Defects within the grain boundaries (GBs) of halide perovskite films make fabrication of efficient and stable perovskite solar cells (PSCs) highly challenging. Here, a low-cost tetra-ammonium zinc phthalocyanine (ZnPc) was used to post-treat the MAPbI (MA = CHNH) film. Two-dimensional (ZnPc)MA PbI was successfully constructed within the GBs of MAPbI film achieving a GBs suture for passivating the defects in GBs. Time-resolved photoluminescence showed that the modification increased the decay time from 44 to 57 ns indicating the passivation of GBs reduces trap-assisted recombination. The PSCs with modified perovskite exhibited increased photovoltage, and the best efficiency was improved up to 20.3%. More importantly, the long-term stability of the responding PSCs against humidity and heating was further improved unprecedentedly. Moreover, the modified MAPbI films revealed a self-repairing capability under mild heating. This work provided a novel insight into ongoing fabrication of efficient and stable PSCs by the efficient GBs suture with low-cost phthalocyanine.

Rapid, sensitive, and selective quantitative detection of pyridine dicarboxylic acid (DPA) as biomarker of anthrax spores is in great demand since anthrax spores are highly lethal to human beings and animals and also potential biological warfare agents. Herein, we prepared a ratiometric fluorescence lanthanide functionalized micelle nanoprobe by "one-pot" self-assembly, with an amphiphilic ligand containing β-diketone derivative which can "immobilize" terbium ions through the coordination interaction and a fluorophore as fluorescence reference (FR). The detection strategy was ascribed to Tb ions in lanthanide functionalized micelle, which can be sensitized to emit the intrinsic luminescence upon addition of DPA due to the presence of energy transfer when DPA chromophore coordinated with Tb ion. The fluorescence intensity of FR remained essentially constant, leading to ratiometric fluorescence response toward DPA. The results demonstrate that the terbium functionalized micelle was able to sensitively detect DPA with a linear relation in the range of 0 μM to 7.0 μM in aqueous solution, which also showed remarkable selectivity to DPA over other aromatic ligands. Our work paves a new way in the design of ratiometric fluorescence lanthanide functionalized micelle nanoprobes which can be promising for selective and sensitive detection of bacterial spores or biomolecules.

The formation of defects at surfaces and grain boundaries (GBs) during the fabrication of solution‐processed perovskite film are thought to be responsible for its instability. Herein, Eu‐porphyrin complex (Eu‐pyP) is directly doped into methylammonium lead triiodide (MAPbI 3 ) precursor, perfectly fabricating 2D (Eu‐pyP) 0.5 MA n ‐1 Pb n I 3 n +1 platelets inlaying the GBs of 3D polycrystalline interstices in this protocol. The device based on Eu‐pyP doped perovskite film possesses a champion efficiency of 18.2%. More importantly, the doped perovskite solar cells device shows beyond 85% retention of its pristine efficiency value, whereas the pure MAPbI 3 device has a rapid drop in efficiency down to 10% within 100 h under 45% humidity at 85 °C in AM 1.5 G. The above acquired perovskite films reveal an unpredictable thermodynamic self‐healing ability. Consequently, the findings provide an avenue for defect passivation to synchronously improve resistibility to moisture, heat, and solar light including UV.

CeO x has been widely used in optoelectronic devices due to its special electronic and optical structure. Herein, CeO x was directly doped into ZnO to successfully construct a ZnO/CeO x electron transport material (ETM) used in perovskite solar cells (PSCs). The incorporation of CeO x can regulate the chemical compatibility between ZnO and perovskite, unmatched energy levels, and poor UV stability, further enhancing the cell performance and stability of PSCs. As expected, the best efficiency of fabricated CH3NH3PbI3-PSCs based on ZnO/CeO x as the ETM was up to 19.5%. In contrast, the efficiency of PSCs with pure ZnO was 16.0%. Moreover, compared with PSCs based on ZnO, ZnO/CeO x -based PSCs exhibited significantly enhanced moisture, and thermal and UV stability. These results point to the introduction of rare-earth oxides, which could accelerate the industrialization of PSCs.

The challenges in transparent photovoltaic (TPV) fields are still that the device transparency and efficiency are difficult to be balanced to meet the requirements of practical applications. In this study, we systematically investigated the interrelationship between photovoltaic film properties, optical transmission, and photovoltaic performances in the near-infrared harvesting organic TPVs. The results indicate that the photovoltaic film thickness determines the TPV’s transparency and meanwhile affects the device efficiency; by contrast, the donor–acceptor ratio only affects device efficiency and has little effect on transparency. By controlling the film thickness and donor–acceptor ratio, the average visible transmission (AVT) of TPVs can be precisely managed in the range of 40% - 85%, and the device efficiency can achieve as high as 4.06% and 2.38% while the AVT exceeds 70% and 80%, respectively. Importantly, the large area (~10 cm2) TPV modules and ultra-flexible devices were then successfully prepared based on the systematical study.