High Separation Efficiency Research Articles

Non-enzymatic g-C3N4 supported CuO derived-biochar based electrochemical sensors for trace level detection of malathion

Malathion (MALA), a widely used insecticide, even at trace levels exhibits deleterious effects towards respiratory tracts, and nervous system, necessitating its detection. Herein, we have offered non-enzymatic trace level monitoring of MALA using g-C3N4 supported CuO-derived biochar. The present B-CuO/g-C3N4 based electrochemical sensor is synthesized using hydrothermal approach followed by calcination at high temperature. The result unveiled the strong <pi-pi> interactions, high charge separation efficiency, significant porosity leading to excellent electrochemically active surface area 9.88 × 10−5 cm2 with least charge transfer resistance (RCT) value of 35.2 K Ω. The B-CuO/g-C3N4 based nanocomposite offered excellent complex formation ability with MALA and square wave anodic stripping voltametric method (SWASV) generates an enhanced electrochemical signal due to oxidation of MALA. Following all necessary optimizations, the sensor was capable to exhibit limit of detection (LOD) value of 1.2 pg mL−1 with R2 = 0.968. The modified biosensor offered its potential towards detection of MALA in apple and tomato samples with a recovery ranging from 87.64 to 120.59%. This novel B-CuO/g-C3N4 ternary nanocomposite provides non-enzymatic detection of MALA having excellent electrochemical properties and hence opens new pathways for exploring the use of biochar in other electrochemical applications.

Electroless Deposition for Robust and Uniform Copper Nanoparticles on Electrospun Polyacrylonitrile (PAN) Microfiltration Membranes.

Filtration membranes coated in metals such as copper have dramatically improved biofouling resistance and pathogen destruction. However, existing coating methods on polymer membranes impair membrane performance, lack uniformity, and may detach from their substrate, thus contaminating the permeate. To solve these challenges, we developed the first electroless deposition protocol to immobilize copper nanoparticles on electrospun polyacrylonitrile (PAN) fibers for the design of antimicrobial membranes. The deposition was facilitated by prior silver seeding. Distinct mats with average fiber diameters of 232 ± 36 nm, 727 ± 148 nm and 1017 ± 80 nm were evaluated for filtration performance. Well-dispersed copper nanoparticles were conformal to the fibers, preserving the open-cell architecture of the membranes. The copper particle sizes ranged from 20 to 140 nm. Infrared spectroscopy revealed the PAN fiber mats' relative chemical stability/resistance to the copper metallization process. In addition, the classical cyclization of the cyano functional group in PAN was observed. For model polystyrene beads with average sizes of 3 μm, Cu NP-PAN fiber mats had high water flux and separation efficiency with negligible loss of Cu NP from the fibers during flow testing. Fiber size increased flux and somewhat decreased separation efficiency, though the efficiency values were still high.

PTFE composite membrane with peroxymonosulfate activation self-cleaning for highly-efficient oil-water emulsion separation and dye degradation

Combining membrane separation with advanced oxidation technology can make the membrane self-cleaning, extending its service life. However, the preparation of composite membranes with excellent catalytic ability, self-cleaning performance, and stability remains a key research direction. In this study, a PTFE composite membrane with peroxymonosulfate activation self-cleaning ability was successfully prepared by in-situ growth of CoOOH and ZIF-67 on the surface of a l-DOPA/PEI modified PTFE membrane. The as-prepared membrane is superhydrophilic and has significant superoleophobic surfaces underwater, the separation efficiency of the as-prepared membrane for multiple oil-water emulsions exceeded 98.4 %. Meanwhile, the effective degradation of several organic dyes under visible light was simulated, with still high degradation efficiency (>99 %) after 10 cycles. Overall, this study puts forward a approach towards self-cleaning membranes based on PTFE material; the resulting composite membrane's high separation efficiency, stability under repeated use conditions as well as its self-cleaning ability position it as an attractive candidate for long-term wastewater purification applications.

