A sodium-ion-conducted asymmetric electrolyzer to lower the operation voltage for direct seawater electrolysis

Hao Shi, Tanyuan Wang, Jianyun Liu, Weiwei Chen, Shenzhou Li, Jiashun Liang, Shuxia Liu, Xuan Liu, Zhao Cai, Chao Wang, Dong Su, Yunhui Huang, Lior Elbaz, Qing Li

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53 Scopus citations

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 languageEnglish
Article number3934
JournalNature Communications
Volume14
Issue number1
DOIs
StatePublished - 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.

FundersFunder number
National Natural Science Foundation of China22122202, 22072051, 21972051
Huazhong University of Science and Technology
Natural Science Foundation of Hubei Province2021CFB329
National Key Research and Development Program of China2021YFA1600800

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