Self-template construction of hollow Co3O4 microspheres from porous ultrathin nanosheets and efficient noble metal-free water oxidation catalysts

被引:200
作者
Zhao, Jun [1 ]
Zou, Yongcun [1 ]
Zou, Xiaoxin [1 ]
Bai, Tianyu [1 ]
Liu, Yipu [1 ]
Gao, Ruiqin [1 ]
Wang, Dejun [1 ,2 ]
Li, Guo-Dong [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN EVOLUTION REACTION; COBALT OXIDE; LITHIUM-ION; STRUCTURAL REQUIREMENTS; GENERALIZED SYNTHESIS; MESOPOROUS CO3O4; SPHERES; NANOCRYSTALS; ELECTROCATALYSTS; NANOPARTICLES;
D O I
10.1039/c4nr00002a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing noble metal-free water oxidation catalysts is essential for many energy conversion/storage processes (e. g., water splitting). Herein, we report the facile synthesis of hollow Co3O4 microspheres composed of porous, ultrathin (<5 nm), single-crystal-like nanosheets via a novel "self-template" route. The successful preparation of these hollow Co3O4 nanomaterials includes three main steps: (1) the synthesis of solid cobalt alkoxide microspheres, (2) their subsequent self-template conversion into hollow cobalt hydroxide microspheres composed of ultrathin nanosheets, and finally (3) thermal treatment of hollow cobalt hydroxide microspheres into the hollow Co3O4 material. The as-obtained hollow Co3O4 nanomaterial possesses a high BET surface area (similar to 180 m(2) g(-1)), and can serve as an active and stable water oxidation catalyst under both electrochemical and photochemical reaction conditions, owing to its unique structural features. In the electrochemical water oxidation, this catalyst affords a current density of 10 mA cm(-2) (a value related to practical relevance) at an overpotential of similar to 0.40 V. Moreover, with the assistance of a sensitizer [Ru(bpy)(3)](2+) (bpy 2,2'-bipyridine), this nanomaterial can catalyze water oxidation reactions under visible light irradiation with an O-2 evolution rate of similar to 12 218 mmol g(-1) h(-1). Our results suggest that delicate nanostructuring can offer unique advantages for developing efficient water oxidation catalysts.
引用
收藏
页码:7255 / 7262
页数:8
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