Ionic liquids based azeotropic separation of refrigerants R410A (R32+R125) and R508B (R23+R116) through hybrid extractive distillation

ABSTRACT The increment in GreenHouse Gases (GHGs) promotes high Global Warming Potential (GWP) due to the production and consumption of hydrofluorocarbons (HFCs) that diverts the aim toward the recycling and reclaiming of refrigerant gases. However, the presence of azeotrope in refrigerant mixtures restricts the recycling process. Therefore, in this work, the refrigerant R410A and R508B have been separated through the hybrid extractive distillation method by using [HMIM][TF2N] and [BMIM][BF4] as a solvent in ASPEN Plus. UNIFAC model has been used for the correlation of ionic liquid in ASPEN Plus. For thermodynamic properties, Cosmotherm has been used with the collaboration of TurbromoleX. The Vapor-liquid Equilibrium (VLE) data has been predicted by using the UNIFAC group contribution method. The Total Annual Cost (TAC) analysis with optimization has been performed. Besides that, the energy analysis has also been performed. In the overall separation process and (TAC) analysis, [BMIM][BF4] proves to be more efficient with high separation efficiency and minimal TAC requirements. Whereas, [HMIM][TF2N]/R508B provides less CO2 emission.

Ultrafast Charge Transfer in a Core-shell CdS@Cu-TCPP-Pt Heterojunction for Photocatalytic Hydrogen Production Coupled with Selective Benzylamine Oxidation.

Photocatalytic selective oxidation of organic substances coupled with hydrogen production is believed to be one of the most favorable pathways to make full use of photogenerated charge carriers. However, this catalytic reaction is often discouraged due to the rapid recombination of photogenerated carriers in practical applications. In this work, a core-shell CdS@Cu-TCPP-Pt nanorod heterojunction was dexterously designed for boosting the photocatalytic dehydrogenation performance of benzylamine. The transient absorption results revealed that the photogenerated electron-holes could be effectively separated by properly matching the energy levels in CdS@Cu-TCPP. Surprisingly, Pt embedded in Cu-TCPP not only provided abundant hydrogen production active sites but also facilitated ultrafast charge transfer, which endowed CdS@Cu-TCPP-Pt with remarkable photocatalytic performances for the coproductions of N-benzylidenebenzylamine (1 mL) with a conversion of 23.48% and H2 (20.75 mmol g-1 h-1) under visible irradiation, far surpassing those of CdS and Cu-TCPP. Obviously, the present work verifies that designing and fabricating a hybrid photocatalyst with high separation efficiency of electron-hole pairs is also a significant avenue for other high-performance cooperative dual-functional photocatalytic reactions.

A Novel Size-Based Centrifugal Microfluidic Design to Enrich and Magnetically Isolate Circulating Tumor Cells from Blood Cells through Biocompatible Magnetite-Arginine Nanoparticles.

This paper presents a novel centrifugal microfluidic approach (so-called lab-on-a-CD) for magnetic circulating tumor cell (CTC) separation from the other healthy cells according to their physical and acquired chemical properties. This study enhances the efficiency of CTC isolation, crucial for cancer diagnosis, prognosis, and therapy. CTCs are cells that break away from primary tumors and travel through the bloodstream; however, isolating CTCs from blood cells is difficult due to their low numbers and diverse characteristics. The proposed microfluidic device consists of two sections: a passive section that uses inertial force and bifurcation law to sort CTCs into different streamlines based on size and shape and an active section that uses magnetic forces along with Dean drag, inertial, and centrifugal forces to capture magnetized CTCs at the downstream of the microchannel. The authors designed, simulated, fabricated, and tested the device with cultured cancer cells and human cells. We also proposed a cost-effective method to mitigate the surface roughness and smooth surfaces created by micromachines and a unique pulsatile technique for flow control to improve separation efficiency. The possibility of a device with fewer layers to improve the leaks and alignment concerns was also demonstrated. The fabricated device could quickly handle a large volume of samples and achieve a high separation efficiency (93%) of CTCs at an optimal angular velocity. The paper shows the feasibility and potential of the proposed centrifugal microfluidic approach to satisfy the pumping, cell sorting, and separating functions for CTC separation.

