Metastable Cu(I)-Niobate Semiconductor with a Low-Temperature, Nanoparticle-Mediated Synthesis

被引:40
作者
Choi, Jonglak [1 ]
King, Nacole [1 ]
Maggard, Paul A. [1 ]
机构
[1] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
基金
美国国家科学基金会;
关键词
nanoscale synthesis; solar energy; metastability; copper niobate; lithium niobate; LITHIUM-NIOBATE; NIOBIUM OXIDE; CU5TA11O30; CUNBO3; ENERGY;
D O I
10.1021/nn305707f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A nanoparticle synthetic strategy for the preparation of a new metastable Cu(I)-niobate Is described, and that involves multipored Li3NbO4 nanoparticles as a precursor. A hydrothermal reaction of HNbO3 and LiOH center dot H2O In PEG200 and water at similar to 180 degrees C yields similar to 15-40 nm Li3NbO4 particles. These particles are subsequently used in a solvothermal copper(I)-exchange reaction with excess CuCl at 150 degrees C. Heating these products within the used CuCl flux (mp = 430 degrees C) to 450 degrees C for 30 mm yields similar to 4-12 nm Cu2Nb8O21 crystalline nanoparticles, and for a heating time of 24 h yields mu m-sized, rod-shaped crystals. The new structure was characterized by single-crystal X-ray diffraction to have a condensed network consisting of NbO7 polyhedra and chains of elongated CuO4 tetrahedra. The compound thermally decomposes starting at similar to 250 degrees C and higher temperatures, depending on the particle sizes, owing to the loss of the weakly coordinated Cu(I) cations from the structure and a concurrent disproportionation reaction at its surfaces. Thus, conventional solid-state reactions involving higher temperatures and bulk reagents have proven unsatisfactory for its synthesis. The measured bandgap size Is similar to 1.43-1.65 eV (indirect) and shows a dependence on the particle sizes. Electronic structure calculations based on density functional theory show that the bandgap transition results from the excitation of electrons at the band edges between filled Cu(I) 3d(10)-orbitals and empty Nb(V) 4d(0)-orbitals, respectively. The p-type nature of the Cu2Nb8O21 particles was confirmed in photoelectrochemical measurements on polycrystalline films that show a strong photocathodic current under visible-light irradiation in aqueous solutions. These results demonstrate the general utility of reactive nanoscale precursors in the synthetic discovery of new Cu(I)-based semiconducting oxides and which also show promise for use in solar energy conversion applications.
引用
收藏
页码:1699 / 1708
页数:10
相关论文
共 42 条
  • [1] Archer M.D., 2008, NANOSTRUCTURED PHOTO
  • [2] Effects of Particle Surface Areas and Microstructures on Photocatalytic H2 and O2 Production over PbTiO3
    Arney, David
    Watkins, Tylan
    Maggard, Paul A.
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2011, 94 (05) : 1483 - 1489
  • [3] Flux synthesis of AgNbO3: Effect of particle surfaces and sizes on photocatalytic activity
    Arney, David
    Hardy, Christopher
    Greve, Benjamin
    Maggard, Paul A.
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2010, 214 (01) : 54 - 60
  • [4] BOND-VALENCE PARAMETERS OBTAINED FROM A SYSTEMATIC ANALYSIS OF THE INORGANIC CRYSTAL-STRUCTURE DATABASE
    BROWN, ID
    ALTERMATT, D
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1985, 41 (AUG): : 244 - 247
  • [5] *BRUK NON, 2004, SAINT VERS 7 07B
  • [6] Bruker-Nonius, 2004, SADABS VERSION 2 10
  • [7] Channu VSR, 2010, INT J ELECTROCHEM SC, V5, P1355
  • [8] First principles methods using CASTEP
    Clark, SJ
    Segall, MD
    Pickard, CJ
    Hasnip, PJ
    Probert, MJ
    Refson, K
    Payne, MC
    [J]. ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 2005, 220 (5-6): : 567 - 570
  • [9] SYNTHESIS, STRUCTURE AND MAGNETIC-PROPERTIES OF MONOCLINIC CUNB2O6 AND THE ELECTRONIC-SPECTRA OF BOTH POLYMORPHS OF CUNB2O6
    DREW, MGB
    HOBSON, RJ
    PADAYATCHY, VT
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 1995, 5 (11) : 1779 - 1783
  • [10] Preparation and Photoelectrochemical Properties of p-type Cu5Ta11O30 and Cu3Ta7O19 Semiconducting Polycrystalline Films
    Fuoco, Lindsay
    Joshi, Upendra A.
    Maggard, Paul A.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (19) : 10490 - 10497