In situ FTIR insights into the electrooxidation mechanism of glucose as a function of the surface facets of Cu2O-based electrocatalytic sensors

• Published in: Journal of catalysis 2019-07, Vol.375, p.95-103
• Main Authors: Dourado, André H.B., da Silva, Anderson G.M., Pastrián, Fabián A.C., Munhos, Renan L., de Lima Batista, Ana P., de Oliveira-Filho, Antonio G.S., Quiroz, Jhon, de Oliveira, Daniela C., Camargo, Pedro H.C., Córdoba de Torresi, Susana I.
• Format: Article
• Language: English
• Subjects: Controlled surface facets; Cu2O; FTIR; In situ techniques
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2019.05.032

[Display omitted] •Mechanism investigation of glucose oxidation as function of shape in Cu2O NPs.•In situ results showed that the mechanism displayed shape-dependent behavior.•Glucose molecule can selectively adsorb on the Cu2O {1 0 0} facets.•Cu3+ species do not participate in the reaction mechanism. We focus herein on understanding how the oxidation mechanism of glucose may be affected by the nature of the surface facets of Cu2O-based electrocatalytic sensors. To this end, we performed a series of in situ FTIR spectroelectrochemical experiments and DFT simulations by employing Cu2O cubes and octahedra as electrocatalytic sensors for glucose and other interferents. Interestingly, our in situ results demonstrated that the glucose oxidation mechanism displayed shape-dependent behavior, indicating that the glucose molecule can selectively adsorb on the Cu2O {1 0 0} facets relative to ascorbate and urate interferents in a process that probably occurs without the need for an external potential. However, when the same reaction was performed in the presence of Cu2O octahedra ({1 1 1} facets), the reaction was not selective, and the final product remained on the surface, blocking the sites for further glucose oxidation and leading to significantly lower electrocatalytic activities. Surprisingly, no bands related to the formation of Cu3+ species were detected, indicating that Cu3+ species do not participate in the reaction mechanism. This is very important because these species have been assumed to be the catalytically active sites for glucose oxidation. We believe that the results presented herein provide new insights into different aspects of the oxidation of carbohydrates and may inspire a deeper mechanistic investigation of other semiconductor materials and the development of optimized electrocatalysts.