期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 142, 期 28, 页码 12306-12313出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c04231
关键词
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资金
- National Natural Science Foundation of China [U1932212, U1932109, 11875257]
- Fundamental Research Funds for the Central Universities [WK2310000070]
The structural dynamics of the solid-liquid interfaces (SLEIs) determines the chemistry in all electrochemical processes. Here, by combining multiple operando synchrotron spectroscopies, we identify at the atomic level a general evolution of single-atom Ni at SLEIs into a near-free atom state in the electrochemical oxygen reduction reaction (ORR). We uncover that the single-atom Ni at SLEIs tends to be dynamically released from the nitrogen-carbon substrate and then forms a near-free, isolated-zigzag active site (Ni1(2-delta)+N2) during the reaction. This isolated-zigzag Ni1(2-delta)+N2 active site facilitates the adsorption and dissociation of O-2 into a crucial *O intermediate within the electrical double layers, realizing a highly efficient single-atom catalyst with the best ORR performance in alkaline solutions reported thus far. These findings may pave a general way for dissecting other important structural dynamic processes at SLEIs, such as hydrogen evolution, oxygen evolution, and CO2 reduction reactions.
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