Oxygen Functionalities Research Articles

Electrochemical Insights into Hydrogen Peroxide Generation on Carbon Electrodes: Influence of Defects, Oxygen Functional Groups, and Alkali Metals in the Electrolyte

Electrochemical Insights into Hydrogen Peroxide Generation on Carbon Electrodes: Influence of Defects, Oxygen Functional Groups, and Alkali Metals in the Electrolyte

Engineering MXene Surface via Oxygen Functionalization and Au Nanoparticle Deposition for Enhanced Electrocatalytic Hydrogen Evolution Reaction.

MXene, a family of 2D transition metal carbides and nitrides, presents promising applications in electrocatalysis. Maximizing its large surface area is key to developing efficient non-noble-metal catalysts for the hydrogen evolution reaction (HER). In this study, oxygen-functionalized Ti3C2Tx MXene (Ti3C2Ox) is synthesized and deposited gold nanoparticles (Au NPs) onto it, forming a novel composite material, Au-Ti3C2Ox. By selectively removing other functional groups, mainly -O functional groups are retained on the surface, directing electron transfer from Au NPs to MXene due to electronic metal-support interaction (EMSI), thereby improving the catalytic activity of the MXene surface. Additionally, the interaction between Au NPs and -O functional groups further enhanced the overall catalytic activity, achieving an overpotential of 62 mV and a Tafel slope of 40.1 mV dec-1 at a current density of -10 mA cm-2 in 0.5 m H2SO4 solution. Density functional theory calculations and scanning electrochemical microscopy with ≤150 nm resolution confirmed the enhanced catalytic efficiency due to the specific interaction between Au NPs and Ti3C2Ox. This work provides a surface modification strategy to fully utilize the MXene surface and enhance the overall catalytic activity of MXene-based catalysts.

Effects of combined anesthesia on pulmonary oxygenation function, hemodynamics, and respiratory compliance in elderly patients undergoing pulmonary lobectomy for lung cancer.

Traditional general anesthesia in elderly lung cancer patients undergoing pulmonary lobectomy may lead to hemodynamic fluctuations and postoperative complications. To optimize anesthesia efficacy, this study explores the application of combined anesthesia (general anesthesia combined with thoracic paravertebral block) in such surgeries. We evaluated the improvement of pulmonary oxygenation function, hemodynamic stability, and respiratory compliance in elderly lung cancer patients undergoing pulmonary lobectomy with combined anesthesia. This retrospective study analyzed 100 elderly lung cancer patients who underwent pulmonary lobectomy at our hospital from February 2020 to December 2023. Patients were divided into 2 groups: the control group received general anesthesia, while the treatment group received combined anesthesia (general anesthesia plus thoracic paravertebral block). By comparing intraoperative hemodynamic parameters, postoperative pulmonary oxygenation function, respiratory compliance, cognitive function, sleep quality, and postoperative complication rates between the 2 groups, we assessed the application efficacy of combined anesthesia. Compared to the control group, the treatment group exhibited better hemodynamic stability intraoperatively, significantly improved postoperative pulmonary oxygenation function and respiratory compliance. Additionally, patients in the treatment group showed faster recovery of cognitive function, better sleep quality, and a relatively lower incidence of postoperative complications. Combined anesthesia demonstrates unique advantages in pulmonary lobectomy for elderly lung cancer patients, optimizing intraoperative hemodynamic stability, promoting postoperative pulmonary function recovery, accelerating cognitive function recovery, improving sleep quality, and potentially reducing the risk of postoperative complications. This finding provides a new effective strategy for anesthesia management in elderly lung cancer patients.

Research on modeling method of providing oxygen functional architecture based on model

Abstract The provision of oxygen is an important function of commercial aircraft, which is defined as providing the necessary oxygen for the safety of everyone on board, including crew oxygen, passenger oxygen, and portable oxygen. This article adopts SysML modelling language and proposes a model-based architecture modelling method for providing oxygen function for commercial aircraft. It transforms traditional experience and document-based system engineering work into functional architecture system engineering work, and utilises the correlation and traceability relationships of models to achieve state machine modelling for providing oxygen functional architecture. Through simulation verification, the functional architecture modelling method that provides oxygen can be effectively applied to the architecture of other systems.

