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dc.date.accessioned 2020-09-15T13:22:46Z
dc.date.available 2020-09-15T13:22:46Z
dc.date.issued 2013-12
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/104632
dc.description.abstract Electrochemical conversions at fuel cell electrodes are complex processes. In particular, the oxygen reduction reaction has substantial overpotential limiting the electrical power output efficiency. Effective and inexpensive catalytic interfaces are therefore essential for increased performance. Taking inspiration from enzymes, earth-abundant metal centres embedded in organic environments present remarkable catalytic active sites. Here we show that these enzyme-inspired centres can be effectively mimicked in two-dimensional metal-organic coordination networks self-assembled on electrode surfaces. Networks consisting of trimesic acid and bis-pyridyl-bispyrimidine coordinating to single iron and manganese atoms on Au(111) effectively catalyse the reduction and reveal distinctive catalytic activity in alkaline media. These results demonstrate the potential of surface-engineered metal-organic networks for electrocatalytic conversions. Specifically designed coordination complexes at surfaces inspired by enzyme cofactors represent a new class of nanocatalysts with promising applications in electrocatalysis. en
dc.language en es
dc.subject Nanoscale materials es
dc.subject STM es
dc.subject UHV es
dc.subject Electrocatalysis es
dc.title Bio-inspired nanocatalysts for the oxygen reduction reaction en
dc.type Articulo es
sedici.identifier.uri http://hdl.handle.net/11336/5313 es
sedici.identifier.other https://doi.org/10.1038/ncomms3904 es
sedici.identifier.other hdl:11336/5313 es
sedici.identifier.issn 2041-1723 es
sedici.creator.person Grumelli, Doris Elda es
sedici.creator.person Wurtser, Benjamin es
sedici.creator.person Stepanow, Sabastian es
sedici.creator.person Kern, Klaus es
sedici.subject.materias Física es
sedici.description.fulltext true es
mods.originInfo.place Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Nature Communications es
sedici.relation.journalVolumeAndIssue vol. 4, no. 1 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)