High-performance bimetallic In-Pb for electrocatalytic hydrogenation of levulinic acid

被引:6
作者
Zhang, Yunfei [1 ]
Wang, Xilun [2 ]
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
关键词
Bimetallic electrocatalysts; Levulinic acid; Valeric acid; Metallic lead; Metallic indium; GAMMA-VALEROLACTONE GVL; ELECTROCHEMICAL CONVERSION; FURANIC COMPOUNDS; FURFURYL ALCOHOL; BIOMASS; REDUCTION; NANOPARTICLES; ELECTRICITY; GENERATION; EVOLUTION;
D O I
10.1016/j.fuel.2023.127787
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
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.
引用
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页数:11
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