MXene@c-MWCNT Adhesive Silica Nanofiber Membranes Enhancing Electromagnetic Interference Shielding and Thermal Insulation Performance in Extreme Environments

A lightweight flexible thermally stable composite is fabricated by com-bining silica nanofiber membranes(SNM)with MXene@c-MWCNT hybrid film.The flexible SNM with outstanding thermal insulation are prepared from tetraethyl orthosilicate hydrolysis and condensation by electrospinning and high-temperature calcination;the MXene@c-MWCNT_(x:y)films are prepared by vacuum filtration tech-nology.In particular,the SNM and MXene@c-MWCNT_(6:4)as one unit layer(SMC_(1))are bonded together with 5 wt%polyvinyl alcohol(PVA)solution,which exhibits low thermal conductivity(0.066 W m^(-1)K^(-1))and good electromagnetic interference(EMI)shielding performance(average EMI SE_(T),37.8 dB).With the increase in func-tional unit layer,the overall thermal insulation performance of the whole composite film(SMC_(x))remains stable,and EMI shielding performance is greatly improved,especially for SMC_(3)with three unit layers,the average EMI SET is as high as 55.4 dB.In addition,the organic combination of rigid SNM and tough MXene@c-MWCNT_(6:4)makes SMC_(x)exhibit good mechanical tensile strength.Importantly,SMC_(x)exhibit stable EMI shielding and excellent thermal insulation even in extreme heat and cold environment.Therefore,this work provides a novel design idea and important reference value for EMI shielding and thermal insulation components used in extreme environmental protection equipment in the future.

Noncovalent cross-linked engineering hydrogel with low hysteresis and high sensitivity for flexible self-powered electronics

In this study,the hydrogel network was reinforced by covalent-like hydrogen bonding,and the strong binding ability of boron-nitrogen coordination served as the main driving force.Among them,acrylamide(AM)and 3-acrylamidophenylboronic acid(AAPBA)were the main body,and the numerous hydroxyl groups in the trehalose(Treh)molecule and other polymer groups formed strong hydrogen bonding interactions to improve the mechanical properties of the PAM/PAAPBA/Treh(PAAT)hydrogel and ensured the simplicity of the synthesis process.The hydrogel possessed high strain at break(1239%),stress(64.7 kPa),low hysteresis(100%to 500%strain,corresponding to dissipation energy from 1.37 to 7.80 kJ/m^(3)),and outstanding cycling stability(retained more than 90%of maximum stress after 200 ten-sile cycles).By integrating carbon nanotubes(CNTs)into PAAT hydrogel(PAATC),the PAATC hydrogel with excellent strain response performance was successfully constructed.The PAATC conductive hydro-gel exhibited high sensitivity(gauge factor(GF)=10.58 and sensitivity(S)=0.304 kPa^(-1)),wide strain response range(0.5%-1000%),fast response time(450 ms),and short recovery time(350 ms),excellent fatigue resistance,and strain response stability.Furthermore,the PAATC-based triboelectric nanogener-ator(TENG)displayed outstanding energy harvesting performance,which shows its potential for appli-cation in self-powered electronic devices.

The Capture and Catalytic Conversion of CO_(2) by Dendritic Mesoporous Silica-Based Nanoparticles

Dendritic mesoporous silica nanoparticles own three-dimensional center-radial channels and hierarchical pores,which endows themselves with super-high specific surface area,extremely large pore volumes,especially accessible internal spaces,and so forth.Dissimilar guest species(such as organic groups or metal nanoparticles)could be readily decorated onto the interfaces of the channels and pores,realizing the functionalization of dendritic mesoporous silica nanoparticles for targeted applications.As adsorbents and catalysts,dendritic mesoporous silica nanoparticles-based materials have experienced nonignorable development in CO_(2)capture and catalytic conversion.This comprehensive review provides a critical survey on this pregnant subject,summarizing the designed construction of novel dendritic mesoporous silica nanoparticles-based materials,the involved chemical reactions(such as CO_(2)methanation,dry reforming of CH_(4)),the value-added chemicals from CO_(2)(such as cyclic carbonates,2-oxazolidinones,quinazoline-2,4(1H,3H)-diones),and so on.The adsorptive and catalytic performances have been compared with traditional silica mesoporous materials(such as SBA-15 or MCM-41),and the corresponding reaction mechanisms have been thoroughly revealed.It is sincerely expected that the in-depth discussion could give materials scientists certain inspiration to design brand-new dendritic mesoporous silica nanoparticles-based materials with superior capabilities towards CO_(2)capture,utilization,and storage.

