Electrochemical Impedance Spectra Research Articles

Communication—Prediction of Area Specific Resistance of Solid Oxide Cell Stacks from Electrochemical Impedance Spectra

A support vector regression model was trained to predict the area specific resistance of solid oxide cell stacks from electrochemical impedance spectroscopy measurements. In particular, the minimum necessary frequency range required for accurate predictions was investigated. Therefore, 711 pairs of DC polarization and electrochemical impedance spectroscopy measurements, conducted at the same stage of stack degradation and under similar measurement conditions, were evaluated. Prediction accuracies of less than 8% mean absolute percentage error and coefficients of determination greater than 93% were achieved. The 101–102 Hz range is sufficient for accurate predictions, allowing an efficient and non-destructive etimation of DC polarization measurements.

Enhancing corrosion resistance of Al alloy sheets with potential gradient by arc-sprayed Zn coatings

To improve the corrosion resistance and wide the application of Al alloy sheet in the engineering production, a corrosion potential gradient along the thickness of the Al alloy sheet was fabricated using the sprayed Zn layer. The process of arc spraying was employed to obtain the Zn coating with optimizing the parameters. Electrochemical testing was conducted on the surface of Al alloy sprayed with Zn layers at different depths. As the depth in the thickness direction increases, the content of Zn alloy elements gradually decreases and the potential gradually increases. This exhibits a gradual decrease in corrosion tendency. The results of electrochemical impedance spectra (EIS) revealed the existence of pitting corrosion on the surface of the Al alloy. This even extended to the underlying substrate material. In contrast, the Zn coating, when exposed to a corrosive environment, demonstrated the beneficial cathodic effect as a sacrificial anode and the protective function of a passivating film, thus mitigating corrosion. The gradual increase in charge transfer resistance in the impedance spectrum suggested that the corrosion resistance of the sample is increasingly improved. Therefore, it exhibited remarkable resistance to corrosion. Additionally, the SEM surface morphology and XRD pattern were utilized to further explain the corrosion mechanism of the arc-sprayed Zn coating. The Zn coating can provide sacrificial protection to the Al layer due to its higher negative potential and localized corrosion reactivity. This is attributed to the micro-galvanic couples formed between the Zn and Al layer, thus increasing the corrosion resistance of the sheets.

Hydrogen Spillover-Bridged Interfacial Water Activation of WCx and Hydrogen Recombination of Ru as Dual Active Sites for Accelerating Electrocatalytic Hydrogen Evolution.

Tungsten carbide (WCx) is a promising alternative to platinum catalysts for hydrogen evolution reaction (HER). However, strong tungsten-hydrogen bond hinders hydrogen desorption while favoring H+ reduction, thus limiting HER kinetics. Inspired by the phenomenon of hydrogen spillover in heterogeneous catalysis, a ruthenium (Ru) doped-driven activated hydrogen migration from WCx surface to Ru is reported. This approach achieved high activity with an ultralow overpotential of 9.0mV at 10 mA·cm-2 and superior stability at an industrial-grade current density of 1.0 A·cm-2 @ 1.65V. In situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS)and operando electrochemical impedance spectra revealed that this exceptional hydrogen production-which surpasses that of previously reported Pt/C catalysts-is attributable to the outstanding ability of WCx to induce water dissociation and hydrogen spillover from WCx to Ru surface. During the HER process, the rigid interfacial water network negatively affected the HER efficiency under alkaline conditions. The WCx sites disrupted this rigid structure, facilitating the contact between activated hydrogen (H*) and WCx sites. Subsequently, H* migrates to Ru surface, where hydrogen recombination occurs to produce H2. This work paves a new avenue for the construction of coupled catalysts at the atomic scale to facilitate HER electrocatalysis.

Regulating hardness homogeneity and corrosion resistance of Al-Zn-Mg-Cu alloy via ECAP combined with inter-pass aging

The novel processing strategies of Equal Channel Angular Pressing (ECAP) combined with inter-pass aging was designed, and XRD, SEM, TEM, electrochemical testing, and hardness testing were used to evaluate the relationship between microstructure and performance of alloys in this work. The results indicate that the hardness uniformity of the circular cross-section perpendicular to the extrusion direction was improved by combining ECAP with inter-pass aging, resulting in a hardness inhomogeneity factor (∼0.030) that was lower than that achieved by peak aging and double-stage aging alloys. Polarization curves and electrochemical impedance spectra show that a more negative corrosion potential and a smaller corrosion current density were possessed by the alloy, with the maximum intergranular corrosion depth (IGC) being reduced to 38 μm. Microstructure observation indicates that the improvement in hardness uniformity is due to the uniformity of grain size and the improved distribution and size of the η’ phase, which is attributed to the interaction between the pinning and shear effects of precipitates and dislocations during deformation. The enhanced corrosion resistance was attributed to an orderly combination of deformation and aging that increases the grain boundary volume and disrupts the η phase continuity within grain boundaries.

