Liquid Metal-Modified 3D Cu Foam for Dendrite-Free Sodium Plating.

Sodium metal is regarded as one of the most promising anode materials due to its high theoretical capacity (1166 mAh g-1) and low redox potential (-2.714 V vs standard hydrogen electrode). However, the practical application of sodium metal is hindered by the formation of dendrites during Na stripping and plating, which can degrade performance and cause potential safety hazards. To address this issue, previous work focuses on leveraging either 3D current collectors or liquid metal modification on current collectors. In this work, both strategies are simultaneously leveraged to design a 3D Cu foam with liquid metal modification (LM@Cu) for dendrite-free sodium plating. The 3D configuration of Cu effectively reduces local current density and evenly distributes electric fields, while the introduction of liquid metal enhances the sodiophilicity of Cu to lower the nucleation barrier for sodium, thereby promoting its uniform plating. As a result, symmetric cells of Na with LM@Cu maintain stable cycling for over 2800 h. Additionally, full cells comprising Na-LM@Cu and Na3V2(PO4)3 sustain 97.5% of the capacity upon 1000 cycles, underscoring the great potentiality of liquid metal-mediated 3D current collectors in energy storage.

Heat transfer and flow characteristics of a plate-fin heat sink equipped with copper foam and twisted tapes.

The objective of this paper is to present new heat transfer enhancement approaches in plate-fin heat sinks (PFHS) using copper foam and twisted tapes. The motivation behind these concepts is to reduce pressure drop while enhancing heat transfer compared to PFHSs fully inserted with copper foam. The impact of twisted tape type, twist ratio, and Reynolds number (Re) on the heat and flow behaviors inside the PFHS equipped with copper foam (PFHSCF) is investigated. Copper foam has a porosity of 0.932 and a pore density of 40 pores per inch. Stationary and rotating twisted tapes with twist ratios between 2.7 and 4 are tested at Re between 3000 and 6000. The experimental results indicated that the pressure drop of the airflow inside a PFHS equipped with copper foam and a stationary twisted tape (PFHSCF_STT) as well as a PFHS equipped with copper foam and rotating twisted tapes (PFHSCF_RTT) decreased by an average of 34.8 % and 37.9 %, respectively, compared to a PFHSCF. When the twist ratio is decreased from 4 to 2.7, the thermal resistances of PFHSCF_STT and PFHSCF_RTT are reduced by 14.2 and 14.8 %, respectively. Based on assessment, the thermal-hydraulic performance of a PFHSCF_RTT with twist ratios of 2.7 and 3.3 is higher than that of a PFHSCF. To facilitate practical applications, correlations are proposed to predict the Nusselt number and friction factor. Additionally, considering the outcomes of the current study, conducting numerical investigations on the thermal performance of PFHS under different pore densities of copper foam and wider twist ratios of twisted tapes is recommended to determine optimal working conditions for future research.

Bilayer Porous Electrocatalysts for Stable and Selective Electrochemical Reduction of CO2 to Formate in the Presence of Flue Gas Containing NO and SO2.

The development of stable and selective electrocatalysts for converting CO2 to value-added chemicals or fuels has gained much interest in terms of their potential to mitigate anthropogenic carbon emissions. Most of the electrocatalysts are tested under pure CO2; however, industrial outlet flue gas contains numerous impurities, such as NO and SO2, which poison the electrocatalysts and alter the product selectivity. Developing electrocatalysts that are resistant to such impurities is essential for commercial implementation. Herein, we prepared bilayer porous electrocatalysts, namely, Sn, Bi, and In, on porous Cu foam mesh (Sn/Cu-f, Bi/Cu-f, and In/Cu-f) by a two-step electrodeposition process and employed these electrodes for the electrochemical reduction of CO2 to formate. It was observed that the bilayer porous electrocatalysts exhibited high CO2 reduction activity compared to catalysts coated on a Cu mesh. Among bilayer porous electrocatalysts, Sn/Cu-f and Bi/Cu-f electrocatalysts showed more than 80% faradaic efficiency (FE) toward formate production, with a formate partial current density of around -16 and -10.4 mA cm-2, respectively, at -1.02 V vs RHE. In/Cu-f electrocatalyst showed nearly 40% formate FE with formate partial current density of -15 mA cm-2 at -1.22 V vs RHE. We investigated the effect of NO and SO2 impurities (500 ppm of NO, 800 ppm of SO2, and 500 ppm of NO + 800 ppm of SO2) on these electrocatalysts' selectivity and stability toward formate. It was observed that the Bi/Cu-f electrocatalyst showed 50 h stability with 80 ± 5% formate FE, and Sn/Cu-f showed 18 h stability with above 80 ± 5% efficiency in the presence of NO and SO2 mixed with CO2. Furthermore, we studied the effect of CO2 concentration with Sn/Cu-f and Bi/Cu-f catalysts in the range of 15-100% CO2, for which formate FEs of 45-80% were observed.

