Surface‐Modified Metallic Ti3C2Tx MXene as Electron Transport Layer for Planar Heterojunction Perovskite Solar Cells

MXenes are a large and rapidly expanding family of 2D materials that, owing to their unique optoelectronic properties and tunable surface termination, find a wide range of applications including energy storage and energy conversion. In this work, Ti₃C₂T_x MXene nanosheets are applied as a novel type of electron transport layer (ETL) in low‐temperature processed planar‐structured perovskite solar cells (PSCs). Interestingly, simple UV‐ozone treatment of the metallic Ti₃C₂T_x that increases the surface Ti? O bonds without any change in its bulk properties such as high electron mobility improves its suitability as an ETL. Improved electron transfer and suppressed recombination at the ETL/perovskite interface results in augmentation of the power conversion efficiency (PCE) from 5.00% in the case of Ti₃C₂T_x without UV‐ozone treatment to the champion PCE of 17.17%, achieved using the Ti₃C₂T_x film after 30 min of UV‐ozone treatment. As the first report on the use of pure MXene layer as an ETL in PSCs, this work shows the great potential of MXenes to be used in PSCs and displays their promise for applications in photovoltaic technology in general.     

Revealing the Pseudo‐Intercalation Charge Storage Mechanism of MXenes in Acidic Electrolyte

Since the discovery of Ti₃C₂T_x in 2011, the family of two‐dimensional transition metal carbides, carbonitrides, and nitrides (collectively known as MXenes) has quickly attracted the attention of those developing energy storage applications such as electrodes for supercapacitors with acidic aqueous electrolytes. The excellent performance of these MXenes is attributed to a pseudocapacitive energy storage mechanism, based on the non‐rectangular shape of cyclic voltammetry curves and changes in the titanium oxidation state detected by in situ X‐ray absorption spectroscopy. However, the pseudocapacitive mechanism is not well understood and no dimensional changes due to proton insertion have been reported. In this work, in situ X‐ray diffraction and density functional theory are used to investigate the charge storage mechanism of Ti₃C₂T_x in 1 m H₂SO₄. Results reveal that a 0.5 Å expansion and shrinkage of the c‐lattice parameter of Ti₃C₂T_x occur during cycling in a 0.9 V voltage window, showing that the charge storage mechanism is intercalation pseudocapacitance with implication for MXene use in energy storage and electrochemical actuators.     

Flexible Ti3C2Tx@Al electrodes with Ultrahigh Areal Capacitance: In Situ Regulation of Interlayer Conductivity and Spacing

Although Ti₃C₂ MXene has shown great potential in energy storage field, poor conductivity and restacking between MXene flakes seriously hinders the maximization of its capacitance. Herein, a new strategy to solve the problems is developed. Gallery Al atoms in Ti₃AlC₂ are partially removed by simple hydrothermal etching to get Ti₃C₂T_x reserving appropriate Al interlayers (Ti₃C₂T_x@Al). Ti₃C₂T_x@Al keeps stable layered structure rather than isolated Ti₃C₂T_x flakes, which avoids flake restacking. The removal of partial Al frees up space for easy electrolyte infiltration while the reserved Al as “electron bridges” ensures high interlayer conductivity. As a result, the areal capacitance reaches up to 1087 mF cm^?2 at 1 mA cm^?2 and over 95% capacitance is maintained after 6000 cycles. The all‐solid‐state supercapacitor (ASSS) based on Ti₃C₂T_x@Al delivers a high capacitance of 242.3 mF cm^?2 at 1 mV s^?1 and exhibits stable performance at different bending states. Two ASSSs in tandem can light up a light‐emitting diode under the planar or wrapping around an arm. The established strategy provides a new avenue to improve capacitance performances of MXenes.     

