Anodic Current Research Articles

Application of SECM to detect a local electrolyte acidification due to the hydrogen flux desorption from a cathodic charged stainless steel

This work aims to estimate local pH variations of a hydrogen charged sample using Scanning ElectroChemical Microscopy (SECM). For that purpose, the microelectrode is polarized in the cathodic domain, where the proton reduction takes place. An initial calibration suggests that cathodic current of the platinum tip is sensitive to pH variations. Then, this system was applied near the surface of stainless steel previously charged with hydrogen. Coupling this result with the analysis of the uncharged samples at two different pH, it appears that hydrogen desorption induces a local acidification which could explain the increase in dissolution kinetics after hydrogen absorption, which has been reported in many studies.

Anionic Ionomer: Released Surface-Immobilized Cations and an Established Hydrophobic Microenvironment for Efficient and Durable CO2-to-Ethylene Electrosynthesis at High Current over One Month.

Electrosynthesis of multicarbon products, such as C2H4, from CO2 reduction on copper (Cu) catalysts holds promise for achieving carbon neutrality. However, maintaining a steady high current-level C2H4 electrosynthesis still encounters challenges, arising from unstable alkalinity and carbonate precipitation caused by undesired ion migration at the cathode under a repulsive electric field. To address these issues, we propose a universal "charge release" concept by incorporating tiny amounts of an oppositely charged anionic ionomer (e.g., perfluorinated sulfonic acid, PFSA) into a cationic covalent organic framework on the Cu surface (cCOF/PFSA). This strategy effectively releases the hidden positive charge within the cCOF, enhancing surface immobilization of cations to impede both outward migration of generated OH- and inward migration of cations, inhibiting carbonate precipitation and creating a strong alkaline microenvironment. Meanwhile, the ionomer's hydrophobic chains create a hydrophobic environment within the cCOF, facilitating efficient gas transport. In situ characterizations and theoretical calculations demonstrate that the cCOF/PFSA catalyst establishes a hydrophobic strong alkaline microenvironment, optimizing the adsorption strength and configuration of *CO intermediates to promote the C2H4 formation. The optimized catalyst achieves a 70.5% Faradaic efficiency for C2H4 with a partial current density over 470 mA cm-2. Notably, it delivers a high single-pass carbon efficiency of 96.5% for CO2RR and sustains an exceptional stability over 760 h. When implemented in a large-area MEA electrolyzer and a 5-cell MEA stack, the system achieves an industrial current of 15 A and continuous C2H4 production exceeding 19 mL min-1, marking a significant step toward industrial feasibility in CO2RR-to-C2H4 conversion.

Tandem Electroreduction of Nitrate to Ammonia Using a Cobalt–Copper Mixed Single‐Atom/Cluster Catalyst with Synergistic Effects

AbstractElectrochemical conversion of waste nitrate (NO3−) to ammonia (NH3) for environmental applications, such as carbon‐neutral energy sources and hydrogen carriers, is a promising alternative to the energy‐intensive Haber–Bosch process. However, increasing the energy efficiency is limited by the high overpotential and selectivity. Herein, a Co─Cu mixed single‐atom/cluster catalyst (Co─Cu SCC) is demonstrated—with well‐dispersed Co and Cu active sites anchored on a carbon support—that delivers high NH3 Faradaic efficiency of 91.2% at low potential (–0.3 V vs. RHE) due to synergism between the heterogenous active sites. Electrochemical analyses reveal that Cu in Co─Cu SCC preferentially catalyzes the NO3−‐to‐NO2− pathway, whereupon Co catalyzes the NO2−‐to‐NH3 pathway. This tandem electroreduction bypasses the rate‐determining steps (RDSs) for Co and Cu to lower the reaction energy barrier and surpass scaling relationship limitations. The electrocatalytic performance is amplified by the subnanoscale catalyst to increase the partial current density of NH3 by 2.3 and 5.4 times compared to those of individual Co, Cu single‐atom/cluster catalysts (Co SCC, Cu SCC), respectively. This Co─Cu SCC is operated stably for 32 h in a long‐term bipolar membrane (BPM)‐based membrane electrode assembly (MEA) system for high‐concentration NH3 synthesis to produce over 1 m NH3 for conversion into high‐purity NH4Cl at 2.1 g day−1.

