Electrochemical Activity Research Articles

Electrochemically Driven Nickel-Catalyzed Enantioselective Hydro-Arylation/Alkenylation of Enones.

Herein, the study reports the first electrochemical nickel-catalyzed enantioselective hydro-arylation/alkenylation of enones in an undivided cell with low-cost electrodes in the absence of external reductants and supporting electrolytes. Aryl bromides/iodides/triflates or alkenyl bromides are employed as electrophiles for the efficient preparation of more than 56 valuable β-arylated/alkenylated ketones in a simple manner (up to 97% yield, 97% ee). With the advantages of electrochemistry, excellent functional group tolerance and late-stage modification of complex natural products and pharmaceuticals made the established protocol greener and more economic. Mechanism investigation suggests that a NiI/NiIII cycle may be involved in this electro-reductive reaction rather than metal reductant driven Ni0/NiII cycle. Overall, the efficient electrochemical activation and turnover of the nickel catalyst avoid the drawbacks posed by the employment of stoichiometric amount of sensitive metal powder reductants.

Chelation approach to long-lived and reversible chromium anolytes for aqueous flow batteries

Iron chromium flow battery (ICFB) has the advances of low cost, safety, and independent design of power and capacity, but is restricted by the deactivation of chromium anolytes. Here, a complex of diethylenetriaminepentaacetic acid with chromium ion (CrDTPA) is designed with minimum capacity loss rate and best cycling stability. DTPA is an octadentate ligand and chelates with chromium ions in a seven-coordinated manner. The coordination structure was studied by Nuclear Magnetic Resonance, Fourier transform infrared and UV–vis absorption spectra, and identified as a robust structure. CrDTPA has good electrochemical activity and reversibility with a redox potential of −1.145 V versus saturated calomel electrode. A novel iron chromium flow battery (NICFB) is designed by coupling CrDTPA anolytes and Fe(CN)6 catholytes. NICFB displays high energy conversion efficiency with coulombic efficiency of 99.0 % and energy efficiency of 82.2 % at 40 mA cm−2. Importantly, NICFB shows superior cycling stability without performance decay for 160 cycles, ranking the best among recently reported ICFBs. This chelation approach provides a simple and practical method to solve chromium anolytes deactivation and improve cycling stability.

Tailoring Sb-F doped ZnO nanoparticles for dual-functionality: Photocatalytic and supercapacitor applications

In the present work, pure zinc oxide nanoparticles (ZnO NPs), antimony doped ZnO nanoparticles (Sb-ZnO NPs), fluorine doped ZnO nanoparticles (F-ZnO NPs), and antimony and fluorine co-doped ZnO nanoparticles (Sb/F-ZnO NPs) with various dopant concentrations are synthesized by co-precipitation method. The optical, structural, morphological, photocatalytic, and electrochemical activities of ZnO nanostructures by the influence of Sb and F doping were investigated. XRD showed crystallite size decreased with increasing Sb/F content, while BET showed 64.25 m2/g surface area for ZnO-5 %Sb-10 %F. SEM and TEM images suggesting Sb/F doping changed the ZnO morphology from spherical to bricks-built and nanorod-built flower structures. XPS verified Sb (+3) and F (−1) oxidation states, while absorption spectroscopy showed increased energy bandgap with 5 % Sb and 10 % F doping in ZnO. The photocatalytic activity for mixture of congo red, rhodamine B, and methylene blue are closer to real polluted water. All the samples exhibited good photocatalytic activity for the methylene blue with degradation efficiency reaching to 99 %. At a constant current density of 1 A/g, symmetric supercapacitors utilizing Sb/F-ZnO electrodes exhibited a specific capacitance of 762 Fg−1, underscoring their superior electrochemical performance and potential for advancing energy storage technologies. Further, physiochemical and electrochemical properties of ZnO can be perfectly tuned by the optimal setting for co-doping in ZnO up to 5 % Sb and 10 % F by the co-precipitation approach.

