Why Is Bulk Thermochemistry a Good Descriptor for the Electrocatalytic Activity of Transition Metal Oxides

It is well known that transition metal oxides can efficiently catalyze electrochemical reactions of interest in electrolyzers and fuel cells. The question is how to describe and rationalize the variations in catalytic activity among a given class of oxides, so that known materials can be improved and new active materials be predicted. In this context, descriptor-based analyses are a powerful tool, as they help to rationalize the trends in catalytic activity through correlations with other properties of the material. Particularly, bulk thermochemistry has long been used to describe the trends in catalytic activity of oxide surfaces. Here we explain the reason for the apparent success of this descriptor on the basis of perovskite oxides and monoxides and the oxygen evolution reaction: essentially, bulk thermochemistry and surface adsorption energetics depend similarly on the number of outer electrons of the transition metal in the oxide. This correspondence applies to a wide number of transition metals and ...

[1]  Kristian Sommer Thygesen,et al.  Calculated Pourbaix Diagrams of Cubic Perovskites for Water Splitting: Stability Against Corrosion , 2014, Topics in Catalysis.

[2]  Y. Schuurman,et al.  Periodic trends in the selective hydrogenation of styrene over silica supported metal catalysts , 2013 .

[3]  Yang Shao-Horn,et al.  Double perovskites as a family of highly active catalysts for oxygen evolution in alkaline solution , 2013, Nature Communications.

[4]  Tom Regier,et al.  An advanced Ni-Fe layered double hydroxide electrocatalyst for water oxidation. , 2013, Journal of the American Chemical Society.

[5]  J. Rossmeisl,et al.  Generalized trends in the formation energies of perovskite oxides. , 2013, Physical chemistry chemical physics : PCCP.

[6]  John R. Kitchin,et al.  Number of outer electrons as descriptor for adsorption processes on transition metals and their oxides , 2013 .

[7]  Maria Chan,et al.  Trends in activity for the water electrolyser reactions on 3d M(Ni,Co,Fe,Mn) hydr(oxy)oxide catalysts. , 2012, Nature materials.

[8]  J. Rossmeisl,et al.  Physical and chemical nature of the scaling relations between adsorption energies of atoms on metal surfaces. , 2012, Physical review letters.

[9]  Thomas Olsen,et al.  Computational screening of perovskite metal oxides for optimal solar light capture , 2012 .

[10]  J. Goodenough,et al.  A Perovskite Oxide Optimized for Oxygen Evolution Catalysis from Molecular Orbital Principles , 2011, Science.

[11]  D. Morgan,et al.  Prediction of solid oxide fuel cell cathode activity with first-principles descriptors , 2011 .

[12]  Jan Rossmeisl,et al.  Density functional studies of functionalized graphitic materials with late transition metals for Oxygen Reduction Reactions. , 2011, Physical chemistry chemical physics : PCCP.

[13]  John Kitchin,et al.  Universality in Oxygen Evolution Electrocatalysis on Oxide Surfaces , 2011 .

[14]  Anubhav Jain,et al.  Formation enthalpies by mixing GGA and GGA + U calculations , 2011 .

[15]  J. Rossmeisl,et al.  Trends in stability of perovskite oxides. , 2010, Angewandte Chemie.

[16]  K. Domen,et al.  Photocatalytic Water Splitting: Recent Progress and Future Challenges , 2010 .

[17]  D. J. Mowbray,et al.  Trends in Metal Oxide Stability for Nanorods, Nanotubes, and Surfaces , 2010, 1002.4834.

[18]  Thomas F. Jaramillo,et al.  Accelerating materials development for photoelectrochemical hydrogen production: Standards for methods, definitions, and reporting protocols , 2010 .

[19]  Heine Anton Hansen,et al.  Formation energies of rutile metal dioxides using density functional theory , 2009 .

[20]  J. Nørskov,et al.  Scaling relationships for adsorption energies on transition metal oxide, sulfide, and nitride surfaces. , 2008, Angewandte Chemie.

[21]  J. Nørskov,et al.  Electrolysis of water on oxide surfaces , 2007 .

[22]  N. Lewis,et al.  Powering the planet: Chemical challenges in solar energy utilization , 2006, Proceedings of the National Academy of Sciences.

[23]  H. Gasteiger,et al.  Activity benchmarks and requirements for Pt, Pt-alloy, and non-Pt oxygen reduction catalysts for PEMFCs , 2005 .

[24]  H. Jónsson,et al.  Origin of the Overpotential for Oxygen Reduction at a Fuel-Cell Cathode , 2004 .

[25]  P. Raybaud,et al.  Kinetic interpretation of catalytic activity patterns based on theoretical chemical descriptors , 2003 .

[26]  J. Bockris,et al.  The origin of ideas on a Hydrogen Economy and its solution to the decay of the environment , 2002 .

[27]  E. Sato,et al.  Electrocatalytic properties of transition metal oxides for oxygen evolution reaction , 1986 .

[28]  S. Trasatti Electrocatalysis in the anodic evolution of oxygen and chlorine , 1984 .

[29]  J. Bockris,et al.  The Electrocatalysis of Oxygen Evolution on Perovskites , 1984 .

[30]  S. Trasatti Electrocatalysis by oxides — Attempt at a unifying approach , 1980 .

[31]  Robert L. Burwell,et al.  The mechanism of heterogeneous Catalysis , 1966 .

[32]  J. M. García‐Lastra,et al.  Oxygen reduction and evolution at single-metal active sites: Comparison between functionalized graphitic materials and protoporphyrins , 2013 .

[33]  C. Delmas,et al.  Review of the structure and the electrochemistry of nickel hydroxides and oxy-hydroxides , 1982 .