Cited by 1,019Electrocatalysts for Energy ConversionIron oxide chemistry and applicationsCO2 Reduction Techniques and Catalysts

Solar-driven, highly sustained splitting of seawater into hydrogen and oxygen fuels

Open access
Kuang, Yun, Kenney, Michael J., Meng, Yongtao, Hung, Wei-Hsuan, Liu, Yijin, Huang, Jianan Erick, Prasanna, Rohit, Li, Pengsong +6 more·2019·Proceedings of the National Academy of Sciences

Abstract

Significance: Electrolysis of water to generate hydrogen fuel could be vital to the future renewable energy landscape. Electrodes that can sustain seawater splitting without chloride corrosion could address the issue of freshwater scarcity on Earth. Herein, a hierarchical anode consisting of a nickel–iron hydroxide electrocatalyst layer uniformly coated on a sulfide layer formed on Ni substrate was developed, affording superior catalytic activity and corrosion resistance in seawater electrolysis. In situ-generated polyanion-rich passivating layers formed in the anode are responsible for chloride repelling and high corrosion resistance, leading to new directions for designing and fabricating highly sustained seawater-splitting electrodes and providing an opportunity to use the vast seawater on Earth as an energy carrier.

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Crossref · 10.1073/pnas.1900556116

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  • Even at a larger current density of 500 mA cm−2, the required overpotential was merely 320 mV, far below the overpotential of 490 mV required to initiate the reaction of chloride oxidation to hypochlorite.

    “Notably, even at a larger current density of 500 mA cm− 2, the required overpotential was merely 320 mV, far below the overpotential of 490 mV required to initiate the reaction of chloride oxidation to hypo chlorite [13].”

    From Wood aerogel-derived sandwich-like layered nanoelectrodes for alkaline overall seawater electrosplitting (2021) · cites this paper as [13]

    The passage describing the three-electrode measurements (Fig. 2B; page unavailable) reports about 300 mV at 400 mA/cm² and a 490 mV threshold for chloride oxidation to hypochlorite. The higher-current passage (Fig. 3B; page unavailable) reports about 380 mV at 1,500 mA/cm². Our copy does not state the claimed 320 mV at 500 mA/cm². (LLM, conf=0.83)

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  • Seawater-splitting was first investigated by Bennett, involving the HER at the cathode and the chlorine evolution reaction (CIER) at the anode-a two-electron process that yields chlorine or hypochlorite as the value-added product.

    “Seawater-splitting was first investigated by Bennett, [215] involving the HER at the cathode and the chlorine evolution reaction (CIER) at the anode-a two-electron process that yields chlorine or hypochlorite as the value-added product.[42]”

    From Advances in Blue Energy Fuels: Harvesting Energy from Ocean for Self‐Powered Electrolysis (2025) · cites this paper as [42]

    The paper’s introductory discussion (indexed under Abstract; page unavailable) describes chlorine evolution as a two-electron reaction, calls chlorine a high-value product, and shows a two-electron pathway to hypochlorite. It does not describe hypochlorite as a value-added product; it treats hypochlorite formation as a competing reaction that its seawater-splitting system seeks to avoid. The Bennett priority claim is attached to a different citation, [215], rather than this source’s [42]. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • The main issue for seawater splitting is competition between the oxygen evolution reaction (OER) and the chlorine evolution reaction (CER) at the anode.

    “The main issue for seawater splitting technique lies in the competion between the OER and the chlorine evolution reaction (CER) at the anode [13,14].”
  • Under alkaline conditions, chlorine is converted into hypochlorite with an onset potential of around 490 mV, which is higher than that of the OER.

    “Under alkaline conditions, chlorine is converted into hypo chlorite, with an onset potential of around 490 mV, which is higher than that of the OER.”

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Cites

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Research works printed but not linked: 20

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Authors
Kuang, Y., Kenney, M. J., Meng, Y., Hung, W.-H., Liu, Y., Huang, J. E., Prasanna, R., Li, P., Li, Y., Wang, L., Lin, M.-C., McGehee, M. D., Sun, X., & Dai, H.
Affiliations
  • State Key Laboratory of Chemical Resource Engineering (CN)
  • Stanford University (US)
  • Shandong University of Science and Technology (CN)
  • Feng Chia University (TW)
  • SLAC National Accelerator Laboratory (US)
  • Tianjin University of Technology (CN)
  • University of Colorado Boulder (US)
Corresponding author
  • Sun, Xiaoming
  • Dai, Hongjie
Venue
Proceedings of the National Academy of Sciences
Published
2019-03-18
Volume
116
Issue
14
Pages
6624-6629
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2922256802
Cited by
1,019
References
0
Citations by year
2026: 147 · 2025: 184 · 2024: 196 · 2023: 176 · 2022: 130 · 2021: 112 · 2020: 63 · 2019: 11
FWCI
16.81
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion, cc-by-nc-nd)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
Funders
  • U.S. Department of Energy (DE-SC0016165, DE-AC02-76SF00515)
  • National Science Foundation (ECCS-1542152)
  • National Key Research and Development Project (2016YFF0204402)
Topics
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Electrocatalysts for Energy Conversion
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Iron oxide chemistry and applications
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › CO2 Reduction Techniques and Catalysts
Keywords
seawater electrolysis, hydrogen production, chloride corrosion resistance, anode design, renewable energy carriers

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