Stable Lithium Metal Batteries Enabled by Lithiophilic Core-Shell Nanowires on Copper Foam.

Lithium (Li) metal batteries have attracted considerable research attention due to their exceptionally high theoretical capacity. However, the commercialization of Li metal batteries faces challenges, primarily attributed to uncontrolled growth of Li dendrites, which raises safety concerns and lowers coulombic efficiency. To mitigate Li dendrites growth and attain dense Li deposition, the hybrid SiO2-Cu2O lithiophilic film applied to a 3D copper foam current collector is developed to regulate the interfacial properties for achieving even and dense Li deposition. The SiO2-Cu2O possesses strong Li+ trapping capability through strong lithiophilicity from Cu2O. Additionally, the SiO2-Cu2O enables uniform ion diffusion through the domain-limiting effect of the holes in the SiO2 layer, inducing an even and dense Li plating/stripping behavior at a large capacity. Furthermore, the SiO2 layer promotes the formation of an initial high inorganic content Solid Electrolyte Interphase (SEI) through selective preferential binding with anion and solvent molecules. When the SiO2-Cu2O@Li anode is coupled with a LiFePO4 (LFP) cathode, the resulting full cell exhibits superior cycling stability and rate performance. These results provide a facile approach to construct a lithiophilic current collector for practical Li metal anodes.

Achieving Long Cycle Life of Zn-Ion Batteries through Three-Dimensional Copper Foam.

Metallic zinc anodes in aqueous zinc-ion batteries (ZIBs) suffer from dendritic growth, low Coulombic efficiency, and high polarization during cycling. To mitigate these challenges, current collectors based on three-dimensional (3D) commercial copper foam (CCuF) are generally preferred. However, their utilization is constrained by their thickness, low electroactive surface area, and increased manufacturing expenses. In this study, the synthesis of cost-effective current collectors with exceptionally large surface areas designed for ZIBs that can be cycled hundreds of times is reported. A zinc-coated CuF anode (Zn/CuF) was prepared with a 3D porous CuF current collector produced by the dynamic hydrogen bubble template (DHBT) method. Electrochemically generated copper foam could be obtained within seconds while offering a thickness as low as 30-40 µm (CuF5 achieved a thickness of ∼38 µm in 5 s) via the DHBT method. The excellent electrical conductivity and open pore structure of the 3D porous copper scaffold ensured the uniform deposition/stripping of Zn during cycling. During the 500 h Zn deposition/stripping process, the as-synthesized CuF5 current collector offered fast electrochemical kinetics and low polarization as well as a relatively high average Coulombic efficiency of 99% (at a current density of 5 mA cm-2 and a capacity of 1 mAh cm-2). Furthermore, the symmetric cell exhibited low voltage polarization and a stable voltage profile for 1000 h at a current density of 0.1 mA cm-2. In addition, full cells containing the Zn/CuF anode coupled with an as-synthesized α-MnO2 nanoneedle cathode in aqueous electrolyte were also prepared. Capacities of 266 mAh g-1 at 0.1 A g-1 and 94 mAh g-1 at 2 A g-1 were achieved after 200 charge/discharge cycles with a stable Coulombic efficiency value close to 99.9%.

Enhanced visible-light activation of persulfate for the removal of RhB by supported nano-(C,N,B)-tridoped TiO2/copper foam mixed-crystals.

