Host-guest chemistry for tuning colloidal solubility, self-organization and photoconductivity of inorganic-capped nanocrystals.
Host-guest chemistry for tuning colloidal solubility, self-organization and photoconductivity of inorganic-capped nanocrystals.
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DOI:
10.1038/ncomms10142
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发表时间:
2015-12-09
影响因子:
16.6
通讯作者:
Kovalenko MV
中科院分区:
文献类型:
--
作者:
Bodnarchuk MI;Yakunin S;Piveteau L;Kovalenko MV
Colloidal inorganic nanocrystals (NCs), functionalized with inorganic capping ligands, such as metal chalcogenide complexes (MCCs), have recently emerged as versatile optoelectronic materials. As-prepared, highly charged MCC-capped NCs are dispersible only in highly polar solvents, and lack the ability to form long-range ordered NC superlattices. Here we report a simple and general methodology, based on host–guest coordination of MCC-capped NCs with macrocyclic ethers (crown ethers and cryptands), enabling the solubilization of inorganic-capped NCs in solvents of any polarity and improving the ability to form NC superlattices. The corona of organic molecules can also serve as a convenient knob for the fine adjustment of charge transport and photoconductivity in films of NCs. In particular, high-infrared-photon detectivities of up to 3.3 × 1011 Jones with a fast response (3 dB cut-off at 3 kHz) at the wavelength of 1,200 nm were obtained with films of PbS/K3AsS4/decyl-18-crown-6 NCs. The high polarity of colloidal inorganic-ligand-functionalized nanocrystals can be problematic for their processing, limiting their optoelectronic applications. Here, by complexation with macrocycles, the authors enabled broad amphiphilicity of such nanocrystals and processing from a variety of solvents.