Synergic process of molybdenum recovery and ceramic preparation for clean and efficient utilization of industrial leaching residues

Ammonia-leaching residues of roasted molybdenite concentrates are intractable wastes and are mostly stockpiled in factories. Common treatments suffer from low Mo recovery and secondary pollution. This study has developed a synergistic process involving a single-step roasting with the addition of Al2O3 and MoO3 to recover Mo and simultaneously prepare porous refractories from the residues containing 5.6% Mo. The Mo separation efficiency, ceramic properties, and thermal behaviors—including chemical reactions, melting transformations, ceramic structure evolutions, and Mo species migrations—were comprehensively investigated. It was found that the addition of Al2O3 facilitated CaMoO4 decomposition to release volatile MoO3, thus promoting Mo recovery. The mullite started to form at about 900 °C, grew into whiskers, and further into interconnected clusters, under the catalytic effect of liquid MoO3 and the sintering effect of glassy melt. Liquid MoO3 was scattered on the outer surface of whisker clusters, achieving a high separation efficiency of over 98% after roasting at 1300 °C for 150 min. Meanwhile, a ceramic with a high porosity of 64.2% and a high compressive strength of 21.2 MPa was obtained, exhibiting promise for serving as a high-temperature insulation refractory. Overall, this study presents a novel approach for both the profound recovery of Mo and the value-added utilization of gangue minerals derived from CaMoO4-bearing wastes.

Stearic acid modified Fe3O4/Y2O3 composite membranes for efficient oil-water separation

Traditional oil-water separation methods have low separation efficiency and are prone to environmental pollution. The development of low-cost and environmentally friendly novel oil-water separation membranes is of wide interest nowadays. In this work, stearic acid modified Fe3O4/Y2O3 (Fe3O4/Y2O3/SA) composite membranes are prepared on PET and cotton fabric using spraying and impregnation methods. Both Y2O3 and Fe3O4 nanoparticles are compounded on the surface of the substrate and modified using stearic acid impregnation. The results show that Fe3O4/Y2O3/SA composite membrane has a water contact angle of 152.5° and exhibits super hydrophobicity/lipophilicity. At the same time, the composite membrane has excellent oil-water separation performance, including high separation efficiency (99.92 %) for a variety of oil-water mixtures, and good stability in 15 cycles of separation tests. The mechanism of oil-water separation is discussed.

Theoretical study on structural stability and electronic properties of CH3NH3PbI3/ZnO heterojunction

The structural stability and electronic properties of CH3NH3PbI3/ZnO heterojunctions were investigated using first-principles method. Our results show that the interfacial termination of CH3NH3PbI3 influences the orientational order of C–N bonds and structural stability of heterojunction. For the first time, it was confirmed that the ionic polarization of CH3NH3PbI3 material in CH3NH3PbI3/ZnO induced by interfacial electrostatic interaction plays an important role in high efficient separation and transport of photo-generated carriers, which is a new physical mechanism. This study could provide an in-depth understanding of the properties of CH3NH3PbI3/ZnO, and improve the stability and performance of perovskite solar cells.

