Phosphate-decorated Ni
Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, p...
Ausführliche Beschreibung
Autor*in: |
Li, Tianshui [verfasserIn] Zhao, Xiuping [verfasserIn] Getaye Sendeku, Marshet [verfasserIn] Zhang, Xingheng [verfasserIn] Xu, Ling [verfasserIn] Wang, Zhaolei [verfasserIn] Wang, Shiyuan [verfasserIn] Duan, Xinxuan [verfasserIn] Liu, Hai [verfasserIn] Liu, Wei [verfasserIn] Zhou, Daojin [verfasserIn] Xu, Haijun [verfasserIn] Kuang, Yun [verfasserIn] Sun, Xiaoming [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: The chemical engineering journal - Amsterdam : Elsevier, 1997, 460 |
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Übergeordnetes Werk: |
volume:460 |
DOI / URN: |
10.1016/j.cej.2023.141413 |
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Katalog-ID: |
ELV062643754 |
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520 | |a Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. | ||
650 | 4 | |a Seawater splitting | |
650 | 4 | |a Near-neutral solutions | |
650 | 4 | |a Oxygen evolution reaction | |
650 | 4 | |a Non-precious metals | |
650 | 4 | |a Phosphate-decorated | |
700 | 1 | |a Zhao, Xiuping |e verfasserin |4 aut | |
700 | 1 | |a Getaye Sendeku, Marshet |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xingheng |e verfasserin |4 aut | |
700 | 1 | |a Xu, Ling |e verfasserin |4 aut | |
700 | 1 | |a Wang, Zhaolei |e verfasserin |4 aut | |
700 | 1 | |a Wang, Shiyuan |e verfasserin |4 aut | |
700 | 1 | |a Duan, Xinxuan |e verfasserin |4 aut | |
700 | 1 | |a Liu, Hai |e verfasserin |4 aut | |
700 | 1 | |a Liu, Wei |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Daojin |e verfasserin |4 aut | |
700 | 1 | |a Xu, Haijun |e verfasserin |4 aut | |
700 | 1 | |a Kuang, Yun |e verfasserin |4 aut | |
700 | 1 | |a Sun, Xiaoming |e verfasserin |4 aut | |
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10.1016/j.cej.2023.141413 doi (DE-627)ELV062643754 (ELSEVIER)S1385-8947(23)00144-4 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Li, Tianshui verfasserin aut Phosphate-decorated Ni 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. Seawater splitting Near-neutral solutions Oxygen evolution reaction Non-precious metals Phosphate-decorated Zhao, Xiuping verfasserin aut Getaye Sendeku, Marshet verfasserin aut Zhang, Xingheng verfasserin aut Xu, Ling verfasserin aut Wang, Zhaolei verfasserin aut Wang, Shiyuan verfasserin aut Duan, Xinxuan verfasserin aut Liu, Hai verfasserin aut Liu, Wei verfasserin aut Zhou, Daojin verfasserin aut Xu, Haijun verfasserin aut Kuang, Yun verfasserin aut Sun, Xiaoming verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 460 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:460 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 460 |
spelling |
10.1016/j.cej.2023.141413 doi (DE-627)ELV062643754 (ELSEVIER)S1385-8947(23)00144-4 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Li, Tianshui verfasserin aut Phosphate-decorated Ni 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. Seawater splitting Near-neutral solutions Oxygen evolution reaction Non-precious metals Phosphate-decorated Zhao, Xiuping verfasserin aut Getaye Sendeku, Marshet verfasserin aut Zhang, Xingheng verfasserin aut Xu, Ling verfasserin aut Wang, Zhaolei verfasserin aut Wang, Shiyuan verfasserin aut Duan, Xinxuan verfasserin aut Liu, Hai verfasserin aut Liu, Wei verfasserin aut Zhou, Daojin verfasserin aut Xu, Haijun verfasserin aut Kuang, Yun verfasserin aut Sun, Xiaoming verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 460 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:460 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 460 |
allfields_unstemmed |
10.1016/j.cej.2023.141413 doi (DE-627)ELV062643754 (ELSEVIER)S1385-8947(23)00144-4 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Li, Tianshui verfasserin aut Phosphate-decorated Ni 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. Seawater splitting Near-neutral solutions Oxygen evolution reaction Non-precious metals Phosphate-decorated Zhao, Xiuping verfasserin aut Getaye Sendeku, Marshet verfasserin aut Zhang, Xingheng verfasserin aut Xu, Ling verfasserin aut Wang, Zhaolei verfasserin aut Wang, Shiyuan verfasserin aut Duan, Xinxuan verfasserin aut Liu, Hai verfasserin aut Liu, Wei verfasserin aut Zhou, Daojin verfasserin aut Xu, Haijun verfasserin aut Kuang, Yun verfasserin aut Sun, Xiaoming verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 460 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:460 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 460 |
allfieldsGer |
