Oxidation Reaction Research Articles

Scale-up of Sodium Persulfate Mediated, Nitroxide Catalyzed Oxidative Functionalization Reactions.

Oxidation is a valuable tool in preparative organic chemistry. Oxoammonium salts and nitroxides have proven valuable as reagents and catalysts in this endeavor. The objective of this study is to scale up the oxidative amidation, ester formation, and nitrile formation using nitroxide as an organocatalyst. Oxidative functionalization reactions were scaled from the 1 mmol to the 1 mole level. Sodium persulfate was used as the primary oxidant, and a nitroxide was employed as a catalyst. The products of the reactions were isolated in analytically pure form by extraction with no need for column chromatography. The oxidative amidation and esterification of aldehydes can be scaled up from 1 mmol to 1 mole effectively, with comparable product yields being obtained at each increment. This work shows that conditions developed on a small scale can be transferred to a larger scale without reoptimization. The oxidative functionalization of aldehydes to prepare nitriles is not amenable to direct scale-up due to the concomitant formation of significant quantities of the corresponding carboxylic acid, thereby compromising the product yield. Two of the three oxidative transformations studied here can be scaled up successfully from the 1 mmol to the 1 mole level.

In-situ fabrication of defect rich Cu2+1O on electrodeposited Cu cone arrays for promoting electrocatalytic anode hydrogen production

The low-potential formaldehyde oxidation reaction (FOR) is a significant replacement for oxygen evolution reaction, as FOR can couple with the cathode hydrogen evolution reaction (HER) to obtain a bipolar H2 production system with an extra low cell voltage. Cu-based electrocatalysts offer cost advantages in FOR but suffer from poor intrinsic activity and stability. Herein, a novel defect rich CF-Cu@Cu2+1O/Cu pinecone-shaped array electrocatalyst is fabricated by in-situ solution immersion of electrodeposited Cu cone arrays on foam for efficient and stable formaldehyde selective oxidation reaction to co-produce hydrogen and valuable formate. Benefitting from the partially mixed Cu2+1O in metallic copper and concomitant production of defect rich oxygen vacancies, only 0.04 VRHE is required for electrocatalytic FOR at 100 mA·cm−2 under alkaline conditions. FOR current density of CF-Cu@Cu2+1O/Cu electrode exhibits 2.35 times than that of CF-Cu (144 mA·cm−2) and 77 times than that of copper foam (4.4 mA·cm−2) at 0.5 VRHE. Moreover, the special pinecone-shaped structure is constructed to modify Cu-based catalysts with substantially enhanced stability. A FOR-HER co-electrolysis device of CF-Cu@Cu2+1O/Cu(+)||Pt/C(−) can achieve bipolar H2 production with an approaching 200 % Faradaic efficiency, requiring an extremely low electrical energy consumption of only ∼ 0.35 kWh per m3 of H2 and potential of 0.291 V at 100 mA·cm−2 at room temperature.

Enhanced single-atom cobalt layer in MAX phase for biomass electrooxidation integrated with hydrogen evolution

MAX phases have attracted considerable interest due to their structural diversities and potential applications. More than 150 MAX phases have been synthesized, especially expanding the range of A-site atoms from traditional main group elements to subgroup elements with outer layer d electronic structure. However, the functional applications for MAX phases remain somewhat limited. The A-site elements in MAX phases can amplify their inherent properties, transforming primary structural materials into multifunctional materials. As highly catalytic elements, introducing cobalt into the A-site of MAX phases can reveal surprising catalytic activities. Hence, the MAX phase with single-atom-thick cobalt layers was synthesized via an A-site alloying strategy in this work. The obtained V2(Sn2/3Co1/3)C MAX phase demonstrates efficient electrocatalysis in 5-hydroxymethylfurfural (HMF) oxidation reaction along with hydrogen evolution reaction (HER). In-situ electrochemical studies discover that HMF can prevent the self-reconstruction of MAX phase and oxygen evolution reaction (OER). The overall reaction reaches 94.4 % yield to 2,5-furandicarboxylic acid (FDCA) at 1.60 V. Density functional theory calculations suggest that the Co-Sn bimetallic synergy in the A-site promotes the reaction. This groundbreaking investigation into using MAX phases for biomass upgrading highlights their potential in green chemistry and beyond.

