Tetramethylammonium Hydroxide Research Articles

Synthesis and Characterization of ZnO Quantum Dot-Functionalized Mesoporous Nanocarriers for Controlled Drug Delivery

In this study, ZnO quantum dots (ZnO@QDs) were synthesized and functionalized with 2nd generation poly amido amine (2GPD) using 3-amino-propyl tri-methoxy silane as the initiator core, facilitated by tetramethylammonium hydroxide (TMAH) to enhance stability against oleate coating. Concurrently, a mesoporous substrate with a unique morphology was developed as a drug reservoir for doxorubicin loading. ZnO quantum dots displayed photoluminescence radiation, with dimensions ranging from 5 to 7 nm and exhibiting spherical morphology. The cubic structure of the synthesized mesoporous nanocatalysts was also confirmed. Brunauer-Emmett-Teller analysis indicated a multidimensional porous structure of the nanocarriers, while zeta potential analysis showed a stable system (approximately -9.6 mV). Fourier transform infrared spectroscopy, X-ray diffraction, and energy dispersive spectroscopy corroborated these findings. Drug release studies demonstrated sustained release under acidic conditions (pH 5.5), with an efficiency of approximately 94%. These results highlight the potential applications of this nanosystem for controlled drug delivery, underscoring its practical implications in the field of nanotechnology.

Dissolution dynamics of partially protected poly(4-hydroxystyrene) in organic developers investigated by quartz crystal microbalance (QCM) method

Abstract Poly(4-hydroxystyrene) (PHS) molecules in solid films are connected each other through polar and nonpolar molecular interaction and hydrogen bonds. Although the dissociation of phenolic hydroxyl groups plays the major role in the dissolution of PHS films in tetramethylammonium hydroxide (TMAH) aqueous developer, it is important to clarify the effects of other interactions. In this study, we investigated the dissolution dynamics of partially protected PHS in organic developers by a quartz crystal microbalance method to deepen the fundamental understanding of the dissolution dynamics of chemically amplified resists. The dissolution dynamics in the solvents, in which the phenolic hydroxyl groups are hardly dissociated, was measured. In 50 vol% methanol aqueous developer, a large swelling was observed. By decreasing the polarity of developer, the dissolution dynamics was significantly changed. In the hexyl acetate, the dissolution kinetics of PHS films became similar to that in TMAH aqueous developer although the dissolution mechanism is different.

Rejection of PFAS and priority co-contaminants in semiconductor fabrication wastewater by nanofiltration membranes

Use of high-pressure membranes is an effective means for treatment of per-and polyfluoroalkyl substances (PFAS) that is less sensitive than adsorption processes to variable water quality and specific PFAS structure. This study evaluated the use of nanofiltration (NF) membranes for the removal of PFAS and industry relevant co-contaminants in semiconductor fabrication (fab) wastewater. Initial experiments using a flat sheet filtration cell determined that the NF90 (tight NF) membrane provided superior performance compared to the NF270 (loose NF) membrane, with NF90 rejection values exceeding 97% for all PFAS evaluated, including the ultrashort trifluoromethane sulfonic acid (TFMS). Cationic fab co-contaminants diaryliodonium (DIA), triphenylsulfonium (TPS), and tetramethylammonium hydroxide (TMAH) were not as highly rejected as anionic PFAS likely due to electrostatic effects. A spiral wound NF90 module was then used in a pilot system to treat a lab solution containing PFAS and co-contaminants and fab wastewater effluent. Treatment of the fab wastewater, containing high concentrations of perfluorocarboxylic acids (PFCAs), including trifluoroacetic acid (TFA: 96,413 ng/L), perfluoropropanoic acid (PFPrA: 11,796 ng/L), and perfluorobutanoic acid (PFBA: 504 ng/L), resulted in ≥92% rejection of all PFAS while achieving 90% water recovery in a semi batch configuration. These findings demonstrate nanofiltration as a promising technology option for incorporation in treatment trains targeting PFAS removal from wastewater matrices.

