Superstructured NiMoO4@CoMoO4 core-shell nanofibers for supercapacitors with ultrahigh areal capacitance.

High areal capacitance for a practical supercapacitor electrode requires both large mass loading and high utilization efficiency of electroactive materials, which presents a great challenge. Herein, we demonstrated the unprecedented synthesis of superstructured NiMoO4@CoMoO4 core-shell nanofiber arrays (NFAs) on a Mo-transition-layer-modified nickel foam (NF) current collector as a new material, achieving the synergistic combination of highly conductive CoMoO4 and electrochemical active NiMoO4. Moreover, this superstructured material exhibited a large gravimetric capacitance of 1,282.2 F/g in 2 M KOH with a mass loading of 7.8 mg/cm2, leading to an ultrahigh areal capacitance of 10.0 F/cm2 that is larger than any reported values of CoMoO4 and NiMoO4 electrodes. This work provides a strategic insight for rational design of electrodes with high areal capacitances for supercapacitors.

Biomass-Derived-Carbon-Supported Spinel Cobalt Molybdate as High-Efficiency Electrocatalyst for Oxygen Evolution Reaction.

Ananas comosus leaves were converted to a porous graphitized carbon (GPLC) material via a high-temperature pyrolysis method by employing iron salt as a catalyst. A cobalt molybdate (CoMoO4)-and-GPLC composite (CoMoO4/GPLC) was then prepared by engineering CoMoO4 nanorods in situ, grown on GPLC. N2 adsorption-desorption isothermal curves and a pore size distribution curve verify that the proposed composite possesses a porous structure and a large specific surface area, which are favorable for charge and reactant transport and the rapid escape of O2 bubbles. Consequently, the as-synthesized CoMoO4/GPLC shows low overpotentials of 289 mV and 399 mV to afford the current densities of 10 mA cm-2 and 100 mA cm-2 towards the oxygen evolution reaction (OER), which is superior to many CoMoO4-based catalysts in previous studies. In addition, the decrease in current density is particularly small, with a reduction rate of 3.2% after a continuous OER procedure for 30 h, indicating its good stability. The excellent performance of the CoMoO4/GPLC composite proves that the GPLC carrier can obviously impel the catalytic activity of CoMoO4 by improving electrical conductivity, enhancing mass transport and exposing more active sites of the composite. This work provides an effective strategy for the efficient conversion of waste ananas comosus leaves to a biomass-derived-carbon-supported Co-Mo-based OER electrocatalyst with good performance, which may represent a potential approach to the development of new catalysts for OER, as well as the treatment of waste biomass.

Synthesis of CoMoO4 Nanofibers by Electrospinning as Efficient Electrocatalyst for Overall Water Splitting.

To improve the traditional energy production and consumption of resources, the acceleration of the development of a clean and green assembly line is highly important. Hydrogen is considered one of the most ideal options. The method of production of hydrogen through water splitting constitutes the most attractive research. We synthesized CoMoO4 nanofibers by electrospinning along with post-heat treatment at different temperatures. CoMoO4 nanofibers show a superior activity for hydrogen evolution reaction (HER) and only demand an overpotential of 80 mV to achieve a current density of 10 mA cm-2. In particular, the CoMoO4 catalyst also delivers excellent performances of oxygen evolution reaction (OER) in 1 M KOH, which is a more complicated process that needs extra energy to launch. The CoMoO4 nanofibers also showed a superior stability in multiple CV cycles and maintained a catalytic activity for up to 80 h through chronopotentiometry tests. This is attributed mainly to a synergistic interaction between the different metallic elements that caused the activity of CoMoO4 beyond single oxides. This approach proved that bimetallic oxides are promising for energy production.

Efficient Degradation of Congo Red in Water by UV-Vis Driven CoMoO4/PDS Photo-Fenton System.