High valence metals engineering strategies of Fe/Co/Ni-based catalysts for boosted OER electrocatalysis

Electrocatalysis for the oxygen evolution reactions(OER)has attracted much attention due to its important role in water splitting and rechargeable metal-air batteries.Therefore,designing highly efficient and low-cost catalysts for OER process is essential as the conventional catalysts still rely on precious metals.Transition metal-based compounds have been widely investigated as active OER catalysts,and renewed interest in the high valence metals engineered compounds has been achieved for superior catalytic activity and stability.However,an in-depth understanding of the construction strategies and induced effects for the high valence metals engineered catalysts is still lacking and desired.In this review,we have summarized the construction strategies of high valence metals as dopants or formed heterostructures with the iron/cobalt/nickel(Fe/Co/Ni)-based catalysts.Then the induced effects on Fe/Co/Ni-based catalysts by incorporating high valence metals,e.g.,accelerating the surface reconstruction,forming amorphous structure,generating vacancies/defects,and acting as stabilizers,are highlighted.The impacts of high valence metals on OER performance are elucidated based on different elements,including molybdenum(Mo),tungsten(W),cerium(Ce),vanadium(V),chromium(Cr),manganese(Mn),niobium(Nb),zirconium(Zr).The correlations of construction strategies,induced effects,catalytic activity and OER reaction pathways are elaborated.Finally,the remaining challenges for further enhancements of OER performance induced by high valence metals are presented.

Advancing the pressure sensing performance of conductive CNT/PDMS composite film by constructing a hierarchical-structured surface

Flexible pressure sensors have attracted wide attention due to their applications to electronic skin,health monitoring,and human-machine interaction.However,the tradeoff between their high sensitivity and wide response range remains a challenge.Inspired by human skin,we select commercial silicon carbide sandpaper as a template to fabricate carbon nanotube(CNT)/polydimethylsiloxane(PDMS)composite film with a hierarchical structured surface(h-CNT/PDMS)through solution blending and blade coating and then assemble the h-CNT/PDMS composite film with interdigitated electrodes and polyurethane(PU)scotch tape to obtain an h-CNT/PDMS-based flexible pressure sensor.Based on in-situ optical images and finite element analysis,the significant compressive contact effect between the hierarchical structured surface of h-CNT/PDMS and the interdigitated electrode leads to enhanced pressure sensitivity and a wider response range(0.1661 kPa^(-1),0.4574 kPa^(-1)and 0.0989 kPa^(-1)in the pressure range of 0–18 kPa,18–133 kPa and 133–300 kPa)compared with planar CNT/PDMS composite film(0.0066 kPa^(-1)in the pressure range of 0–240 kPa).The prepared pressure sensor displays rapid response/recovery time,excellent stability,durability,and stable response to different loading modes(bending and torsion).In addition,our pressure sensor can be utilized to accurately monitor and discriminate various stimuli ranging from human motions to pressure magnitude and spatial distribution.This study supplies important guidance for the fabrication of flexible pressure sensors with superior sensing performance in next-generation wearable electronic devices.

Influence of UVB-Irradiation on the Structures and Solid Particle Erosion Resistance for CF/PC Composites

The service life and properties of Carbon fiber reinforced polycarbonate (CF/PC) composites are seriously affected by ultraviolet radiation from outdoor exposure during aging. In this work, the changes of structure and solid particle erosion resistance for CF/PC composites after ultraviolet irradiation were studied. It was shown that ultraviolet irradiation causes photo-oxygen aging and photo-fries re-arrangement of the composite, and the result was confirmed by FTIR. We correlated the solid particle erosion resistance with aging time, and found that the solid particle erosion resistance of CF/PC composites greatly decreased by UVB irradiation during 15 hours. Furthermore, the eroded material surface was analyzed using scanning electron microscope (SEM). It suggests that ultraviolet aging leads to plasticization and degradation, resulting in reduction of erosion resistance of the composite.

