Operando Spectroscopic Analysis of CoP Films Electrocatalyzing the Hydrogen-Evolution Reaction
Creators
- 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 periodAdditional details
Identifiers
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
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 49012735
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; CATALYSIS; COBALT PHOSPHIDES; CURRENT DENSITY; ELECTROCHEMISTRY; ELECTRODEPOSITION; HYDROGEN PRODUCTION; RAMAN SPECTROSCOPY; SULFURIC ACID; X-RAY SPECTROSCOPY
- Descriptors DEC
- CHEMISTRY; COBALT COMPOUNDS; DEPOSITION; ELECTROLYSIS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; LASER SPECTROSCOPY; LYSIS; OXYGEN COMPOUNDS; PHOSPHIDES; PHOSPHORUS COMPOUNDS; PNICTIDES; SPECTROSCOPY; SULFUR COMPOUNDS; SURFACE COATING; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Contract/Grant/Project number
- AC02-05CH11231; SC0004993; AC02-76SF00515
- Funding organization
- USDOE Office of Science - SC, Basic Energy Sciences (BES) (SC-22) (United States); USDOE Office of Science - SC, Biological and Environmental Research (BER) (SC-23) (United States); National Institutes of Health (NIH) (United States)
- Secondary number(s)
- OSTIID--1398516