Fast acquisition method of battery electrochemical impedance spectra based on impedance fragments

Electrochemical impedance spectroscopy (EIS) is often used for battery characterization and monitoring. However, there are still difficulties in acquiring battery impedance spectra in large quantities and wide frequency bands in practical applications. The lower the frequency range of acquisition, the longer the measurement time spent, and the higher the frequency range of measurement, the more expensive the measurement equipment, and these problems seriously limit the wide application of impedance information. To address this problem, this study proposes a method for fast acquisition of electrochemical impedance spectra of lithium-ion batteries based on impedance fragments. Firstly, impedance segments at specific frequencies in the EIS are selected as features based on the distribution of relaxation times (DRT). Then, a Long Short-Term Memory (LSTM) neural network model is used to reconstruct the complete impedance spectrum, and a population optimization algorithm is used to optimize the hyperparameters in the model. The validation results indicate that the reconstructed RMSE error is only 14.26 mΩ, corresponding to a MAPE of 1.65 %, while the measurement time is reduced to 27.01 % of the original measurement time. Finally, the performance of this method in identifying fractional-order model parameters is further discussed.

Porous biochar supported PET plastic waste MOF heterostructure as a novel, efficient and recyclable catalyst for acetaminophen degradation

Herein, the innovative hybrid photocatalyst PET-based Zn-MOF on orange peel biochar (BC)(PZM/BC) was designed and synthesized via the hydrothermal method. Electrochemical methods have been used to demonstrate the action of the PET-MOF in the PZM/BC photocatalyst as a medium for electron transfer. The latter involved the synthesis of a zinc-containing metal–organic framework (MOF) in which the linkers were derived from the depolymerization of polyethylene terephthalate (PET) originating from plastic wastes. According to research, the catalytic reactions are sped up when porous BC and linker PET are assimilated into PZM/BC photocatalyst hetero-junction. Furthermore, BC stored electrons under light and released these electrons under dark conditions. When BC was combined with PET-MOF, the electrons on the biochar activated the catalytic redox activity of acetaminophen. Additionally, it lowers the reassimilation rate due to the combined meshed nanostructures and functionality of PET-MOF and PZM/BC. UV–Vis DRS, Mott-Schottky, Photoluminescence(PL), and Electrochemical Impedance spectra(EIS) results showed that the PZM/BC exhibited efficient spatial separation and transportation of photogenerated charge carriers and exhibited superior photocatalytic ability. Electron spin resonance(ESR) analysis confirmed that ⋅OH and h+ were the predominant radical species responsible for the degradation of acetaminophen(ACT). The optimum conditions for ACT removal were observed at pH 6.07, with a PZM/BC dosage of 0.1 g L−1, and an initial ACT concentration of 50 mg L−1, highlighting the pivotal role of the PZM/BC system in ACT degradation. Furthermore, potential photocatalytic degradation pathways of ACT were inferred renders on the identified intermediates which are responsible for the degradation of refractory intermediates. Regeneration trials were carried out to assess the stability of the photocatalyst. Additionally, the degraded intermediates generated during the degradation processes were examined, providing a comprehensive elucidation of the degradation mechanism.Graphical

Surface Morphology Analysis of Graphene Transfer on SiO2 with BPA Aptasensor Detection using Electrochemical Impedance Spectroscopy

