Oxygen Vacancies Research Articles

Alanine Production by Chemical Upcycling of Polylactic Acid Waste Over Fe-Doped Ru/CeO2.

Biodegradable polyesters, such as polylactic acid (PLA), is one of the most promising plastics with great potential to contribute to enabling a sustainable global circular economy. However, the efficient chemical upcycling of PLA plastic waste into high-value chemicals remains a grand challenge. Herein, a series of Ru/CeFeOx catalysts with varying Ru loadings were developed for the catalytic amination of PLA plastic waste to alanine in the presence of ammonia. The as-prepared catalysts exhibited exceptional catalytic activity, high selectivity, and excellent recyclability, achieving an alanine yield of 70.5 % at 180 °C for 18 h, significantly surpassing previous reports. The outstanding catalytic performance can be primarily attributed to the presence of Fe species in Ru/CeFeOx, which generated more oxygen vacancies, provided abundant base sites, and enhanced reducibility, therefore accelerating the reaction rate and enhancing catalytic efficiency. This study presents an alternative strategy for the sustainable chemical upcycling of PLA plastic waste into alanine and the realization of a circular economy.

Multifaceted Synergism of Dual Active Sites in Oxygen Vacancies Enriched Plasmonic Ag-BiOI Nanosheets for Enhanced Piezo-Photocatalytic Degradation of Trimethoprim

Multifaceted Synergism of Dual Active Sites in Oxygen Vacancies Enriched Plasmonic Ag-BiOI Nanosheets for Enhanced Piezo-Photocatalytic Degradation of Trimethoprim

Metalloid Phosphorus Induces Tunable Defect Engineering in High Entropy Oxide Toward Advanced Lithium‐Ion Batteries

AbstractThe inferior electrical conductivity and sluggish lithium storage kinetics of conventional high‐entropy oxide (HEO) are critical issues hindering their commercialization. The high electronegativity of metalloids can ameliorate this predicament by altering the electronic configuration of HEO compared to metals. Herein, metalloid phosphorus doping in spinel‐type HEO (PxA1‐x)B2O4 (A/B = Cr, Mn, Fe, Co, Ni) (P‐HEO) is achieved through a facile sol–gel process. The metalloid phosphorus doping facilitates the transfer of electrons from transition metal sites to phosphorus‐doped sites, resulting in the formation of electron‐rich and electron‐deficient local regions on the HEO surface and is conducive to an increase in the total number of active lithium sites in the electrochemical reaction process. Density functional theory calculation reveals Li adsorption energy on the synthesized P‐HEO is only −1.102 eV, demonstrating that the phosphorus doping enables a strong electronic coupling between lithium ions and P‐HEO. Furthermore, metalloid phosphorus doping also leads to oxygen vacancies formation and lattice distortion, which significantly enhances charge transfer efficiency and diffusion kinetics and results in the enhanced lithium storage performance with impressive rate capability and long‐term stability. These findings provide valuable insights for the design of lattice‐engineered HEO as versatile electrodes for future energy storage applications.

Impact of N+ Ion Irradiation on the Electrochemical Behavior of ZnO Thin Film Electrode-Electrolyte Interfaces.

Defect engineering serves as a crucial technique for enhancing the performance of advanced next-generation devices. Ion beam irradiation stands out as a highly promising method for introducing defects in a controlled manner. This study investigates the impact of nitrogen ion (N+) irradiation-induced defects on the electrochemical behavior of ZnO thin-film electrode-electrolyte interface. The oxygen vacancy defects were introduced and tuned by varying the fluence of ion irradiation. The increased Urbach energy in the irradiated samples confirms the enhanced disorder. Photoluminescence data show the emergence of new defect states upon irradiation. The behavior of the ZnO thin-film electrode-electrolyte interface was studied using cyclic voltammetry and electrochemical impedance spectroscopy. At a fixed scan rate, the enhanced peak current was observed in cyclic voltammetry in N+ Irradiated electrodes. Furthermore, reduced charge transfer resistance was observed in the case of irradiated electrodes. To unravel the underlying mechanism, we analyze the AC conductivity, which shows varying dependency on the frequency. It shows the existence of multiple ion-ion correlations in irradiated electrodes. Furthermore, the AC conductivity in the entire frequency region is enhanced significantly. Dielectric permittivity spectra suggest low-frequency dipole interactions and increased dielectric losses after irradiation, indicating non-Debye type relaxation processes. Understanding irradiation-induced changes will help engineer thin film electrodes for batteries, supercapacitors, and other electrochemical applications.

