期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 113, 期 15, 页码 5984-5990出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp810155r
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资金
- National Natural Science Foundation of China [20773104]
- New Century Excellent Talents in University [NCET-06-0891]
- Ministry of Education of China [208143]
- Key Laboratory of Shaanxi Province [08JZ81]
- Natural Science Foundation of Shaanxi Provincial Education Office [07JK435]
Novel three-dimensional (3D) dendritic CdS nanoarchitectures were synthesized via a facile template-free hydrothermal process only using CdSO4 and thiourea as precursors and cetylpyridinium chloride (CPC) as a capping reagent. The morphology of CdS nanoarchitecture is strongly dependent on the reaction conditions such as the ratio of thiourea/CdSO4, concentration of CPC, and hydrothermal time. A growth mechanism of dendritic CdS nanoarchitectures is proposed by capturing the shape evolution based on SEM observation, and the detailed formation procedures are as follows: (a) formation of CdS nanoparticles; (b) CdS nanoparticles form larger aggregates via hydrogen-bond interaction; (c) formation of nanopetal by H-bonding effects; (d) formation of the dendritic CdS nanoarchitectures by Ostwald Ripening. Furthermore, the photocatalytic activity experiment illustrated that as-synthesized dendritic CdS nanoarchitectures exhibited an excellent photocatalytic performance to decolorize methyl orange aqueous solution under the visible-light illumination.
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