Dissolution dynamics of poly(4-hydroxystyrene) partially protected with t-butoxycarbonyl group in alkyltrimethylammonium hydroxide aqueous developers

Novel developers with low biotoxicity have attracted considerable attention with respect to ensuring environmental sustainability. In this study, the dissolution dynamics of poly(4-hydroxylstyrene) (PHS) partially protected with a t-butoxycarbonyl (t-Boc) group in alkyltrimethylammonium hydroxide and tetraethylammonium hydroxide aqueous solutions (0.26 N) were investigated by the quartz crystal microbalance method. One of the methyl groups of tetramethylammonium hydroxide (TMAH) was substituted by ethyl, propyl, and butyl groups. Depending on the developer used, the dissolution dynamics of PHS and t-Boc-protected PHS (t-Boc PHS) films showed different tendencies. The dissolution rate of PHS was higher in the TMAH developer than in the butyltrimethylammonium hydroxide (B-TMAH) developer, whereas that of the t-Boc PHS (30 mol%-protected) film was higher in the B-TMAH developer than in the TMAH developer. The elongation of one of the alkyl chains is beneficial for the penetration of the developer and the separation of nonpolar molecular interactions among t-Boc PHS molecules.

Hydroxide-Derived Nanostructures: Scalable Synthesis, Characterization, Properties, and Potential Applications.

Metal oxide nanostructures have received an increasing attention owing to their unique chemical and physical properties along with their widespread applications in various fields. This article provides an overview of the recent discovery - christened Hydroxides-Derived Nanostructures, or HDNs - in which hydroxide aqueous solutions (mostly tetramethylammonium hydroxide, TMAH) are reacted at temperatures < 100°C and under atmospheric pressure with various metal-containing precursors to scalably prepare novel metal oxide nanostructures. In one case, a dozen commercial and earth abundant Ti-containing powders such as binary carbides, nitrides, borides, among others, are converted into new, 1D TiO2-based lepidocrocite (1DL) nanofilaments (NFs). Application-wise, the 1DLs show outstanding performance in a number of energy, environmental, and biomedical fields such as photo- and electrocatalysis, water splitting, lithium-sulfur and lithium-ion batteries, water purification, dye degradation, cancer therapy, and polymer composites. In addition to 1DL, the HDNs family encompasses other metal oxides nanostructures including magnetic Fe3O4 nanoparticles and MnO2 birnessite-based crystalline 2D flakes. The latter showed promise in electrochemical energy conversion and storage applications. The developed recipe provides a new vista in the molecular self-assembly synthesis of nanomaterials that can advance the field with a library of novel nanostructures with substantial implications in a multitude of fields.

Deep eutectic solvent (TMAH·5H2O/Urea) with low viscosity for cellulose dissolution at room temperature

A deep eutectic solvent (DES) formulated with tetramethylammonium hydroxide pentahydrate /urea (TMAH·5H2O/Urea) was designed for the first time to dissolve cellulose at room temperature. The optimized system, characterized by a 1:3 M ratio, demonstrates the capability to dissolve approximately 7.5 wt% cellulose, boasting a high degree of polymerization (DP = 526). Notably, both the pure DES and 4.0 wt% cellulose/TMAH·5H2O/Urea mixtures manifests low viscosity, establishing its potential as an effective spinning aid in fiber manufacturing. The structural analyses shows that the cellulose crystal type shifts from type I to type II form, accompanied by a reduction in both crystallinity and DP. A pivotal aspect of this research involves determining Kamlet-Taft parameters for TMAH·5H2O/Urea-DES with different molar ratios. The results reveal these solvate DESs exhibit the high hydrogen bond basicity, which enables them to easily form hydrogen bonds with hydroxyl groups of cellulose and demonstrate good cellulose solubility. In conclusion, this solvent system presents notable advantages, including straightforward synthesis procedures, low viscosity, and well cellulose solubility, paving the way for new approaches and techniques in cellulose utilization.

Hydroxide Ion Conduction through Viologen-Based Covalent Organic Frameworks (vCOFs): An Approach toward the Advancement.

Alkaline fuel cells rely on the movement of hydroxide anions (OH-) for their operation, yet these anions face challenges in efficient conduction due to their limited diffusion coefficient and substantial mass compared to proton (H+) transport. Within the covalent organic framework structure, ordered channels offer a promising solution for the OH- ion transport. Herein, we synthesized a cationic covalent organic framework (vTAPA) via the solvothermal-assisted Zincke reaction. vTAPA showcases excellent stability in harsh basic solution (12 M) and a wide range of pH. This framework facilitates OH- conduction through its one-dimensional network through the anion exchange process. We employed various tertiary ammonium salts (tetramethyl, tetraethyl, and tetrabutyl ammonium hydroxide) to exchange trapped anionic chloride ions inside the vTAPA structure with OH- ions. The density functional theory (DFT) study exhibited that the anion exchange process is very favorable, as the vTAPA framework offers preferable interaction sites for OH- ions. The impact of steric hindrance from these tertiary ammonium salts on the OH- conduction performance was extensively investigated. Butyl@vTAPA exhibited a high OH- ion conductivity of 1.05 × 10-4 S cm-1 at 90 °C under 98% relative humidity (RH). Our uniquely designed cationic covalent organic frameworks (COF) created a platform for a preferential transport network of hydroxide ions, and this is the first report of directly used COFs for hydroxide ion conduction without any vigorous postsynthetic modification.

