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Power conversion efficiency (PCE) and long‐term stability are two vital issues for perovskite solar cells (PSCs). However, there is still a lack of suitable hole transport layers (HTLs) to endow PSCs with both high efficiency and stability. Here, NiOx nanoparticles are promoted as an efficient and 85 °C/85%‐stable inorganic HTL for high‐performance n‐i‐p PSCs, with the introduction of perovskite quantum dots (QDs) between perovskite and NiOx as systematic interfacial engineering. The QD intercalation enhances film morphology and assembly regulation of NiOx HTLs. Due to structure–function correlations, hole mobility within NiOx HTL is improved. And the hole extraction from perovskite to NiOx is also facilitated, resulting from reduced trap states and optimized energy level alignments. Hence, the promoted NiOx‐based n‐i‐p PSCs exhibit high PCE (21.59%) and excellent stability (sustaining 85 °C aging in air without encapsulation). Furthermore, encapsulated solar modules with QDs‐promoted NiOx HTLs show impressive stability during 85 °C/85% aging test for 1000 hours. With high transparency, QDs‐promoted NiOx is also demonstrated to be an advanced HTL for semitransparent PSCs. This work develops promising NiOx inorganic HTL in n‐i‐p PSCs for manufacturing next‐generation photovoltaic devices. [ABSTRACT FROM AUTHOR]

As an inorganic hole transport material (HTM), nickel oxide (NiOx) is widely used in perovskite solar cells (PSCs) due to its low cost and intrinsic stability. However, on account of its poor film formation on perovskite, the low power conversion efficiency (PCE) and stability of regular NiOx‐based PSCs is a main obstacle for commercialization. Here, a solution‐processed inorganic/organic hybrid hole transporting system is developed to resolve this issue, thereby improving the PCE from 16.0% to 21.2%. Poly(3‐hexylthiophene) (P3HT) is studied as the typical case, revealing that the performance improvement mainly lies in the synergistic interaction between NiOx and P3HT: 1) the introduction of P3HT improves assembly regularity and film uniformity of NiOx; 2) electron redistribution between P3HT and NiOx increases the Ni3+/Ni2+ ratio for higher hole mobility; 3) the feed‐back impact of NiOx on P3HT enhances molecular orientation of polymer chains in P3HT for better hole transport through polymer framework. Finally, the encapsulated solar cell modules with P3HT‐promoted NiOx maintains 91% of the initial efficiency after 1000 h aging at a harsh 85 °C/85% relative humidity condition. This finding provides a feasible approach for using NiOx‐based HTMs to realize high‐performance regular PSCs, paving the way for their commercialization. [ABSTRACT FROM AUTHOR]

During the last two decades, large-scale high biomass algal blooms of the dinoflagellate Prorocentrum donghaiense Lu have occurred frequently in the East China Sea (ECS). The role of increasing nutrient concentrations in driving those blooms is well-established, but the source population that initiates them is poorly understood. We hypothesized that the front of Taiwan Warm Current (TWC) may serve as a ‘seed bank’ that initiates P. donghaiense blooms in the ECS, as the physiochemical conditions in the TWC are suitable for the growth of P. donghaiense. In order to test this hypothesis, two surveys at different spatio-temporal scales were conducted in 2010 and 2011. We found a strong correlation in space and time between the abundance of P. donghaiense and the TWC. The spatial extent of the P. donghaiense bloom coincided with the TWC front in both 2010 and 2011. During the early development of the blooms, P. donghaiense concentration was highest at the TWC front, and then the bloom mass shifted inshore over the course of our 2011 survey. The TWC also moved inshore, albeit after the appearance of P. donghaiense. Overall, these results support our hypothesis that P. donghaiense blooms develop from the population at the TWC front in the ECS, suggesting the role of the ocean current front as a seed bank to dinoflagellate blooms. [ABSTRACT FROM AUTHOR]

Metal halide perovskite materials inherently possess imperfections, particularly under nonequilibrium conditions, such as exposure to light or heat. To tackle this challenge, we introduced stearate ligand-capped nickel oxide (NiO x ), a redox-sensitive metal oxide with variable valence, into perovskite intermediate films. The integration of NiO x improved the efficiency and stability of perovskite solar cells (PSCs) by offering multifunctional roles: (1) chemical passivation for ongoing defect repair, (2) energetic passivation to bolster defect tolerance, and (3) field-effect passivation to mitigate charge accumulation. Employing a synergistic approach that tailored these three passivation mechanisms led to a substantial increase in the devices' efficiencies. The target cell (0.12 cm 2 ) and module (18 cm 2 ) exhibited efficiencies of 24.0 and 22.9%, respectively. Notably, the encapsulated modules maintained almost 100 and 87% of the initial efficiencies after operating for 1100 h at the maximum power point (60 °C, 50% RH) and 2000 h of damp-heat testing (85 °C, 85% RH), respectively. Outdoor real-time tests further validated the commercial viability of the NiO x -assisted PSMs. The proposed passivation strategy provides a practical and uncomplicated approach for fabricating high-efficiency and stable photovoltaics.

Power conversion efficiency (PCE) and long-term stability are two vital issues for perovskite solar cells (PSCs). However, there is still a lack of suitable hole transport layers (HTLs) to endow PSCs with both high efficiency and stability. Here, NiO x nanoparticles are promoted as an efficient and 85 °C/85%-stable inorganic HTL for high-performance n-i-p PSCs, with the introduction of perovskite quantum dots (QDs) between perovskite and NiO x as systematic interfacial engineering. The QD intercalation enhances film morphology and assembly regulation of NiO x HTLs . Due to structure-function correlations, hole mobility within NiO x HTL is improved. And the hole extraction from perovskite to NiO x is also facilitated, resulting from reduced trap states and optimized energy level alignments. Hence, the promoted NiO x -based n-i-p PSCs exhibit high PCE (21.59%) and excellent stability (sustaining 85 °C aging in air without encapsulation). Furthermore, encapsulated solar modules with QDs-promoted NiO x HTLs show impressive stability during 85 °C/85% aging test for 1000 hours. With high transparency, QDs-promoted NiO x is also demonstrated to be an advanced HTL for semitransparent PSCs. This work develops promising NiO x inorganic HTL in n-i-p PSCs for manufacturing next-generation photovoltaic devices., (© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.)