Construction of Ternary Zn0.5Cu0.5Co2O4 Spinel Structure on Nickel Foam: A Comprehensive Theoretical and Experimental Study from Single to Ternary Metal Oxides for High-Energy-Density Asymmetric Supercapacitor Application.

Developing nanostructured multi-transition metal-based spinel architectures represents a strategic approach for boosting the energy density of supercapacitors while preserving high power density. Here, the influence of incorporating Zn and Cu into Co3O4 spinel systems on supercapacitor performance is investigated by synthesizing single (ZnO, CuO, Co3O4), binary (ZnCo2O4, CuCo2O4), and ternary (Zn0.5Cu0.5Co2O4) oxides on nickel foam substrates. Theoretical and experimental analyses highlight that the flower-like structures of Zn0.5Cu0.5Co2O4, comprising nanowires and nanoribbons, effectively reduced transport barriers and enhanced ion adsorption, thereby improving electron/ion reaction kinetics. Oxygen vacancies induced defect states in Zn0.5Cu0.5Co2O4, shifting the d- and p-band center values closer to the Fermi level and enhancing electrochemical performance. The Zn0.5Cu0.5Co2O4 exhibits a specific capacity of 271 mA h g-1 (1776 F g-1) at 1 A g-1 with 97% capacity retention after 5000 charge/discharge cycles. In a Zn0.5Cu0.5Co2O4//activated carbon configuration, the device demonstrates superior energy and power densities of 122.2 Wh kg-1 and 800 W kg-1, respectively, maintaining 91% capacitance after 10000 cycles at 30 A g-1 with high coulombic efficiency. This study presents an effective strategy to enhance ion/charge transfer and adsorption in multi-transition metal spinel architectures, advancing the development of supercapacitor electrodes.

A Facile Microwave-Promoted Formation of Highly Photoresponsive Au-Decorated TiO2 Nanorods for the Enhanced Photo-Degradation of Methylene Blue

The integration of noble metal nanoparticles (NPs) effectively modifies the electronic properties of semiconductor photocatalysts, leading to improved charge separation and enhanced photocatalytic performance. TiO2 nanorods decorated with Au NPs were successfully synthesized using a cost-effective, rapid microwave-assisted method in H2O2 and HF media for methylene blue (MB) degradation under visible light illumination. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 physisorption, and UV–vis spectroscopy were employed to characterize the structures, morphologies, compositions, and photoelectronic properties of the as-synthesized materials. The fusing of Au NPs effectively alters the electronic structure of TiO2, enhancing the charge separation efficiency and improved electrical conductivity. The HF treatment promotes the exposure of the highly reactive (001) and (101) crystalline facets. The improved photocatalytic activity of Au/TiO2, achieving 97% efficiency, is attributed to the surface plasmon resonance (SPR) effect of the Au NPs and the presence of oxygen vacancies. The photodegradation of MB using the TiO2/Au photocatalysts follows pseudo-first-order kinetics, highlighting the enhanced catalytic efficiency of the synthesized nanostructures. The exceptional properties of the binary Au/TiO2 photocatalysts, including the SPR effect, exposed crystallographic faces, and efficient charge carrier separation through a decrease in the recombination of electrons and holes, contribute to the photocatalytic degradation of MB.

Bio‐Realistic Synaptic‐Replicated “V” Type Oxygen Vacancy Memristor

AbstractThe development of an artificial synaptic device is essential for the construction of a brain‐like neuromorphic computing architecture. In this study, the goal is to create a multi‐layer HfOx memristor with a “V” type oxygen vacancy (Vo) distribution to mimic the function of calcium ions (Ca2+) during synaptic information transmission. By adjusting voltage and compliance current (Icc), the HfOx memristor can open or close different levels of volt‐controlled Ca2+ channels, thus enabling the replication of synaptic structure, neurotransmitter release/acceptor, and information transmission. A mathematical model is adopted to describe the behavior of volt‐controlled Ca2+ channels, which demonstrates that the device exhibits consistent characteristics with biological synapses. The device forms an “hourglass” conductive filament (CF) within its middle functional layer, allowing for precise control over filament formation and positioning. This results in ultra‐low power consumption for erasing (581 fJ), fast erasing speed (10 ns), and a low resistance difference coefficient of only 1.8%. Furthermore, the device successfully simulates the physical dynamics of Ca2+ during short‐term potentiation (STP) and long‐term potentiation (LTP) in biological synapses while replicating various guided synaptic behaviors. This study provides a straightforward method for memristors to realize bio‐realistic artificial neuromorphic applications.

