CeO2 Nanorods Research Articles

AuAg plasmonic nanoalloys with asymmetric charge distribution on CeO2 nanorods for selective photocatalytic CO2‐to‐CH4 conversion

AbstractConverting CO2 under mild conditions by employing semiconductor photocatalysts is promising to address global environmental issues. However, the current CO2 conversion efficiency is limited by the difficulty activating the thermodynamically stable CO2 molecules. Constructing plasmonic nanoalloy‐based photocatalytic systems with significant localized surface plasmon resonance (LSPR) is full of potential but remains a vast challenge. In this work, AuAg plasmonic nanoalloys were incorporated on CeO2 nanorods (designated as AuAg–CeO2) to achieve selective photoreduction of CO2. The result displays that Ag can serve as a superior electron modifier to promote the electron enrichment of Au, thus producing asymmetric charge distributions to boost the selective conversion of CO2. Furthermore, the improved LSPR effect on AuAg–CeO2 induces the generation of high‐energy hot electrons under irradiation, enhancing the reactivity of electrons for CO2 photoreduction. Due to the aforementioned effects, AuAg–CeO2 exhibits a high CO2‐to‐CH4 performance of 92.6 μmol g−1 through a 3‐h test and a high CH4 selectivity of 94.5%, up to 2.6, 8.7, and 17.1 times higher than the activity of Au–CeO2, pure CeO2, and Ag–CeO2, respectively. This work can provide a new perspective for constructing high‐performance catalysts for photocatalytic CO2 reduction.

Ultrasensitive ECL immunoassay for CA15-3 via self-enhanced L012-loaded ZnNi-MOF as an emitter and CeO2–Pt as a co-reaction accelerator

Improvement in the sensitivity and accuracy of ECL-based biosensors, to a great extent, depends on the fabrication of high-performance electrochemiluminescence (ECL) sensors. Herein, polyethyleneimine (PEI)-grafted bimetallic ZnNi metal-organic framework (ZnNi-MOF/PEI) nanospheres were synthesized to prepare a L012-based ECL immunosensor for detecting carbohydrate antigen 15-3 (CA15-3). The introduced PEI was utilized not only as a bridging element for L012 luminophore and detection antibody (Ab2) immobilization but also as a co-reactant for generating the self-enhanced ZnNi-MOF/PEI-L012@Ab2 ECL signal probe. Furthermore, Pt nanoparticle-functionalized CeO2 nanorods (CeO2–Pt) featuring high-efficiency electrocatalytic properties, as a co-reaction accelerator, could catalyze H2O2 to generate abundant reactive oxygen species (ROS), further augmenting the ECL signal of ZnNi-MOF/PEI-L012@Ab2. In the presence of CA15-3 antigen, the capture antibody (Ab1)-conjugated CeO2–Pt complex (CeO2–Pt@Ab1) and ZnNi-MOF/PEI-L012@Ab2 would get closer to each other, with the formation of a “signal-on” sandwich-type ECL immunosensor. The ZnNi-MOF-assisted ECL biosensor achieved a detection limit of down to 5.75✕10−5 U mL−1. This work shows distinguished potential for measuring low levels of biomarkers that may help in the clinical diagnosis of breast cancer.

Comparative Assessment of First-Row 3d Transition Metals (Ti-Zn) Supported on CeO2 Nanorods for CO2 Hydrogenation

Comparative Assessment of First-Row 3d Transition Metals (Ti-Zn) Supported on CeO2 Nanorods for CO2 Hydrogenation

Sonocatalytic degradation of caffeine using CeO2 nanorods: Modeling by artificial neural network

