Enhanced Stability and Efficiency for Photoelectrochemical Iodide Oxidation by Methyl Termination and Electrochemical Pt Deposition on n-Type Si Microwire Arrays AITranslate
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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.
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DOI:https://doi.org/10.1021/acsenergylett.9b01529
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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.
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| GB/T 7714-2015 | [1] Shane Ardo, Elizabeth A. Santori, Hal S. Emmer, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b01529. |
| MLA | [1] Shane Ardo, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b01529. |
| APA | [1] Shane Ardo, Elizabeth A. Santori, Hal S. Emmer, Ronald L. Grimm, Matthew J. Bierman, Bruce S. Brunschwig, Harry A. Atwater, & Nathan S. Lewis. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b01529 |
| IEEE | [1] Shane Ardo, Elizabeth A. Santori, Hal S. Emmer, Ronald L. Grimm, Matthew J. Bierman, Bruce S. Brunschwig, Harry A. Atwater, and Nathan S. Lewis, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b01529. |
