Well-dispersed Pt/Nb2O5on zeolitic imidazolate framework derived nitrogen-doped carbon for efficient oxygen reduction reaction.

In this work, an advanced hybrid material was constructed by incorporating niobium pentoxide (Nb2O5) nanocrystals with nitrogen-doped carbon (NC) derived from ZIF-8 dodecahedrons, serving as a support, referred to as Nb2O5/NC. Pt nanocrystals were dispersed onto Nb2O5/NC using a simple impregnation reduction method. The obtained Pt/Nb2O5/NC electrocatalyst showed high oxygen reduction reaction (ORR) activity due to three-phase mutual contacting structure with well-dispersed Pt and Nb2O5NPs. In addition, the conductive NC benefits electron transfer, while the induced Nb2O5can regulate the electronic structure of Pt element and anchor Pt nanocrystals, thereby enhancing the ORR activity and stability. The half-wave potential (E1/2) for Pt/Nb2O5/NC is 0.886 V, which is higher than that of Pt/NC (E1/2= 0.826 V). The stability examinations demonstrated that Pt/Nb2O5/NC exhibited higher electrocatalytic durability than Pt/NC. Our work provides a new direction for synthesis and structural design of precious metal/oxides hybrid electrocatalysts.

Synthesis of freestanding binder- and additive-free carbon nanofiber with graphene-wrapped Nb2O5composite anode for lithium-ion batteries.

Niobium pentoxide (Nb2O5)-based materials have attracted significant interest for application in diverse fields. Unfortunately, the employment of these materials as electrodes of lithium-ion batteries (LIBs) is limited by several inherent drawbacks. The present study demonstrated the synthesis of composites comprising homogeneous graphene-wrapped niobium pentoxide (GNbO) encapsulated in carbon nanofibers (CNFs) for utilization as binder- and additive-free anodes in LIBs. The composites were synthesized via electrospinning and subsequent carbonization; the presence of graphene (G) ensured the homogenous dispersion of the Nb2O5particles in the CNF matrix. The CNFs formed a highly conductive network that resulted in high physical flexibility, electrical conductivity, and structural stability during charge-discharge cycles, thereby facilitating rapid ion/electron transmission. Consequently, the CNF/GNbO composite anodes exhibited outstanding electrochemical performances. CNF/GNbO_5 (one of the synthesized composites with an Nb2O5concentration of 5 wt% relative to GO) delivered a specific capacity of 361 mAh g-1after 100 cycles, corresponding to a capacity retention of 58.3%. In addition, it exhibited an excellent rate capability with a capacity of 317 mAh g-1at 10 C. The outcomes of the present study will facilitate the extensive application of the synthesized composites as high-performance anodes in next-generation LIBs.

Hybrid Aqueous/Nonaqueous Water-in-Bisalt Electrolyte Enables Safe Dual Ion Batteries.

Dual ion batteries (DIBs) have recently attracted ever-increasing attention owing to the potential advantages of low material cost and good environmental friendliness. However, the potential safety hazards, cost, and environmental concerns mainly resulted from the commonly used nonaqueous organic solvents severely hinder the practical application of DIBs. Herein, a hybrid aqueous/nonaqueous water-in-bisalt electrolyte with both broad electrochemical stability window and excellent safety performance is developed. The lithium-based DIB assembled using KS6 graphite and niobium pentoxide as the active materials in the cathode and anode exhibits good comprehensive performance including capacity, cycling stability, rate performance, and medium discharge voltage. Initial capacities of ≈47.6 and 29.6 mAh g-1 retention after 300 cycles can be delivered with a medium discharge voltage of around 2.2 V in the voltage window of 0-3.2 V at the current density of 200 mA g-1 . Good rate performance for the battery can be indicated by 29.7 mAh g-1 discharge capacity retention at 400 mA g-1 . It is noteworthy that the coulombic efficiency of the battery can reach as high as 93.9%, which is comparable to that of the corresponding DIBs using nonaqueous organic electrolytes.

Porous Nb2O5 Formed by Anodic Oxidation as the Sulfur Host for Enhanced Performance Lithium-Sulfur Batteries.

