Pulse Electrochemical Deposition Method Research Articles

Novel High-Entropy FeCoNiMoZn-Layered Hydroxide as an Efficient Electrocatalyst for the Oxygen Evolution Reaction

The exploration of catalysts for the oxygen evolution reaction (OER) with high activity and acceptable price is essential for water splitting to hydrogen generation. High-entropy materials (HEMs) have aroused increasing interest in the field of electrocatalysis due to their unusual physicochemical properties. In this work, we reported a novel FeCoNiMoZn-OH high entropy hydroxide (HEH)/nickel foam (NF) synthesized by a facile pulsed electrochemical deposition method at room temperature. The FeCoNiMoZn-OH HEH displays a 3D porous nanosheet morphology and polycrystalline structure, which exhibits extraordinary OER activity in alkaline media, including much lower overpotential (248 mV at 10 mA cm−2) and Tafel slope (30 mV dec−1). Furthermore, FeCoNiMoZn-OH HEH demonstrates excellent OER catalytic stability. The enhanced catalytic performance of the FeCoNiMoZn-OH HEH primarily contributed to the porous morphology and the positive synergistic effect between Mo and Zn. This work provides a novel insight into the design of HEMs in catalytic application.

Strontium doped electrospinning fiber membrane with antibacterial and osteogenic properties prepared by pulse electrochemical method

• Composite fibers were prepared by electrostatic spinning and pulse electrochemical deposition. • PPy controls the slow release of Sr 2+ and Cu 2+ for a long time. • Good physiological stability and long-term antibacterial effect. • Fiber has good osteogenic and angiogenic properties. The osteogenic differentiation and new bone formation are commonly delayed by bacterial infection of orthopedic implants, which is urgent to be resolved quickly in the clinic. The current paper prepared a strontium-doped electrospinning fiber membrane with antibacterial and osteogenic properties by pulse electrochemical method. Polylactic acid/hydroxyapatite (PLLA/HA) composite fiber substrate was fabricated by electrospinning technology, and strontium doped SrHA/Cu/Polypyrrole (PPy) composite coating was constructed with pulse electrodeposition method on its surface. The strontium doping technique, degradation of Sr 2+ and Cu 2+ , cellular compatibility, and the antibacterial activity of the fiber membrane were examined. The results revealed that the deposition of phosphorus and calcium on composite fiber was the highest, indicating good biological activity. The release of Sr 2+ and Cu 2+ was stable and gradual due to the modulation of PPy. The composite fiber presented excellent antibacterial performance and the antibacterial rate was close to 100% against Staphylococcus aureus and Escherichia coli. Furthermore, it is conducive to the adhesion, spread, and proliferation of vascular endothelial cells and osteoblasts, namely outstanding osteogenesis and angiogenesis abilities. In conclusion, the multifunctional PLLA/HA@SrHA/Cu/PPy composite fiber membrane with good antibacterial and osteogenic activity by electrospinning technology and pulsed electrochemical deposition method provides an effective strategy for the poor bone healing of infected bone defects. Strontium doped antibacterial osteogenic PLLA/HA@SrHA/Cu/PPy composite fiber was constructed by electrostatic spinning and pulsed electrochemical deposition technology, which showed good antibacterial properties and had the ability to promote bone induction and angiogenesis.

Current density-induced emergence of soft and hard magnetic phases in Fe nanowire arrays

The capability of generating magnetically soft and hard phases in a material is important in many aspects, ranging from basic science to applications. Here, the emergence of soft and hard magnetic phases is reported in Fe nanowire (NW) arrays with a diameter of 35 nm fabricated by using a pulsed electrochemical deposition method in porous aluminum oxide templates under different current density (C d ) values in the range of 25–100 mA cm−2. The variation of C d influences the grain size, crystallinity, electrodeposition efficiency and length of the Fe NWs, as characterized by x-ray diffraction, high-resolution transmission electron microscopy, vibrating sample magnetometry and field-emission scanning electron microscopy. Increasing C d from 25 to 80 mA cm−2 results in a significant decrease in coercivity and squareness from 1590 to 900 Oe and 0.9 to 0.5, respectively, inducing the soft and hard phases along the length of Fe NWs. Further increasing the C d leads to the separation of the phases, as evidenced by first-order reversal curve analysis. From a theoretical aspect, the emergence of the soft phase may lead to the occurrence of the fanning reversal mode in the NWs, for which there is no precedent in previous experimental investigations.

