Efficient Screening of Bi–Metallic Electrocatalysts for Glycerol Valorization

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作者
dos Santos, Egon Campos [1 ,4 ]
Araujo, Rafael B. [1 ]
Valter, Mikael [1 ]
Salazar-Alvarez, German [2 ]
Johnsson, Mats [3 ]
Bajdich, Michal [4 ]
Abild-Pedersen, Frank [4 ]
Pettersson, Lars Gunnar Moody [1 ]
机构
[1] Department of Physics, AlbaNova University Center, Stockholm University, Stockholm,SE-106 91, Sweden
[2] Department of Materials Science and Engineering, Ångström Laboratory, Uppsala University, Box 35, Uppsala,751 03, Sweden
[3] Department of Materials and Environmental Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm,SE-106 91, Sweden
[4] SUNCAT- Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park,CA,94025, United States
关键词
Electrocatalysts - Glycerol - Hydrogen production - Silver alloys - Copper alloys - Cost effectiveness - Electrodes - Electrooxidation - Gold alloys - Indium alloys - Bismuth alloys - Ruthenium alloys - Cobalt alloys - Metals - Palladium alloys - Platinum alloys - Sustainable development - Tin alloys - Methanol - Catalyst selectivity - Biodiesel - Gallium alloys - Toxicity;
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摘要
Glycerol is a byproduct of biodiesel production and, as such, it is of limited economic value. By means of electrooxidation, glycerol can be used as a feedstock for scalable hydrogen production, in addition to conversion to value-added products. The development of novel and efficient catalytic electrode materials for the anodic side of the reaction is a key towards a hydrogen-based energy economy. In the present study, a computational screening protocol combining DFT, scaling relations, and microkinetic modeling allows for a rational selection of novel catalysts that can deliver efficient glycerol electrooxidation, low cost of production, and environmental sustainability. Activity and chemical selectivity towards hydrogen production on pure metal catalysts is discussed in terms of volcano-shaped plots. We find that the selectivity in the glycerol oxidation reaction is influenced by a different energy landscape when in the presence of water and best classified by a comparison of O[sbnd]H and C[sbnd]H bond-breaking barriers. In addition, we screened 3570 bi-metallic catalysts in the AB (L10) and A3B (L12) ordered structures for activity, stability, price, and toxicity. By filtering based on the criteria for toxicity, resistance to oxidation, miscibility, and price, we have identified 5 L10 structured catalysts (AgPd, AuPd, PtSb, CuPt, and AgPt) and 20 L12 catalysts (Ga3Ta, In3Ta, Ir3W, Ir3Mo, Cu3Pt, Ir3Ta, Ir3Re, Pd3Bi, Pd3Cu, Pd3W, Pd3Co, Pd3Sn, Pd3Mo, Pd3Ag, Pd3Ga, Pd3Ta, Au3Ru, Pd3In, Au3Ir, and Pd3Au) that are all predicted to show high activity. We also identify an additional 37 L10 and 92 L12 structured electrocatalysts with an anticipated medium-high activity. © 2021 The Author(s)
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