Lithium-sulfur batteries (LSBs), with their high theoretical specific capacity and energy density, have great potential to be a candidate for secondary batteries in the future. However, Li-S batteries suffer from multiple issues and challenges, for example, uneven growth of lithium dendrites, low utilization of the active material (sulfur), and low specific capacity. This paper reports a low-cost and anodic oxidation method to produce niobium pentoxide with a porous structure (P-Nb2O5). A simple one-step process was used to synthesize P-Nb2O5 with porous structures by anodizing niobium at 40 V in fluorinated glycerol. The porous Nb2O5 showed excellent rate capability and good capacity retention by maintaining its structural integrity, allowing us to determine the advantages of its porous structure. As a result of the highly porous structure, the sulfur was not only provided with adequate storage space and abundant adsorption points, but it was also utilized more effectively. The initial discharge capacity with the P-Nb2O5 cathode rose to 1106.8 mAh·g-1 and dropped to 810.7 mAh·g-1 after 100 cycles, which demonstrated the good cycling performance of the battery. This work demonstrated that the P-Nb2O5 prepared by the oxidation method has strong adsorption properties and good chemical affinity.

Competitive Redox Chemistries in Vanadium Niobium Oxide for Ultrafast and Durable Lithium Storage.

Niobium pentoxide (Nb2O5) anodes have gained increasing attentions for high-power lithium-ion batteries owing to the outstanding rate capability and high safety. However, Nb2O5 anode suffers poor cycle stability even after modified and the unrevealed mechanisms have restricted the practical applications. Herein, the over-reduction of Nb5+ has been demonstrated to be the critical reason for the capacity loss for the first time. Besides, an effective competitive redox strategy has been developed to solve the rapid capacity decay of Nb2O5, which can be achieved by the incorporation of vanadium to form a new rutile VNbO4 anode. The highly reversible V3+/V2+ redox couple in VNbO4 can effectively inhibit the over-reduction of Nb5+. Besides, the electron migration from V3+ to Nb5+ can greatly increase the intrinsic electronic conductivity for VNbO4. As a result, VNbO4 anode delivers a high capacity of 206.1 mAh g-1 at 0.1 A g-1, as well as remarkable cycle performance with a retention of 93.4% after 2000 cycles at 1.0 A g-1. In addition, the assembled lithium-ion capacitor demonstrates a high energy density of 44 Wh kg-1 at 5.8 kW kg-1. In summary, our work provides a new insight into the design of ultra-fast and durable anodes.

Superior functionality of niobium pentoxide nano-rod/tripod photocatalyst synthesized using polyethyleneimine as a soft template for the abatement of methylene blue under UV and visible irradiation.

Polyethyleneimine (PEI) capping agent-cum-template-mediated synthesis of niobium oxide nanoparticles is reported to explore its impact on the resultant morphology, porosity, crystallinity, phase complexation, and thus on the photocatalytic activity. The resultant niobium oxides calcined at 800°C and 1000°C crystallized into highly ordered nano-rod/tripod nanostructure with inter-rod angle <120° having orthorhombic phase and heavily agglomerated rod-like nanostructures having monoclinic crystal phase, respectively. Contrary to the expectations, the nano-rod/tripods showed superior photocatalytic degradation kinetics and high adsorption of methylene blue dye in the hydrocolloid than formerly reported monoclinic nanoparticles. The best adsorption capability and photocatalytic activity are observed for the sample calcined at 800°C, resulting in a combined degradation efficiency of 98.8% of methylene blue dye. The adsorption characteristics, stability of the hydrocolloid system, the existence of oxygen vacancies, and the distinct morphology of the photocatalytic nano-rod/tripods are mainly responsible for this behavior. The process and the performance of unique nanostructure over others presents a superior alternative.

Calcium hydroxide and niobium pentoxide treatment effects before MTA placement.

The aim of this study was to evaluate the effect of calcium hydroxide (CH) and niobium pentoxide (NP) pretreatment on pH, dentin microhardness and sealing of Mineral Trioxide Aggregate (MTA; Angelus). The pH of CH, NP and CH-NP (3:1) was evaluated in neutral and acidic simulated tissue fluid over 28 days. The Vickers microhardness was measured in forty 4 mm coronal root slices filled with pretreatment materials stored in medium for 1, 7, 28 days. Forty 10 mm roots were packed with pretreatment materials, irrigated after 24 h, then a 3 mm MTA plug was placed. Sealing ability was evaluated after 7 days using fluid filtration method. Statistics was performed using ANOVA and post hoc Tukey HSD tests. Addition of NP to CH maintained the alkalinity of CH, increased the microhardness of root dentin and reduced the microleakage. CH-NP can be effectively used as a pretreatment medicament in root canals requiring placement of MTA under acidic conditions.

Wear behaviour of titanium based composites reinforced with niobium pentoxide in saline and acidic environments.

