共查询到20条相似文献,搜索用时 16 毫秒
1.
Juliana Isabel Clodt Volkan Filiz Sofia Rangou Kristian Buhr Clarissa Abetz Daniel Höche Janina Hahn Adina Jung Volker Abetz 《Advanced functional materials》2013,23(6):731-738
Double stimuli‐responsive membranes are prepared by modification of pH‐sensitive integral asymmetric polystyrene‐b‐poly(4‐vinylpyridine) (PS‐b‐P4VP) diblock copolymer membranes with temperature‐responsive poly(N‐isopropylacrylamide) (pNIPAM) by a surface linking reaction. PS‐b‐P4VP membranes are first functionalized with a mild mussel‐inspired polydopamine coating and then reacted via Michael addition with an amine‐terminated pNIPAM‐NH2 under slightly basic conditions. The membranes are thoroughly characterized by nuclear magnetic resonance (1H‐NMR), Fourier transform infrared spectroscopy and X‐ray‐induced photoelectron spectroscopy. Additionally dynamic contact angle measurements are performed comparing the sinking rate of water droplets at different temperatures. The pH‐ and thermo‐double sensitivities of the modified membranes are proven by determining the water flux under different temperature and pH conditions. 相似文献
2.
Anping Cao Roel J. H. van Raak Xinglong Pan Dirk J. Broer 《Advanced functional materials》2019,29(28)
Azobenzene‐containing liquid crystal polymer networks (LCNs) are developed for temperature‐ and light‐regulated gas permeation. The order in a chiral‐nematic LCN (LCN*) is found to be essential to couple the unique structure of the membrane and its gas permeation responses to external stimuli such as temperature and varying irradiation conditions. An LCN membrane polymerized in the isotropic phase exhibits enhanced N2 permeation with increasing temperature, like most traditional polymers, but barely responds to exposure with 455 and 365 nm light. In sharp contrast, a reversible decrease of N2 transport is observed for the LCN* membrane of exactly the same chemical composition, but molecularly ordered, when submitted to an elevated temperature. More importantly, alternating in situ illumination with 455 and 365 nm light modulates reversibly N2 permeation performance of the LCN* membrane, through the trans–cis isomerization of azo moieties. The authors postulate that, besides the anisotropic deformation of LCN*, the decreased order in LCN* membrane caused by external stimuli (i.e., increasing temperature or UV light illumination) is responsible for an inhibition of gas permeation. These results show potential applications of liquid crystal polymers in the gas transport and separation, and also contribute to the development of “smart” membranes. 相似文献
3.
Ultrathin β‐MnOOH nanofibers can be produced on a large scale via a green‐chemical method using an aqueous solution of very dilute Mn(NO3)2 and aminoethanol at room temperature. High‐magnification electron microscopy demonstrates that the β‐MnOOH nanofibers are 3–5 nm thin and up to 1 micrometer long and the nanofibers are parallel assembled into bundles with an average diameter of 25 nm. By a filtration process, ultrathin mesoporous membranes with strong mechanical, thermal, and chemical stabilities are prepared from the β‐MnOOH nanofiber bundles. The membranes can separate 10‐nm nanoparticles from water at a flux of 15120 L m?2·h?1·bar?1, which was 2–3 times higher than that of commercial membranes with similar rejection properties. Based on the Young‐Laplace equation, β‐MnOOH nanofiber/polydimethylsiloxane composite membranes are developed through a novel downstream‐side evaporation process. From nanoporous to dense separation membranes can be achieved by optimizing the experimental conditions. The membranes show desirable separation performance for proteins, ethanol/water mixtures, and gases. The synthesis method of β‐MnOOH nanofibers is simple and environmentally friendly, and it is easily scalable for industry and applicable to other metal oxide systems. These composite membranes constitute a significant contribution to advanced separation technology. 相似文献
4.
