Tributylphosphine-assisted greener synthesis of ultrasmall PbS quantum dots and their high performance in luminescent solar concentrator application.

As compared to the great effort made on improving the power conversion efficiency of quantum dot (QD) solar cells, investigations on relevant stability, regarded as another crucial factor for their widespread implementation, are still limited. In this perspective, we discuss the stability of QD solar cells from different aspects, all highly relying on the surface chemistry of QDs. Specifically, three types of stabilities, closely relevant to the realization of the actual application of QD solar cells, are presented: (i) air-processability, which allows QDs to be processed in air with high batch-to-batch reproducibility; (ii) long-term stability of QD solar cells, directly related to their performance degradation in the long run; and (iii) QD ink stability that is concerned with the storage lifetime of QDs in solution and is compatible with low-cost solution processing techniques. Both air processability and excellent QD ink stability are critical for achieving the desired low-cost, large-scale roll-to-toll manufacturing of solar cells.

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Semiconductor nanocrystals that show plasmonic resonance represent an emerging class of highly promising plasmonic materials with potential applications in diverse fields, such as sensing and optical and optoelectronic devices. We report a new approach to synthesizing homogeneous covellite CuS nanoplatelets in air and the almost complete disappearance of their plasmonic resonance once coupled with multiwalled carbon nanotubes (MWCNTs). These nanoplatelets were rapidly synthesized by a simple microwave-assisted approach at a relatively low reaction temperature in air, instead of under N2 as reported previously. These less severe synthesis conditions were enabled by appropriately selecting a Cu precursor and preparing a precursor sulfur solution (instead of using solid sulfur) and by using microwave radiation as the heat source. The advantages of utilizing microwave irradiation, including uniform and rapid heating, became clear after comparing the results of the synthesis with those achieved using a conventional oil-bath method under N2. The CuS nanoplatelets prepared in this way showed very strong plasmon resonance at c. 1160 nm as a result of their free charge carriers at the calculated density of nh = 1.5 × 10(22) cm(-3) based on the Drude model. With the aim of exploring their potential for near-infrared responsive optoelectronic devices, they were hybridized with functionalized MWCNTs. Their strong plasmon resonance almost completely disappeared on hybridization. Detailed investigations excluded the effect of possible structural changes in the CuS nanoplatelets during the hybridization process and a possible effect on the plasmon resonance arising from the chemical bonding of surface ligands. Charge transfer was considered to be the main reason for the almost complete disappearance of the plasmon resonance, which was further confirmed by terahertz (THz) time-domain spectrometry and THz time-resolved spectrometry measurements performed on the CuS-MWCNT nanohybrids. By extracting the rising and relaxation constants through fitting a single-exponential rising function and a bi-exponential relaxation function, in combination with the results of THz differential transmission as a function of the NIR pump fluence, it was found that hole injection changed the electronic properties of the MWCNTs only subtly on a short picosecond time scale, whereas the nature of the band structure of the MWCNTs remained largely unchanged. These findings aid our understanding of recently emerging semiconductor plasmonics and will also help in developing practical applications.

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Stretching-induced orientation of both silver nanorice and silver nanocarrots dispersed in or deposited on the surface of poly(vinyl alcohol) (PVA) films was investigated using polarized UV-visible-near-infrared (NIR) spectroscopy and atomic force microscopy (AFM). The results show that the film stretching not only aligns the long axis of individual nanorice or nanocarrots preferentially along the stretching direction, but also induces assembly of these nanostructures into oriented arrays of random lengths in the deformation process. Consequently, the longitudinal surface plasmon resonance peaked at 820 nm for nanorice and 1050 nm for nanocarrots before stretching can be replaced by continuous extinction over the entire 800-1800 nm NIR spectral range after stretching. Stretched PVA films containing either silver nanorice or nanocarrots thus display polarization-dependent transmission of NIR light.

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