| The rise of perovskite solar cells(PSCs)provides a new solution for mankind to achieve more efficient use of solar energy.Although the power conversion efficiency(PCE)of organic-inorganic hybrid perovskite solar cells keeps hitting new highs,its instability under high light intensity and high heat restricts its application and development.In this context,the inorganic perovskite material CsPbX3(X=Cl,Br,I)with better light and thermal stability has received extensive attention.At present,the fabrication of PSCs based on spin coating technique has been fully researched.However,the research based on vacuum evaporation technology,which is more widely used in industrial production,is far from enough.In this paper,based on the sequential evaporation technique and two-step sintering method,we optimize the critical process parameters and perovskite light absorbing layer,thus improving the performance of thermally evaporated CsPbX3 PSCs and fabricating functional PSCs for specific application scenarios.In general,the main results are listed as following:1.We fabricated CsPbBr3 perovskite films through sequential evaporation technique and two-step sintering method.By optimizing the parameters of evaporation and sintering process,the crystallinity and morphology of perovskite films were significantly enhanced,and the resistance of charge transmission between layers was reduced.Finally,an all-inorganic PSC based on the FTO/SnO2/CsPbBr3/Carbon structure achieved an efficiency of 9.41%and an open circuit voltage(Voc)of 1.467 V.In addition,the unencapsulated device retained 95%of its initial efficiency after aging at 100℃ for 90 days,which shows excellent thermal stability.To further reduce the trap density of thermally evaporated CsPbBr3perovskite films and the open-circuit voltage loss of CsPbBr3 PSCs,we incorporated Ba I2 additive into CsPbBr3 perovskite based on sequential evaporation technique.It is found that Ba2+ions can enter the CsPbBr3 perovskite lattice,while I-ions induced iodine vacancies during the annealing process,both leading to the passivation of CsPbBr3 perovskite defects and the modification of Fermi level.By adjusting the thickness of Ba I2 additive,we improved the efficiency of the all-inorganic perovskite solar cell based on the FTO/SnO2/CsPbBr3/Carbon structure to 10.09%and the Vocto 1.551 V.In addition,the unencapsulated device retained 93%of its initial efficiency after aging at 100℃ for 90 days.2.By optimizing the process parameters of thermal evaporation,we successfully obtained CsPbBr3 perovskite film with excellent performance,and then we explored the application of CsPbBr3 perovskite in semitransparent solar cells.We selected Spiro-OMeTAD as the hole transport material,and compared the transmittance,photovoltaic properties and stability of the semitransparent CsPbBr3 perovskite with MoO3/Au/MoO3 and ITO as transparent electrodes,respectively.3.In order to improve the phase stability of CsPbI2Br,we explored the effects of Ba2+doping,replacement of a hydrophobic hole transport layer,and secondary annealing after phase transformation on the phase stability and device performance of PSCs. |