A general synthesis approach for supported bimetallic nanoparticles via surface inorganometallic chemistry
Abstract
Here, the synthesis of ultrasmall supported bimetallic nanoparticles (between 1 and 3 nanometers in diameter) with well-defined stoichiometry and intimacy between constituent metals remains a substantial challenge. We synthesized 10 different supported bimetallic nanoparticles via surface inorganometallic chemistry by decomposing and reducing surface-adsorbed heterometallic double complex salts, which are readily obtained upon sequential adsorption of target cations and anions on a silica substrate. For example, adsorption of tetraamminepalladium(II) [Pd(NH3)42+] followed by adsorption of tetrachloroplatinate [PtCl42–] was used to form palladium-platinum (Pd-Pt) nanoparticles. These supported bimetallic nanoparticles show enhanced catalytic performance in acetylene selective hydrogenation, which clearly demonstrates a synergistic effect between constituent metals.
- Authors:
-
[1];
[2];
[1];
[3];
[1];
[2];
[1]
- Louisiana State Univ., Baton Rouge, LA (United States)
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
- Chinese Academy of Sciences, Shanxi (People's Republic of China); Synfuels China Co., Ltd., Beijing (People's Republic of China)
- Publication Date:
- Research Org.:
- Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1483180
- Grant/Contract Number:
- AC05-00OR22725
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Science
- Additional Journal Information:
- Journal Volume: 362; Journal Issue: 6414; Journal ID: ISSN 0036-8075
- Publisher:
- AAAS
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Citation Formats
Ding, Kunlun, Cullen, David A., Zhang, Laibao, Cao, Zhi, Roy, Amitava D., Ivanov, Ilia N., and Cao, Dongmei. A general synthesis approach for supported bimetallic nanoparticles via surface inorganometallic chemistry. United States: N. p., 2018.
Web. doi:10.1126/science.aau4414.
Ding, Kunlun, Cullen, David A., Zhang, Laibao, Cao, Zhi, Roy, Amitava D., Ivanov, Ilia N., & Cao, Dongmei. A general synthesis approach for supported bimetallic nanoparticles via surface inorganometallic chemistry. United States. https://doi.org/10.1126/science.aau4414
Ding, Kunlun, Cullen, David A., Zhang, Laibao, Cao, Zhi, Roy, Amitava D., Ivanov, Ilia N., and Cao, Dongmei. Fri .
"A general synthesis approach for supported bimetallic nanoparticles via surface inorganometallic chemistry". United States. https://doi.org/10.1126/science.aau4414. https://www.osti.gov/servlets/purl/1483180.
@article{osti_1483180,
title = {A general synthesis approach for supported bimetallic nanoparticles via surface inorganometallic chemistry},
author = {Ding, Kunlun and Cullen, David A. and Zhang, Laibao and Cao, Zhi and Roy, Amitava D. and Ivanov, Ilia N. and Cao, Dongmei},
abstractNote = {Here, the synthesis of ultrasmall supported bimetallic nanoparticles (between 1 and 3 nanometers in diameter) with well-defined stoichiometry and intimacy between constituent metals remains a substantial challenge. We synthesized 10 different supported bimetallic nanoparticles via surface inorganometallic chemistry by decomposing and reducing surface-adsorbed heterometallic double complex salts, which are readily obtained upon sequential adsorption of target cations and anions on a silica substrate. For example, adsorption of tetraamminepalladium(II) [Pd(NH3)42+] followed by adsorption of tetrachloroplatinate [PtCl42–] was used to form palladium-platinum (Pd-Pt) nanoparticles. These supported bimetallic nanoparticles show enhanced catalytic performance in acetylene selective hydrogenation, which clearly demonstrates a synergistic effect between constituent metals.},
doi = {10.1126/science.aau4414},
journal = {Science},
number = 6414,
volume = 362,
place = {United States},
year = {Fri Nov 02 00:00:00 EDT 2018},
month = {Fri Nov 02 00:00:00 EDT 2018}
}
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