Bisphenol A or BPA is one of the highest produced chemicals in the world. The production of polycarbonate plastic and epoxy resin are used to make variety of consumer goods and it is frequently employed BPA as a raw material. BPA is one of the endocrine disruptors which is related to a wide range of adverse health effects that can cause reproductive disorders and many kinds of cancers. In the work, the novelty of electrochemical sensor of BPA was constructed on a raphene modified electrode using graphene transfer method. In this work, High-power microscope and scanning electron microscopy were used to study the production and characterization of the graphene, with two significant mapping graphene at 20% and 80%. The existence of graphene on silicon oxide was analyzed using Raman Spectroscopy while the composition of the materials was analyze using Fourier-Transform Infrared Spectroscopy. In this analysis, both analysis data from Raman and FTIR clearly shown that 80% mapping graphene is the best option which resulting to the high surface coverage. The electrochemical performance of the mapping 80% graphene electrode was examined using Electrochemical Impedance Spectra. The increase in charge transfer resistance (Rct) both before and after the addition of BPA denotes the development of the charge at the electrode surface. The equivalent circuit shows the Rct of graphene increased from 0.4 k Ω to 1.2 k Ω and drastically increased to 300 kΩ when the device was introduced with BPA due to the existence of a negative charge carrier and the repelling contact.

Real-time in-situ coatings corrosion monitoring using machine learning-enhanced triboelectric nanogenerator

Current methods for monitoring coating corrosion are limited by their inability to provide real-time data and dependence on external power sources. This study presents a novel in-situ corrosion monitoring system using a solid-liquid triboelectric nanogenerator (TENG) that converts mechanical energy into electrical signals for self-powered sensing. TENG signals and electrochemical impedance spectra were measured on a dopamine-modified lignin-polydimethylsiloxane coating on steel in 1 M NaCl solution under no corrosion, indentation, pitting, and broken conditions, respectively. We extract time-frequency features from the TENG signals to predict the coating’s corrosion condition by applying a customised convolutional neural network (CNN). By extracting time-frequency features from the TENG signals and applying a custom CNN, a prediction accuracy of 99 % for corrosion classification was achieved. Furthermore, the CNN regression model predicted coating impedance values with a high coefficient of determination (R² = 0.98), demonstrating its effectiveness in tracking corrosion progression. The developed TENG also facilitates defect localisation via a matrix electrode beneath the coating. Our approach introduces a promising real-time technology for in-situ corrosion monitoring.

SnIn4S8/FeNi2P Z-scheme heterojunction hollow nanorods for photocatalytic hydrogen production

Climate change and natural disasters have stimulated the exploration of renewable energy, photocatalytic hydrogen production utilizing solar energy is considered an effective way. In this study, hollow FeNi2-MIL-88 nanorods were synthesized by the hydrothermal method, and then FeNi2P was obtained by gas phase phosphorization. Finally, SnIn4S8 was utilized to coat the surface of FeNi2P through an in-situ growth method to obtain rod-like SnIn4S8/FeNi2P. The results showed that the hydrogen production of SnIn4S8/FeNi2P reached 18083.93 μmol/g within 3 h. And SnIn4S8/FeNi2P showed good stability. The photocurrent response spectra and electrochemical impedance spectra confirmed that SnIn4S8/FeNi2P had good carrier conductivity and effectively inhibited the reorganization of photogenerated carriers. The modification of SnIn4S8 enabled the construction of a Z-scheme heterojunction between SnIn4S8 and FeNi2P. It provided more active sites and promoted the separation of photogenerated carriers, ultimately improving the hydrogen production performance of the SnIn4S8/FeNi2P photocatalyst. It would offer essential insights into the design and development of efficient MOFs-derived photocatalysts.

Platinum oxide-based peracetic acid activation for efficient degradation of typical antibiotic

Peracetic acid (PAA)-based Advance Oxidation Process (AOP) is now used to treat pharmaceutically contaminated wastewater. Herein, PAA is heterogenically activated to degrade sulfamethoxazole (SMX) taking platinum oxide (PtO2) as a catalyst for the first time. PtO2/PAA system with good synergetic effect achieved 100 % SMX degradation in 75 min.Its corresponding kinetic rate constant (0.072 min−1) was exceptionally higher than six other Transition Metal/PAA-based systems tested as well as than PtO2 or PAA alone. The degradation improved by augmenting PAA and PtO2 inputs. Radical scavenging and electron paramagnetic resonance pointed acetylperoxy (CH3C(O)OO·) and acetoxyl (CH3C(O)O·) as the main reactive radicals attributing SMX abatement. X-ray photoelectron spectroscopy and diffraction along with electrochemical tests (cyclic voltammetric curve, electrochemical impedance spectra, and I-t curve) recommended that the electron transfer of Pt2+/Pt4+ also facilitated PAA activation. Density Functional Theory (DFT) assisted in predicting the reaction sites on SMX molecules. Four degradation pathways are proposed with the help of DFT calculations and eight intermediate products identified by High-Performance Liquid Chromatography Mass-Spactrometry. Dissolved organic matter, anions and different waterbodies had tolerable degradation inhibition. Efficient reactivity and adequate stability attest PtO2 as an ideal catalyst for oxidative degradations. The findings offer valuable insights into a novel, sustainable, and efficient approach to treat drug-contaminated wastewater.

