Quantitative 3D evolution of colloidal nanoparticle oxidation in solution

被引:138
作者
Sun, Yugang [1 ]
Zuo, Xiaobing [2 ]
Sankaranarayanan, Subramanian K. R. S. [3 ]
Peng, Sheng [3 ]
Narayanan, Badri [3 ]
Kamath, Ganesh [3 ]
机构
[1] Temple Univ, Dept Chem, 1901 North 13th St, Philadelphia, PA 19122 USA
[2] Argonne Natl Lab, Xray Sci Div, Adv Photon Source, 9700 South Cass Ave, Argonne, IL 60439 USA
[3] Argonne Natl Lab, Ctr Nanoscale Mat, 9700 South Cass Ave, Argonne, IL 60439 USA
关键词
LITHIUM ION BATTERIES; IN-SITU; HOLLOW NANOCRYSTALS; OXIDE NANOPARTICLES; ELECTRON-MICROSCOPY; GROWTH; SCATTERING; CELL;
D O I
10.1126/science.aaf6792
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Real-time tracking of the three-dimensional (3D) evolution of colloidal nanoparticles in solution is essential for understanding complex mechanisms involved in nanoparticle growth and transformation. We used time-resolved small-angle and wide-angle x-ray scattering simultaneously to monitor oxidation of highly uniform colloidal iron nanoparticles, enabling the reconstruction of intermediate 3D morphologies of the nanoparticles with a spatial resolution of similar to 5 angstroms. The in situ observations, combined with large-scale reactive molecular dynamics simulations, reveal the details of the transformation from solid metal nanoparticles to hollow metal oxide nanoshells via a nanoscale Kirkendall process-for example, coalescence of voids as they grow and reversal of mass diffusion direction depending on crystallinity. Our results highlight the complex interplay between defect chemistry and defect dynamics in determining nanoparticle transformation and formation.
引用
收藏
页码:302 / 304
页数:4
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