Strategy Toward Semiconducting Ti3C2Tx-MXene: Phenylsulfonic Acid Groups Modified Ti3C2Tx as Photosensitive Material for Flexible Visual Sensory-Neuromorphic System

The excellent electronic and electrochemical properties make 2D MXenes suitable candidates for sensors, batteries, and supercapacitors. However, the metallic-like behavior of MXenes hinders their potential for optoelectronic devices such as photodetectors. In this study, the band gap of metalloid Ti₃C₂T_x MXene is successfully opened to 1.53 eV with phenylsulfonic acid groups and realized a transistor and high-performance near-infrared photodetector array for a flexible vision sensory-neuromorphic system. The phenylsulfonic acid groups modified Ti₃C₂T_x MXene (S-Ti₃C₂T_x)-based flexible photodetector has a maximum responsivity of 8.50×10² A W⁻¹ and a detectivity of 3.69×10¹¹ Jones under 1064 nm laser irradiation. Moreover, the fabricated flexible vision sensory-neuromorphic system for image recognition realizes a high recognition rate >0.99, leading to great potential in the field of biological visual simulation and biomimetic eye. Besides conventional devices with Au as the conductive electrodes, all Ti₃C₂T_x MXene-based devices are also fabricated with S-Ti₃C₂T_x as the photosensitive material and unmodified Ti₃C₂T_x as the conductive electrodes, exhibiting comparable optoelectronic performances.     

2D Titanium Carbide (MXene) Based Films: Expanding the Frontier of Functional Film Materials

2D titanium carbide (Ti₃C₂T_x) MXene films, with their well-defined microstructures and chemical functionality, provide a macroscale use of nano-sized Ti₃C₂T_x flakes. Ti₃C₂T_x films have attractive physicochemical properties favorable for device design, such as high electrical conductivity (up to 20 000 S cm^–1), impressive volumetric capacitance (1500 F cm^–3), strong in-plane mechanical strength (up to 570 MPa), and a high degree of flexibility. Here, the appealing features of Ti₃C₂T_x-based films enabled by the layer-to-layer arrangement of nanosheets are reviewed. We devote attention to the key strategies for actualizing desirable characteristics in Ti₃C₂T_x-based functional films, such as high and tunable electrical conductivity, outstanding mechanical properties, enhanced oxidation-resistance and shelf life, hydrophilicity/hydrophobicity, adjustable porosity, and convenient processability. This review further discusses fundamental aspects and advances in the applications of Ti₃C₂T_x-based films with a focus on illuminating the relationship between the structural features and the resulting performances for target applications. Finally, the challenges and opportunities in terms of future research, development, and applications of Ti₃C₂T_x-based films are suggested. A comprehensive understanding of these competitive features and challenges shall provide guidelines and inspiration for the further development of Ti₃C₂T_x-based functional films, and contribute to the advances in MXene technology.     

Bimetal Organic Framework–Ti3C2Tx MXene with Metalloporphyrin Electrocatalyst for Lithium–Oxygen Batteries

The gravest oxidation of MXenes has become a critical problem due to the formation of metal oxides, leading to the loss of their intrinsic properties. Herein, bimetallic cobalt–manganese organic framework (CMT) directly grown on a Ti₃C₂T_x MXene sheet via solvothermal treatment to obtain strong oxidation resistance in an open structured application and to enhance electrocatalytic properties for oxygen evolution and reduction reaction is reported. Inspired by ligand chemistry, the carboxyl acids in tetrakis(4–carboxyphenyl)porphyrin acting as an organic linker are grafted with the surface terminators of Ti₃C₂T_x MXene through the Fischer esterification and substitution reaction of fluorine, thereby greatly enhancing the antioxidation stability. Furthermore, the as-formed metalloporphyrin structure and unpaired electrons, produced between CMT and Ti₃C₂T_x MXene during solvothermal treatment, improve their electrocatalytic activity, durability, and electrical conductivity through an electron hopping mechanism. Consequently, the CMT@MXene demonstrates high stability as a bifunctional electrocatalyst at a fixed specific capacity of 1000 mAh g⁻¹ and a current density of 500 mA g⁻¹ for 247 cycles in lithium–oxygen (Li O₂) battery. This approach suggests new strategies for the synergistic coupling of MXenes and MOFs for future open structured applications.     

3D Metal Carbide@Mesoporous Carbon Hybrid Architecture as a New Polysulfide Reservoir for Lithium‐Sulfur Batteries

3D metal carbide@mesoporous carbon hybrid architecture (Ti₃C₂T_x@Meso‐C, T_X ≈ F_xO_y) is synthesised and applied as cathode material hosts for lithium‐sulfur batteries. Exfoliated‐metal carbide (Ti₃C₂T_x) nanosheets have high electronic conductivity and contain rich functional groups for effective trapping of polysulfides. Mesoporous carbon with a robust porous structure provides sufficient spaces for loading sulfur and effectively cushion the volumetric expansion of sulfur cathodes. Theoretical calculations have confirmed that metal carbide can absorb sulfur and polysulfides, therefore extending the cycling performance. The Ti₃C₂T_x@Meso‐C/S cathodes have achieved a high capacity of 1225.8 mAh g^?1 and more than 300 cycles at the C/2 current rate. The Ti₃C₂T_x@Meso‐C hybrid architecture is a promising cathode host material for lithium‐sulfur batteries.     