ZIF-67 derivatives of NiCo2S4 Decorated in Salen-Complex Amine Functionalization GO Layers for High-Performance Applications in Supercapacitor Devices.

The study develops polyamine-functionalized graphene oxide-supported NiCo2S4 nanomaterial using a metal-organic framework (MOF). This modification adds free amines and oxygen functionality to the graphene oxide electrode surface, resulting in the decrease in the 2 theta value from 11.2 to 7.1 and an increase in the interlayer spacing value from 1.4 to 7.8 nm. This modification enhances the surface properties, leading to improved wettability and dispersion stability. Additionally, bimetallic nanoparticles of NiCo2S4, synthesized via the ZIF-67 MOF template, further enhance performance. Analysis confirms the successful fabrication of ZIF-67/f-GO/NiCo2S4 electrode material through various techniques such as XPS spectra, FE-SEM, XRD, and Raman spectra. The resulting Salen-fGO@NiCo2S4 composite exhibits impressive specific capacitance, reaching 2581.65 F g-1 at 10 A g-1 with 82% capacity retention after 5000 cycles. Employing this composite in a hybrid supercapacitor yields remarkable energy and power densities of 40 and 920 W kg-1, individually, while maintaining 74% capacity retention rate at 10 A g-1. These findings offer promising prospects for advanced energy storage applications.

Trajectories and sex differences of brain structure, oxygenation and perfusion functions in normal aging

Background: Brain structure, oxygenation and perfusion are important factors in aging. Coupling between regional cerebral oxygen consumption and perfusion also reflects functions of neurovascular unit (NVU). Their trajectories and sex differences during normal aging important for clinical interpretation are still not well defined. In this study, we aim to investigate the relationship between brain structure, functions and age, and exam the sex disparities.Method: A total of 137 healthy subjects between 20∼69 years old were enrolled with conventional MRI, structural three-dimensional T1-weighted imaging (3D-T1WI), 3D multi-echo gradient echo sequence (3D-mGRE), and 3D pseudo-continuous arterial spin labeling (3D-pCASL). Oxygen extraction fraction (OEF) and cerebral blood flow (CBF) were respectively reconstructed from 3D-mGRE and 3D-pCASL images. Cerebral metabolic rate of oxygen (CMRO2) were calculated as follows: CMRO2=CBF·OEF·[H]a, [H]a=7.377 μmol/mL. Brains were segmented into global gray matter (GM), global white matter (WM), and 148 cortical subregions. OEF, CBF, CMRO2, and volumes of GM/WM relative to intracranial volumes (rel_GM/rel_WM) were compared between males and females. Generalized additive models were used to evaluate the aging trajectories of brain structure and functions. The coupling between OEF and CBF was analyzed by correlation analysis. P or PFDR < 0.05 was considered statistically significant.Results: Females had larger rel_GM, higher CMRO2 and CBF of GM/WM than males (P < 0.05). With control of sex, CBF of GM significantly declined between 20 and 32 years, CMRO2 of GM declined subsequently from 33 to 41 years and rel_GM decreased significantly at all ages (R2 = 0.27, P < 0.001; R2 = 0.17, P < 0.001; R2 = 0.52, P < 0.001). In subregion analysis, CBF declined dispersedly while CMRO2 declined widely across most subregions of the cortex during aging. Robust negative coupling between OEF and CBF was found in most of the subregions (r range = -0.12∼-0.48, PFDR < 0.05).Conclusion: The sex disparities, age trajectories of brain structure and functions as well as the coupling of NVU in healthy individuals provide insights into normal aging which are potential targets for study of pathological conditions.

