Ti 3 C 2 T x (MXene) exhibits attractive properties in different applications. However, traditional synthesis leads to unsatisfactory yield of two-dimensional (2D) Ti 3 C 2 T x , e.g., lower than 20%, which stems from the strong interactions of potential Ti−Ti bonds and residual Ti−Al bonds between the adjacent Ti 3 C 2 layers, hindering the effective intercalation and delamination. Herein, we propose a facile hydrothermalassisted intercalation (HAI) strategy to boost the yield of 2D sheets, achieving a record high value of 74%. This HAI assists the diffusion and intercalation of reagent effectively, promoting the subsequent delamination; meanwhile, an antioxidant is applied to protect these Ti 3 C 2 T x from oxidation during the HAI process. Therefore, massive Ti 3 C 2 T x 2D sheets can be easily synthesized. Thanks to the synergistic effect of high conductivity and substantial terminated functionalities, these Ti 3 C 2 T x 2D sheets show promising application in supercapacitor, providing a high capacitance of 482 F g −1 . Besides, the ultrafast carrier dynamics results of Ti 3 C 2 T x 2D sheets clearly imply the promising application in photocatalysis due to the relatively long bleaching relaxation time. Our work not only paves the way for the mass production of Ti 3 C 2 T x 2D sheets but also provides insights into their electronic and optical properties. KEYWORDS: hydrothermal-assisted intercalation (HAI), Ti 3 C 2 T x , MXene, high yield, facile

A brand new polysulfide entrapping strategy based on the ferroelectric effect has been demonstrated for the first time. By simply adding the nano-ferroelectrics (BaTiO nanoparticles) into the cathode, the heteropolar polysulfides can be anchored within the cathode due to the internal electric field originated from the spontaneous polarization BaTiO nanoparticles, and thus significantly improving the cycle stability of Li-S batteries.

A new Fe-based metallic glass with composition Fe76B12Si9Y3 (at. %) is found to have extraordinary degradation efficiency towards methyl orange (MO, C14H14N3SO3) in strong acidic and near neutral environments compared to crystalline zero-valent iron (ZVI) powders and other Fe-based metallic glasses. The influence of temperature (294–328 K) on the degradation reaction rate was measured using ball-milled metallic glass powders revealing a low thermal activation energy barrier of 22.6 kJ/mol. The excellent properties are mainly attributed to the heterogeneous structure consisting of local Fe-rich and Fe-poor atomic clusters, rather than the large specific surface and strong residual stress in the powders. The metallic glass powders can sustain almost unchanged degradation efficiency after 13 cycles at room temperature, while a drop in degradation efficiency with further cycles is attributed to visible surface oxidation. Triple quadrupole mass spectrometry analysis conducted during the reaction was used to elucidate the underlying degradation mechanism. The present findings may provide a new, highly efficient and low cost commercial method for azo dye wastewater treatment.

A highly textured (111)-oriented Pb0.8Ba0.2ZrO3 (PBZ) relaxor thin film with the coexistence of antiferroelectric (AFE) and ferroelectric (FE) phases was prepared on a Pt/TiOx/SiO2/Si(100) substrate by using a sol-gel method. A large recoverable energy storage density of 40.18 J/cm(3) along with an efficiency of 64.1% was achieved at room temperature. Over a wide temperature range of 250 K (from room temperature to 523 K), the variation of the energy density is within 5%, indicating a high thermal stability. The high energy storage performance was endowed by a large dielectric breakdown strength, great relaxor dispersion, highly textured orientation, and the coexistence of FE and AFE phases. The PBZ thin film is believed to be an attractive material for applications in energy storage systems over a wide temperature range.

Novel S-doped carbon quantum dots are synthesized and used for the detection of Fe3+ in an extremely strong acid environment.

Luminescent water-induced shape memory polymer (SMP) composites with tunable shape recovery rate are developed by blending poly(vinyl alcohol) (PVA) and carbon quantum dots (CQDs). The oxygen and active hydrogen-rich CQDs can serve as extra physical cross-linking points in PVA via strong hydrogen bonding interaction, which largely improves the shape memory performances of PVA. At room temperature, water can successfully actuate the shape recovery of deformed PVA/CQDs composite. It is demonstrated that this water-induced shape recovery is mainly attributed to the plasticizing effect of water and its competitive hydrogen bonding. Furthermore, a quantitative bending test suggests that the shape recovery time of this water-induced SMP is tunable by altering the environmental pH value and temperature, and a relatively large shape recovery time window (from 20 to 200 s) can be achieved. In addition, the introduction of CQDs endows the PVA/CQDs SMP composites with excellent luminescent property, which makes the shape change of SMP visible under UV light. It should be noted that the mild stimulus condition and tunable shape recovery performances make the luminescent visible PVA/CQDs SMP feasible for diverse biological applications in smart medical devices, stimuli-responsive drug-release, and intelligent sensors in vivo and in vitro.

Modification of an FTO surface using tetramethylammonium hydroxide achieves 20.1% efficiency for ETL-free perovskite solar cells with a reduced hysteresis.

Sn-doped InO (ITO) electrodes were deposited on transparent and flexible muscovite mica. The use of mica substrate makes a high-temperature annealing process (up to 500 °C) possible. ITO/mica retains its low electric resistivity even after continuous bending of 1000 times on account of the unique layered structure of mica. When used as a transparent flexible heater, ITO/mica shows an extremely fast ramping (<15 s) up to a high temperature of over 438 °C. When used as a transparent electrode, ITO/mica permits a high-temperature annealing (450 °C) approach to fabricate flexible perovskite solar cells (PSCs) with high efficiency.