Bifunctionalized MOFs modified poly (aryl ether ketone sulfone) ultrafiltration membranes with high-efficient BSA separation and dye adsorption

In this study, by connecting the amino ligand in ZIF-8-NH2 with an alkyl side chain containing sulfonic acid groups in a one-step method, a novel nanofiller (ZIF-8-NS) with bifunctional amino and sulfonic acid groups was formed. Sulfonated poly (aryl ether ketone sulfone) containing fluorene group (F-SPAEKS) was chosen as the polymer matrix. The nanofiller not only had good hydrophilicity but also had electrostatic interaction with the polymer matrix, which effectively promoted the compatibility problem among the polymer matrix and the filler. The nanofillers were characterized by XRD, FT-IR, SEM and XPS. The composite membranes were prepared by the NIPs method. The antifouling and separation properties of the prepared mixed matrix membranes (MMMs) were investigated using positively charged dye (RHB) and negative charge bovine serum albumin (BSA) as model contaminants. The water flux of the pure membrane achieved 529.16 L/m2 h. When the addition amount of ZIF-8-NS was 0.1 %, the water flux of M4 (F-SPAEKS/ZIF-8-NS-0.1 %) could reach 838.84 L/m2 h. The retention rate of the BSA solution could reach 99.06 %, and the FRR value was kept at a high level (81.45 %). Meanwhile, the dynamic retention of M4 on the primary adsorption of the dye RHB could even reach 99.89 %. Therefore, the innovative design of the novel MMMs not only improved the flux, retention, and other separation properties but also enhanced their excellent adsorption capacity for RHB dyes. This result indicated that the nanofiller ZIF-8-NS provided an interesting reference for the study of ultrafiltration membranes.

One-pot fabrication of hydrophobic, superelastic, harakeke-derived nanocellulose aerogels with excellent shape recovery for oil adsorption and water-in-oil emulsion separation

Cellulose-based aerogels have attracted significant attention for oil/water separation due to their high porosity, large specific surface area and high adsorption capacity. However, their intrinsic hydrophilicity, and inadequate mechanical properties have often limited their practical applications. Traditional freeze-dried cellulose aerogels exhibit unsatisfactory elasticity and require a separate surface modification process to adjust the surface wettability. In this study, we present a novel one-pot fabrication strategy which simultaneously achieves the crosslinking of individual cellulose nanofibers and the hydrophobic modification of the surface wettability. Following directional freeze-drying, hydrophobic, superelastic, and anisotropic cellulose-based aerogel was prepared from the 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO)-oxidized cellulose nanofibers, isolated from harakeke (New Zealand native flax). The resulting aerogel exhibits a high water contact angle of 142°, good compressive recovery performance (85 % recovery of the original height after 100 compression cycles at 70 % strain), and outstanding adsorption capacity for various types of oil and organic solvents (80–105 g/g). Furthermore, the aerogel could also be used as a filter to separate surfactant stabilized water-in-oil emulsions with a high flux (782 L m−2 h−1) and a high separation efficiency (98.7–99.2 %). The novel aerogel prepared in this study is expected to have great potential for practical applications in oily wastewater remediation.

Getting the Best out of Capillary Electrophoresis and Capillary Electrophoresis-Mass Spectrometry by Quantifying Sources of Peak Broadening for Proteins Using Polyelectrolyte Multilayer Coated Fused Silica Capillaries.

Capillary electrophoresis (CE) has emerged as a relevant technique for protein and biopharmaceutical analysis, as it combines high separation efficiency, sensitivity, and versatility. The use of capillary coatings, including successive multiple ionic-polymer layers (SMILs), reduces interactions between analytes and the capillary, further improving the CE performance. Nevertheless, separations done on SMIL coatings rarely surpass 500 × 103 plates/m. To obtain the best out of the CE, it is interesting to have a detailed look at the sources of peak dispersion. Separations of a mix of model proteins were performed on (poly(diallyldimethylammonium chloride)/poly(styrenesulfonate))2.5-coated capillaries at different electrical field strengths, leading to plate height H against migration velocity u plots that enabled a quantitative analysis of each contribution. Using this model, capillary lengths and injected volumes were systematically varied. For the first time, the contribution of sample electrophoretic heterogeneity to the total peak dispersion was deciphered for model proteins and a monoclonal antibody. Dispersion due to electromigration was seen to have an impact on plate heights in the case of triangular peaks of small molecules but not for proteins under the present conditions. UV and mass spectrometry detections were compared on the same capillary, providing valuable information on the impact of the detection type on separation efficiency. Close to 1 million plates/m were reached in the best conditions.

