Electrochemical Water Oxidation Catalysed by CoO-Co2O3-Co(OH)2 Multiphase-Nanoparticles Prepared by Femtosecond Laser Ablation in Water

被引:18
作者
Nishi, Teppei. [1 ]
Hayasaka, Yuichiro. [2 ]
Suzuki, Tomiko. M. [1 ]
Sato, Shunsuke. [1 ]
Isomura, Noritake. [1 ]
Takahashi, Naoko. [1 ]
Kosaka, Satoru. [1 ]
Nakamura, Takahiro. [3 ]
Sato, Shunichi. [3 ]
Morikawa, Takeshi. [1 ]
机构
[1] Toyota Cent Res & Dev Labs Inc, 41-1 Yokomichi, Nagakute, Aichi 4801192, Japan
[2] Tohoku Univ, Electron Microscopy Ctr, Aoba Ku, Katahira 2-1-1, Sendai, Miyagi 9808577, Japan
[3] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Katahira 2-1-1, Sendai, Miyagi 9808577, Japan
关键词
electrochemistry; laser ablation; nanoparticles; supported catalysts; water oxidation; GOLD NANOPARTICLES; CONDUCTION-BAND; VISIBLE-LIGHT; OXIDE; PHOTOANODES; ELECTROCATALYSTS; IRRADIATION; EVOLUTION; PERFORMANCE; STABILITY;
D O I
10.1002/slct.201800943
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoparticle formation via laser ablation in liquid is known to produce functional materials. However, there have been few applications of this technique to the synthesis of electrochemical catalysts for energy conversion. Herein, we report the detailed effects of femtosecond laser ablation in water on the structure and activity of a catalyst intended to promote the electrochemical oxygen evolution reaction (OER) in association with water oxidation. The femtosecond laser ablation of submicron-sized Co-CoO particles induced a drastic size reduction (from approximately 500 to 5nm) to give highly dispersed CoO nanoparticles. X-ray absorption near edge structure (XANES) and X-ray diffraction (XRD) data demonstrated that these particles also contained Co3O4 and CoO(OH) but not metallic Co. These 5nm-CoO nanoparticles showed higher mass-based-activity and lower over-potential values than those of submicron-sized Co-CoO during the OER in a nearly neutral solution. XANES data suggest that Co containing Co2O3 and Co(OH)(2) formed during the OER functioned as the actual OER catalyst.
引用
收藏
页码:4979 / 4984
页数:6
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