Electrocatalytic Mechanism Research Articles

Recent advances and future perspectives of metal-organic frameworks as efficient electrocatalysts for CO2 reduction

AbstractThe conversion of carbon dioxide (CO2) to the reduced chemical compounds offers substantial environmental benefits through minimizing the emission of greenhouse gas and fostering sustainable practices. Recently, the unique properties of metal-organic frameworks (MOFs) make them attractive candidates for electrocatalytic CO2 reduction reaction (CO2RR), providing many opportunities to develop efficient, selective, and environmentally sustainable processes for mitigating CO2 emissions and utilizing CO2 as a valuable raw material for the synthesis of fuels and chemicals. Here, the recent advances in MOFs as efficient catalysts for electrocatalytic CO2RR are summarized. The detailed characteristics, electrocatalytic mechanisms, and practical approaches for improving the electrocatalytic efficiency, selectivity, and durability of MOFs under realistic reaction conditions are also clarified. Furthermore, the outlooks on the prospects of MOF-based electrocatalysts in CO2RR are provided.

Hydrogen Evolution Reactivity of Pentagonal Carbon Rings and p‐d Orbital Hybridization Effect with Ru

AbstractTopological defects are inevitable existence in carbon‐based frameworks, but their intrinsic electrocatalytic activity and mechanism remain under‐explored. Herein, the hydrogen evolution reaction (HER) of pentagonal carbon‐rings is probed by constructing pentagonal ring‐rich carbon (PRC), with optimized electronic structures and higher HER activity relative to common hexagonal carbon (HC). Furthermore, to improve the reactivity, we couple Ru clusters with PRC (Ru@PRC) through p‐d orbital hybridization between C and Ru atoms, which drives a shortcut transfer of electrons from Ru clusters to pentagonal rings. The electron‐deficient Ru species leads to a notable negative shift in d‐band centers of Ru and weakens their binding strength with hydrogen intermediates, thus enhancing the HER activity in different pH media. Especially, at a current density of 10 mA cm−2, PRC greatly reduces alkaline HER overpotentials from 540 to 380 mV. And Ru@PRC even exhibits low overpotentials of 28 and 275 mV to reach current densities of 10 and 1000 mA cm−2, respectively. Impressively, the mass activity and price activity of Ru@PRC are 7.83 and 15.7 times higher than that of Pt/C at the overpotential of 50 mV. Our data unveil the positive HER reactivity of pentagonal defects and good application prospects.

In-situ Reconstruction of Catalyst in Electrocatalysis.

Reconstruction of catalysts is now well recognized as a common phenomenon in electrocatalysis. As the reconstructed structure may promote or hamper the electrochemical performance, how to achieve the designed active surface for highly enhanced catalytic activity through the reconstruction needs to be carefully investigated. In this review, the genesis and electrochemical effects of reconstruction in various electrochemical catalytic processes, such as hydrogen evolution reaction (HER), oxygen evolution reaction (OER), carbon dioxide reduction reaction (CO2RR), and nitrate reduction reaction (NO3RR) are first described. Then, the strategies for optimizing the reconstruction, such as valence states control, active phase retention, phase evolution engineering, and surface poisoning prevention are comprehensively discussed. Finally, the general rules of reconstruction optimization are summarized and give perspectives for future study. It is believed that the review shall provide deep insights into electrocatalytic mechanisms and guide the design of pre-catalysts with highly improved activity.

The breakthrough of oxide pathway mechanism in stability and scaling relationship for water oxidation

Abstract An in-depth understanding of electrocatalytic mechanisms is essential for advancing electrocatalysts for the oxygen evolution reaction (OER). The emerging oxide pathway mechanism (OPM) streamlines direct O–O radical coupling, circumventing the formation of oxygen vacancy defects characteristic of the lattice oxygen mechanism (LOM) and bypassing additional reaction intermediates (*OOH) inherent to the adsorbate evolution mechanism (AEM). With only *O and *OH as intermediates, OPM-driven electrocatalysts stand out for their ability to disrupt traditional scaling relationships while ensuring stability. This review compiles the latest significant advances in OPM-based electrocatalysis, detailing design principles, synthetic methods, and sophisticated techniques to identify active sites and pathways. We conclude with prospective challenges and opportunities for OPM-driven electrocatalysts, aiming to advance the field into a new era by overcoming traditional constraints.

