LAPSE:2023.17066
Published Article

LAPSE:2023.17066
Catalytic and Sulfur-Tolerant Performance of Bimetallic Ni−Ru Catalysts on HI Decomposition in the Sulfur-Iodine Cycle for Hydrogen Production
March 6, 2023
Abstract
The sulfur-iodine (SI) cycle holds great promise as an alternative large-scale process for converting water into hydrogen without CO2 emissions. A major issue regarding the long-term stability and activity of the catalysts is their poor sulfur deactivation resistance in the HI feeding process. In this work, the effect of Ru addition for enhancing the activity and sulfur resistance of SiO2-supported Ni catalysts in the HI decomposition reaction has been investigated. The presence of H2SO4 molecules in the HI results in severe sulfur deactivation of the Ru-free Ni/SiO2 catalysts by blocking the active sites. However, Ni−Ru/SiO2 catalysts show higher catalytic activity without sulfur-poisoning by 25% and exhibit more superior catalytic performance than the Ru-free catalyst. The addition of Ru to the Ni/SiO2 catalyst promotes the stability and activity of the catalysts. The experimental trends in activity and sulfur tolerance are consistent with the theoretical modeling, with the catalytic activities existing in the order Ni/SiO2 < Ni−Ru/SiO2. The effect of Ru on the improvement in sulfur resistance over Ni-based catalysts is attributed to electronic factors, as evidenced by theory modeling analysis and detailed characterizations.
The sulfur-iodine (SI) cycle holds great promise as an alternative large-scale process for converting water into hydrogen without CO2 emissions. A major issue regarding the long-term stability and activity of the catalysts is their poor sulfur deactivation resistance in the HI feeding process. In this work, the effect of Ru addition for enhancing the activity and sulfur resistance of SiO2-supported Ni catalysts in the HI decomposition reaction has been investigated. The presence of H2SO4 molecules in the HI results in severe sulfur deactivation of the Ru-free Ni/SiO2 catalysts by blocking the active sites. However, Ni−Ru/SiO2 catalysts show higher catalytic activity without sulfur-poisoning by 25% and exhibit more superior catalytic performance than the Ru-free catalyst. The addition of Ru to the Ni/SiO2 catalyst promotes the stability and activity of the catalysts. The experimental trends in activity and sulfur tolerance are consistent with the theoretical modeling, with the catalytic activities existing in the order Ni/SiO2 < Ni−Ru/SiO2. The effect of Ru on the improvement in sulfur resistance over Ni-based catalysts is attributed to electronic factors, as evidenced by theory modeling analysis and detailed characterizations.
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Keywords
bimetallic catalysts, HI decomposition, hydrogen production, SI cycle, sulfur-tolerant
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Suggested Citation
Wang L, Zhang K, Qiu Y, Chen H, Wang J, Wang Z. Catalytic and Sulfur-Tolerant Performance of Bimetallic Ni−Ru Catalysts on HI Decomposition in the Sulfur-Iodine Cycle for Hydrogen Production. (2023). LAPSE:2023.17066
Author Affiliations
Wang L: Zhejiang Institute of Metrology, Hangzhou 310018, China [ORCID]
Zhang K: State Grid Zhejiang Electric Power Research Institute, Hangzhou 310014, China
Qiu Y: Zhejiang Institute of Metrology, Hangzhou 310018, China
Chen H: Zhejiang Institute of Metrology, Hangzhou 310018, China
Wang J: Zhejiang Institute of Metrology, Hangzhou 310018, China
Wang Z: State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou 310027, China [ORCID]
Zhang K: State Grid Zhejiang Electric Power Research Institute, Hangzhou 310014, China
Qiu Y: Zhejiang Institute of Metrology, Hangzhou 310018, China
Chen H: Zhejiang Institute of Metrology, Hangzhou 310018, China
Wang J: Zhejiang Institute of Metrology, Hangzhou 310018, China
Wang Z: State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou 310027, China [ORCID]
Journal Name
Energies
Volume
14
Issue
24
First Page
8539
Year
2021
Publication Date
2021-12-17
ISSN
1996-1073
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Original Submission
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PII: en14248539, Publication Type: Journal Article
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LAPSE:2023.17066
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Mar 6, 2023
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