Ni Flower/MXene-Melamine Foam Derived 3D Magnetic/Conductive Networks for Ultra-Efficient Microwave Absorption and Infrared Stealth

The development of multifunctional and efficient electromagnetic wave absorbing materials is a challenging research hotspot.Here,the magnetized Ni flower/MXene hybrids are successfully assembled on the surface of melamine foam(MF)through electrostatic self-assembly and dip-coating adsorption process,realizing the integration of microwave absorption,infrared stealth,and flame retardant.Remarkably,the Ni/MXene-MF achieves a minimum reflection loss(RLmin)of−62.7 dB with a corresponding effective absorption bandwidth(EAB)of 6.24 GHz at 2 mm and an EAB of 6.88 GHz at 1.8 mm.Strong electromagnetic wave absorption is attributed to the three-dimensional magnetic/conductive networks,which provided excellent impedance matching,dielectric loss,magnetic loss,interface polarization,and multiple attenuations.In addition,the Ni/MXene-MF endows low density,excellent heat insulation,infrared stealth,and flame-retardant functions.This work provided a new development strategy for the design of multifunctional and efficient electromagnetic wave absorbing materials.

Vertically Aligned Silicon Carbide Nanowires/Boron Nitride Cellulose Aerogel Networks Enhanced Thermal Conductivity and Electromagnetic Absorbing of Epoxy Composites

With the innovation of microelectronics technology, the heat dissipation problem inside the device will face a severe test. In this work, cellulose aerogel(CA) with highly enhanced thermal conductivity(TC) in vertical planes was successfully obtained by constructing a vertically aligned silicon carbide nanowires(SiC NWs)/boron nitride(BN) network via the ice template-assisted strategy. The unique network structure of SiC NWs connected to BN ensures that the TC of the composite in the vertical direction reaches 2.21 W m^(-1) K^(-1) at a low hybrid filler loading of 16.69 wt%, which was increased by 890% compared to pure epoxy(EP). In addition, relying on unique porous network structure of CA, EP-based composite also showed higher TC than other comparative samples in the horizontal direction. Meanwhile, the composite exhibits good electrically insulating with a volume electrical resistivity about 2.35 × 10^(11) Ω cm and displays excellent electromagnetic wave absorption performance with a minimum reflection loss of-21.5 dB and a wide effective absorption bandwidth(<-10 dB) from 8.8 to 11.6 GHz. Therefore, this work provides a new strategy for manufacturing polymer-based composites with excellent multifunctional performances in microelectronic packaging applications.

Structural engineering of cathodes for improved Zn-ion batteries

Aqueous zinc-ion batteries(ZIBs) are attracting considerable attention because of their low cost,high safety and abundant anode material resources.However,the major challenge faced by aqueous ZIBs is the lack of stable and high capacity cathode materials due to their complicated reaction mechanism and slow Zn-ion transport kinetics.This study reports a unique 3 D ’flower-like’ zinc cobaltite(ZnCo_(2)O_(4-x)) with enriched oxygen vacancies as a new cathode material for aqueous ZIBs.Computational calculations reveal that the presence of oxygen vacancies significantly enhances the electronic conductivity and accelerates Zn^(2+) diffusion by providing enlarged channels.The as-fabricated batteries present an impressive specific capacity of 148.3 mAh g^(-1) at the current density of 0.05 A g^(-1),high energy(2.8 Wh kg^(-1)) and power densities(27.2 W kg^(-1)) based on the whole device,which outperform most of the reported aqueous ZIBs.Moreover,a flexible solid-state pouch cell was demonstrated,which delivers an extremely stable capacity under bending states.This work demonstrates that the performance of Zn-ion storage can be effectively enhanced by tailoring the atomic structure of cathode materials,guiding the development of low-cost and eco-friendly energy storage materials.

Flexible Ag Microparticle/MXene-Based Film for Energy Harvesting

Ultra-thin flexible films have attracted wide attention because of their excellent ductility and potential versatility.In particular,the energy-harvesting films(EHFs)have become a research hotspot because of the indispensability of power source in various devices.However,the design and fabrication of such films that can capture or transform di erent types of energy from environments for multiple usages remains a challenge.Herein,the multifunctional flexible EHFs with e ective electro-/photo-thermal abilities are proposed by successive spraying Ag microparticles and MXene suspension between on waterborne polyurethane films,supplemented by a hot-pressing.The optimal coherent film exhibits a high electrical conductivity(1.17×10^(4)S m^(-1)),excellent Joule heating performance(121.3℃)at 2 V,and outstanding photo-thermal performance(66.2℃ within 70 s under 100 mW cm^(-1)).In addition,the EHFs-based single-electrode triboelectric nanogenerators(TENG)give short-circuit transferred charge of 38.9 nC,open circuit voltage of 114.7 V,and short circuit current of 0.82μA.More interestingly,the output voltage of TENG can be further increased via constructing the double triboelectrification layers.The comprehensive ability for harvesting various energies of the EHFs promises their potential to satisfy the corresponding requirements.

