Yunna Guo, Hantao Cui, Peng Jia, Zhangran Ye, Lei Deng, Hui Li, Baiyu Guo, Xuedong Zhang, Jie Huang, Yong Su, Jianyu Huang, Bin Wen, Yang Lu, Liqiang Zhang
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Bottom-up assembly and joining of silica nanoparticles to form complicated geometries up to three-dimensional (3D) glass structures are attractive for nanoscale optical, optoelectronics, etc. Most existing silica 3D printing techniques can only achieve submicron-level precision due to the optical limit of vat photopolymerization, which presents critical challenges for sub-100 nm printing. In this context, we introduce an electron-beam-assisted cold welding technique for nanoscale glass that is capable of achieving precision at the tens-of-nanometers scale. This method enables the direct fusion of two amorphous silica nanospheres within a few seconds while keeping the diameter smaller than 100 nm. Meanwhile, the strength, composition, and structure of the as-welded junctions appear the same as those of the pristine silica. Our approach would potentially allow ultra-high-resolution 3D bottom-up assembly and printing of silica nanostructures with ultimate resolution subject to the nanoparticle size only, which offers a new approach for additive manufacturing of nanoscale glass devices.
期刊介绍:
ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to:
* Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials.
* Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets.
* Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance.
* Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents.
* Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota.
* Small molecule vaccine adjuvants for infectious disease.
* Viral and bacterial biochemistry and molecular biology.