Selective methanol production via CO2 reduction on Cu2O revealed by micro-kinetic study combined with constant potential model

High efficiency electrocatalysis of greenhouse gas CO2 to liquid fuel methanol attracts great attentions that allows energy transformation from renewable electric energy to storable chemical energy. Catalytically converting CO2 to methanol using green hydrogen is a promising pathway to achieve carbon neutrality. In this work, the catalytic activity and product selectivity of the electrochemical CO2 reduction reaction on Cu2O were studied using a micro-kinetic model based on Marcus charge transfer theory. The constant potential model under the grand-canonical ensemble enables the accurate description of binding energies and ground-state charge transfer upon surface adsorption as a function of electrode potential. Firstly, the potential-dependent activation energies and rate constants of all possible elementary reactions involved in CO2 reduction are calculated. Then, the surface coverage and its derivative can be obtained in a steady-state approximation. Finally, the total reaction rate and partial reaction rate can be deduced, allowing for direct comparison with catalytic activity (current density) and product selectivity (Faradaic efficiency). It is found that CH3OH is the dominant product on the Cu2O(111) surface, while CO is the main product on the Cu2O(110) surface. Based on the derived total and partial reaction rates under the steady-state approximation, it is demonstrated that Cu2O(111) exhibits the highest electrocatalytic activity and methanol selectivity at U = −0.6 V vs. SHE. This research presents a methodology for predicting apparent electrocatalytic performance from microscopic reaction energy calculations, which can be applied to other important electrocatalytic reaction mechanisms and performance predictions.

Template‐Sacrificing Synthesis of Asymmetrically Coordinated Zn Single‐Atom Sites for High‐Performance Sodium–Sulfur Batteries

AbstractMetal single‐atom catalysts (SACs) are extensively investigated to accelerate the sulfur redox kinetics in room‐temperature sodium─sulfur (Na─S) batteries. Nevertheless, the influence of the structure symmetry of SACs center on the electrocatalytic mechanism and the precise pathway in which single‐atom active sites facilitate sodium polysulfides (Na2Sn) conversion remain unknown. To enable controlled construction of highly active single‐atom configuration, herein, Zn SACs with an asymmetrical Zn─N3O configuration are designed for sodium polysulfides conversion. Both theoretical and experimental explorations reveal that the Zn─N3O single‐atom center displays higher electrocatalytic activity for polysulfides conversion than the Zn─N4 single‐atom center. The N/O co‐coordination induces the localized charge at Zn single‐atom center, which strengthens the d‐p hybridization with Na2Sn and stretches Na─S bond length of Na2Sn, thus accelerating the sulfur redox reaction kinetics. Consequently, the as‐assembled Na─S batteries achieve a high capacity of 1016 mAh g−1 at 1.0 C with a capacity decay of 0.0186% per cycle over 1000 cycles. This work uncovers the subtle relationship between the electrocatalytic activity of species conversion and the local coordination environment of SACs, and offers a guidance for the design of efficient asymmetrical SACs for different catalysis applications.

Trifunctional Graphene-Sandwiched Heterojunction-Embedded Layered Lattice Electrocatalyst for High Performance in Zn-Air Battery-Driven Water Splitting.

Zn-air battery (ZAB)-driven water splitting holds great promise as a next-generation energy conversion technology, but its large overpotential, low activity, and poor stability for oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER) remain obstacles. Here, a trifunctional graphene-sandwiched, heterojunction-embedded layered lattice (G-SHELL) electrocatalyst offering a solution to these challenges are reported. Its hollow core-layered shell morphology promotes ion transport to Co3S4 for OER and graphene-sandwiched MoS2 for ORR/HER, while its heterojunction-induced internal electric fields facilitate electron migration. The structural characteristics of G-SHELL are thoroughly investigated using X-ray absorption spectroscopy. Additionally, atomic-resolution transmission electron microscopy (TEM) images align well with the DFT-relaxed structures and simulated TEM images, further confirming its structure. It exhibits an approximately threefold smaller ORR charge transfer resistance than Pt/C, a lower OER overpotential and Tafel slope than RuO₂, and excellent HER overpotential and Tafel slope, while outlasting noble metals in terms of durability. Ex situ X-ray photoelectron spectroscopy analysis under varying potentials by examining the peak shifts and ratios (Co2+/Co3+ and Mo4+/Mo6+) elucidates electrocatalytic reaction mechanisms. Furthermore, the ZAB with G-SHELL outperforms Pt/C+RuO2 in terms of energy density (797Wh kg-1) and peak power density (275.8mW cm-2), realizing the ZAB-driven water splitting.