锂-空气电池的实用化之路:规避二氧化碳负面效应

与其他的锂电池体系相比,锂-空气电池具有最高的理论比能量,被认为有潜力成为终极能量转换和储存装置。目前的锂-空气电池常常使用气体钢瓶提供纯氧气,而非空气中的氧气,这种电池设计极大降低了锂-空气电池的能量密度和实用性。然而,当空气作为锂-空气电池的氧气供给源时,二氧化碳作为杂质会引起严重的副反应,从而降低锂-空气电池的性能。要解决二氧化碳引起的副反应,理解其反应机制至关重要。本文综述了锂-空气电池中有关二氧化碳诱发的化学/电化学反应的研究进展;总结了可缓解二氧化碳负面效应的有效策略。此外,对二氧化碳选透膜材料和分离技术用于锂-空气电池进行了展望。

Poly(vinyl alcohol)/Graphene Nanocomposite Hydrogel Scaffolds for Control of Cell Adhesion

Poly(vinyl alcohol)(PVA)/reduced graphene oxide(rGO)nanocomposites is prepared by the immersion of PVA/graphene oxide(GO)nanocomposites in the reducing agent aqueous solution.The PVA/graphene nanocomposites can be used as scaffold after treatment by chemical crosslinking agents.The surface hydrophilicity of the nanocomposite scaffolds decreased with the addition of GO or rGO by measuring the contact angles of scaffolds.The electrical conductivity of PVA/rGO nanocomposite scaffold increased with rGO content increased.The highest conductivity of PVA/rGO nanocomposite scaffolds with 10 wt%rGO could reach to 12.16×10^(−3)S/m.The NIH-3T3 fibroblasts attach and grow well on the surface of PVA/rGO nanocomposite scaffolds with increasing the content of rGO.The number of cells obviously increases on the PVA/rGO nanocomposite scaffolds,especially,at 5 wt%and 10 wt%rGO.Furthermore,a good level of conductivity and a variation in the surface property of the PVA/rGO nanocomposite scaffolds have affected NIH-3T3 fibroblasts grow.

Correction to: Ni Flower/MXene-Melamine Foam Derived 3D Magnetic/Conductive Networks for Ultra-Efficient Microwave Absorption and Infrared Stealth

The original version of this article unfortunately contained some mistakes.The corrections are updated as follows:Error 1:We found that Equations 3,4 and 6 were wrong in the published paper:Error 2:In the page 7,“Since N Ni/MXene-MF possessed numer-ous heterogeneous interfaces and abundant functional groups,the dielectric loss mechanism was explored.”

Improving Strength of Carbon Fiber Grafted Carbon Nanotube Reinforced Thermoplastic Composites by 3D-Printed Molding

To improve the strength of carbon fiber(CF) reinforced Polycaprolactam(PA6) composites, controlled amounts of carbon nanotubes(CNTs) were grafted onto the surface of CF to prepare the hybrid reinforcement(HR). We used HR to fabricate laminate and H-sample to test the interfacial bonding strength(IBS) of the composites by means of a novel process called three-dimensional printed molding(3 D-PM). By using the melt drop printing method, we measured the contact angles between PA6 and CF(without sizing) and between PA6 and HR. The IBS and the mechanical properties of the composites were obtained by the tensile test. The experimental result indicated that CF grafted by 0.25% weight fraction of CNT or more could develop a special microstructure similar to the micro-pits on the surface of CF, which improved the wettability of CF and PA6 due to the increased surface area and the roughness of CF. When the weight fraction of CNT reached 0.25%, the IBS increased by 41.8%, the tensile strength by 130%, and the interfacial shear strength(IFSS) by 238%. The interfacial dimple fracture was observed by Scanning Electron Microscope(SEM), which revealed that the composites were able to absorb more deforming energy before fracture. The modified surface microstructure of CF would prevent crack propagation at the interface and increase the mechanical properties of thermoplastic composites(TPCs).

