TY - JOUR
T1 - Retrosynthetic Design of Morphologically Complex Metal Sulfide Nanoparticles Using Sequential Partial Cation Exchange and Chemical Etching
AU - Butterfield, Auston G.
AU - Steimle, Benjamin C.
AU - Schaak, Raymond E.
N1 - Funding Information:
This work was supported by the U.S. National Science Foundation under Grant DMR-1904122. TEM/STEM imaging, EDS mapping and X-ray diffraction were performed at the Materials Characterization Laboratory of the Penn State Materials Research Institute.
Funding Information:
This work was supported by the U.S. National Science Foundation under Grant DMR-1904122. TEM/STEM imaging, EDS mapping, and X-ray diffraction were performed at the Materials Characterization Laboratory of the Penn State Materials Research Institute.
Publisher Copyright:
© 2020 American Chemical Society.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/9/8
Y1 - 2020/9/8
N2 - Designer nanoparticles with complex morphologies are of growing interest for a wide range of applications, but making them rationally and scalably remains challenging. Here, we demonstrate a retrosynthetic approach to access morphologically complex colloidal nanoparticles by combining partial sequential cation exchange reactions with chemical etching. Rational synthesis of the targeted nanoparticles containing ZnS, CdS, or CoS began by identifying heterostructured nanorod precursors that contained precisely located regions of Cu1.8S, which were subsequently etched with trioctylphosphine in the presence of oxygen to generate the desired product. Appropriate heterostructured nanorod precursors were then synthesized by replacing some of the Cu+ cations in colloidal Cu1.8S nanorods with Zn2+, Cd2+, or Co2+, using exchange sequences that were known to produce the desired features. The residual Cu1.8S was then dissolved, converting the Cu1.8S regions into void space. Mixed-population samples were also used to explore and identify a wider swath of potential retrosynthetic pathways and targeted morphologies, as well as morphological tunability. Collectively, several new classes of complex nanoparticles were synthesized, including nanoparticles having a flat end on one side and a faceted tip on the other, nanoparticles having a different material on the top and bottom, and nanoparticles having various protrusions and notches.
AB - Designer nanoparticles with complex morphologies are of growing interest for a wide range of applications, but making them rationally and scalably remains challenging. Here, we demonstrate a retrosynthetic approach to access morphologically complex colloidal nanoparticles by combining partial sequential cation exchange reactions with chemical etching. Rational synthesis of the targeted nanoparticles containing ZnS, CdS, or CoS began by identifying heterostructured nanorod precursors that contained precisely located regions of Cu1.8S, which were subsequently etched with trioctylphosphine in the presence of oxygen to generate the desired product. Appropriate heterostructured nanorod precursors were then synthesized by replacing some of the Cu+ cations in colloidal Cu1.8S nanorods with Zn2+, Cd2+, or Co2+, using exchange sequences that were known to produce the desired features. The residual Cu1.8S was then dissolved, converting the Cu1.8S regions into void space. Mixed-population samples were also used to explore and identify a wider swath of potential retrosynthetic pathways and targeted morphologies, as well as morphological tunability. Collectively, several new classes of complex nanoparticles were synthesized, including nanoparticles having a flat end on one side and a faceted tip on the other, nanoparticles having a different material on the top and bottom, and nanoparticles having various protrusions and notches.
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U2 - 10.1021/acsmaterialslett.0c00287
DO - 10.1021/acsmaterialslett.0c00287
M3 - Article
AN - SCOPUS:85092179973
SN - 2639-4979
VL - 2
SP - 1106
EP - 1114
JO - ACS Materials Letters
JF - ACS Materials Letters
IS - 9
ER -