Hydrogen Evolution Reactivity of Pentagonal Carbon Rings and p-d Orbital Hybridization Effect with Ru.

Topological defects are inevitable existence in carbon-based frameworks, but their intrinsic electrocatalytic activity and mechanism remain under-explored. Herein, the hydrogen evolution reaction (HER) of pentagonal carbon-rings is probed by constructing pentagonal ring-rich carbon (PRC), with optimized electronic structures and higher HER activity relative to common hexagonal carbon (HC). Furthermore, to improve the reactivity, we couple Ru clusters with PRC (Ru@PRC) through p-d orbital hybridization between C and Ru atoms, which drives a shortcut transfer of electrons from Ru clusters to pentagonal rings. The electron-deficient Ru species leads to a notable negative shift in d-band centers of Ru and weakens their binding strength with hydrogen intermediates, thus enhancing the HER activity in different pH media. Especially, at a current density of 10 mA cm-2, PRC greatly reduces alkaline HER overpotentials from 540 to 380 mV. And Ru@PRC even exhibits low overpotentials of 28 and 275 mV to reach current densities of 10 and 1000 mA cm-2, respectively. Impressively, the mass activity and price activity of Ru@PRC are 7.83 and 15.7 times higher than that of Pt/C at the overpotential of 50 mV. Our data unveil the positive HER reactivity of pentagonal defects and good application prospects.

Theoretical Study on the Electrocatalytic CO2 Reduction Mechanism of Single-Atom Co Complexed Carbon-Based (Co-Nχ@C) Catalysts Supported on Carbon Nanotubes.

Electrocatalytic CO2 reduction serves as an effective strategy to tackle energy crises and mitigate greenhouse gas effects. The development of efficient and cost-effective electrocatalysts has been a research hotspot in the field. In this study, we designed four Co-doped single-atom catalysts (Co-Nχ@C) using carbon nanotubes as carriers, these catalysts included tri- and dicoordinated N-doped carbon nanoribbons, as well as tri- and dicoordinated N-doped graphene, respectively denoted as H3(H2)-Co/CNT and 3(2)-Co/CNT. The stable configurations of these Co-Nχ@C catalysts were optimized using the PBE+D3 method. Additionally, we explored the reaction mechanisms of these catalysts for the electrocatalytic reduction of CO2 into four C1 products, including CO, HCOOH, CH3OH and CH4, in detail. Upon comparing the limiting potentials (UL) across the Co-Nχ@C catalysts, the activity sequence for the electrocatalytic reduction of CO2 was H2-Co/CNT > 3-Co/CNT > H3-Co/CNT > 2-Co/CNT. Meanwhile, our investigation of the hydrogen evolution reaction (HER) with four catalysts elucidated the influence of acidic conditions on the electrocatalytic CO2 reduction process. Specifically, controlling the acidity of the solution was crucial when using the H3-Co/CNT and H2-Co/CNT catalysts, while the 3-Co/CNT and 2-Co/CNT catalysts were almost unaffected by the solution's acidity. We hope that our research will provide a theoretical foundation for designing more effective CO2 reduction electrocatalysts.

Pt and Mo2C nanoparticles embedded in hollow carbon nanofibers as an effective electrocatalyst for hydrogen evolution reaction in acidic and alkaline electrolytes

Efficient catalysts for water electrolysis are essential for the advancement of hydrogen energy, aiding in carbon neutrality. Herein, a novel Pt and Mo2C embedded in hollow carbon nanofibers (referred to as Pt/Mo2C-HCNFs) electrocatalyst is devised and manufactured by coaxial electrostatic spinning and subsequent carbonization process in this work. Molybdenum carbide (Mo2C) and Pt share similar electronic structures, Mo2C is thought to be a possible alternative to Pt in hydrogen evolution reaction (HER). The synergistic interaction between Pt nanoparticles (NPs) and Mo2C NPs, the abundance of active sites, the hollow structure, the exceptional conductivity of carbon nanofibers, and the suppression of nanoparticle agglomeration by carbon nanofibers jointly make Pt/Mo2C-HCNFs exhibit excellent HER performances in both acidic and alkaline electrolytes. At a current density of 10 mA cm−2, the overpotentials of Pt/Mo2C-HCNFs in acidic and alkaline electrolytes are respectively 27 and 41 mV, demonstrating superior HER performance compared to commercial 20 wt% Pt/C. Electrocatalytic mechanisms are reasonably advanced. The formative mechanisms of the Pt/Mo2C-HCNFs are proposed, and corresponding technology is founded. This work offers a novel approach for synthesizing simple, efficient, and cost-effective Pt-based electrocatalysts.