This study has investigated the utilization of CeO2 nanorods (NRs) in the sonocatalytic degradation of caffeine. The degradation performance was determined by examining the influence of three parametric conditions, namely, the initial pH of the solution (3.5 – 7.5), initial concentration of caffeine (5 – 30 mg/L), and dosage of CeO2 NRs (0.5 – 2.0 g/L). All experiments were conducted in an ultrasonic bath (37 kHz, 150 W) that served as a sonocatalytic reactor. The mathematical modeling of the process with the catalyst was developed using Feedforward artificial neural networks (FFNN). The FFNN was employed to develop suitable modeling for determining the performance of the sonocatalytic degradation of caffeine (%) using CeO2 NRs. A three-layer FFNN with [4−10-1] topology was successfully developed to predict the sonocatalytic degradation of caffeine using CeO2 NRs. The FFNN was able to offer highly accurate predictions with the overall R2 and MSE validation values of 0.991 and 0.00225, respectively. The ANN model has also provided excellent predictive performance by achieving the highest R2 value. Thus, these results showed the promising finding of the sonocatalysis degradation of caffeine using CeO2 NRs via experiments and the ANN model.

Influence of Ni Doping on Oxygen Vacancy-Induced Changes in Structural and Chemical Properties of CeO2 Nanorods

In recent years, cerium dioxide (CeO2) has attracted considerable attention owing to its remarkable performance in various applications, including photocatalysis, fuel cells, and catalysis. This study explores the effect of nickel (Ni) doping on the structural, thermal, and chemical properties of CeO2 nanorods, particularly focusing on oxygen vacancy-related phenomena. Utilizing X-ray powder diffraction (XRD), alterations in crystal structure and peak shifts were observed, indicating successful Ni doping and the formation of Ni2O3 at higher doping levels, likely due to non-equilibrium reactions. Thermal gravimetric analysis (TGA) revealed changes in oxygen release mechanisms, with increasing Ni doping resulting in the release of lattice oxygen at lower temperatures. Raman spectroscopy corroborated these findings by identifying characteristic peaks associated with oxygen vacancies, facilitating the assessment of Ni doping levels. Ni-doped CeO2 can catalyze the ultrasonic degradation of methylene blue, which has good application prospects for catalytic ultrasonic degradation of organic pollutants. Overall, this study underscores the substantial impact of Ni doping on CeO2 nanorods, shedding light on tailored catalytic applications through the modulation of oxygen vacancies while preserving the nanorod morphology.

Boosting hydrocarbon conversion via Cu-doping induced oxygen vacancies on CeO2 in CO2 electroreduction

Conversion of CO2 back to hydrocarbons is the most direct way of closing the “carbon cycle”, and its significance is further enlarged if this process is driven by renewable energies such as electricity. However, precisely controlling the product selectivity towards hydrocarbons against the competitive hydrogen evolution remains challenging, especially for Cu-based catalysts. Herein, we report a novel defect engineering strategy, by which Cu-doping-induced oxygen vacancies on CeO2 nanorods were effectively created, with adjustable vacancy/Cu ratio. The resulting optimum catalyst shows up to 79% catalytic current density to hydrocarbons (excluding CO), with 49% faradaic efficiency to CH4. Experiments and density functional theory unveil that the ratio between oxygen vacancy and Cu affects significantly the formation of *CHO and activation of H2O, which leads to the following deep hydrogenation to hydrocarbons. These findings may spur new insights for designing and developing more controllable chemical process relevant to CO2 utilization.

Enhancement of photocatalytic activity of CeO2 nanorods through lanthanum doping (La–CeO2) for the degradation of Congo red dyes