Stamping of Flexible,Coplanar Micro‐Supercapacitors Using MXene Inks

The fast growth of portable smart electronics and internet of things have greatly stimulated the demand for miniaturized energy storage devices. Micro‐supercapacitors (MSCs), which can provide high power density and a long lifetime, are ideal stand‐alone power sources for smart microelectronics. However, relatively few MSCs exhibit both high areal and volumetric capacitance. Here rapid production of flexible MSCs is demonstrated through a scalable, low‐cost stamping strategy. Combining 3D‐printed stamps with arbitrary shapes and 2D titanium carbide or carbonitride inks (Ti₃C₂T_x and Ti₃CNT_x, respectively, known as MXenes), flexible all‐MXene MSCs with controlled architectures are produced. The interdigitated Ti₃C₂T_x MSC exhibits high areal capacitance: 61 mF cm^?2 at 25 µA cm^?2 and 50 mF cm^?2 as the current density increases by 32 fold. The Ti₃C₂T_x MSCs also showcase capacitive charge storage properties, good cycling lifetime, high energy and power densities, etc. The production of such high‐performance Ti₃C₂T_x MSCs can be easily scaled up by designing pad or cylindrical stamps, followed by a cold rolling process. Collectively, the rapid, efficient production of flexible all‐MXene MSCs with state‐of‐the‐art performance opens new exciting opportunities for future applications in wearable and portable electronics.     

Engineering the Interlayer Spacing by Pre-Intercalation for High Performance Supercapacitor MXene Electrodes in Room Temperature Ionic Liquid

MXenes exhibit excellent capacitance at high scan rates in sulfuric acid aqueous electrolytes, but the narrow potential window of aqueous electrolytes limits the energy density. Organic electrolytes and room-temperature ionic liquids (RTILs) can provide higher potential windows, leading to higher energy density. The large cation size of RTIL hinders its intercalation in-between the layers of MXene limiting the specific capacitance in comparison to aqueous electrolytes. In this work, different chain lengths alkylammonium (AA) cations are intercalated into Ti₃C₂T_x, producing variation of MXene interlayer spacings (d-spacing). AA-cation-intercalated Ti₃C₂T_x (AA-Ti₃C₂), exhibits higher specific capacitances, and cycling stabilities than pristine Ti₃C₂T_x in 1 m 1-ethly-3-methylimidazolium bis-(trifluoromethylsulfonyl)-imide (EMIMTFSI) in acetonitrile and neat EMIMTFSI RTIL electrolytes. Pre-intercalated MXene with an interlayer spacing of ≈2.2 nm, can deliver a large specific capacitance of 257 F g⁻¹ (1428 mF cm⁻² and 492 F cm⁻³) in neat EMIMTFSI electrolyte leading to high energy density. Quasi elastic neutron scattering and electrochemical impedance spectroscopy are used to study the dynamics of confined RTIL in pre-intercalated MXene. Molecular dynamics simulations suggest significant differences in the structures of RTIL ions and AA cations inside the Ti₃C₂T_x interlayer, providing insights into the differences in the observed electrochemical behavior.     

Pristine Titanium Carbide MXene Films with Environmentally Stable Conductivity and Superior Mechanical Strength

2D titanium carbide (Ti₃C₂T_x MXene) has potential application in flexible/transparent conductors because of its metallic conductivity and solution processability. However, solution‐processed Ti₃C₂T_x films suffer from poor hydration stability and mechanical performance that stem from the presence of intercalants, which are unavoidably introduced during the preparation of Ti₃C₂T_x suspension. A proton acid colloidal processing approach is developed to remove the extrinsic intercalants in Ti₃C₂T_x film materials, producing pristine Ti₃C₂T_x films with significantly enhanced conductivity, mechanical strength, and environmental stability. Typically, pristine Ti₃C₂T_x films show more than twofold higher conductivity (10 400 S cm^?1 vs 4620 S cm^?1) and up to 11‐ and 32‐times higher strength and strain energy at failure (112 MPa, 1,480 kJ m^?3, vs 10 MPa, 45 kJ m^?3) than films prepared without proton acid processing. Simultaneously, the conductivity and mechanical integrity of pristine films are also largely retained during the long‐term storage in H₂O/O₂ environment. The improvement in mechanical performance and conductivity is originated from the intrinsic strong interaction between Ti₃C₂T_x layers, and the absence of extrinsic intercalants makes pristine Ti₃C₂T_x films stable in humidity by blocking the intercalation of H₂O/O₂. This method makes the material more competitive for real‐world applications such as electromagnetic interference shielding.     

