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]
日期:2022-10-25
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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