Journal
JOURNAL OF ENERGY CHEMISTRY
Volume 68, Issue -, Pages 556-563Publisher
ELSEVIER
DOI: 10.1016/j.jechem.2021.12.029
Keywords
Ethanol electrooxidation; Formic acid dehydrogenation; AuPd; Nanoclusters; Bi-functional catalyst
Funding
- National Natural Science Foun-dation of China [51901083]
- Fundamental Research Funds for the Central Universities
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A facile wet-chemical method was developed to synthesize ultrasmall metal nanoclusters with high catalytic activities. The resulting AuPd nanoclusters exhibited significantly improved specific and mass activities for ethanol electrooxidation compared to commercial Pd/C catalysts. Moreover, the nanoclusters showed a much higher initial turnover frequency for formic acid dehydrogenation than most reported AuPd catalysts, indicating their potential for various applications.
The synthesis of ultrasmall metal nanoclusters (NCs) with high catalytic activities is of great importance for the development of clean and renewable energy technologies but remains a challenge. Here we report a facile wet-chemical method to prepare similar to 1.0 nm AuPd NCs supported on amine-functionalized carbon blacks. The AuPd NCs exhibit a specific activity of 5.98 mA cm(AuPd)(-2) and mass activity of 5.25 A mg(AuPd)(-1) for ethanol electrooxidation, which are far better than those of commercial Pd/C catalysts (1.74 mA cm(Pd)(-2) and 0.54 A mg(Pd)(-1)). For formic acid dehydrogenation, the AuPd NCs have an initial turn over frequency of 49339 h(-1) at 298 K without any additive, which is much higher than those obtained for most of reported AuPd catalysts. The reported synthesis may represent a facile and low-cost approach to prepare other ultrasmall metal NCs with high catalytic activities for various applications. (C) 2021 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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