Increase In Current Density Research Articles

Tailoring d–p Orbital Hybridization to Decipher the Essential Effects of Heteroatom Substitution on Redox Kinetics

AbstractThe heteroatom substitution is considered as a promising strategy for boosting the redox kinetics of transition metal compounds in hybrid supercapacitors (HSCs) although the dissimilar metal identification and essential mechanism that dominate the kinetics remain unclear. It is presented that d‐p orbital hybridization between the metal and electrolyte ions can be utilized as a descriptor for understanding the redox kinetics. Herein, a series of Co, Fe and Cu heteroatoms are respectively introduced into Ni3Se4 cathodes, among them, only the moderate Co‐substituted Ni3Se4 can hold the optimal d‐p orbital hybridization resulted from the formed more unoccupied antibonding states π*. It inevitably enhances the interfacial charge transfer and ensures the balanced OH− adsorption‐desorption to accelerate the redox kinetics validated by the lowest reaction barrier (0.59 eV, matching well with the theoretical calculations). Coupling with the lower OH− diffusion energy barrier, the prepared cathode delivers ultrahigh rate capability (~68.7 % capacity retention even the current density increases by 200 times), and an assembled HSC also presents high energy/power density. This work establishes the principles for determining heteroatoms and deciphers the underlying effects of the heteroatom substitution on improving redox kinetics and the rate performance of battery‐type electrodes from a novel perspective of orbital‐scale manipulation.

Tailoring d-p Orbital Hybridization to Decipher the Essential Effects of Heteroatom Substitution on Redox Kinetics.

The heteroatom substitution is considered as a promising strategy for boosting the redox kinetics of transition metal compounds in hybrid supercapacitors (HSCs) although the dissimilar metal identification and essential mechanism that dominate the kinetics remain unclear. It is presented that d-p orbital hybridization between the metal and electrolyte ions can be utilized as a descriptor for understanding the redox kinetics. Herein, a series of Co, Fe and Cu heteroatoms are respectively introduced into Ni3Se4 cathodes, among them, only the moderate Co-substituted Ni3Se4 can hold the optimal d-p orbital hybridization resulted from the formed more unoccupied antibonding states π*. It inevitably enhances the interfacial charge transfer and ensures the balanced OH- adsorption-desorption to accelerate the redox kinetics validated by the lowest reaction barrier (0.59 eV, matching well with the theoretical calculations). Coupling with the lower OH- diffusion energy barrier, the prepared cathode delivers ultrahigh rate capability (~68.7 % capacity retention even the current density increases by 200 times), and an assembled HSC also presents high energy/power density. This work establishes the principles for determining heteroatoms and deciphers the underlying effects of the heteroatom substitution on improving redox kinetics and the rate performance of battery-type electrodes from a novel perspective of orbital-scale manipulation.

Strategic Development of Ni–Cu–Fe2O3 Composite Coatings to Strengthen Mild Steel Against Corrosion

Mild steel is extensively employed in various industries due to its affordability and versatility. However, its susceptibility to corrosion poses a significant challenge. This study explores the efficacy of protecting mild steel by applying coatings composed of highly noble copper and its alloys. In this direction, Ni–Cu alloy and Ni–Cu–Fe2O3 coating have been developed from a sulfate citrate bath on mild steel through the electrodeposition method. The alloy and composite coating deposition was done at different current densities 1 A dm−2, 2 A dm−2, 3 A dm−2, and 4 A dm−2. The copper content of the coating has increased with an increase in current density in both alloy and composite coatings. The deposit with a high Copper content showed lower crystallite size with a lower corrosion rate value at a current density of 3 A dm−2. The trace addition of Fe2O3 into the Ni–Cu alloy matrix has improved the overall corrosion resistance of the mild steel materials as compared to bare Ni–Cu alloy coating.