The discharge of synthetic dyes into water bodies poses severe environmental risks due to their toxic and recalcitrant nature. This study explores the enhancement of photocatalytic properties of cerium dioxide (CeO2) nanorods by doping with lanthanum (La) to improve their efficacy in degrading aqueous solutions of Congo red dye. The CeO2 nanorods were synthesized via a hydrothermal method and subsequently doped with varying concentrations of La. The scanning electron microscopy (SEM) images confirmed the rod-like structures (nanorods) were observed for all samples, while the energy-dispersive X-ray spectroscopy (EDX) confirmed the homogeneous incorporation of La into the CeO2 matrix. The X-ray diffraction (XRD) spectra demonstrate lattice distortion due to substitutional defect. Photocatalytic experiments revealed that La-doped CeO2 nanorods exhibited significantly enhanced degradation capabilities compared to undoped counterparts, achieving up to a 3-fold photocatalytic kinetics ((30 ± 2) × 10−3 min−1) compared to the undoped counterparts ((11.5 ± 0.4) × 10−3 min−1). Influence of various parameters that affect the photocatalysis performance (i.e., contact time, initial dye concentration, catalyst dosage, and dye solution pH value) were also investigated. Radical scavenger experiments reveal that superoxide radicals play a dominant role in the photocatalytic process. Collectively, these findings confirm that the strategic incorporation of lanthanum into CeO2 nanorods not only enhances their overall photocatalytic efficiency but also tailors their activity towards specific pollutants through radical-mediated pathways.

Antifouling and antimicrobial wearable electrochemical sweat sensors for accurate dopamine monitoring based on amyloid albumin composite hydrogels

Wearable electrochemical sweat sensors are potentially promising for health monitoring in a continuous and non-invasive mode with high sensitivity. However, due to the complexity of sweat composition and the growth of skin bacteria, the wearable sweat sensors may gradually lose their sensitivity or even fail over time. To deal with this issue, herein, we proposed a new strategy to construct wearable sweat sensors with antifouling and antimicrobial capabilities. Amyloid albumin hydrogels (ABSAG) were doped with two-dimensional (2D) nanomaterial MXene and CeO2 nanorods to obtain the antifouling and antimicrobial amyloid albumin composite hydrogels (ABSACG, CeO2/MXene/ABSAG), and the wearable sensors were prepared by modifying flexible screen-printed electrodes with the ABSACG. Within this sensing system, the hydrophilic ABSAG possesses strong hydration capability, and it can form a hydration layer on the electrode surface to resist biofouling in sweat. The 2D nanomaterial MXene dispersed in the hydrogel endows the hydrogel with good conductivity and electrocatalytic capability, while the doping of CeO2 nanorods further improves the electrocatalytic performance of the hydrogel and also provides excellent antimicrobial capability. The designed wearable electrochemical sensors based on the ABSACG demonstrated satisfying antifouling and antimicrobial abilities, and they were capable of detecting dopamine accurately in human sweat. It is expected that wearable sensors utilizing the antifouling and antimicrobial ABSACG may find practical applications in human body fluids analysis and health monitoring.

Can Subsurface Oxygen Species in Oxides Participate in Catalytic Reactions? An 17O Solid-State Nuclear Magnetic Resonance Study.

The impacts of subsurface species of catalysts on reaction processes are still under debate, largely due to a lack of characterization methods for distinguishing these species from the surface species and the bulk. By using 17O solid-state nuclear magnetic resonance (NMR) spectroscopy, which can distinguish subsurface oxygen ions in CeO2 (111) nanorods, we explore the effects of subsurface species of oxides in CO oxidation reactions. The intensities of the 17O NMR signals due to surface and subsurface oxygen ions decrease after the introduction of CO into CeO2 nanorods, with a more significant decrease observed for the latter, confirming the participation of subsurface oxygen species. Density functional theory calculations show that the reaction involves subsurface oxygen ions filling the surface oxygen vacancies created by the direct contact of surface oxygen with CO. This new approach can be extended to the study of the role of oxygen species in other catalytic reactions.

Highly sensitive hydrolytic nanozyme-based sensors for colorimetric detection ofaluminum ions.

