production circular routes.Taking Ni and NiFe catalysts supported over g-Al_(2)O_(3) oxide as reference materials,this work evaluates the potentiality of Ni and NiFe supported biochar catalysts for CO_(2) methanation.The development of competitive biochar catalysts was found dependent on the creation of basic sites on the catalyst surface.Displaying lower Turn Over Frequencies than Ni/Al catalyst,the absence of basic sites achieved over Ni/C catalyst was related to the depleted catalyst performances.For NiFe catalysts,analogous Ni_(5)Fe_(1) alloys were constituted over both alumina and biochar supports.The highest specific activity of the catalyst series,exhibited by the NiFe/C catalyst,was related to the development of surface basic sites along with weaker NiFe-C interactions,which resulted in increased Ni0:NiO surface populations under reaction conditions.In summary,the present work establishes biochar supports as a competitive material to consider within the future low-carbon energetic panorama.

Ni替换Fe对FeNiSiB合金非晶形成能力和性能的影响

利用单铜辊甩带法制备(Fe_(1-x)Ni_(x))_(83)Si_(1)B_(16)(x=0,0.1,0.2,0.3,0.4,0.5)非晶合金带材,并进行退火处理。采用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、差示扫描量热仪(DSC)、振动样品磁强计(VSM)、直流/交流磁化特性自动测试分析仪(BH)、维氏硬度计、Instron机械试验机分析研究不同的Fe/Ni比例对于FeNiSiB合金带材的非晶形成能力、软磁性能和力学性能的影响。结果表明随着Ni元素不断替换Fe元素,FeNiSiB合金带材会有晶化的趋势,并且有α-Fe相析出,第一晶化温度T x1不断降低,力学性能有所提升,维氏硬度和抗拉强度分别高达770.0和2452 MPa。适当的Fe/Ni比例会使得材料的软磁性能显著提升,其中(Fe_(0.8)Ni_(0.2))83-Si 1B 16在退火处理后饱和磁感应强度Bs为1.62 T,矫顽力Hc仅为0.5 A/m,初始磁导率μi为33000。

Fe@Cu-Ni材料降解罗丹明B的机理与途径

文章采用直接还原法制备了Fe@Cu-Ni微电解材料,并探究了其对罗丹明B(Rh B)的降解效果。采用SEM、XRD和XPS对Fe@Cu-Ni进行了表征,分析了Fe@Cu-Ni对Rh B的降解机理和降解路径。Fe@Cu-Ni的枝晶结构为电子传递和富集提供了发散路径,有利于电荷转移。电子转移通道末端的Cu_(2)O和Fe与Ni掺杂对氧还原反应生成H_(2)O_(2)起着重要作用。由原位产生的H_(2)O_(2)催化生成的·OH是降解Rh B的关键活性物质。通过LC-MS/MS对Rh B的降解中间体进行了鉴定,结果表明,Rh B的降解主要来自于·H和·OH的协同作用。当pH=2、Fe@Cu-Ni催化剂用量为0.5 g/L、Rh B初始浓度为20 mg/L时,Rh B的降解效率可达98.7%。该研究强调了Fe@Cu-Ni复合材料在消除染料残留方面的潜力。