The present study reports on the wet wear behaviour of spark plasma sintered commercial pure titanium (Cp Ti) and Ti-based composites containing 5, 10, and 15 wt% Nb2O5 in acidic and saline environments. The wear properties in wet (3.5 wt% NaCl and 0.3 M H2SO4 solutions) environments were assessed using a tribometer. The wear volumes and wear rates, irrespective of the environment, decreased with an increase in the Nb2O5 wt.%, which was linked to the harder Nb2O5 particles. Furthermore, the wear rate was relatively higher in the acidic environment than in the saline environment. This was connected to the higher chemical attack likely in the acidic environment due to the aggressive nature of the SO4 - ions compared to the less aggressive 3.5 wt% NaCl solution. Abrasive wear prevalence, combined with chemical attack-induced particle scratch-off and subdued adhesive wearing, were mechanisms acknowledged to be operational for wet environments.

Enhanced Photocatalytic Activity of Nonuniformly Nitrogen-Doped Nb2O5 by Prolonging the Lifetime of Photogenerated Holes.

The narrow band gap and significant separation of photogenerated carriers are essential aspects in practical photocatalytic applications. Nitrogen doping usually narrows the band gap of semiconductor oxides, and it enhances photocatalytic activity. Nitrogen-doped Nb2O5 was prepared by a multiple hydrothermal method. The non-metal element N inside the nanostructure, working as the trapping sites for the holes, which were effectively incorporated into the crystal lattice of Nb2O5 semiconductor oxide, remarkably shorten the band gap (3.1 eV) to enhance the visible light response, effectively reducing the photoinduced electron-hole pair recombination and prolonging carrier lifetime. The multilayer coating structure with a gradient concentration distribution and the type of nitrogen doped is favorable for the migration of photoexcited carriers in the bulk of catalysts. The unique multi-layer coating with the micro-concentration gradient of doped nitrogen provides a fast separation channel and jump steps for the separation of electron-hole pairs.

On the Sintering Behavior of Nb2O5 and Ta2O5 Mixed Oxide Powders.

A mixed oxide system consisting of Nb2O5 and Ta2O5, was subjected to annealing in air/hydrogen up to 950 °C for 1-4 h to study its sintering behavior. The thermogravimetric-differential scanning calorimetry (TGA-DSC) thermograms indicated the formation of multiple endothermic peaks at temperatures higher than 925 °C. Subsequently, a 30% Ta2O5 and 70% Nb2O5 (mol%) pellet resulted in good sintering behavior at both 900 and 950 °C. The scanning electron microscope (SEM) images corroborated these observations with necking and particle coarsening. The sintered pellets contained a 20.4 and 20.8% mixed oxide (Nb4Ta2O15) phase, along with Ta2O5 and Nb2O5, at both 900 and 950 °C, indicating the possibility of the formation of a solid solution phase. In situ high-temperature X-ray diffraction (XRD) scans also confirmed the formation of the ternary oxide phase at 6 and 19.8% at 890 and 950 °C, respectively. The Hume-Rothery rules could explain the good sintering behavior of the Ta2O5 and Nb2O5 mixed oxides. An oxide composition of 30% Ta2O5 and 70% Nb2O5 (mol%) and a sintering temperature of 950 °C appeared adequate for fabricating well-sintered oxide precursors for subsequent electrochemical polarization studies in fused salts.

Unraveling the Origin of Enhanced Activity of the Nb2O5/H2O2 System in the Elimination of Ciprofloxacin: Insights into the Role of Reactive Oxygen Species in Interface Processes.

The overlooked role of reactive oxygen species (ROS), formed and stabilized on the surface of Nb2O5 after H2O2 treatment, was investigated in the adsorption and degradation of ciprofloxacin (CIP), a model antibiotic. The contribution of ROS to the elimination of CIP was assessed by using different niobia-based materials in which ROS were formed in situ or ex situ. The formation of ROS was confirmed by electron paramagnetic resonance (EPR) and Raman spectroscopy. The modification of the niobia surface charge by ROS was monitored with zeta potential measurements. The kinetics of CIP removal was followed by UV-vis spectroscopy, while identification of CIP degradation products and evaluation of their cytotoxicity were obtained with liquid chromatography-mass spectrometry (LC-MS) and microbiological studies, respectively. Superoxo and peroxo species were found to significantly improve the efficiency of CIP adsorption on Nb2O5 by modifying its surface charge. At the same time, it was found that improved removal of CIP in the dark and in the presence of H2O2 was mainly determined by the adsorption process. The enhanced adsorption was confirmed by infrared spectroscopy (IR), total organic carbon measurements (TOC), and elemental analysis. Efficient chemical degradation of adsorbed CIP was observed upon exposure of the Nb2O5/H2O2 system to UV light. Therefore, niobia is a promising inorganic adsorbent that exhibits enhanced sorption capacity toward CIP in the presence of H2O2 under dark conditions and can be easily regenerated in an environmentally benign way by irradiation with UV light.