Exploring the potential of induced dipole-dominated electrorheological effect: advancing ER elastomers

Abstract Prior research has predominantly focused on traditional electrorheological (ER) effects while overlooking the transformative potential of induced dipoles in enhancing the overall performance of ER materials. In this study, we introduced a novel type of ER elastomer called induced dipole-dominated ER elastomer (ID-ERE). Through high-energy ball milling (HEBM) of the filler particles, the oxygen vacancies were produced within the particles that acted as local charge centers. In the presence of an external electric field (E), these oxygen vacancies induced the dipoles with significant dipole moments, thus amplifying the local electric field EL within the particle gaps. The powerful interactions of these dipoles significantly improved the overall performance of elastomer; the phenomenon referred to as the ID-ER effect. The viscoelastic results showed that ID-EREs have high field-induced storage modulus (G’ = 395.7 kPa), a significant increment in storage modulus (ΔG’ = 270.5 kPa) and high relative ER effect (ΔG’/G0 = 217.2%) at 3 kV mm−1. Additionally, after testing ID-EREs viscoelastic properties, it was discovered that excessive powder content leads to a decline in the elastomer’s performance. The results showed that ID-ERE’s viscoelastic, mechanical, dielectric, and overall efficiency is finer than the control ER elastomer (C-ERE) having unmilled TiO2 particles. Besides, the preparation method is straightforward, easily replicated, scalable, and cost effective. Thus, these ID-EREs should be a new generation of elastomer with the potential to be used in various automotive, robotics, construction, and electroactive actuators industries.

Oxygen Defect Site Filling Strategy Induced Moderate Enrichment of Reactants for Efficient Electrocatalytic Biomass Upgrading.

The electrocatalytic oxidation of 5-hydroxymethylfurfural (HMF) provides a feasible approach for the efficient utilization of biomass. Defect regulation is an effective strategy in the field of biomass upgrading to enhance the adsorption capacity of reactants and thus increase the activity. However, how to select appropriate strategies to regulate the over-enrichment of reactants induced by excessive oxygen vacancy is still a huge challenge. In this work, the defect-filling strategy to design and construct an element-filled oxygen vacancy site layered double hydroxide (S─Ov─LDH) is adopted, which achieves a significant reduction in the electrolysis potential of biomass platform molecule HMF oxidation reaction and a significant increase in current density. Physical characterizations, electrochemical measurements, and theoretical calculations prove that the formation of metal─S bond in the second shell effectively regulates the electronic structure of the material, thus weakening the over-strong adsorption of HMF and OH- induced by excessive oxygen vacancy, promoting the formation of high-valence Co3+ during the reaction, and forming new adsorption sites. This work discusses the catalytic enhancement mechanism of defect filling in detail, fills the gap of defect filling in the field of biomass upgrading, and provides favorable guidance for the further development of defect regulation strategies.

The Activation of Oxygen Species on the Pt/CeO2 Catalyst by H2 for NO Oxidation

The Pt/CeO2 catalyst has attracted significant attention due to its exceptional performance in NO oxidation. This study comprehensively examines the effects of calcination temperature and H2 pretreatment on the structure and activity of the Pt/CeO2 catalyst. Experimental findings indicate that the calcination temperature significantly affects the catalyst’s redox performance, thereby modulating its efficacy in NO oxidation reactions. H2 pretreatment facilitates the creation of oxygen vacancies on the catalyst, assisted by the reduction in PtOx to Pt, enhancing the formation of activated oxygen and thereby improving NO oxidation. This study offers valuable insights into the design and optimization of Pt/CeO2 catalysts for environmental applications, particularly in the development of exhaust gas after-treatment technologies.

Stable Long-Persistent Luminescence from Self-Activated CaSb2O6 Induced by Intrinsic Defects.