Investigation of corrosion resistance offered by the Fe-based clad layer under salt spray and electrochemical workstations

The present work aims to evaluate the electrochemical characteristics of the Fe–based alloy coating formed on the 27SiMn steel substrate under neutral salt spray and 3.5 wt% NaCl environments. By adopting the high-speed laser cladding technique, the Fe-based clad layer was fabricated to perform microstructural and electrochemical characterizations. The microstructure and phase of the coating were analyzed using a scanning electron microscope (SEM), electron backscatter diffraction (EBSD) and X-ray diffraction (XRD), and its corrosion performance was also discussed using the salt spray corrosion chamber and the electrochemical workstation. The results show that the microstructure of the coating surface contains equiaxed crystals and long dendritic crystals which arise due to the higher solidification rate after the cladding process. The Fe–based coating was rich in FeCr phase throughout its microstructure without the formation of the intermetallic compounds. Compared to the substrate, the corroded surface of the coating tends to be compact containing a few corrosion pits after different corrosion times, which is attributed to the formation of Cr oxide on it. The electrochemical tests on the potentiodynamic polarization curve (PPC) and electrochemical impedance spectrum (EIS) indicate that the corrosion resistance of the coating is superior to the substrate, presenting a higher corrosion potential (−0.298 V), lower passive current density (1.36 × 10−6 A•cm2), and higher charge transfer resistance (8.23 × 106 Ω·cm2). Additionally, the corrosion mechanism of coating in salt spray and electrochemical tests is the local pitting corrosion due to the autocatalytic effect on the localized region, which facilitates Cl− ions penetrating the coating and leads to the dissolution of Fe and Cr oxides.

Trace RuO2 nanoparticles loaded nickel-coated multi-walled carbon nanotubes to boost hydrogen evolution reaction under acidic and alkaline media

Developing low-cost catalysts with high activity for the Hydrogen Evolution Reaction (HER) is a main challenge to reduce the dependence on precious metals while maintaining the catalytic activity. In this study, nickel-plated multi-walled carbon nanotubes (Ni-MWCNTs) with a large number of active sites were selected, and Ni-MWCNTs electrocatalysts loaded with trace amounts of RuO2 nanoparticles were prepared by annealing treatment, which exhibited excellent HER performances in both acidic and alkaline media. The RuO2 nanoparticles loaded nickel-coated multi-walled carbon nanotubes (RuO2@Ni-MWCNTs) had a small electrochemical impedance spectrum (EIS) and a large electrochemically active surface area (ECSA). Notably, RuO2@Ni-MWCNTs with less than 1 % Ru content exhibited excellent catalytic activities in both acidic and alkaline solutions. The results showed that the overpotentials of RuO2@Ni-MWCNTs were 20.2 mV (alkaline) and 73.7 mV (acidic), respectively. After stabilization at 20 mA cm−2 for 90 h, the evaluation results showed that RuO2@Ni-MWCNTs could maintain their catalytic efficiency without significant degradation.

N-(4-(1,3-benzothiazol-2-ylcarbamoyl)phenyl)isonicotinamide as corrosion mitigator for mild steel in 1 M HCl: A multifaceted study integrating synthesis, characterization, and molecular modelling

Newly synthesized, cost-effective corrosion inhibitor, N-(4-(1,3-benzothiazol-2-ylcarbamoyl)phenyl)isonicotinamide (BIA) was evaluated for mild steel/1M HCl interface. BIA showed a maximum inhibition efficiency of 90.40 % at 100 ppm and 303 ± 1 K, with efficiency increasing with concentration but decreasing with temperature. Inhibitor’s adsorption followed Langmuir isotherm via physicochemical interactions. Activation parameters revealed BIA retards both metal dissolution and hydrogen evolution held in unimolecular process. Potentiodynamic polarization (PDP) divulged BIA as a mixed-type, impeding charge-transfer. Electrochemical impedance spectra (EIS) confirmed BIA forms a protective double layer, blocking active sites at the interface. Surface analysis supported a protective film formation. Global and local reactivity descriptors using DFT/B3LYP/6-311G++(d,p) were calculated to relate inhibition efficiency with BIA’s electronic properties. Molecular dynamics simulation (MDS) showed an interaction energy of −224.7 kJ/mol between BIA and Fe(110) at 303 K, with Radial Distribution Function (RDF) showing bond lengths under 3.5 Å, confirming a chemical interaction. Theoretical results align with experimental data.