Eco-friendly Synthesis of Silver-Doped Reduced Graphene Oxide Nanocomposite, The Characterization, and Evaluation of Electrochemical Activity

In this study, Orobanche aegyptiaca Pers., which is an important holoparasite plant, was used for green synthesis of reduced graphene oxide silver nanocomposites (rGO-AgNCs). The obtained rGO-AgNCs were characterizated using UV–Vis spectroscopy, Fourier transformation infrared spectroscopy (FT-IR), X-Ray diffractiometer (XRD), Scanning electron microscope (SEM), Transmission electron microscope (TEM), and X-Ray photoelectron spectroscopy (XPS). The synthesized rGO-AgNCs structure were used to modify carbon paste electrode (rGO-AgNCs@CPE) for electrochemical determination of metronidazole (MNZ). It was observed that the obtained rGO-AgNCs@CPE showed higher sensitivity in MNZ determination than the unmodified CPE, and DPV measurements showed a low detection limit of 0.039 μM over a linear concentration range of 5–300 μM. Real sample analysis of the proposed sensor shows that it responds well in MNZ analysis of human urine.

Hierarchical 2D/1D MOFs/electrospun ZIF-67 modified carbon nanofibers heterostructure electrode for high-performance asymmetric supercapacitor

In this paper, a 2 dimensional (2D) metal–organic frameworks (MOFs) nanosheets grown on 1D ZIF-67 modified carbon nanofibers (CNFs) was designed and fabricated with a hierarchical heterostructure. The hierarchical 2D/1D MOFs/CCNF offers rich electrochemical active sites and favorable ion/electron diffusion pathways. The synergistic effect of Co, CNFs and MOFs from heterostructures contributes to superb electrochemical activities. Benefiting from the hierarchical heterostructures optimized by the mass ratio of ZIF-67/PAN and CCNF/NiMOF as well as the type of substrates, CCNF-20@MOF showed a specific capacity of 361.50 C g−1 at 0.5 A g−1, whose charge storage mechanism is dominated by diffusion control. Meanwhile, a bamboo-derived carbon material (BBC) was designed in the solid-state asymmetric supercapacitor (CCNF-20@MOF//BBC). The device exhibited an energy density of 38.89 Wh kg−1 at the power density of 800.02 W kg−1 and excellent cycling stability, that exceed many MOFs based devices. Moreover, it could be successfully used for LED light-emitting, demonstrating a good application prospect. This work provides a feasible strategy for the improved performance of MOFs and CNFs based materials in the field of energy storage.

The comprehensive understanding of intrinsic contribution of nickel foam as a conductive substrate in water splitting

Using nickel foam as a substrate for an electrocatalyst to report overpotential in a manuscript is a popular method in electrochemical testing or water-splitting i.e., the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER). However, use of coated Nickel foam as substrate methodology is, in essence, not reasonable for studying the intrinsic chemistry difference of electrocatalysts. To assess water-splitting devices, Ni-foam is a valid substrate if nanoparticles are grown uniformly; however, when drop-casted ink methodology is used or there is inhomogeneous growth of nanoparticles, it becomes difficult to determine whether a particular electrocatalyst is intrinsically active or not. In order to gain a rational understanding of the electrochemical activity and overpotential findings of a specific catalyst, it is essential to recognize the limitations of Ni-foam in reflecting its intrinsic role in electrocatalytic activity. In this study, the same catalyst was drop-casted on three different substrates, namely glassy carbon electrode (GCE), carbon fiber paper (CFP) and nickel foam (NF). It was observed that electrochemical results, such as overpotential, Tafel slope, turnover frequency, and others, varied significantly between NF and CFP or GCE. Therefore, it is concluded that NF should not be preferred as a conductive substrate during electrochemical testing (ET). On the contrary, other neutral substrates like CFP and GCE should be employed.