Long-persistent luminescence (LPL) materials have attracted intensive attention due to their fascinating emission after excitation. However, current LPL materials typically depend on external doping to introduce traps or emitting centers, resulting in a complex synthesis and controllability. For the first time, we develop another category of undoped LPL materials based on antimonate CaSb2O6, which exhibits blue LPL for over 8000 s. Both experimental and theoretical evidence indicate that excitons are trapped by intrinsic oxygen vacancies. Then, they are detrapped and recombine through singlet and triplet emission of Sb3+ to form LPL. Moreover, CaSb2O6 maintains approximately 100% of its initial LPL performance and structural integrity even after being treated under 1000 °C, UV irradiation, and extreme conditions (pH = 1 or 13). This study highlights the significant potential of antimonates as robust and versatile luminescent materials.

Effects of Charge Imbalance on Field‐Induced Instability of HfO2‐Based Ferroelectric Tunnel Junctions

AbstractFerroelectricity in hafnium‐based materials has attracted significant research attention and is used in various applications owing to their complementary metal‐oxide‐semiconductor compatibility, scalability, and low‐power operation. However, their widespread integration into various technologies is hindered by reliability and stability problems, particularly field‐induced instability, which causes fluctuations in polarization characteristics during operation. Herein, on the underlying mechanism of field‐induced instability is reported in pure hafnium oxide films within metal‐ferroelectric‐insulator‐semiconductor (MFIS) ferroelectric tunnel junctions (FTJs). The comprehensive material analysis combined with low‐frequency noise (LFN) measurements reveals that the presence of oxygen vacancies and interface traps within the ferroelectric and dielectric layers induces a charge imbalance in the FTJ, leading to distortion in its polarization characteristics and the onset of cyclic evolution in field‐induced instability. Furthermore, high‐pressure annealing effectively mitigates field‐induced instability by reducing the defects within the film, thereby alleviating the associated charge imbalance. These findings contribute to a deeper understanding of the internal dynamics of FTJs and provide an efficient approach to enhancing their stability.

Sustainable photocatalytic hydrogen peroxide production over octonary high-entropy oxide

The direct utilization of solar energy for the artificial photosynthesis of hydrogen peroxide (H2O2) provides a reliable approach for producing this high-value green oxidant. Here we report on the utility of high-entropy oxide (HEO) semiconductor as an all-in-one photocatalyst for visible light-driven H2O2 production directly from H2O and atmospheric O2 without the need of any additional cocatalysts or sacrificial agents. This high-entropy photocatalyst contains eight earth-abundant metal elements (Ti/V/Cr/Nb/Mo/W/Al/Cu) homogeneously arranged within a single rutile phase, and the intrinsic chemical complexity along with the presence of a high density of oxygen vacancies endow high-entropy photocatalyst with distinct broadband light harvesting capability. An efficient H2O2 production rate with an apparent quantum yield of 38.8% at 550 nm can be achieved. The high-entropy photocatalyst can be readily assembled into floating artificial leaves for sustained on-site production of H2O2 from open water resources under natural sunlight irradiation.

Oxygen Vacancy-Electron Polarons Featured InSnRuO2 Oxides: Orderly and Concerted In-Ov-Ru-O-Sn Substructures for Acidic Water Oxidation.

Polymetallic oxides with extraordinary electrons/geometry structure ensembles, trimmed electron bands, and way-out coordination environments, built by an isomorphic substitution strategy, may create unique contributing to concertedly catalyze water oxidation, which is of great significance for proton exchange membrane water electrolysis (PEMWE). Herein, well-defined rutile InSnRuO2 oxides with density-controllable oxygen vacancy (Ov)-free electron polarons are firstly fabricated by in situ isomorphic substitution, using trivalent In species as Ov generators and the adjacent metal ions as electron donors to form orderly and concerted In-Ov-Ru-O-Sn substructures in the tetravalent oxides. For acidic water oxidation, the obtained InSnRuO2 displays an ultralow overpotential of 183 mV (versus RHE) and a mass activity (MA) of 103.02 A mgRu -1, respectively. For a long-term stability test of PEMWE, it can run at a low and unchangeable cell potential (1.56 V) for 200 h at 50 mA cm-2, far exceeding current IrO2||Pt/C assembly in 0.5 m H2SO4. Accelerated degradation testing results of PEMWE with pure water as the electrolyte show no significant increase in voltage even when the voltage is gradually increased from 1 to 5 A cm-2. The remarkably improved performance is associated with the concerted In-Ov-Ru-O-Sn substructures stabilized by the dense Ov-electron polarons, which synergistically activates band structure of oxygen species and adjacent Ru sites and then boosting the oxygen evolution kinetics. More importantly, the self-trapped Ov-electron polaron induces a decrease in the entropy and enthalpy, and efficiently hinder Ru atoms leaching by increasing the lattice atom diffusion energy barrier, achieves long-term stability of the oxide. This work may open a door to design next-generation Ru-based catalysts with polarons to create orderly and asymmetric substructures as active sites for efficient electrocatalysis in PEMWE application.