In order to improve the catalytic activity of cobalt molybdate (CoMoO4), a PDS-activated and UV-vis assisted system was constructed. CoMoO4 was prepared by coprecipitation and calcination, and characterized by XRD, FTIR, Raman, SEM, TEM, XPS, TGA Zeta potential, BET, and UV-Vis DRS. The results showed that the morphology of the CoMoO4 nanolumps consisted of stacked nanosheets. XRD indicated the monoclinic structures with C2/m (C32h, #12) space group, which belong to α-CoMoO4, and both Co2+ and Mo6+ ions occupy distorted octahedral sites. The pH of the isoelectric point (pHIEP) of CMO-8 at pH = 4.88 and the band gap of CoMoO4 was 1.92 eV. The catalytic activity of CoMoO4 was evaluated by photo-Fenton degradation of Congo red (CR). The catalytic performance was affected by calcination temperature, catalyst dosage, PDS dosage, and pH. Under the best conditions (0.8 g/L CMO-8, PDS 1 mL), the degradation efficiency of CR was 96.972%. The excellent catalytic activity of CoMoO4 was attributed to the synergistic effect of photo catalysis and CoMoO4-activated PDS degradation. The capture experiments and the ESR showed that superoxide radical (·O2-), singlet oxygen (1O2), hole (h+), sulfate (SO4-·), and hydroxyl (·OH-) were the main free radicals leading to the degradation of CR. The results can provide valuable information and support for the design and application of high-efficiency transition metal oxide catalysts.

Defects enriched cobalt molybdate induced by carbon dots for a high rate Li-ion battery anode.

A defects-enriched CoMoO4/carbon dot (CD) with CoMoO4around 37 nm is achieved via hydrothermal reaction by introducing CDs to buffer large volume changes of CoMoO4during lithiation-delithiation and enhance rate performance. The phase, morphology, microstructure, as well as the interface of the CoMoO4/CD composites were investigated by x-ray diffraction, scanning electron microscopy, transmission electron microscopy and x-ray photoelectron spectroscopy. When employed as Li-ion battery anode, the CoMoO4/CD exhibits a reversible capacity of ∼531 mAh g-1after 400 cycles at a current density of 2.0 A g-1. Under the scan rate at 2 mV s-1, the CoMoO4/CD shows accounts for 81.1% pseudocapacitance. It may attribute to the CoMoO4with surface defects given more reaction sites to facilitate electrons and lithium ions transfer at high current densities. Through galvanostatic intermittent titration technique, the average lithium ion diffusion coefficient calculated is an order of magnitude larger than that of bulk CoMoO4, indicating that the CoMoO4/CD possesses promising electrons and lithium ions transportation performance as anode material.

High Catalytic Efficiency of Nanostructured ß-CoMoO4 in the Reduction of the Ortho-, Meta- and Para-Nitrophenol Isomers.

Nanostructured ß-CoMoO4 catalysts have been prepared via the thermal decomposition of an oxalate precursor. The catalyst was characterized by infrared spectroscopy (FTIR), X-ray diffraction (XRD), Brunauer-Emmett-Teller method (BET), energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The efficiency of these nanoparticles in the reduction of ortho- and meta-nitrophenol isomers (2-NP, 3-NP, and 4-NP) to their corresponding aminophenols was tested using UV-visible spectroscopy measurements. It was found that, with a ß-CoMoO4 catalyst, NaBH4 reduces 3-NP instantaneously, whilst the reduction of 2-NP and 4-NP is slower at 8 min. This difference is thought to arise from the lower acidity of 3-NP, where the negative charge of the phenolate could not be delocalized onto the oxygen atoms of the meta-nitro group.

Synergistic Charge Storage Enhancement in Supercapacitors via Ti3C2Tx MXene and CoMoO4 Nanoparticles.

MXene has emerged as a highly promising two-dimensional (2D) layered material with inherent advantages as an electrode material, such as a high electrical conductivity and spacious layer distances conducive to efficient ion transport. Despite these merits, the practical implementation faces challenges due to MXene's low theoretical capacitance and issues related to restacking. In order to overcome these limitations, we undertook a strategic approach by integrating Ti3C2Tx MXene with cobalt molybdate (CoMoO4) nanoparticles. The CoMoO4 nanoparticles bring to the table rich redox activity, high theoretical capacitance, and exceptional catalytic properties. Employing a facile hydrothermal method, we synthesized CoMoO4/Ti3C2Tx heterostructures, leveraging urea as a size-controlling agent for the CoMoO4 precursors. This innovative heterostructure design utilizes Ti3C2Tx MXene as a spacer, effectively mitigating excessive agglomeration, while CoMoO4 contributes its enhanced redox reaction capabilities. The resulting CoMoO4/Ti3C2Tx MXene hybrid material exhibited 698 F g-1 at a scan rate of 5 mV s-1, surpassing that of the individual pristine Ti3C2Tx MXene (1.7 F g-1) and CoMoO4 materials (501 F g-1). This integration presents a promising avenue for optimizing MXene-based electrode materials, addressing challenges and unlocking their full potential in various applications.