Synthesis of SnC@Au@Apta by electrospinning as an electrochemical sensor for detection of tetracycline

A highly efficient electrochemical aptamer sensor for the detection of tetracycline (TC) was prepared by using SnC@Au@Apta. Metal tin has good electrochemical activity and high conductivity. It is often used as an electrochemical sensing material. The nanofibers prepared by electrospinning machine make the metal distribution more uniform, not easy to agglomerate, and have a certain porosity, which can improve the sensitivity of sensor detection. Carbonization further enhances conductivity. The gold nanoparticles (AuNPs) on the surface of SnC nanomaterials improve the electrochemical detection performance, and also act as the binding site of the TC aptamer, which is stably combined with the thiol group at the end of the TC aptamer. The TC aptamer specifically binds to TC to detect TC in the sample. The electrochemical performance of SnC@Au@Apta was evaluated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Under the optimal conditions, the detection range of SnC@Au@Apta is wide (0.001–100 μM), the detection limit is low (0.83 nM), and it has excellent selectivity, stability and reproducibility. In addition, SnC@Au@Apta can be used to detect TC in milk samples.

The Effect of Hatch Spacing on the Electrochemistry and Discharge Performance of a CeO2/Al6061 Anode for an Al-Air Battery via Selective Laser Melting

To improve the electrochemical activity and discharge performance of an aluminum-air (Al-air) battery, a commercial 6061 alloy (Al6061) was selected as the anode, and CeO2 was also added inside the anode to enhance its performance. The CeO2/Al6061 composite was prepared using selective laser melting (SLM) technology. The influence of hatch spacing on the forming quality, corrosion resistance, and discharge performance of the anode was studied in detail. The results showed that with an increase in hatch spacing, the density, corrosion resistance, and discharge performance of the anode first increased and then decreased. When the hatch spacing is 0.13 mm, the anode has the best forming quality. At this point, the density reaches 98.39%, and the self-corrosion rate (SCR) decreases to 2.596 × 10−4 g·cm−2·min−1. Meanwhile, the anode exhibits its highest electrochemical activity and discharge voltage, which is up to −1.570 V. The change in anode performance is related to the defects generated during the SLM forming process. For samples with fewer defects, the anode can dissolve uniformly, while for samples with more defects, the electrode solution is prone to penetrate the defects, causing uneven corrosion and reducing electrochemical and discharge activity.

Formation Characteristics of Pt-Ni Alloy Nanoparticles Fabricated by Nanolamination of Atomic Layer Deposition in Hydrogen.

Forced-flow atomic layer deposition nanolamination is employed to fabricate Pt-Ni nanoparticles on XC-72, with the compositions ranging from Pt94Ni6 to Pt67Ni33. Hydrogen is used as a co-reactant for depositing Pt and Ni. The growth rate of Pt is slower than that using oxygen reactant, and the growth exhibits preferred orientation along the (111) plane. Ni shows much slower growth rate than Pt, and it is only selectively deposited on Pt, not on the substrate. Higher ratios of Ni would hinder subsequent stacking of Pt atoms, resulting in lower overall growth rate and smaller particles (1.3-2.1nm). Alloying of Pt with Ni causes shifted lattice that leads to larger lattice parameter and d-spacing as Ni fraction increases. From the electronic state analysis, Pt 4f peaks are shifted to lower binding energies with increasing the Ni content, suggesting charge transfer from Ni to Pt. Schematic of the growth behavior is proposed. Most of the alloy nanoparticles exhibit higher electrochemical surface area and oxygen reduction reaction activity than those of commercial Pt. Especially, Pt83Ni17 and Pt87Ni13 show excellent mass activities of 0.76 and 0.59AmgPt -1, respectively, higher than the DOE target of 2025, 0.44AmgPt -1.

