Electrochemical Oxidation Research Articles

Effects of ion mass transport on electrochemical reaction pathways in aluminum-anthraquinone batteries

Aluminum anodes and quinone-based organic cathodes couple as earth abundant, sustainable, and safe battery electrodes. However, different numbers of galvanostatic discharge plateaus have been observed in aluminum-quinone cells depending on the experimental conditions, a phenomenon that has not yet been explained and furthermore affects cell energy density. Here, in aluminum-anthraquinone batteries, we show that ion mass transport affects the electrochemical reaction pathway and controls the occurrence of either one or two reduction plateaus during galvanostatic discharge. The effects of electrode mass loading, porosity, rest periods, and cycling rates were analyzed on the reduction potential and relative specific capacity of the galvanostatic plateaus. When AlCl2+ cations charge compensate the electrochemically reduced carbonyl groups concurrently, a single reduction plateau is observed. When ion mass transport is limiting, sequential reduction and charge compensation of each carbonyl group results in two distinct reduction plateaus. The second plateau occurs at a potential approximately 0.3 V lower than the first, thus decreasing the cell energy density. The potential of the electrochemical oxidation reaction where AlCl2+ cations dissociate, however, is not affected. Ion mass transport is thus shown to be a critical variable that can control the electrochemical reaction pathway, redox potentials, and practical energy densities of aluminum-quinone batteries.

Multiple Enzyme-Mimicking CuMOF-Driven Self-Cascading Antioxidant Reaction for Synergistic Electrochemiluminescence Modulation in Ultrasensitive Biosensing.

Developing nanozyme-based free radical scavenging is a promising signal modulation approach for ECL sensing. Nevertheless, the relatively low antioxidant activity and inherent pro-oxidant activity of numerous nanozymes have significantly hindered the development of this strategy. Here a biofunctional copper-based metal-organic framework (CuMOF) with multiple enzyme-mimicking activities was employed for the modulation of the ECL immunosensor, guided by the self-cascade antioxidant reaction. The inherent SOD, CAT, and the capacity to eliminate ·OH endow CuMOF with powerful synergistic antioxidant effects while little pro-oxidant activities were displayed, enabling efficient scavenging of the O2·- produced during the electrochemical oxidation of H2O2. Subsequently, the nanoconfinement effect of the layered double hydroxide was introduced to ensure a steady ECL signal. The suggested ECL immunosensor, using aflatoxin B1 as a proof-of-concept target, demonstrated a detection range spanning from 0.001 pg/mL to 10 ng/mL, with the detection limit calculated to be 0.18 fg/mL. This exceptional achievement greatly broadens the range of possible uses for nanozyme-based radical scavenging modulated ECL analysis.

Electrochemical oxidation of bisphenol A with a Fe-N-C/persulfate three-dimensional electrochemical system

In this study, an effective three-dimensional (3D) electrochemical system based on persulfate was developed, utilizing Fe-N-C compostie as the particle electrodes, and its electrocatalytic performance for the oxidation of bisphenol A was evaluated. With the synergetic effect of Fe-N-C catalyst and electric current, peroxydisulfate is activated to generate highly oxidative sulfate radicals (SO4•−) and hydroxyl radicals (•OH), and the •OH playing a leading role in the oxidation of BPA. In this process, the redox cycle of Fe2+/Fe3+ acts as the main catalytic active center to produce SO4•−, •OH and O2•−, while pyridine N and graphite carbon cooperate to catalyze the formation of 1O2 and promote direct electron transfer, with their reduction by 37.19 % and 3.34 %, respectively, highlighting their crucial role in these processes. During the degradation of bisphenol A, coupling polymerization occurred at the same time, which may be due to the stabilization and instantaneous resonance of the intermediate on the surface of the catalyst caused by direct electron transfer, which induced the polymerization of oxide intermediate. 1O2 not only oxidizes BPA into low molecular weight products, but also extracts hydrogen atoms to form phenoxy free radicals. The coupling of these free radicals promotes the formation of macromolecular polymers and separation from water. This parallel treatment mechanism of degradation and polymerization effectively reduces the emission of CO2 and the mineralization of organic matter. Based on the above findings, the E/PDS/Fe-N-C system has broad potential in the treatment of environmental pollutants.