Fast, Sensitive, and Highly Selective Room-Temperature Hydrogen Sensing of Defect-Rich Orthorhombic Nb2O5-x Nanobelts with an Abnormal p-Type Sensor Response.

The research and development of low-power-consumption and room-temperature hydrogen sensors are of great significance for the safe application of hydrogen energy. Herein, orthorhombic Nb2O5-x nanobelts are prepared through a combined procedure of hydrothermal, ion exchange, and annealing treatment in Ar. The topological transformation process results in the formation of abundant surface defects including chemical defects such as Nb4+, oxygen vacancies, and disordered microregions, which lead to the abnormal p-type conducting and hydrogen sensing behavior. Moreover, the orthorhombic Nb2O5-x nanobelts exhibit fast and sensitive room-temperature hydrogen sensing performance, which shows greater advancement than the monoclinic, tetragonal, and hexagonal Nb2O5 one-dimensional (1D) nanostructures. The response time and lowest limit of detection of the as-fabricated room-temperature sensor decrease to 28 s and 3.5 ppm, respectively. The sensor also exhibits a highly selective hydrogen response against CO, CH4, ethanol, H2S, and NH3. The hydrogen response of the Nb2O5-x nanobelts can be attributed to the redox reaction between hydrogen and preadsorbed oxygens. The defective surface structure and the prolonged dimension of the nanobelts give rise to the highly reactive surface and the suppression of the negative nanojunction effect, which greatly improves the sensing performance. The orthorhombic lattice structure can also promote gas adsorption and diffusion behavior due to its specific catalytic and pathway effect. The results of this work can be helpful for the rational design and defect engineering of the Nb2O5-based 1D nanostructures for room-temperature hydrogen sensing applications.

Investigation of phase transition employing strain mapping in TT- and T-Nb2O5 obtained by HRTEM micrographs.

This work aimed to study the crystalline structure of TT-,T-phases of Nb2O5 nanoparticles through XRD, Rietveld refinement, and HRTEM, using geometric phase analysis (GPA). The results show the presence of distorted NbO6 and NbO7 polyhedral, producing strain effects, mainly in the plane boundaries and along the b-c plane. XRD and HRTEM analyses show the TT→T transition at 700 °C, with increased particle size and increased strain in the boundaries between nanoparticles. The sample calcinated at 700 °C presents segregation of the TT-(001), (100), and T-(130) planes, where the strain effect is more relevant along the [100] zone axis and between phases.

Nb2O5 nanoparticles decorated with magnetic ferrites for wastewater photocatalytic remediation.

Nanotechnology has been studied on environmental remediation processes to foster greater photocatalysts efficiency and reuse in wastewater. This study investigated the photocatalytic efficiency and viability of niobium pentoxide (Nb2O5) nanoparticles decorated with magnetic ferrite (cobalt ferrite (CoFe2O4) or magnesium ferrite (MgFe2O4)) for atrazine photodegradation. Thus, the decorated Nb2O5 was synthesized by the polymeric precursor method, forming nanoparticles with sizes ranging from 25 to 50 nm. Nanocomposite elementary analyses showed a homogeneous distribution of elements on all particles surface. Efficient magnetic saturation was observed for pure CoFe2O4 (53 emu g-1) and MgFe2O4 (19 emu g-1) nanoparticles, promoting the magnetic removal of Nb2O5:CoFe2O4 and Nb2O5:MgFe2O4 nanocomposites. Photocatalytic assays showed 88% efficiency for atrazine photodegradation with all nanomaterials, which represented a 21% increase compared to photolysis in the 1st cycle. The magnetic nanocomposites when applied to a 5th cycle maintained the atrazine photodegradation activity. In this way, magnetic Nb2O5-based nanocomposites decorated with ferrite nanoparticles showed an efficient photocatalytic response, in addition to posterior magnetic removal from the aqueous medium. Therefore, the evaluated magnetic Nb2O5 nanocomposites may be an alternative to enhance the wastewater removal process and foster the reuse in advanced oxidative processes.

