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Scalable Synthesis of High Entropy Alloy Nanoparticles by Microwave Heating.

Authors :
Qiao H
Saray MT
Wang X
Xu S
Chen G
Huang Z
Chen C
Zhong G
Dong Q
Hong M
Xie H
Shahbazian-Yassar R
Hu L
Source :
ACS nano [ACS Nano] 2021 Sep 28; Vol. 15 (9), pp. 14928-14937. Date of Electronic Publication: 2021 Aug 23.
Publication Year :
2021

Abstract

High entropy alloy nanoparticles (HEA-NPs) are reported to have superior performance in catalysis, energy storage, and conversion due to the broad range of elements that can be incorporated in these materials, enabling tunable activity, excellent thermal and chemical stability, and a synergistic catalytic effect. However, scaling the manufacturing of HEA-NPs with uniform particle size and homogeneous elemental distribution efficiently is still a challenge due to the required critical synthetic conditions where high temperature is typically involved. In this work, we demonstrate an efficient and scalable microwave heating method using carbon-based materials as substrates to fabricate HEA-NPs with uniform particle size. Due to the abundant functional group defects that can absorb microwave efficiently, reduced graphene oxide is employed as a model substrate to produce an average temperature reaching as high as ∼1850 K within seconds. As a proof-of-concept, we utilize this rapid, high-temperature heating process to synthesize PtPdFeCoNi HEA-NPs, which exhibit an average particle size of ∼12 nm and uniform elemental mixing resulting from decomposition nearly at the same time and liquid metal solidification without diffusion. Various carbon-based materials can also be employed as substrates, including one-dimensional carbon nanofibers and three-dimensional carbonized wood, which can achieve temperatures of >1400 K. This facile and efficient microwave heating method is also compatible with the roll-to-roll process, providing a feasible route for scalable HEA-NPs manufacturing.

Details

Language :
English
ISSN :
1936-086X
Volume :
15
Issue :
9
Database :
MEDLINE
Journal :
ACS nano
Publication Type :
Academic Journal
Accession number :
34423972
Full Text :
https://doi.org/10.1021/acsnano.1c05113