Integrated electrochemical-adsorption for simultaneous removal of pharmaceuticals from water: Process optimization and synergistic insights

Water contamination with pharmaceuticals has become an evident environmental challenge. Treatment processes such as electrochemical oxidation (EO) and adsorption have limitations in the simultaneous removal of pharmaceuticals from water. Therefore, this study examined the potential of coupled process (EO followed by adsorption) in binary pharmaceuticals (acetaminophen (ACM) + ciprofloxacin (CIP)) removal from water, with an emphasis on coupled process optimization. Consequently, optimized coupled process conditions including current density (22 mA/cm2), pH (5.5), EO time (40 min), adsorbent dose (0.1 g/L) and adsorption time (60 min) were obtained. Under optimal conditions, removal efficiencies of 94.6% (ACM)+92% (CIP), 94.07% (ACM)+91.15% (CIP), and > 99.8% (ACM + CIP) were recorded for 20 mg/L (ACM + CIP) removal in EO, adsorption and EO + adsorption, respectively. Further, the coupled process was employed in multiple pharmaceuticals (20 mg/L of ACM + CIP + ATN (atenolol) + AMX (amoxicillin)) removal from water and removal of > 97.56% (ACM + CIP + ATN + AMX) was achieved. Removal efficiencies of ACM (83.35%) + CIP (73.1%) + ATN (68.52%) + AMX (63.05%) and ACM (80.37%) + CIP (66.5%) + ATN (73.07%) + AMX (60.5%) were obtained in EO and adsorption, respectively. The noted lower removal efficiencies in EO and adsorption are associated with the diverse nature of the pharmaceuticals, limited adsorbent active sites, and the shared utilization of reactive oxygen species (ROS) among the pharmaceuticals in EO. The total organic carbon (TOC) removal of 40.24%, and 99% and chemical oxygen demand (COD) removal of 72.45%, and 99.6% were obtained under optimal conditions of EO, and coupled process, respectively. These findings indicate that the pharmaceuticals are only partially mineralized in EO and the subsequent adsorption effectively eliminated the remaining target pharmaceuticals, and degradation by-products from water. Additionally, integrating EO with adsorption reduced the electrical energy consumption of the EO process from 31.6 kWh/m³ to 6 kWh/m³ under optimal conditions. Overall, coupling EO with adsorption offers the utmost advantages when removing multiple pharmaceuticals from complex water matrices.

A Green and Efficient Electrocatalytic Route for the Highly‐Selective Oxidation of C–H Bonds in Aromatics over 1D Co3O4‐Based Nanoarrays

Electrocatalytic oxidation of C‐H bonds in hydrocarbons represents an efficient and sustainable strategy for the synthesis of value‐added chemicals. Herein, a highly selective and continuous‐flow electrochemical oxidation process of toluene to various oxygenated products (benzyl alcohol, benzaldehyde, and benzyl acetate) is developed with the electrocatalytic membrane electrodes (ECMEs). The selectivity of target products can be manipulated via surface and interface engineering of Co3O4‐based electrocatalysts. We achieved a high benzaldehyde selectivity of 90% at a toluene conversion of 47.6% using 1D‐Co3O4 nanoneedles (NNs) loaded on a microfiltration (MF) titanium (Ti) membrane, i.e, Co3O4 NNs/Ti. In contrast, the main product shifted to benzyl alcohol with a selectivity of 90.1% at conversion of 32.1% after modifying MnO2 nanosheets (NSs) on Co3O4 NNs/Ti (Co3O4@MnO2/Ti) catalyst. Moreover, benzyl acetate product can be obtained with selectivity of 92% at a conversion of 58.5% at high current density (> 1.5mA cm‐2), demonstrating that the pathway of toluene oxidation is readily maneuvered. DFT results reveal that modifying MnO2 on Co3O4 optimizes the electron structure of Co3O4@MnO2/Ti and modulates the adsorption behavior of intermediate species. This work demonstrates a sustainable, and continuous‐flow process for precise control over production selectivity of value‐added oxygenated derivatives in electrochemical oxidation of aromatic hydrocarbons.

A Green and Efficient Electrocatalytic Route for the Highly-Selective Oxidation of C-H Bonds in Aromatics over 1D Co3O4-Based Nanoarrays.

