4.8 Article

Role of Ni in PtNi Bimetallic Electrocatalysts for Hydrogen and Value-Added Chemicals Coproduction via Glycerol Electrooxidation

Journal

ACS CATALYSIS
Volume 12, Issue 23, Pages 14492-14506

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c03907

Keywords

glycerol oxidation; electrocatalysis; PtNi nanoparticles; glycerol adsorption; operando spectroscopy; product distribution

Funding

  1. European Research Council (ERC) under the European Union [866402]
  2. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo - FAPESP [2017/11986-5, 2020/04431-0]
  3. Shell
  4. ANP (Brazil's National Oil, Natural Gas and Biofuels Agency) through the R & D levy regulation
  5. National Council for Scientific and Technological Development - CNPq [130741/2021-3]
  6. UK Catalysis Hub
  7. EPSRC [EP/R027129/1]
  8. European Research Council (ERC) [866402] Funding Source: European Research Council (ERC)

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PtNi2 catalyst with a moderate Ni content and a homogenously alloyed structure exhibited the highest reaction activity in the electrochemical oxidation of glycerol among all materials studied. The role of Ni in PtNi is to tailor the electronic structure of pure Pt sites, influencing the glycerol oxidation reaction.
Pt-based bimetallic electrocatalysts are promising candidates to convert surplus glycerol from the biodiesel industry to value-added chemicals and coproduce hydrogen. It is expected that the nature and content of the elements in the bimetallic catalyst can not only affect the reaction kinetics but also influence the product selectivity, providing a way to increase the yield of the desired products. Hence, in this work, we investigate the electrochemical oxidation of glycerol on a series of PtNi nanoparticles with increasing Ni content using a combination of physicochemical structural analysis, electrochemical measurements, operando spectroscopic techniques, and advanced product characterizations. With a moderate Ni content and a homogenously alloyed bimetallic Pt-Ni structure, the PtNi2 catalyst displayed the highest reaction activity among all materials studied in this work. In situ FTIR data show that PtNi2 can activate the glycerol molecule at a more negative potential (0.4 VRHE) than the other PtNi catalysts. In addition, its surface can effectively catalyze the complete C-C bond cleavage, resulting in lower CO poisoning and higher stability. Operando X-ray absorption spectroscopy and UV-vis spectroscopy suggest that glycerol adsorbs strongly onto surface Ni(OH)x sites, preventing their oxidation and activation of oxygen or hydroxyl from water. As such, we propose that the role of Ni in PtNi toward glycerol oxidation is to tailor the electronic structure of the pure Pt sites rather than a bifunctional mechanism. Our experiments provide guidance for the development of bimetallic catalysts toward highly efficient, selective, and stable glycerol oxidation reactions.

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