Heterogeneous Wet Chemical Synthesis of Superlattice-Type Hierarchical ZnO Architectures for Concurrent H2 Production and N2 Reduction

被引:95
作者
Janet, C. M. [1 ]
Navaladian, S. [1 ]
Viswanathan, B. [1 ]
Varadarajan, T. K. [1 ]
Viswanath, R. P. [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Natl Ctr Catalysis Res, Madras 600036, Tamil Nadu, India
关键词
ZINC-OXIDE; WATER; NANOPARTICLES; GROWTH; SHAPE; NANOCRYSTALS; PARTICLES; PRECURSOR; NANORODS; NITROGEN;
D O I
10.1021/jp908683x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two wet chemical methods, namely, wet etching (heterogeneous) and chemical precipitation (homogeneous), have been exploited for the formation of hierarchical ZnO architectures without any specific templates, catalysts, or capping agents. As-synthesized ZnO have been extensively characterized by X-ray diffraction, UV-visible absorbance studies, Fourier transform infrared analysis, scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive analysis of X-rays, selected area electron diffraction, photoluminescence (PL), and textural analysis. Wet etching resulted in the formation of self-assembled hexagonal plates with a disordered superlattice-type texture and ultimately ended up in crystallites with high-defect concentration showing a red PL emission. Mechanistic aspects of the growth process in both the methods have been analyzed, and a rational explanation is presented for their observed morphologies. ZnO prepared by both methods have been tested for their photocatalytic water splitting abilities in producing H-2. Crystalline, spectral, textural, and activity analyses have been carried out for commercial ZnO for a comparison. Pt loaded ZnO was used for the concurrent hydrogen generation and dinitrogen fixation yielding a maximum of 86 mu mol of ammonia/(h/0.1 g of catalyst), thus achieving the activation of N-2 at room temperature and atmospheric pressure.
引用
收藏
页码:2622 / 2632
页数:11
相关论文
共 54 条
[1]   Zinc oxalate nanorods: a convenient precursor to uniform nanoparticles of ZnO [J].
Ahmad, T ;
Vaidya, S ;
Sarkar, N ;
Ghosh, S ;
Ganguli, AK .
NANOTECHNOLOGY, 2006, 17 (05) :1236-1240
[2]   PHOTOCATALYTICALLY INDUCED FIXATION OF MOLECULAR NITROGEN BY NEAR UV-RADIATION [J].
BICKLEY, RI ;
VISHWANATHAN, V .
NATURE, 1979, 280 (5720) :306-308
[3]  
Boltz D.F., 1978, COLORIMETRIC DETERMI, P210
[4]   HIGHLY EFFICIENT HETEROGENEOUS PHOTOOXIDATION OF 2-PROPANOL TO ACETONE WITH AMORPHOUS MANGANESE OXIDE CATALYSTS [J].
CAO, H ;
SUIB, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (12) :5334-5342
[5]   Synthesis, structure and ferromagnetic properties of Mn-doped ZnO nanoparticles [J].
Cong, CJ ;
Liao, L ;
Li, JC ;
Fan, LX ;
Zhang, KL .
NANOTECHNOLOGY, 2005, 16 (06) :981-984
[6]   THERMAL-DECOMPOSITION OF MIXED OXALATES .1. THERMOGRAVIMETRIC ANALYSIS OF COPRECIPITATED ZINC-COPPER OXALATES IN NITROGEN [J].
DALVI, BD ;
CHAVAN, AM .
JOURNAL OF THERMAL ANALYSIS, 1978, 14 (03) :331-334
[7]   STABILITY OF ZNO PARTICLES IN AQUEOUS SUSPENSIONS UNDER UV ILLUMINATION [J].
DOMENECH, J ;
PRIETO, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1986, 90 (06) :1123-1126
[8]   The effect of the rate of precursor production on the purity and aggregation morphology of nanoparticulate zinc oxide [J].
Duffy, Grainne M. ;
Pillai, Suresh C. ;
McCormack, Declan E. .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (02) :181-184
[9]  
Fullam S, 2000, ADV MATER, V12, P1430, DOI 10.1002/1521-4095(200010)12:19<1430::AID-ADMA1430>3.0.CO
[10]  
2-8