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null (Ed.)In addition to ocean acidification, a significant recent warming trend in Chinese coastal waters has received much attention. However, studies of the combined effects of warming and acidification on natural coastal phytoplankton assemblages here are scarce. We conducted a continuous incubation experiment with a natural spring phytoplankton assemblage collected from the Bohai Sea near Tianjin. Experimental treatments used a full factorial combination of temperature (7 and 11°C) and pCO 2 (400 and 800 ppm) treatments. Results suggest that changes in pCO 2 and temperature had both individual and interactive effects on phytoplankton species composition and elemental stoichiometry. Warming mainly favored the accumulation of picoplankton and dinoflagellate biomass. Increased pCO 2 significantly increased particulate organic carbon to particulate organic phosphorus (C:P) and particulate organic carbon to biogenic silica (C:BSi) ratios, and decreased total diatom abundance; in the meanwhile, higher pCO 2 significantly increased the ratio of centric to pennate diatom abundance. Warming and increased pCO 2 both greatly decreased the proportion of diatoms to dinoflagellates. The highest chlorophyll a biomass was observed in the high pCO 2 , high temperature phytoplankton assemblage, which also had the slowest sinking rate of all treatments. Overall, there were significant interactive effects of increased pCO 2 and warming on dinoflagellate abundance, pennate diatom abundance, diatom vs. dinoflagellates ratio and the centric vs. pennate ratio. These findings suggest that future ocean acidification and warming trends may individually and cumulatively affect coastal biogeochemistry and carbon fluxes through shifts in phytoplankton species composition and sinking rates.more » « less
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Quasi‐2D perovskites are attractive because of their improved stability compared with 3D perovskites counterparts; however, they suffer from poor performance due to the insulating organic cation spacers. To resolve this issue, a strategy of replacing the insulating spacer with conducting spacer is proposed which successfully converts the spacer from a charge‐transporting “barrier” to charge‐transporting “bridge.” Specifically, an alkyl linker‐free, fully conjugated aromatic 2,2′‐biimidazolium (BIDZ) cation is introduced as a spacer to compose quasi‐2D perovskites. Density functional theory (DFT) simulation results show that the lowest unoccupied molecular orbital (LUMO) level localizes on BIDZ and the highest occupied molecular orbital (HOMO) level is on the perovskite. However, both HOMO and LUMO levels localize on perovskite slabs for the well‐known phenethylammonium (PEA)‐based 2D perovskites. The strong electronic coupling between BIDZ and 3D perovskite slabs improves carrier mobilities even for a low‐weak‐crystallinity and random‐orientated quasi‐2D perovskite film. As a result, a remarkable power conversion efficiency up to 11.4% (
n = 5) is achieved, which is much higher than that of PEA‐based random‐orientated quasi‐2D perovskites with the same processing condition (6.5%). The strategy paves the way to highly efficient and stable quasi‐2D perovskites solar cells through designing new organic spacer cations.