Mechanistic studies on the oxidation reaction of n-pentane

The oxidation reaction mechanism of n-pentane is investigated using density functional theory and transition state theory as a case study to elucidate the combustion characteristics of liquids with low boiling points. This study divides the oxidation reaction of n-pentane into four steps. First, n-pentane decomposes to form n-pentyl radicals C5H11 and H, CH3 and C4H9, and C2H5 and C3H7 radicals. Second, n-pentane primarily undergoes H-abstraction reactions with H, CH3, C2H5, and C3H7 radicals to form the C5H11 radicals. Subsequently, C5H11 radicals react with O2 in an addition reaction to form n-pentyl peroxy radicals ROO. Finally, ROO radical undergoes internal H-atom transfer to form hydroperoxy pentyl radicals QOOH, which then undergoes cyclization and bond scission to produce cyclic ethers, alkenes, aldehydes, OH radicals, and HO2 radicals. Results indicate that n-pentane readily decomposes into C2H5 and C3H7 radicals, with a bond dissociation energy of 367.1 KJ/mol. The H-abstraction reactions involving H and CH3 radicals have the fastest rates, which require the lowest energy barriers of 21.6 and 41.9 KJ/mol, respectively. The reaction between C5H11 and O2 is a barrierless addition reaction. The oxidation of n-pentane, which leads to the formation of 2-methyloxirane and OH radicals, exhibits the fastest reaction rate.

Sulfur-containing cellulose esters for selectively anchoring gold for water catalytic decontamination

The facile preparation of sustainable sulfur-containing polymer functional materials has been obtained great attention due to their chemical reactivity and metal complexing ability. In this study, taking the solution properties advantages of the newly developed cellulose solvent system of DBU/DMSO/CO2, thiol and disulfide bond functionalized cellulose ester (TDSCE) was facilely prepared via in-situ tandem transesterification and oxidation reaction by using methyl 3-mercaptopropionate, without adding any external catalyst. The synthetic protocol was featured by that the DBU not only acted as reagent for the dissolution of cellulose, but also catalysts for the transesterification of cellulose with methyl 3-mercaptopropionate to yield cellulose 3-mercaptopropionate (Cell-MP) with maximum degrees of substitution (DS) of 0.77, and an oxidant for the partial oxidation of Cell-MP to produce a cellulose methyl 3,3′-disulfanediyldipropionate (Cell-MDSP) with maximum DS of 0.36 mixed ester, respectively. With successful introduction of thiol and disulfide bond into the cellulose backbone, the TDSCEs indicated desirable selective absorption of Au3+ from mimic heavy mental ions waste water due to the sulfur-Au chemistry with maximal adsorption capacity for Au3+ of 415.2 mg/g. The subsequent reduction of Au3+ into gold nanoparticles (Au NPs) fabricated a robust TDSCE-2@Au NPs composite catalyst with high catalytic activity for the hydrogenation treatment of water pollutes, such as 4-nitrophenol (4-NP)and azo dyes.

