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      Recent studies on small molecular and polymeric hole‐transporting materials for high‐performance perovskite solar cells

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          Abstract

          A decade of significant research has led to the emergence of photovoltaic solar cells based on perovskites that have achieved an exceptionally high‐power conversion efficiency of 26.08%. A key breakthrough in perovskite solar cells (PSCs) occurred when solid hole‐transporting materials (HTMs) replaced liquid electrolytes in dye‐sensitized solar cells (DSSCs), because HTMs play a crucial role in improving photovoltaic performance as well as cell stability. This review is mainly focused on the HTMs that are responsible for hole transport and extraction in PSCs, which is one of the crucial components for efficient devices. Here, we have reviewed small molecular as well as polymeric HTMs that have been reported in the last two years and discussed their performance based on the analysis of their molecular architectures. Finally, we include a perspective on the molecular engineering of new functional HTMs for highly efficient stable PSCs.

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          Organometal halide perovskites as visible-light sensitizers for photovoltaic cells.

          Two organolead halide perovskite nanocrystals, CH(3)NH(3)PbBr(3) and CH(3)NH(3)PbI(3), were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells. When self-assembled on mesoporous TiO(2) films, the nanocrystalline perovskites exhibit strong band-gap absorptions as semiconductors. The CH(3)NH(3)PbI(3)-based photocell with spectral sensitivity of up to 800 nm yielded a solar energy conversion efficiency of 3.8%. The CH(3)NH(3)PbBr(3)-based cell showed a high photovoltage of 0.96 V with an external quantum conversion efficiency of 65%.
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            Efficient hybrid solar cells based on meso-superstructured organometal halide perovskites.

            The energy costs associated with separating tightly bound excitons (photoinduced electron-hole pairs) and extracting free charges from highly disordered low-mobility networks represent fundamental losses for many low-cost photovoltaic technologies. We report a low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight. This "meso-superstructured solar cell" exhibits exceptionally few fundamental energy losses; it can generate open-circuit photovoltages of more than 1.1 volts, despite the relatively narrow absorber band gap of 1.55 electron volts. The functionality arises from the use of mesoporous alumina as an inert scaffold that structures the absorber and forces electrons to reside in and be transported through the perovskite.
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              Is Open Access

              Lead Iodide Perovskite Sensitized All-Solid-State Submicron Thin Film Mesoscopic Solar Cell with Efficiency Exceeding 9%

              We report on solid-state mesoscopic heterojunction solar cells employing nanoparticles (NPs) of methyl ammonium lead iodide (CH3NH3)PbI3 as light harvesters. The perovskite NPs were produced by reaction of methylammonium iodide with PbI2 and deposited onto a submicron-thick mesoscopic TiO2 film, whose pores were infiltrated with the hole-conductor spiro-MeOTAD. Illumination with standard AM-1.5 sunlight generated large photocurrents (JSC) exceeding 17 mA/cm2, an open circuit photovoltage (VOC) of 0.888 V and a fill factor (FF) of 0.62 yielding a power conversion efficiency (PCE) of 9.7%, the highest reported to date for such cells. Femto second laser studies combined with photo-induced absorption measurements showed charge separation to proceed via hole injection from the excited (CH3NH3)PbI3 NPs into the spiro-MeOTAD followed by electron transfer to the mesoscopic TiO2 film. The use of a solid hole conductor dramatically improved the device stability compared to (CH3NH3)PbI3 -sensitized liquid junction cells.
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                Author and article information

                Journal
                Journal of the Chinese Chemical Society
                J Chinese Chemical Soc
                Wiley
                0009-4536
                2192-6549
                December 2023
                October 28 2023
                December 2023
                : 70
                : 12
                : 2046-2063
                Affiliations
                [1 ] Department of Chemistry, and Research Center of New Generation Light Driven Photovoltaic Modules, National Central University Taoyuan Taiwan
                [2 ] Department of Materials Science and Engineering National Taiwan University Taipei Taiwan
                [3 ] Department of Chemistry PSG College of Arts and Science Coimbatore India
                Article
                10.1002/jccs.202300326
                4ae2a8e4-5c17-462a-8a80-b7d84fac8ce8
                © 2023

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