Probing the Anti-Corrosion Behavior of X65 Steel Underwater FSW Joint in Simulated Seawater

To detect the corrosion resistance of a friction stud welding (FSW) joint in simulated seawater (a 3.5 wt% NaCl solution), the pulse electrochemical deposition method was used for electroplating Ni coating with different duty ratios (50%, 80%, and 100%) on the surface of FSW joint. The microstructure and surface structure of the coating were observed by micro-spectroscopy and other characterization methods. The corrosion behavior of the coating was analyzed by means of macroscopic electrochemical testing. The local corrosion law of joint surface and coating surface defects were innovatively explored by using micro-zone electrochemical scanning system. The coating characterization results showed that, as the duty ratio continues to increase, the coating surface becomes denser and smoother, and the corrosion products such as Fe2O3, Fe3O4, and FeOOH are generated. The results of macroscopic electrochemical experiment indicated that the coating with 100% duty ratio has the lowest corrosion current density and the maximum polarization resistance. The scanning vibrating electrode technique results showed that the corrosion current density in the defect area is higher than that in the coating area, and the maximum corrosion current density decreases with the increase of duty ratio. The localized electrochemical impedance spectroscopy results indicated that the localized impedance at the welded zone was the largest, and with the increase of the pulse duty ratio, the impedance diffusion in the defect area was decreasing.

Polypyrrole doping-regulated construction of dexamethasone/hydroxyapatite composite coating on titanium surface for sustained osteoinduction

Nano-hydroxyapatite (HA-NPs) coating on the surface of titanium is an effective way to improve the osteoinductivity of implants. However, particle agglomeration and uncontrollable structure of HA-NPs results in limited osteogenic capability. In this study, pulse electrochemical deposition method was used to drive PPy in situ, and HA-NPs as well as the osteoinductive drug Dex were introduced to PPy based on its doping characteristics to endow the titanium-based composite coating with long-term osteoinductivity during the osseointegration process. During the oxidative polymerization of PPy, PO43− and Dex− were doped into the main chain of PPy, and HA was formed due to the electrostatic interaction of PO43− and Ca2+, finally realizing the co-deposition of HA-NPs and Dex. Dex drug release experiments showed that the doping effect of PPy has reduced the release rate of Ca2+ from the coating and increased the physiological stability of the coating. The in vitro evaluation of osteoblasts and vascular endothelial cells showed that the number of cells increased steadily with good proliferation conditions, showing promising osteogenic ability and angiogenic property. In summary, a bioactive PPy@HA/Dex nanocomposite coating with sustained osteoinductivity was successfully constructed on the titanium surface using pulse electrochemical method.

Bifunctional and binder-free S-doped Ni-P nanospheres electrocatalyst fabricated by pulse electrochemical deposition method for overall water splitting

Due to their excellent electrocatalytic properties, transition metal phosphides have been considered as desirable and cost-effective electrocatalysts in recent years. However, in many cases, the synthesis of phosphide-based nanostructures requires expensive conditions and toxic phosphorous-containing compounds. Therefore, the emergence of an economical and eco-friendly method for creating phosphides-based nanostructures can be very effective. Here, S-doped Ni-P nanospheres were created using a novel pulse electrochemical deposition method, and its hydrogen evolution reaction (HER), as well as oxygen evolution reaction (OER) electrocatalytic activity and stability were investigated. Inspired by the high electrochemically active surface area, the synergistic effect between S and P, the rapid detachment of the gasses from the surface and thus the lowered resistance resulted from bubbles pinning, and ultimately the increased wettability due to nanostructuring, the electrode exhibited outstanding electrocatalytic activity for HER and OER processes. The electrode requires only 55 mV and 229 mV overproduction to be able to afford the current density of 10 mA.cm−2 for HER and OER processes, respectively. Furthermore, at a current density of 100 mA.cm−2, these electrodes showed minor changes in potential, indicating the superb electrocatalytic stability of the synthesized electrode. Moreover, in the overall water splitting process, the S-doped Ni-P electrode requires only 1.51 V to generate a current of 10 mA.cm−2. The results of this study indicate the successful use of pulse electrochemical deposition method to create active electrocatalysts.