Photocatalytic persulfate activation by TiO2 and its application in sewage treatment have aroused great interest because of its high decontamination ability and strong adaptability, but the low light energy utilization rate and poor recycling of TiO2 limited its practical application. Herein, by using C-, N-, and B-modified TiO2 and immobilizing it on copper foam, we prepared a new and efficient (C,N,B)-TiO2/copper foam photocatalyst with enhanced visible-light activation performance of persulfate for the removal of RhB. It almost completely degraded RhB within 15 min of UV-vis light photocatalysis-assisted persulfate oxidation reaction with TOC removal of 53.17% in 30 min and presented the excellent long-term recyclability and stability, which is much better or comparative than those photocatalysts in the related literatures. (C,N,B)-TiO2/copper foam exhibited the largest apparent rate constant (0.149 min-1), 1.16 times higher than (C,N,B)-TiO2 (0.128 min-1), and 2.40 times higher than that of TiO2 (0.062 min-1), respectively. C,N,B doping modified the crystalline phase of TiO2, narrowed its band gap, and reduced charge-carrier recombination rate. These, together with the synergistic effect between photocatalysis and persulfate activation for enhancing generation of active species, jointly promoted the performance enhancement of TiO2. The 1O2 was the primary oxidation active species for the degradation of RhB, and the radical species (SO4•-, •O2-, and •OH) could further accelerate the photocatalytic activation of persulfate reaction.

Multi-Functional Janus Hollow Solar Evaporator Based on Copper Foam for Non-Contact High-Efficiency Solar Interfacial Distillation.

As a sustainable, clean, and friendly technology with a minimal carbon footprint when treating seawater or wastewater, interfacial solar vapor generation (ISVG) technology is a great alternative to traditional desalination and water purification methods (e.g., reverse osmosis and ultrafiltration). So far, it presents tremendous potential for applications in realizing desalination of seawater or brine, wastewater treatment, and so forth. However, the precipitated salt particles during conventional ISVG inevitably block the evaporator surface, resulting in the degradation of photothermal conversion and decrease of evaporation rate. Herein, a multi-functional non-contact Janus hollow evaporator based on copper foam was prepared, which was assembled by a hydrophobic light-to-heat conversion layer and a hydrophilic interfacial water evaporation layer as two separate parts. Accordingly, the precipitated salt in the ISVG system does not block the photothermal interface, increasing the stability of solar capture and reusability of the evaporator. Notably, the hollow structure of the evaporator has a local interfacial heating effect, endowing the evaporation system with a high seawater evaporation rate of 2.249 kg m-2 h-1. The evaporator is capable of stable operation for 10 h under 1 sun illumination even when evaporating concentrated brine (15 wt %). Moreover, the evaporation rate of water under one sun irradiation reached 2.284 kg m-2 h-1 and the solar-to-vapor efficiency reached 96.6%. Not only that, the evaporator was able to successfully purify wastewater containing dyes and heavy metal ions. The multi-functional Janus hollow interfacial solar evaporator will provide inspiration for upcoming research on the production of safety water.

Cobalt Oxide Arrays Anchored to Copper Foam as Efficient Binder-free Anode for Lithium Ion Batteries.

The development of lithium-ion batteries with simplified assembling steps and fast charge capability is crucial for current battery applications. In this study, we propose a simple in-situ strategy for the construction of high-dispersive cobalt oxide (CoO) nanoneedle arrays, which grow vertically on a copper foam substrate. It is demonstrated that this nanoneedle CoO electrodes provide abundant electrochemical surface area. The resulting CoO arrays directly act as binder-free anodes in lithium-ion batteries with the copper foam functioning as the current collector. The highly-dispersed feature of the nanoneedle arrays enhances the effectiveness of active materials, leading to outstanding rate capability and superior long-term cycling stability. These impressive electrochemical properties are attributed to the highly-dispersed self-standing nanoarrays, the advantages of binder-free constituent, and the high exposed surface area of the copper foam substrate compared to copper foil, which enrich active surface area and facilitate charge transfer. The proposed approach to prepare binder-free lithium-ion battery anodes streamlines the electrode fabrication steps and holds significant promise for the future development of the battery industry.

A facile heat-treatment solid phase microextraction method for SERS detection of isocarbophos in tea using a hand-held Raman spectrometer.

A facile sensor system based on heat-treatment solid phase microextraction and Surface-Enhanced Raman Scattering (HT-SPME-SERS) was established for in-situ detection of isocarbophos in complex tea matrix. Starting from the action optimization of temperature control unit and air flow control unit, pesticide molecules volatilizing from solution are efficiently captured by substrate and generate real-time SERS signals by a hand-held Raman spectrometer, and the sensor system based on HT-SPME-SERS was finally established. A novel SERS substrate of Cu@rGO@Ag was developed as HT-SPME-SERS material, where reduced graphene oxide (rGO) enriched pesticide molecules by π-π stacking. A superior detection sensitivity brought by the ultra-high enhancement effect of Cu@rGO@Ag substrate was obtained. A good linear relationship between Raman intensity and isocarbophos concentration was obtained and the limit of detection (LOD) was as low as 0.00451 ppm. The detection results obtained from the sensor system have been verified by gas chromatography-mass spectrometer (GC-MS), showing its great application potential for the safety of agricultural products.

