Multipulse electrochemical/chemical synthesis of CdS/S core/shell nanocrystals exhibiting ultranarrow photoluminescence emission lines

被引:31
作者
Gorer, S
Penner, RM [1 ]
机构
[1] Univ Calif Irvine, Inst Surface & Interface Sci, Irvine, CA 92679 USA
[2] Univ Calif Irvine, Dept Chem, Irvine, CA 92679 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1999年 / 103卷 / 28期
关键词
D O I
10.1021/jp991141u
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
Ensembles of sulfur capped, cadmium sulfide nanocrystals (CdS/S NCs) which exhibit photoluminescence (PL) emission line widths of 15-35 meV at 20 K have been obtained. These CdS/S NCs were synthesized using a new variant of the electrochemical/chemical (E/C) method: Cadmium (Cd-o) NCs were first electrodeposited from an aqueous Cd2+ plating solution using a train of 8-10 ms plating pulses separated by approximate to 1.0 s "mixing" segments at the open circuit potential. These Cd-o nanoparticles were then oxidized to Cd(OH)(2), and CdS/S NCs were obtained by exposure of Cd(OH)(2) nanoparticles to H2S at 300 degrees C. Ensembles of 200 000-400 000 CdS/S NCs prepared using this "multipulse" technique exhibited PL emission lines narrower than 35 meV. CdS/S NCs were also synthesized using the same E/C method except that a single Cd-o plating pulse was employed, and these CdS/S NCs exhibited PL emission line widths of 125-180 meV. TEM analysis of Cd(OH)(2) precursor particles confirms that the narrower lines obtained using multipulse Cd-o electrodeposition result from improved size monodispersity of the CdS core, which is attributed to the diffusional decoupling of Cd-o nanoparticles during growth.
引用
收藏
页码:5750 / 5753
页数:4
相关论文
共 21 条
  • [1] Alivisatos AP, 1998, ADV MATER, V10, P1297
  • [2] Semiconductor clusters, nanocrystals, and quantum dots
    Alivisatos, AP
    [J]. SCIENCE, 1996, 271 (5251) : 933 - 937
  • [3] A hybrid electrochemical/chemical synthesis of supported, luminescent cadmium sulfide nanocrystals
    Anderson, MA
    Gorer, S
    Penner, RM
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (31): : 5895 - 5899
  • [4] THE QUANTUM-MECHANICS OF LARGER SEMICONDUCTOR CLUSTERS (QUANTUM DOTS)
    BAWENDI, MG
    STEIGERWALD, ML
    BRUS, LE
    [J]. ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 : 477 - 496
  • [5] PHOTOLUMINESCENCE OF SINGLE SEMICONDUCTOR NANOCRYSTALLITES BY 2-PHOTON EXCITATION MICROSCOPY
    BLANTON, SA
    DEHESTANI, A
    LIN, PC
    GUYOTSIONNEST, P
    [J]. CHEMICAL PHYSICS LETTERS, 1994, 229 (03) : 317 - 322
  • [6] Chemical approaches to semiconductor nanocrystals
    Brus, L
    [J]. JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1998, 59 (04) : 459 - 465
  • [7] FRANSAER J, 1999, UNPUB J PHYS CHEM B
  • [8] Size-selective and epitaxial electrochemical/chemical synthesis of sulfur-passivated cadmium sulfide nanocrystals on graphite
    Gorer, S
    Ganske, JA
    Hemminger, JC
    Penner, RM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (37) : 9584 - 9593
  • [9] A hybrid electrochemical/chemical synthesis of semiconductor nanocrystals on graphite: a new role for electrodeposition in materials synthesis
    Gorer, S
    Hsiao, GS
    Anderson, MG
    Stiger, RM
    Lee, J
    Penner, RM
    [J]. ELECTROCHIMICA ACTA, 1998, 43 (19-20) : 2799 - 2809
  • [10] Hybrid electrochemical/chemical synthesis of supported, luminescent semiconductor nanocrystallites with size selectivity: Copper(I)iodide
    Hsiao, GS
    Anderson, MG
    Gorer, S
    Harris, D
    Penner, RM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (06) : 1439 - 1448