Published 2017 | Version v1
Journal article

Operando Spectroscopic Analysis of CoP Films Electrocatalyzing the Hydrogen-Evolution Reaction

  • 1. California Institute of Technology (CalTech), Pasadena, CA (United States). Division of Engineering and Applied Sciences, Joint Center for Artificial Photosynthesis
  • 2. California Institute of Technology (CalTech), Pasadena, CA (United States). Division of Chemistry and Chemical Engineering
  • 3. Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States). Molecular Biophysics and Integrated Bioimaging Division
  • 4. California Institute of Technology (CalTech), Pasadena, CA (United States). Joint Center for Artificial Photosynthesis

Description

Transition metal phosphides exhibit high catalytic activity toward the electrochemical hydrogen-evolution reaction (HER) and resist chemical corrosion in acidic solutions. For example, an electrodeposited CoP catalyst exhibited an overpotential, η of -η < 100 mV at a current density of -10 mA cm-2 in 0.500 M H2SO4 (aq). To obtain a chemical description of the material as-prepared and also while effecting the HER in acidic media, such electrocatalyst films were investigated using Raman spectroscopy and X-ray absorption spectroscopy both ex situ as well as under in situ and operando conditions in 0.500 M H2SO4 (aq). Ex situ analysis using the tandem spectroscopies indicated the presence of multiple ordered and disordered phases that contained both near-zerovalent and oxidized Co species, in addition to reduced and oxygenated P species. Lastly, operando analysis indicated that the active electrocatalyst was primarily amorphous and predominantly consisted of near-zerovalent Co as well as reduced P.

Availability note (English)

Available from http://www.osti.gov/pages/biblio/1398516; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period

Additional details

Publishing Information

Journal Title
Journal of the American Chemical Society
Journal Volume
139
Journal Issue
37
Journal Page Range
p. 12927-12930
ISSN
0002-7863