Highly flexible and transparent colorless polyimide substrate sandwiched between plasma polymerized fluorocarbon and InGaTiO for high performance flexible perovskite solar cells

ABSTRACT We integrated transparent antireflective coatings and transparent electrodes onto flexible colorless polyimide (CPI) substrates to fabricate high-performance flexible perovskite solar cells. Multifunctional PPFC/CPI/IGTO substrates were fabricated by sputtering the optimal plasma-polymerized fluorocarbon (PPFC) antireflective coating and InGaTiO (IGTO) electrode films on both sides of the CPI substrate. By applying PPFC with a low refractive index (1.38) as an antireflective coating, the transparency of the PPFC/CPI/IGTO substrate increased by an additional 1.2%. In addition, owing to the amorphous characteristics of the PPFC and IGTO layers, the PPFC/CPI/IGTO substrate showed constant sheet resistance and transmittance change even after 10,000 cycles during the bending tests. The flexible perovskite solar cells, fabricated on the PPFC/CPI/IGTO substrate, exhibited an increase in current density of 1.48 mA/cm2 after the deposition of the PPFC antireflective coating. These results confirmed that the PPFC/CPI/IGTO substrate was durable against high-temperature treatment, flexible, and exhibited excellent electrical characteristics. This enhanced the efficiency and durability of the flexible perovskite solar cells. Moreover, the hydrophobic PPFC layer allowed the self-cleaning of inflexible perovskite solar cells. Given these attributes, the PPFC/CPI/IGTO structure has been recognized as a good choice for multifunctional substrates of flexible perovskite solar cells, presenting the potential for enhancing performance.

Elucidating the effects of Cr–S variations in Cr-doped CZTS for intermediate band solar cell applications

Intermediate band (IB) materials, such as chromium-doped Cu2ZnSnS4 (CZTS:Cr) show promise for surpassing the Shockley-Queisser limit in solar cells. This study explores the effects of sulphur variation in this film. Sulphurization results in a layered structure, with Cr-poor micron-sized grains on top and Cr-rich nanograins at the bottom preventing complete crystallization. Optimization improves the Cu2ZnSnS4 (CZTS) crystallization and introduces additional absorption peaks at 1.15 eV and 1.31 eV, alongside the fundamental 1.55 eV absorption using 47.1 mg of sulphur content. CZTS:Cr device fabricated achieve a threefold increase in current density (Jsc) compared to undoped samples. These findings are crucial for advancing intermediate band solar cell (IBSC) based on CZTS:Cr IB material.

Sliding Memristor in Parallel-Stacked Hexagonal Boron Nitride.

Sliding ferroelectricity in 2D materials, arising from interlayer sliding-induced interlayer hybridization and charge redistribution at the van der Waals interface, offers a means to manipulate spontaneous polarization at the atomic scale through various methods such as stacking order, interfacial contact, and electric field. However, the practical application of extending 2D sliding ferroelectricity remains challenging due to the contentious mechanisms and the complex device structures required for ferroelectric switching. Here, a sliding memristor based on a graphene/parallel-stacked hexagonal boron nitride/graphene tunneling device, featuring a stable memristive hysteresis induced by interfacial polarizations and barrier height modulations, is presented. As the tunneling current density increases, the memristive window broadens, achieving an on/off ratio of ≈103 and 2 order decrease of the trigger current density, attributed to the interlayer migration of positively charged boron ions and the formation of conductive filaments, as supported by the theoretical calculations. The findings open a path for exploring the sliding memristor via a tunneling device and bridge the gap between sliding ferroelectricity and memory applications.

Phase structure and electrochemical properties of A5B19 La0.8-xPrxMg0.2Ni3.8 (x = 0–0.3) hydrogen storage alloy anode material

The La0.8-xPrxMg0.2Ni3.8 (x = 0, 0.05, 0.1, 0.2, 0.3) alloy were synthesized useing the induction melting method. X-ray diffraction, scanning electron microscope, electron probe micro analyzer, and electrochemical tests were used to analyze the structure and electrochemical performance of the La0.8-xPrxMg0.2Ni3.8 (x = 0–0.3) alloy. It was studied how the Pr element affected the electrochemical characteristics and microstructure of the A5B19 La-Mg-Ni based hydrogen storage alloy. The results show that the alloy consists of the CaCu5-LaNi5 phase, 2 H-Pr5Co19 phase, and 3R-Ce5Co19 phase. The abundance of the A5B19 phase increase with the increase of Pr content, while the abundance of the LaNi5 phase decrease, and the addition of Pr promotes the formation of the 2 H-Pr5Co19 phase. According to the results of the electrochemical test, every sample has good activation qualities, and the activation can be completed in 3–4 times. The activation properties are not significantly altered by the addition of Pr. The maximum discharge capacity increases at first, then decreases, reaching the highest 371.15 mAh g−1 at x = 0.2. The cyclic stability gradually improves with increasing content of Pr, and the maximum capacity retention rate reaches 85.80 % after 100 cycles. The primary factor influencing the alloy's high rate discharge ability is the exchange current density. With the increase of the exchange current density, the high rate discharge performance is gradually enhanced.