An effective strategy to construct pH-responsive microemulsion for cobalt recovery and its responsive mechanisms

Microemulsions for heavy metal separation show advantages of fast separation rate, high separation efficiency and extraction capacity. However, it remains challenging in destabilizing microemulsions for back-extraction due to their thermodynamic stability. This study describes an effective strategy to construct pH-responsive microemulsion by adding N,N-dimethylethanolamine (DMEA) during back-extraction to avoid the negative impact of responsive materials on the extraction, meanwhile the back-extraction can be realized through a mild pH stimulus compared to traditional strong acid demulsifier. Cetyltrimethylammonium bromide (CTAB)-stabilized microemulsion was formulated and optimized for the selective Co(II) extraction reaching 95.4 %, while extraction efficiency of Ni(II) kept low at 10.5 %. The back-extraction efficiency of Co(II) reached 99.53 %. The responsive mechanism was studied by measuring the dynamic interfacial tension and interfacial dilatational rheology of CTAB solution in heptane under the effects of NaCl, DMEA and pH. By pH stimulus, DMEA protonated and increased the ionic strength, consequently inducing a “salting-out” effect and deactivating CTAB at oil-water interface, ultimately destabilizing the microemulsion. This study proposes a new approach for constructing responsive microemulsions for recovering heavy metals and also provides useful information on its responsive mechanisms by establishing a relationship between interfacial property and macroscopic stability of microemulsions.

High throughput PTFE@PPS /ACFs porous membrane for continuous highly effective oil-water separation

We proposed a feasible and straightforward approach for fabricating a superhydrophobic polytetrafluoroethylene coated polyphenylene sulfide/aramid composite film (PTFE@PPS/ACFs porous membrane) for oil-water separation. This process involves utilizing a wet paper making process combined with a spray coating technique. The PPS/ACFs composite membrane displays a three-dimensional network structure by the application of wet papermaking approach. The uniformly spray coating of PTFE on its surface results in a superhydrophobic PTFE@PPS/ACFs porous membrane (PPAM). The membrane obtained through this method can effectively separate oil and water. It is remarkable in separating oil-water lotion stabilized by surfactant, achieving a separation efficiency of up to 99.9 % with a high flux of 8000 L/m2·h−1. Additionally, owing to the inherent thermal stability of the membrane, the PPAM is recyclable. In summary, the PTFE@PPS/ACFs porous membrane is a promising for separating various oil-water emulsions. Its outstanding performance, including high separation efficiency, flux, and recyclability, underscores its potential for practical applications for oil-water separation.

Simulation and Experimental Validation of a New Separator Design for a Wide Range of Gas Volume Fractions

Summary For downhole gas-liquid separation, it is crucial to maintain high separation efficiency across a wide range of inlet gas volume fractions. In this paper, we present a numerical investigation into the flow field characteristics and separation mechanism of a new gas-liquid separator that utilizes centrifugal and gravity separation methods. An experimental system was built to validate the accuracy of the numerical model, and the numerical results show similar characteristics with experimental data in phase distribution as well as separation efficiency. In addition, we examine the impact of various operational parameters on the separation performance in this study. The findings indicate that the separator is capable of achieving a separation efficiency of approximately 100% within the inlet gas volume fraction range of 40–80%. Furthermore, it is crucial to control the liquid level to ensure effective separation of gas from the water layer. Altering the inlet liquid flow rate and gas volume fraction has a direct influence on the water content of the gas outlet, resulting in a decrease in separation efficiency. Consequently, optimization of the upper region of the separator is necessary to improve the separation performance.

