Cu-Based Bimetallic Catalysts for Electrocatalytic Oxidative Dehydrogenation of Furfural with Practical Rates

被引:6
|
作者
Liu, Hengzhou [1 ]
Yu, Jiaqi [2 ]
Chen, Yifu [1 ]
Lee, Jungkuk [1 ]
Huang, Wenyu [2 ]
Li, Wenzhen [1 ]
机构
[1] Iowa State Univ, Dept Chem & Biol Engn, 618 Bissell Rd, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Chem, 618 Bissell Rd, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
hydrogen; biomass; bimetal; electrocatalyticoxidative dehydrogenation; aldehyde; HYDROGEN-PRODUCTION; ADDITIVE-FREE; FORMALDEHYDE; COPPER; GENERATION; EVOLUTION; PLATFORM;
D O I
10.1021/acsami.3c06783
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Electrocatalytic oxidative dehydrogenation (EOD) of aldehydesenablesultra-low voltage, bipolar H-2 production with co-generationof carboxylic acid. Herein, we reported a simple galvanic replacementmethod to prepare CuM (M = Pt, Pd, Au, and Ag) bimetallic catalyststo improve the EOD of furfural to reach industrially relevant currentdensities. The redox potential difference between Cu/Cu2+ and a noble metal M/My+ can incorporate the noble metalon the Cu surface and enlarge its surface area. Particularly, dispersingPt in Cu (CuPt) achieved a record-high current density of 498 mA cm(-2) for bipolar H-2 production at a low cellvoltage of 0.6 V and a Faradaic efficiency of >80% to H-2. Future research is needed to deeply understand the synergisticeffects of Cu-M toward EOD of furfural, and improve the Cu-Mcatalyst stability, thus offering great opportunities for future distributedmanufacturing of green hydrogen and carbon chemicals with practicalrates and low-carbon footprints.
引用
收藏
页码:37477 / 37485
页数:9
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