Enhancing OLED electroluminescence by surface modification and work function adjustment of anode through NiO:Co coating

This study presents an approach to improve the electroluminescence (EL) of organic light-emitting diodes (OLEDs) by coating an ultra-thin NiO:Co (NCO) layer on the anode. The NCO layer was pivotal in modifying anodic properties, including surface roughness, hydrophilicity, and work function, thereby promoting ohmic hole injection from the anode into the NPB layer and enhancing the current density and carrier recombination in OLEDs. Compared to OLEDs with a pristine ITO anode, the OLEDs with an NCO-coated ITO anode showed a significant enhancement in EL performance, including a 24.5 % increase in current density, an 84.9 % enhancement in brightness, and a 48.7 % boost in efficiency. Notably, coating NCO on the anode consistently enhanced hole injection regardless of whether ITO or PEDOT:PSS was used as the anode.

Understanding the Effects of Anode Catalyst Conductivity and Loading on Catalyst Layer Utilization and Performance for Anion Exchange Membrane Water Electrolysis.

Anion exchange membrane water electrolysis (AEMWE) is a promising technology to produce hydrogen from low-cost, renewable power sources. Recently, the efficiency and durability of AEMWE have improved significantly due to advances in the anion exchange polymers and catalysts. To achieve performances and lifetimes competitive with proton exchange membrane or liquid alkaline electrolyzers, however, improvements in the integration of materials into the membrane electrode assembly (MEA) are needed. In particular, the integration of the oxygen evolution reaction (OER) catalyst, ionomer, and transport layer in the anode catalyst layer has significant impacts on catalyst utilization and voltage losses due to the transport of gases, hydroxide ions, and electrons within the anode. This study investigates the effects of the properties of the OER catalyst and the catalyst layer morphology on performance. Using cross-sectional electron microscopy and in-plane conductivity measurements for four PGM-free catalysts, we determine the catalyst layer thickness, uniformity, and electronic conductivity and further use a transmission line model to relate these properties to the catalyst layer resistance and utilization. We find that increased loading is beneficial for catalysts with high electronic conductivity and uniform catalyst layers, resulting in up to 55% increase in current density at 2 V due to decreased kinetic and catalyst layer resistance losses, while for catalysts with lower conductivity and/or less uniform catalyst layers, there is minimal impact. This work provides important insights into the role of catalyst layer properties beyond intrinsic catalyst activity in AEMWE performance.

Fabrication of innovative ZnCo2O4/Ti3C2Tx MXene nanocomposite counter electrode to replace Pt in dye-sensitized solar cells and improve solar cell performance

This study focuses on the fabrication and optimization of Ti3C2Tx/ZnCo2O4 (ZCO) hybrid counter electrodes (CEs) for Dye-Sensitized Solar Cells (DSSCs). The Ti3C2Tx Max phase was initially prepared through a solid-state reaction method and subsequently transformed into the MXene phase using the minimally intensive layer delamination (MILD) technique. ZnCo2O4 was synthesized via the sol-gel method. Various analyses, including FESEM, XRD, EDS, CV, Tafel, XPS, IPCE, and HRTEM, were employed to characterize the prepared materials. The key parameter investigated involved CEs with different weight ratios of Ti3C2Tx to ZnCo2O4 (0 %, 20 %, 30 %, and 40 %). Results revealed that the optimized DSSC with 30 % Ti3C2Tx to ZCO exhibited a remarkable efficiency of 8.61 %, surpassing both the cell without MXene (5.59 % efficiency) and the one with a Pt CE (8.12 % efficiency). The enhanced performance was attributed to a significant increase in current density primarily driven by the higher electrocatalytic activity of the ZM30 CE and improved conductivity.

Mechanically robust and self-cleaning antireflective coatings for photovoltaic modules

