Nian Cheng

Low-temperature plasma-enhanced atomic layer deposition of tin oxide electron selective layers for highly efficient planar perovskite solar cells

Recent progress has shown that low-temperature processed tin oxide (SnO2) is an excellent electron selective layer (ESL) material for fabricating highly efficient organic–inorganic metal-halide perovskite solar cells with a planar cell structure. Low-temperature processing and a planar cell structure are desirable characteristics for large-scale device manufacturing due to their associated low costs and processing simplicity. Here, we report that plasma-enhanced atomic layer deposition (PEALD) is able to lower the deposition temperature of SnO2 ESLs to below 100 °C and still achieve high device performance. With C60-self-assembled monolayer passivation, our PEALD SnO2 ESLs deposited at ∼100 °C led to average power conversion efficiencies higher than 18% (maximum of 19.03%) and 15% (maximum of 16.80%) under reverse voltage scan for solar cells fabricated on glass and flexible polymer substrates, respectively. Our results thus demonstrate the potential of the low-temperature PEALD process of SnO2 ESLs for large-scale manufacturing of efficient perovskite solar cells.

One-pot stirring-free synthesis of silver nanowires with tunable lengths and diameters via a Fe3+ & Cl− co-mediated polyol method and their application as transparent conductive films

The properties of nanomaterials are highly dependent on their size, shape and composition. Compared with zero-dimensional nanoparticles, the increased dimension of a one-dimensional silver nanowire (AgNW/Ag NW) leads to extra challenges on synthesizing it with controllable sizes. Here, a convenient way for the synthesis of AgNWs with tunable sizes has been developed simply by adjusting the amount of salt additives, i.e., ferric chloride (FeCl3), or Fe(NO3)3 & KCl. The average diameter and length of nanowires are readily tailored within 45-220 nm and 10-230 μm, respectively. The distinctive roles of Fe3+ and Cl- played during the growth stages of Ag NWs were revealed by comparative experiments and a heterogeneous nucleation model with the assistance of oxidative etching was proposed to elucidate the growth mechanism. Afterwards, transformations in XRD patterns from nanometer-size effects and quantitative relation for size-dependent peak wavelength of surface plasmon resonances (SPRs) in UV-vis spectroscopy of these nanowires were studied. In addition, as transparent conductive materials (TCMs), these metal nanowires were utilized to fabricate transparent conductive films (TCFs), and the effects of their diameters and lengths were elucidated. Very/ultra-long nanowires with a high aspect ratio up to 1600 achieved impressive properties of R = 12.4 ohm sq-1 at T% = 90.1% without any post treatment. This facile method for the size-tunable growth of uniform AgNWs with high yield is attractive and ready to be home-made, which is believed to promote research in their potential applications, especially in optoelectronic devices and flexible electronics.

Self-amplified piezoelectric nanogenerator with enhanced output performance: The synergistic effect of micropatterned polymer film and interweaved silver nanowires

A piezoelectric nanogenerator with self-amplified output is prepared with a polydimethylsiloxane (PDMS)/silver nanowire (Ag NW)/poly(vinylidene fluoride-trifluoroethylene) sandwich structure. The Ag NWs facilitate the collection of induced charge generated by the piezoelectric film, and the micro-patterned PDMS films multiply the devices sensitivity under external compression. The nanogenerator exhibits good performance, with a peak open circuit voltage of 1.2 V, and a peak short circuit current of 82 nA. These findings highlight the potential of the nanogenerator in self-powered devices and wearable energy harvesters.