Formation of calcium phosphate coating on carbon fibre with pyrolytic carbon interlayer

ABSTRACTPyrolytic carbon interlayer modified carbon fibers (PCF) were fabricated by chemical vapour deposition method. The original carbon fibers (OCF) and carbon fibers treated by H2O2 (HCF) were used as control samples. The CaP coatings were applied on OCF, HCF and PCF using pulse electrochemical deposition (PED) method. The morphology, microstructure and element composition of the CaP coatings for OCF, HCF and PCF were analyzed. The results showed that PCF exhibited smooth surface, whereas OCF and HCF had a grooved surface. More CaP crystals were formed on PCF than those on OCF and HCF using same deposition parameters. The introduction of pyrolytic carbon interlayer resulted in that the CaP coatings on carbon fibers transformed from octacalcium phosphate (OCP) to hydroxyapatite (HA). Simulated body fluid (SBF) immersion behavior of the CaP coating for PCF showed that the CaP coating could induce the formation of new apatite layer and exhibited good in-vitro bioactivity.

Characterization of Co–Cr–Fe–Mn–Ni High-Entropy Alloy Thin Films Synthesized by Pulse Electrodeposition: Part 2: Effect of Pulse Electrodeposition Parameters on the Wettability and Corrosion Resistance

Co–Cr–Fe–Mn–Ni high-entropy alloy thin films were synthesized by pulse electrochemical deposition method. The films were co-deposited in an electrolyte based on a DMF-CH3CN organic system consisting of Co, Cr, Fe, Mn, and Ni cations via the pulse electrodeposition method at 2500 and 5000 Hz frequencies, as well as 50% and 60% duty cycles. The GXRD patterns indicated that films consisted of a single face-centered-cubic structure. The effect of pulsed electrodeposition parameters on wettability and corrosion resistance of coatings was investigated as well. The results of the hydrophobic/hydrophilic test showed that all coatings were completely hydrophilic; the largest wettability angle is for the prepared film at a duty cycle of 50% in frequency of 5000 Hz (56°). The potentiodynamic polarization test results showed that same sample with a corrosion density of 0.067 μA/cm2, improved the corrosion resistance of the substrate due to the superhydrophilic properties of those by about 34 times, and therefore, was chosen as optimal conditions. Also, it was shown that none of the samples were sensitive to pitting corrosion. The results of the EIS test showed an outstanding performance of coatings in improving corrosion resistance compared to similar alloy samples, with a conservation efficiency of about 95%. In addition, it enables the evaluation of continuous changes in the metal-coating system. In such conditions, prepared film at 50% duty cycle in frequency of 5000 Hz improved the corrosion resistance of the substrate by about 40 times.

Stable ZnO-doped hydroxyapatite nanocoating for anti-infection and osteogenic on titanium

Titanium and titanium alloys have been widely used in orthopedics and related fields. However, their clinical applications are limited due to the lack of anti-infection, osteoinductivity and angiogenic ability. In the present study, we utilized pulse electrochemical deposition method to prepare polypyrrole (PPy) by the in-situ oxidative polymerization of pyrrole (Py), and through the coordination and doping of ions, the function of PPy as a dual regulator of hydroxyapatite nanoparticles (HA-NPs) and zinc oxide nanoparticles (ZnO-NPs) was achieved. Bioactivity test showed that the composite coating could induce the formation of apatite, and the apatite was in a neat arrangement preferentially grew along the (002) crystal plane, indicating good bioactivity. The release test showed that the dual regulation effect of PPy coordination and doping reduced the release rate of Ca2+ and Zn2+ from the composite coating. Antibacterial tests showed that the composite coating against Escherichia coli and Staphylococcus aureus. Besides, bone marrow-derived mesenchymal stem cells (BMSCs) exhibited good adhesion, proliferation and differentiation on the composite coating, and fluorescence staining experiments demonstrated good osteoinductivity of the composite coating. In this study, a multifunctional composite coating with anti-infection, angiogenic and osteoinductivity was successfully constructed on the titanium surface via pulse electrochemical deposition method.

Investigation of plasmonic Cu with controlled diameter over TiO2 photoelectrode for solar-to-hydrogen conversion

Plasmonic metal nanoparticles (NPs) have been used to improve the solar-to-hydrogen conversion efficiency. Relative to Au and Ag, Cu is cheaper and more abundant. In the present work, Cu NPs with the controlled diameter were deposited on TiO2 nanotube arrays (TNTAs) by using a pulse electrochemical deposition method. When the deposition was cycled 3600 times, the size of Cu NPs can be tuned to approximately 30 nm with the most uniform distribution, resulting in the remarkable characteristic peak of surface plasmon resonance and higher photocurrent density. The hydrogen production rates remained unchanged during irradiation (AM 1.5, 100 mW/cm2) of 2 h, indicating a good stability of the resultant Cu/TNTAs electrode. The photoelectrochemical performances of as-prepared Cu/TNTAs can also be comparable to those of Ag/TNTAs electrode fabricated by the same method.

