@article{80b93a333b604bd09ddf0a677e190883,
title = "Morphology Engineering in Multicomponent Hollow Metal Chalcogenide Nanoparticles",
abstract = "Hollow metal chalcogenide nanoparticles are widely applicable in environmental and energy-related processes. Herein, we synthesized such particles with large compositional and morphological diversity by combining scanning probe block copolymer lithography with a Kirkendall effect-based sulfidation process. We explored the influence of temperature-dependent diffusion kinetics, elemental composition and miscibility, and phase boundaries on the resulting particle morphologies. Specifically, CoNi alloys form single-shell sulfides for the synthetic conditions explored because Co and Ni exhibit similar diffusion rates, while CuNi alloys form sulfides with various types of morphologies (yolk-shell, double-shell, and single-shell) because Cu and Ni have different diffusion rates. In contrast, Co-Cu heterodimers form hollow heterostructured sulfides with varying void numbers and locations depending on synthesis temperature and phase boundary. At higher temperatures, the increased miscibility of CoS2and CuS makes it energetically favorable for the heterostructure to adopt a single alloy shell morphology, which is rationalized using density functional theory-based calculations.",
keywords = "Heterostructures, Hollow nanoparticles, Kirkendall effect, Metal chalcogenide, Nanolithography",
author = "Bo Shen and Liliang Huang and Jiahong Shen and Xiaobing Hu and Peichen Zhong and Zheng, {Cindy Y.} and Chris Wolverton and Mirkin, {Chad A.}",
note = "Funding Information: The project described was supported by the Sherman Fairchild Foundation Inc., the Toyota Research Institute Inc., and the Air Force Office of Scientific Research Award FA9550-17-1-0348. C.Y.Z. was supported by the U.S. Department of Energy, Office of Science, Office of Workforce Development for Teachers and Scientists, Office of Science Graduate Student Research (SCGSR) program. The SCGSR program is administered by the Oak Ridge Institute for Science and Education for the DOE under contract number DE-SC0014664. J.S. and C.W. were supported by the Materials Research Science and Engineering Centers (MRSEC) program (NSF Grant DMR-1720139) at the Materials Research Center of Northwestern University. The computational resources are supported by the National Energy Research Scientific Computing Center, a U.S. Department of Energy Office of Science User Facility operated under Contract DE-AC02-05CH11231 and the Quest high-performance computing facility at Northwestern University. This work made use of the Electron Probe Instrumentation Center facility of the Northwestern University Atomic and Nanoscale Characterization Experimental Center, which has received support from the Soft and Hybrid Nanotechnology Experimental Resource (NSF Grant ECCS1542205); the MRSEC program (NSF Grant DMR-1720139) at the Materials Research Center; the International Institute for Nanotechnology (IIN); the Keck Foundation; and the State of Illinois, through the IIN. We thank Dr. S. H. Petrosko and Dr. J. K. H. Orbeck (Northwestern University) for providing editorial input. Publisher Copyright: {\textcopyright} 2023 American Chemical Society. All rights reserved.",
year = "2023",
month = mar,
day = "14",
doi = "10.1021/acsnano.2c10667",
language = "English (US)",
volume = "17",
pages = "4642--4649",
journal = "ACS Nano",
issn = "1936-0851",
publisher = "American Chemical Society",
number = "5",
}