Multi-Functional Regulation on Buried Interface for Achieving Efficient Triple-Cation Perovskite Solar Cells.

Mixed-cation perovskite solar cells (PSCs) have attracted much attention because of the advantages of suitable bandgap and stability. It is still a challenge to rationally design and modify the perovskite/tin oxide (SnO) heterogeneous interface for achieving highly efficient and stable PSCs. Herein, a strategy of one-stone-for-three-birds is proposed to achieve multi-functional interface regulation via introducing N-Chlorosuccinimide (NCS) into the solution of SnO: i) C═O functional group in NCS can induces strong binding affinity to uncoordinated defects (oxygen vacancies, free lead ions, etc) at the buried interface and passivate them; ii) incomplete in situ hydrolysis reactions can occur spontaneously and adjust the pH value of the SnO solution to achieve a more matchable energy level; iii) effectively releasing the residual stress of the underlying perovskite.

Constructing Additives Synergy Strategy to Doctor-Blade Efficient CH NH PbI Perovskite Solar Cells under a Wide Range of Humidity from 45% to 82.

Perovskite solar cells (PSCs) have emerged as one of the most promising and competitive photovoltaic technologies, and doctor-blading is a facile and robust deposition technique to efficiently fabricate PSCs in large scale, especially matching with roll-to-roll process. Herein, it demonstrates the encouraging results of one-step, antisolvent-free doctor-bladed methylammonium lead iodide (CH NH PbI MAPbI ) PSCs under a wide range of humidity from 45% to 82%. A synergy strategy of ionic-liquid methylammonium acetate (MAAc) and molecular phenylurea additives is developed to modulate the morphology and crystallization process of MAPbI perovskite film, leading to high-quality MAPbI perovskite film with large-size crystal, low defect density, and ultrasmooth surface.

Manipulating the Migration of Iodine Ions via Reverse-Biasing for Boosting Photovoltaic Performance of Perovskite Solar Cells.

Perovskite solar cells (PSCs) are being developed rapidly and exhibit greatly potential commercialization. Herein, it is found that the device performance can be improved by manipulating the migration of iodine ions via reverse-biasing, for example, at -0.4 V for 3 min in dark.

Restricting the Formation of Pb-Pb Dimer via Surface Pb Site Passivation for Enhancing the Light Stability of Perovskite.

Poor light stability hinders the potential applications of perovskite optoelectronic devices. Recent experiments have demonstrated that the passivation surface via forming strong chemical bonds (SO -Pb, PO -Pb, Cl-Pb, O-Pb, and S-Pb) could effectively improve the light stability of perovskite solar cells. However, the underlying reasons are not clear.