Effects of Thermal Compressive Strain on the Orientation Recovery for Ultra-Thin CNT-Filled Polypropylene Molding

Due to the strong shearing field during processing,untra-thin injection molded CNT-filled polypropylene(PP) always forms a strong CNT orientation along the flow direction,which results in its anisotropic conductivity.In order to evaluate the mechanism on recovery of the orientation,we processed the molding under the condition of different thermal compressive strains with modified hot-rolling machine.The stability of the molding's conductivity after rolling was studied under the action of alternated loading.The disoriented behavior of the microstructures during rolling was observed by SEM and 2 D-WAXD,and the degree of orientation of CNT was calculated.The conductivity of the sample was measured using a standard two-terminal DC resistor.The results showed that the deformation resistance in the rolling direction was greater than that in the transverse deformation under the action of large thermal compressive strain.The samples would mainly deform in the transverse direction and not elongate in the direction of the rolling,which could speed up the recovery of the orientation structure and reduce the anisotropy of the conductivity.The recovery speed of the orientation was related to the level of the thermal compressive strain.After the hotrolling processing,the stability of the sample's conductivity under the alternating load was improved because of the effect induced by polymer strengthening.

分子间相互作用调控丝素蛋白/聚丙烯酰胺水凝胶的网络形貌和β片结晶,赋予水凝胶优异的黏附、应变和传感性能

丝素蛋白(SF)作为一种特殊的天然聚合物,具有优异的生物相容性、生物降解性和双亲性,是制备柔性传感器的良好候选者.然而,丝素蛋白的高结晶度和结晶不可控性使获得这种出色的仿生水凝胶传感器具有挑战性.纯SF水凝胶是脆性的,没有黏性.在此,我们通过引入聚丙烯酰胺(PAM)到SF水凝胶中来解决这一问题.由于SF/PAM水凝胶具有较强的分子间相互作用,其网络形貌由欧几里得孔改变为非欧几里得孔.同时,其β片结晶很容易被抑制到纳米尺度.这些演变不仅使SF/PAM水凝胶具有优异的机械性能,而且具有出色的黏附性能.与纯PAM水凝胶相比,SF8/PAM水凝胶的拉伸强度、拉伸破坏应变、抗压强度(80%应变下)和黏附性能(在猪皮上)分别提高了133.1%、120.9%、610.8%和104.8%.此外,SF的双亲性可以使碳纳米管(CNTs)在水凝胶中分散良好.制备的CNT0.3/SF8/PAM水凝胶继承并进一步改善了上述性能.除此之外,它还表现出优异的自黏附传感性能,最大灵敏度因子高达10.13,工作应变范围超过1000%,大应变下稳定循环拉伸达500次以上.同时,六种人类活动的精确检测也得到了验证.本工作为实现高性能SF基水凝胶提供了新策略,并证实SF/PAM水凝胶在柔性可穿戴应变传感器中具有广阔的应用前景.

Regulating microstructure and composition by carbonizing in-situ grown metal-organic frameworks on cotton fabrics for boosting electromagnetic wave absorption

High-temperature carbonized metal-organic frameworks(MOFs)derivatives have demonstrated their superiority for promising electromagnetic wave(EMW)absorbers,but they still suffer from limited EMW absorption capacity and narrow bandwidth.Considering the advantage of microstructure and chemical composition regulation for the design of EMW absorber,hierarchical heterostructured MoS_(2)/CoS_(2)-Co_(3)O_(4)@cabonized cotton fabric(CF)(MCC@CCF)is prepared by growing ZIF-67 MOFs onto CF surface,chemical etching,and carbonization.Aside from the dual loss mechanism of magnetic-dielectric multicomponent carbonized MOFs,chemical etching and carbonization process can effectively introduce abundant micro-gap structure that can result in better impedance matching and stronger absorption capacity via internal reflection,doped heteroatoms(Mo,N,S)to supply additional dipolar polarization loss,and numerous heterointerfaces among MoS_(2),CoS_(2),Co_(3)O_(4),and CCF that produce promoted conduction loss and interfacial polarization loss.Thus,a minimal reflection loss of−52.87 dB and a broadest effective absorption bandwidth of 6.88 GHz were achieved via tunning the sample thickness and filler loading,showing excellent EMW absorption performances.This research is of great value for guiding the research on MOFs derivatives based EMW absorbing materials.