Synergistic Pd‐Au Catalyst for Selective Electrosynthesis of Dimethyl Carbonate in Conjunction with High‐Rate Redox System

AbstractThis study reports ambient electrosynthesis of dimethyl carbonate with a palladium–gold catalyst. Material screening identifies a region of intermediate‐catalyst binding energy that facilitates interfacial electron and proton transfers for selective carbonylation, achieving a distinct maximum of 92% faradaic efficiency to dimethyl carbonate. Structural and electrochemical analyses suggest that the alloying of palladium and gold effectively modulates the CO* binding energy to the catalytic surface, in accord with subsequent computational studies. With an extended heterogeneous–homogeneous catalytic environment with a halide redox mediator, a remarkable partial current density of 52 mA cm−2 is observed for dimethyl carbonate for 100 h of continuous operation.

Electron-Efficient Co-Electrosynthesis of Formates from CO2 and Methanol Feedstocks.

The electrochemical conversion of CO2 into valuable chemicals using renewable electricity shows significant promise for achieving carbon neutrality and providing alternative energy storage solutions. However, its practical application still faces significant challenges, including high energy consumption, poor selectivity, and limited stability. Here, we propose a hybrid acid/alkali electrolyzer that couples the acidic CO2 reduction reaction (CO2RR) at the cathode with alkaline methanol oxidation reaction (MOR) at the anode. This dual electro-synthesis cell is implemented by developing Bi nanosheets as cathode catalysts and oxide-decorated Cu2Se nanoflowers as anode catalysts, enabling high-efficiency electron utilization for formate production with over 180 % coulombic efficiency and more than 90 % selectivity for both CO2RR and MOR conversion. The hybrid acid/alkali CO2RR-MOR cell also demonstrates long-term stability exceeding 90 hours of continuous operation, delivers a formate partial current density of 130 mA cm-2 at a voltage of only 2.1 V, and significantly reduces electricity consumption compared to the traditional CO2 electrolysis system. This study illuminates an innovative electron-efficiency and energy-saving techniques for CO2 electrolysis, as well as the development of highly efficient electrocatalysts.

Optical and Structural Properties of V2O5 Electrochromic Thin Films

The increase in global temperature has led to a significant surge in energy consumption within the air conditioning industry, resulting in environmental deterioration. Electrochromic (EC) windows have emerged as a promising solution to address these challenges. Vanadium pentoxide (V2O5) stands out among all metal oxide materials due to its remarkable EC properties, including substantial Li+ ion insertion capacity and multicolor capabilities. Despite the potential of V2O5, there remains a lack of comprehensive research on the structural and optical properties of V2O5 films with varying thicknesses. Therefore, this study aims to investigate the structural and optical properties of V2O5 thin films with thicknesses ranging from 46 to 344 nm. By employing the sol-gel spin coating method, V2O5 thin films were fabricated and analyzed using X-ray diffraction (XRD) spectroscopy and ultraviolet-visible (UV-Vis) spectrophotometry. The fabricated V2O5 thin films with thicknesses of 46-274 nm demonstrated an average film transparency of 83 %. XRD analysis further revealed that the V2O5 thin films reached their peak crystallinity at a thickness of 344 nm. Moreover, CV analysis revealed that the V2O5 device, with a thickness of 274 nm, exhibited a cathodic peak current of -1.63 mA, indicating its excellent ability to facilitate Li+ ion diffusion. Additionally, CA measurements displayed a high optical modulation of 37.78 %. Ultimately, this research contributes to the development of energy-efficient solutions for sustainable environmental practices.

Increasing electrochemical carbon dioxide reduction to methane via a novel copper-based conductive metal organic framework

The development of a new system for the electrochemical carbon dioxide reduction reaction (ECO2RR) to methane (CH4) is challenging, and novel conductive metal organic frameworks (c-MOFs) for efficient ECO2RR to CH4 are critical to this system. Here, we report a novel c-MOF, copper-pyromellitic dianhydride-2-methylbenzimidazole (Cu-PD-2-MBI), in which the introduction of electron-withdrawing 2-methylbenzimidazole (2-MBI) into the copper-pyromellitic dianhydride (Cu-PD) interlayer elevated the valence of copper (Cu) ions, which improved the ECO2RR performance of Cu-PD-2-MBI. Cu-PD-2-MBI was tested in a flow cell, and the Faradaic efficiency of CH4 reached 73.7 %, with a corresponding partial current density of −428.3 mA·cm−2 at −1.3 V, which was higher than those of most reported Cu-based catalysts. Further exploration via theoretical calculations indicated that the intercalated 2-MBI in Cu-PD-2-MBI induced a shift in the d-band center in the Cu sites from −2.63 to −1.86 eV and reduced the formation energy of the *COOH and *CHO intermediates in the process of generating CH4 compared with those of the reference Cu-PD catalyst.