Loren A. Perelman Troy Moore Jennifer Singelyn Michael J. Sailor Ester Segal 《Advanced functional materials》2010,20(5):826-833
A multifunctional nanohybrid composed of a pH‐ and thermoresponsive hydrogel, poly(N‐isopropylacrylamide‐co‐acrylic acid) [poly(NIPAM‐co‐AAc)], is synthesized in situ within the mesopores of an oxidized porous Si template. The hybrid is characterized by electron microscopy and by thin film optical interference spectroscopy. The optical reflectivity spectrum of the hybrid displays Fabry–Pérot fringes characteristic of thin film optical interference, enabling direct, real‐time observation of the pH‐induced swelling, and volume phase transitions associated with the confined poly(NIPAM‐co‐AAc) hydrogel. The optical response correlates to the percentage of AAc contained within the hydrogel, with a maximum change observed for samples containing 20% AAc. The swelling kinetics of the hydrogel are significantly altered due to the nanoscale confinement, displaying a more rapid response to pH or heating stimuli relative to bulk polymer films. The inclusion of AAc dramatically alters the thermoresponsiveness of the hybrid at pH 7, effectively eliminating the lower critical solution temperature (LCST). The observed changes in the optical reflectivity spectrum are interpreted in terms of changes in the dielectric composition and morphology of the hybrids. 相似文献
5.
Santosh B. Rahane J. Alaina Floyd Andrew T. Metters S. Michael Kilbey II 《Advanced functional materials》2008,18(8):1232-1240
Surface‐initiated photoiniferter‐mediated photopolymerization (SI‐PMP) in presence of tetraethylthiuram disulfide is used to directly synthesize surface‐grafted poly(methacrylic acid)‐block‐poly(N‐isopropylacrylamide) (PMAA‐b‐PNIPAM) layers. The response of these PMAA‐b‐PNIPAM bi‐level brushes to changes in pH, temperature and ionic strength is investigated by using in‐situ multi‐angle ellipsometry to measure changes in solvated layer thickness. As expected for a block copolymer architecture, PMAA blocks swell as pH is increased, with the maximum change in the thickness occurring near pH = 5, and PNIPAM blocks exhibit lower critical solution temperature (LCST) behavior, marked by a broad transition between swollen and collapsed states. The response of the bi‐level brushes to changes in added salt at constant pH is complex, as the swelling behaviors of both the weak polyelectrolyte, PMAA, and thermoresponsive PNIPAM are affected by changes in ionic strength. This work demonstrates not only the robustness of SI‐PMP for making novel, bi‐level stimuli‐responsive brushes, but also the complex links between synthesis, structure, and response of these materials. 相似文献
6.
J.‐B. Qu L.‐Y. Chu M. Yang R. Xie L. Hu W.‐M. Chen 《Advanced functional materials》2006,16(14):1865-1872
In this study, we report on a novel composite membrane system for pH‐responsive controlled release, which is composed of a porous membrane with linear grafted, positively pH‐responsive polymeric gates acting as functional valves, and a crosslinked, negatively pH‐responsive hydrogel inside the reservoir working as a functional pumping element. The proposed system features a large responsive release rate that goes effectively beyond the limit of concentration‐driven diffusion due to the pumping effects of the negatively pH‐responsive hydrogel inside the reservoir. The pH‐responsive gating membranes were prepared by grafting poly(methacrylic acid) (PMAA) linear chains onto porous polyvinylidene fluoride (PVDF) membrane substrates using a plasma‐graft pore‐filling polymerization, and the crosslinked poly(N,N‐dimethylaminoethyl methacrylate) (PDM) hydrogels were synthesized by free radical polymerization. The volume phase‐transition characteristics of PMAA and PDM were opposite. The proposed system opens new doors for pH‐responsive “smart” or “intelligent” controlled‐release systems, which are highly attractive for drug‐delivery systems, chemical carriers, sensors, and so on. 相似文献
7.
Extremely long and thin nanocomposite fibers are prepared by oxidative polymerization of pyrrole (or aniline) around the surfaces of copper hydroxide nanostrands. The individual nanostrands of 2.5 nm are uniformly coated with a polypyrrole layer of 3 to 4 nm, resulting in hybrid core/shell fibers of about 10 nm in diameter and a few micrometers in length, as confirmed by high‐resolution electron microscopy. The as‐prepared nanocomposite fibers are dispersive in water and can be converted into thin free‐standing films by simply filtering a small volume of the aqueous solution using a polycarbonate membrane filter. The films covering the submicrometer pores of the membrane filter have a thickness of a few tens of nanometers, and provide a mechanically stable nanofiber network with abundant pores of a few nanometers. The network is stable in acidic and basic media, and can be used for protein separation under pressures of at least 90 kPa. The permeation rates of cytochrome c, myoglobin, and ferritin were examined by changing the pH around their isoelectric points. It is seen that the nanofibrous free‐standing films on the polycarbonate membrane filter show clear size selectivity for the proteins, retaining extremely high filtration rates for water. We demonstrate herein durable mesoporous separation membranes made of organic–inorganic nanocomposite fibers and their outstanding performance. 相似文献
8.