Efficient adsorption of antibiotics using MXene nanosheet delaminated by Taylor vortex flow

MXenes are emerging as a promising class of two-dimensional (2D) adsorbents suitable for various environmental applications. The present study explores the use of Ti3C2Tx MXene nanosheet, delaminated by Taylor vortex flow (TVF), namely d-MXene-CT, as an efficient adsorbent for fluoroquinolones (FQs). The TVF induced in the gap between two coaxial cylinders of the Couette-Taylor reactor enhances the delamination process, yielding larger and thinner MXene nanosheets with a specific surface area 12 fold higher than that of nanosheets delaminated by turbulent eddy flow (TEF), namely d-MXene-MT in a conventional mixing tank (MT) reactor. As a result, the d-MXene-CT exhibited superior adsorption performance, with removal capacity for ciprofloxacin (CIP) of 349 mg/g and for levofloxacin (LEV) of 290.51 mg/g, representing 40 ∼ 60 % improvement over d-MXene-MT (249 mg/g for CIP and 180.22 mg/g for LEV). The adsorption process follows the pseudo-second-order kinetics model and fits the Langmuir isotherm, indicating the involvement of a monolayer chemisorption mechanism. Further investigation revealed that the removal of CIP and LEV was mainly driven by electrostatic attraction between oxygen functionality of MXene and protonated nitrogen group of FQs. The study highlights the potential of d-MXene-CT as a promising adsorbent for treating (FQs) from contaminant water.

Desulfurization of simulated and commercial liquid fuel on nano-ZnO fabricated walnut shells.

The current investigation involved the development of activated carbon, juglans regia activated carbon (JRACs), from walnut shells, scientifically known as Juglans regia. The ZnO nanorods were loaded on the activated carbon and referred to as ZnO@JRACs. Desulfurization efficiency was assessed through batch adsorption and compared to commercial activated carbon known as DARCO. The materials were characterized using PXRD (powder X-ray diffraction), FTIR (Fourier-transform infrared spectroscopy), ICP-AES (inductively coupled plasma atomic emission spectroscopy), BET (Brunauer-Emmett-Teller) surface area analysis, TEM (transmission electron microscopy) imaging, and TGA (thermal gravimetric analysis). The findings indicated that the materials have oxygen functionalities, a porous morphology, and a substantial specific surface area (BET) of 1269.92 m2/g for ZnO@JRACs. Zn atom concentration in the ZnO@JRACs surface was determined to be 1.16 atomic percent using ICP-AES. Desulfurization experiments were conducted on three liquid fuels, namely a single component model fuel, MSF (multicomponent simulated fuel), and commercial fuel (kerosene), under optimized conditions (8g/L adsorbent dosage in 10mL of fuel, 15min of contact time at room temperature). The conditions effectively removed ~ 98.9% of dibenzothiophene (DBT) from the single component model fuel. The observed order for adsorption capacity is as follows: ZnO@JRACs (63.6mgg-1) > JRACs (46.3mgg-1) > DARCO (26.1mgg-1). The analysis of multicomponent simulated fuel (MSF) using gas chromatography-flame photometric detector (GC-FPD) revealed significant removal percentages for different types of thiophenic sulfur. Specifically, the removal percentages were ~ 46.2%, 97.6%, and 99.4% for benzothiophene, dibenzothiophene, and 4, 6-dimethyldibenzothiophene, respectively. Kinetic studies have shown that the adsorption process is governed by a pseudo second-order reaction. Additional thermodynamic studies were conducted to further investigate the mechanism of adsorption. The spent synthesized composite ZnO@JRACs were thermally regenerated and can be reused for up to four cycles.