Evaluating diffusivity for efficient electrocatalytic conversion of carbon dioxide into multicarbon products using dealloyed hierarchically nanoporous copper

Hierarchical nanoporous copper (Hi-NPC) is a promising catalyst for carbon dioxide reduction reaction (CO2RR) due to its high surface area and excellent mass transport properties. To evaluate the effect of its architecture, eutectic-phased Cu18Al82 and single-phased Cu33Al67 were potentiostatically dealloyed to produce Hi-NPC and homogeneous nanoporous copper (Ho-NPC), respectively. At a comparable overpotential, the Hi-NPC electrocatalyst exhibited a significantly higher C2+ partial current density (jC2+) in CO2RR, reaching 510 mA/cm2, compared to both Ho-NPC (72 mA/cm2) and Cu electrodes (23 mA/cm2). When the current density was normalized by the electrochemically active surface area, the CO production among three electrodes demonstrated similar electrochemical behavior. However, notable differences were observed in the formation of C2H4 and C2H5OH, which can be attributed to the hierarchical structure of Hi-NPC facilitating C–C coupling to form C2 products. Although the Tafel plot indicated the CO2RR kinetics were identical for all three electrodes, linear sweep voltammetry experiments revealed that Hi-NPC exhibited the steepest current variation slope. Furthermore, the improved diffusivity was further confirmed by conducting oxygen reduction reactions with varying partial O2/N2 flow rates and electrochemical impedance spectroscopies. The hydrophobic properties of the electrode under various CO2RR current densities were also evaluated by water contact angle test.

Atomic Defects Engineering Boosts Urea Synthesis toward Carbon Dioxide and Nitrate Coelectroreduction.

The atomic defect engineering could feasibly decorate the chemical behaviors of reaction intermediates to regulate catalytic performance. Herein, we created oxygen vacancies on the surface of In(OH)3 nanobelts for efficient urea electrosynthesis. When the oxygen vacancies were constructed on the surface of the In(OH)3 nanobelts, the faradaic efficiency for urea reached 80.1%, which is 2.9 times higher than that (20.7%) of the pristine In(OH)3 nanobelts. At -0.8 V versus reversible hydrogen electrode, In(OH)3 nanobelts with abundant oxygen vacancies exhibited partial current density for urea of -18.8 mA cm-2. Such a value represents the highest activity for urea electrosynthesis among recent reports. Density functional theory calculations suggested that the unsaturated In sites adjacent to oxygen defects helped to optimize the adsorbed configurations of key intermediates, promoting both the C-N coupling and the activation of the adsorbed CO2NH2 intermediate. In-situ spectroscopy measurements further validated the promotional effect of the oxygen vacancies on urea electrosynthesis.

Atomically dispersed nickel-bismuth dual-atom sites for high rate electrochemical CO2 reduction

We report a diatomic-site catalyst configuration constituted by Ni-N3 and Bi-N4 embedded in ultrathin nitrogenated carbon nanosheets (Ni/Bi-N-C) which showed dramatically improved activity and selectivity for the conversion of CO2 to CO. Specifically, the catalyst exhibited high CO Faradaic efficiency (FECO) of above 90 % over a wide potential window from −0.76 to −2.22 versus reversible hydrogen electrode with the maximum CO partial current density up to 312 mA cm−2 in a flow cell, and coupled with robust durability. Ni/Bi-N-C-based membrane electrode assembly (MEA) device presented ultrahigh FECO of 95.7 % at 750 mA and over 100 h of continuous operation without decay under constant current density of 100 mA cm−2. Mechanistic studies and density functional theory calculations reveal that regulating the CO2RR catalytic performance via nearby Ni and Bi active sites can potentially break the activity benchmark of the single metal counterparts because the neighboring Ni and Bi active sites work in synergy to decrease the reaction barrier for the formation of *COOH and desorption of *CO. This work presents an efficient combination of two metal atomic sites which was designed by optimizing the interaction between the atomic sites and key reaction intermediates, resulting in the high-rate electrocatalytic CO2 reduction.