Hydrolytic nanozyme-based visual colorimetry has emerged as a promising strategy for the detection of aluminum ions. However, most studies focus on simulating the structure of natural enzymes while neglecting to regulate the rate of hydrolysis-related steps, leading to low enzyme-like activity for hydrolytic nanozymes. Herein, we constructed a ruthenium dioxide (RuO2) in situ embedded cerium oxide (CeO2) nanozyme (RuO2/CeO2) with aLewis acid-base pair (Ce-O-Ru-OH), which can simulate the catalytic behavior of phosphatase (PPase) and can be quantitatively quenched by Al3+ to achieve accurate and sensitive Al3+ colorimetric sensing detection. The incorporation of Ru into CeO2 nanorods accelerates the dissociation of H2O, followed by subsequent combination of hydroxide species to Lewis acidic Ce-O sites. This synergistic effect facilitates substrate activation and significantly enhances the hydrolysis activity of the nanozyme. The results show that the RuO2/CeO2 nanozyme exhibits a limit of detection as low as 0.5ng/mL. We also demonstrate their efficacy in detecting Al3+ in various practical food samples. This study offers novel insights into the advancement of highly sensitive hydrolytic nanozyme engineering for sensing applications.

Oxygen Vacancy-Driven Heterointerface Breaks the Linear-Scaling Relationship of Intermediates toward Electrocatalytic CO2 Reduction.

Smart metal-metal oxide heterointerface construction holds promising potentials to endow an efficient electron redistribution for electrochemical CO2 reduction reaction (CO2RR). However, inhibited by the intrinsic linear-scaling relationship, the binding energies of competitive intermediates will simultaneously change due to the shifts of electronic energy level, making it difficult to exclusively tailor the binding energies to target intermediates and the final CO2RR performance. Nonetheless, creating specific adsorption sites selective for target intermediates probably breaks the linear-scaling relationship. To verify it, Ag nanoclusters were anchored onto oxygen vacancy-rich CeO2 nanorods (Ag/OV-CeO2) for CO2RR, and it was found that the oxygen vacancy-driven heterointerface could effectively promote CO2RR to CO across the entire potential window, where a maximum CO Faraday efficiency (FE) of 96.3% at -0.9 V and an impressively high CO FE of over 62.3% were achieved at a low overpotential of 390 mV within a flow cell. The experimental and computational results collectively suggested that the oxygen vacancy-driven heterointerfacial charge spillover conferred an optimal electronic structure of Ag and introduced additional adsorption sites exclusively recognizable for *COOH, which, beyond the linear-scaling relationship, enhanced the binding energy to *COOH without hindering *CO desorption, thus resulting in the efficient CO2RR to CO.

Interface reconstruction of MXene-Ti3C2 doped CeO2 nanorods for remarked photocatalytic ammonia synthesis

Prospective photocatalytic ammonia synthesis process has received more attentions but quite challenging with the low visible light utilization and weak N2 molecule absorption ability around the photocatalysts. Herein, interface reconstruction of MXene-Ti3C2/CeO2 composites with high-concentration active sites through the carbon-doped process are presented firstly, and obvious transition zones with the three-phase reaction interface are formed in the as-prepared catalysts. The optimal co-doped sample demonstrates an excellent photo response in the visible light region, the strongest chemisorption activity and the most active sites. Moreover, much more in-situ extra oxygen defects are also produced under light irradiation. It is expected that the double decorated catalyst shows a remarked ammonia production rate of above 0.76 mmol gcal−1·h−1 under visible-light illumination and a higher apparent quantum efficiency of 1.08 % at 420 nm, which is one of the most completive properties for the photocatalytic N2 fixation at present.