Optical-Concentrating Solar Distillation Based on Three-Dimensional Copper Foam Cubes Coated with CuS Nanoparticles and Agarose Gel.

Solar distillation by interfacial evaporation is a promising method for relieving the freshwater crisis. However, the solar-to-water generation rate inside an enclosed system is usually lower than the solar-to-vapor evaporation rate in an open system due to the lower mass transfer rate. In this work, we demonstrate high rate solar distillation based on a three-dimensional copper foam (CF) cube, which offers five surfaces for absorbing direct and reflected sunlight to achieve optical concentration. The CF surface was first oxidized into black CuO and then dip-coated with a mixture of CuS nanoparticles (CuSNPs) and agarose gel (AG) for enhancing near-infrared (NIR) absorption and water transport. The open interconnected pores within the CF cube provide a large surface area for evaporation and steam escape. In an open space, the CuSNPs/AG-coated oxidized CF cube with the five surfaces illuminated by sunlight can achieve the solar-to-vapor evaporation rate equal to 5.83 kg m-2 h-1. When the same CF cube was placed in an enclosed distillation chamber with the five chamber surfaces illuminated by sunlight, the solar-to-water generation rate is equal to 4.14 kg m-2 h-1, which is 5.34 times higher than the case with only the top chamber surface illuminated. Lastly, when real seawater was used for distillation, although the solar-to-water generation rate was decreased by about 30%, the distillation efficiency was consistent after repeated cycles and no obvious salt accumulation was observed on the light absorbing surface. This work presents an efficient and reliable method of optical concentration for enhancing the solar distillation rate in an enclosed system.

3D Solar Evaporation Enhancement by Superhydrophilic Copper Foam Inverted Cone and Graphene Oxide Functionalization Synergistic Cooperation.

Solar evaporation has become a promising and sustainable technique for harvesting freshwater from seawater and wastewater. However, the applicability and efficacy of solar evaporation need further improvement to achieve high production closer to theoretical limits in compact systems. A 3D (three-dimensional) hierarchical inverted conical solar evaporation is developed, which consists of a 3D copper foam skeleton cone decorated with micro-/nano-structures functionalized with graphene oxide, fabricated via easy and scalable wet oxidation, impregnation, and drying at room temperature. The proposed configuration empowers high-efficiency solar absorption, continuous liquid film spreading and transport, enhanced interfacial local evaporation, and rapid vapor diffusion through the pores. More notably, the 3D conical evaporator realizes thermal localization at the skeleton interface and allows evaporation to occur along the complete structure with unimpeded liquid and vapor rapid diffusion. The solar-thermal evaporation efficiency under 1-Sun is as high as 93% with a maximum evaporation rate per unit area of 1.71 kg·m-2 ·h-1 . This work highlights the benefits of synergistic cooperation of an easily scalable 3D hierarchical functiomicro-/nano-structured copper foam skeletons and functionalized graphene oxide for high-efficient solar evaporation of interest to numerous applications.

A copper foam-based surface-enhanced Raman scattering substrate for glucose detection.

Raman spectroscopy can quickly achieve non-destructive, qualitative and quantitative detection, and analysis the molecular structure of substances. Herein, a facile and low-cost method for preparation of highly sensitivity SERS substrates was implemented through the displacement reaction of copper foam immersed in AgNO3 ethanol solution. Due to the 3D structure of copper film and homogenous displacement, the Ag-Cu substrate showed high performance SERS enhancement (1.25 × 107), and the lowest detection concentration for R6G reached 10-10 Mol/L. For glucose detection, mixed decanethiol (DT)/mercaptohexanol (MH) interlayer was used to enable glucose attach to the substrate surface, and the limit of detection reached to 1 uM/L. SERS substrate makes the Ag-Cu SERS substrate promising for biological applications.

Achieving Self-Supported Hierarchical Cu(OH)2/Nickel-Cobalt Sulfide Electrode for Electrochemical Energy Storage.