Highly oriented MXene/polyvinyl alcohol films prepared by scalable layer-by-layer blade coating for efficient electromagnetic interference shielding and infrared stealth

Controlling the orientation of two-dimensional MXene within layered films is essential to optimize or tune their mechanical properties and electromagnetic interference shielding(EMI)performance,but achieving the high orientation MXene layers on an industrial scale remains a challenging goal.In this paper,a scalable layer-by-layer blade coating(LbLBC)method was employed to fabricate highly oriented MXene/polyvinyl alcohol(PVA)films.During the LbLBC process,MXene/PVA colloid suffered a strong shearing effect,which induced the ordered alignment of MXene nanosheets along the direction of the blade movement.The orientation of MXene can be effectively adjusted by changing the scraping gap of LbLBC,achieving a maximum Herman orientation factor f of 0.81.As a result,the mechanical properties and EMI performance of the as-prepared MXene/PVA films are in direct proportion to their orientation,with the optimal values of tensile strength of 145.5 MPa,fracture strain of 19.6%,toughness of 17.7 MJ·m^(−3),and EMI shielding effectiveness of 36.7 dB.Furthermore,the inherently low mid-infrared(mid-IR)emissivity of MXene,combined with the densely oriented structure affords the composite films with IR stealth,resulting in a substantial decrease from 150 to 66.1℃in the radiative temperature of a surface.Conclusively,these scalable MXene/PVA films exhibit remarkable potential for integration into the next generation of multifunctional protective camouflage materials.

Polyzwitterionic cross-linked double network hydrogel electrolyte enabling high-stable Zn anode

Zn metal anode suffers from dendrite issues and passive byproducts,which severely plagues the practical application of aqueous Zn metal batteries.Herein,a polyzwitterionic cross-linked double network hydrogel electrolyte composed of physical crosslinking(hyaluronic acid)and chemical crosslinking(synthetic zwitterionic monomer copolymerized with acrylamide)is introduced to overcome these obstacles.On the one hand,highly hydrophilic physical network provides an energy dissipation channel to buffer stress and builds a H_(2)O-poor interface to avoid side reactions.On the other hand,the charged groups(sulfonic and imidazolyl)in chemical crosslinking structure build anion/cation transport channels to boost ions’kinetics migration and regulate the typical solvent structure[Zn(H_(2)O)_(6)]^(2+)to R-SO_(3)^(−)[Zn(H_(2)O)_(4)]^(2+),with uniform electric field distribution and significant resistance to dendrites and parasitic reactions.Based on the above functions,the symmetric zinc cell exhibits superior cycle stability for more than 420 h at a high current density of 5 mA·cm^(−2),and Zn||MnO_(2)full cell has a reversible specific capacity of 150 mAh·g^(−1)after 1000 cycles at 2 C with this hydrogel electrolyte.Furthermore,the pouch cell delivers impressive flexibility and cyclability for energy-storage applications.

Assembly of a core–shell MOF with stability into polyacrylamide hydrogel for boosting extraction of uranium from seawater

Efficient and selective extraction of uranium(U(VI))from seawater is essential for sustainable nuclear power production.This study reports a novel adsorbent zeolitic imidazolate framework(ZIF)-67@SiO_(2)-A/polyacrylamide(PAM)which was synthesized by grafting the core–shell metal–organic frameworks(MOFs)-based nanostructures coated with the 3-aminopropyl triethoxysilane(APTES)functionalized SiO_(2)(SiO_(2)-A)onto PAM hydrogel.The SiO_(2) shell was grown on the surface of MOF,which improved the acid-base resistance of MOF.The introduction of ZIF-67@SiO_(2)-A enhances the specific surface area and adsorption efficiency of the PAM.The ZIF-67@SiO_(2)-A/PAM shows remarkable adsorption capacity,fast adsorption kinetics,and good reusability for uranium.It has excellent adsorption property(6.33 mg·g^(-1),30 d)in natural seawater.The X-ray photoelectron spectroscopy(XPS),Fourier transform infrared(FTIR),energy dispersive spectroscopy(EDS)mappings,and density functional theory reveal that the coordination by N and O in ZIF-67@SiO_(2)-A/PAM with uranium is the main mechanism of uranium adsorption.Thus,ZIF-67@SiO_(2)-A/PAM has great potential to capture uranium from natural seawater.