Electrocatalytic oxidation of C-H bonds in hydrocarbons represents an efficient and sustainable strategy for the synthesis of value-added chemicals. Herein, a highly selective and continuous-flow electrochemical oxidation process of toluene to various oxygenated products (benzyl alcohol, benzaldehyde, and benzyl acetate) is developed with the electrocatalytic membrane electrodes (ECMEs). The selectivity of target products can be manipulated via surface and interface engineering of Co3O4-based electrocatalysts. We achieved a high benzaldehyde selectivity of 90% at a toluene conversion of 47.6% using 1D-Co3O4 nanoneedles (NNs) loaded on a microfiltration (MF) titanium (Ti) membrane, i.e, Co3O4 NNs/Ti. In contrast, the main product shifted to benzyl alcohol with a selectivity of 90.1% at conversion of 32.1% after modifying MnO2 nanosheets (NSs) on Co3O4 NNs/Ti (Co3O4@MnO2/Ti) catalyst. Moreover, benzyl acetate product can be obtained withselectivity of 92% at a conversion of 58.5% at high current density (> 1.5mA cm-2), demonstrating that the pathway of toluene oxidation is readily maneuvered. DFT results reveal that modifying MnO2 on Co3O4 optimizes the electron structure of Co3O4@MnO2/Ti and modulates the adsorption behavior of intermediate species. This work demonstrates a sustainable,and continuous-flow process for precise control over production selectivity of value-added oxygenated derivatives in electrochemical oxidation of aromatic hydrocarbons.

Enhanced electrocatalytic activity of hafnium doped tungsten oxide (Hf-WO3) for ultrasensitive detection of nonsteroidal anti-inflammatory drug

Efficient hafnium-doped tungsten oxide nanoparticles (Hf-WO3) were developed by hydrothermal approach and characterization was carried out by X-ray diffraction pattern (XRD), transmission electron microscopy (TEM), high resolution-transmission electron microscopy (HR-TEM), scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS) and electrochemical impedance spectroscopy (EIS) techniques. Cyclic voltammetry (CV) and square wave voltammetry (SWV) techniques were employed to assess the electrochemical response of the fabricated carbon paste electrodes (CPE) for the analysis of mefenamic acid (MA). The objective of this work is to develop and optimize parameters to enhance the selectivity and sensitivity of Hf-WO3 modified sensor for the trace-level detection of MA, addressing its critical importance in both pharmaceutical and environmental analysis. The Hf-WO3 predominantly showed a monoclinic phase with some hexagonal peaks, confirming its good crystallinity and 1-D structure, which enhances charge transport and catalytic sites. XPS analysis confirmed the formation of pure Hf-WO3 by showing distinct W and Hf peaks and verifying their valences: W in the +6 state and Hf in the +4 state. CV showed that the Hf-WO3/CPE greatly enhances the electrochemical oxidation of MA compared to unmodified and tungsten oxide-modified electrodes, with a six-fold increase in peak current and notable redox activity attributed to improved surface properties and charge transfer efficiency. Under optimum experimental conditions, the Hf-WO3/CPE exhibits a low limit of detection (LOD) of 3.94 nM with dynamic concentration linearity ranging from 0.01 to 100.0 μM with good sensitivity of 1.74 μAμM−1cm−2. Furthermore, the Hf-WO3/CPE was employed in real-time analysis of MA in spiked urine samples and pharmaceutical tablet samples, which showed satisfactory recovery results ⁓ 98 %. Moreover, the electrode showed good stability over multiple measurements, and these results demonstrate that Hf-WO3/CPE is a promising sensor for MA detection.

Boosting Zn2+ Intercalation in High‐Performance Aqueous Zinc‐Ion Batteries with Coupling‐Induced Biphase Interface

AbstractEffectively addressing the trade‐off between fast charging kinetics and long cycle life of aqueous zinc ion batteries (AZIBs) has proven challenging due to JahnTeller distortion and high lattice strain induced by inserted Zn2+ ions in cathode structures. Herein, a hybrid cathode of NiCo2O4‐MnO2 with abundant electrochemical phase interfaces and interface coupling induced defects is developed via a simple electrochemical oxidation strategy to boost rich redox reactions. The formation of Ni─O─Mn and Co─O─Mn bonds promoted the electron transfer between the biphase interface, adjusted the electron density of the material body, effectively alleviated the electrostatic effect between Zn2+ embedding and the main frame, and further maintained the stability of the structure and alleviated the dissolution of manganese. The resulting NiCo2O4‐MnO2 cathode exhibited a high reversible specific capacity of 343.5 mA h g−1 at a current density of 100 mA g−1 and retained 95.5 % of its initial capacity after 1000 cycles at a current density of 1 A g−1. This discovery enriches insights into performance mechanisms at interfaces and paves the way for designing advanced energy storage materials.