Preparation of Ni nanocone/Grid electrodes by laser-electrodeposition combined process as an efficient and stable electrocatalyst for hydrogen evolution reaction

Hydrogen is a renewable and environmentally friendly energy carrier and is considered a viable alternative to fossil fuels. Consequently, developing electrodes with excellent hydrogen evolution electrocatalysis is a top priority in research. However, the use of flat electrodes as cathode substrates by most researchers limits the electrocatalytic active area of the prepared electrode. To address this issue, it is essential to prepare a micro-nano structure on a cathode substrate before electrodeposition. This study introduced a novel Ni nanocone/Grid electrode, obtained through a combined laser-electrodeposition process to investigate its electrocatalytic activity and stability for the hydrogen evolution reaction (HER). Various techniques, including linear sweep voltammetry (LSV), electrochemical impedance spectra (EIS), cyclic voltammetry (CV), and chronopotentiometry (CP) in 1 M KOH solution, were employed to assess the HER electrocatalytic performance of the Ni nanocone/Grid electrodes. The experimental results demonstrated that the electrodes could achieve current densities of -10, -20, and -100 mA/cm2 with corresponding overpotentials of -281, -308, and -390 mV, respectively. Additionally, the Tafel slope of these electrodes was found to be only -82.05 mV/dec. The enhanced catalytic performance of the electrode was attributed to the synergistic effect of the grid-like and nanocone structures, which significantly increased the electrocatalytically active area and improved surface hydrophilicity, thereby boosting electrocatalytic performance. The simplicity of the preparation method and the exceptional performance of the electrode provide a promising new avenue for future research on HER electrocatalysts.

Numerical Modeling of Water Transport in a Microporous Layer-Coated Porous Transport Layer for a Polymer Electrolyte Membrane Water Electrolyzer with an Interdigitated Flow Field for Internal Gas-Liquid Separation

A novel design for interdigitated flow fields in polymer electrolyte membrane electrolyzers has been developed for both ground and space applications. This design separates oxygen and liquid water internally, eliminating the need for water circulators to remove bubbles and external gas-liquid separators with buoyancy. The capillary pressure in the hydrophobic microporous layer (MPL) of the anode porous transport layer facilitates internal separation of oxygen gas and pressurized liquid water. A finite element model (COMSOL Multiphysics) simulates water transport in the MPL, while electrochemical impedance spectra determine the electrochemical kinetic parameters for the model. The model takes into account the oxygen bubble coverage of the cathode, liquid water saturation in the MPL, and the current ratio between liquid water and water vapor at the MPL-cathode layer interface. The vapor from liquid water in the MPL is modeled to mix with oxygen for diffusion. A volumetric water evaporation rate as a linear function of liquid water saturation in the MPL is assumed, where the rate constant is estimated from vapor permeation tests.

Spatially Resolved Analysis of the Influence of Three-Dimensional Flow Field Structures on Loss Processes in PEMFCs

This study introduces a novel measurement device and technique to spatially resolve the influence of 3D flow field structures consisting of extended metal meshes on the performance distribution in PEMFCs. The newly designed segmented cell enables not only the measurement of the current distribution but also local electrochemical impedance spectra, subsequently analyzed by the distribution of relaxation times. The 3D flow field structures provide, despite of an increased HFR, an advantage at high current densities. The spatially resolved DRT analysis enabled the identification of polarization processes revealing that the gas diffusion process is greatly reduced compared to a conventional channel-rib design. In particular, the 3D coarse mesh shows promising advantages for application under high current densities. The findings from this study provide valuable insights into the local power and resistance distribution, enabling optimization of the flow field design and improvement of the performance of fuel cells with large active areas.