Ferricyanide-Mediated, Electrocatalytic Mechanism of Electrochemical Aptamer-Based Sensor Supports Ultrasensitive Analysis of Cardiac Troponin I in Clinical Samples.

Rapid, reagent-free, and ultrasensitive analysis of cardiac troponin I (cTnI) is of significance for early diagnosis of acute myocardial infarction (AMI). The electrochemical aptamer-based (EAB) sensors are promising candidates to fill this role as they are reagentless and can be directly interrogated in complex matrices (e.g., blood). To achieve high sensitivity, EAB sensors typically require nanomaterials or other amplification strategies, which often involves a cumbersome fabrication process. To circumvent this, here we develop a simple yet effective electrocatalytic electrochemical aptamer-based (Ec-EAB) sensor that utilizes target-induced regulation of the catalytic mechanism to achieve ultrasensitive measurement of cTnI. In this assay, we employed a probe-attached redox reporter (i.e., methylene blue, MB) and a solution-diffusive redox reporter (i.e., Fe(CN)63-) to generate two signals, of which the latter is used to catalyze MB to amplify aptamer-mediated charge transfer. The recognition of target altered the diffusion of catalysts (2.2 × 10-9 mol/cm2 in the target-free state versus 1.2 × 10-9 mol/cm2 in the target-bound state) and thus electrocatalytical efficiency, enabling ultrasensitive measurement of cTnI with a 1000-fold improvement in their sensitivity (a limit of detection value: 10 pg/mL).

Influence of Particle Size on Mass Transport during the Oxygen Reduction Reaction at Single Silver Particles Using Scanning Electrochemical Cell Microscopy.

Single entity electrochemical measurements enable insight into the electrocatalytic activity of individual particles based on composition, shape, and crystallographic orientation. In addition to structural effects, particle size can further influence electrocatalytic activity and reaction mechanisms through mass transport effects. In this work, electrodeposition was used to grow well-separated silver particles of varying sizes from 100 to 500 nm in radius. Using a multimicroscopy approach of scanning electrochemical cell microscopy combined with scanning electron microscopy, the electrocatalytic current of individual silver particles toward the oxygen reduction reaction was evaluated as a function of their size. It was found that the current density increased with decreasing particle radius, which was correlated to the mass transport of oxygen to the silver particle, demonstrating the importance of size dependent mass transport effects that can occur at the single particle level using scanning electrochemical cell microscopy and opening new opportunities for quantitative electrocatalysis measurements.

(Invited) Insights into the Electrocatalytic Behavior of Mxenes

The continued rise in global energy consumption, along with the associated environmental hazards, pose a significant risk to our society’s infrastructure unless the main source is changed. Electrocatalysis involving hydrogen evolution reaction (HER), nitrogen reduction reaction (NRR), and oxygen reduction reaction (ORR), provide a pathway for energy storage and conversion due to their enhanced environmental friendliness and efficient energy input compared to their thermocatalytic counterparts. Currently, the state-of-the-art electrocatalysts suffer from scarcity and high cost. MXenes, a novel family of two-dimensional (2D) transition metal carbide and nitride materials, show potential as cost-efficient and highly abundant electrocatalysts with limited knowledge on their electrocatalytic mechanisms. This is especially true when considering the often-overlooked nitride family of MXenes. Herein, we investigate the electrocatalytic performance of a Ti2N nitride MXene under different electrocatalytic conditions. The effect of surface phenomena is investigated through manipulation of the surface passivation layer, as evidenced by Raman and Fourier-transform infrared (FTIR) spectroscopies, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Successful decoupling of the bulk and surface phenomena is achieved through Raman laser power attenuation. Under acidic medium, the surface reactivity towards HER is poor but the bulk reactivity for NRR is favored, making it an optimal NRR catalyst. Under alkaline medium, the surface reactivity of the pristine Ti2N MXene for ORR is high, but also leads to surface passivation and thus hinders the electrocatalytic activity. Overall, these results provide fundamental insights into future optimization strategies of the Ti2N nitride MXene, along with other MXene electrocatalysts, towards electrocatalytic applications.