Mechanisms of Thermal Decomposition in Spent NCM Lithium-Ion Battery Cathode Materials with Carbon Defects and Oxygen Vacancies.

Resource recovery from retired electric vehicle lithium-ion batteries (LIBs) is a key to sustainable supply of technology-critical metals. However, the mainstream pyrometallurgical recycling approach requires high temperature and high energy consumption. Our study proposes a novel mechanochemical processing combined with hydrogen (H2) reduction strategy to accelerate the breakdown of ternary nickel cobalt manganese oxide (NCM) cathode materials at a significantly lower temperature (450 °C). Particle refinement, material amorphization, and internal energy storage are considered critical success factors for the accelerated decomposition of NCM cathode materials. In our proposed approach, NCM cathode materials can develop active sites with carbon defects (Cv) and oxygen vacancies (Ov), which improve the reduction and breakdown of H2. The adsorbed H2 on the surface of NCM decomposes into H* and combines with oxygen to form OH species, which can be facilitated by Ov via the enhanced charge transfer. The introduced Cv can enhance H2 cracking and generate *C-H species to promote the thermal decomposition of NCM. The presence of defects proves to foster the preferential reduction of Mn(IV) by H2, leading to a lower activation energy for the NCM decomposition (from 139 to 110 kJ/mol) with less H2 consumption. Life cycle assessment suggests a reduction of 4.42 kg CO2 eq for the recycling of every 1.0 kg of retired batteries. This study can promote material circularity and minimize the environmental burden of mining technology-critical metals for a low-carbon transition.

Enhanced photocatalytic performance of TiO2 with tunable oxygen vacancies induced by H2/N2 mixture treatment

Surface treatment can effectively modulate the surface properties of a photocatalyst to hasten the separation and transfer of photoinduced charges, ultimately achieving high photocatalytic performance. Herein, surface treatment of anatase-phase TiO2 prepared by a hydrothermal method was performed under H2/N2 mixed atmosphere. The experimental results demonstrate that roasting TiO2 in a H2/N2 atmosphere can effectively reduce partial Ti4+ to Ti3+, thereby facilitating the production of tunable oxygen vacancies (OVs) by disrupting Ti-O-Ti bonds. OVs can construct defective energy levels to bring about a decrease in the bandgap of TiO2 and an extension of light absorption range. Moreover, OVs remarkedly improve the separation of photoinduced charges of TiO2 and accelerate the photocatalytic reaction as active sites. The photocatalytic experimental results demonstrate that TiO2 exhibits the highest performance when roasting TiO2 in a H2/N2 atmosphere for 2 h, and the photocatalytic degradation rate constant of rhodamine B (RhB) and tetracycline (TC) on this sample under simulated solar light irradiation is 2.24 and 1.11 times higher than that on the reference TiO2, respectively. These findings provide valuable insights for designing highly efficient photocatalysts for effective water pollution treatment.

Porous and defective NiCo2O4 spinel derived from bimetallic NiCo-based Prussian blue analogue for enhanced hydrogen production via the urea electro-oxidation reaction

The efficient hydrogen production via overall water splitting is seriously restrained by the slow kinetics of the oxygen evolution reaction (OER). The substantially low potential for the urea electro-oxidation reaction (UOR) can tackle this problem by replacing the OER at the electrolyzer anode. Herein, the NiCo2O4 spinel with rich oxygen vacancies (Ov) and embedded within mesoporous carbon network (Ov-NiCo2O4@mC) was derived from NiCo-based Prussian blue analogous (NiCo PBA) and exploited as the bifunctional electrocatalyst of the UOR and OER for boost the hydrogen production via the overall water splitting. Benefiting to the regular skeleton and abundant dual metal sites of NiCo PBA, the derived Ov-NiCo2O4@mC comprises abundant oxygen vacancies, lattice defects, and adjustable electron structure. These features afford Ov-NiCo2O4@mC the improved UOR ability, showing the potential of 1.33 V versus reversible hydrogen electrode (RHE) at the current density of 10 mA cm−2, along with a small Tafel slopes of 31 mV dec-1, remarkably lower than that of the OER (1.51 V versus RHE, Tafel slope = 85 mV dec-1). The UOR performance of Ov-NiCo2O4@mC substantially outperforms to most of the reported Co and/or Ni-based electrocatalysts. Impressively, the assembled two-electrode urea-assisted overall water splitting device shows the small voltage for the hydrogen production (1.43 V versus RHE) and good long-term stability. The present work can provide a new alternative for the efficient hydrogen production using the MOFs-derivatives.