Enhancement of device performance in β-Ga2O3 Schottky barrier diodes with tetramethylammonium hydroxide treatment

Schottky barrier diodes were fabricated on tetramethylammonium hydroxide (TMAH)-treated β-Ga2O3 surfaces with Ni/Au as Schottky metal contacts. TMAH wet surface treatment efficiently reduced the roughness of the β-Ga2O3 surface. An X-ray photoelectron emission analysis of the TMAH-treated β-Ga2O3 surface chemical binding features indicates the effective removal of unwanted surface oxides and contaminants formed unintentionally by chemisorption during exposure to ambient conditions. The TMAH-treated Au/Ni/β-Ga2O3 Schottky diode displayed improved rectification behavior with an increment of barrier height by 0.30 eV compared to the untreated diode. The breakdown voltages (Vbr) for the untreated and TMAH-treated Au/Ni/β-Ga2O3 Schottky barrier diode are 298 and 358 V, respectively. The decrease in the turn-on resistance (Ron) in the Au/Ni/β-Ga2O3 Schottky barrier diode by TMAH treatment can be ascribed to the improved surface morphology. The improved electrical behavior of the Au/Ni/β-Ga2O3 Schottky barrier diode formed on the TMAH-treated β-Ga2O3 surface can be accredited to the oxygen vacancies reduction, that deceased the carrier concentration in the β-Ga2O3 epilayer and to the improved the surface morphology. These results demonstrate the effectiveness of TMAH wet surface treatment on β-Ga2O3 and its potential as a simple method for fabricating β-Ga2O3-based devices with improved performance.

Synthesis of ω-Chloroalkyl Aryl Ketones via C-C Bond Cleavage of tert-Cycloalkanols with Tetramethylammonium Hypochlorite.

An oxidative C-C bond cleavage of tert-cycloalkanols with tetramethylammonium hypochlorite (TMAOCl) has been developed. TMAOCl is easy to prepare from tetramethylammonium hydroxide, and the combination of TMAOCl and AcOH effectively promoted the C-C bond cleavage in a two-phase system without additional phase-transfer reagents. Unstrained tert-cycloalkanols were transformed into ω-chloroalkyl aryl ketones in moderate to excellent yields under metal-free and mild reaction conditions.

Effect of Oxidizing Agent on the Synthesis of ZnO Nanoparticles for Inverted Phosphorescent Organic Light-Emitting Devices without Multiple Interlayers.

Inverted organic light-emitting devices (OLEDs) have been aggressively developed because of their superiorities such as their high stability, low driving voltage, and low drop of brightness in display applications. The injection of electrons is a critical issue in inverted OLEDs because the ITO cathode has an overly high work function in injecting electrons into the emission layer from the cathode. We synthesized hexagonal wurtzite ZnO nanoparticles using different oxidizing agents for an efficient injection of electrons in the inverted OLEDs. Potassium hydroxide (KOH) and tetramethylammonium hydroxide pentahydrate (TMAH) were used as oxidizing agents for synthesizing ZnO nanoparticles. The band gap, surface defects, surface morphology, surface roughness, and electrical resistivity of the nanoparticles were investigated. The inverted devices with phosphorescent molecules were prepared using the synthesized nanoparticles. The inverted devices with ZnO nanoparticles using TMAH exhibited a lower driving voltage, lower leakage current, and higher maximum external quantum efficiency. The devices with TMAH-based ZnO nanoparticles exhibited the maximum external quantum efficiency of 19.1%.