Pulsed electrochemical deposition of porous WO3 on silver networks for highly flexible electrochromic devices

Uniform and lamellar-porous WO3 films were successfully prepared on a flexible Ag nanofiber (Ag NF) network film via a pulsed electrochemical deposition method for highly flexible electrochromic devices.

Synthesis, characterization and cytocompatibility assessment of hydroxyapatite-polypyrrole composite coating synthesized through pulsed reverse electrochemical deposition

Composite coating of hydroxyapatite-polypyrrole is synthesized with the help of pulsed reverse electrochemical deposition method from aqueous bath through in-situ formation and co-deposition of both phases simultaneously over metallic stainless steel surface. The inter phase bonding along with surface energy variation and morphology is tuned with the help of deposition current density, deposition time and reverse duty cycle. Hydroxyapatite (HA) lattice exhibits unidirectional growth along the highest atomic plane of 〈111〉 parallel to the coating surface. Different kind of deposited hydroxyapatite structures, namely lamellar and spherical particle scaffold, are observed at moderate and high current densities respectively together with the incorporation of polypyrrole (PPy) phase in between. Pyrrole ring stretching and bond strengthening represent the bonding with hydroxyapatite lattice, which in turn helps to increase the overall corrosion resistance of composite coating by ten-fold as compared to bare PPY coating. The coating deposited with moderate current density (10 mA/cm2) seems to be the optimum one regarding the faster-interconnected growth of MG63 cells over the coating surface along with highest corrosion resistance and anodic passivation capability. Presence of sub-micron level ceramic hydroxyapatite scaffold along with polymer filler material makes this composite biocompatible coating as a potential candidate to use over the load bearing metallic implant surfaces due to its sufficient elasticity along with superior toughness.

Mo(SxOy) thin films deposited by electrochemistry for application in organic photovoltaic cells

In this study, Mo(SxOy) thin films were deposited onto fluorine doped tin oxide (FTO) using pulsed electrochemical deposition method. It is shown by scanning electron microscopy, energy-dispersive spectroscopy and X-ray photoelectron spectroscopy that after water cleaning the deposited Mo(SxOy) film corresponds to a hybrid layer MoSx:MoO3. This hybrid is used as anode buffer layer (ABL) in planar organic photovoltaic cells (OPVCs) based on the couple copper-phthalocyanine/fullerene. It is shown that it is necessary to proceed to a soft annealing-5 min at 150 °C- of the anode FTO/Mo(SxOy) to clean the ABL surface in order to obtain efficient contact with the organic material. The OPVC with the optimum Mo(SxOy) thickness, 12 nm, showed a power conversion efficiency, PCE = 1.41% under an illumination of AM1.5, which is 12% higher than that achieved with a simple MoO3 ABL. This improvement is attributed to the fact that using a hybrid MoS2:MoO3 ABL allows to combine the advantages of its both constituents. The MoSx blocks the electrons, while the high work function of MoO3 induces a high hole extraction efficiency at the interface electron donor/anode.

Next-Generation Multifunctional Electrochromic Devices.