Inhibition of LPS-induced inflammatory response in RAW264.7 cells by natural Chlorogenic acid isomers involved with AKR1B1 inhibition

Inflammation is the physiological response of the immune system to injury or infection, typically manifested by local tissue congestion, swelling, heat, and pain. Prolonged or excessive inflammation can lead to tissue damage and the development of many diseases. The anti-inflammatory effects of natural ingredients have been extensively researched and confirmed. This study investigated the effects of Chlorogenic acid (CGA) isomers —— 3-Caffeolyquninic acid (3-CQA), 4-Caffeolyquninic acid (4-CQA), and 5-Caffeolyquninic acid (5-CQA) —— on the inflammatory response and oxidative stress reaction induced by LPS in RAW264.7 cells. Overall, 3-CQA exhibited the most significant reduction in levels of TNF-α, IL-6, NO, and ROS. 4-CQA showed superior inhibition of TNF-α compared to 5-CQA (p < 0.05), while no significant difference in other parameters. We further used DARTS and CETSA to demonstrate that CGA isomers have stable affinity with AKR1B1. As a positive control, the AKR1B1 antagonist epalrestat exhibited similar effects to the CGA isomers. 3-CQA having the smallest half-inhibitory concentration (IC50) for AKR1B1, while 4-CQA and 5-CQA have similar values. AutoDock simulations of the docking conformations revealed minimal differences in the average binding energies of the CGA isomers. The main differences were that VAL47 formed a hydrogen bond with 3-CQA, whereas GLN49 formed hydrogen bonds with 4-CQA and 5-CQA. Additionally, the number of hydrophobic bonds involving PHE122 and LEU300 varies. Our conclusion is that differences in non-covalent interactions result in the varying inhibitory abilities of CGA isomers on AKR1B1, which further affect the anti-inflammatory and antioxidant effects of CGA isomers.

Natural DNA-Derived Ultrafine Ir/Ir2P Hybrid on Porous N, P-Codoped Carbon for pH-Universal Energy-Saving Hydrogen Production Assisted by Electrocatalytic Hydrazine Oxidation

Due to the intrinsic slow kinetics and high potential of the anodic oxygen evolution reaction (OER), hydrazine oxidation reaction (HzOR) with ultralow potential is a viable substitute to combine the cathodic hydrogen evolution reaction (HER) for the energy-saving hydrogen generation. Therefore, it is a compelling demand to explore high-performance electrocatalysts for bifunctional HER and HzOR. Herein, natural DNA was employed to prepare the uniform and ultrafine Ir/Ir2P hybrids loaded on N, P-codoped porous carbon (Ir/PNPC) through a facile “mix-and-pyrolyze” approach. Benefitting from abundant heteroatom doping, large surface area and high degree of graphitization, Ir/PNPC only requires the ultrasmall potentials of -22/-347/-54 mV at 100 mA cm-2 for HER, 46/172/227 mV at 10 mA cm-2 for HzOR, and 167/836/864 mV at 100 mA cm−2 for the constructed two-electrode overall hydrazine splitting (OHzS) in the alkaline, neutral and acidic electrolytes, respectively, all exceeding Pt/C and also showing the remarkable energy-efficient superiority over the conventional water splitting. Furthermore, the OHzS system can be readily driven by the as-prepared direct N2H4/H2O2 fuel cell and commercial solar cell with decent H2 generation rate of 1.245 and 1.392 mmol h-1, respectively. This study provides lights on the preparation of the advanced pH-universal HER and HzOR bifunctional electrocatalysts by natural DNA and is also encouraging for the energy-saving H2 production.

Cathodic corrosion induced selective nano-crystallization of Nickel oxo/hydroxo complex on (NiFeCr)SiB amorphous ribbon for alkaline oxygen evolution reaction and methanol oxidation reaction

The study focuses on the development and optimization of (Ni87Fe4Cr9)78Si8B14 amorphous ribbons as self-supported electro-catalysts for oxygen evolution reaction (OER) and methanol oxidation reaction (MOR). Electro-catalytically active nano α-Ni(OH)2 phase (5–10nm) was generated in the amorphous ribbon surface through potentiostatic cathodic corrosion for different time intervals (0–120 min). The X-ray diffraction and scanning electron microscopy results shows the favourable occurrence of dense nanocrystallization of α-Ni(OH)2 between 45 and 90 min of corrosion time. For OER in 1 M KOH, the 60-min surface modified ribbon exhibits an overpotential of 295 mV at 10 mA/cm2 current density and tafel slope of 51 mV dec−1. In case of MOR in 1 M KOH +1 M MeOH, the 90-min corroded ribbon shows lowest potential of 1.38 V vs RHE, at 10 mA/cm2 and tafel slope of 34 mV dec−1. In addition to superior electro-catalytic activity, the optimal surface-modified ribbons show superior long-term stability for OER and MOR studies, indicating its potential application in hydrogen generation and direct methanol fuel cell.

