Perovskite‐based solar cells (PSCs) are some of the most promising devices for capturing photovoltaic energy. Efficiency has increased from single digits to a certified 25.7%, an unprecedented improvement for any solar cell technology. Incorporating carbon materials into perovskite solar cells promises to be revolutionary in the solar cell field by increasing stability, decreasing manufacturing costs, and making them attractive for commercialization. Here, an overview of the advances in carbon‐based perovskite solar cells (C–PSCs) that incorporate different carbon materials as back contact on different device architectures is presented. An overview of PSC architectures and high‐ and low‐temperature C–PSCs is provided. Additionally, recent advances in the main carbon materials applied in the field, such as graphene, carbon nanotubes, carbon dots, and biocarbon, are presented. Finally, a summary of carbon materials applied to C–PSCs is provided.
The present work evaluated the effect on charge transfer in functionalized TiO 2 nanostructured systems using different binders. We highlight the conditions required to form self-assembled systems by varying the number of layers, as well as by substituting them for an organic binder, cysteine. Additionally, we study the pH effect of the precursor solution (HAuCl 4 ) on gold nanoparticles (AuNPs) formation. The morphological characterization allowed us to determine the percentage of Au atoms on the surface of the synthesized nanoparticles. Inductively coupled plasma mass spectrometry (ICP-MS) analysis determined the amount of gold deposited on the TiO 2 surface, which ranged from 4.56 to 253.00 ng mm -2 depending on the system used. Based on Fourier-transform infrared spectroscopy (FTIR) and Raman analysis, it was possible to propose a photolysis mechanism for AuNP formation in accordance with the change in the binders. The different systems were subjected to hydrogen photogeneration by a water splitting process, resulting in 2.02 μmol cm -2 of hydrogen production for cysteine binder [Cys+HAuCl 4 -2.7]. There proved to be an excellent synergy between the morphological aspects, crystallinity, and stability of this arrangement.
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