Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 41, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202208215
Keywords
Bifunctionality; Chlorine Evolution Reaction; Inherent Oxide Anchoring Strategy; Nitrate Reduction Reaction; Single Atom Monolithic Electrode
Categories
Funding
- National Natural Science Foundation of China [22102100, 21936003]
- Natural Science Foundation of Shanghai [22ZR1431700]
- National Key Research and Development Program of China [2021YFA1201701, 2018YFC1800801]
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By regulating the metal-support interactions, ligand-free isolated Ru atoms were successfully anchored on the amorphous layer of a monolithic Ti support, resulting in the preparation of a Ru single atom electrode. This electrode exhibited exceptional electrochemical performance, with high chlorine evolution activity and selective reduction of nitrate to ammonia. Moreover, the size of the monolithic electrode can be scaled up, indicating its potential for industrial electrocatalytic applications.
Fabricating single-atom electrodes via atomic dispersion of active metal atoms into monolithic metal supports is of great significance to advancing the lab-to-fab translation of the electrochemical technologies. Here, we report an inherent oxide anchoring strategy to fasten ligand-free isolated Ru atoms on the amorphous layer of monolithic Ti support by regulating the electronic metal-support interactions. The prepared Ru single atom electrode exhibited exceptional electrochemical chlorine evolution activity, three orders of magnitude higher mass activity than that of commercial dimensionally stable anode, and also selectively reduced nitrate to ammonia with an unprecedented ammonia yield rate of 22.2 mol g(-1) h(-1) at -0.3 V. Furthermore, the Ru single atom monolithic electrode can be scaled up from 2x2 cm to 25x15 cm at least, thus demonstrating great potential for industrial electrocatalytic applications.
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