Photocatalytic degradation of real textile wastewater using carbon black-Nb2O5 composite catalyst under UV/Vis irradiation.

This work investigated the impregnation of Nb2O5 into carbon black (CB) in different ratios and its effect in photocatalytic degradation of real wastewater from a dyeing factory by advanced oxidative processes (AOP). Synthesized catalysts were characterized regarding their crystalline structure (DRX, micro-Raman), morphology (MEV), textural (BET area) and optical properties (bandgap energy by diffuse reflectance) and pH at the point of zero charge (pHpzc). Preliminary tests showed better photodegradation results in the acidic medium after 5 h of irradiation with NCB-0.5 (Nb2O5:CB 0.5:1). Treatment parameters optimization was carried out using response surface methodology based on Box-Behnken experimental design. Catalyst concentration, solution pH and irradiation time were varied, analysing absorbance reduction (285 and 574 nm), COD and TOC removal after treatment as responses. The composite catalyst showed improved photocatalytic activity, attributed to an increase in adsorption capacity and the bandgap narrowing, redshifting the absorption edge wavelength to the visible region, brought by CB impregnation. Optimal conditions were found at 0.250 g L-1 of catalyst, pH 2.0 and 5 h of irradiation, removing 72.19% and 93.52% of absorbance in 285 and 574 nm, respectively, 51.29% of COD and 70.70% of TOC using NCB-0.5.

Three-Dimensional Cross-Linked Nb2O5 Polymorphs Derived from Cellulose Substances: Insights into the Mechanisms of Lithium Storage.

Niobium pentoxide (Nb2O5)-based materials have been regarded as promising anodic materials for lithium-ion batteries due to their abundant crystalline phases and stable and safe lithium storage performances. However, there is a lack of systematic studies of the relationship among the crystal structures, electrochemical characteristics, and lithium storage mechanisms for the various Nb2O5 polymorphs. Herein, pure pseudohexagonal Nb2O5 (TT-Nb2O5), orthorhombic Nb2O5 (T-Nb2O5), tetragonal Nb2O5 (M-Nb2O5), and monoclinic Nb2O5 (H-Nb2O5) with three-dimensional interconnected structures are reported, which were synthesized via a hydrothermal method using the commercial filter paper as the structural template followed by specific annealing processes. Impressively, the TT- and T-Nb2O5 species both possess bronze-like phases with "room and pillar" structures, while M- and H-Nb2O5 ones are both in the Wadsley-Roth phases with crystallographic shear structures. Among the pristine Nb2O5 materials, H-Nb2O5 exhibits the highest initial specific capacity (270 mA h g-1), while T-Nb2O5 performs with the lowest (197 mA h g-1) at 0.02 A g-1, meaning that crystallographic shear structures provide more lithium storage sites. TT-Nb2O5 realizes the best rate capability (207 mA h g-1 at 0.02 A g-1 and 103 mA h g-1 at 4.0 A g-1), indicating that the "room and pillar" crystal structures favor fast lithium storage. Electrochemical analyses reveal that the TT- and T-Nb2O5 phases with "room and pillar" crystal structures utilize a pseudocapacitive intercalation mechanism, while the M- and H-Nb2O5 phases with the Wadsley-Roth shear structures follow a typical battery-type intercalation mechanism. A fresh insight into the further understanding of the intercalation pseudocapacitance on the basis of the unit cells of the electrode materials and a meaningful guidance for crystalline structural design/construction of the electrode materials for the next-generation LIBs are thus provided.

Noise Tailoring in Memristive Filaments.

In this study, the possibilities of noise tailoring in filamentary resistive switching memory devices are investigated. To this end, the resistance and frequency scaling of the low-frequency 1/f-type noise properties are studied in representative mainstream material systems. It is shown that the overall noise floor is tailorable by the proper material choice, as demonstrated by the order-of-magnitude smaller noise levels in Ta2O5 and Nb2O5 transition-metal oxide memristors compared to Ag-based devices. Furthermore, the variation of the resistance states allows orders-of-magnitude tuning of the relative noise level in all of these material systems. This behavior is analyzed in the framework of a point-contact noise model highlighting the possibility for the disorder-induced suppression of the noise contribution arising from remote fluctuators. These findings promote the design of multipurpose resistive switching units, which can simultaneously serve as analog-tunable memory elements and tunable noise sources in probabilistic computing machines.