Ultra-hydrophilic MOF-303 on electrospun nanofibers with Burr Puzzles structure for the purification of oily wastewater containing heavy metal ions

The current oil-water separation field is extremely complex and the material system is variable. Therefore, the full process applicability of membrane technology is extremely demanding, both in terms of high oil-water separation efficiency and the treatment of soluble substances in wastewater, such as heavy metal ions. The high demand for membrane performance is accompanied by the complexity of the membrane manufacturing process, resulting in the development of membrane technology being hindered. If we can purify heavy metal ions from wastewater while meeting the conditions of oil-water treatment, and simplify the process flow, it is an innovation that we are happy to see. Herein, the use of a seed pre-embedded growth strategy is taking polyacrylamide (PEI) as a breakthrough point, we take advantage of blending to introduce embedding sites in polyacrylonitrile (PAN) membranes. Uniform growth of MOF-303 with Burr Puzzle structure on membrane surface using in situ hydrothermal growth method. The Burr Puzzles structure on the membrane surface is not only able to effectively deal with nanoscale stabilized oil-water mixture and effectively adsorb heavy metal ions, but also enables the MOF-303 crystals to grow more firmly on the membrane surface, so that the modified membrane still maintains good performance in harsh environments. The separation fluxes of the oil-in-water emulsions were all higher than 6987 L m−2 h−1 for oil-in-water emulsion with a separation efficiency of 98.4 %, and the adsorption efficiency of heavy metal ions was also as high as 98.3 %. After 20 cycles, the membrane maintains its promising performance. Due to its simple preparation process and excellent efficiency of emulsions separation and heavy metal ions separation, simplifies complex membrane processes while meeting the rigors of wastewater treatment. it has great prospects for development in the current complex wastewater treatment process.

Superhydrophilic‐underwater superoleophobic polyvinyl alcohol membranes for oily water treatment

AbstractPolyvinyl alcohol (PVA) and potato starch‐based porous hydrogels have been fabricated and studied for their wettability. The starting material was crosslinked by glutaraldehyde performed via co‐polymerization reaction at room temperature and low temperature (freeze–thaw). The gels were characterized by Fourier transform infrared (FT‐IR), field emission scanning electron microscope (FE‐SEM), thermogravimetric (TG), and powder X‐ray diffraction (PXRD) analysis. The wetting studies of the gels were evaluated at ambient and submerged conditions by considering both oil and water drops as probe liquids. The gels tend to absorb oil and water in air, however, water‐wet gels demonstrated a very high oil contact angle (&gt;150°). The gels demonstrated superoleophobicity, and the underwater oil CA &gt;172° as the concentration (wt%) of PVA was increased in the gels. Overall, the freeze–thaw gels demonstrated higher underwater oil CA, however, both (room temperature and freeze–thaw fabricated) gels demonstrated similar affinity for under‐oil–water absorption and separation. The hydrogel can retain water easily and thus remove water (even dye dissolved in water) with high separation efficiency and recyclability.

Smart anti‐fouling and self‐repairing polymer brushes for efficient oil–water separation

AbstractThe increasing water pollution problem poses a demand for oil–water separation materials, but preparing separation materials with high efficiency and excellent durability remains a great challenge. In this work, we use a diblock polymer brush of polydimethylsiloxane (PDMS) and poly(N,N‐dimethylaminoethyl methacrylate) (PDMAEMA) based on cotton fabric to prepare oil–water separation membranes with high efficiency, good durability, and intelligent self‐repairing properties. Lubricating PDMS brushes reduces the fouling adhesion due to its low surface energy and high flexibility. pH‐responsive PDMAEMA brushes provide good hydrophobicity and an intelligent self‐repairing effect. The prepared Co‐PDMS‐PDMAEMA has high oil flux (&gt;30,000 L m−2 h−1) and high separation efficiency (&gt;99%) even after 10 cycles and its surface character can be recovered under acidic conditions. Overall, the modified cotton fabric made by such a versatile technique is promising in oil–water separation.