A multifunctional solution to enhance capacity and stability in lithium-sulfur batteries: Incorporating hollow CeO2 nanorods into carbonized non-woven fabric as an interlayer

Lithium-sulfur batteries (LSBs) hold promise as the next-generation lithium-ion batteries (LIBs) due to their ultra-high theoretical capacity and remarkable cost-efficiency. However, these batteries suffer from the serious shuttle effect, challenging their practical application. To address this challenge, we have developed a unique interlayer (HCON@CNWF) composed of hollow cerium oxide nanorods (CeO2) anchored to carbonized non-woven viscose fabric (CNWF), utilizing a straightforward template method. The prepared interlayer features a three-dimensional (3D) conductive network that serves as a protective barrier and enhances electron/ion transport. Additionally, the CeO2 component effectively chemisorbs and catalytically transforms lithium polysulfides (LiPSs), offering robust chemisorption and activation sites. Moreover, the unique porous structure of the HCON@CNWF not only physically adsorbs LiPSs but also provides ample space for sulfur’s volume expansion, thus mitigating the shuttle effect and safeguarding the electrode against damage. These advantages collectively contribute to the battery’s outstanding electrochemical performance, notably in retaining a reversible capacity of 80.82 % (792 ± 5.60 mAh g−1) of the initial value after 200 charge/discharge cycles at 0.5C. In addition, the battery with HCON@CNWF interlayer has excellent electrochemical performance at high sulfur loading (4 mg cm−2) and low liquid/sulfur ratio (7.5 µL mg−1). This study, thus, offers a novel approach to designing advanced interlayers that can enhance the performance of LSBs.

Comparative study on CeO2 catalysts with different morphologies and exposed facets for catalytic ozonation: performance, key factor and mechanism insight

Morphology and facet effects of metal oxides in heterogeneous catalytic ozonation (HCO) are attracting increasing interests. In this paper, the different HCO performances for degradation and mineralization of phenol of seven ceria (CeO2) catalysts, including four with different morphologies (nanorod, nanocube, nanooctahedron and nanopolyhedron) and three with the same nanorod morphology but different exposed facets, are comparatively studied. CeO2 nanorods with (110) and (100) facets exposed show the best performance, much better than that of single ozonation, while CeO2 nanocubes and nanooctahedra show performances close to single ozonation. The underlying reason for their different HCO performances is revealed using various experimental and density functional theory (DFT) calculation results and the possible catalytic reaction mechanism is proposed. The oxygen vacancy (OV) is found to be pivotal for the HCO performance of the different CeO2 catalysts regardless of their morphology or exposed facet. A linear correlation is discerned between the rate of catalytic decomposition of dissolved ozone (O3) and the density of Frenkel-type OV. DFT calculations and in-situ spectroscopic studies ascertain that the existence of OV can boost O3 activation on both the hydroxyl (OH) and Ce sites of CeO2. Conversely, various facets without OV exhibit similar O3 adsorption energies. The OH group plays an important role in activating O3 to produce hydroxyl radical (∙OH) for improved mineralization. This work may offer valuable insights for designing Facet- and OV-regulated catalysts in HCO for the abatement of refractory organic pollutants.

Frustrated Lewis pairs on Al-doped CeO2 for efficient reverse water–gas shift reaction

The reverse water–gas shift (RWGS) reaction holds promise for producing high value-added CO from CO2, serving as a crucial intermediate to feedstock for producing various hydrocarbons through Fischer-Tropsch synthesis reactions. Metallic catalysts often yield significant methane production as a by-product during operation, whereas non-metallic oxide catalysts offer potential for high CO selectivity. We prepare Al doped CeO2 nanorod by atomic layer deposition (ALD). The incorporation of Al creates more oxygen vacancies on the surface, resulting in increased Frustrated Lewis Pair (FLP) sites. Particularly, the CO yield of ALD-modified CeO2 was enhanced by 134 % compared to that of pristine CeO2 nanorods (CeO2-NR) at 500 °C, with CO selectivity reached 100 %. Density Functional Theory (DFT) calculations reveal a lower energy barrier for H2 dissociation facilitated by the formation of FLP sites, potentially leading to heightened activity in the Reverse Water Gas Shift (RWGS) reaction.

