Facet Impact of CuMn2O4 Spinel Nanocatalysts on Enhancement of the Oxygen Reduction Reaction in Alkaline Media

纳米材料基催化剂 尖晶石 催化作用 材料科学 纳米晶 化学工程 价(化学) 八面体 纳米颗粒 无机化学 化学 冶金 晶体结构 纳米技术 结晶学 工程类 有机化学
作者
Ming Zhou,Hongsen Wang,Lihua Zhang,Can Li,Amar Kumbhar,Héctor D. Abruña,Jiye Fang
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:12 (21): 13663-13670 被引量:35
标识
DOI:10.1021/acscatal.2c03275
摘要

Surface-structure engineering represents an attractive strategy to optimize the energy conversion performance of nanocatalysts using their deliberately controlled exposed facets. To further exploit the potential of non-PGM-based spinel catalysts for alkaline oxygen reduction reaction (ORR), a cathodic fuel cell reaction, we hereby report a strategy of ORR improvement by controlling the crystallographic facets of ultra-small CuMn<sub>2</sub>O<sub>4</sub> spinel nanocatalysts through a developed colloidal synthesis approach. The synthesis of CuMn<sub>2</sub>O<sub>4</sub> nanocrystals with morphological control relies on the design and selection of the Cu-/Mn-precursors with striking discrepancies in reaction kinetics. Following carbon loading and an annealing post-treatment of the as-synthesized nanocatalysts, the exclusively {101} facet-exposed CuMn<sub>2</sub>O<sub>4</sub> spinel nano-octahedra exhibit improved electrocatalytic activity toward ORR in 1 M KOH, when compared to their spherical counterparts, exhibiting a mass activity (MA) of 37.6 A/g at 0.85 V. After 10,000 cycles of ORR durability test, the nano-octahedra still retain an MA of 24.5 A/g, which is twice that of the CuMn<sub>2</sub>O<sub>4</sub> spinel nanospheres. Structural characterizations after durability testing indicate that the MA decay is likely associated with a decrease in the Mn<sup>3+</sup> fraction and the emergence of Cu<sup>+</sup> on CuMn<sub>2</sub>O<sub>4</sub> nano-octahedral surfaces. Finally, as a paradigm, this synthesis approach could be extended to other Mn-based spinel nanocatalysts with precise shape control, enabling us to understand and establish the relationship between the surface lattice/valence state and electrocatalytic properties.
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