Ru doping induced interface engineering in flower-liked CoMoO4-RuO2 boosts oxygen electrocatalysis for rechargeable Zn-air battery.

Constructing heterogeneous catalysts can significantly boost the electrocatalytic activity due to the improved intrinsic catalytic activity induced by tailored electronic structure and optimized chemisorption to the reaction intermediates. RuO2 based electrocatalysts are especially attractive due to the high catalytic activity of RuO2. To reduce the usage of noble metal and improve the catalytic activity of catalyst, CoMoO4-RuO2 micro-flower was synthesized using a facile hydrothermal-calcination method in this work. CoMoO4-RuO2 exhibits a low overpotential of 177 mV at 10 mA cm-2 for oxygen evolution reaction (OER) and a high half-wave potential of 0.858 V for oxygen reduction reaction (ORR). Moreover, the Zn-air battery assembled using CoMoO4-RuO2 exhibit shows a high maximum discharge power density of 149 mW cm-2 and a large open circuit voltage of 1.38 V. The good performance can be attributed to the incorporation of RuO2, which not only induces extra catalytic active sites, but also forms heterojunction with CoMoO4 to optimize the electronic structure of CoMoO4-RuO2, thereby achieving a better equilibrium of absorption and desorption of intermediates. The work provides insights into designing RuO2 based electrocatalysts for advanced electrocatalysis.

Hybridization of bimetallic cobalt-molybdenum oxide multihole nanosheets with selenium adulteration as advanced bifunctional electrocatalysts for boosting overall water splitting.

Electrocatalytic water splitting produces green and pollution-free hydrogen as a clean energy carrier, which can effectively alleviate energy crisis. In this paper, bimetallic and selenium doped cobalt molybdate (Se-CoMoO4) nanosheets with rough surface are resoundingly prepared. The multihole Se-CoMoO4 nanosheets display ultrathin and rectangular architecture with the dimensions of âˆ¼ 3.5 µm and 700 nm for length and width, respectively. The Se-CoMoO4 electrocatalyst shows remarkable water electrolysis activity and stability. The overpotentials of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are 270 and 63.3 mV at 10 mA cm-2, along with low Tafel slopes of 51.6 and 62.0 mV dec-1. Furthermore, the Se-CoMoO4 couple electrolyzer merely requires a cell voltage of 1.48 V to achieve 10 mA cm-2 current density and presents no apparent attenuation for 30 h. This investigation declares that the hybridization of transition bimetallic oxide with nonmetallic adulteration can afford a tactic for the preparation of bifunctional non-precious metal-based electrocatalysts.

Transforming crystal structures of cobalt molybdate to generate electron-rich sites for electrochemical detection of Pb(II).

BACKGROUND: Most of the investigations on distinct crystal structures of catalysts are individually focused on the difference of surface functional groups or adsorption properties, but rarely explore the changes of active sites to affect the electrocatalytic performance. Catalysts with diverse crystal structures had been applied to modified electrodes in different electrocatalytic reactions. However, there is currently a lack of an essential understanding for the role of real active sites in catalysts with crystalline structures in electroanalysis, which is crucial for designing highly sensitive sensing interfaces. RESULTS: Herein, cobalt molybdate with divergent crystal structures (α-CoMoO4 and ß-CoMoO4) were synthesized by adjusting the calcination temperature, indicating that α-CoMoO4 (800 °C) (60.00 µA µM-1) had the highest catalytic ability than ß-CoMoO4 (700 °C) (38.68 µA µM-1) and α-CoMoO4 (900 °C) (29.55 µA µM-1) for the catalysis of Pb(II). It was proved that the proportion of Co(II) and Mo(IV) as electron-rich sites in α-CoMoO4 (800 °C) were higher than ß-CoMoO4 (700 °C) and α-CoMoO4 (900 °C), possessing more electrons to participate in the valence cycles of Co(II)/Co(III) and Mo(IV)/Mo(VI) to boost the catalytic reduction of Pb(II). Specifically, Co(II) transferred a part of electrons to Mo(VI), promoting the formation of Mo(IV). Co(II) and Mo(IV), as the electron-rich sites, providing electrons to Pb(II), further accelerating the conversion of Pb(II) into Pb(0). SIGNIFICANCE: In the process of detecting Pb(II), the CoMoO4 structures under different temperatures have distinct content of electron-rich sites Co(II) and Mo(IV). α-CoMoO4 (800 °C), with the highest content are benefited to detect Pb(II). This work is conducive to understanding the effect of the changes of active sites resulting from crystal transformation on the electrocatalytic performance, and provides a way to construct sensitive electrochemical interfaces of distinct active sites.