Stabilized Cu0 -Cu1+ dual sites in a cyanamide framework for selective CO2 electroreduction to ethylene

Electrochemical reduction of carbon dioxide to produce high-value ethylene is often limited by poor selectivity and yield of multi-carbon products. To address this, we propose a cyanamide-coordinated isolated copper framework with both metallic copper (Cu0) and charged copper (Cu1+) sites as an efficient electrocatalyst for the reduction of carbon dioxide to ethylene. Our operando electrochemical characterizations and theoretical calculations reveal that copper atoms in the Cuδ+NCN complex enhance carbon dioxide activation by improving surface carbon monoxide adsorption, while delocalized electrons around copper sites facilitate carbon-carbon coupling by reducing the Gibbs free energy for *CHC formation. This leads to high selectivity for ethylene production. The Cuδ+NCN catalyst achieves 77.7% selectivity for carbon dioxide to ethylene conversion at a partial current density of 400 milliamperes per square centimeter and demonstrates long-term stability over 80 hours in membrane electrode assembly-based electrolysers. This study provides a strategic approach for designing catalysts for the electrosynthesis of value-added chemicals from carbon dioxide.

Fabrication of fMW@TiO2@MoS2-Sm2S3/GCE electrochemical nanosensor for simultaneous measurement of sertraline and buspirone neuroleptic drugs

In this paper for the first time, due to the importance of simultaneous administration of sertraline (SRT) and buspirone (BPH), a sensitive electrochemical nanosensor was fabricated and used for simultaneous measurement of them. Firstly, fMW@TiO2@MoS2-Sm2S3 was synthesized and characterized by different techniques. The performance of fMW@TiO2@MoS2-Sm2S3/GCE nanocomposite was investigated for simultaneous quantifications of SRT and BPH using different electrochemical methods. Response surface methodology (RSM) indicated that pH 7.0 for phosphate buffer solutions (PBS), scan rate of 0.08 V s-1, accumulation potential of 0.4 V and accumulation time of 125 s in CHA get maximum anodic currents. The anodic peak current densities of SRT and BPH drugs were improved excellently on the surface of fMW@TiO2@MoS2-Sm2S3/GCE compared to bare GCE. With the DPV method, the linear response 1.53–38.46, 38.46–74.07 µM and 1.11–29.12, 29.12–90.90 µM were obtained for SRT and BPH, respectively. Also, the detection limit of 0.50 µM and 0.36 µM were acquired for SRT and BPH, respectively. The catalytic rate constants were calculated to be 3.63 × 107 and 2.80 × 107 cm3 mol-1 s-1 for SRT and BPH, respectively. The practical application of the fMW@TiO2@MoS2-Sm2S3 for measurements of the SRT and BPH in human plasma and tablets showed good recovery percentage.

Potential-driven structural distortion in cobalt phthalocyanine for electrocatalytic CO2/CO reduction towards methanol

Cobalt phthalocyanine immobilized on carbon nanotube has demonstrated appreciable selectivity and activity for methanol synthesis in electrocatalytic CO2/CO reduction. However, discrepancies in methanol production selectivity and activity between CO2 and CO reduction have been observed, leading to inconclusive mechanisms for methanol production in this system. Here, we discover that the interaction between cobalt phthalocyanine molecules and defects on carbon nanotube substrate plays a key role in methanol production during CO2/CO electroreduction. Through detailed operando X-ray absorption and infrared spectroscopies, we find that upon application of cathodic potential, this interaction induces the transformation of the planar CoN4 center in cobalt phthalocyanine to an out-of-plane distorted configuration. Consequently, this potential induced structural change promotes the transformation of linearly bonded *CO at the CoN4 center to bridge *CO, thereby facilitating methanol production. Overall, these comprehensive mechanistic investigations and the outstanding performance (methanol partial current density over 150 mA cm−2) provide valuable insights in guiding the activity and selectivity of immobilized cobalt phthalocyanine for methanol production in CO2/CO reduction.