Flexible Ag@Au core–shell nanowires electrode fabrication with controllable nanogold size and thickness on silver nanowires/PDMS substrate toward enhanced ethanol electrooxidation

The synthesis of gold nanowires (AuNWs) is challenging due to difficulties in obtaining AuNWs of variable diameters and lengths. In this study, an effective approach to fabricating AuNWs with controllable lengths and diameters was developed on a flexible silver nanowires (AgNWs)/polydimethylsiloxane (PDMS) substrate. Gold nanoparticles were uniformly electrodeposited onto the flexible AgNWs/PDMS to form bimetallic Ag@Au core–shell NWs/PDMS. The results showed that the diameters and the lengths of the Ag@Au NWs were easily fine-tuned. The flexible Ag@Au NWs/PDMS electrode exhibited excellent mechanical, electrical, and electrochemical properties. In ethanol oxidation reaction (EOR), the Ag@Au NWs/PDMS achieved a peak current density of 28541.55 μA cm−2 (10 times higher than that of a commercial Au electrode) and 63.39% retaining activity in a stability test by chronoamperometry (over 2 times stable than values in literature). Finally, EOR and chromium (VI) determination by the Ag@Au NWs/PDMS in flexible integrated electrodes were performed to showcase the versatile feasibilities of this new material.

Utilizing cationic vacancies to enhance nickel-cobalt layered double hydroxides for efficient electrocatalytic urea oxidation reaction

Electrocatalytic urea oxidation reaction (UOR) is a promising approach for urea-rich wastewater splitting, which benefits for reducing energy consumption in hydrogen production accompanying environmental protection and sustainable energy development. To address the limitations posed by the self-oxidation of nickel-based catalysts on the activity of UOR, we here developed a NiCo LDH nanosheet catalyst with abundant Ni vacancies to initiate the UOR process prior to nickel oxidation. Electrochemical impedance spectroscopy and In-situ spectroscopic characterizations confirm that the UOR process primarily occurs on the surface of the catalyst, rather than being driven by nickel oxidation products. The favorable electronic structure modulation induced by Ni vacancies makes the catalyst more energetically favorable for the UOR compared to nickel self-oxidation. The catalyst exhibits excellent UOR activity, only requiring 1.27 V vs. RHE at 10 mA cm−2 and 1.34 V vs. RHE at 100 mA cm−2, with no significant decay observed after over 120 h of operation. Furthermore, it can function as a bifunctional catalyst, requiring only 1.66 V to achieve 100 mA cm−2 for the UOR||HER system. This study expands the pathway for the application of cationic vacancies in UOR.

Regulating the electronic structure of Ni3Se4-MoSe2 by coupling with ZIF-derived Co@C promotes boosted urea-assisted water splitting at industrial current density