Pseudocapacitive Ti-Doped Niobium Pentoxide Nanoflake Structure Design for a Fast Kinetics Anode toward a High-Performance Mg-Ion-Based Dual-Ion Battery.

Magnesium-ion batteries (MIBs) have received increasing attention for next-generation energy storage recently because of the natural abundance, high capacity, and dendrite-free deposition of Mg. However, their applications are hindered by irreversible Mg anode plating in conventional electrolytes and the lack of cathode materials, demonstrating high working voltage, satisfactory Mg2+ diffusivity, and long cycling life. In this work, we first developed a novel magnesium-ion based dual-ion battery (Mg-DIB) by utilizing expanded graphite as the cathode and Ti-doped niobium pentoxide nanoflakes (Ti-Nb2O5 NFs) as the anode. The Ti-Nb2O5 NFs showed hierarchical structures of microspheres with diameters of 4-5 µm assembled by nanoflakes. For the first time, the Mg-ion storage mechanism in Ti-Nb2O5 NFs was investigated. Benefiting from the hierarchical structure design and pseudocapacitive intercalation behavior of Mg ions, the Ti-Nb2O5 NF anode exhibited fast Mg-ion diffusion. Consequently, the Mg-DIB exhibited a high discharge capacity of 93 mA h g-1 at 1 C (1 C corresponding to 100 mA g-1), along with good long-term cycling performance with a capacity retention of 79% at 3 C after 500 cycles. The Mg-DIB also demonstrated a capacity retention of 77% at 5C, indicating its good rate performance. Moreover, the Mg-DIB exhibited a high discharge medium voltage of ∼1.83 V, thus enabling a high energy density of 174 W h kg-1 at 183 W kg-1 and 122 W h kg-1 at a high power density of 845 W kg-1, among the best of the reported magnesium-ion full batteries. Our work provides a new strategy to improve the performance of MIBs and other rechargeable batteries.

Fabrication of electrospun poly(lactic acid) nanoporous membrane loaded with niobium pentoxide nanoparticles as a potential scaffold for biomaterial applications.

Tissue engineering aims to regenerate and restore damaged human organs and tissues using scaffolds that can mimic the native tissues. The requirement for modern and efficient biomaterials that are capable of accelerating the healing process has been considerably increased. In this work, a novel electrospun poly(lactic acid) (PLA) nanoporous membrane incorporated with niobium pentoxide nanoparticles (Nb2 O5 ) for biomaterial applications was developed. Nb2 O5 nanoparticles were obtained by microwave-assisted hydrothermal synthesis, and different concentrations (0, 1, 3, and 5% wt/wt) were tested. Chemical, morphological, mechanical, and biological properties of membranes were evaluated. Cell viability results demonstrated that the membranes presented nontoxic effects. The incorporation of Nb2 O5 improved cell proliferation without impairing the wettability, porosity, and mechanical properties of membranes. Membranes containing Nb2 O5 nanoparticles presented biocompatible properties with suitable porosity, which facilitated cell attachment and proliferation while allowing diffusion of oxygen and nutrients. This study has demonstrated that Nb2 O5 nanoparticle-loaded electrospun PLA nanoporous membranes are potential candidates for drug delivery and wound dressing applications.

"Water in salt/ionic liquid" electrolyte for 2.8 V aqueous lithium-ion capacitor.

Development of high-voltage electrolytes with non-flammability is significantly important for future energy storage devices. Aqueous electrolytes are inherently non-flammable, easy to handle, and their electrochemical stability windows (ESWs) can be considerably expanded by increasing electrolyte concentrations. However, further breakthroughs of their ESWs encounter bottlenecks because of the limited salt solubility, leading to that most of the high-energy anode materials can hardly function reversibly in aqueous electrolytes. Here, by introducing a non-flammable ionic liquid as co-solvent in a lithium salt/water system, we develop a "water in salt/ionic liquid" (WiSIL) electrolyte with extremely low water content. In such WiSIL electrolyte, commercial niobium pentoxide (Nb2O5) material can operate at a low potential (-1.6 V versus Ag/AgCl) and contribute its full capacity. Consequently, the resultant Nb2O5-based aqueous lithium-ion capacitor is able to operate at a high voltage of 2.8 V along with long cycling stability over 3000 cycles, and displays comparable energy and power performance (51.9 Wh kg-1 at 0.37 kW kg-1 and 16.4 Wh kg-1 at 4.9 kW kg-1) to those using non-aqueous electrolytes but with improved safety performance and manufacturing efficiency.