On-line enrichment and separation of glycoprotein by capillary electrophoresis based on pH response coating column

A capillary column coated with 3-aminophenylboronic acid (APBA)-functionalized gold nanoparticles (AuNPs@APBA) was prepared via electrostatic self-assembly. The coated column exhibited anti-nonspecific adsorption of glycoproteins, enabling selective online enrichment during capillary electrophoresis (CE). First, gold nanoparticles (AuNPs) were synthesized using the sodium citrate reduction method. Then, APBA was self-assembled electrostatically on the surface of the AuNPs to obtain AuNPs@APBA. This nanomaterial was bonded to the inner wall of a capillary through ion adsorption to produce a AuNPs@APBA-coated capillary column. Glycoproteins were adsorbed via bond formation with boric acid groups under alkaline conditions (pH 8) to generate borate esters. Under acidic conditions (pH 3), the borate esters dissociated to release the glycoproteins, thereby achieving the selective online enrichment and separation of glycoproteins. The AuNPs and AuNPs@APBA were characterized using Fourier transform infrared spectroscopy, and their sizes and Zeta potentials were determined. In addition, the electroosmotic flow (EOF) of the AuNPs@APBA-coated capillary column was measured. The results showed that the surface of the AuNPs was successfully modified with APBA and that AuNPs@APBA was adsorbed on the inner wall of the capillary. The peak area of ovalbumin (OVA) on the AuNPs@APBA-coated column was 26.46 times higher than that on a bare column via conventional electrophoresis. In contrast, the peak area of bovine serum albumin (BSA) only increased by 8.47 times, indicating that the AuNPs@APBA coated column selectively enriched glycoproteins. Evaluation of the reproducibility and stability of this method revealed that the AuNPs@APBA coated capillary column could be used continually for 33-67 h. The relative standard deviations (RSDs) of the peak areas for intra-day (n=5) and inter-day (n=6) analyses were 2.2% and 3.0%, respectively. The developed method was successfully applied to enrich glycoproteins in a 1×106-fold diluted egg white sample. Glycoproteins were not detected using conventional electrophoresis on the bare column, whereas the AuNPs@APBA-coated capillary column effectively enriched and separated glycoproteins, resulting in a peak area of 10469 mAU·ms. Furthermore, the entire enrichment and separation process was completed within 3 min. This new online enrichment and separation method for glycoproteins has the advantages of low sample consumption, simple operation, and high separation efficiency.

Surface-Integrating Oxygen Vacancy and CuxO Nanodots Enabling Synergistic Electric Field and Dual Catalytic Sites Boosting CO2 Photoreduction.

High carrier separation efficiency and rapid surface catalytic reaction are crucial for enhancing catalytic CO2 photoreduction reaction. Herein, integrated surface decoration strategy with oxygen vacancies (Ov) and anchoring CuxO (1 < x < 2) nanodots below 10nm is realized on Bi2MoO6 for promoting CO2 photoreduction performance. The charge interaction between Ov and anchored CuxO enables the formation of enhanced internal electric field, which provides a strong driving force for accelerating the separation of photocharge carriers on the surface of Bi2MoO6 (ηsurf ≈71%). They can also cooperatively reduce the surface work function of Bi2MoO6, facilitating the migration of carrier to the surface. Meanwhile, surface-integrated Ov and CuxO nanodots allowing dual catalytic sites strengthens the adsorption and activation CO2 into *CO2 over Bi2MoO6, considerably boosting the progression of CO2 conversion process. In the absence of co-catalyst or sacrificial agent, Bi2MoO6 with Ov and CuxO nanodots achieves a photocatalytic CO generation rate of 12.75µmol g-1 h-1, a remarkable increase of over ≈15 times that of the original counterpart. This work provides a new idea for governing charge movement behaviors and catalytic reaction thermodynamics on the basis of synergistic improvement of electric field and active sites by coupling of the internal defects and external species.