3,8-Disubstituted Pyrazolo[1,5-a]quinazoline as GABAA Receptor Modulators: Synthesis, Electrophysiological Assays, and Molecular Modelling Studies

As a continuation of our study in the field of GABAA receptor modulators, we report the design and synthesis of new pyrazolo[1,5-a]quinazoline (PQ) bearing at the 8-position an oxygen or nitrogen function. All the final compounds and some intermediates, showing the three different forms of the pyrazolo[1,5-a]quinazoline scaffold (5-oxo-4,5-dihydro, -4,5-dihydro, and heteroaromatic form), have been screened with an electrophysiological technique on recombinant GABAAR (α1β2γ2-GABAAR), expressed in Xenopus laevis oocytes, by evaluating the variation in produced chlorine current, and permitting us to identify some interesting compounds (6d, 8a, 8b, and 14) on which further functional assays were performed. Molecular modelling studies (docking, minimization of complex ligand–receptor, and MD model) and a statistical analysis by a Hierarchical Cluster Analysis (HCA) have collocated these ligands in the class corresponding to their pharmacological profile. The HCA results are coherent with the model we recently published (Proximity Frequencies), identifying the residues γThr142 and αHis102 as discriminant for the agonist and antagonist profile.

Light‐Driven Site‐Selective Glycosylation of Native Carbohydrates

Carbohydrates constitute the largest source of biomass on Earth, but their synthetic modification is highly challenging due to their high content of oxygen functionalities. The site‐ and stereoselective modification of native sugars is a definitive goal of glycochemistry research. Recent efforts to bypass the need for protecting groups, leveraging selective activation through photochemical mechanisms for site‐selective C‐C bond formation from native sugars, are likely to largely impact all glycochemistry‐related areas. Davis, Koh, and co‐workers have recently presented their use of photocatalysis to develop a “cap and glycosylate” approach for the site‐ and stereoselective C‐glycosylation of native sugars. The modernization of a direct radical functionalization of in situ formed thioglycoside using photocatalysis was used in the synthetic manipulation of unprotected carbohydrates. This allowed reaching complex saccharides, and post‐translational modification of proteins.

Light-Driven Site-Selective Glycosylation of Native Carbohydrates.

Carbohydrates constitute the largest source of biomass on Earth, but their synthetic modification is challenging due to their high content in oxygen functionalities. The site- and stereoselective modification of native sugars is a definite goal of glycochemistry research. Recent efforts to bypass the need for protecting groups, leveraging selective activation through photochemical mechanisms for site-selective C-C bond formation from native sugars, are likely to largely impact all glycochemistry-related areas. Davis, Koh, and co-workers have recently presented their use of photocatalysis to develop a "cap and glycosylate" approach for the site- and stereoselective C-glycosylation of native sugars. A modernized direct radical functionalization of in situ formed thioglycoside using photocatalysis was used in the synthetic manipulation of unprotected carbohydrates. This allowed reaching complex saccharides, and post-translational modification of proteins.

Improved interfacial properties of carbon fiber reinforced epoxy resin composite by in‐situ self‐assembled mental‐phenolic networks

AbstractThe chemical modification of carbon fiber surface often uses toxic reagents and harsh reaction conditions, while the preparation process of metal‐phenol networks (MPNs) is simple, rapid, non‐toxic and harmless, which provides a direction for alleviating environmental problems. In this study, tannic acid (TA) was coordinated with Fe3+ to form MPNs, which was coated on the surface of carbon fibers through π‐π interaction. The results indicated that oxygen functionalities on the surface of the MPN coating can facilitate better adhesion between the carbon fiber and the epoxy resin, when the molar ratio of TA to Fe3+ is 1:3 and the pH is 4, the interlaminar shear strength (ILSS) performance of the composite material reaches its optimal level. In addition, a green and non‐destructive method is provided for the surface modification of carbon fiber, which can effectively optimize the interfacial properties of carbon fiber reinforced polymer (CFRP) composites.