Adopting urea oxidation reaction (UOR) as an alternative to oxygen evolution reaction (OER) is a prospective approach to achieve energy-saving H2 generation as well as purify wastewater with abundant urea, while the industrial application of bifunctional catalysts for hydrogen evolution reaction (HER) and UOR still remains challenge. Herein, novel coleslaw-like arrays Ni3Se4-MoSe2/Co@C electrocatalyst is fabricated by coupling Ni3Se4-MoSe2 heterointerface with Co-ZIF derived Co@C, in which the synergistic effects of Ni3Se4-MoSe2 and Co@C can tailor the electronic state caused by Ni, Mo, Se and Co atoms, contributing to the modulated d-band center and charge redistribution, hence balancing the absorption and desorption of HER and UOR reaction intermediates and realizing facilitated HER and UOR activities. Furthermore, the coleslaw-like arrays could expose more active sites as well as speed up mass transport. As a result, Ni3Se4-MoSe2/Co@C shows ultralow potentials of 189 mV and 1.427 V to achieve industrial current density of 1000 mA·cm−2 with small Tafel slopes of 56.5 and 30.2 mV·dec-1 towards HER and UOR with exceptional long durability, respectively. Impressively, a remarkably decreased cell voltage of 1.98 V is seen to achieve 1000 mA·cm−2 for urea-assisted water splitting. This study introduces a new strategy to producing non-noble-based selenides with ZIF derivative to realize bifunctional application in energy-saving H2 production with industrial treatment of urea wastewater.

Enhancing CO tolerance in hydrogen oxidation reaction through synergy of surface-modified MoOx with PtRu alloy

Even trace amounts of CO impurities present in low-cost crude hydrogen can severely poison Pt-based catalysts. For proton exchange membrane fuel cells (PEMFCs), the development of hydrogen oxidation reaction (HOR) catalysts capable of enduring CO contamination is of significant economic importance. In this study, we propose a new strategy to synergistically enhance the CO tolerance of PtRu alloys by incorporating MoOx. The MoOx modified on PtRu/C catalysts can initiate the oxidation of CO adsorbed on its surface at potentials as low as 0.125 V. The synergy effect of MoOx and bifunctional PtRu ensures sufficient HOR stability even under hydrogen containing high CO concentrations. The resulting PtRu-MoOx/C catalyst exhibits a 4.6-fold increase in remained HOR current compared to commercial PtRu/C, after two hours in a hydrogen environment containing 10,000 ppm CO. Under typical testing condition of H2/1,000 ppm CO, PtRu-MoOx/C maintains over 80 % of the initial current density even after ten hours, significantly outperforming PtRu/C (30 %) and most previously reported catalysts.

Chemical thermodynamics of biomass, cellulose, and cellulose derivatives: A review

This article provides a review of the research on the chemical thermodynamics and thermochemistry of biomass, cellulose, and its derivatives such as ethers, esters, and oxycelluloses. For diverse biomass types, gross and net heating values were studied. It has been established that these energetical characteristics of biomass can be calculated using a superposition of the energetical characteristics of the main components of biomass such as cellulose, hemicelluloses, lignin, lipids, proteins, etc. The pelletization of biomass improves its fuel performance. It was shown that, if the ultimate goal is to generate the maximum amount of thermal energy, then it is more profitable to directly burn the initial biomass in the form of pellets than to burn the amount of solid or liquid biofuel that can be extracted from this biomass. After the cellulose study, the direct and exact thermochemical method for determining the crystallinity degree of this biopolymer was proposed. In addition, the standard combustion and formation enthalpies of various cellulose samples were studied. As a result, the thermodynamic characteristics of four crystalline allomorphs of cellulose, CI, CII, CIII, and CIV, were obtained and their thermodynamic stability was evaluated. The thermochemistry of enzymatic hydrolysis of cellulose was studied. In addition. The thermodynamical characteristics of various cellulose derivatives were determined, and the thermochemistry of the reactions of cellulose alkalization, etherification, esterification, and oxidation was studied.

Well-Defined Microenvironment in Metal–Organic Frameworks Enable Green, Benign, and Isolation-Free Catalytic Oxidation Reaction

Well-Defined Microenvironment in Metal–Organic Frameworks Enable Green, Benign, and Isolation-Free Catalytic Oxidation Reaction

Suppression of Structural Heterogeneity in High-Entropy Intermetallics for Electrocatalytic Upgrading of Waste Plastics.

