001     89524
005     20250731122354.0
024 7 _ |a 1432-8488
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024 7 _ |a 1433-0768
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024 7 _ |a 10.1007/s10008-008-0711-3
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082 _ _ |a 540
100 1 _ |a Simonsen, V. L. E.
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110 1 _ |a DESY
|b Experiments with synchrotron radiation
245 _ _ |a Electrochemical reduction of NO on $La{2-x}SrxNiO_4$ based electrodes
260 _ _ |a Berlin
|c 2009
|b Springer
300 _ _ |a 1529
336 7 _ |a article
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336 7 _ |a Journal Article
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440 _ 0 |a J Solid State Electrochem
|0 PERI:(DE-600)1478940-1
|v 13
|y 10
|x 1432-8488
500 _ _ |a © Springer-Verlag; Post referee fulltext in progress; Embargo 12 months from publication
|3 Converted on 2013-05-30 13:41
500 _ _ |3 Converted on 2013-06-21 19:20
520 _ _ |a The series La$_2$ − $_x$ Sr $_x$ NiO$_4$(x = 0.0, 0.05, 0.15, 0.25, 0.35, and 1.0) was tested for functionality as electrode materials for direct electrochemical reduction of NO. The materials were tested using cyclic voltammetry in 1% NO and 10% O$_2$ in Ar on a cone-shaped electrode. The best materials for the electrochemical reduction of NO are La$_2$NiO$_4$ and LaSrNiO$_4$, which have current densities for NO reduction 1.82 and 7.09 times higher, respectively, than for O$_2$ at 400 °C. Increasing the temperature decreased the ability to reduce NO before O$_2$ while the activity increased. The adsorbed species during direct decomposition was attempted, clarified using X-ray absorption near-edge structure experiments and thermogravimetry, but no conclusive results were obtained
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700 1 _ |a Noerskov, L.
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700 1 _ |a Hagen, A.
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700 1 _ |a Hansen, K.
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773 _ _ |a 10.1007/s10008-008-0711-3
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