SONOCHEMICAL SYNTHESIS OF SILVER NANOPARTICLES FOR GAS-DIFFUSION ELECTRODES APPLICATION

The aim of the current study is to explore the application of silver nanoparticles (AgNPs) as a catalyst in air gas-diffusion electrodes (AGDE). AgNPs have been successfully synthesized through an original sonochemical method. The effects of reagent concentrations, temperature and reaction time were studied as well. Composites of AgNPs and activated carbon (Norit NK) were prepared by using two adsorption methods to demonstrate the catalytic activity. Method 1 involves homogenizing preliminary prepared AgNPs colloid solution and Norit NK followed by evaporation of the suspension. One-step route was used for Method 2, i.e. all components were mixed altogether and sonicated, resulting in the AgNPs formation directly on the surface and inside the pores of Norit NK. Additionally,some of the samples were thermally treated at 300°C for 1h under air and argon. The composites were characterized by X-ray diffraction (XRD), scanning electron microscopy with energy dispersive X-Ray analysis (SEM/EDX) and transmission electron microscopy (TEM). The catalytic activity of the obtained composites regarding oxygen reduction reaction (ORR) was investigated in AGDE using an aqueous 4M NaCl electrolyte. The thermally treated composite obtained via Method 2 appears to show improved electrochemical catalytic activity regarding ORR in comparison to the Method 1 samples.

Composite Modified Graphite Felt Anode for Iron–Chromium Redox Flow Battery

The iron–chromium redox flow battery (ICRFB) has a wide range of applications in the field of new energy storage due to its low cost and environmental protection. Graphite felt (GF) is often used as the electrode. However, the hydrophilicity and electrochemical activity of GF are poor, and its reaction reversibility to Cr3+/Cr2+ is worse than Fe2+/Fe3+, which leads to the hydrogen evolution side reaction of the negative electrode and affects the efficiency of the battery. In this study, the optimal composite modified GF (Bi-Bio-GF-O) electrode was prepared by using the optimal pomelo peel powder modified GF (Bio-GF-O) as the matrix and further introducing Bi3+. The electrochemical performance and material characterization of the modified electrode were analyzed. In addition, using Bio-GF-O as the positive electrode and Bi-Bio-GF-O as the negative electrode, the high efficiency of ICRFB is realized, and the capacity attenuation is minimal. When the current density is 100 mA·cm−2, after 100 cycles, the coulomb efficiency (CE), voltage efficiency (VE), and energy efficiency (EE) were 97.83%, 85.21%, and 83.36%, respectively. In this paper, the use of pomelo peel powder and Bi3+ composite modified GF not only promotes the electrochemical performance and reaction reversibility of the negative electrode but also improves the performance of ICRFB. Moreover, the cost of the method is controllable, and the process is simple.

Optimizing Reversible Exsolution and Phase Transformation in Double Perovskite Sr2Fe1.5-xCoxMo0.5O6-δ Electrodes for High-Performance Symmetric Solid Oxide Cells.

Double perovskite (DP) oxides are promising electrode materials for symmetric solid oxide cells (SSOCs) due to their excellent electrochemical activity and stability. B-site cation doping in DP oxides affects the reversibility ofphase transformation and exsolution, which plays a crucial role in the catalyst recovery. Yet, few studies have been conducted on this topic. In this study, the Sr2Fe1.5-xCoxMo0.5O6-δ (CSFM, x = 0, 0.1, 0.3, 0.5) DP system demonstrates modulated exsolution and phase transformation reversibility by manipulating the oxygen vacancy concentration. The correlation between Co-doping level and oxygen vacancy concentration is investigated to optimize the exsolution and phase transformation properties. Sr2Fe1.2Co0.3Mo0.5O6-δ (3CSFM) exhibits reversible transformation between DP and Ruddlesden-Popper phases with a high density of exsolved CoFe nanoparticles under redox atmospheres. The quasi-symmetric cell with 3CSFM shows a peak power density of 1.27Wcm-2 at 850°C in H2 fuel cell mode and a current density of 2.33Acm-2 at 1.6V and 800°C in H2O electrolysis mode. The 3CSFM electrode exhibits robust stability during continuous operation for ≈700h. These results demonstrate the significant role of B-site doping in designing DP materials capable of dynamic phase transformation in diverse environments.

