All inorganic metal halide perovskite shows great application potential in the field of photoelectric devices due to its excellent physical and chemical properties,such as ultra-high quantum yield,high absorption coefficient,large carrier mobility,bipolar carrier transport capacity,high stability and simple synthesis schemes.Considering the balance of light absorption capacity,band gap width and phase stability,mixed halide inorganic perovskite is considered as an ideal photoactive material.Among them,CsPbI2Br has a suitable bandgap width and good stability,making it a photosensitive material for photodetectors.However,the defects in CsPbI2Br perovskite thin films and the low energy level matching between CsPbI2Br and electrodes limit the performance of CsPbI2Br photodetectors.Therefore,optimizing the material preparation scheme and device structure is of great significance for improving the performance of CsPbI2Br perovskite photodetectors.This paper constructs heterostructures of CsPbI2Br thin films with CsPbBr3 quantum dots and Ag2S quantum dots,respectively,to improve the energy level matching between CsPbI2Br and electrodes,reduce non radiative recombination of charge carriers,and thereby enhance the performance of CsPbI2Br perovskite photodetectors.In addition,by adding CsBr and H2O to the precursor solution of CsPbI2Br,the quality of CsPbI2Br thin films is improved,the requirements for environmental conditions during device preparation and testing are reduced,and the photoelectric conversion ability of CsPbI2Br photodetectors is improved.The construction of heterostructures and additive passivation strategies provide solutions for improving the quality of perovskite materials and improving the detection performance of perovskite photodetectors.The main research contents of this paper are as follows:1.A high response perovskite photodetector with CsPbBr3/CsPbI2Br layer heterojunction was prepared by solution method.As a sensitizer,CsPbBr3 can improve the light absorption capacity of the device.Due to the different energy levels of CsPbBr3 and CsPbI2Br,layer heterojunction is formed,so as to construct bipolar carrier transport channel and improve carrier transmission performance.At 405 nm,the CsPbBr3/CsPbI2Br layer heterojunction photodetector showed a high responsivity(R)of 66 A/W,a specific detectivity(D*)of 1.17×1011 Jones,and a rise/fall time of38/81 ms.This work provides a feasible strategy for preparing layer heterojunction perovskite devices.2.The Ag2S/CsPbI2Br bulk heterojunction photodetector is studied.By adding Ag2S quantum dot aqueous solution to CsPbI2Br perovskite precursor,film defects are passivated and the quality of perovskite films is improved.Moreover,the construction of Ag2S/CsPbI2Br bulk heterojunction optimized the energy level arrangement between CsPbI2Br and gold(Au)electrodes,improving the carrier transport ability.This comprehensive strategy improves the performance of perovskite photodetectors.The Ag2S/CsPbI2Br bulk heterojunction photodetector has an ultra-low dark current of 7.74 p A,an ultra-fast response time of 2.95/3.07μs and a high switching ratio of7.67×105.This work provides a method for the preparation of high quality perovskite materials and a strategy for the development of high performance perovskite photodetectors based on bulk heterojunction.3.High performance CsPbI2Br photodetectors enhanced by excess CsBr and a certain amount of H2O are studied.Excess CsBr helps to generate micro-strain in the lattice,thus stabilizing the cubic phase of CsPbI2Br at low temperature.H2O molecules fine-regulate the balance of proton transfer reaction in the precursor solution,manipulate the thermodynamic favorable phase by adjusting the size of perovskite microcrystals,reduce the surface free energy,and passivate the film defects.Excess CsBr and a certain amount of H2O enhanced CsPbI2Br photodetectors have excellent photoelectric detection performance,with R up to 160 A/W,D*is 4.9×1011 Jones,the response time is 5.5/6.8 ms.This work provides experience for passivation strategies of perovskite optoelectronic devices. |