Preparation of transparent AlON ceramics with controlled shapes by a novel spontaneous coagulation casting and pressureless sintering method

Aluminum oxynitride (AlON) exhibits excellent mechanical properties and good optical transparency in the ultraviolet to near-infrared range and can be used in military and civilian fields. However, the troublesome molding of AlON, especially for complex shapes, limits its promotion and application. Therefore, transparent AlON ceramics with complex morphologies were prepared for the first time by a novel spontaneous coagulation casting (SCC) and pressureless sintering method. In this study, we report a simple carbothermal reduction and nitridation (CRN) method for synthesizing high-purity AlON powder, which is especially suitable for wet casting without anti-hydration treatment. The dispersion and gelation behavior of AlON slurries by isobutene maleic anhydride copolymer (Isobam104) and tetramethylammonium hydroxide (TMAH) were extensively investigated. With the addition of 0.9 wt% Isobam104 and 15 mL/L TMAH, the AlON slurries can achieve a solids loading of up to 45 vol% with the lowest viscosity (460.4 mPa·s-10 r/min) and the AlON green body is free of cracks and deformation during drying and demolding processes. Finally, the AlON green bodies with square and polygonal irregular morphologies were fabricated via a simple SCC method. High transparent AlON ceramics of a maximum transmittance up to 77.3% at 2000 nm and 72.2% at 632 nm were obtained by pressureless sintered at 2000 °C for 6 h. The SCC method has great potential in preparing ceramics with controllable shapes.

Effect of Wet Etching on AlGaN‐Based Ultraviolet‐B Laser Diodes Grown on Wet‐Etched Periodic AlN Nanopillars

The effect of wet etching on the characteristics of ultraviolet‐B (UV‐B) lasers fabricated on AlGaN templates grown as crystals or wet‐etched AlN nanopillars is compared in detail. Specifically, a tetramethylammonium hydroxide (TMAH) solution is used to form templates with AlN nanopillars of different diameters, followed by determining the dependence of the dislocation density in AlGaN crystals grown on the templates, the threshold power density (Pth) of an optically pumped UV‐B laser, and the threshold current density (Jth) of a UV‐B laser diode (LD) on the extent of etching. It is observed that the pillar diameter decreases almost linearly as the etching time with the TMAH solution increases. The dislocation density of AlGaN crystals grown on AlGaN templates is almost independent of the etching time. Meanwhile, Pth of the optically pumped UV‐B laser is almost halved upon etching with TMAH. Finally, the Jth of the UV‐B LD tends to decrease by 10%–20% upon etching. The optical gain is estimated by optical excitation; wet etching of AlN nanopillars with TMAH solution results in a larger optical gain at the same excitation intensity, indicating that nonradiative recombination centers, such as point defects, are reduced.

A proposal and simulation analysis for a novel architecture of gate-all-around polycrystalline silicon nanowire field effect transistor

A proposal for a novel gate-all-around (GAA) polycrystalline silicon nanowire (poly-SiNW) field effect transistor (FET) is presented and discussed in this paper. The device architecture is based on the realization of poly-SiNW in a V-shaped cavity obtained by tetra methyl ammonium hydroxide (TMAH) etch of monocrystalline silicon (100). The device’s behavior is simulated using Silvaco commercial software, including the density of states (DOS) model described by the double exponential distribution of acceptor trap density within the gap. The electric field, potential, and free electron concentration are analyzed in different nanowire regions to investigate the device's performance. The results show good performance despite the high density of deep states in poly-SiNW. This can be explained by the strong electric field caused by the corner effect in the nanowire, which favors the ionization of the acceptor traps and increases the free electron concentration.

Mechanism of catalyst on morphological evolution of Al(OH)3 during Al–H2O reaction

The morphologies of Al(OH)3 crystals prepared via the Al–H2O reactions with various catalysts and the growth mechanisms of these crystals were investigated. The reaction was carried out with NaOH, KOH, tetramethylguanidine (TMG), and tetramethylammonium hydroxide (TMAH) as catalysts. The evolution of the obtained product was observed in situ, and the products obtained after 120 min of reaction have the shapes of the hexagonal prism, long-hexagonal prism, long rod, and irregular rod, respectively. In the NaOH and KOH systems, the products are gibbsite, and the gibbsite crystals grow along the (110), (001), and (100) faces in the NaOH system, and the (100), (102), and (110) faces in the KOH system. However, in the TMG and TMAH systems, the products are bayerite, and the bayerite crystals grow along the (110), (111), and (001) faces. It is worth mentioning that gibbsite has more Al—O bonds than bayerite, giving rise to the formation of columnar crystals.

Piezoelectric Micromachined Ultrasonic Transducers with Micro-Hole Inter-Etch and Sealing Process on (111) Silicon Wafer.

