Controlled deposition of size-selected MnO nanoparticle thin films for water splitting applications: reduction of onset potential with particle size

被引:5
作者
Khojasteh, Malak [1 ,2 ]
Haghighat, Shima [2 ,3 ]
Dawlaty, Jahan M. [3 ]
Kresin, Vitaly V. [1 ]
机构
[1] Univ Southern Calif, Dept Phys & Astron, Los Angeles, CA 90089 USA
[2] Univ Southern Calif, Mork Family Dept Chem Engn & Mat Sci, Los Angeles, CA 90089 USA
[3] Univ Southern Calif, Dept Chem, Los Angeles, CA 90089 USA
基金
美国国家科学基金会;
关键词
water splitting; water oxidation; nanocluster thin films; size-selective deposition; nanoparticle catalysts; gas aggregation source; manganese nanoparticles; OXYGEN EVOLUTION REACTION; PHOTOSYSTEM-II; CUO PHOTOCATHODE; MANGANESE OXIDES; GAS-AGGREGATION; OXIDATION; CATALYSTS; EFFICIENT; CLUSTER; MECHANISM;
D O I
10.1088/1361-6528/aab543
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Emulating water oxidation catalyzed by the oxomanganese clusters in the photosynthetic apparatus of plants has been a long-standing scientific challenge. The use of manganese oxide films has been explored, but while they may be catalytically active on the surface, their poor conductivity hinders their overall performance. We have approached this problem by using manganese oxide nanoparticles with sizes of 4, 6 and 8 nm, produced in a sputter-gas-aggregation source and soft-landed onto conducting electrodes. The mass loading of these catalytic particles was kept constant and corresponded to 45%-80% of a monolayer coverage. Measurements of the water oxidation threshold revealed that the onset potential decreases significantly with decreasing particle size. The final stoichiometry of the catalytically active nanoparticles, after exposure to air, was identified as predominantly MnO. The ability of such a sub-monolayer film to lower the reaction threshold implies that the key role is played by intrinsic size effects, i.e., by changes in the electronic properties and surface fields of the nanoparticles with decreasing size. We anticipate that this work will serve to bridge the knowledge gap between bulk thick film electrocatalysts and natural photosynthetic molecular-cluster complexes.
引用
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页数:9
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