The key to fully realizing the potential of high-entropy alloys (HEAs) lies in balancing their inherent local chemical disordering with the long-range ordering required for electrochemical applications. Herein, we synthesized a distinctive L10-(PtIr)(FeMoBi) high-entropy intermetallics (HEIs) exhibiting nanoscale long-range order and atomic scale short-range disorder via a lattice compensation strategy to mitigate the entropy reduction tendency. The (PtIr)(FeMoBi) catalyst exhibited remarkable activity and selectivity of glycollic acid (GA) production via electrocatalytic waste polymer-derived ethylene glycol oxidation reaction (EGOR). With a mass activity of 5.2 A mgPt-1 and a Faradic efficiency (FE) for GA of 95 %, it outperformed most previously reported electrocatalysts for selective GA production. The lattice-compensation effect promotes the homogeneity of Pt and Fe actives sites, facilitating co-adsorption of EG and OH and reducing the energy barriers for dehydrogenation and OH-combination processes. This approach effectively avoids the formation of low-active sites commonly encountered in HEA solid solutions, offering a promising avenue for exploring the complex interplay between catalytic activity and HEI structures.

Vanadium-Doped Heterointerfaced Ni3N-MoOx Nanosheets with Optimized H and H2O Adsorption for Effective Alkaline Hydrogen Electrocatalysis.

Nickel (Ni)-based materials represent a compelling avenue as platinum alternatives in the realm of alkaline hydrogen electrocatalysis. However, conventional nickel nitrides (Ni3N) have long been hindered by sluggish hydrogen evolution kinetics in alkaline environments, owing to inadequate adsorption strengths of both hydrogen and water molecules. Herein, a novel approach is presented involving the design of vanadium (V)-doped Ni3N/MoOx heterogeneous nanosheets (V-Ni3N@MoOx), engineered to achieve optimized adsorption strengths for hydrogen evolution and oxidation reactions (HER/HOR). Theoretical insights underscore the superior catalytic performance of this composite, attributed to a synergistic interplay between unique V doping and the heterointerfaced structure. This synergistic effect not only fine-tunes the electronic structure, establishing an optimal d band center to mitigate proton over-bonding, but also ameliorates the energy barrier through enhanced H2O dissociation capability. Consequently, V-Ni3N@MoOx manifests remarkable catalytic activities, evincing an overpotential of 56mV at 10mAcm-2 for HER and an exchange current density of 1.91mAcm-2 for HOR in alkaline media. Notably, the stability assessment reveals the enduring performance of V-Ni3N@MoOx for HER/HOR, exhibiting no activity decay over extended operational durations. This study underscores the efficacy of heterogeneous interface modulation as a transformative strategy in designing Ni-based materials for alkaline hydrogen electrocatalysis.

The Swiss Army Knife of Electrodes: Pillar[6]arene-Modified Electrodes for Molecular Electrocatalysis Over a Wide pH Range.

Molecularly-modified electrode materials that maintain stability over a broad pH range are rare. Typically, each electrochemical transformation necessitates a specifically tuned system to achieve strong binding and high activity of the catalyst. Here, we report the functionalisation of mesoporous indium tin oxide (mITO) electrodes with the macrocyclic host molecule pillar[6]arene (PA[6]). These electrodes are stable within the pH range of 2.4-10.8 and can be equipped with electrochemically active ruthenium complexes through host-guest interactions to perform various oxidation reactions. Benzyl alcohol oxidation serves as a model reaction in acidic media, while ammonia oxidation is conducted to assess the systems performance under basic conditions. PA[6]-modified electrodes demonstrate catalytic activity for both reactions when complexed to different guest molecules and can be reused by reabsorption of the catalyst after its degradation. Furthermore, the system can be employed to perform subsequent reactions in electrolyte with varying pH, enabling the same electrode to be utilised in multiple different electrocatalytic reactions.