Dual-donor D-A-D types electrochromic conjugated polymers employed quinoxaline as the acceptor: Synthesis, electrochemistry, and electrochromism

In this work, two donor-acceptor-donor (D-A-D) type electrochromic conjugated polymers were prepared upon electrochemical oxidation through their precursors employed dual-thiophene derivatives as the donor units and quinoxaline as the acceptor unit. The effects of different donor substituents on the polymers’ electrochemical and electrochromic properties were carefully examined. Owing to the introduction of stronger electron donor ability of 3,4-ethylenedioxythiophene (EDOT), P(Q-T-E) demonstrated good coplanarity and dense surface morphology, outstanding redox activity and stability (retained 97 % after 1000 cycles), low optical band gap (1.45 eV). P(Q-T-T) exhibited excellent electrochromic performance of above 30 % transmittance changes in both the NIR region and the visible region, as fast as 0.75 s response time, and high coloration efficiency value of 212.8 cm2 C−1. The Dual-donor strategy may provide a new research idea to achieve high-performance electrochromic D-A-D conjugated polymers.

Low-Loaded Pt Nanoparticles Supported on Electrochemically Exfoliated Graphene as a Sustainable Catalyst for Electrochemical Ethanol Oxidation

Low-Loaded Pt Nanoparticles Supported on Electrochemically Exfoliated Graphene as a Sustainable Catalyst for Electrochemical Ethanol Oxidation

Tandem Oxidation Activation of Carbon for Enhanced Electrochemical Synthesis of H2O2: Unveiling the Role of Quinone Groups and Their Operando Derivatives

AbstractOxygen‐doped carbon materials show great promise to catalyze two‐electron oxygen reduction reaction (2e‐ORR) for electrochemical synthesis of hydrogen peroxide (H2O2), but the identification of the active sites is the subject of ongoing debate. In this study, a tandem oxidation strategy is developed to activate carbon black for achieving highly efficient electrochemical synthesis of H2O2. Acetylene black (AB) is processed with O2 plasma and subsequent electrochemical oxidation, resulting in a remarkable selectivity of >96% over a wide potential range, and a record‐setting high yield of >10 mol gcat−1 h−1 with good durability in gas diffusion electrode. Comprehensive characterizations and calculations revealed that the presence of abundant C═O groups at the edge sites positively correlated to and accounted for the excellent 2e‐ORR performance. Notably, the edge hydroquinone group formed from quinone under operando conditions, which is overlooked in previous research, is identified as the most active catalytic site.

Improving biodegradability of dissolved organic matter (DOM) in old landfill leachate by electrochemical pretreatment: The effect mechanism of polarity

Enhancing the biodegradability of old landfill leachate is vital for the efficient treatment or resource utilization of municipal solid waste. Electrochemical pretreatment emerges as a promising technology for transformation of refractory dissolved organic matter (DOM). However, the specific impact of polarity on improving biodegradability of DOM remains unclear. In this study, a divided electrolyzer was used to explore the changes in the biodegradability of DOM in old landfill leachate during electrolysis. Meanwhile, the correlation mechanism between BOD5 variation and DOM evolution was explored by spectroscopy and Maldi-TOF-MS analysis. Results shown that different polarities all have positive effect on enhancing the biodegradability of DOM, while the structural changes related with BOD5 are depending on the polarity. In the anode chamber, electrochemical oxidation (EO) generates and eliminates carboxyl groups. Additionally, EO concurrently eliminates humic-like substances, which are challenging for microorganisms to degrade, and protein-like substances, which are easily degradable by microorganisms. This creates a competitive mechanism that coexist the promotion and inhibition for biodegradability. In the cathode chamber, electrochemical reduction (ER) transforms DOM components, accumulating easily useable protein components for microorganisms. Kinetic studies show that EO related BOD5 changes are aptly described by a competition model, considering both generation and removal of bioavailable components. ER related BOD5 changes suit a pseudo-first-order kinetic model. These insights into the transformation of old leachate DOM support the development of methods predicting BOD5 evolution, crucial for future process optimization.

Enhanced selectivity of reactive intermediates by modifying electrodes with layered materials for the green high-salinity wastewater treatment

Improving the selectivity of the reactive intermediates such as ClO− and •OH by modifying nickel foam electrodes with ion exchangeable layered materials would greatly enhance the efficiency of high-salinity wastewater treatment. A universal pattern was verified herein that through functioning as a permeable overlayer regulating the transport of cations/anions, ClO− and •OH could be the predominant intermediates in the anionic/cationic layered material modified electrode. The significance of selectivity enhancement includes improving electrochemical efficiency and reducing the usage of chemical reagents. For instance, it is demonstrated that electrochemically degrading high salinity azo wastewater using decorated electrodes would be as effective as chemical treatment. Furthermore, electrochemical oxidation using cation layered material modified electrode could reduce the pKa of the oxidized cellulose filter paper as effectively as using H2O2.