As the conversion efficiency of solar cells approaches its theoretical upper limit, the importance of photon management in enhancing photovoltaic modules performance becomes paramount. One promising approach involves the application of antireflective coatings to the surface of the photovoltaic glass to improve its transmittance. However, balancing mechanical durability, self-cleaning characteristics, and optical performance for photovoltaic applications remains challenging. This study focuses on synthesizing a composite coating through the sol-gel method, aiming to achieve high optical transmittance and superior mechanical properties. Hollow silica nanoparticles (HSN) are employed to achieve a reduced refractive index, while a composite sol of zirconium dioxide (ZrO2) and titania (TiO2) is utilized to enhance mechanical strength and hydrophilicity. The prepared composite coatings demonstrate notable improvements, with the photovoltaic transmittance (TPV) increasing from 88.31 % to 94.03 % in the 300–1100 nm wavelength range, with peak transmittance reaching 98.01 %. Additionally, the coatings exhibited a pencil hardness rating of 3H alongside exceptional abrasion resistance, affirming their potential for enduring practical deployment. When compared to uncoated glass, modules integrated with these composite coatings showed a significant increase in short-circuit current density (JSC) by 1.28 mA cm-2 and in photoelectric conversion efficiency (PCE) by 0.70 %. These results highlight the composite coatings' capacity to enhance the conversion efficiency of photovoltaic modules significantly. By attempting to prepare anti reflective coatings with high mechanical strength and self-cleaning properties, this study is expected to make a valuable contribution to the advancement of sustainable and durable solar cell technology.

Suppressing Competing Solvent Reduction in CO2 Electroreduction with a Magnetic Field.

The presence of an external magnetic field is found to affect the competition between the H2O and CO2 reduction reactions by increasing mass transport via the Lorentz force. Increasing the magnetic field strength at the electrode surface from 0 to 325 mT increases the selectivity of CO over H2 by 3×, while an increase in current density from 0.5 to 5 mA/cm2 increases the selectivity of CO production by 5×. Cyclic voltammetry and finite-element simulations reveal that the origin of the enhanced CO selectivity is attributable to a magnetic field lowering the electrode-electrolyte interfacial pH. A drop in interfacial pH enables increased production of CO from CO2 reduction due to a decrease in the activity of H2O reduction and increase in CO2 solubility near the electrode surface. The insight provided in this study offers new opportunities to control reaction selectivity in electrocatalysis with magnetic field vectors.

In Situ Observation and Electrical Signal Analysis of Different Bubble Detachment Modes on Microelectrode Surface

The deactivation of the reaction surface caused by bubble covering is an important factor that causes the decrease in the efficiency of water electrolysis. By combining an electrochemical workstation with a high-speed camera, the evolutionary properties of hydrogen bubble and potential were obtained on a horizontal microelectrode with a diameter of 100 μm. During the electrolysis, individual bubbles evolved periodically on the electrode surface. Under the influence of electrode adsorption, the detachment diameter of the bubble is independent of current density, but with the increase of current density, the bubble detachment frequency increases. With the increase of ethylene glycol (EG) concentration, the bubble detachment frequency increased. When the concentration of EG is greater than 7.5 g l−1, the surface tension of the solution is lower than that of water, at which time the detachment mode of the bubble changes. Separating the resistance caused by the bubbles from the total resistance, it was found that the additional resistance caused by the bubbles rapidly became smaller as the EG concentration increased until the EG concentration reached 7.5 g l−1. The total resistance decreases first and then increases when the EG concentration is greater than 3 g l−1.

Influence of anodic treatment of a copper-nickel alloy in a eutectic mixture of choline chloride and urea on the surface morphology and electrocatalytic behavior in the hydrogen evolution reaction

For the first time, we investigated the process of potentiostatic anodic treatment of the surface of a copper (≈55%)-nickel alloy in a eutectic mixture of urea and choline chloride (reline), which is a typical representative of a new generation of ionic liquids, deep eutectic solvents. The anodic behavior of the alloy in the used solvent was characterized by cyclic voltammetry, and the nature of the electrochemical dissolution reactions of individual components of the alloy corresponding to several anodic current waves registered in voltammograms was determined. It was established that the anodic dissolution of the alloy occurs under conditions of salt surface passivation due to the formation of a layer of poorly soluble products of the electrode reaction. It was shown that under conditions of prolonged (150 min) potentiostatic polarization of the alloy in reline for various values of the electrode potential (in the range from 0.1 to 1.7 V relative to the Ag reference electrode), the chemical composition of the surface remained unchanged (i.e., there was no selective etching of individual components of the alloy), but an evolution of surface morphology patterns was observed, the specific type of which depended on the value of the applied potential. Anodic treatment of the Cu-Ni alloy in the reline solvent at any of the investigated anodic potentials led to an increase in the surface roughness coefficient, and electrochemical polishing did not occur. Analysis of kinetic data related to the hydrogen evolution reaction on the surfaces of reline-treated copper-nickel alloys in a 1 M NaOH aqueous solution showed a significant increase in exchange current density. This indicates enhancement of electrocatalytic activity compared to the untreated surface. The observed effect is likely associated with an increase in the true surface area of the alloy available for electrochemical reaction and an increase in the surface concentration of electrocatalytic sites resulting from the anodic dissolution of the alloy. The obtained results can be used in the development of highly efficient and relatively inexpensive electrocatalysts for hydrogen energy.

