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Recently, perovskite solar cells (PSCs) and organic solar cells (OSCs) have emerged as solution-processable photovoltaic (PV) technologies with certified power conversion efficiencies (PCEs) surpassing 26% and 20%, respectively. However, challenges such as charge generation, separation, transport, collection, and recombination at the nanoscale still exist in fully controlling and understanding the performance-limiting factors in the photoactive layers of OSC and PSC devices. Although several efforts have been reported to address the above phenomena, the origin of the nanoscale defects and how they lead to performance losses have not yet been fully understood. This perspective provides an in-depth discussion of nanoscale spatial and time-resolved mapping for OSCs and PSCs to understand their roles in improving PV performance. A comprehensive multimodal technique to map the charge carrier photodynamics at the nanoscale, such as charge generation, separation, transport, collection, and recombination in OSCs and PSCs, is presented, which has the potential to evaluate the photodynamics related to local heterogeneities in the active layers of the corresponding devices. [ABSTRACT FROM AUTHOR]

Perovskite solar cells (PSCs) have made great strides in recent years, operating inside the theoretical Scholkely–Quisser efficiency limit with a certified power conversion efficiency (PCE) of 26.1%. However, lead toxicity from Pb‐based PSCs can harm the environment. As a result, the search for nontoxic and environmentally friendly substances to replace Pb in perovskites is the need of the hour. Tin has emerged as the most viable choice to replace Pb, due to its favorable electronic properties and smaller bandgaps of Sn‐based perovskites between 1.1 and 1.4 eV, strong charge carrier mobility, and high theoretical efficiency of 32%. Sn vacancies and point defects, on the other hand, are easily produced in Sn perovskites, leading to nonradiative recombination. Furthermore, interfacial flaws and traps impede further performance improvement. In this research, to produce high‐quality Pb‐free perovskites for high‐performance PSCs, a Lewis‐base thioacetamide (TAA) is added to the simple FASnI3 perovskite solution. FASnI3 and TAA additive‐based films effectively control perovskite film crystallinity and grain size via Lewis acid–base reaction. The champion FASnI3 + TAA‐based PSC achieves a maximum PCE of 10.67% while paving a facile way for other compositional perovskite analogues to be integrated into highly efficient and operationally stable PSCs. [ABSTRACT FROM AUTHOR]

The increasing need to control anthropogenic CO 2 emissions and conversion to fuels features the necessity for innovative solutions, one of which is photoelectrochemical system. This approach, capable of yielding gaseous production progressively, is facing challenges for liquid fuels generation due to optical, electrical, and catalytic properties. This study employs a standalone photoelectrochemical setup, in which InGaP/GaAs/Ge photoanode is integrated with tin-modified bismuth oxide cathode to convert CO 2 into liquid formic acid. In unassisted two-electrode assembly, setup exemplifies its operational durability for 100 h, during which it maintains an average Faradaic efficiency of 88% with 17.3 mmol L -1  h -1 of yield, thereby excelling in average solar-to-fuel conversion efficiency at 12% with 60% of electrical energy efficiency under one sun illumination. This significant performance is further associated with metal-semiconductor interface formation between tin and bismuth oxide, which bridges electronic structures and generates an electric field at their interfaces. This study outperforms conventional solar-driven systems in operational durability and liquid fuel production., (© 2024. The Author(s).)