Morphological control of hydrothermal Ni(OH)2 in the presence of polymers and surfactants:: Nanocrystals, mesocrystals, and superstructures

被引:33
作者
Buscaglia, Maria Teresa [1 ]
Buscaglia, Vincenzo [1 ,2 ]
Bottino, Carlo [1 ]
Viviani, Massimo [1 ,2 ]
Fournier, Roxane [3 ]
Sennour, Mohamed [4 ]
Presto, Sabrina [5 ]
Marazza, Rinaldo [2 ,5 ]
Nanni, Paolo [1 ,2 ,6 ]
机构
[1] CNR, Inst Energet & Interphases, I-16149 Genoa, Italy
[2] Italian Interuniv Consortium Mat Sci & Technol IN, I-50121 Florence, Italy
[3] Univ Bourgogne, ESIREM, F-21078 Dijon, France
[4] Ecole Mines Paris, Ctr Mat, F-91000 Evry, France
[5] Univ Genoa, Dept Chem & Ind Chem, I-16146 Genoa, Italy
[6] Univ Genoa, Dept Proc & Chem Engn, I-16149 Genoa, Italy
关键词
D O I
10.1021/cg800555x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymers with different hydrophilic groups [polyvinylpyrrolidone (PVP), ammonium polyacrylate (APA), and hydroxypropylmethyl cellulose (HPMC)] and surfactants [cetyltrimethylammonium bromide (CTAB) and sodium dodecylbenzensulfonate (SDBS)] were used as additives to modify the crystallization of beta-Ni(OH)(2) in hydrothermal conditions. Marked morphological changes in the beta-Ni(OH)(2) particles were observed depending on the additive concentration and on the duration of the hydrothermal treatment. The final morphology is the result of a complex, time-dependent self-assembly and growth process. Well-defined particles with sizes from submicrometer range to a few micrometers corresponding to hexagonal lamellae, hexagonal tabular mesocrystals, rosette- and flowerlike aggregates of lamellae, hexagonal prismatic mesocrystals, and acicular nanocrystals were easily obtained after a short time (2-24 h) aging at 150-200 degrees C. With PVP and CTAB, there is evidence of a growth process dominated by self-assembly of nanocrystals to produce mesocrystals. The formation of spherical superstructures (with SDBS, up to 70 mu m in diameter) and hollow spheres (with PVP) is observed at long times (>24 h) as a result of solvent-mediated recrystallization processes, like Ostwald ripening. The overall results show that hydrothermal synthesis of beta-Ni(OH)(2) in the presence of polymers with hydrophilic groups and surfactants is a versatile tool for crystal morphogenesis.
引用
收藏
页码:3847 / 3855
页数:9
相关论文
共 60 条
[1]  
Busch S, 1999, EUR J INORG CHEM, P1643
[2]   Ni(OH)2 tubes with mesoscale dimensions as positive-electrode materials of alkaline rechargeable batteries [J].
Cai, FS ;
Zhang, GY ;
Chen, J ;
Gou, XL ;
Liu, HK ;
Dou, SX .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (32) :4212-4216
[3]   Self-assembled nickel hydroxide three-dimensional nanostructures: A nanomaterial for alkaline rechargeable batteries [J].
Cao, Minhua ;
He, Xiaoyan ;
Chen, Jun ;
Hu, Changwen .
CRYSTAL GROWTH & DESIGN, 2007, 7 (01) :170-174
[4]   A new and facile route to ultrafine nanowires, superthin flakes and uniform nanodisks of nickel hydroxide [J].
Chen, DL ;
Gao, L .
CHEMICAL PHYSICS LETTERS, 2005, 405 (1-3) :159-164
[5]   Polymer-directed formation of unusual CaCO3 pancakes with controlled surface structures [J].
Chen, SF ;
Yu, SH ;
Wang, TX ;
Jiang, J ;
Cölfen, H ;
Hu, B ;
Yu, B .
ADVANCED MATERIALS, 2005, 17 (12) :1461-1465
[6]   Controlled synthesis of hierarchically porous β-Ni(OH)2 microspheres and NiO nanoparticles with the optical property of NiO nanoparticles [J].
Chen, Xiangying ;
Zhang, Zhongjie ;
Shi, Chengwu ;
Li, Xueliang .
MATERIALS LETTERS, 2008, 62 (03) :346-351
[7]   Self-construction of core-shell and hollow zeolite analcime icositetrahedra: A reversed crystal growth process via oriented aggregation of nanocrystallites and recrystallization from surface to core [J].
Chen, Xueying ;
Qiao, Minghua ;
Xie, Songhai ;
Fan, Kangnian ;
Zhou, Wuzong ;
He, Heyong .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (43) :13305-13312
[8]   Higher-order organization by mesoscale self-assembly and transformation of hybrid nanostructures [J].
Cölfen, H ;
Mann, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (21) :2350-2365
[9]   Mesocrystals:: Inorganic superstructures made by highly parallel crystallization and controlled alignment [J].
Cölfen, H ;
Antonietti, M .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (35) :5576-5591
[10]  
Cölfen H, 2001, CHEM-EUR J, V7, P106