Dispersed CeO2 Nanorods with Low-Speed Mixing for Mechanical Properties Promotion of PTA Steel Coatings

The plasma-transferred arc technology has been observed to induce preferential grain orientation in multiple directions, leading to nonuniform grain growth within the alloy coating material. The addition of nano-oxides can act as heterogeneous nucleation sites, reducing the preferred orientation of grains. In this study, a low-speed mixing method was employed to coat highly dispersed CeO2 nanorods (CNRs) onto the surface of 14Cr2NiSiVMn alloy powder particles. The aim was to analyze the influence of dispersed CNRs on grain growth orientation in different directions and the refinement and heterogeneous nucleation effect of CNR additives. The addition of 0.5 wt.% CNRs resulted in the refinement of dendritic grains along both the perpendicular and parallel directions to the coating cladding direction, leading to the formation of more uniform equiaxed crystals. The combination of Ce with Si and V elements formed submicron particles, which promoted grain nucleation and reduced defects in the coating. Consequently, the mechanical performance of the sample significantly improved. In the deposition direction, there was a notable improvement in microhardness (20.4%), tensile strength (97.6%), and elongation (59.0%). In the perpendicular deposition direction, the tensile strength increased by 88.1%, and the elongation increased by 33.9%. Additionally, the weight loss due to wear decreased by 44.2%, and the relative wear resistance improved by 79.3%.

Catalytically Self‐Supplied Oxygen to Alleviate Hypoxia for Treatment of Acute Kidney Injury

AbstractOvercoming hypoxia is an urgent clinical challenge in acute kidney injury (AKI) treatment. Specifically, hypoxia upregulates xanthine oxidase (XO) expression and induces reactive oxygen species (ROS) generation, which exacerbates renal injury. Herein, a therapeutic strategy of self‐supply oxygen for highly efficient AKI therapy is developed, in which the biocompatible CeO2 nanorods modified by poly(ethylene glycol)‐folic acid conjugate (CeFA) catalytically convert ROS into oxygen and effectively relieve hypoxia in injured renal tissues. Modification with poly(ethylene glycol)‐folic acid conjugate allows the catalysts to be accumulated in injured renal tissues, and the high activity of CeFA guaranteed long‐lasting endogenous ROS decomposition to continuously supply oxygen. This resulted in the relief of renal hypoxia, which inhibits XO expression, reduces ROS generation and thereafter essentially alleviates kidney injury. Moreover, CeFA significantly reduces lipopolysaccharide‐induced ROS injury and reverses hypoxia in the murine AKI model, where the levels of kidney function indicators remain normal, and inflammation is alleviated without negative effects. This study offers a promising strategy for relieving hypoxia and protecting the kidney from AKI. This methodology is anticipated to provide a valuable approach for treating other oxygen‐dependent diseases and events, such as tumors and stroke.

Operando investigation of catalytic trichloroethylene combustion over metal-doped CeO2 nanorods

The remediation of chlorinated volatile organic compounds is an intractable issue for it typically requires high temperatures and generates undesirable byproducts. This work utilized a series of representative transition metals (i.e., Cr, Cu, V) to modify the morphology, surface oxygen, and acidity of the CeO2 nanorods for trichloroethylene (TCE) treatment. A spectroscopic operando DRIFT − online GCMS reactor was introduced to examine the catalytic performance and elucidate the reaction pathway. Among them, Cr-CeO2 exhibited 50 % (T50) and 90 % (T90) TCE conversions with no byproduct at 171 °C and 241 °C, respectively. The performances of Cu-CeO2 (T90 = 391 °C), V-CeO2 (T90 = 423 °C) and CeO2 (T90 = 494 °C) were inferior to Cr-CeO2 (T90 = 241 °C), with obvious C2Cl4 generated in the TCE oxidation. It reveals that TCE adsorbed on Cr-CeO2 is dechlorinated on acidic sites and oxidized to carbonate/formate intermediates by the surface oxygen then facilely to generate carbon oxides, while TCE is adsorbed as chlorinated species (CH2ClCH2O−) on the other three catalysts which occupy the surface and require higher temperature to be oxidized. The abundant medium-strong acidic sites and surface oxygen species of Cr-CeO2 nanorods are responsible for the low-temperature activation via C-Cl cleavage on acidic sites and fast oxidation of hydrocarbon intermediates in the TCE oxidation, respectively.

