Sustainable ZIF-67/Mo-MXene-Derived Nanoarchitecture Synthesis: An Enhanced Durable Performance of Lithium-Selenium Batteries.

Selenium-based electrodes have garnered attention for their high electrical conductivity, compatibility with carbonate electrolytes, and volumetric capacity comparable to sulfur electrodes. However, real-time application is hindered by rapid capacity deterioration from the "shuttle effect" of polyselenides and volume fluctuations. To address these challenges, a hybrid Se@ZIF-67/Mo-MXene-derived (Se@Co-NC/Mo2C) nanoarchitecture is developed via an economically viable in situ electrostatic self-assembly of ZIF-67 and Mo2C nanosheets. The catalytic effects and porous framework of Co-NC/Mo2C enhance electrode attributes, promoting superior adsorption and conversion of lithium polyselenides and facile ion/electron transport within the electrode, resulting in stable electrochemical performance. Lithium-selenium batteries (LSeBs) exhibit remarkable characteristics, boasting high specific capacity and exceptional durability. The Se@Co-NC/Mo2C electrode delivers a reversible capacity of 503.5 mAh g-1 at 0.5 C with 98% capacity retention, 100% Coulombic efficiency, and exceptional cyclic durability through 8600 cycles. In sustainability tests at 10C/1C charging/discharging, the Se@Co-NC/Mo2C electrode demonstrates an optimistic and stable capacity of ≈370.6 mAh g-1 with 93% capacity retention at the 3100th cycle in a carbonate-based electrolyte and ≈181.3 mAh g-1 with 92% capacity retention after 5000 cycles in an ether-based electrolyte, indicating exceptional stability for practical rechargeable batteries. This cost-effective and efficient approach holds significant potential for high-performance and durable LSeBs.

Designing a Se-intercalated MOF/MXene-derived nanoarchitecture for advancing the performance and durability of lithium-selenium batteries.

Lithium-selenium batteries have emerged as a promising alternative to lithium-sulfur batteries due to their high electrical conductivity and comparable volume capacity. However, challenges such as the shuttle effect of polyselenides and high-volume fluctuations hinder their practical implementation. To address these issues, we propose synthesizing Fe-CNT/TiO2 catalyst through high-temperature sintering of an amalgamated nanoarchitecture of carbon nanotubes decorated metal-organic framework (MOF) and MXene, optimized for efficient selenium hosting, leveraging the distinctive physicochemical properties. The catalytic features inherent in the porous Se@Fe-CNT/TiO2 nanoarchitecture were instrumental in promoting efficient ion and electron transport, and lithium-polyselenide kinetics, while its inherent porosity could play a crucial role in inhibiting electrode stress during cycling. This nanoarchitecture exhibits remarkable battery performance, retaining 99.7% of theoretical capacity after 425 cycles at 0.5 C rate and demonstrating 95.8% capacity retention after 2000 cycles at 1 C rate, with ∼100% Coulombic efficiency. Additionally, the Se@Fe-CNT/TiO2 electrode exhibited an impressive recovery of 297.5 mAh/g (97.9%) capacity after undergoing 450 cycles at a charging rate of 10 C and a discharging rate of 1 C. This synergistic integration of MOF- and MXene-derived materials unveils new possibilities for high-performance and durable LSeBs, thus advancing electrochemical energy storage systems.

Rational Design of Oil-Resistant and Electrically Conductive Fluorosilicone Rubber Foam Nanocomposites for Sensitive Detectability in Complex Solvent Environments.

Recent years have witnessed the explosive development of highly sensitive smart sensors based on conductive polymer foam materials. However, the design and development of multifunctional polymeric foam composites as smart sensors applied in complex solvent and oil environments remain a critical challenge. Herein, we design and synthesize vinyl-terminated polytrifluoropropylmethylsiloxane through anionic ring-opening polymerization to fabricate fluorosilicone rubber foam (FSiRF) materials with nanoscale wrinkled surfaces and reactive Si-H groups via a green and rapid chemical foaming strategy. Based on the strong adhesion between FSiRF materials and consecutive oxidized ketjen black (OKB) nano-network, multifunctional FSiRF nanocomposites were prepared by a dip-coating strategy followed by fluoroalkylsilane modification. The optimized F-OKB@FSiRF nanocomposites exhibit outstanding mechanical flexibility in wide-temperature range (100 cycle compressions from -20 to 200 °C), structure stability (no detached particles after being immersed into various aqueous solutions for up to 15 days), surface superhydrophobicity (water contact angle of 154° and sliding angle of ∼7°), and tunable electrical conductivity (from 10-5 to 10-2 S m-1). Additionally, benefiting from the combined actions of multiple lines of defense (low surface energy groups, physical barriers, and "shielding effect"), the F-OKB@FSiRF sensor presents excellent anti-swelling property and high sensitivity in monitoring both large-deformation and tiny vibrations generated by knocking the beaker, ultrasonic action, agitating, and sinking objects in weak-polar or nonpolar solvents. This work conceivably provides a chemical strategy for the fabrication of multifunctional polymeric foam nanocomposite materials as smart sensors for broad applications.