TY - JOUR
T1 - Thermal Atomization of Platinum Nanoparticles into Single Atoms
T2 - An Effective Strategy for Engineering High-Performance Nanozymes
AU - Chen, Yuanjun
AU - Wang, Peixia
AU - Hao, Haigang
AU - Hong, Juanji
AU - Li, Haijing
AU - Ji, Shufang
AU - Li, Ang
AU - Gao, Rui
AU - Dong, Juncai
AU - Han, Xiaodong
AU - Liang, Minmin
AU - Wang, Dingsheng
AU - Li, Yadong
N1 - Publisher Copyright:
©
PY - 2021/11/10
Y1 - 2021/11/10
N2 - Although great progress has been made in artificial enzyme engineering, their catalytic performance is far from satisfactory as alternatives of natural enzymes. Here, we report a novel and efficient strategy to access high-performance nanozymes via direct atomization of platinum nanoparticles (Pt NPs) into single atoms by reversing the thermal sintering process. Atomization of Pt NPs into single atoms makes metal catalytic sites fully exposed and results in engineerable structural and electronic properties, thereby leading to dramatically enhanced enzymatic performance. As expected, the as-prepared thermally stable Pt single-atom nanozyme (PtTS-SAzyme) exhibited remarkable peroxidase-like catalytic activity and kinetics, far exceeding the Pt nanoparticle nanozyme. The following density functional theory calculations revealed that the engineered P and S atoms not only promote the atomization process from Pt NPs into PtTS-SAzyme but also endow single-atom Pt catalytic sites with a unique electronic structure owing to the electron donation of P atoms, as well as the electron acceptance of N and S atoms, which simultaneously contribute to the substantial enhancement of the enzyme-like catalytic performance of PtTS-SAzyme. This work demonstrates that thermal atomization of the metal nanoparticle-based nanozymes into single-atom nanozymes is an effective strategy for engineering high-performance nanozymes, which opens up a new way to rationally design and optimize artificial enzymes to mimic natural enzymes.
AB - Although great progress has been made in artificial enzyme engineering, their catalytic performance is far from satisfactory as alternatives of natural enzymes. Here, we report a novel and efficient strategy to access high-performance nanozymes via direct atomization of platinum nanoparticles (Pt NPs) into single atoms by reversing the thermal sintering process. Atomization of Pt NPs into single atoms makes metal catalytic sites fully exposed and results in engineerable structural and electronic properties, thereby leading to dramatically enhanced enzymatic performance. As expected, the as-prepared thermally stable Pt single-atom nanozyme (PtTS-SAzyme) exhibited remarkable peroxidase-like catalytic activity and kinetics, far exceeding the Pt nanoparticle nanozyme. The following density functional theory calculations revealed that the engineered P and S atoms not only promote the atomization process from Pt NPs into PtTS-SAzyme but also endow single-atom Pt catalytic sites with a unique electronic structure owing to the electron donation of P atoms, as well as the electron acceptance of N and S atoms, which simultaneously contribute to the substantial enhancement of the enzyme-like catalytic performance of PtTS-SAzyme. This work demonstrates that thermal atomization of the metal nanoparticle-based nanozymes into single-atom nanozymes is an effective strategy for engineering high-performance nanozymes, which opens up a new way to rationally design and optimize artificial enzymes to mimic natural enzymes.
UR - http://www.scopus.com/inward/record.url?scp=85119277949&partnerID=8YFLogxK
U2 - 10.1021/jacs.1c08581
DO - 10.1021/jacs.1c08581
M3 - Article
C2 - 34726407
AN - SCOPUS:85119277949
SN - 0002-7863
VL - 143
SP - 18643
EP - 18651
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 44
ER -