Functionalization of pyrolyzed hydrochar with nitrogen containing deep eutectic solvent for carbon capture at low and high pressure

The purpose of this research is to evaluate the effectiveness of pyrolyzed hydrochar functionalized with nitrogen containing deep eutectic solvent (DES) in the absorption of CO2 under low- and high-pressure conditions. Pyrolyzed hydrochars were synthesized by hydrothermally carbonizing pine at the temperature of 200°C and 260°C, followed by pyrolysis at 600°C. These pyrolyzed hydrochars were impregnated with 3 different nitrogen containing DES namely choline chloride: urea, choline chloride: glycerol, and tetrabutylammonium bromide: glycerol all in 1:2 molar ratio. It was found that the functionalized pyrolyzed hydrochars were enhanced with nitrogen and oxygen functionalities (N-H, C-N, and CO). The results also show a substantial reduction in surface area for the functionalized pyrolyzed hydrochars, ranging from 10.19 to 227.74 m2g−1, compared to the surface areas of pyrolyzed hydrochars of 306–337 m2g−1. On the other hand, an increase in N content up to 38 % was identified after functionalization of pyrolyzed hydrochars. Upon conducting CO2 uptake at low (0.1–1 bar) and high (2.5–3.5 bar) pressure, the functionalized pyrolyzed hydrochars exhibited an CO2 uptake of up to 9.5 mmol/g at high pressure, which was attributed to the increased total nitrogen content, enhanced surface functionalities, and available micropore volume. The low-pressure isotherm for functionalized pyrolyzed hydrochars showed Langmuir-type isotherm, suggesting a monolayer adsorption. In contrast, the high-pressure isotherms were better fitted to the Freundlich isotherm, suggesting a multilayer adsorption behavior. It was concluded that the enhanced CO2 uptake is the result of the combined impact of increased surface functionalities and porosity, which results in improved physical and chemical adsorption mechanisms at the high pressure.

Oxygen Functionalization of Carbon Nanotubes Shifted the Formation Pathway of Hydroxyl Radicals in Catalytic Ozonation: The Overlooked Role of Hydrogen Peroxide

Oxygen Functionalization of Carbon Nanotubes Shifted the Formation Pathway of Hydroxyl Radicals in Catalytic Ozonation: The Overlooked Role of Hydrogen Peroxide

Impact of Mechanochemical Activation (MChA) on Characteristics and Dye Adsorption Behavior of Sawdust-Based Biocarbons.

The increase in environmental pollution due to the development of industry and human activity has resulted in intensive development of research on the possibility of its purification. A very effective method is the pollutants' adsorption from the air and water environment. For adsorption to be effective, materials with a specific structure and a well-developed surface decorated with numerous functionalities, e.g., biocarbons (BC), are necessary. An effective method of activating biocarbons is mechanochemical milling, an environmentally friendly procedure. This paper describes the possibility of using mechanochemical activation (MChA) of non-porous biocarbons to develop surface and porosity for their use in processes of pollutant adsorption. BC was characterized based on N2 adsorption, thermogravimetry (TGA), SEM/EDS imaging, Fourier (ATR-FTIR) and Raman spectroscopies, as well as titration using the Boehm method and determination of zeta potential. The adsorption capacity of BC for methylene blue (MB) was studied. It was proven that the solvent-free MChA made it possible to obtain microporous biocarbons, causing an intensive increase in the surface area and pore volume and the generation of oxygen functionalities. The biocarbons had predominantly acidic (mainly carboxylic) or basic functionalities and exhibited an amorphous structure. BC proved to be effective in adsorbing MB from aqueous solutions.

Enhancing electrochemical carbon dioxide capture with supercapacitors

Supercapacitors are emerging as energy-efficient and robust devices for electrochemical CO2 capture. However, the impacts of electrode structure and charging protocols on CO2 capture performance remain unclear. Therefore, this study develops structure-property-performance correlations for supercapacitor electrodes at different charging conditions. We find that electrodes with large surface areas and low oxygen functionalization generally perform best, while a combination of micro- and mesopores is important to achieve fast CO2 capture rates. With these structural features and tunable charging protocols, YP80F activated carbon electrodes show the best CO2 capture performance with a capture rate of 350 mmolCO2 kg–1 h–1 and a low electrical energy consumption of 18 kJ molCO2–1 at 300 mA g–1 under CO2, together with a long lifetime over 12000 cycles at 150 mA g–1 under CO2 and excellent CO2 selectivity over N2 and O2. Operated in a “positive charging mode”, the system achieves excellent electrochemical reversibility with Coulombic efficiencies over 99.8% in the presence of approximately 15% O2, alongside stable cycling performance over 1000 cycles. This study paves the way for improved supercapacitor electrodes and charging protocols for electrochemical CO2 capture.