Piezoelectric micromachined ultrasound transducers (PMUTs) have gained significant popularity in the field of ultrasound ranging and medical imaging owing to their small size, low power consumption, and affordability. The scar-free "MIS" (micro-hole inter-etch and sealing) process, a novel bulk-silicon manufacturing technique, has been successfully developed for the fabrication of pressure sensors, flow sensors, and accelerometers. In this study, we utilize the MIS process to fabricate cavity diaphragm structures for PMUTs, resulting in the formation of a flat cavity diaphragm structure through anisotropic etching of (111) wafers in a 70 °C tetramethylammonium hydroxide (TMAH) solution. This study investigates the corrosion characteristics of the MIS technology on (111) silicon wafers, arranges micro-pores etched on bulk silicon around the desired cavity structure in a regular pattern, and takes into consideration the distance compensation for lateral corrosion, resulting in a fully connected cavity structure closely approximating an ortho-hexagonal shape. By utilizing a sputtering process to deposit metallic molybdenum as upper and lower electrodes, as well as piezoelectric materials above the cavity structure, we have successfully fabricated aluminum nitride (AlN) piezoelectric ultrasonic transducer arrays of various sizes and structures. The final hexagonal PMUT cells of various sizes that were fabricated achieved a maximum quality factor (Q) of 251 and a displacement sensitivity of 18.49 nm/V across a range of resonant frequencies from 6.28 MHz to 11.99 MHz. This fabrication design facilitates the achievement of IC-compatible and cost-effective mass production of PMUT array devices with high resonance frequencies.

Quantitative analysis of iodine and bromine in soil using an energy-dispersive X-ray fluorescence spectrometer with three-dimensional polarized optics.

A nondestructive and simple method for the determination of bromine and iodine in soil was investigated using an energy-dispersive X-ray fluorescence spectrometer equipped with three-dimensional polarized optics. Using a gadolinium X-ray tube and Mo and Al2O3 as optimal secondary target materials, K-lines were detected for bromine and iodine. The minimum detection limits for bromine and iodine were calculated using JSAC0411, a certified reference material of soil for metal composition analysis, and were 0.77mg/kg for bromine and 2.3mg/kg for iodine at a measurement time of 600s. The results of the determination of bromine and iodine in soil samples by the standard addition method were 256 ± 8mg/kg for iodine and 67.9 ± 1.3mg/kg for bromine with JSAC0411, which were in close agreement with the results measured by inductively coupled plasma mass spectrometry (ICP-MS) after alkaline extraction with tetramethylammonium hydroxide (TMAH) solution. The method developed in this study is an excellent technique for direct analysis of soil by X-ray fluorescence analysis without any pretreatment such as alkaline extraction. It is expected to be a practical analytical method for elucidating the dynamics of bromine and iodine in agricultural land and soil.

Comprehensive synthesis of Ti3C2Tx from MAX phase to MXene.

MXenes are a large family of two-dimensional materials that have attracted attention across many fields due to their desirable optoelectronic, biological, mechanical and chemical properties. There currently exist many synthesis procedures that lead to differences in flake size, defects and surface chemistry, which in turn affect their properties. Herein, we describe the steps to synthesize Ti3C2Tx-the most important and widely used MXene, from a Ti3AlC2 MAX phase precursor. The procedure contains three main sections: synthesis of Ti3AlC2 MAX, wet chemical etching of the MAX in hydrofluoric acid/HCl solution to yield multilayer Ti3C2Tx and its delamination into single-layer flakes. Three delamination options are described; these use LiCl, tertiary amines (tetramethyl ammonium hydroxide/ tetrabutyl ammonium hydroxide) and dimethylsulfoxide respectively. These procedures can be adapted for the synthesis of MXenes beyond Ti3C2Tx. The MAX phase synthesis takes about 1 week, with the etching and delamination each requiring 2 d. This protocol requires users to have experience working with hydrofluoric acid, and it is recommended that users have experience with wet chemistry and centrifugation; characterization techniques such as X-ray diffraction and particle size analysis are also essential for the success of the protocol. While alternative synthesis methods, such as minimally intensive layer delamination, are desirable for certain MXenes (such as Ti2CTx) or specific applications, this protocol aims to standardize the more commonly used hydrofluoric acid/HCl etching method, which produces Ti3C2Tx with minimal concentration of defects and the highest conductivity and serves as a guideline for those working with MXenes for the first time.

