Volcanic activity is one of the main sources of natural nanoparticles. It has been found earlier that the concentration of toxic metals/metalloids in nanoparticles of volcanic ash may be one or two orders of magnitude higher than in bulk sample. However, fate and behavior of toxic metals/metalloids depend on the type of their binding to nanoparticles. Hence, element species adsorbed onto pyroclastic nanoparticles and individual nanophases of metal/metalloid oxides or salts should be distinguished. For the first time, the single particle inductively coupled plasma mass spectrometry has been applied to the nanospeciation of volcanic particles. Ashes of four volcanoes of Kamchatka (Russia) were under study. Nanoparticles were separated from bulk ash samples using coiled-tube field-flow fractionation. It has been shown that the nanospeciation of Ni, Zn, Ag, Cd, Tl, As, Pb, Bi, Te, and Hg is dependent on element and volcano. In most cases these elements can be found both as species absorbed onto pyroclastic nanoparticles and as individual nanophases. The ratios of individual nanophases and adsorbed species vary with the sample. In nanoparticles of Tolbachik volcano ash, Ni, Zn, Tl, and Hg are present only as individual nanophases, while Bi, As, Pb, Ag, Cd, and Te are found both as adsorbed species and individual nanophases. The results obtained open a new door into study on the chemical composition of volcanic ash nanoparticles and their fate in the environment.
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http://dx.doi.org/10.1016/j.chemosphere.2021.130950 | DOI Listing |
Nanophotonics
May 2024
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
Color centers in diamond play a central role in the development of quantum photonic technologies, and their importance is only expected to grow in the near future. For many quantum applications, high collection efficiency from individual emitters is required, but the refractive index mismatch between diamond and air limits the optimal collection efficiency with conventional diamond device geometries. While different out-coupling methods with near-unity efficiency exist, many have yet to be realized due to current limitations in nanofabrication methods, especially for mechanically hard materials like diamond.
View Article and Find Full Text PDFAdv Mater
November 2024
Department of Materials Science and Engineering, University of California, Los Angeles, CA, 90095, USA.
ACS Nano
July 2024
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, United States.
Multimaterial heterostructures have led to characteristics surpassing the individual components. Nature controls the architecture and placement of multiple materials through biomineralization of nanoparticles (NPs); however, synthetic heterostructure formation remains limited and generally departs from the elegance of self-assembly. Here, a class of block polymer structure-directing agents (SDAs) are developed containing repeat units capable of persistent (covalent) NP interactions that enable the direct fabrication of nanoscale porous heterostructures, where a single material is localized at the pore surface as a continuous layer.
View Article and Find Full Text PDFACS Nano
July 2024
Department of Mechanical Engineering, Boston University, 110 Cummington Mall, Boston, Massachusetts 02215, United States.
Soft gels with spatially defined mesoscale distributions of chemical activity that guide and accelerate reactions by chemical nanoconfinement are found ubiquitously in nature but are rare in artificial systems. In this study, we introduce chemically nanostructured bulk organogels with periodically ordered morphologies from self-assembled block copolymer monoliths with a single selectively cross-linked block (xBCP). Ordered bulk organogels are fabricated with various distinct morphologies including hexagonally packed cylinders and two gyroidal three-dimensionally periodic network structures that exhibit macroscopic and nanoscopic structural integrity upon swelling.
View Article and Find Full Text PDFRev Sci Instrum
May 2024
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
We report an algorithm to identify and correct distorted wavefronts in atomic resolution scanning tunneling microscope images. This algorithm can be used to correct nonlinear in-plane distortions without prior knowledge of the physical scanning parameters, the characteristics of the piezoelectric actuator, or individual atom positions. The 2D image is first defined as a sum of sinusoidal plane waves, where a nonlinear distortion renders a curve for an otherwise ideal linear wavefront.
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