Redox Energetics and Kinetics of Water Oxidation in Neutral versus Alkaline Electrolyte: an In-Operando Time-Resolved X-Ray Absorption Study

Author(s):  
Chiara Pasquini ◽  
Holger Dau
1997 ◽  
Vol 497 ◽  
Author(s):  
S. Chaturvedi ◽  
J. A. Rodriguez ◽  
J. C. Hanson ◽  
A. Albornoz ◽  
J. L. Brito

ABSTRACTX-ray absorption near-edge spectroscopy (XANES) was used to characterize the structural and electronic properties of a series of cobalt- and nickel-molybdate catalysts (AMoO4.nH20, α-AMoO4, β-AMoO4; A= Co or Ni). The results of XANES indicate that the Co and Ni atoms are in octahedral sites in all these compounds, while the coordination of Mo varies from octahedral in the a-phases to tetrahedral in the β-phases and hydrate. Time-resolved x-ray diffraction shows a direct transformation of the hydrates into the β-AMoO4 compounds (following a kinetics of first order) at temperatures between 200 and 350 °C. This is facilitated by the similarities that the AMoO4.nH20 and β-AMoO4 compounds have in their structural and electronic properties. The molybdates react with H 2 at temperatures between 400 and 600 °C, forming gaseous water and oxides in which the oxidation state of Co and Ni remains +2 while that of Mo is reduced to +5 or +4. After exposing α-NiMoO4 and P-NiMoO4 to H2S, both metals get sulfided and a NiMoSx phase is formed. For the β phase of NiMoO4 the sulfidation of Mo is more extensive than for the a phase, making the former a better precursor for catalysts of hydrodesulfurization reactions.


2010 ◽  
Vol 97 (3-4) ◽  
pp. 381-388 ◽  
Author(s):  
Konstantinos Alexopoulos ◽  
Mettu Anilkumar ◽  
Marie-Françoise Reyniers ◽  
Hilde Poelman ◽  
Sylvain Cristol ◽  
...  

Author(s):  
Chiara Pasquini ◽  
Si Liu ◽  
Petko Chernev ◽  
Diego Gonzalez-Flores ◽  
Mohammad Reza Mohammadi ◽  
...  

AbstractTransition metal oxides are promising electrocatalysts for water oxidation, i.e., the oxygen evolution reaction (OER), which is critical in electrochemical production of non-fossil fuels. The involvement of oxidation state changes of the metal in OER electrocatalysis is increasingly recognized in the literature. Tracing these oxidation states under operation conditions could provide relevant information for performance optimization and development of durable catalysts, but further methodical developments are needed. Here, we propose a strategy to use single-energy X-ray absorption spectroscopy for monitoring metal oxidation-state changes during OER operation with millisecond time resolution. The procedure to obtain time-resolved oxidation state values, using two calibration curves, is explained in detail. We demonstrate the significance of this approach as well as possible sources of data misinterpretation. We conclude that the combination of X-ray absorption spectroscopy with electrochemical techniques allows us to investigate the kinetics of redox transitions and to distinguish the catalytic current from the redox current. Tracking of the oxidation state changes of Co ions in electrodeposited oxide films during cyclic voltammetry in neutral pH electrolyte serves as a proof of principle. Graphical abstract


1986 ◽  
Vol 60 (5) ◽  
pp. 1774-1783 ◽  
Author(s):  
H. C. Gerritsen ◽  
H. van Brug ◽  
F. Bijkerk ◽  
K. Murakami ◽  
M. J. van der Wiel

1989 ◽  
Vol 158 (1-3) ◽  
pp. 52-53 ◽  
Author(s):  
J.M. Lee ◽  
M.A. Paesler ◽  
D.E. Sayers ◽  
Alain Fontaine

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