The rational design and exploration of electrochromic devices will find a wide range of applications in smart windows for energy-efficient buildings, low-power displays, self-dimming rear mirrors for automobiles, electrochromic e-skins, and so on. Electrochromic devices generally consist of multilayer structures with transparent conductors, electrochromic films, ion conductors, and ion storage films. Synthetic strategies and new materials for electrochromic films and transparent conductors, comprehensive electrochemical kinetic analysis, and novel device design are areas of active study worldwide. These are believed to be the key factors that will help to significantly improve the electrochromic performance and extend their application areas. In this Account, we present our strategies to design and fabricate electrochromic devices with high performance and multifunctionality. We first describe the synthetic strategies, in which a porous tungsten oxide (WO3) film with nearly ideal optical modulation and fast switching was prepared by a pulsed electrochemical deposition method. Multiple strategies, such as sol-gel/inkjet printing methods, hydrothermal/inkjet printing methods, and a novel hybrid transparent conductor/electrochromic layer have been developed to prepare high-performance electrochromic films. We then summarize the recent advances in transparent conductors and ion conductor layers, which play critial roles in electrochromic devices. Benefiting from the developments of soft transparent conductive substrates, highly deformable electrochromic devices that are flexible, foldable, stretchable, and wearable have been achieved. These emerging devices have great potential in applications such as soft displays, electrochromic e-skins, deformable electrochromic films, and so on. We finally present a concept of multifunctional smart glass, which can change its color to dynamically adjust the daylight and solar heat input of the building or protect the users' privacy during the daytime. Energy can also be stored in the smart windows during the daytime simultaneously and be discharged for use in the evening. These results reveal that the electrochromic devices have potential applications in a wide range of areas. We hope that this Account will promote further efforts toward fundamental research on electrochromic materials and the development of new multifunctional electrochromic devices to meet the growing demands for next-generation electronic systems.

Ultra-high-performance core-shell structured Ru@Pt/C catalyst prepared by a facile pulse electrochemical deposition method.

Core–shell structured catalysts, made by placing either a monolayer or a thin layer of a noble metal on relatively cheap core-metal nanoparticles, are fascinating and promising fuel cell catalysts due to their high utilization of noble metals. Here, we report our development of a core–shell structured catalyst, Ru@Pt/C, generated by a novel and facile pulse electrochemical deposition (PED) approach. We demonstrate that compared with a commercial Pt/C catalyst, this novel catalyst achieves over four times higher mass activity towards the anodic oxidation of methanol, and 3.6 times higher mass activity towards the cathodic reduction of oxygen. Importantly, we find that the intrinsic activity of Pt in this Ru@Pt/C catalyst is doubled due to the formation of the core–shell structure. The catalyst also shows superior stability: even after 2000 scans, it still retains up to 90% of the peak current. Our findings demonstrate that this novel PED approach is a promising method for preparing high-performance core–shell catalysts for fuel cell applications.

Non-noble metal copper nanoparticles-decorated TiO2 nanotube arrays with plasmon-enhanced photocatalytic hydrogen evolution under visible light

Cu nanoparticles (Cu NPs) were successful deposited on the TiO2 nanotube arrays (TNAs) through pulsed electrochemical deposition method. By adjusting the number of deposition cycles, the amount of Cu NPs can be controlled. Compared with pure TNAs, a new strong absorption peak appeared on Cu/TNAs under visible light region due to the surface plasmon resonance (SPR) of Cu NPs. Photoelectrochemical performance and photocatalytic hydrogen evolution characteristic of the Cu/TNAs catalysts were investigated under visible light irradiation. The novel Cu/TNAs heterogenous architectures show a stable and high photocatalytic activity for hydrogen evolution without the Pt co-catalyst.

A pulse electrochemical deposition method to prepare membrane electrode assemblies with ultra-low anode Pt loadings through in situ construction of active core–shell nanoparticles on an electrode

Ultra-low Pt loading membrane electrode assemblies (ULP MEAs) are prepared through in situ construction of core–shell Ir@Pt nanoparticles (Ir/Vulcan XC-72R as the core) on the surface of an electrode via a pulse electrochemical deposition (PED) approach. The core material is coated on a membrane with a conventional catalyst-coated membrane process prior to the deposition of the shell metal (Pt in this case). The ULP MEAs are characterized by X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and X-ray Photoelectron Spectroscopy (XPS). The effects of a number of preparation parameters on cell performance are investigated in detail. The performance of the ULP MEA, in which the anode loadings of Pt and metals are ∼0.012 mg cm−2 and 0.044 mg cm−2(0.012 mg cm−2 Pt + 0.032 mg cm−2 Ir) respectively, is found to be competitive with that of an MEA prepared with an anode Pt loading of 0.1 mg cm−2 (commercial Pt/C catalyst from Johnson Matthey), manifesting the solid advantage of this in situ PED method.

