Source abstract
Abstract
Arrays of Si microwires doped n-type (n-Si) and surface-functionalized with methyl groups have been used, with or without deposition of Pt electrocatalysts, to photoelectrochemically oxidize I–(aq) to I3–(aq) in 7.6 M HI(aq). Under conditions of iodide oxidation, methyl-terminated n-Si microwire arrays exhibited stable short-circuit photocurrents over a time scale of days, albeit with low energy-conversion efficiencies. In contrast, electrochemical deposition of Pt onto methyl-terminated n-Si microwire arrays consistently yielded energy-conversion efficiencies of ∼2% for iodide oxidation, with an open-circuit photovoltage of ∼400 mV and a short-circuit photocurrent density of ∼10 mA cm–2 under 100 mW cm–2 of simulated air mass 1.5G solar illumination. Platinized electrodes were stable for >200 h of continuous operation, with no discernible loss of Si or Pt. Pt deposited using electron-beam evaporation also resulted in stable photoanodic operation of the methyl-terminated n-Si microwire arrays but yielded substantially lower photovoltages than when Pt was deposited electrochemically.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Division of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Blvd., Pasadena, California 91125, United States
Thomas J. Watson Laboratories of Applied Physics, California Institute of Technology, 1200 East California Blvd., Pasadena, California 91125, United States
Beckman Institute, California Institute of Technology, 1200 East California Blvd., Pasadena, California 91125, United States
Kavli Nanoscience Institute, California Institute of Technology, 1200 East California Blvd., Pasadena, California 91125, United States
Funding
Division of Chemistry · Office of Energy Efficiency and Renewable Energy
References (73)
Show source-provided references
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