Abstract
Hydrogen produced from neutral seawater electrolysis faces many challenges including high energy consumption, the corrosion/side reactions caused by Cl-, and the blockage of active sites by Ca2+/Mg2+ precipitates. Herein, we design a pH-asymmetric electrolyzer with a Na+ exchange membrane for direct seawater electrolysis, which can simultaneously prevent Cl- corrosion and Ca2+/Mg2+ precipitation and harvest the chemical potentials between the different electrolytes to reduce the required voltage. In-situ Raman spectroscopy and density functional theory calculations reveal that water dissociation can be promoted with a catalyst based on atomically dispersed Pt anchored to Ni-Fe-P nanowires with a reduced energy barrier (by 0.26 eV), thus accelerating the hydrogen evolution kinetics in seawater. Consequently, the asymmetric electrolyzer exhibits current densities of 10 mA cm−2 and 100 mA cm−2 at voltages of 1.31 V and 1.46 V, respectively. It can also reach 400 mA cm−2 at a low voltage of 1.66 V at 80 °C, corresponding to the electricity cost of US$1.36 per kg of H2 ($0.031/kW h for the electricity bill), lower than the United States Department of Energy 2025 target (US$1.4 per kg of H2).
Original language | English |
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Article number | 3934 |
Journal | Nature Communications |
Volume | 14 |
Issue number | 1 |
DOIs | |
State | Published - 4 Jul 2023 |
Bibliographical note
Publisher Copyright:© 2023, The Author(s).
Funding
This work was financially supported by the National Key Research and Development Program of China (2021YFA1600800 to Q.L. and T.W.), National Natural Science Foundation of China (22122202 to Q.L., 22072051 to T.W., 21972051 to Q.L.), the Natural Science Foundation of Hubei Province (2021CFB329 to T.W.). The authors thank the Analytical and Testing Center of Huazhong University of Science and Technology (HUST) for carrying out the SEM, XPS, and XRD measurements. This work was financially supported by the National Key Research and Development Program of China (2021YFA1600800 to Q.L. and T.W.), National Natural Science Foundation of China (22122202 to Q.L., 22072051 to T.W., 21972051 to Q.L.), the Natural Science Foundation of Hubei Province (2021CFB329 to T.W.). The authors thank the Analytical and Testing Center of Huazhong University of Science and Technology (HUST) for carrying out the SEM, XPS, and XRD measurements.
Funders | Funder number |
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National Natural Science Foundation of China | 22122202, 22072051, 21972051 |
Huazhong University of Science and Technology | |
Natural Science Foundation of Hubei Province | 2021CFB329 |
National Key Research and Development Program of China | 2021YFA1600800 |