Sub‐10 nm Wide Cellulose Nanofibers for Ultrathin Nanoporous Membranes with High Organic Permeation
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Qiu Gen Zhang Chao Deng Faizal Soyekwo Qing Lin Liu Ai Mei Zhu 《Advanced functional materials》2016,26(5):792-800
There are increasing requirements for highly efficient and solvent‐resistant nanoporous membranes in various separation processes. Traditional membranes usually have a poor solvent resistance and a thick skin layer leading to a low permeation flux. Currently, the major challenge lies in fabrication of ultrathin few‐nanometers‐pore membranes for fast organic filtration. Herein, a facile approach is presented to prepare ultrafine cellulose nanofibers for fabrication of ultrathin nanoporous membranes. The obtained nanofibers have a uniform diameter of 7.5 ± 2.5 nm and are homogeneously dispersed in aqueous solutions that are favorable to the fabrication of ultrathin nanoporous membranes. The resulting cellulose nanoporous membranes have an adjustable thickness down to 23 nm and pore sizes ranging from 2.5 to 12 nm. They allow fast permeation of water and organics during pressure‐driven filtration. Typically, the 30 nm thick membrane has high fluxes of 1.14 and 3.96 × 104 L h?1 m?2 bar?1 for pure water and acetone respectively. Furthermore, the as‐prepared cellulose nanofibers are easily employed to produce a novel syringe filter with sub‐10 nm pores that have a wide application in fast separation and purification of nanoparticles on few‐nanometers scale. 相似文献
9.
Maria Giovanna Buonomenna Giovanni Golemme Caterina Maria Tone Maria Penelope De Santo Federica Ciuchi Enrico Perrotta 《Advanced functional materials》2012,22(8):1759-1767
The preparation and characterization of new, tailor‐made polymeric membranes using poly(styrene‐b‐butadiene‐b‐styrene) (SBS) triblock copolymers for gas separation are reported. Structural differences in the copolymer membranes, obtained by manipulation of the self‐assembly of the block copolymers in solution, are characterized using atomic force microscopy, transmission electron microscopy, and the transport properties of three gases (CO2, N2, and CH4). The CH4/N2 ideal selectivity of 7.2, the highest value ever reported for block copolymers, with CH4 permeability of 41 Barrer, is obtained with a membrane containing the higher amount of polybutadiene (79 wt%) and characterized by a hexagonal array of columnar polystyrene cylinders normal to the membrane surface. Membranes with such a high separation factor are able to ease the exploitation of natural gas with high N2 content. The CO2/N2 ideal selectivity of 50, coupled with a CO2 permeability of 289 Barrer, makes SBS a good candidate for the preparation of membranes for the post‐combustion capture of carbon dioxide. 相似文献
10.
T. Cui J. Zhang J. Wang F. Cui W. Chen F. Xu Z. Wang K. Zhang B. Yang 《Advanced functional materials》2005,15(3):481-486
In this paper we describe the combined use of surface‐initiated atom transfer radical polymerization (ATRP) and a gas/solid reaction in the direct preparation of CdS‐nanoparticle/block‐copolymer composite shells on silica nanospheres. The block copolymer, consisting of poly(cadmium dimethacrylate) (PCDMA) and poly(methyl methacrylate) (PMMA), is obtained by repeatedly performing the surface‐initiated ATRP procedures in N,N‐dimethylformamide (DMF) solution at room temperature, using cadmium dimethacrylate (CDMA) and methyl methacrylate (MMA) as the monomers. CdS nanoparticles with an average size of about 3 nm are generated in situ by exposing the silica nanospheres coated with block‐copolymer shells to H2S gas. These synthetic core–shell nanospheres were characterized using transmission electron microscopy (TEM), dynamic light scattering (DLS), thermogravimetric analysis (TGA), diffuse reflectance UV‐vis spectroscopy, X‐ray photoelectron spectroscopy (XPS), and powder X‐ray diffraction (XRD). These composite nanospheres exhibit strong red photoluminescence in the solid state at room temperature. 相似文献
11.
