TY - JOUR
T1 - Tunable intraparticle frameworks for creating complex heterostructured nanoparticle libraries
AU - Fenton, Julie L.
AU - Steimle, Benjamin C.
AU - Schaak, Raymond E.
N1 - Funding Information:
TEM imaging was performed in the Penn State Microscopy and Cytometry facility. HRTEM imaging, STEM imaging, and EDS mapping were performed at the Materials Characterization Laboratory of the Penn State Materials Research Institute. The authors thank K. Wang and J. L. Gray for assistance with TEM experiments and helpful discussions. This work was supported by the U.S. National Science Foundation under grant DMR-1607135.
Publisher Copyright:
© 2017 The Authors, some rights reserved;
PY - 2018/5/4
Y1 - 2018/5/4
N2 - Complex heterostructured nanoparticles with precisely defined materials and interfaces are important for many applications. However, rationally incorporating such features into nanoparticles with rigorous morphology control remains a synthetic bottleneck. We define a modular divergent synthesis strategy that progressively transforms simple nanoparticle synthons into increasingly sophisticated products. We introduce a series of tunable interfaces into zero-, one-, and two-dimensional copper sulfide nanoparticles using cation exchange reactions. Subsequent manipulation of these intraparticle frameworks yielded a library of 47 distinct heterostructured metal sulfide derivatives, including particles that contain asymmetric, patchy, porous, and sculpted nanoarchitectures. This generalizable mix-and-match strategy provides predictable retrosynthetic pathways to complex nanoparticle features that are otherwise inaccessible.
AB - Complex heterostructured nanoparticles with precisely defined materials and interfaces are important for many applications. However, rationally incorporating such features into nanoparticles with rigorous morphology control remains a synthetic bottleneck. We define a modular divergent synthesis strategy that progressively transforms simple nanoparticle synthons into increasingly sophisticated products. We introduce a series of tunable interfaces into zero-, one-, and two-dimensional copper sulfide nanoparticles using cation exchange reactions. Subsequent manipulation of these intraparticle frameworks yielded a library of 47 distinct heterostructured metal sulfide derivatives, including particles that contain asymmetric, patchy, porous, and sculpted nanoarchitectures. This generalizable mix-and-match strategy provides predictable retrosynthetic pathways to complex nanoparticle features that are otherwise inaccessible.
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U2 - 10.1126/science.aar5597
DO - 10.1126/science.aar5597
M3 - Article
C2 - 29724950
AN - SCOPUS:85046442664
SN - 0036-8075
VL - 360
SP - 513
EP - 517
JO - Science
JF - Science
IS - 6388
ER -