Research on carbon and nitrogen removal of tetramethylammonium hydroxide containing wastewater by combined anaerobic/integrated fixed film activated sludge process

Tetramethylammonium hydroxide (TMAH) is widely used as a developer and etchant in the thin-film transistor liquid crystal display industry, which is the main component of developer wastewater with low C/N ratio. This study investigated TMAH degradation by combined anaerobic/integrated fixed film activated sludge (A/IFAS) process, especially for nitrogen removal. Effects of process condition on the TMAH degradation were studied, including dissolved oxygen concentration in IFAS reactor and the temperature of anaerobic reactor. Especially, the nitrogen removal was studied through the monitoring of intermediate products during TMAH biodegradation. The results indicated that lower the anaerobic treatment temperature can provide more available organic matters to enhance the denitrification in the subsequent IFAS reactor. Less oxygen supply in the IFAS reactor contributed to simultaneous nitrification and denitrification. Removal efficiency of total organic carbon and total nitrogen was up to 95.8% and 80.7%, when the temperature of anaerobic treatment was controlled at 30 °C with the DO kept at 0.7 mg/L. It indicated that A/IFAS process was efficient in carbon and nitrogen removal for TMAH degradation. The results also confirmed intermediate products of TMAH biodegradation can be used as the electron donor during denitrification, including trimethylamine, dimethylamine and methylamine. Illumina MiSeq sequencing showed that Proteobacteria was the dominant phylum contribute to nitrogen removal. Compared to sludge flocs in IFAS reactor, richer community and higher microbial diversity were observed in the biofilm.

Exploring monolayer Ta4C3Tx MXene for quick ammonia detection at room temperature

Two-dimensional (2D) MXenes have emerged as promising gas sensor materials due to their abundant surface functional groups, excellent conductivity, and large surface area. In this work, we synthesized 2D Ta4C3Tx nanosheets via hydrofluoric acid (HF) etching followed by a tetramethylammonium hydroxide (TMAOH) intercalation treatment. Systematical characterization reveals the as-prepared 2D Ta4C3Tx exhibits promising monolayer morphology with abundant oxygen containing functional groups. The sensor device based on monolayer Ta4C3Tx presents a brilliant response to ammonia gas at room temperature, well surpassing those based on other previously reported MXenes. The high selectivity of Ta4C3Tx for ammonia gas was explored through first-principle calculations. This study highlights the significant potential of monolayer Ta4C3Tx for developing high-performance room-temperature ammonia gas sensors.

Flower-like ZnO modified TiO2@Ti3C2Tx composite for efficient adsorption of malachite green and oil-water separation

The intensification of industrial production has led to a sharp increase in the discharge of toxic organic chemicals and wastewater from printing and dyeing industry. In this study, flower-like ZnO modified TiO2@Ti3C2Tx composites (ZnO/TiO2@Ti3C2Tx) were prepared by in-situ oxidation solvothermal method from zinc nitrate hexahydrate and tetramethylammonium hydroxide intercalated Ti3C2Tx. During the solvothermal processes, sodium hydroxide acted as an etchant to further exfoliated the accordion-like Ti3C2Tx into single or few-layer; and at the same time, TiO2 was formed in-situ on the surface of Ti3C2Tx with simultaneous deposition of flower-like ZnO. The layer structural Ti3C2Tx facilitates the loading and dispersion of ZnO and TiO2 on its surface. After the in-situ oxidation by solvothermal method, TiO2 was evenly distributed on the surface of Ti3C2Tx, adjusting the functional groups on the surface of the ZnO/TiO2@Ti3C2Tx composite, and improving its adsorption performance. ZnO/TiO2@Ti3C2Tx can be used as an efficient adsorbent for malachite green with a high maximum adsorption capacity of 1232.7 mg g−1, which is higher than that of TiO2@Ti3C2Tx (628.57 mg g−1). Moreover, a superhydrophilic and underwater superoleophobic ZnO/TiO2@Ti3C2Tx@PU sponge was prepared by loading ZnO/TiO2@Ti3C2Tx onto polyurethane (PU) sponge. The introduction of ZnO enhances the surface roughness of the ZnO/TiO2@Ti3C2Tx@PU sponge, which can effectively separate six oil-water mixtures, and has a high separation flux of 171784 L m−2 h−1 and separation efficiency of 99.6% for cyclohexane-water mixture.