Boosting quantum-structured solar cell light absorption through compressively strained superlattices

The escalating demand for improved energy conversion efficiency in vehicular applications of solar cells underscores the need for innovative solutions. This study focuses on enhancing the current density of GaAs middle cells within conventional Ge-based triple-junction solar cells to realize unprecedented levels of energy conversion efficiency. We introduced a novel superlattice configuration termed a compressively strained superlattice (CSSL) and demonstrated its integration into a p-i-n junction GaAs solar cell, achieving a current density increase of 1.03 mA cm−2 over conventional GaAs solar cells. Prior investigations have explored a strain-balanced superlattice (SBSL) to enhance GaAs middle cell current density. However, our findings establish the superiority of the CSSL over the SBSL in terms of current density improvement, with the CSSL featuring 1.59 times more quantum wells per unit length than the SBSL. This increase in quantum well quantity significantly enhances light absorption efficiency and consequently, the current density.

Optimization and mass transfer analysis under the ribs of multi-serpentine flow fields

This study aims to enhance the performance of Proton Exchange Membrane Fuel Cell (PEMFC) by optimizing the design of a three-channel serpentine flow field. The focus is on the introduction of sub-channels beneath the flow field ribs, utilizing the pressure differential between the main and sub-channels to strengthen lateral convection under the ribs, thus achieving uniform distribution of reaction gases. Using Computational Fluid Dynamics (CFD) methods, the performance of traditional and optimized flow fields were compared across various metrics. The results show that the introduction of sub-channels significantly improves gas mass transfer efficiency, enhances the uniformity of oxygen concentration and current density, and optimizes water content on the proton exchange membrane. At a voltage of 0.5 V, the Improved Serpentine Flow Field (ISCF) exhibits a notable enhancement in current density, increasing from 1.501 A/cm2 in the Traditional Serpentine Flow Field (TCSF) to 1.654 A/cm2 in the ISCF. This represents a significant 10 % increase in current density. Concurrently, the uniformity index climbs from 0.84 to 0.898, marking a 7 % improvement in uniformity. Furthermore, the ISCF design achieves a substantial reduction in pressure drop, decreasing from 1631 Pa to 1212 Pa, a reduction of 26 %. Additionally, the expansion of sub-channel width markedly boosts cell performance, whereas the Increase in sub-channel height reaches a saturation point beyond a certain threshold, indicating an optimal range for dimensional adjustments.

Nanoscale interface engineering for enhanced performance in light-emitting-diode devices: ITO/Ag-SRCOOH

In light-emitting diode (LED) devices, the hole-injection layer (HIL) reduces the hole injection barrier (HIB) between the anode and organic layers to obtain favorable conditions for hole transport, which considerably affects device efficiency and performance. However, the fabrication of ultrathin silver (Ag) films for electron and hole transport layers remains challenging. We demonstrated the design of a nanoscale HIL interface with chemisorption-bonded carboxylic acid-terminated alkanethiol self-assembled layers on ultrathin Ag. The device structure consisted of indium tin oxide (ITO)/Ag-mercaptan acid (Ag-SRCOOH)/N, Nj-Di (1-naphthyl)-N,Nj-diphenyl-(1,1-biphenyl)-4,4-diamine (NPB)/tris-(8-hydroxyquinoline) aluminum (Alq3)/ETL(LiF/Al. Notably, a chemical bond peak was not detected between ITO and ultrathin Ag. However, X-ray photoelectron spectroscopy (XPS) measurements confirmed Ag binding to the thiol group of 3-mercaptopropionic acid (MPA) and 11-mercaptoundecanoic acid (MUA) on the Ag island surface, which is evident from -S-Ag- and -RS-Ag- association peaks. Ultraviolet photoelectron spectroscopy analysis results revealed a reduction in the HIB of device from 0.68 to 0.19 eV. Consequently, the luminance and current density, and current density of the AgNP–MPA device increased by 63-fold, 5.8-fold, and 1.1-fold, respectively. Similarly, the AgNP-MUA device exhibited enhanced performance with a 61-fold increase in luminance, 43-fold increase in current density, and a 1.4-fold increase in current efficiency, respectively. The results of this study not only opened novel avenues for future applications, including operation requiring flexibility and transparency of LEDs, but also proposed the optimization of nanoscale interfaces to enhance LED performance.

