4.8 Article

Ultrathin Silicon Oxide Overlayers Enable Selective Oxygen Evolution from Acidic and Unbuffered pH-Neutral Seawater

期刊

ACS CATALYSIS
卷 11, 期 3, 页码 1316-1330

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c04343

关键词

seawater electrolysis; oxygen evolution reaction; chlorine evolution reaction; membrane-coated electrocatalysts; hydrogen; silicon oxide; coatings

资金

  1. Netherlands Organization for Scientific Research (NWO) [731.015.204 ELECTROGAS]
  2. Akzo Nobel Chemicals/Nouryon
  3. Shell Global Solutions
  4. Magneto Special Anodes (an Evoqua Brand)
  5. Elson Technologies
  6. Deresiewicz Research Fellowship
  7. Columbia University Materials Research Science and Engineering Center REU program
  8. Columbia Engineering Dean's Office Research Fellowship
  9. American Membrane Technology Association Fellowship
  10. National Science Foundation (NSF) [CBET-1752340]
  11. Qatar National Research Fund under its National Priorities Research Program award [NPRP12S-0131-190024]
  12. Qatar Shell Research and Technology Center (QSRTC)

向作者/读者索取更多资源

The study demonstrates that ultrathin silicon oxide (SiOx) overlayers on model platinum anodes effectively suppress chlorine evolution reaction (CER) in the presence of chloride ions, while still allowing oxygen evolution reaction (OER) to occur.
Seawater electrolysis is an attractive approach for producing clean hydrogen fuel in scenarios where freshwater is scarce and renewable electricity is abundant. However, chloride ions (Cl-) in seawater can accelerate electrode corrosion and participate in the undesirable chlorine evolution reaction (CER). This problem is especially acute in acidic conditions that naturally arise at the anode as a result of the desired oxygen evolution reaction (OER). Herein, we demonstrate that ultrathin silicon oxide (SiOx) overlayers on model platinum anodes are highly effective at suppressing the CER in the presence of 0.6 M Cl- in both acidic and unbuffered pH-neutral electrolytes by blocking the transport of Cl- to the catalytically active buried interface while allowing the desired oxygen evolution reaction (OER) to occur there. The permeability of Cl- in SiOx overlayers is 3 orders of magnitude less than that of Cl- in a conventional salt-selective membrane used in reverse osmosis desalination. The overlayers also exhibit robust stability over 12 h in chronoamperometry tests at moderate overpotentials. SiOx overlayers demonstrate a promising step toward achieving selective and stable seawater electrolysis without the need to adjust the pH of the electrolyte.

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