Synergistic effects of layered Ti3C2TX MXene/MIL-101(Cr) heterostructure as a sonocatalyst for efficient degradation of sulfadiazine and acetaminophen in water.

In this work, different mass loadings of MXene-coupled MIL-101(Cr) (MXe/MIL-101(Cr)) nanocomposites were generated through a hydrothermal process in order to investigate the potential of this nanocomposite as a novel sonocatalyst for the elimination of sulfadiazine (SD) and acetaminophen (AAP) in aqueous media. The sonocatalytic activity of different MXe/MIL-101(Cr) compositions and surface functionalities was investigated. In addition, the sonocatalytic activities at various pH values, temperatures, pollutant concentrations, catalyst dosages, initial H2O2 concentrations, and organic matter contents were investigated. The experiments on the sonocatalytic elimination of SD and AAP revealed that MXe/MIL-101(Cr) exhibited a catalytic efficiency of âˆ¼ 98% in 80 min when the MXene loading was 30 wt% in the nanocomposite. Under optimized reaction conditions, the degradation efficiency of MXe/MIL-101(Cr) reached 91.5% for SD and 90.6% for AAP in 60 min; these values were 1.2 and 1.8 times greater than those of MXene and MIL-101(Cr), respectively. The high surface area of the MXe/MIL-101(Cr) nanocomposite increased from 4.68 m2/g to 294.21 m2/g, and the band gap of the tagged MIL-101(Cr) on the MXene surface was minimized. The superior sonocatalytic activity of MXe/MIL-101(Cr) was attributed to the effective contact interface, the effective separation rate of e- - h+ pairs through the type II heterostructure interface, and the favorable high free •OH radical production rates that promoted the degradation of SD and AAP. The solid heterointerface between MIL-101(Cr) and MXene was confirmed through Raman and FTIR analysis and was found to promote accessible •OH radical production under sonication, thus maximizing the catalytic activity of nanocomposites. The present results present an effective strategy for the design of a highly efficient, low-cost, reliable sonocatalyst that can eradicate pharmaceutical pollutants in our environment.

Zn-ion Batteries: Charge Storing Mechanism and Development Challenges.

Improving the energy share of renewable energy technologies is the only solution to reduce greenhouse gas emissions and air pollution. The high-performing green battery energy storage technologies are critical for storing energy to address the intermittent nature of renewable energy resources. In recent years, aqueous batteries, particularly Zn-ion batteries (ZIBs), have achieved and shown great potential for stationary energy storage systems owing to their low cost and safer operation. However, the practical applications of the ZIBs have significantly been impeded due to the gap between the breakthroughs achieved in academic research and industrial developments. The present review discusses the ZIB's advantages, possibilities, and shortcomings for stationary energy storage systems. The Review begins with a brief introduction to the ZIBs and their charge storage mechanisms based on the structural properties of cathode materials. The scientific and technical challenges that obstruct the commercialization of the ZIBs are discussed in detail concerning their impact on accelerating the utilization of the ZIBs for real-life applications. The final section highlights the outlook on research in this flourishing field.

Fabrication of a High-Performance Hybrid Supercapacitor Based on Hydrothermally Synthesized Highly Stable Cobalt Manganese Phosphate Thin Films.

In the present study, cobalt manganese phosphate (H-CMP-series) thin films with different compositions of Co/Mn are prepared on stainless steel (SS) substrate via a facile hydrothermal method and employed as binder-free cathode electrodes in a hybrid supercapacitor. The XRD study reveals a monoclinic crystal structure, and the FE-SEM analysis confirmed that H-CMP-series samples displayed a nano/microarchitecture (microflowers to nanoflakes) on the surface of SS substrate with excess available surfaces and unique sizes. Interestingly, the synergy between cobalt and manganese species in the cobalt manganese phosphate thin film electrode demonstrates a maximum specific capacitance of 571 F g-1 at a 2.2 A g-1 current density in 1 M KOH. Besides, the nano/microstructured cobalt manganese phosphate was able to maintain capacitance retention of 88% over 8000 charge-discharge cycles. More importantly, the aqueous/all-solid-state asymmetric supercapacitor manufactured with the cobalt manganese phosphate thin film as the cathode and reduced graphene oxide (rGO) as the anode displays a high operating potential window of 1.6 V. The aqueous asymmetric device exhibited a maximum specific capacitance of 128 F g-1 at a current density of 1 A g-1 with an energy density of 45.7 Wh kg-1 and a power density of 1.65 kW kg-1. In addition, the all-solid-state asymmetric supercapacitor device provides a high specific capacitance of 37 F g-1 at 1 A g-1 with 13.3 Wh kg-1 energy density and 1.64 kW kg-1 power density in a polymer gel (PVA-KOH) electrolyte. The long cyclic life of both devices (87 and 84%, respectively, after 6000 cycles) and practical demonstration of the solid-state device (lighting of a LED lamp) suggest another alternative choice for cathode materials to develop stable energy storage devices with high energy density. Furthermore, the aforementioned study paves the way to investigate phosphate-based materials as a new class of materials for supercapacitor applicability.