- Volumes 84-95 (2024)
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Volumes 72-83 (2023)
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Volume 83
Pages 1-258 (December 2023)
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Volume 82
Pages 1-204 (November 2023)
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Volume 81
Pages 1-188 (October 2023)
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Volume 80
Pages 1-202 (September 2023)
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Volume 79
Pages 1-172 (August 2023)
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Volume 78
Pages 1-146 (July 2023)
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Volume 77
Pages 1-152 (June 2023)
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Volume 76
Pages 1-176 (May 2023)
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Volume 75
Pages 1-228 (April 2023)
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Volume 74
Pages 1-200 (March 2023)
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Volume 73
Pages 1-138 (February 2023)
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Volume 72
Pages 1-144 (January 2023)
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Volume 83
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Volumes 60-71 (2022)
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Volume 71
Pages 1-108 (December 2022)
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Volume 70
Pages 1-106 (November 2022)
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Volume 69
Pages 1-122 (October 2022)
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Volume 68
Pages 1-124 (September 2022)
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Volume 67
Pages 1-102 (August 2022)
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Volume 66
Pages 1-112 (July 2022)
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Volume 65
Pages 1-138 (June 2022)
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Volume 64
Pages 1-186 (May 2022)
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Volume 63
Pages 1-124 (April 2022)
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Volume 62
Pages 1-104 (March 2022)
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Volume 61
Pages 1-120 (February 2022)
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Volume 60
Pages 1-124 (January 2022)
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Volume 71
- Volumes 54-59 (2021)
- Volumes 48-53 (2020)
- Volumes 42-47 (2019)
- Volumes 36-41 (2018)
- Volumes 30-35 (2017)
- Volumes 24-29 (2016)
- Volumes 18-23 (2015)
- Volumes 12-17 (2014)
- Volume 11 (2013)
- Volume 10 (2012)
- Volume 9 (2011)
- Volume 8 (2010)
- Volume 7 (2009)
- Volume 6 (2008)
- Volume 5 (2007)
- Volume 4 (2006)
- Volume 3 (2005)
- Volume 2 (2004)
- Volume 1 (2003)
• CdS multipods were synthesized by using Cd xanthate as single precursor in EDA.
• A synergistic effect between temperature and concentration determined the growth of CdS pods.
• EDA and xanthate ligands acted as co-capping agents in the growth of CdS multipods.
CdS nanocrystals of various shapes were synthesized by using cadmium ethyldithiocarbonatio (xanthate) as a single precursor under solvothermal condition. The reaction temperature, cadmium concentration, and solvents determine the CdS morphology. Multipodal CdS structures of different fractions of all particles were obtained at temperatures ranging from 100 to 180 °C with the corresponding precursor concentrations in ethylenediamine (EDA) solution. This approach is different from that reported in the literature, where EDA is regarded as a solvent favorable to the formation of CdS nanorods instead of pods. Uniform CdS multipods were prepared at 160 °C with 1.0 g of cadmium xanthate. The formation of CdS multipods in EDA solution may be attributed to a synergistic effect between the reaction temperature and Cd concentration, i.e., thermodynamically and kinetically controlled growth of the CdS wurtzite (WZ) and zinc blende (ZB) phases, as confirmed by the structural characterization of the component CdS crystals. EDA and xanthate ligands act as co-assisted capping agents in the growth of CdS multipods. When using N,N-dimethylformamide (DMF) and ethylene glycol (EG) as solvents, the CdS appears as triangular particles and flower-like microspheres assembled by polyhedrons, respectively.