Influence of umbilical cord clamping time on cerebral oxygenation and early cardiac function in term infants.

Delayed cord clamping is the standard of care for both term and preterm infants worldwide. The aim of this study was to evaluate the effect of 60-second or 180-second delayed cord clamping during labor on cerebral oxygenation and cardiac function. Healthy newborns were divided into two groups: a 60-second delay in cord clamping (60-s DCC) and a 180-second delay in cord clamping (180-s DCC) at birth. Pulse oximetry and cerebral near-infrared spectroscopy (cNIRS) probes were placed during postnatal care. A total of 84 healthy newborns were included in this study. Preductal oxygen saturation (SpO2), heart rate, and cNIRS values were recorded at 5 and 10 minutes after delivery. The cardiac function of the infants was assessed by echocardiography at 3-7 days postnatally. There was no significant difference between the groups in SpO2 and cNIRS values at 5 and 10 min. While there was no significant difference in the number of neonates with targeted SpO2 at the 5th and 10th min and targeted cNIRS values at the 10th min, there was a significant difference in the number of neonates with target cNIRS values at the 5th min between groups (p < 0.001). Echocardiographic findings showed that pulmonary flow velocity was increased in the 180-s DCC group; the difference was statistically significant (p = 0.04). Our results showed that the number of infants with normal cNIRS values regarding cerebral oxygenation was higher in the 180-s DCC group. The pulmonary flow velocity was significantly increased in the 180-s DCC group in terms of echocardiographic findings.

Assessment of Accelerated Aging Effect of Bio-Oil Fractions Utilizing Ultrahigh-Resolution Mass Spectrometry and k-Means Clustering of van Krevelen Compositional Space.

Bio-oils contain a substantial number of highly oxygenated hydrocarbons, which often exhibit low thermal stability during storage, handling, and refining. The primary objectives of this study are to characterize the hydroxyl group in bio-oil fractions and to investigate the relationship between the type of hydroxyl group and accelerated aging behavior. A bio-oil was fractionated into five solubility-based fractions, classified in two main groups: water-soluble and water-insoluble fractions. These fractions were then subjected to chemoselective reactions to tag molecules containing hydroxyl groups and analyzed by negative-ion electrospray ionization 21 T Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The fractions were also subjected to accelerated aging experiments and characterized by FT-ICR MS and bulk viscosity measurements. Extracting insightful information from ultrahigh-resolution data to aid in predicting upgrading methodologies and instability behaviors of bio-oils is challenging due to the complexity of the data. To address this, an unsupervised learning technique, k-means clustering analysis, was used to semiquantify molecular compositions with a close Euclidean distance within the (O/C, H/C) chemical space. The combination of k-means analysis with findings from chemoselective reactions allowed the distinctive hydroxyl functionalities across the samples to be inferred. Our results indicate that the hexane-soluble fraction contained numerous molecules containing primary and secondary alcohols, while the water-soluble fraction displayed diverse groups of oxygenated compounds, clustered near to carbohydrate-like and pyrolytic humin-like materials. Despite its high oxygen content, the water-soluble fraction showed minimal changes in viscosity during aging. In contrast, a significant increase in viscosity was observed in the water-insoluble materials, specifically, the low- and high-molecular-weight lignin fractions (LMWL and HMWL, respectively). Among these two fractions, the HMWL exhibited the highest increase in viscosity after only 4 h of accelerated aging. Our results indicate that this aging behavior is attributed to an increased number of molecular compositions containing phenolic groups. Thus, the chemical compositions within the HMWL are the major contributors to the viscosity changes in the bio-oil under accelerated aging conditions. This highlights the crucial role of oxygen functionality in bio-oil aging, suggesting that a high oxygen content alone does not necessarily correlate with an increase of viscosity. Unlike other bio-oil categorization methods based on constrained molecule locations within the van Krevelen compositional space, k-means clustering can identify patterns within ultrahigh-resolution data inherent to the unique chemical fingerprint of each sample.

