Perovskite solar cell

Summary

A perovskite solar cell (PSC) is a type of solar cell that includes a perovskite-structured compound, most commonly a hybrid organic–inorganic lead or tin halide-based material as the light-harvesting active layer. Perovskite materials, such as methylammonium lead halides and all-inorganic cesium lead halide, are cheap to produce and simple to manufacture. Solar-cell efficiencies of laboratory-scale devices using these materials have increased from 3.8% in 2009 to 25.7% in 2021 in single-junction architectures, and, in silicon-based tandem cells, to 29.8%, exceeding the maximum efficiency achieved in single-junction silicon solar cells. Perovskite solar cells have therefore been the fastest-advancing solar technology . With the potential of achieving even higher efficiencies and very low production costs, perovskite solar cells have become commercially attractive. Core problems and research subjects

Official source

https://en.wikipedia.org/wiki/Perovskite_solar_cell

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Cooperative effects of Dopant-Free Hole-Transporting materials and polycarbonate film for sustainable perovskite solar cells

Jianxing Xia

Dopant-free hole-transporting materials (HTMs) and interface modification are two effective approaches for developing sustainable perovskite solar cells (PSCs). In this work, dopant-free HTM (GW-4) containing an N- ethyl-carbazole with two rotatable vinyl linkages is first synthesized by a green chemical method without any metal catalysts. The GW-4 cost is only 22.43% of the price of commercial 2,2'7,7'-tetrakis[N,N-di(4-methox-yphenyl)amino]-9,9 & PRIME;-spirobifluorene (spiro-OMeTAD). In the device fabrication, the concentrations of doped GW-4 (20 mg mL(-1)) and pristine GW-4 solutions (10 mg mL(-1)) are much lower than that of spiro-OMeTAD solution (doped, 72.3 mg mL-1). The power conversion efficiency (PCE) of doped GW-4-based cell is 20.45%, superior to that of spiro-OMeTAD-based cell (19.59%). As the optimal concentration of dopant-free GW-4 is insufficient to completely cover the perovskite layer, a polycarbonate (PC) polymer with carbonyl groups is first introduced to modulate perovskite grain boundaries and improve film-forming property of pristine GW-4. The cell with PC/pristine GW-4 has a slightly higher PCE (17.92%) than the cell with pristine GW-4 (17.66%). Regarding humid stability, after 455 h, the doped GW-4 and spiro-OMeTAD based PSCs retain only 11.71% and 2.27% of the initial efficiency, respectively. In striking contrast, after 850 h, the pristine GW-4 and PC/pristine GW-4 based devices retain 69.74% and 97.53% of the initial efficiency, respectively. This study provides both a new molecular design strategy to develop highly efficient dopant-free HTMs and an ingenious interfacial contrivance to overcome the defects of incomplete coverage of HTM film on perovskite layer and understand the charge dynamics at interfacial layers.

ELSEVIER SCIENCE SA2022

A Porphyrin-Involved Benzene-1,3,5-Tricarboxamide Dendrimer (Por-BTA) as a Multifunctional Interface Material for Efficient and Stable Perovskite Solar Cells

Yi Zhang, Bing Zhang, Peng Zhao

Surface defects of perovskite films are the major sources of nonradiative recombination which limit the efficiency and stability of perovskite solar cells. Surface passivation represents one of the most efficient strategies to solve this problem. Herein, for the first time we designed a porphyrin-involved benzene-1,3,5-tricarboxamide dendrimer (Por-BTA) as a multifunctional interface material between the interface of the perovskite and the hole-transporting layer (spiro-OMeTAD) for the surface passivation of perovskite films. The results suggested that Por-BTA not only efficiently passivated the perovskite surface defects via the coordination of the exposed Pb2+ with the carbonyl unit and basic sites of pyrrole units in Por-BTA but also improved the interface contact and the charge transfer between the perovskite and spiro-OMeTAD ascribed to the strong intermolecular p-p stacking of Por-BTA. It was shown that the PSC devices with the Por-BTA treatment exhibited improved power conversion efficiency with the champion of 22.30% achieved (21.30% for the control devices), which is mainly attributed to the increased short-circuit current density and fill factor. Interestingly, the stability of moisture for the Por-BTA-treated device was also enhanced compared to those without the Por-BTA treatment. This work presents a promising direction toward the design of multifunctional organic molecules as the interface materials to improve the cell performance of PSCs.

AMER CHEMICAL SOC2021