Numerical Modeling of Water Transport in a Microporous Layer-Coated Porous Transport Layer for a Polymer Electrolyte Membrane Water Electrolyzer with an Interdigitated Flow Field for Internal Gas-Liquid Separation

A novel design for interdigitated flow fields in polymer electrolyte membrane electrolyzers has been developed for both ground and space applications. This design separates oxygen and liquid water internally, eliminating the need for water circulators to remove bubbles and external gas-liquid separators with buoyancy. The capillary pressure in the hydrophobic microporous layer (MPL) of the anode porous transport layer facilitates internal separation of oxygen gas and pressurized liquid water. A finite element model (COMSOL Multiphysics) simulates water transport in the MPL, while electrochemical impedance spectra determine the electrochemical kinetic parameters for the model. The model takes into account the oxygen bubble coverage of the cathode, liquid water saturation in the MPL, and the current ratio between liquid water and water vapor at the MPL-cathode layer interface. The vapor from liquid water in the MPL is modeled to mix with oxygen for diffusion. A volumetric water evaporation rate as a linear function of liquid water saturation in the MPL is assumed, where the rate constant is estimated from vapor permeation tests.

Spatially Resolved Analysis of the Influence of Three-Dimensional Flow Field Structures on Loss Processes in PEMFCs

This study introduces a novel measurement device and technique to spatially resolve the influence of 3D flow field structures consisting of extended metal meshes on the performance distribution in PEMFCs. The newly designed segmented cell enables not only the measurement of the current distribution but also local electrochemical impedance spectra, subsequently analyzed by the distribution of relaxation times. The 3D flow field structures provide, despite of an increased HFR, an advantage at high current densities. The spatially resolved DRT analysis enabled the identification of polarization processes revealing that the gas diffusion process is greatly reduced compared to a conventional channel-rib design. In particular, the 3D coarse mesh shows promising advantages for application under high current densities. The findings from this study provide valuable insights into the local power and resistance distribution, enabling optimization of the flow field design and improvement of the performance of fuel cells with large active areas.

PEDOT: PSS Doped Activated Biochar as a Novel Composite Material for Photocatalytic and Efficient Energy Storage Application

Herein, we report the synthesis of activated biochar from green algae and the effect of its doping on the structural, photocatalytic, and energy storage properties of PEDOT-PSS. The morphology of pure and doped samples was investigated with Fourier Transform Infrared Spectroscopy (FTIR), Atomic Force Microscopy (AFM), Brunauer–Emmett–Teller (BET) analysis, and thermogravimetric analysis (TGA). AFM results for PEDOT-PSS@6wt.% of BC indicate that the calculated average peak height, particle size, and roughness were 283 nm, 136 nm, and 71 nm, respectively. Adding biochar to PEDOT-PSS significantly improved the thermal stability of PEDOT-PSS up to 550 °C. The novel photocatalyst PEDOT-PSS@6wt.% BC improved photocatalytic performance by approximately 17% in Methylene Blue (MB) dye removal. The electrochemical performance in terms of supercapacitors for the synthesized samples was investigated using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), specific capacitance, stability, and electrochemical impedance spectra (EIS). PEDOT-PSS@6wt.% of BC as a novel electrode material in supercapacitors exhibits an initial specific capacitance of 1300 Fg−1. Moreover, the PEDOT-PSS@6wt.% of BC electrode shows excellent stability up to 1000 cycles of operation. The EIS studies suggest the presence of charge transfer resistance. Considering the economical biosynthesis and multifunctional features, the PEDOT-PSS@6wt.% of BC could potentially be used as a photocatalyst to remove organic dyes and supercapacitors in energy storage applications.

Benzodiazole-Based Covalent Organic Frameworks for Enhanced Photocatalytic Dehalogenation of Phenacyl Bromide Derivatives.

Covalent organic frameworks (COFs) have garnered significant interest within the scientific community due to their distinctive ability to act as organic semiconductors responsive to visible light. This unique attribute makes them up-and-coming candidates for facilitating photocatalytic organic reactions. Herein, two donor-acceptor COFs, TPE-BSD-COF and TPE-BD-COF, have been designed and synthesized by incorporating electron-rich tetraphenylethylene and electron-deficient benzoselenadiazole and benzothiadiazole units into the framework through a Schiff-base polycondensation reaction. Both COFs exhibit exceptional crystallinity and enduring porosity. TPE-BSD-COF and TPE-BD-COF exhibit broad light absorption capabilities, a narrow optical band gap, and low electrochemical impedance spectrum (EIS) levels, indicating that the two COFs are effective heterogeneous photocatalysts for the reductive dehalogenation of phenacyl bromide derivatives under blue LED irradiation. A high photocatalytic yield of 98% and 95% was achieved by TPE-BSD-COF and TPE-BD-COF catalysts, respectively, within only one hour.