Herein, nickel-cobalt sulfide (NCS) nanoflakes covering the surface of Cu(OH)2 nanorods were achieved by a facile two-step electrodeposition strategy. The effect of CH4N2S concentration on formation mechanism and electrochemical behavior is investigated and optimized. Thanks to the synergistic effect of the selected composite components, the Cu(OH)2/NCS composite electrode can deliver a high areal specific capacitance (Cs) of 7.80 F cm-2 at 2 mA cm-2 and sustain 5.74 F cm-2 at 40 mA cm-2. In addition, coulombic efficiency was up to 84.30% and cyclic stability remained 82.93% within 5000 cycles at 40 mA cm-2. This innovative work provides an effective strategy for the design and construction of hierarchical composite electrodes for the development of energy storage devices.

A Tin Oxide-Coated Copper Foam Hybridized with a Gas Diffusion Electrode for Efficient CO2 Reduction to Formate with a Current Density Exceeding 1 A cm-2.

The electrochemical CO2 reduction reaction (CO2 RR) is a promising strategy for closing the carbon cycle. Increasing the current density ( J) for CO2 RR products is a critical requirement for the social implementation of this technology. Herein, nanoscale tin-oxide-modified copper-oxide foam is hybridized with a carbon-based gas-diffusion electrode (GDE). Using the resultant electrode, the Jformate is increased to -1152 mA cm-2 at -1.2 V versus RHE in 1 m KOH, which is the highest value for CO2 -to-formate electrolysis. The formate faradaic efficiency (FEformate ) reaches ≈99% at -0.6 V versus RHE. The achievement of ultra-high-rate formate production is attributable to the following factors: i) homogeneously-modified Sn atoms suppressing H2 evolution and ii) the hydrophobic carbon nanoparticles on GDEs penetrating the macroporous structure of the foam causing the increase in the thickness of triple-phase interface. Additionally, the FEformate remains at ≈70% under a high J of -1.0 A cm-2 for more than 20 h.

SiOxCy Microspheres with Homogeneous Atom Distribution for a High-Performance Li-Ion Battery.

The broad application of silicon-based materials is limited by large volume fluctuation, high preparation costs, and complicated preparation processes. Here, we synthesized SiOxCy microspheres on 3D copper foams by a simple chemical vapor deposition method using a low-cost silane coupling agent (KH560) as precursors. The SiOxCy microspheres are available with a large mass loading (>3 mg/cm2) on collectors and can be directly used as the electrode without any binders or extra conductive agents. As a result, the as-prepared SiOxCy shows a high reversible capacity of ∼1240 mAh g-1 and can be cycled more than 1900 times without decay. Ex situ characterizations show that the volume change of the microspheres is only 55% and the spherical morphology as well as the 3D structure remain intact after cycles. Full-cell electrochemical tests paired with LiFePO4 as cathodes show 87% capacity retention after 500 cycles, better than most reported results, thus showing the commercial potential of the material.

Ultraviolet-Driven Janus Foams with Wetting Gradients: Unidirectional Penetration Control for Underwater Bubbles.

Understanding the behavior of underwater bubbles and enabling their effective manipulation is important for bubble capture, collection, and transport. Here, to discuss the underwater permeation behavior of bubbles and critical influencing parameters in this process, the copper foams with tunable wettability were fabricated by utilizing the light-stimulated wettability response of TiO2. The Janus copper foams had different wettability gradients from superhydrophobic/hydrophobic to superhydrophobic/hydrophilic after UV irradiation at different times, and the bubbles on the surfaces showed distinctly diverse penetration behaviors. In particular, the constructed superhydrophobic/hydrophilic surfaces showed more difficult to achieve bubble penetration than the fully superhydrophobic, superhydrophobic/hydrophobic surface. It was found that the wetting states of the foams exposed to different irradiation times underwater plays a crucial role in the bubble penetration behavior. In other words, the difficulty of bubble penetration depends on the difficulty of bubble transition from gas-liquid contact to gas-solid contact. This facile and low-cost fabrication approach for Janus foams provided a valuable approach to understand the penetration behaviors of underwater bubbles, which is significant for expanding potential applications in bubble capture, bubble transport, and control of unstable gas reactions in underwater conditions.

Copper Foam as Active Catalysts for the Borylation of α, ß-Unsaturated Compounds.