A Novel, Selective, and Fast Electrochemical Sensor Based on an 8-Nitroquinoline-Coated Pencil Graphite Electrode for Rutin Determination in Orange Juice

In this study, we developed a facile and low-cost method to prepare a modified electrode by coating the pencil graphite electrode (PGE) surface with 8-nitroquinoline (8-NQ). The surface modification process was carried out by electrochemical reduction of 8-NQ on the PGE surface in ethanol solution. The optimum conditions were determined for the experimental studies. The differential pulse voltammetry was used to determine rutin with the modified electrode (8-NQ/PGE). The developed electrode showed excellent performance for rutin oxidation in a pH 3.0 Britton Robinson buffer (BR). In this media, linearly increasing anodic peak currents were observed with the concentration of rutin in two wide concentration ranges (i.e., 0.016–0.96 μM and 0.96‒19.73 μM), the sensor showed a low detection limit (i.e., 4.14 nM) (3 s m−1). It displayed good stability and selectivity. Also, it was used successfully for the determination of rutin in orange juice samples.

Kinetic investigation of discharge performance for Xe, Kr, and Ar in a miniature ion thruster using a fast converging PIC-MCC-DSMC model

Abstract The present work develops a full particle-based model that couples the particle-in-cell plus Monte Carlo collision (PIC-MCC) simulation for plasma dynamics and the direct simulation Monte Carlo (DSMC) method for neutral dynamics in a synergistic iterative manner. This new model overcomes the slow convergence issue in the conventional direct coupling approach caused by the disparity of the time scales between the plasma and neutral dynamics. This model is applied to simulate the behavior of xenon (Xe) and its potential alternatives, krypton (Kr) and argon (Ar), in the discharge chamber of a miniature direct current (DC) ion thruster. The results show that a stable discharge is difficult to achieve for Kr and Ar under the operating conditions optimal for Xe. While increasing the discharge voltage can effectively improve the stability of discharge for Kr and Ar, other common strategies such as changing the magnetic field strength, propellant flow rate, and cathode current are not successful. The propellant utilization efficiency and discharge efficiency are affected by both discharge voltage and propellant flow rate. A maximum utilization efficiency and an optimal discharge efficiency are observed for all three propellants, with the values decreasing in the order of Xe, Kr, and Ar. Moreover, the discharge voltage corresponding to the optimal efficiency is inversely proportional to the square root of the propellant mass, indicating that the ion diffusional loss to the wall, rather than the ionization energy, is the dominant factor affecting the discharge performance for alternative propellants in a miniature DC thruster.

A Multi‐Scale Particle‐In‐Cell Simulation of Plasma Dynamics From Magnetotail Reconnection to the Inner Magnetosphere

AbstractDuring magnetospheric substorms, plasma from magnetic reconnection in the magnetotail is thought to reach the inner magnetosphere and form a partial ring current. We simulate this process using a fully kinetic 3D particle‐in‐cell (PIC) numerical code along with a global magnetohydrodynamics (MHD) model. The PIC simulation extends from the solar wind outside the bow shock to beyond the reconnection region in the tail, while the MHD code extends much further and is run for nominal solar wind parameters and a southward interplanetary magnetic field. By the end of the PIC calculation, ions and electrons from the tail reconnection reach the inner magnetosphere and form a partial ring current and diamagnetic current. The primary source of particles to the inner magnetosphere is bursty bulk flows (BBFs) that originate from a complex pattern of reconnection in the near‐Earth magnetotail at to . Most ion acceleration occurs in this region, gaining from 10 to 50 keV as they traverse the sites of active reconnection. Electrons jet away from the reconnection region much faster than the ions, setting up an ambipolar electric field allowing the ions to catch up after approximately 10 ion inertial lengths. The initial energy flux in the BBFs is mainly kinetic energy flux from the ions, but as they move earthward, the energy flux changes to enthalpy flux at the ring current. The power delivered from the tail reconnection in the simulation to the inner magnetosphere is W, which is consistent with observations.

Facile Synthesis of Porous Zinc Nanosheets for Highly Selective Electrochemical CO2 Reduction to CO

AbstractWith the increasing levels of CO2 emissions and the decreasing availability of energy resources, the electrocatalytic CO2 reduction reaction (CO2RR) offers a promising method for utilizing CO2 as a valuable resource using sustainable electrical energy. However, developing cost‐effective and highly efficient catalysts remains a significant challenge. Although zinc, an abundant element on Earth, has shown potential for converting CO2 into CO, its effectiveness as a catalyst for CO2 reduction is hindered by its low selectivity and stability. This study introduces a fast, efficient, and simple electrochemical deposition method for preparing porous zinc nanosheets (NS) using the hydrogen bubble template approach. The as‐prepared zinc NS catalyst demonstrates exceptional catalytic activity due to its highly porous structure and high specific surface area. At a voltage of −1 V versus RHE, it achieves a maximum CO Faradaic efficiency of 89.5 %. The performance of this system is characterized by a partial current density of around −6.17 mA cm−2 in an H‐cell configuration. Additionally, our catalyst exhibits remarkable durability over 10 h, highlighting its significant potential for real‐world utilization in CO2RR.

