A unique family of II−VI based nanostructured inorganic−organic hybrid semiconductors exhibit nearly zero uniaxial thermal expansion in the temperature range of 95−295 K. Both their optoelectronic and thermal expansion properties are systematically tunable. The diamine molecules show a strong negative thermal expansion effect, and the extent of such an effect increases as the length of the organic molecules increases.
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Li et al. (2007) studied this question.
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