Promoting effect of interfacial hole accumulation on photoelectrochemical water oxidation in BiVO4 and Mo-doped BiVO4

Hole transfer at the semiconductor-electrolyte interface is a key elementary process in (photo)electrochemical (PEC) water oxidation. However, up to now, a detailed understanding of the hole transfer and the influence of surface hole density on PEC water oxidation kinetics is lacking. In this work, we propose a model for the first time in which the surface accumulated hole density in BiVO4 and Mo-doped BiVO4 samples during water oxidation can be acquired via employing illumination-dependent Mott-Schottky measurements. Based on this model, some results are demonstrated as below: (1) Although the surface hole density increases when increasing light intensity and applied potential, the hole transfer rate remains linearly proportional to surface hole density on a log-log scale. (2) Both water oxidation on BiVO4 and Mo-doped BiVO4 follow first-order reaction kinetics at low surface hole densities, which is in good agreement with literature. (3) We find that water oxidation active sites in both BiVO4 and Mo-doped BiVO4 are very likely to be Bi5+, which are produced by photoexcited or/and electro-induced surface holes, rather than VOx species or Mo6+ due to their insufficient redox potential for water oxidation. (4) Introduction of Mo doping brings about higher OER activity of BiVO4, as it suppresses the recombination rate of surface holes and increases formation of Bi5+. This surface hole model offers a general approach for the quantification of surface hole density in the field of semiconductor photoelectrocatalysis.

New spacious SrWO4/PEDOT-PPy nanohybrids and their electrochemical and photocatalytic activities.

A novel SrWO4-poly(3,4-ethylene dioxythiophene) (PEDOT)-polypyrrole (PPy) nanocomposite was synthesized via chemically oxidative polymerization and considered by using numerous method of the techniques. The resulting SrWO4/PEDOT-PPy nanocomposite demonstrated remarkable electrochemical sensing capabilities for sulfadiazine (SFA). As a modified glassy carbon electrode (SrWO4/PEDOT-PPy/GCE) revealed for superior catalytic activity in the electrochemical oxidation of sulfadiazine, enabling sensitive detection with quantification and detection limits of 1.0936 × 10-9M µA-1 and 2.2104 × 10-9M µA-1, respectively. This technique effectively determined SFA content in real samples. Additionally, SrWO4/PEDOT-PPy demonstrated extraordinary photocatalytic ability, achieving a Methylene Blue (MB) degradation rate of up to 99.1% under halogen light irradiation within 80min. Hybrid photocatalyst has exhibited to strong reusability and photocatalytic stability under frequent light exposure. A contrivance for the photocatalytic deprivation of MB by SrWO4/PEDOT-PPy is proposed. These results underscore the crucial role of SrWO4/PEDOT-PPy in practical environmental remediation analysis. The fluorescence investigations have betrothed to terephthalic acid radical formations of SrWO4/PEDOT-PPy hybrids, which were modulated by different approaches, and its mainly driven for higher illumination aptitudes. Meanwhile, this was more supporting for physio-chemical properties of the phenomenon, at this consequential with significantly well improved to the photocatalytic performances. Because of this, SrWO4/PEDOT-PPy hybrid materials were comprehended to deliver excellent kinetics, and better recyclable activities.

Electrochemical unzipping of multiple-walled WS2 nanotubes for synthesis of WS2 nanoribbons being an attractive H2 evolution catalyst

We report the unzipping of multiple-walled WS2 nanotubes (WS2-MWNTs) to produce WS2 nanoribbons by employing an electrochemical oxidation process. When conditioning the WS2-MWNTs in an acidic solution at 1.2 V vs. RHE, W-S bond was oxidized inducing a longitudinal unzipping of WS2 walls. The resultant WS2 nanoribbons displayed a significant superior catalytic activity in comparison to the WS2-MWNTs.

An Electrosynthesis of 1,3,4-Oxadiazoles from N-Acyl Hydrazones.