A Robust,Freestanding MXene‐Sulfur Conductive Paper for Long‐Lifetime Li–S Batteries

Freestanding, robust electrodes with high capacity and long lifetime are of critical importance to the development of advanced lithium–sulfur (Li–S) batteries for next‐generation electronics, whose potential applications are greatly limited by the lithium polysulfide (LiPS) shuttle effect. Solutions to this issue have mostly focused on the design of cathode hosts with a polar, sulfurphilic, conductive network, or the introduction of an extra layer to suppress LiPS shuttling, which either results in complex fabrication procedures or compromises the mechanical flexibility of the device. A robust Ti₃C₂T_x/S conductive paper combining the excellent conductivity, mechanical strength, and unique chemisorption of LiPSs from MXene nanosheets is reported. Importantly, repeated cycling initiates the in situ formation of a thick sulfate complex layer on the MXene surface, which acts as a protective membrane, effectively suppressing the shuttling of LiPSs and improving the utilization of sulfur. Consequently, the Ti₃C₂T_x/S paper exhibits a high capacity and an ultralow capacity decay rate of 0.014% after 1500 cycles, the lowest value reported for Li–S batteries to date. A robust prototype pouch cell and full cell of Ti₃C₂T_x/S paper // lithium foil and prelithiated germanium are also demonstrated. The preliminary results show that Ti₃C₂T_x/S paper holds great promise for future flexible and wearable electronics.     

Tetrabutylammonium Bromide Functionalized Ti3C2Tx MXene as Versatile Cathode Buffer Layer for Efficient and Stable Inverted Perovskite Solar Cells

2D Ti₃C₂T_x MXene, possessing facile preparation, high electrical conductivity, flexibility, and solution processability, shows good application potential for enhancing device performance of perovskite solar cells (PVSCs). In this study, tetrabutylammonium bromide functionalized Ti₃C₂T_x (TBAB-Ti₃C₂T_x) is developed as cathode buffer layer (CBL) to regulate the PCBM/Ag cathode interfacial property for the first time. By virtue of the charge transfer from TBAB to Ti₃C₂T_x demonstrated by electron paramagnetic resonance and density functional theory, the TBAB-Ti₃C₂T_x CBL with high electrical conductivity exhibits significantly reduced work function of 3.9 eV, which enables optimization of energy level alignment and enhancement of charge extraction. Moreover, the TBAB-Ti₃C₂T_x CBL can effectively inhibit the migration of iodine ions from perovskite layer to Ag cathode, which synergistically suppresses defect states and reduce charge recombination. Consequently, utilizing MAPbI₃ perovskite without post-treatment, the TBAB-Ti₃C₂T_x based device exhibits a dramatically improved power conversion efficiency of 21.65% with significantly improved operational stability, which is one of the best efficiencies reported for the devices based on MAPbI₃/PCBM with different CBLs. These results indicate that TBAB-Ti₃C₂T_x shall be a promising CBL for high-performance inverted PVSCs and inspire the further applications of quaternary ammonium functionalized MXenes in PVSCs.     

Electrochromic Effect in Titanium Carbide MXene Thin Films Produced by Dip‐Coating

MXenes, a large family of 2D transition metal carbides and nitrides, have shown potential in energy storage and optoelectronic applications. Here, the optoelectronic and pseudocapacitive properties of titanium carbide (Ti₃C₂T_x) are combined to create a MXene electrochromic device, with a visible absorption peak shift from 770 to 670 nm and a 12% reversible change in transmittance with a switching rate of <1 s when cycled in an acidic electrolyte under applied potentials of less than 1 V. By probing the electrochromic effect in different electrolytes, it is shown that acidic electrolytes (H₃PO₄ and H₂SO₄) lead to larger absorption peak shifts and a higher change of transmittance than the neutral electrolyte (MgSO₄) (Δλ is 100 nm vs 35 nm and ΔT_{770 nm} is ≈12% vs ≈3%, respectively), hinting at the surface redox mechanism involved. Further investigation of the mechanism by in situ X‐ray diffraction and Raman spectroscopy reveals that the reversible shift of the absorption peak is attributed to protonation/deprotonation of oxide‐like surface functionalities. As a proof of concept, it is shown that Ti₃C₂T_x MXene, dip‐coated on a glass substrate, functions as both transparent conductive coating and active material in an electrochromic device, opening avenues for further research into optoelectronic and photonic applications of MXenes.     