Composition and photoelectrochemical properties of WO3/TNAs photoelectrodes fabricated by in situ electrochemical method

TiO2/Ti Nanotube arrays (TNAs) and WO3/TNAs photoelectrodes were fabricated by in situ anodization and cycle pulse electrochemical deposition method. The morphology and structure were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectra and X-ray photoelectron spectroscopy (XPS). Optical properties and photoelectrochemical (PECH) properties were investigated by surface photovoltage (SPV), ultra UV–vis diffuse reflectance spectra (UV/vis/DRS), open-circuit potential (OCP), and photocurrent density The results showed that WO3/TNAs photoelectrodes have excellent photoresponse performance. WO3 would enhance the photovoltage and photocurrent of TNAs photoelectrodes. The presence of WO3 caused red shift and enhanced the photosensitivity of TNAs photoelectrodes in whole light region.

Honeycomb Cupric Oxide and Hematite Nanotubes Synergism Photoelectro-reduction CO2

Vertically aligned Fe2O3 nanotubes (Fe2O3 NTs) arrays were prepared on the iron foil by potentiostatic anodization method. The anodization experiments were performed under 30 V for 2 h (20 degrees C). The ferrous foil was working electrode and titanium foil was counter electrode. The electrolytes were consisted of 0.25 wt% NH4F in an aqueous solution (Volume of water : glycol=3 : 97). After sonicating for 5 min, the samples were put under oxygen atmosphere with the flow rate of 60 sccm (standard cubic centimeters/min) and heated to 500 degrees C with the rate of 3 degrees C.min(-1) and maintained at 500 degrees C for 2 h. Then cooled to room temperature with the rate of 3 degrees C.min(-1). Honeycomb structure cupric oxide (CuO HCs) were decorated on the surface of Fe2O3 NTs by the pulse electrochemical deposition method. This was done by CHI660D potentiostat in 1 mol.L-1 CuSO4 solution (40 degrees C) in a three-electrode configuration. The Fe2O3 NTs electrode worked as counter electrode, Hg/Hg2Cl2 in saturated KCl solution as reference electrode, and platinum wire as working electrode, respectively. A 10 ms cathodic pulse with a current density of -70 mA.cm(-2) was employed. After that followed by a 1 ms anodic pulse and its density was +70 mA.cm(-2) to prevent damage of the Fe2O3 NTs structure. Finally was a 1000 ms rest time. The electrodeposition time was 36 s, with a forward duty cycle of 0.99% (considering cathodic, anodic and rest components). Then the samples were annealed under oxygen atmosphere with the flow rate of 60 sccm then heated to 300 degrees C with the rate of 3 degrees C.min(-1) and maintained at 300 degrees C for 2 h. Then cooled to room temperature with the rate of 3 degrees C.min(-1). Then the CuO HCs/Fe2O3 NTs catalysis was obtained. The SEM images showed that CuO HCs distributed uniformly on the surface of Fe2O3 NTs that arranged in order were volcano-like. Measured by UV-vis DRS (ultraviolet-visible diffuse reflection spectrum) and valence band photoemission spectrum, its band energy has been narrowed from 2.03 eV to 1.84 eV after CuO decorating. It also has admirable photocatalytic and electrocatalytic reduction performance. The main product of photoelectrocatalytic CO2 reduction identified by chromatography was methanol and its concentration reached 3.77 mmol/L after 6 h. The study has some guidance and reference significance for photoelectrocatalytic CO2 reduction.

Reduction of CO2 to low carbon alcohols on CuO FCs/Fe2O3 NTs catalyst with photoelectric dual catalytic interfaces

In this paper, the CuO FCs/Fe2O3 NTs catalyst was obtained after Fe2O3 nanotubes (Fe2O3 NTs) were decorated with CuO flower clusters (CuO FCs) by the pulse electrochemical deposition method. The in situ vertically aligned Fe2O3 NTs were prepared on the ferrous substrate by a potentiostatic anodization method. The SEM result showed the volcano-like Fe2O3 NTs were arranged in order and the CuO FCs constituted of flaky CuO distributed on the Fe2O3 NTs surface uniformly. After CuO FCs were loaded on Fe2O3 NTs, the absorption of visible light was enhanced noticeably, and its band gap narrowed to 1.78 eV from 2.03 eV. The conduction band and valence band locating at -0.73 eV and 1.05 eV, respectively were further obtained. In the PEC reduction of CO2 process, methanol and ethanol were two major products identified by chromatography. Their contents reached 1.00 mmol L(-1) cm(-2) and 107.38 μmol L(-1) cm(-2) after 6 h, respectively. This high-efficiency catalyst with photoelectric dual catalytic interfaces has a great guidance and reference significance for CO2 reduction to liquid carbon fuels.