Metal-Organic-Framework Derived Co-Mo Multimetal Oxide Semiconductors: Selective Trace-Level Hydrogen Sulfide Detection.

The development of a highly selective and trace-level gas sensing platform for detecting hydrogen sulfide (H2S) remains a formidable challenge. To solve this problem, Co-Mo multimetal oxide semiconductors are rationally tailored by employing metal organic frameworks (MOFs) as self-sacrificial templates. The MOF-derived Co3O4/ß-CoMoO4 based gas sensors displays high sensitivity (Rg/Ra = 22) to 10 ppm of H2S and ultralow limit of detection (10 ppb H2S). The formation of p-p heterojunction and multivalence states of Mo play a crucial role in electron transfer and oxygen adsorption. A sensor array constructed from four Co3O4/ß-CoMoO4 materials with different Co/Mo ratios demonstrates a superior selective discrimination of H2S from other VOCs and malodorous gases by principal component analysis (PCA). Besides, a H2S gas sensing and alarming platform was designed for monitoring the environment contaminated with H2S. This finding provides a feasible approach for the discovery of highly efficient gas sensors to monitor environmental H2S concentration.

Selective oxidation decontamination in cobalt molybdate activated Fenton-like oxidation via synergic effect of cobalt and molybdenum.

In this study, cobalt molybdate (CoMoO4) activated peracetic acid (PAA) was developed for water purification. CoMoO4/PAA system could remove 95% SMX with pseudo-first-order reaction rate constant of 0.15410 min-1, which was much higher than CoFe2O4/PAA, FeMoO4/PAA, and CoMoO4/persulfate systems. CoMoO4/PAA system follows a non-radical species pathway dominated by the high-valent cobalt (Co(IV)), and CH3C(O)OO• shows a minor contribution to decontamination. Density functional theory (DFT) calculation indicates that the generation of Co(IV) is thermodynamically more favorable than CH3C(O)OO• generation. The abundant Co(IV) generation was attributed to the special structure of CoMoO4 and effect of molybdenum on redox cycle of Co(II)/Co(III). DFT calculation showed that the atoms of SMX with higher ƒ0 and ƒ- values are the main attack sites, which are in accordance with the results of degradation byproducts. CoMoO4/PAA system can effectively reduce biological toxicity after the reaction. Benefiting from the selective of Co(IV) and CH3C(O)OO•, the established CoMoO4/PAA system exhibits excellent anti-interference capacity and satisfactory decontamination performance under actual water conditions. Furthermore, the system was capable of good potential practical application for efficient removal of various organics and favorable reuse. Overall, this study provides a new strategy by CoMoO4 activated PAA for decontamination with high efficiency, high selectivity and favorable anti-interference.

Cobalt molybdate nanoflowers decorated bio-waste derived porous activated carbon nanocomposite: A high performance electrode material for supercapacitors.

In this work, we report a supercapacitor electrode material based on nano-flower like cobalt molybdate decorated on porous activated carbon derived from waste onion peels (ß-CoMoO4-POAC). The obtained POAC exhibits highly porous structure and after the hydrothermal treatment with salts of cobalt and molybdenum, we observed a uniform distribution of ß-cobalt molybdate (ß-CoMoO4) as nano-flowers on the surface of POAC. The chemical composition, morphology and porosity of the materials were thoroughly analyzed using field emission scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, infrared spectroscopy and Brunauer-Emmet-Teller surface area measurement. Due to its flower like and highly porous morphology, ß-CoMoO4@POAC exhibits a high specific capacitance of 1110.72 F/g at a current density of 1 mA/cm2 with superior cyclic retention of 96.03% after 2000 cycles. The best electrochemical performance exhibited by ß-CoMoO4@POAC is mainly due to its high surface area and porous nature of the material which assists in active transport of ions. This study reveals the exceptional electrochemical properties of ß-CoMoO4@POAC which could be considered as a potential material for advanced energy storage devices.