Constructed Mott–Schottky Heterostructure Catalyst to Trigger Interface Disturbance and Manipulate Redox Kinetics in Li-O2 Battery

HighlightsA carbon free self supported Mott-Schottky heterostructure was constructed as an efficient cathode catalyst for lithium oxygen batteries, achieving homogeneous contact between the two materials for strong interfacial interactions.The heterostructure triggered interfacial perturbations and band structure changes, which accelerated oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) kinetics, resulting in an extremely long cycle life of 800 cycles and an extremely low overpotential of 0.73 V.Combined with advanced characterization techniques and density functional theory calculations, the underlying mechanism behind the boosted ORR/OER activities and the electrocatalytic mechanism were revealed.

Recent Advances in Revealing the Electrocatalytic Mechanism for Hydrogen Energy Conversion System.

In light of the intensifying global energy crisis and the mounting demand for environmental protection, it is of vital importance to develop advanced hydrogen energy conversion systems. Electrolysis cells for hydrogen production and fuel cell devices for hydrogen utilization are indispensable in hydrogen energy conversion. As one of the electrolysis cells, water splitting involves two electrochemical reactions, hydrogen evolution reaction and oxygen evolution reaction. And oxygen reduction reaction coupled with hydrogen oxidation reaction, represent the core electrocatalytic reactions in fuel cell devices. However, the inherent complexity and the lack of a clear understanding of the structure-performance relationship of these electrocatalytic reactions, have posed significant challenges to the advancement of research in this field. In this work, the recent development in revealing the mechanism of electrocatalytic reactions in hydrogen energy conversion systems is reviewed, including in situ characterization and theoretical calculation. First, the working principles and applications of operando measurements in unveiling the reaction mechanism are systematically introduced. Then the application of theoretical calculations in the design of catalysts and the investigation of the reaction mechanism are discussed. Furthermore, the challenges and opportunities are also summarized and discussed for paving the development of hydrogen energy conversion systems.

Efficient degradation of halogenated disinfection by products in a three-dimensional electrode reactor with MnO2/NiMn-LDH/C as particle electrodes: Performance prediction and mechanism exploration

In this work, an in situ novel MnO2/NiMn-LDH/C composite material was designed and used as a particle electrode in a three-dimensional electrochemical continuous flow system, which degraded dichloroacetamide (DCAcAm) because a suitable nickel-manganese metal ratio leads to the construction of MnO2 and NiMn-LDH, and the addition of carbon contributes to the formation of a hierarchical structure. The effects of different conditions were explored by single factor experiments and response surface design experiments. A high removal rate of 89 % was obtained under optimal conditions (current density of 12 mA/cm2, flow rate of 0.5 mL/min, electrolyte concentration of 0.175 mol/L, and a pollutant concentration of 10.5 g/L). According to density functional theory (DFT) calculations, electron paramagnetic resonance (EPR) measurements and free radical quenching experiments, the corresponding electrocatalytic mechanism and reaction pathways were clarified. The application of response surfaces was utilized to predict degradation performance. The results of the recycling experiments show the good stability of this electrode. Finally, the actual chlorin wastewater degradation experiment results showed that the COD and TOC of this wastewater decreased by 76.03 % and 72.41 %, respectively, after 90 min of electrocatalytic degradation. This study offers a novel theoretical framework and technical support for the control of HAcAms.

Elucidating the local structure and electronic properties of a highly active overall alkaline water splitting NixCo1-xO/hollow carbon sphere catalyst

A NixCo1-xO/HCS catalyst with superior water-splitting is presented. High water-splitting reaction kinetics and enhanced durability were observed. The structure-function relationship was investigated with XPS, which demonstrated the presence of dominant Ni2+ and Co2+ species and a functionalized HCS support where nucleation of small metal oxide nanoparticles occurred. The PDF showed broadened Nickel/Cobalt-oxide bonds and expansion of the metal-metal pair distances. The alteration of the Metal-Oxide and Metal-Metal-Oxide bonds favored better HER and OER electrocatalysis, also as supported by DFT. EXAFS showed the existence of the bimetallic oxide catalyst and the stretching of the Ni–O bonds due to the coordination of the Ni–O with the Co. The composite exhibited higher activity and enhanced electrocatalytic mechanism towards water splitting through higher exchange current densities (0.615 and 0.886 mA cm−2) and low charge transfer resistance (14 and 10 Ω) respectively. Chronoamperometry proved the catalyst's stability during prolonged electrolysis.