10.1016/j.cej.2023.141413 doi (DE-627)ELV062643754 (ELSEVIER)S1385-8947(23)00144-4 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Li, Tianshui verfasserin aut Phosphate-decorated Ni 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. Seawater splitting Near-neutral solutions Oxygen evolution reaction Non-precious metals Phosphate-decorated Zhao, Xiuping verfasserin aut Getaye Sendeku, Marshet verfasserin aut Zhang, Xingheng verfasserin aut Xu, Ling verfasserin aut Wang, Zhaolei verfasserin aut Wang, Shiyuan verfasserin aut Duan, Xinxuan verfasserin aut Liu, Hai verfasserin aut Liu, Wei verfasserin aut Zhou, Daojin verfasserin aut Xu, Haijun verfasserin aut Kuang, Yun verfasserin aut Sun, Xiaoming verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 460 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:460 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 460 |
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10.1016/j.cej.2023.141413 doi (DE-627)ELV062643754 (ELSEVIER)S1385-8947(23)00144-4 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Li, Tianshui verfasserin aut Phosphate-decorated Ni 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. Seawater splitting Near-neutral solutions Oxygen evolution reaction Non-precious metals Phosphate-decorated Zhao, Xiuping verfasserin aut Getaye Sendeku, Marshet verfasserin aut Zhang, Xingheng verfasserin aut Xu, Ling verfasserin aut Wang, Zhaolei verfasserin aut Wang, Shiyuan verfasserin aut Duan, Xinxuan verfasserin aut Liu, Hai verfasserin aut Liu, Wei verfasserin aut Zhou, Daojin verfasserin aut Xu, Haijun verfasserin aut Kuang, Yun verfasserin aut Sun, Xiaoming verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 460 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:460 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 460 |
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Li, Tianshui @@aut@@ Zhao, Xiuping @@aut@@ Getaye Sendeku, Marshet @@aut@@ Zhang, Xingheng @@aut@@ Xu, Ling @@aut@@ Wang, Zhaolei @@aut@@ Wang, Shiyuan @@aut@@ Duan, Xinxuan @@aut@@ Liu, Hai @@aut@@ Liu, Wei @@aut@@ Zhou, Daojin @@aut@@ Xu, Haijun @@aut@@ Kuang, Yun @@aut@@ Sun, Xiaoming @@aut@@ |
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2023-01-01T00:00:00Z |
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Li, Tianshui |
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Li, Tianshui ddc 660 bkl 58.10 misc Seawater splitting misc Near-neutral solutions misc Oxygen evolution reaction misc Non-precious metals misc Phosphate-decorated Phosphate-decorated Ni |
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660 VZ 58.10 bkl Phosphate-decorated Ni Seawater splitting Near-neutral solutions Oxygen evolution reaction Non-precious metals Phosphate-decorated |
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ddc 660 bkl 58.10 misc Seawater splitting misc Near-neutral solutions misc Oxygen evolution reaction misc Non-precious metals misc Phosphate-decorated |
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Li, Tianshui Zhao, Xiuping Getaye Sendeku, Marshet Zhang, Xingheng Xu, Ling Wang, Zhaolei Wang, Shiyuan Duan, Xinxuan Liu, Hai Liu, Wei Zhou, Daojin Xu, Haijun Kuang, Yun Sun, Xiaoming |
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phosphate-decorated ni |
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Phosphate-decorated Ni |
abstract |
Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. |
abstractGer |
Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. |
abstract_unstemmed |
Direct seawater splitting technique can produce clean hydrogen energy without a complicated water desalination process. However, the oxygen evolution reaction (OER) confronts with selectivity challenge in competing with chlorine evolution and severe corrosion issues of the electrode. In this work, phosphate-decorated Ni3Fe-layered double hydroxides grown on cobalt phosphide nanoarray with both high intrinsic activity and 100 % selectivity towards seawater oxidation in a near neutral electrolyte is reported. The as-prepared electrode shows a low overpotential of 370 mV10 mA cm−2 with high durability in near-neutral seawater oxidation for 350 h. The phosphate layer on the catalyst surface contributes to the enhanced selectivity by weakening the adsorption of Cl–, and thus avoiding the competing chlorine evolution. Meanwhile, the phosphate layer with a strong proton accepting ability can resist the local pH change on the electrode surface in the neutral electrolyte, affording highly stable seawater splitting for prolonged operations in neutral seawater electrolyte. |
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Phosphate-decorated Ni |
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Zhao, Xiuping Getaye Sendeku, Marshet Zhang, Xingheng Xu, Ling Wang, Zhaolei Wang, Shiyuan Duan, Xinxuan Liu, Hai Liu, Wei Zhou, Daojin Xu, Haijun Kuang, Yun Sun, Xiaoming |
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up_date |
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|
score |
7.3996515 |