A novel CoMoO4 enwrapped ZIF-8 nanocomposite with enhanced visible light photocatalytic activity.

A hybrid nano catalyst, CoMoO4 anchored zeolitic imidazolate framework-8 (ZIF-8) has been synthesized by simplest in-situ chemical method. The characterization results showed that the CoMoO4@ZIF-8 composites had a crystalline structure with a uniform distribution of the Cobalt molybdate particles on the ZIF-8 surface. The FTIR spectra revealed the presence of characteristic peaks for both ZIF-8 and CoMoO4, indicating the successful incorporation of the metal molybdate into the ZIF-8 framework. The SEM-EDS analysis showed that the CoMoO4 nanoparticles (NPs) have been evenly distributed on the ZIF-8 surface. In HRTEM, some rod-like CoMoO4 is observed on the surface of the ZIF-8 material, which is stacked in a disorderly manner and a porous channel structure is formed. The photocatalytic activity of the CoMoO4@ZIF-8 has been evaluated using the degradation of methylene blue (MB) and antibiotic Ciprofloxacin (CIP) under visible light. The optimal photocatalytic activity was achieved with the CoMoO4@ZIF-8 composite, which showed a degradation efficiency of 100% under visible light after 40 min of irradiation. In conclusion, the CoMoO4@ZIF-8 composites showed enhanced photocatalytic activity under visible light, and it exhibited the best performance compared with pure CoMoO4 and ZIF-8.

Polyphosphazene-derived P/S/N-doping and carbon-coating of yolk-shelled CoMoO4 nanospheres towards enhanced pseudocapacitive lithium storage.

Transition metal oxides as potentialanodes of lithium-ion batteries (LIBs) possess high theoretical capacity but suffer from large volume expansion and poor conductivity. To overcome these drawbacks, we designed and fabricated polyphosphazene-coated yolk-shelled CoMoO4 nanospheres, in which polyphosphazene with abundant C/P/S/N species was readily converted into carbon shells and provided P/S/N dopants. This resulted in the formation of P/S/N co-doped carbon-coated yolk-shelled CoMoO4 nanospheres (PSN-C@CoMoO4). The PSN-C@CoMoO4 electrode exhibits superior cycle stability of 439.2 mA h g-1at 1000 mA g-1after 500 cycles and rate capability of 470.1 mA h g-1at 2000 mA g-1. The electrochemical and structural analyses reveal that PSN-C@CoMoO4 with yolk-shell structure, coated with carbon and doped with heteroatom not only greatly enhances the charge transfer rate and reaction kinetics, but also efficiently buffers the volume variation upon lithiation/delithiation cycling. Importantly, the use of polyphosphazene as coating/doping agent can be a general strategy for developing advanced electrode materials.

Tuning the oxygen vacancy of mixed multiple oxidation states nanowires for improving Li-air battery performance.

Mixed multiple oxidation states CoMoO4 nanowires (electrocatalysts) with tunable intrinsic oxygen vacancies were fabricated. CoMoO4 with proper oxygen vacancy can be employed to construct a Li-air battery with a high capacity and stable cyclability. This is possible because CoMoO4 contains surface oxygen vacancies, which result in the unit of CoMo bond, that is important for electrocatalysts used in Li-air batteries. Both the experimental and theoretical results demonstrate that the surface oxygen vacancies containing CoMoO4 nanowires have a higher electrocatalytic activity. This shows that the highly efficient electrocatalysts used for Li-air batteries were designed to modify the redox properties of the mixed metal oxide in the catalytic active sites. This successful material design led to an improved strategy for high oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activities based on the fast formation and extinction of ORR products.

Construction of Core-Shell CoMoO4@γ-FeOOH Nanosheets for Efficient Oxygen Evolution Reaction.

The oxygen evolution reaction (OER) occurs at the anode in numerous electrochemical reactions and plays an important role due to the nature of proton-coupled electron transfer. However, the high voltage requirement and low stability of the OER dramatically limits the total energy converting efficiency. Recently, electrocatalysts based on multi-metal oxyhydroxides have been reported as excellent substitutes for commercial noble metal catalysts due to their outstanding OER activities. However, normal synthesis routes lead to either the encapsulation of excessively active sites or aggregation during the electrolysis. To this end, we design a novel core-shell structure integrating CoMoO4 as support frameworks covered with two-dimensional γ-FeOOH nanosheets on the surface. By involving CoMoO4, the electrochemically active surface area is significantly enhanced. Additionally, Co atoms immerge into the γ-FeOOH nanosheet, tuning its electronic structure and providing additional active sites. More importantly, the catalysts exhibit excellent OER catalytic performance, reducing overpotentials to merely 243.1 mV a versus 10 mA cm-2. The current strategy contributes to advancing the frontiers of new types of OER electrocatalysts by applying a proper support as a multi-functional platform.

