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Stepan Demchyshyn

Publications and source records attributed to Stepan Demchyshyn.

2 recordsLinked to original sources

CsCl seed layer homogenizes co-evaporated perovskite growth for high-efficiency fully textured perovskite-silicon tandem solar cells

Monolithic perovskite-silicon tandem solar cells experienced a significant increase in efficiency, making them viable for industrial applications. Among the various scalable and industry-compatible metal halide perovskite deposition techniques, co-evaporation stands out as particularly well-suited for perovskite-silicon tandem solar cells due to its ability to conformally cover textured silicon bottom cells. Solution-processed [2-(3,6-Dimethoxy-9H-carbazol-9-yl)ethyl]phosphonic acid (MeO-2PACz) is commonly used as a hole-transporting material for co-evaporated metal halide perovskites. However, we show that it covers the textured surface of silicon bottom cells unevenly, impacting the film growth and leading to the formation of residual PbI2 at the buried interface. The present study reveals via X-ray photoemission electron microscopy (XPEEM) and infrared scattering-type scanning near-field optical microscope (IR s-SNOM) that a CsCl seed layer fosters organic precursor incorporation across the MeO-2PACz/perovskite interface, even in the areas with a thin MeO-2PACz layer, thereby preventing the formation of interfacial PbI2 and leading to larger apparent grains. The improvement of the metal halide perovskite film quality on the MeO-2PACz/perovskite interface and the bulk perovskite film led to 30.3% (29.7% certified) efficient perovskite-silicon tandem solar cell. The present work highlights the importance of a seed layer for a robust growth of co-evaporated metal halide perovskite and represents an important milestone for the transfer of perovskite-silicon tandem solar cells from laboratory to industry.

cond-mat.mtrl-sci

Confining Metal-Halide Perovskites in Nanoporous Thin Films

Controlling size and shape of semiconducting nanocrystals advances nanoelectronics and photonics. Quantum confined, inexpensive, solution derived metal halide perovskites offer narrow band, color-pure emitters as integral parts of next-generation displays and optoelectronic devices. We use nanoporous silicon and alumina thin films as templates for the growth of perovskite nanocrystallites directly within device-relevant architectures without the use of colloidal stabilization. We find significantly blue shifted photoluminescence emission by reducing the pore size; normally infrared-emitting materials become visibly red, green-emitting materials cyan and blue. Confining perovskite nanocrystals within porous oxide thin films drastically increases photoluminescence stability as the templates auspiciously serve as encapsulation. We quantify the template-induced size of the perovskite crystals in nanoporous silicon with microfocus high-energy X-ray depth profiling in transmission geometry, verifying the growth of perovskite nanocrystals throughout the entire thickness of the nanoporous films. Low-voltage electroluminescent diodes with narrow, blue-shifted emission fabricated from nanocrystalline perovskites grown in embedded nanoporous alumina thin films substantiate our general concept for next generation photonic devices.

cond-mat.mtrl-sci