Layered Orthorhombic Nb2O5@Nb4C3Tx and TiO2@Ti3C2Tx Hierarchical Composites for High Performance Li‐ion Batteries

Engineering electrode nanostructures is critical in developing high‐capacity, fast rate‐response, and safe Li‐ion batteries. This study demonstrates the synthesis of orthorhombic Nb₂O₅@Nb₄C₃T_x (or @Nb₂CT_x) hierarchical composites via a one‐step oxidation —in flowing CO₂ at 850 °C —of 2D Nb₄C₃T_x (or Nb₂CT_x) MXene. The composites possess a layered architecture with orthorhombic Nb₂O₅ nanoparticles decorated uniformly on the surface of the MXene flakes and interconnected by disordered carbon. The composites have a capacity of 208 mAh g^?1 at a rate of 50 mA g^?1 (0.25 C) in 1–3 V versus Li⁺/Li, and retain 94% of the specific capacity with 100% Coulombic efficiency after 400 cycles. The good electrochemical performances could be attributed to three synergistic effects: (1) the high conductivity of the interior, unoxidized Nb₄C₃T_x layers, (2) the fast rate response and high capacity of the external Nb₂O₅ nanoparticles, and (3) the electron “bridge” effects of the disordered carbon. This oxidation method was successfully extended to Ti₃C₂T_x and Nb₂CT_x MXenes to prepare corresponding composites with similar hierarchical structures. Since this is an early report on producing this structure, there is much room to push the boundaries further and achieve better electrochemical performance.     

Covalent Assembly of Two-Dimensional COF-on-MXene Heterostructures Enables Fast Charging Lithium Hosts

2D heterostructured materials combining ultrathin nanosheet morphology, defined pore configuration, and stable hybrid compositions, have attracted increasing attention for fast mass transport and charge transfer, which are highly desirable features for efficient energy storage. Here, the chemical space of 2D–2D heterostructures is extended by covalently assembling covalent organic frameworks (COFs) on MXene nanosheets. Unlike most COFs, which are generally produced as solid powders, ultrathin 2D COF-LZU1 grows in situ on aminated Ti₃C₂T_x nanosheets with covalent bonding, producing a robust MXene@COF heterostructure with high crystallinity, hierarchical porosity, and conductive frameworks. When used as lithium hosts in Li metal batteries, lithium storage and charge transport are significantly improved. Both spectroelectrochemical and theoretical analyses demonstrate that lithiated COF channels are important as fast Li⁺ transport layers, by which Li ions can be precisely nucleated. This affords dendrite-free and fast-charging anodes, which would be difficult to achieve using individual components.     

Nonoxidized MXene Quantum Dots Prepared by Microexplosion Method for Cancer Catalytic Therapy

Nanocatalysts based on Fenton or Fenton‐like reactions for amplification of intracellular oxidative stress has become a frontier research area of tumor precise therapy. However, the major translational challenges are low catalytic efficiency, poor biocompatibility, and even potential toxicities. Here, a Ti‐based material with excellent biocompatibility is proposed for cancer treatment. The nonoxidized MXene‐Ti₃C₂T_x quantum dots (NMQDs‐Ti₃C₂T_x) are successfully prepared by a self‐designed microexplosion method. Surprisingly, it has an apparent inhibitory and killing effect on cancer cells, and excellent biocompatibility with normal cells. Moreover, the suppression rate of NMQDs‐Ti₃C₂T_x on xenograft tumor models can reach 91.9% without damaging normal tissues. Mechanistically, the Ti³⁺ of NMQDs‐Ti₃C₂T_x can react with H₂O₂ in the tumor microenvironment and high‐efficiently produce excessive toxic hydroxyl radicals to increase tumor microvascular permeability to synergistically kill cancer cells. This work should pave the way for tumor catalytic therapy applications of Ti‐based material as a promising and safer route.     

