High-performance bimetallic In-Pb for electrocatalytic hydrogenation of levulinic acid
被引:6
作者:
Zhang, Yunfei
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South China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R ChinaSouth China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
Zhang, Yunfei
[1
]
Wang, Xilun
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Sun Yat Sen Univ, Fine Chem Ind Res Inst, Sch Chem, Guangzhou 510275, Peoples R ChinaSouth China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
Wang, Xilun
[2
]
Shen, Yi
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South China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
China Singapore Int Joint Res Inst, Guangzhou Knowledge City, Guangzhou 510663, Peoples R ChinaSouth China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
Shen, Yi
[1
,3
]
机构:
[1] South China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
[2] Sun Yat Sen Univ, Fine Chem Ind Res Inst, Sch Chem, Guangzhou 510275, Peoples R China
[3] China Singapore Int Joint Res Inst, Guangzhou Knowledge City, Guangzhou 510663, Peoples R China
The challenge in the electrochemical reduction of levulinic acid (LA) lies in designing highly selective, energy -efficient, and non-precious-metal electrocatalysts that minimize the competitive hydrogen evolution reaction during LA conversion. Herein, we reported a facile pulsed electrodeposition strategy to fabricate bimetallic electrocatalysts with different combinations of lead (Pb), indium (In), tin, and cadmium supported by free-standing carbon felts (CFs). The as-prepared bimetallic self-supporting electrodes were examined for the elec-trochemical hydrogenation (ECH) of LA. The resulting InPb/CF electrocatalysts showed superior performance among the bimetallic catalysts. In addition, it was demonstrated that the catalytic performance of bimetallic samples was better than that of the corresponding monometallic samples. Notably, the In72.4Pb27.6/CF exhibited the best performance for ECH of LA, leading to 86.1 % of LA conversion, 99.7 % of selectivity towards valeric acid and 60.8 % of Faradaic efficiency at-1.5 V vs RHE. The excellent performance is mainly attributed to the modification of the electronic structures by the ligand and strain effects. Meanwhile, the relatively high elec-trochemically active surface area and the low charge transfer resistance are also conducive to improving the catalytic performance.
机构:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
Sun Hongmei
Cao Linyuan
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
Cao Linyuan
Lu Lehui
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
机构:
Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Mizugaki, T.
Nagatsu, Y.
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Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Nagatsu, Y.
Togo, K.
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Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Togo, K.
Maeno, Z.
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Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Maeno, Z.
Mitsudome, T.
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Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Mitsudome, T.
Jitsukawa, K.
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Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Jitsukawa, K.
Kaneda, K.
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Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
Osaka Univ, Res Ctr Solar Energy Chem, Toyonaka, Osaka 5608531, JapanOsaka Univ, Grad Sch Engn Sci, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
机构:
Gurukula Kangri Univ, Dept Chem, Haridwar 249404, Uttarakhand, India
CSIR Indian Inst Petr Dehradun, Dehra Dun 248005, Uttarakhand, IndiaGurukula Kangri Univ, Dept Chem, Haridwar 249404, Uttarakhand, India
Andola, Suresh Chandra
Pandey, Ankit
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CSIR Indian Inst Petr Dehradun, Dehra Dun 248005, Uttarakhand, India
Uttaranchal Univ, Dept Chem, Dehra Dun 248007, Uttarakhand, IndiaGurukula Kangri Univ, Dept Chem, Haridwar 249404, Uttarakhand, India
Pandey, Ankit
Poddar, Mukesh Kumar
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CSIR Indian Inst Petr Dehradun, Dehra Dun 248005, Uttarakhand, IndiaGurukula Kangri Univ, Dept Chem, Haridwar 249404, Uttarakhand, India