The 1,3,4-oxadiazole is a widely encountered motif in the areas of pharmaceuticals, materials, and agrochemicals. This work has established a mild, mediated electrochemical synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from N-acyl hydrazones. Using DABCO as the optimal redox mediator has enabled a mild oxidative cyclisation, without recourse to stoichiometric oxidants. In contrast to previous methods, this indirect electrochemical oxidation has enabled a broad range of substrates to be accessed, with yields of up to 83%, and on gram scale. The simplicity of the method has been further demonstrated by the development of a one-pot procedure, directly transforming readily available aldehydes and hydrazides into valuable heterocycles.

Reviewing the Phenomenon of Antimicrobial Resistance in Hospital and Municipal Wastewaters: The Crisis, the Challenges and Mitigation Methods

Antibiotic resistance is a major crisis that the modern world is confronting. This review highlights the abundance of different types of antibiotic resistance genes (ARGs) in two major reservoirs in the environment, namely hospital and municipal wastewater, which is an unforeseen threat to human lives across the globe. The review helps understand the current state of affairs and the whereabouts on the dissemination of ARGs in both these environments. The various traditional wastewater treatment methods, such as chlorination and UV treatment, and modern methods, such as electrochemical oxidation, are discussed, and the gaps in these technologies are highlighted. The need for the development of newer techniques for wastewater treatment with enhanced efficiency is urgently underscored. Nanomaterial applications for ARG removal were observed to be less explored. This has been discussed, and prospective nanomaterials and nanocomposites for these applications are proposed.

Removal of refractory humic acid-like components from UF filtrate of landfill leachate through pH adjustment and coupled electrochemical process

Mature landfill leachate contains large quantities of a wide range of hazardous and refractory pollutants, especially humic acid-like (HA) and fulvic acid-like (FA) substances. These have poor biodegradability and a considerable ultraviolet-light quenching capacity, severely inhibiting the performance of wastewater treatment and post ultraviolet-light disinfection, but this aspect has attracted little previous research. The Fenton reaction has proved to be a feasible method for removing ultraviolet-quenching substances (UVQSs) but in conventional systems it is unable to completely mineralize organic contaminants. In this study, a novel electro-oxidation process was developed consisting of a flow-through reactor with a Cu2O cathode to catalyze Fenton-type reactions, and oxidation at a RuO2 anode. The combination of pH adjustment and electro-oxidation was evaluated for the treatment of real ultrafiltration (UF) filtrate of mature landfill leachate. A series of analytical techniques were used to determine the performance for the removal of HA and FA. Under optimal conditions, the elimination of fluorescence characteristics of HA and FA reached 100 % and 99.3 %, respectively, according to PARAFAC results based on EEM spectra. TOC was removed by 25.5 %∼30.4 % during the pH adjustment step and 51 % by electrochemical oxidation. Changes in the molecular weight distribution and fluorescence content showed that pH adjustment played an important and significant role in removing UVQSs, and the remaining TOC after electrochemical oxidation was attributed to bioavailable amino acid-like substances. Overall, the results have demonstrated the successful development of an effective method of treating the UF filtrate from mature landfill leachate, with particular respect to the removal of the problematic HA and FA content.

Electrobiofabrication of antibody sensor interfaces within a 3D printed device yield rapid and robust electrochemical measurements of titer and glycan structure.

We report the integration of 3D printing, electrobiofabrication, and protein engineering to create a device that enables near real-time analysis of monoclonal antibody (mAb) titer and quality. 3D printing was used to create the macroscale architecture that can control fluidic contact of a sample with multiple electrodes for replicate measurements. An analysis "chip" was configured as a "snap-in" module for connecting to a 3D printed housing containing fluidic and electronic communication systems. Electrobiofabrication was used to functionalize each electrode by the assembly of a hydrogel interface containing biomolecular recognition and capture proteins. Specifically, an electrochemical thiol oxidation is used to assemble a thiolated polyethylene glycol hydrogel, that in turn is covalently coupled to either a cysteine-tagged protein G that binds the antibody's Fc region or a lectin that binds the glycans of target mAb analytes. We first show the design, assembly, and testing of the hardware device. Then, we show the transition of a step-by-step sensing methodology (e.g., mix, incubate, wash, mix, incubate, wash, measure) into the current method where functionalization, antibody capture, and assessment are performed in situ and in parallel channels. Both titer and glycan analyses were found to be linear with antibody concentration (to 0.2 mg/L). We further found the interfaces could be reused with remarkably similar results. Because the interface assembly and use are simple, rapid, and robust, we suggest this assessment methodology will be widely applicable, including for other biomolecular process development and manufacturing environments.