Performance of proton exchange membrane fuel cell system by considering the effects of the gas diffusion layer thickness, catalyst layer thickness, and operating temperature of the cell

BackgroundIn this research, the effect of anode and cathode channel cross-sectional shape on the performance of PEM fuel cell was investigated and the appropriate length and dimensions of the channel were determined. Finally, for the determined geometric conditions, the cell performance at different voltages was investigated. MethodsThe purpose of this study was to investigate the structural characteristics of the fuel cell on its performance. The results show that the pressure and temperature in the catalyst layer (CL) of the cathode side are greater than the anode, and the temperature in the central regions of the catalyst layer is higher than the lateral regions. Also, the channel with a length of 100 mm is optimal in terms of producing the maximum current density and the amount of pressure drop is much lower than the channel with a length of 150 mm, which reduces the power consumption of the cell. Significant findingsIn general, a higher electric current is produced by increasing the thickness of the gas diffusion layer (GDL) and the catalyst layer. At a voltage of 0.8 V, with increasing thickness from 0.25 mm to 0.5 mm, the current density increases above 6 %. The percentage increase in current density at 60 °C–80 °C for 0.85 V and 0.75 V voltages is 42.1 % and 9.28 %, respectively.

Characterization of resistance welded hybrid sandwich sheets with additively manufactured core structure

Abstract Production of additively manufactured sandwich sheets is limited to small sizes. In the new introduced process route, additively manufactured core structures are joined with rolled face sheets by resistance welding, and the formability of the hybrid sandwich sheets is investigated. The necessity of developing the humps to improve the quality of resistance welding is initially investigated. Two different core structures, namely honeycomb and hollow sphere, are selected, and electrical-thermal coupled simulations with the ABAQUS software are performed to study the temperature distribution during resistance welding without and with hump. The strength of the joints for the fabricated sandwich sheets is verified by a quasi-static shear test. It is experimentally proven that the sandwich sheets without a hump in the core structure are not fully joined, and desired temperature localization is possible only by applying the hump. This is because the hump reduces the contact area, which leads to an increase in current density at the point where the resistance ratios are changed. This leads to higher temperatures in the intended joining zone. Different hump geometries for the core structure are designed, fabricated, and joined to the face sheets under different process parameters. The spot contact yields up to 50% higher shear strength than the linear or area contact. The free air bending results show that the double weld is essential for successful subsequent bending. It is also concluded that increasing the resistance welding time by more than 120 ms does not affect the joining strength of hybrid sheets.

Mechanical behavior and underlying mechanism of nickel-based superalloy during coupling electrical pulse and ultrasonic treatment

Coupling electric pulse and ultrasonic treatment (CEPUT) is a multi-energy field-assisted forming technology that can improve the forming efficiency of materials. The current research focused on the surface modification of materials by CEPUT, lacking the explanation of its coupling mechanism. In this study, Inconel 718 was adopted as the research object to observe the mechanical behavior and microstructure after CEPUT uniaxial tension experiment. The deformation tendency of grain under coupling multi-energy field was described by analyzing the texture evolution and dislocation morphology. The coupling mechanism of ultrasonic vibration and pulsed current was revealed in CEPUT. The experimental results revealed that there was a nonlinear relationship between the increase of flow stress softening efficiency and the increase of ultrasonic energy density and current density. This phenomenon was the macroscopic manifestation of interference between initial ultrasonic vibration and vibration after energy attenuation, which was related to dislocation slip and recrystallization under coupled multi-field. In addition, more efficient path of dislocation slip was demonstrated through the CEPUT. Among them, ultrasonic vibration caused local resistance to rise at the dislocation source and dislocation pile-up, which strengthened the local Joule heating effect; while the pulsed current reduced the activation energy required for dislocation slip near the waning points. This effectively reduced the resistance of dislocation motion near the pinning point, promoting the chance of dislocation crossing and annihilation. Meanwhile, the high temperature caused by pulsed current and local high strain caused by ultrasonic vibration were more favorable to dynamic recrystallization, and the change of grain orientation was more active. The texture strength and grain orientation of the matrix can be effectively controlled by adjusting the input power of ultrasonic vibration and pulsed current.