Effect of microgravity on the crystallization of a self-assembling layered material

被引:33
作者
Ahari, H
Bedard, RL
Bowes, CL
Coombs, N
Dag, O
Jiang, T
Ozin, GA
Petrov, S
Sokolov, I
Verma, A
Vovk, G
Young, D
机构
[1] UNIV TORONTO,LASH MILLER CHEM LABS,MAT CHEM RES GRP,TORONTO,ON M5S 3H6,CANADA
[2] UOP,DIV RES,DES PLAINES,IL 60017
[3] IMAGETEK ANALYT IMAGING,TORONTO,ON M6J 2K4,CANADA
关键词
D O I
10.1038/42213
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In microgravity, crystals of semiconductors and proteins can be grown with improved crystallinity, offering the prospect of improved structural analyses (for proteins) and better electronic properties (for semiconductors)(1-3). Here we study the effect of a microgravity environment on the crystallization of a class of materials-layered microporous tin(IV) sulphides(4-11)-whose crystal structure is determined by weak interlayer interactions (electrostatic, hydrogen-bonding and van der Waals) as well as strong intralayer covalent bonds. We find that the crystals grown in microgravity (on board the Space Shuttle Endeavour) show improved crystal habits, smoother faces, greater crystallinity, better optical quality and larger void volumes than the materials grown on Earth. These differences are due at least in part to the profound influence of microgravity on the layer registry over length scales of around a nanometre, which is shown by X-ray and electron diffraction to be better in space than on Earth. Thus we can see a clear distinction between the covalent bonds in these materials, which are not significantly affected by microgravity, and the weaker forces (like those that determine the structure of proteins over length scales of around 0.3-0.4 nm) which are more susceptible to the dynamic disturbances that operate in crystallization on Earth.
引用
收藏
页码:857 / 860
页数:4
相关论文
共 13 条
  • [1] NANOPOROUS TIN(IV) CHALCOGENIDES - FLEXIBLE OPEN-FRAMEWORK NANOMATERIALS FOR CHEMICAL SENSING
    AHARI, H
    BOWES, CL
    JIANG, T
    LOUGH, A
    OZIN, GA
    BEDARD, FL
    PETROV, S
    YOUNG, D
    [J]. ADVANCED MATERIALS, 1995, 7 (04) : 375 - 378
  • [2] *COMM MICR RES, 1992, MICR RES STRAT
  • [3] DAG O, IN PRESS ADV MAT
  • [4] Feuerbacher B., 1986, MAT SCI SPACE
  • [5] Hydrothermal synthesis of microporous tin sulfides studied by real-time in situ energy-dispersive X-ray diffraction
    Francis, RJ
    Price, SJ
    Evans, JSO
    OBrien, S
    OHare, D
    Clark, SM
    [J]. CHEMISTRY OF MATERIALS, 1996, 8 (08) : 2102 - 2108
  • [6] NANOPOROUS TIN(IV) SULFIDES - MODE OF FORMATION
    JIANG, T
    OZIN, GA
    BEDARD, RL
    [J]. ADVANCED MATERIALS, 1994, 6 (11) : 860 - 865
  • [7] SYNTHESIS AND STRUCTURE OF THE NOVEL NANOPOROUS TIN(IV) SULFIDE MATERIAL TPA-SNS-3
    JIANG, T
    LOUGH, AJ
    OZIN, GA
    YOUNG, D
    BEDARD, RL
    [J]. CHEMISTRY OF MATERIALS, 1995, 7 (02) : 245 - 248
  • [8] JIANG T, 1997, THESIS U TORONTO
  • [9] Microporous and mesoporous electronic materials: Flexible open-framework nanomaterials for molecular recognition, towards the electronic nose
    Ozin, GA
    [J]. SUPRAMOLECULAR CHEMISTRY, 1995, 6 (1-2) : 125 - &
  • [10] OZIN GA, 1997, P 9 INT S MOL REC IN