Construction of Cu2Y2O5/g-C3N4 Novel Composite for the Sensitive and Selective Trace-Level Electrochemical Detection of Sulfamethazine in Food and Water Samples.

The most frequently used sulfonamide is sulfamethazine (SMZ) because it is often found in foods made from livestock, which is hazardous for individuals. Here, we have developed an easy, quick, selective, and sensitive analytical technique to efficiently detect SMZ. Recently, transition metal oxides have attracted many researchers for their excellent performance as a promising sensor for SMZ analysis because of their superior redox activity, electrocatalytic activity, electroactive sites, and electron transfer properties. Further, Cu-based oxides have a resilient electrical conductivity; however, to boost it to an extreme extent, a composite including two-dimensional (2D) graphitic carbon nitride (g-C3N4) nanosheets needs to be constructed and ready as a composite (denoted as g-C3N4/Cu2Y2O5). Moreover, several techniques, including X-ray diffraction analysis, scanning electron microscopy analysis, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, and Raman spectroscopy were employed to analyze the composites. The electrochemical measurements have revealed that the constructed g-C3N4/Cu2Y2O5 composites exhibit great electrochemical activity. Nevertheless, the sensor achieved outstanding repeatability and reproducibility alongside a low limit of detection (LOD) of 0.23 µM, a long linear range of 2 to 276 µM, and an electrode sensitivity of 8.86 µA µM-1 cm-2. Finally, the proposed GCE/g-C3N4/Cu2Y2O5 electrode proved highly effective for detection of SMZ in food samples, with acceptable recoveries. The GCE/g-C3N4/Cu2Y2O5 electrode has been successfully applied to SMZ detection in food and water samples.

NiFe-spinel oxides with nitrogen-doped carbon quantum dots for enhanced oxygen evolution activity

Designing efficient and stable electro-catalysts for non-precious metal oxygen evolution reactions (OER) is critical to solve the bottleneck of water splitting. The NiFe2O4/NCQDs composite electrode was fabricated by combining nitrogen doped carbon quantum dots (NCQDs) with NiFe2O4 spinel via a hydrothermal method, which showed brilliant OER catalytic performance by modifying on nickel foams (NF). The composites had petal-like structures, and the NiFe2O4 was epitaxially grown on the NF substrates with exposed sites, resulting in enhanced electron transport. The fluorescence quenching of NCQDs was accompanied by binding NCQDs with NiFe2O4, which indicated the energy barrier was greatly reduced during the electron transport as well as electro-catalysis. The higher intrinsic charge transfer was achieved, and the doping combination having a higher conductivity was confirmed. The electrochemical activity of NiFe2O4/NCQDs electrode in OER reaction was evaluated under alkaline conditions. The addition of NCQDs effectively enhanced the OER activity, and over-potentials were decreased from 330 mV to 270 mV at 10 mA cm−2 with Tafel slope lower (66 mV/dec) than counterparts. The NiFe2O4/NCQDs displayed long-term catalytic stability at 1.47 V. Therefore, a facile method for preparing NiFe2O4/NCQDs was developed which had characteristics of low cost, simple process and excellent OER activity.

Assembling Zn2+ on surface of kevlar NanoFibers as functionalized separator for dendrite-free Zn anode and high-performance Zn metal batteries