Direct colour printing on zirconia using 222nm UV-C photons.

To proof the feasibility of direct colour printing on 3Y-TZP using 222nm UV-C through investigating the degree and durability of the colour changes, and testifying whether surface, mechanical and biological properties are influenced by the treatment. 222nm UV-C light (Irradiance: 1.870mW/cm2) was used to treat 3Y-TZP for durations from 15min to 24h. ΔE*, TP, crystalline structure, surface morphology, Sa, BFS and biological activities were investigated before and after irradiation. SPSS 28.0 was used for statistical analysis (α=0.05). 222nm UV-C irradiation was capable to shade white 3Y-TZP into tooth colours. With the increase of ΔE*, TP decreased, such that the longer the irradiation time, the higher the ΔE*(logarithmic relationship) and lower the TP. Despite the induced optical changes being prone to fade, the process can be predicted by inversely proportional relationships between ΔE*, TP and the testing points. The treated surface exhibited enhanced hydrophilicity, while the recovery phenomenon was observed. Other properties were not altered by the treatment. This is the seminal study demonstrating the feasibility of direct colour printing on 3Y-TZP using 222nm UV-C. The new relationship between the colour centre and Eg of 3Y-TZP was established, whereas the induced optical changes were stabilised after a certain period and were highly predictable by controlling the irradiation periods. The irradiation was only correlated to the electron excitation and oxygen vacancies, and would not lead to any changes of other properties. A simple, safe and promising approach to achieve satisfactory colours on 3Y-TZP in clinical practice can be developed.

Molecular mechanisms of iron nanominerals formation in fungal extracellular polymeric substances (EPS) layers during fungus-mineral interactions.

Extracellular polymeric substances (EPS), which envelop on fungal hyphae surface, interact strongly with minerals and play a crucial role in the formation of nanoscale minerals during biomineralization in nature environments. However, it remains poorly understood about the molecular mechanisms of nanominerals (i.e., iron nanominerals) formation in fungal EPS halos during fungus-mineral interactions. This process is vital because fungi typically grow attached to various mineral surfaces in nature. According to the changes of thickness of the fungal cell and EPS layers during the Trichoderma guizhouense NJAU 4742 and hematite cultivation experiments in this study, we found that fungal biomineralization could trigger the formation of EPS layers. Fe-dominated nanominerals, aromatic C (283-286.1 eV), alkyl C (287.6-288.3 eV), and carboxylic C (288.4-289.1 eV) were the dominant chemical groups on the EPS layers, as determined by nanoscale secondary ion mass spectrometry (NanoSIMS), high-resolution transmission electron microscope (HRTEM), and carbon 1s near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. Further, evidence from Fe K-edge X-ray absorption near-edge structure (XANES) and X-ray photoelectron spectroscopy (XPS) spectra indicated that oxygen vacancy (OV) was formed on the Fe-dominated nanomineral surface during fungus-mineral interactions, which played an important role in catalyzing H2O2 decomposition and HO* production. Taken together, the intrinsic peroxidase-like activity by reactive oxygen species (ROS) could modulate the Fe-dominated nanominerals formation in EPS layers to newly form a physical barrier between the cell and the external environments around hyphae, providing novel insights into the effects of ROS-mediated fungal-mineral interactions on fungal nutrient recycling, attenuation of contaminants, and biological control in nature environments.

Insights into the oxygen vacancies in titanium-aluminum composite oxides for Ru-catalyzed bio-oil upgrading using guaiacol as a model compound

Insights into the oxygen vacancies in titanium-aluminum composite oxides for Ru-catalyzed bio-oil upgrading using guaiacol as a model compound