The use of simple, inexpensive, and efficient methods to construct carbon-boron and carbon-oxygen bonds has been a hot research topic in organic synthesis. We demonstrated that the desired ß-boronic acid products can be obtained under mild conditions using copper foam as an efficient heterogeneous catalyst. The structure of copper foam before and after the reaction was investigated by polarized light microscopy (PM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), and the results have shown that the structure of the catalyst copper foam remained unchanged before and after the reaction. The XPS test results showed that the Cu(0) content increased after the reaction, indicating that copper may be involved in the boron addition reaction. The specific optimization conditions were as follows: CH3COCH3 and H2O were used as mixed solvents, 4-methoxychalcone was used as the raw material, 8 mg of catalyst was used and the reaction was carried out at room temperature and under air for 10 h. The yield of the product obtained was up to 92%, and the catalytic efficiency of the catalytic material remained largely unchanged after five cycles of use.

Enhanced reactive oxygen species via in situ producing H2O2 and synchronous catalytic conversion at stable modified copper foam cathode for efficient high-concentration organic wastewater treatment and simultaneous electricity generation.

Efficient high-concentration organics degradation (including 2-CP, phenol, and tetracycline) and simultaneous electricity generation were achieved via in situ producing H2O2 and synchronous catalytic conversion to more reactive oxygen species at stable modified copper foam cathode. The cathode was synthesized using the one-pot electrodeposition method and was used to in-situ generate H2O2 through the two-electron reduction of oxygen. The produced H2O2 was then catalytically converted into ·OH and ·O2- simultaneously. The results showed that the system using the Au-Fe co-modified cathode achieved an optimal rhodamine b (50 mg L-1) removal ratio and the removal ratios of 2-CP, phenol and tetracycline were all higher than 90% in 120 min. Meanwhile, it exhibited a high conversion performance of organics into electricity, which is superior to most of the reported PFC (Photocatalytic Fuel Cell) systems. Electron spin resonance test was conducted to ascertain the role of ·O2- and ·OH in the organics degradation. Furthermore, the Au-Fe-modified cathode exhibited superior stability for long-term application in the pH range of 3-7, which can be attributed to the protection of photocurrent and the interaction between Cu and Fe.

Temperature Effects on the Compressive Behaviors of Closed-Cell Copper Foams Prepared by Powder Metallurgy.

A fabrication technology of closed-cell copper foams (CCCFs) based on powder metallurgy is proposed, by using the expanded polystyrene foams (EPS) spheres with the prescribed diameter as the space holder before sintering. The material characterization and the quasi-static compressive behaviors of both uniform and graded CCCFs at different temperatures were experimentally studied. A high temperature weakens the initial compressive modulus, plateau stress, and effective energy absorption for both uniform and graded CCCFs; meanwhile, the onset strain of densification and the maximum energy absorption efficiency are less sensitive to temperature, especially for the graded CCCFs. Compared with the uniform CCCF, the graded CCCF with even a small relative density exhibits superiority in terms of the effective energy absorption and the maximum energy absorption efficiency, attributed to the much larger onset strain of densification for the gradient pore arrangement. Finite element simulations based on the ideal sphere foam model can basically mimic the compressive performance of the CCCF samples. It is also found that both the decrease of pore diameter and the increase of cell wall thickness could improve the compressive performance of the CCCFs.

Easily Fabricated Low-Energy Consumption Joule-Heated Superhydrophobic Foam for Fast Cleanup of Viscous Crude Oil Spills.

Effective cleanup of viscous crude oil spills remains a persistent and crippling challenge. Herein, this work presents a Joule-heated superhydrophobic flower-like Cu8(PO3OH)2(PO4)4·7H2O-coated copper foam (SHB-CF@CP) for rapid cleanup of viscous crude oil spills via a facile strategy. The SHB-CF@CP shows outstanding water repellency and excellent stability of hydrophobicity in harsh environments. Due to the high electrical conductivity and thermal conductivity, it requires lower power energy consumption (less than 1 V of voltage input) to raise the temperature significantly, which dramatically reduces the viscosity of crude oil (from ∼2 × 105 to ∼60 mPa s) and then increases the oil absorption rate, effectively avoiding the poor mobility and ineffective absorption of viscous crude oil. Notably, the SHB-CF@CP can achieve continuous and quick cleanup of crude oil under in situ pumping force. The high-performance Joule-heated SHB-CF@CP sorbent with a strong porous skeleton, corrosion resistance, and low predicted operational costs holds a promise of promoting its practical applications in the cleanup of intractable and large-area viscous oil spills.