Dual-anions engineering of bimetallic oxides as highly active electrocatalyst for boosted overall water splitting.

Bimetallic oxides have unique advantages in driving both oxygen and hydrogen evolution reactions (OER/HER). Surface engineering of bimetallic oxides is a promising way to boost the catalytic activity by the regulation of electronic structure and surface property. Herein, a dual P, S-anions modification strategy is developed to optimize the catalytic performance of CoMoO4 nanowire arrays. The formations of CoP and Co3S4 species on the CoMoO4 surface bring heterojunction interfaces for more catalytic active sites and strong electronic interaction for faster interfacial charge transfer. Benefiting from these advantages, the P, S-CoMoO4 catalyst on nickel foam (NF) delivers excellent catalytic activity and stability. The overpotentials at 10 mA cm-2 of P, S-CoMoO4/NF for HER are just 31 mV in acid media and 58 mV in alkaline media, respectively. In addition, by assembling the P, S-CoMoO4/NF as bifunctional electrodes for overall water splitting, the electrolyzer exhibits a voltage of as low as 1.66 V at a current density of 50 mA cm-2. This work put forward a new avenue for the development of advanced bifunctional electrocatalysts for water splitting.

Fe(Co)OOH Dynamically Stable Interface Based on Self-Sacrificial Reconstruction for Long-Term Electrochemical Water Oxidation.

FeOOH on the real catalytic interface for the oxygen evolution reaction (OER) is chemically unstable to dissolve in alkaline media. Herein, based on the perspective of the dynamically stable interface, we purposely design the well-dispersed nanorod arrays of CoMoO4 as a host on activated iron foam (IF) to realize the optimal redeposition of FeOOH, constructing a self-sacrificial template rich in the FeOOH surface. Notably, at long-time oxidation potential, the precatalyst FeOOH-CoMoO4 can realize MoO42- dissolution and redeposition of Co oxyhydroxides on FeOOH host simultaneously, constructing a dynamically stable Fe(Co)OOH interface. The introduction of CoOOH improves conductivity and provides synergistic effect with FeOOH to lower the energy barrier for OER and maintain long-time stability, eventually exhibiting a low overpotential of 298 mV to reach the current density of 100 mA cm-2 and high stability over 60 h. This work demonstrates the feasibility of manipulating metal dissolution-redeposition process for a dynamically stable interface.

Selenizing CoMoO4 nanoparticles within electrospun carbon nanofibers towards enhanced sodium storage performance.

Transition metal oxides/selenides as anodes for sodium-ion batteries (SIBs) suffer from the insufficient conductivity and large volumetric expansion, which leads to the poor electrochemical performance. To address these issues, we herein demonstrate a facile selenization method to enhance the sodium storage capability of CoMoO4 nanoparticles which are encapsulated into the electrospun carbon nanofibers (CMO@carbon for short). The partially and fully selenized CoMoO4 within carbon nanofibers (denote as CMOS@carbon and CMS@carbon, respectively) can be readily obtained by controlling the annealing temperature (at 400 and 600 °C, correspondingly). When examined as anode materials for SIBs, the CMOS@carbon nanofibers display an outstanding electrochemical performance with a higher reversible capacity of 396 mA h g-1 after 200 cycles at 0.2 A g-1 and a high-rate capacity of 365 mA h g-1 at 2 A g-1, as compared with the CMO@carbon and CMS@carbon counterparts. The enhanced sodium storage performance of the CMOS@carbon can be owing to the partial selenization of the CoMoO4 nanoparticles which are rooted into the porous electrospun carbon nanofibers, thus endowing them with superior ionic/electronic charge transfer efficiencies and a cushion against the electrode pulverization during cycling. Moreover, this work proposed a useful strategy to enhance the sodium storage performance of metal oxides via controlled selenization, which is promising for exploiting the advanced anode materials for SIBs.