Identifying the Geometric Site Dependence of Spinel Oxides for the Electrooxidation of 5-Hydroxymethylfurfural.
Yuxuan LuChung-Li DongYu-Cheng HuangYuqin ZouZhijuan LiuYanbo LiuYingying LiNihan HeJianqiao ShiShuangyin WangPublished in: Angewandte Chemie (International ed. in English) (2020)
Co-based spinel oxides, which are of mixing valences with the presence of both Co2+ and Co3+ at different atom locations, are considered as promising catalysts for the electrochemical oxidation of 5-hydroxymethylfurfural (HMF). Identifying the role of each atom site in the electroxidation of HMF is critical to design the advanced electrocatalysts. In this work, we found that Co2+ Td in Co3 O4 is capable of chemical adsorption for acidic organic molecules, and Co3+ Oh play a decisive role in HMF oxidation. Thereafter, the Cu2+ was introduced in spinel oxides to enhance the exposure degree of Co3+ and to boost acidic adsorption and thus to enhance the electrocatalytic activity for HMF electrooxidation significantly.