Courtney D. Sorrell Matthew C. D. Carter Michael J. Serpe 《Advanced functional materials》2011,21(3):425-433
A new class of materials that are capable of color tunability over 300 nm with a 15 °C temperature change is introduced. The materials are assembled from thermoresponsive poly (N‐isopropylacrylamide)‐co‐acrylic acid (pNIPAm‐co‐AAc) microgels, which are deposited on Au coated glass substrates. The films are also pH responsive; the temperature‐induced color change was suppressed at high pH and is consistent with the behavior of a solution of suspended microgels. The mechanism proposed to account for the observed optical properties suggests that they result from the two Au layers being separated from each other by the “monolithic” microgel film, much like a Fabry‐Pérot etalon or interferometer. It is the modulation of the distance between these two layers, facilitated by the microgel collapse transition at high temperature, that allows the color to be tuned. The sensitivity of the system presented here will be used for future sensing and biosensing applications, as well as for light filtering applications. 相似文献
12.
Capucine Sassoye Christel Laberty Hung Le Khanh Sophie Cassaignon Cédric Boissière Markus Antonietti Clément Sanchez 《Advanced functional materials》2009,19(12):1922-1929
RuO2‐based mesoporous thin films of optical quality are synthesized from ruthenium‐peroxo‐based sols using micelle templates made of amphiphilic polystyrene‐polyethylene oxide block copolymers. The mesoporous structure and physical properties of the RuO2 films (mesoporous volume: 30%; pore diameter: ~30 nm) can be controlled by the careful tuning of both the precursor solution and thermal treatment (150–350 °C). The optimal temperature that allows control of both mesoporosity and nanocristallinity is strongly dependent on the substrate (silicon or fluorine‐doped tin oxide). The structure of the resulting mesoporous films are investigated using X‐ray diffraction, X‐ray photoelectron spectroscopy, and atomic force microscopy. Mesoporous layers are additionally characterized by transmission and scanning electron microscopy and ellipsometry while their electrochemical properties are analyzed via cyclic voltammetry. Thick mesoporous films of ruthenium oxide hydrates, RuO2 · xH2O, obtained using a thermal treatment at 280 °C, exhibit capacitances as high as 1000 ± 100 F g?1 at a scan rate of 10 mV s?1, indicating their potential application as electrode materials. 相似文献
13.
Markus J. Barthel Tobias Rudolph Anke Teichler Renzo M. Paulus Jürgen Vitz Stephanie Hoeppener Martin D. Hager Felix H. Schacher Ulrich S. Schubert 《Advanced functional materials》2013,23(39):4921-4932
The application of well‐defined poly(furfuryl glycidyl ether) (PFGE) homopolymers and poly(ethylene oxide)‐b‐poly(furfuryl glycidyl ether) (PEO‐b‐PFGE) block copolymers synthesized by living anionic polymerization as self‐healing materials is demonstrated. This is achieved by thermo‐reversible network formation via (retro) Diels‐Alder chemistry between the furan groups in the side‐chain of the PFGE segments and a bifunctional maleimide crosslinker within drop‐cast polymer films. The process is studied in detail by differential scanning calorimetry (DSC), depth‐sensing indentation, and profilometry. It is shown that such materials are capable of healing complex scratch patterns, also multiple times. Furthermore, microphase separation within PEO‐b‐PFGE block copolymer films is indicated by small angle X‐ray scattering (lamellar morphology with a domain spacing of approximately 19 nm), differential scanning calorimetry, and contact angle measurements. 相似文献
14.
Membranes with outstanding performance that are applicable in harsh environments are needed to broaden the current range of organic dehydration applications using pervaporation. Here, well‐intergrown UiO‐66 metal‐organic framework membranes fabricated on prestructured yttria‐stabilized zirconia hollow fibers are reported via controlled solvothermal synthesis. On the basis of the adsorption–diffusion mechanism, the membranes provide a very high flux of up to ca. 6.0 kg m?2 h?1 and excellent separation factor (>45 000) for separating water from i ‐butanol (next‐generation biofuel), furfural (promising biochemical), and tetrahydrofuran (typical organic). This performance, in terms of separation factor, is one to two orders of magnitude higher than that of commercially available polymeric and silica membranes with equivalent flux. It is comparable to the performance of commercial zeolite NaA membranes. Additionally, the membrane remains robust during a pervaporation stability test (≈300 h), including exposure to harsh environments (e.g., boiling benzene, boiling water, and sulfuric acid) where some commercial membranes (e.g., zeolite NaA membranes) cannot survive. 相似文献
15.