The recent progress of single-atom catalysts on amorphous substrates for electrocatalysis

Single-atom catalysts (SACs) have emerged as a focal point in energy catalytic conversion due to their remarkable atomic efficiency and catalytic performance. The challenge lies in efficiently anchoring active sites on a specific substrate to prevent agglomeration, maximizing their effectiveness. Substrate characteristics play a pivotal role in shaping the catalytic performance of SACs, influencing the dispersion and stability of single atoms. In recent years, amorphous materials have gained attention as substrates due to their unique surface structure and abundance of unsaturated coordination sites, offering an ideal platform for capturing and anchoring single atoms effectively, thus enhancing catalytic activity. To clarify the interaction between single atoms and amorphous substrates, this review outlines amorphization methods, the mechanism of single-atom anchoring and the characterization methods of amorphous SACs. Subsequently, it summarizes the physical properties and electrocatalytic mechanisms of amorphous materials. Then, interactions between single atoms and amorphous substrates are categorized and summarized. Finally, the paper consolidates the research progress of amorphous SACs and outlines future development prospects. By exploring the synergistic relationship between single atoms and amorphous substrates, this review aims to deepen the understanding of their interaction mechanisms, thereby propelling advancements in SACs for energy catalytic conversion.

Revealing the Electrocatalytic Reaction Mechanism of Water Splitting by In Situ Raman Technique

AbstractUsing renewable energy for water splitting to produce hydrogen is a crucial step toward achieving the dual carbon goals. However, due to the lack of a clear understanding of the precise localization of catalytic active sites and the complex structural evolution of catalysts during actual reaction conditions, there is still a challenge to reveal the electrocatalytic reaction mechanism of water splitting. In situ electrochemical Raman characterization technique can dynamically monitor the structural evolution of catalysts in real time, reveal the dynamic structure‐performance relationship of catalysts during the reaction process, and explore the catalytic reaction mechanism. This paper focuses on reviewing the latest developments in in situ electrochemical Raman characterization technology in terms of active sites on catalyst surfaces, the behavior of interfacial water molecules, and the structure evolution of electrocatalysts. The future development prospect of advanced in situ electrochemical Raman technology is also prospected.

Mechanism of enhanced degradation of antibiotic wastewater by three-dimensional electrocatalytic oxidation system: Coconut shell biochar as particle electrode

A porous particle electrode, coconut shell biochar (CBC), was prepared using coconut shell as raw material and applied to the treatment of tetracycline (TC) wastewater. Exploring the three-dimensional electrocatalytic oxidation system using a series of key factors such as pH (2−10), current density (20–60 mA/cm2), CBC particle size (0.88–2.36 mm), CBC dosage (3–13 g/L), electrolyte concentration (5000–10,000 mg/L), and electrode spacing (3–5 cm). The optimal conditions for these parameters were 10, 50 mA/cm2, 1.4–1.7 mm, 7 g/L, 8000 mg/L, and 4 cm. Under these conditions, the degradation of TC conformed to pseudo-first-order kinetics. The chemical oxygen demand (COD) and TC removal rates reached 84.01 % and 99.18 % within 45 min, while the two-dimensional system only achieved 29.27 % and 39.83 %, respectively. The degradation mechanism of TC was determined based on the production of H2O2 and •OH. The adsorbed saturated CBC might be regenerated through electrochemical reactions, inducing further adsorption, and forming numerous micro electrolysis cells to promote the production of free radicals, thereby boosting TC mineralization. Finally, the high-performance liquid chromatography-mass spectrometer was applied to identify the transformation products and degradation pathways of TC. Additionally, the CBC still showed excellent catalytic degradation effect after being reused for 4 times. Therefore, this study makes it possible to prepare an efficient and low-cost electrocatalyst for the treatment of antibiotic wastewater, as well as for further understanding the electrocatalytic mechanism, conversion products, and degradation pathways of TC in wastewater.