Improvement of the Thermal Insulation Performance of Silica Aerogel by Proper Heat Treatment: Microporous Structures Changes and Pyrolysis Mechanism.

A simple heat treatment method was used to optimize the three-dimensional network structure of the hydrophobic aerogel, and during the heat treatment process at 200-1000 °C, the thermal conductivity of the aerogel reached the lowest to 0.02240 W/m·K between 250 °C and 300 °C, which was mainly due to the optimization of microstructure and pyrolysis of surface groups. Further Fluent heat-transfer simulation also confirmed the above results. Synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) was used to finely measure the pyrolysis process of aerogels, and the pyrolysis process of aerogel was divided into four stages. (I) Until 419 °C, as the temperature continued to rise, surface methyl groups were oxidized to form hydroxyl. (II) As the temperature reached to 232 °C, the oxidation proceeded. In addition, inside the aerogel, because of lacking oxygen, the reaction produced CH4 and C-Si bonds would form. (III) After 283 °C, Si-OH groups began to condense to form Si-O-Si, which optimized the three-dimensional network structures to be beneficial to improve the thermal insulation performance of silica aerogel. (IV) When it reached 547 °C, the chemical reaction was terminated, and all the primary particles gradually fused into secondary particles and sintered to form clusters.

Mechanically Strong and Tailorable Polyimide Aerogels Prepared with Novel Silicone Polymer Crosslinkers.

Polyimide (PI) aerogels were prepared using self-designed silicone polymer cross-linkers with multi-amino from low-cost silane coupling agents to replace conventional small-molecule cross-linkers. The long-chain structure of silicone polymers provides more crosslinking points than small-molecule cross-linkers, thus improving the mechanical properties of polyimide. To investigate the effects of amino content and degree of polymerization on the properties of silicone polymers, the different silicone polymers and their cross-linked PI aerogels were prepared. The obtained PI aerogels exhibit densities as low as 0.106 g/cm3 and specific surface areas as high as 314 m2/g, and the maximum Young's modulus of aerogel is up to 20.9 MPa when using (T-20) as cross-linkers. The cross-linkers were an alternative to expensive small molecule cross-linkers, which can improve the mechanical properties and reduce the cost of PI aerogels.

"Robust-Soft" Anisotropic Nanofibrillated Cellulose Aerogels with Superior Mechanical, Flame-Retardant, and Thermal Insulating Properties.

Advanced thermal insulation materials with low thermal conductivity and robustness derived from regenerative resources are badly needed for building energy conservation. Among them, nanofibrillated cellulose aerogels have huge application potential in the field of thermal insulation materials, but it is still a challenge to prepare cellulose aerogels of excellent comprehensive properties in a simple way. Herein, we demonstrate a unidirectional freeze-drying strategy to develop a novel "robust-soft" anisotropic nanofibrillated cellulose aerogel (NFC-Si-T) by integrating nanofibrillated cellulose (NFC) and Si-O-Si bonding networks under the catalytic dehydration of p-toluenesulfonic acid (TsOH). The anisotropic structure endows the NFC-Si-T with high flexibility that can be easily bent or even tied with a knot, and in addition, it possesses high Young's modulus (1-3.66 MPa) that can resist the compression weight of 10,000 times of its own weight without deformation. Furthermore, the NFC-Si-T aerogels exhibit anisotropic thermal insulation performances with a low average thermal conductivity (0.028-0.049 W m-1 K-1). More importantly, the limited oxygen index of the NFC-Si-T reaches up to 42.6-51%, showing excellent flame-retardant performance. Therefore, the "robust-soft" anisotropic NFC-Si-T aerogels can be used as an advanced thermal insulation material for building thermal insulation applications.

Mechanically strong polyimide aerogels cross-linked with low-cost polymers.

Polyimide aerogels were prepared using low-cost polymers with different structure capped polyamide oligomers serving as cross-linking agents. To investigate the effects of the anhydride density on cross-linker chain units and side groups of cross-linkers on their properties and microstructures, two kinds of polymers from maleic anhydride, endic anhydride, and styrene were prepared by simple radical polymerization. The polyimide aerogels exhibit densities as low as 0.087 g cm-3 and specific surface areas as high as 456 m2 g-1. And the maximum modulus of the aerogel is up to 21.3 MPa. These cross-linkers are alternatives to expensive small molecule cross-linkers, therefore reducing the cost of PI aerogels.

A long life sodium-selenium cathode by encapsulating selenium into N-doped interconnected carbon aerogels.

Selenium cathodes have attracted a great deal of attention due to their much higher electronic conductivity compared to sulfur cathodes and similar volumetric capacity to them. However, selenium cathodes still suffer from rapid capacity fading because of low utilization of active materials, high volume changes and the shuttle effect of polyselenides. Herein, we prepared selenium-carbon aerogel composites as cathodes for sodium-selenium batteries by infiltrating selenium into the microporous structure of N-doped interconnected carbon aerogels (Se@NCAs). The carbon matrix could effectively accommodate the volume change of Se during cycling and alleviate the shuttle effect of polyselenides. The Se@NCA cathode exhibits an excellent discharge capacity (600 mA h g-1 after 50 cycles at 0.1 A g-1) and a superior rate capability (430 mA h g-1 at 2 A g-1) for Na-Se batteries. In addition, it also shows a superior long cycling life of 407 mA h g-1 at a current density of 0.5 A g-1 after 800 cycles with only 0.04% capacity decline per cycle.

Double-Morphology CoS2 Anchored on N-Doped Multichannel Carbon Nanofibers as High-Performance Anode Materials for Na-Ion Batteries.

Na-ion batteries (NIBs) have attracted increasing attention given the fact that sodium is relatively more plentiful and affordable than lithium for sustainable and large-scale energy storage systems. However, the shortage of electrode materials with outstanding comprehensive properties has limited the practical implementations of NIBs. Among all the discovered anode materials, transition-metal sulfide has been proven as one of the most competitive and promising ones due to its excellent redox reversibility and relatively high theoretical capacity. In this study, double-morphology N-doped CoS2/multichannel carbon nanofibers composites (CoS2/MCNFs) are precisely designed, which overcome common issues such as the poor cycling life and inferior rate performance of CoS2 electrodes. The conductive 3D interconnected multichannel nanostructure of CoS2/MCNFs provides efficient buffer zones for the release of mechanical stresses from Na+ ions intercalation/deintercalation. The synergy of the diverse structural features enables a robust frame and a rapid electrochemical reaction in CoS2/MCNFs anode, resulting in an impressive long-term cycling life of 900 cycles with a capacity of 620 mAh g-1 at 1 A g-1 (86.4% theoretical capacity) and a surprisingly high-power output. The proposed design in this study provides a rational and novel thought for fabricating electrode materials.