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Lars Korte

Publications and source records attributed to Lars Korte.

4 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

Monitoring charge separation of individual cells in perovskite/silicon tandems via transient surface photovoltage spectroscopy

Identification of charge carrier separation processes in perovskite/silicon tandem solar cells and recombination at buried interfaces of charge selective contacts is crucial for photovoltaic research. Here, intensity- and wavelength- dependent transient surface photovoltage (tr-SPV) is used to investigate slot-die-coated perovskite top layers deposited on n-type Heterojunction Silicon bottom cells. We show that using an appropriate combination of photon energy and/or bottom cell polarity, one can individually probe the buried interfaces of the bottom silicon cell or the perovskite`s buried interfaces of a tandem solar cell: For excitation with higher energy photons, time delays before the onset of a strong SPV signal indicate significant hole minority drift before separation in the silicon bottom cells. Furthermore, symmetric bottom Si heterojunction solar cell stacks can serve to investigate the top perovskite stack including its junction to the bottom cell, unhampered by photovoltages from the silicon substrate. Thus, investigation of the buried interfaces in tandem devices using time-resolved surface photovoltage is found to yield valuable information on charge carrier extraction at buried interfaces and demonstrates its unique potential compared to more conventional approaches that rely on photoluminescence decay kinetics.

cond-mat.mtrl-sci

Transient Analysis during Maximum Power Point Tracking (TrAMPPT) to Assess Dynamic Response of Perovskite Solar Cells

Determination of the device performance parameters of perovskite solar cells is far from trivial as transient effects may cause large discrepancies in current-voltage measurements as a function of scan rate and pre-conditioning. Maximum power point tracking, MPPT, enables to determine the steady-state maximum power conversion efficiency. However, the MPPT does not provide any information on the device performance parameters, which are reliable only if extracted from current-voltage curves collected under steady-state conditions. We show that is possible to determine the shorter settling or delay time suitable to carry out J-V measurements under steady-state conditions by analysis of the transient device response around the MPP. This procedure proves to be more time-efficient than measurement J-V measurements at a variety of scan rates. Furthermore, the generic algorithm presented here can be implemented to assess changes in the dynamic response of devices during long-term device ageing.

physics.app-ph

Exploring co-sputtering of ZnO:Al and SiO2 for efficient electron-selective contacts on silicon solar cells

In recent years, considerable efforts have been devoted to developing novel electron-selective materials for crystalline Si (c-Si) solar cells with the attempts to simplify the fabrication process and improve efficiency. In this study, ZnO:Al (AZO) is co-sputtered with SiO2 to form AZO:SiO2 films with different SiO2 content. These nanometer-scale films, deposited on top of thin intrinsic hydrogenated amorphous silicon films and capped with low-work-function metal (such as Al and Mg), are demonstrated to function effectively as electron-selective contacts in c-Si solar cells. On the one hand, AZO:SiO2 plays an important role in such electron-selective contact and its thickness is a critical parameter, thickness of 2 nm showing the best. On the other hand, at the optimal thickness of AZO:SiO2, the open circuit voltage (VOC) of the solar cells is found to be relatively insensitive to either the work function or the band gap of AZO:SiO2. Whereas, regarding the fill factor (FF), AZO without SiO2 content exhibits to be the optimal choice. By using AZO/Al as electron-selective contact, we successfully realize a 19.5%-efficient solar cell with VOC over 700 mV and FF around 75%, which is the best result among c-Si solar cells using ZnO as electron-selective contact. Also, this work implies that efficient carrier-selective film can be made by magnetron sputtering method.

physics.app-ph