In this paper, we modified carbon nanotubes with the thiol‐reactive species, subsequently combined the thiol‐coupling reaction and reversible addition‐fragmentation chain transfer (RAFT) polymerization to prepare temperature‐responsive PNIPAAm (poly(N‐isopropylacrylamide))‐carbon nanotube conjugates. The prepared PNIPAAm‐carbon nanotube conjugates have temperature‐responsive PNIPAAm chain, and disulfide linkages between PNIPAAm and carbon nanotube which are sensitive to bio‐stimuli such as glutathione, therefore dual‐responsive polymer‐carbon nanotube conjugates have been prepared. 相似文献
16.
Nanodot‐Enhanced High‐Efficiency Pure‐White Organic Light‐Emitting Diodes with Mixed‐Host Structures
J.‐H. Jou C.‐C. Chen Y.‐C. Chung M.‐F. Hsu C.‐H. Wu S.‐M. Shen M.‐H. Wu W.‐B. Wang Y.‐C. Tsai C.‐P. Wang J.‐J. Shyue 《Advanced functional materials》2008,18(1):121-126
A relatively high‐efficiency, fluorescent pure‐white organic light‐emitting diode was fabricated using a polysilicic acid (PSA) nanodot‐embedded polymeric hole‐transporting layer (HTL). The diode employed a mixed host in the single emissive layer, which comprised 0.5 wt % yellow 5,6,11,12‐tetra‐phenylnaphthacene doped in the mixed host of 50 % 2‐(N,N‐diphenyl‐amino)‐6‐[4‐(N,N‐diphenylamino)styryl]naphthalene and 50 % N,N′‐bis‐(1‐naphthyl)‐N,N′‐diphenyl‐1,10‐biphenyl‐4‐4′‐diamine. By incorporating 7 wt % 3 nm PSA nanodot into the HTL of poly(3,4‐ethylene‐dioxythiophene)‐poly‐(styrenesulfonate), the efficiency at 100 cd m–2 was increased from 13.5 lm W–1 (14.7 cd A–1; EQE: 7.2 %) to 17.1 lm W–1 (17.6 cd A–1; EQE: 8.3 %). The marked efficiency improvement may be attributed to the introduction of the PSA nanodot, leading to a better carrier‐injection‐balance. 相似文献
17.
Xiao Zhang Piaoping Yang Yunlu Dai Ping'an Ma Xuejiao Li Ziyong Cheng Zhiyao Hou Xiaojiao Kang Chunxia Li Jun Lin 《Advanced functional materials》2013,23(33):4067-4078
Multifunctional nanocarriers based on the up‐conversion luminescent nanoparticles of NaYF4:Yb3+/Er3+ core (UCNPs) and thermo/pH‐coupling sensitive polymer poly[(N‐isopropylacrylamide)‐co‐(methacrylic acid)] (P(NIPAm‐co‐MAA)) gated mesoporous silica shell are reported for cancer theranostics, including fluorescence imaging, and for controlled drug release for therapy. The as‐synthesized hybrid nanospheres UCNPs@mSiO2‐P(NIPAm‐co‐MAA) show bright green up‐conversion fluorescence under 980 nm laser excitation and the thermo/pH‐sensitive polymer is active as a “valve” to moderate the diffusion of the embedded drugs in‐and‐out of the pore channels of the silica container. The anticancer drug doxorubicin hydrochloride (DOX) can be absorbed into UCNPs@mSiO2‐P(NIPAm‐co‐MAA) nanospheres and the composite drug delivery system (DDS) shows a low level of leakage at low temperature/high pH values but significantly enhanced release at higher temperature/lower pH values, exhibiting an apparent thermo/pH controlled “on‐off” drug release pattern. The as‐prepared UCNPs@mSiO2‐P(NIPAm‐co‐MAA) hybrid nanospheres can be used as bioimaging agents and biomonitors to track the extent of drug release. The reported multifunctional nanocarriers represent a novel and versatile class of platform for simultaneous imaging and stimuli‐responsive controlled drug delivery. 相似文献
18.