Copper cluster regulated by N, B atoms for enhanced CO2 electroreduction to formate

Electrochemical CO2 conversion into formate by intermittent renewable electricity, presents a captivating prospect for both the storage of renewable electrical energy and the utilization of emitted CO2. Typically, Cu-based catalysts in CO2 reduction reactions favor the production of CO and other by-products. However, we have shifted this selectivity by incorporating B, N co-doped carbon (BNC) in the fabrication of Cu clusters. These Cu clusters are regulated with B, N atoms in a porous carbon matrix (Cu/BN-C), and Zn2+ ions were added to achieve Cu clusters with the diameter size of ∼1.0 nm. The obtained Cu/BN-C possesses a significantly improved catalytic performance in CO2 reduction to formate with a Faradaic efficiency (FE) of up to 70 % and partial current density (jformate) surpassing 20.8 mA cm−2 at −1.0 V vs RHE. The high FE and jformate are maintained over a 12-hour. The overall catalytic performance of Cu/BN-C outperforms those of the other investigated catalysts. Based on the density functional theory (DFT) calculation, the exceptional catalytic behavior is attributed to the synergistic effect between Cu clusters and N, B atoms by modulating the electronic structure and enhancing the charge transfer properties, which promoted a preferential adsorption of HCOO* over COOH*, favoring formate formation.

Solar energy powered electrochemical reduction of CO2 on In2O3 nanosheets with high energy conversion efficiency at a large current density

Electrochemical CO2 reduction (ECO2R) to value-added chemicals offers a promising approach to both mitigate CO2 emission and facilitate renewable energy conversion. We demonstrate a solar energy powered ECO2R system operating at a relatively large current density (57 mA cm−2) using In2O3 nanosheets (NSs) as the cathode and a commercial perovskite solar cell as the electricity generator, which achieves the high solar to formate energy conversion efficiency of 6.6 %. The significantly enhanced operative current density with a fair solar energy conversion efficiency on In2O3 NSs can be ascribed to their high activity and selectivity for formate production, as well as the fast kinetics for ECO2R. The Faradic efficiencies (FEs) of formate In2O3 NSs are all above 93 %, with the partial current density of formate ranging from 2.3 to 342 mA cm−2 in a gas diffusion flow cell, which is among the widest for formate production on In-based catalysts. In-situ Raman spectroscopy and density functional theory simulations reveal that the exceptional performances of formate production on In2O3 NSs originates from the presence of abundant low coordinated edge sites, which effectively promote the selective adsorption of *OCHO while inhibiting *H adsorption.

Electroreduction of CO2 to HCOOH on 3D-Ag nanosheet array supported on carbon membrane

Regulating local CO2 concentration and pH near the catalytic active sites could induce effective reaction pathways for electroreduction of CO2 to chemicals. Here, a membrane nanofluid reactor for efficient electroreduction of CO2 to formic acid was prepared by constructing high-density active sites of 3D-Ag nanosheet array on the surface and within the pores of carbon membrane (3D-Ag NA/CM). The local microenvironment of CO2 and H+ concentration was controlled by adjusting the pore size, CO2 flow rate, and mass transfer mode. In the flow-through mode, the CO2 was electro-reduced to formic acid with Faraday efficiency of 94% and the partial current density of 35.8 mA/cm2. Both the selectivity and activity were higher than those in flow-by mode. The low local concentration of CO2 in the channel was the key to the high selectivity of formic acid. When CO2 flowed through the membrane nanopores, the high collision frequency of CO2 with catalyst on the pore walls facilitated the electroreduction of CO2. It found that the presence of OV promoted the adsorption of CO2 and reduced the energy barrier for its activation into ∗CHOO. It lays a foundation for the research on optimizing the performance of CO2 electroreduction with nanofluid reactors.