A green approach to synthesis of Ag-doped CeO2 nanorods embedded reduced graphene oxide nanocomposite for excellent photocatalytic and antimicrobial activity

In this paper, the Ag-doped cerium oxide nanorods embedded reduced graphene oxide (Ag@CeO2/rGO) nanocomposite was synthesized via Punica Granatum peel extract for for photocatalytic degradation of methylene blue (MB) and 4-nitrophenol (4-NP). The microstructural results confirmed the successful decoration of Ag-doped CeO2 nanorods on rGO matrix. The photocatalytic properties, including photocatalytic degradation, charge transfer kinetics and photocurrent generation, are systematically investigated using electrochemical impedance spectroscopy (EIS), photocurrent transient response (PCTR) and open circuit voltage decay (OCVD). The results of photocatalytic dye degradation measurements indicated that Ag@CeO2/rGO nanocomposite is more effective than pristine CeO2 to degrade the MB dye, and the degradation rate reached 100 % in 60 min. The decomposition of MB with Ag@CeO2/rGO nanostructure followed first-order reaction kinetics with a reaction rate constant (Ka) of 0.0198 min−1. The EIS and OCVD measurements revealed that the Ag doping and incorporation of rGO could suppress the recombination probability in CeO2 by the separation of photo-generated electron–hole pairs, which leads to the enhanced photocurrent generation and photocatalytic activity. The photocurrent density of Ag@CeO2/rGO, CeO2/rGO and pristine CeO2 are 215, 167.4 and 98.8 mAcm−2, respectively.

Effect of cobalt on CeO2 nanorod supported Pt catalyst: Structure, performance, kinetics and reaction mechanism in CO oxidation

Catalytic oxidation represents a highly efficient and extensively employed approach for the elimination of CO in exhaust gas. Rationally designing and preparing catalysts with exceptional activity and stability in the presence of H2O and SO2 at low temperatures represent crucial avenues for future advancements. In this work, a series of Pt catalysts supported on CeO2 nanorods incorporated with varying amounts of Cobalt (Co/CeO2 ratio ranging from 0 to 10 %) were prepared and evaluated for their catalytic activity in CO oxidation under both dry and wet conditions. The ultrahigh dispersion of Pt, outstanding redox properties, and abundant oxygen vacancies on the surface of Co-doped CeO2 nanorod supported Pt catalysts were revealed by XRD, TEM, Raman spectroscopy and H2-TPR techniques. The catalytic activity for CO oxidation strongly depends on the Co content and reaction conditions. Among them, Pt/Co-CeO2-5 % exhibits the highest CO oxidation performance with a T90 (the temperature to achieve 90 % conversion of CO) of 170 °C under dry conditions, which is significantly lower by 140 °C compared to T90 of Pt/CeO2. Pt/Co-CeO2-1 % demonstrates superior CO oxidation performance with a T90 of 195 °C under wet conditions, exhibiting a reduction in temperature by 65 °C compared to the T90 of Pt/CeO2. Moreover, Pt/Co-CeO2 exhibits excellent resistance to SO2 compared to Pt/CeO2. Kinetic studies, in situ DRIFT analysis and isotopic experiments demonstrated direct participation of H2O in the reaction. On the catalysts with a low Co/Ce ratio (Co/Ce < 0.03), CO readily reacts with hydroxyl groups dissociated from H2O to form carboxyl intermediates, which subsequently undergo rapid decomposition into CO2, resulting in an enhanced reaction rate of CO oxidation at low temperature.