The Swiss Army Knife of Electrodes: Pillar[6]arene‐Modified Electrodes for Molecular Electrocatalysis Over a Wide pH Range

AbstractMolecularly‐modified electrode materials that maintain stability over a broad pH range are rare. Typically, each electrochemical transformation necessitates a specifically tuned system to achieve strong binding and high activity of the catalyst. Here, we report the functionalisation of mesoporous indium tin oxide (mITO) electrodes with the macrocyclic host molecule pillar[6]arene (PA[6]). These electrodes are stable within the pH range of 2.4–10.8 and can be equipped with electrochemically active ruthenium complexes through host–guest interactions to perform various oxidation reactions. Benzyl alcohol oxidation serves as a model reaction in acidic media, while ammonia oxidation is conducted to assess the systems performance under basic conditions. PA[6]‐modified electrodes demonstrate catalytic activity for both reactions when complexed to different guest molecules and can be reused by reabsorption of the catalyst after its degradation. Furthermore, the system can be employed to perform subsequent reactions in electrolyte with varying pH, enabling the same electrode to be utilised in multiple different electrocatalytic reactions.

Electronic Structure of Rh and Ir Single Atom Catalysts Supported on Defective and Doped ZnO: Assessment of Their Activity Towards CO Oxidation

This study investigated the electronic structure of single-atom Rhodium (Rh) and Iridium (Ir) adsorbed on defective and impurity-doped ZnO(0001) surfaces, and assessed their activity towards the CO oxidation reaction. Our findings reveal that surface impurities significantly influence the binding energies and electronic properties of the metal atoms, with Al and Cr serving as particularly effective promoters. While Rh and Ir acquire a positive charge upon incorporation on the unpromoted Zn(0001) surface, adsorption directly on the promoter results in a net negative charge, thus facilitating the activation of both CO and O2 species. These results highlight the potential of impurity-promoted ZnO surfaces in modulating and tailoring the electronic properties of SACs, which can be used for a rational design of active single-atom catalysts.

High uric acid induces vascular endothelial cell injury via XBP1-PKM2 mediated glycolytic inhibition

Abstract Background/Introduction Although not fully understood, hyperuricemia induced endothelial dysfunction exhibits at the early onset of the pathology of atherosclerosis. Since aerobic glycolysis is the predominant energy source of endothelial cells, exploring the key glycolytic regulators that are responsible for maintaining the integrity of endothelial barrier may confer vascular homeostasis and prevent atherosclerosis. Purpose We aimed to investigate the role of high uric acid in the glycolysis of human umbilical vein endothelial cells (HUVECs), and reveal its potential molecular mechanism underlying endothelial cell injury early in their quiescence. Methods Glycolytic metabolism was determined by real-time extracellular flux analysis and seahorse test on the HUVECs exposed to high uric acid (600 and 800μmol/L). We examined the expression of pyruvate kinase muscle isoforms 2 (PKM2), a key enzyme of glycolysis, and transcription factor X-box binding protein 1 (XBP1), which was identified by RNA sequencing and chromatin immunoprecipitation combined with luciferase assay. Then, the effect of glycolytic regulation on the HUVECs functions under hypeuricemic condition was evaluated by molecular manipulating of XBP1-PKM2 signaling pathway. Results We observed that hyperuricemia inhibited glycolysis and led to reduced ATP production of HUVECs in vitro by inhibiting the expression of PKM2. In addition, both unsliced and sliced XBP1-(u/s) were also downregulated under the stimulation of high uric acid. Overexpression of XBP1-s increased the transcriptional level of PKM2 via binding the PKM2 promoter, and effectively recovered the glycolitic activity and ATP synthesis. Moreover, upregulating the XBP1-PKM2 pathway mitigated the HUVECs injury induced by hyperuricemia, including the abnormal release of endothelin-1, von Willebrand Factor, reactive oxygen species and nitric oxide, and poor cell proliferation, migration as well as tube formation. Conclusions Our data reveal that high uric acid induces HUVECs injury by downregulating glycolysis through the XBP1-PKM2 signaling axis.