Responsive Macroscopic Materials From Self‐Assembled Cross‐Linked SiO2‐PNIPAAm Core/Shell Structures
Christian W. Pester Artjom Konradi Birte Varnholt Patrick van Rijn Alexander Böker 《Advanced functional materials》2012,22(8):1724-1731
A way to obtain macroscopic responsive materials from silicon‐oxide polymer core/shell microstructures is presented. The microparticles are composed of a 60 nm SiO2‐core with a random copolymer corona of the temperature responsive poly‐N‐isopropylacrylamide (PNIPAAm) and the UV‐cross‐linkable 2‐(dimethyl maleinimido)‐N‐ethyl‐acrylamide. The particles shrink upon heating and form a stable gel in both water and tetrahydrofuran (THF) at 3–5 wt% particle content. Cross‐linking the aqueous gel results in shrinkage when the temperature is increased above the lower critical solution temperature and it regains its original size upon cooling. By freeze drying with subsequent UV irradiation, thin stable layers are prepared. Stable fibers are produced by extruding a THF gel into water and subsequent UV irradiation, harnessing the cononsolvency effect of PNIPAAm in water/THF mixtures. The temperature responsiveness translates to the macroscopic materials as both films and fibers show the same collapsing behavior as the microcore/shell particle. The collapse and re‐swelling of the materials is related to the expelling and re‐uptake of water, which is used to incorporate gold nanoparticles into the materials by a simple heating/cooling cycle. This allows for future applications, as various functional particles (antibacterial, fluorescence, catalysis, etc.) can easily be incorporated in these systems. 相似文献
19.
J.N. Barsema N.F.A. vanderVegt G.H. Koops M. Wessling 《Advanced functional materials》2005,15(1):69-75
We prepared dense flat‐sheet Ag‐functionalized carbon molecular‐sieve (CMS) membranes from blends of P84 co‐polyimide and a sulfonated poly(ether ether ketone) with a Ag+ counterion (AgSPEEK). These blends offer the possibility of producing new functionalized precursor structures, which were previously not possible, such as integrally skinned asymmetric hollow fibers. Membranes prepared at a pyrolysis end temperature of 800 °C showed a maximum permeability for all tested gases at a Ag content of approximately 2.5 wt.‐% (He permeability PHe = 465 Barrer (1 Barrer = 7.5 × 10–18 m2 s–1 Pa–1), Pequation/tex2gif-inf-2.gif = 366 Barrer, Pequation/tex2gif-inf-4.gif = 91.8 Barrer, Pequation/tex2gif-inf-6.gif = 10.3 Barrer). The maximum achieved selectivity for O2 over N2 with CMS membranes based on these blends was αequation/tex2gif-inf-10.gif = 13.5 (Ag content: 4.5 wt.‐%, Pequation/tex2gif-inf-14.gif = 52.7 Barrer). The CO2 over N2 selectivity reached a value of 48.9 (Ag content: 4.5 wt.‐%, Pequation/tex2gif-inf-18.gif = 191 Barrer). These observations are explained by the formation of selective bypasses around Ag nanoclusters in the CMS matrix. 相似文献
20.
2D Heterostructure Membranes with Sunlight‐Driven Self‐Cleaning Ability for Highly Efficient Oil–Water Separation
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Yanan Liu Yanlei Su Jingyuan Guan Jialin Cao Runnan Zhang Mingrui He Kang Gao Linjie Zhou Zhongyi Jiang 《Advanced functional materials》2018,28(13)
Introducing solar energy into membrane filtration to decrease energy and chemicals consumption represents a promising direction in membrane fields. In this study, a kind of 0D/2D heterojunction is fabricated by depositing biomineralized titanium dioxide (TiO2) nanoparticles with delaminated graphitic carbon nitride (g‐C3N4) nanosheets, and subsequently a kind of 2D heterostructure membrane is fabricated via intercalating g‐C3N4@TiO2 heterojunctions into adjacent graphene oxide (GO) nanosheets by a vacuum‐assisted self‐assembly process. Due to the enlarged interlayer spacing of GO nanosheets, the initial permeation flux of GO/g‐C3N4@TiO2 membrane reaches to 4536 Lm?2 h?1 bar?1, which is more than 40‐fold of GO membranes (101 Lm?2 h?1 bar?1) when utilized for oil/water separation. To solve the sharp permeation flux decline, arising from the adsorption of oil droplets, the a sunlight‐driven self‐cleaning process is followed, maintaining a flux recovery ratio of more than 95% after ten cycles of filtration experiment. The high permeation flux and excellent sunlight‐driven flux recovery of these heterostructure membranes manifest their attractive potential application in water purification. 相似文献