2D Nano‐Quartz Aerogels Cloned via Chemical Vapor Deposition Enable High‐Power Laser Scattering
Source abstract
Abstract
Abstract Artificial synthesis of silica aerogel, either with crystalline quartz building blocks rather than present amorphous ones, or with greater than 0D building blocks rather than present nano‐spherical ones, has become a century‐old problem in light of its invention in 1931. Herein, 2D nano‐quartz aerogels (QAs) with various configurations (e.g., ultrafine or hollow fiber, thin film, lightweight monolith, etc.) are all successfully cloned by chemical vapor deposition of silica source onto graphene aerogel skeletons to form ultrathin ceramic layers with carbon‐leaving‐induced crystallization during subsequent carbon etching. These QAs not only possess large amounts of graphene‐like nanosheets with typical α‐quartz phase, but exhibit ultralow density (as low as 1.5 mg cm −3 ), large specific surface area (up to 836 m 2 g −1 ), superior thermal‐insulation (∼20 mW m −1 ·K −1 in air), configuration‐dependent flexibility, more than 600 °C higher thermal stability than traditional amorphous silica aerogel, and promising high‐power (>10 2 W) light‐scattering ability, indicating these QAs might be used as the distinct diffusers for high‐power laser‐driven lighting and high power laser shielding. This research might open numerous possibilities in developing quartz‐like crystalline aerogels with 2D nano‐building blocks.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Aerogels and thermal insulation · Transition Metal Oxide Nanomaterials · Glass properties and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Suzhou Institute of Nano‐Tech and Nano‐Bionics Chinese Academy of Sciences Suzhou 215123 P. R. China
College of Textile Science and Engineering Jiangnan University Wuxi 214122 China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
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