Correlation between optical phonon softening and superconducting Tc in YBa2Cu3Ox within d-wave Eliashberg theory

Abstract We provide a mathematical description, based on d-wave Eliashberg theory, of the strong correlation between the experimentally observed softening of Raman modes associated with in-plane oxygen motions and the corresponding superconducting critical temperature T c , as a function of oxygen doping x, in YBa2Cu3O x . The theoretical model provides a direct link between physical trends of soft optical Ag (in-plane) oxygen modes, the level of oxygen doping x, and the superconducting T c . Different regimes observed in the trend of T c vs doping can be related to corresponding regimes of optical phonon softening in the Raman spectra. These results provide further evidence related to the physical origin of high-temperature superconductivity in rare-earth cuprate oxides and to the significant role of electron–phonon coupling therein.

Synthesis and characterization of hierarchically porous carbon anodes from furfural biorefinery residues for sustainable lithium-ion batteries

This study aims to valorize abundant lignocellulosic residues from furfural biorefineries into hierarchically porous carbon anodes for sustainable lithium-ion batteries (LIBs). Simultaneously, it addresses the growing demand for high-performance anode materials by leveraging renewable waste feedstocks. Sugarcane bagasse waste residues obtained after furfural extraction were used as the precursor. The furfural-derived bagasse residue (FDBR) underwent pyrolysis at 700 °C to produce a carbon-rich char, which was further activated using KOH and steam at 900 °C for 15–60 minutes to enhance porosity development. Comprehensive physicochemical characterizations, including proximate analysis, N2 adsorption-desorption, SEM-EDX, FTIR, and TGA/DTG, and Raman spectroscopy were performed to evaluate the properties of the synthesized activated carbons. The results demonstrated the successful generation of high surface area (405.8 m2/g) activated carbons with a hierarchical pore structure comprising micropores and mesopores. SEM and EDX analyses revealed a uniform, porous morphology enriched with 10.41 % at oxygen-containing functional groups. FTIR spectra confirmed the presence of hydroxyls, carbonyls, and carboxylic acid groups, beneficial for pseudocapacitive charge storage. The Raman analysis revealed a highly disordered and amorphous carbon structure with a significant concentration of defects, as evidenced by a high-intensity ratio (ID/IG ≈ 1.2–1.4) of the disordered carbon band to the graphitic band. The activated carbons exhibited a high initial discharge capacity of 1055 mAh/g in lithium half-cells, significantly exceeding the theoretical limit of commercial graphite anodes (372 mAh/g). This superior capacity was attributed to the high surface area, hierarchical porosity, and pseudocapacitive contributions from the oxygen functionalities. However, rapid capacity fading from 1055 to ∼250 mAh/g was observed over 100 cycles at a C/2 rate. The capacity retention stabilized at ∼88 % after 47 cycles, indicating irreversible capacity losses. These limitations were ascribed to the disordered amorphous structure, instability of the solid-electrolyte interphase, lithium trapping by oxygen groups, and structural changes during cycling. Optimizing activation conditions, incorporating conductive additives/coatings, exploring alternative binders, and surface functionalization are proposed to improve long-term cycling stability. Overall, this study demonstrates the feasibility of upcycling furfural biorefinery waste into sustainable LIB anodes while highlighting challenges and potential solutions for enhancing their electrochemical performance.