Understanding the atomic structure and structural instability of organic-inorganic hybrid perovskites is the key to appreciate their remarkable photoelectric properties and understand failure mechanism. Here, using low-dose imaging technique by direct-detection electron-counting camera in a transmission electron microscope, we investigate the atomic structure and decomposition pathway of CH3NH3PbI3 (MAPbI3) at the atomic scale. We successfully image the atomic structure of perovskite in real space under ultra-low electron dose condition, and observe a two-step decomposition process, i.e., initial loss of MA+ followed by the collapse of perovskite structure into 6H-PbI2 with their critical threshold doses also determined. Interestingly, an intermediate phase (MA0.5PbI3) with locally ordered vacancies can robustly exist before perovskite collapses, enlightening strategies for prevention and recovery of perovskite structure during the degradation. Associated with the structure evolution, the bandgap gradually increases from ~1.6 eV to ~2.1 eV. In addition, it is found that C-N bonds can be readily destroyed under irradiation, releasing NH3 and HI and leaving hydrocarbons. These findings enhance our understanding of the photoelectric properties and failure mechanism of MAPbI3, providing potential strategies into material optimization.
Joule heating is featured with an extremely high rising rate of temperature with hundreds of kelvin per second, which has shown superiorities of high efficiency and energy conservation in graphene fabrication. Herein, we design a dynamic joule heating system for continuous synthesis of graphene fibers with ultrashort high‐temperature (≈2000 °C), treating time (≈20 min), and low electric energy consumption (≈2000 kJ m−1). During the joule heating fabrication, the current flowing through the fibers can manipulate the configuration of graphene sheets, the basic component units of fiber, and induce their alignment. Theoretical simulations reveal that graphene sheets tend to rotate towards the current direction under the current induced electric field for the highest stability with the lowest electric free energy and zero rotation torque. Therefore, the electrical and mechanical performances of as‐fabricated graphene fibers can be further improved in comparison with thermally annealed graphene fibers without applying current.
The gradual depletion of global fossil energy and environmental pollution make the development of hydrogen energy imminent. Two-dimensional g-C3N4 (CN) based heterostructures have attracted considerable research interest in photocatalytic H2...
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