High Linearity,Low Hysteresis Ti3C2Tx MXene/AgNW/Liquid Metal Self-Healing Strain Sensor Modulated by Dynamic Disulfide and Hydrogen Bonds

Flexible wearable strain sensors have received extensive attention in human–computer interaction, soft robotics, and human health monitoring. Despite significant efforts in developing stretchable electronic materials and structures, developing flexible strain sensors with stable interfaces and low hysteresis remains a challenge. Herein, Ti₃C₂T_x MXene/AgNWs/liquid metal strain sensors (MAL strain sensor) with self-healing function are developed by exploiting the strong interactions between Ti₃C₂T_x MXene/AgNWs/LM and the disulfide and hydrogen bonds inside the self-healing poly(dimethylsiloxane) elastomers. AgNWs lap the Ti₃C₂T_x MXene sheets, and the LM acts as a bridge to increase the lap between Ti₃C₂T_x MXene and AgNWs, thereby improving the interface interaction between them and reducing hysteresis. The MAL strain sensor can simultaneously achieve high sensitivity (gauge factor for up to 3.22), high linearity (R² = 0.98157), a wide range of detection (e.g., 1%–300%), a fast response time (145 ms), excellent repeatability, and stability.In addition, the MAL strain sensor before and after self-healing is combined with a small fish and an electrothermally driven soft robot, respectively, allowing real-time monitoring of the swinging tail of the small fish and the crawling of the soft robot by resistance changes.     

Enhancing the Energy Storage Capabilities of Ti3C2Tx MXene Electrodes by Atomic Surface Reduction

MXenes are a large class of 2D materials that consist of few-atoms-thick layers of transition metal carbides, nitrides, or carbonitrides. The surface functionalization of MXenes has immense implications for their physical, chemical, and electronic properties. However, solution-phase surface functionalization often leads to structural degradation of the MXene electrodes. Here, a non-conventional, single-step atomic surface reduction (ASR) technique is adopted for the surface functionalization of MXene (Ti₃C₂T_x) in an atomic layer deposition reactor using trimethyl aluminum as a volatile reducing precursor. The chemical nature of the modified surface is characterized by X-ray photoelectron spectroscopy and nuclear magnetic resonance techniques. The electrochemical properties of the surface-modified MXene are evaluated in acidic and neutral aqueous electrolyte solutions, as well as in conventional Li-ion and Na-ion organic electrolytes. A considerable improvement in electrochemical performance is obtained for the treated electrodes in all the examined electrolyte solutions, expressed in superior rate capability and cycling stability compared to those of the non-treated MXene films. This improved electrochemical performance is attributed to the increased interlayer spacing and modified surface terminations after the ASR process.     

2D/2D Heterojunction of Ultrathin MXene/Bi2WO6 Nanosheets for Improved Photocatalytic CO2 Reduction

Exploring cheap and efficient cocatalysts for enhancing the performance of photocatalysts is a challenge in the energy conversion field. Herein, 2D ultrathin Ti₃C₂ nanosheets, a kind of MXenes, are prepared by etching Ti₃AlC₂ with subsequent ultrasonic exfoliation. A novel 2D/2D heterojunction of ultrathin Ti₃C₂/Bi₂WO₆ nanosheets is then successfully prepared by in situ growth of Bi₂WO₆ ultrathin nanosheets on the surface of these Ti₃C₂ ultrathin nanosheets. The resultant Ti₃C₂/Bi₂WO₆ hybrids exhibit a short charge transport distance and a large interface contact area, assuring excellent bulk‐to‐surface and interfacial charge transfer abilities. Meanwhile, the improved specific surface area and pore structure endow Ti₃C₂/Bi₂WO₆ hybrids with an enhanced CO₂ adsorption capability. As a result, the 2D/2D heterojunction of ultrathin Ti₃C₂/Bi₂WO₆ nanosheets shows significant improvement on the performance of photocatalytic CO₂ reduction under simulated solar irradiation. The total yield of CH₄ and CH₃OH obtained on the optimized Ti₃C₂/Bi₂WO₆ hybrid is 4.6 times that obtained on pristine Bi₂WO₆ ultrathin nanosheets. This work provides a new protocol for constructing 2D/2D photocatalytic systems and demonstrates Ti₃C₂ as a promising and cheap cocatalyst.