The proliferation of wearable electronic products has made the development of flexible energy storage devices increasingly important. Among various options, aqueous Zn metal batteries are promising due to their low cost, safety, non-toxicity, environmental friendliness, and abundant element storage. However, the growth of dendrites on the anode surface of Zn metal batteries is a significant challenge to efficient transport of Zn2+, which leads to reduced battery capacity or even failure. This limitation hinders practical applications for these batteries. This study develops a functionalized separator with high ion transport performance and excellent mechanical performances by electrostatic assembling deprotonated PPTA− molecular chains with Zn2+ using Kevlar as a raw material. The successful assembly of Zn2+ is confirmed through chemical composition and functional group analysis. The prepared separator significantly shows the increased the transfer number of Zn2+ and decreased activation energy of Zn2+ deposition. The separator is used in Zn||Zn symmetric batteries, achieving a reversible deposition/stripping process of more than 180 h at a current density of 1 mA cm−2 and a deposition capacity of 1 mAh·cm−2. When applied to Zn||MnO2 batteries, an initial discharging specific capacity of up to 220 mAh·g−1 is obtained at a high current density of 2 A g−1, and the battery could be cycled stably for more than 1, 200 cycles, with a smooth and flat Zn anode surface and no obvious dendrite growth. The separator has good potential for flexible energy storage applications due to its excellent mechanical strength, which enables it to maintain high electrochemical activity even after bending 500 times at 180°. Overall, the functionalized separator effectively inhibits dendrite growth, improves the electrochemical stability of Zn metal batteries, and demonstrates significant application potential for other flexible energy storage applications.

Electrowetland Pilot of 50 m2: Operation and Characterization Under Real Conditions for 1 Year

ABSTRACTTraditional wastewater treatment plants (WWTPs) consume a significant amount of energy to clean wastewater. However, for medium‐ and small‐scale WWTPs, it is crucial to have an energetically self‐sustained treatment. In this regard, novel low‐energy demand treatment systems, such as nature‐based solutions (NBS), are highly suitable alternatives. Constructed wetlands coupled with microbial fuel cells (MFC), referred to as electrowetlands (EWs), are NBS able to treat wastewater while recovering electricity. In this study, initially, various granular carbon materials were tested as anode materials in laboratory‐scale MFCs, and anthracite was selected due to its higher electrochemical activity. Then, pre‐pilot scale tests were conducted, evaluating different EW configurations. The one consisting in a horizontal anode yielded the best wastewater treatment efficiencies (chemical oxygen demand [COD] degradation greater than 90%) and electricity production (11 mW m−2; 260 mWh day−1 m−2). Finally, a 50 m2 pilot was constructed in Valladolid, studying its performance under real conditions for 1 year. The pilot showed robust and stable performance, achieving high wastewater treatment efficiencies (COD degradation >85%, outflow COD of 100 ppm) and generating 115 Wh in 1 year (power density of 0.4 mW m−2).

Ligand‐Hybridization Activates Lattice‐Hydroxyl‐Groups of NiCo(OH)x Nanowires for Efficient Electrosynthesis

AbstractElectrochemical dehydrogenation of hydroxides plays a crucial role in the formation of high‐valence metal active sites toward 5‐hydroxymethylfurfural oxidation reaction (HMFOR) to produce the value‐added chemical of 2,5‐furandicarboxylic (FDCA). Herein, we construct benzoic acid ligand‐hybridized NiCo(OH)x nanowires (BZ‐NiCo(OH)x) with ample electron‐deficient Ni/Co sites for HMFOR. The robust electron‐withdrawing capability of benzoic acid ligands in BZ‐NiCo(OH)x speeds up the electrochemical activation and dehydrogenation of lattice‐hydroxyl‐groups (M2+−O−H⇌M3+−O), boosting the formation of abundant electron‐deficient and high‐valence Ni/Co sites. DFT calculation reveals that the deintercalation proton is prone to establishing a hydrogen bridge with the carbonyl group in benzoic acid, facilitating the proton transfer. Coupled with the synergistic oxidation of Ni/Co sites on hydroxyl and aldehyde groups, BZ‐NiCo(OH)x delivers a remarkable current density of 111.20 mA cm−2 at 1.4 V for HMFOR, exceeding that of NiCo(OH)x by approximately fourfold. And the FDCA yield and Faraday efficiency are as high as 95.24 % and 95.39 %, respectively. The ligand‐hybridized strategy in this work introduces a novel perspective for designing high‐performance transition metal‐based electrocatalysts for biomass conversion.

