Boosting Performance of Na-S Batteries Using Sulfur-Doped Ti<inf>3</inf>C<inf>2</inf>T<inf>x</inf> MXene Nanosheets with a Strong Affinity to Sodium Polysulfides

Copyright © 2019 American Chemical Society. Sodium-sulfur batteries using abundant elements offer an attractive alternative to currently used batteries, but they need better sulfur host materials to compete with lithium-ion batteries in capacity and cyclability. We report an in situ sulfur-doping strategy to functionalize MXene nanosheets by introducing heteroatomic sulfur into the MXene structure form the MAX phase precursor. By employing the vacuum freeze-drying method, a three-dimensional (3D) wrinkled MXene nanoarchitecture with the high specific surface area was prepared. The tailor-made wrinkled sulfur-doped MXene (S-Ti3C2Tx) nanosheets were applied as an electrode host material in room temperature sodium-sulfur batteries. The S-Ti3C2Tx matrix shows high polarity with sodium polysulfides, restricting the diffusion of sodium polysulfides. The MXene/sulfur electrode can achieve high areal sulfur loading up to 4.5 mg cm-2 as well as good electrochemical performance (reversible capacity of 577 mAh g-1 at 2 C after 500 cycles)

Two-dimensional vanadium carbide (V2C) MXene as electrode for supercapacitors with aqueous electrolytes

Recently, a large family of 2D materials called MXenes have attracted much attention in the field of supercapacitors, thanks to the excellent performance demonstrated by Ti3C2 MXene-based electrodes. However, research on MXenes for supercapacitor applications has been primarily focused on Ti3C2, even though there are more than 20 other members of this large family of materials already available. Studies on other MXenes are emerging, with promising results already achieved by Ti2C, Mo2C, and Mo1.33C in aqueous electrolytes. Yet, many other MXenes remain unexplored in aqueous supercapacitor applications. In this work, we report on the electrochemical behavior of a vanadium carbide MXene, V2C, in three aqueous electrolytes. Excellent specific capacitances were achieved, specifically 487 F/g in 1 M H2SO4, 225 F/g in 1 M MgSO4, and 184 F/g in 1 M KOH, which are higher than previously reported values for few micrometer-thick delaminated MXene electrodes. This work shows the promise of V2C MXene for energy storage using aqueous electrolytes

SnO2–Ti3C2 MXene electron transport layers for perovskite solar cells

MXenes, a class of two-dimensional (2D) transition metal carbides and nitrides, have a wide range of potential applications due to their unique electronic, optical, plasmonic, and other properties. Herein, we explore the use of the Ti3C2 MXene in organic–inorganic lead halide perovskite solar cells (PSCs). SnO2–Ti3C2 MXene nanocomposites with different contents of Ti3C2 (0, 0.5, 1.0, 2.0, and 2.5 wt‰) were used as electron transport layers (ETLs) in low-temperature processed planar-structured PSCs. Mixing SnO2 with 1.0 wt‰ Ti3C2 effectively increases the power conversion efficiency (PCE) from 17.23% to 18.34%, whereas the device prepared with pristine Ti3C2 as the ETL achieves a PCE of 5.28%. Photoluminescence and electrochemical impedance spectroscopy results reveal that metallic Ti3C2 MXene nanosheets provide superior charge transfer paths, enhancing electron extraction, electron mobility, and decreasing the electron transfer resistance at the ETL/perovskite interface, and thus leading to higher photocurrents. This work proposes a new field of application for MXenes and a promising method to increase the efficiency of solar cells