TY - JOUR
T1 - Direct observation of the formation and stabilization of metallic nanoparticles on carbon supports
AU - Huang, Zhennan
AU - Yao, Yonggang
AU - Pang, Zhenqian
AU - Yuan, Yifei
AU - Li, Tangyuan
AU - He, Kun
AU - Hu, Xiaobing
AU - Cheng, Jian
AU - Yao, Wentao
AU - Liu, Yuzi
AU - Nie, Anmin
AU - Sharifi-Asl, Soroosh
AU - Cheng, Meng
AU - Song, Boao
AU - Amine, Khalil
AU - Lu, Jun
AU - Li, Teng
AU - Hu, Liangbing
AU - Shahbazian-Yassar, Reza
N1 - Funding Information:
This project was not directly funded. We acknowledge the partial support from NSF-DMR award No. 1809439 and NSF-SNM award No. 1635221. This work made use of JOEL 3010 and JOEL JEM-ARM 200CF in the Electron Microscopy Core of UIC’s Research Resources Center. JOEL JEM-ARM 200CF is supported by an MRI-R2 grant from the National Science Foundation DMR-0959470. Y. Liu acknowledges the use of the Center for Nanoscale Materials, an Office of Science user facility, supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under contract no. DE-AC02-06CH11357. A portion of this work was conducted at Argonne National Laboratory. Argonne National Laboratory is operated for DOE Office of Science by UChicago Argonne, LLC, under contract no. DE-AC02-06CH11357. Z. Pang and T. Li acknowledge the University of Maryland supercomputing resources (http://hpcc.umd.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12
Y1 - 2020/12
N2 - Direct formation of ultra-small nanoparticles on carbon supports by rapid high temperature synthesis method offers new opportunities for scalable nanomanufacturing and the synthesis of stable multi-elemental nanoparticles. However, the underlying mechanisms affecting the dispersion and stability of nanoparticles on the supports during high temperature processing remain enigmatic. In this work, we report the observation of metallic nanoparticles formation and stabilization on carbon supports through in situ Joule heating method. We find that the formation of metallic nanoparticles is associated with the simultaneous phase transition of amorphous carbon to a highly defective turbostratic graphite (T-graphite). Molecular dynamic (MD) simulations suggest that the defective T-graphite provide numerous nucleation sites for the nanoparticles to form. Furthermore, the nanoparticles partially intercalate and take root on edge planes, leading to high binding energy on support. This interaction between nanoparticles and T-graphite substrate strengthens the anchoring and provides excellent thermal stability to the nanoparticles. These findings provide mechanistic understanding of rapid high temperature synthesis of metal nanoparticles on carbon supports and the origin of their stability.
AB - Direct formation of ultra-small nanoparticles on carbon supports by rapid high temperature synthesis method offers new opportunities for scalable nanomanufacturing and the synthesis of stable multi-elemental nanoparticles. However, the underlying mechanisms affecting the dispersion and stability of nanoparticles on the supports during high temperature processing remain enigmatic. In this work, we report the observation of metallic nanoparticles formation and stabilization on carbon supports through in situ Joule heating method. We find that the formation of metallic nanoparticles is associated with the simultaneous phase transition of amorphous carbon to a highly defective turbostratic graphite (T-graphite). Molecular dynamic (MD) simulations suggest that the defective T-graphite provide numerous nucleation sites for the nanoparticles to form. Furthermore, the nanoparticles partially intercalate and take root on edge planes, leading to high binding energy on support. This interaction between nanoparticles and T-graphite substrate strengthens the anchoring and provides excellent thermal stability to the nanoparticles. These findings provide mechanistic understanding of rapid high temperature synthesis of metal nanoparticles on carbon supports and the origin of their stability.
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U2 - 10.1038/s41467-020-20084-5
DO - 10.1038/s41467-020-20084-5
M3 - Article
C2 - 33311508
AN - SCOPUS:85097510643
SN - 2041-1723
VL - 11
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 6373
ER -