Ligand-Hybridization Activates Lattice-Hydroxyl-Groups of NiCo(OH)x Nanowires for Efficient Electrosynthesis.

Electrochemical dehydrogenation of hydroxides plays a crucial role in the formation of high-valence metal active sites toward 5-hydroxymethylfurfural oxidation reaction (HMFOR) to produce the value-added chemical of 2,5-furandicarboxylic (FDCA). Herein, we construct benzoic acid ligand-hybridized NiCo(OH)x nanowires (BZ-NiCo(OH)x) with ample electron-deficient Ni/Co sites for HMFOR. The robust electron-withdrawing capability of benzoic acid ligands in BZ-NiCo(OH)x speeds up the electrochemical activation and dehydrogenation of lattice-hydroxyl-groups (M2+-O-H⇌M3+-O), boosting the formation of abundant electron-deficient and high-valence Ni/Co sites. DFT calculation reveals that the deintercalation proton is prone to establishing a hydrogen bridge with the carbonyl group in benzoic acid, facilitating the proton transfer. Coupled with the synergistic oxidation of Ni/Co sites on hydroxyl and aldehyde groups, BZ-NiCo(OH)x delivers a remarkable current density of 111.20 mA cm-2 at 1.4 V for HMFOR, exceeding that of NiCo(OH)x by approximately fourfold. And the FDCA yield and Faraday efficiency are as high as 95.24 % and 95.39 %, respectively. The ligand-hybridized strategy in this work introduces a novel perspective for designing high-performance transition metal-based electrocatalysts for biomass conversion.

Anode‐Electrolyte Interfacial Acidity Regulation Enhances Electrocatalytic Performances of Alcohol Oxidations

AbstractThe local acidity at the anode surface during electrolysis is apparently stronger than that in bulk electrolyte due to the deprotonation from the reactant, which leads to the deteriorated electrocatalytic performances and product distributions. Here, an anode‐electrolyte interfacial acidity regulation strategy has been proposed to inhibit local acidification at the surface of anode and enhance the electrocatalytic activity and selectivity of anodic reactions. As a proof of the concept, CeO2‐x Lewis acid component has been employed as a supporter to load Au nanoparticles to accelerate the diffusion and enrichment of OH− toward the anode surface, so as to accelerate the electrocatalytic alcohol oxidation reaction. As the result, Au/CeO2‐x exhibits much enhanced lactic acid selectivity of 81 % and electrochemical activity of 693 mA⋅cm−2 current density in glycerol oxidation reaction compared to pure Au. Mechanism investigation reveals that the introduced Lewis acid promotes the mass transport and concentration of OH− on the anode surface, thus promoting the generation of lactic acid through the simultaneous enhancements of Faradaic and non‐Faradaic processes. Attractively, the proposed strategy can be used for the electro‐oxidation performance enhancements of a variety of alcohols, which thereby provides a new perspective for efficient alcohol electro‐oxidations and the corresponding electrocatalyst design.

Investigation of the effect of electrodeposited Cu from graphite wrapped in polypyrrole film formed by chemical oxidation

The metallization of graphite substrates is currently confronted by negative issues including insufficient adhesion and inherent instability. In an effort to surmount these challenges, a layer of conductive polypyrrole (PPy) film on a graphite surface is formed through simple polymerization, followed by an electroplating copper layer. The graphite enveloped by the PPy film, subjected to cyclic voltammetry (CV) and linear sweep voltammetry (LSV) analyses, demonstrates enhanced electrochemical activity and thus renders the more efficient electrodeposition of copper. Further investigation was conducted through orthogonal experiments to explore the optimal formulation of electroplating solutions containing popular additives including 3, 3′-dithiobis-1-propanesulfonic acid disodium salt (SPS), Janus Green B (JGB), and polyethylene glycol 8000 (PEG8000)., According to the optimal additive formulation, a dense copper layer with superior adhesion was electroplated on the graphite substrate employing PPy as an intermediate layer.