MAPbBr_(3)(MA=CH_(3)NH_(3)^(+))doping with bismuth increases electric conductivity,charge carrier density and photostability,reduces toxicity,and expands light absorption.However,Bi doping shortens excited-state lifet...MAPbBr_(3)(MA=CH_(3)NH_(3)^(+))doping with bismuth increases electric conductivity,charge carrier density and photostability,reduces toxicity,and expands light absorption.However,Bi doping shortens excited-state lifetimes due to formation of DY−charge recombination centers.Using nonadiabatic molecular dynamics and time-domain density functional theory,we demonstrate that the DY−center forms a deep,highly localized hole trap,which accelerates nonradiative relaxation ten-fold and is responsible for 90%of carrier losses.Hole trapping occurs by coupling between the valence band and the trap state,facilitated by the Br atoms surrounding the Bi dopant.Passivation of the DY−center with chlorines heals the local geometry distortion,eliminates the trap state,and makes the carrier lifetimes longer than even in pristine MAPbBr_(3).The decreased charge recombination arises from reduced nonadiabatic coupling and shortened coherence time,due to diminished electron–hole overlap around the passivated defect.Our study demonstrates accelerated nonradiative recombination in Bi-doped MAPbBr_(3),suggests a strategy for defect passivation and reduction of nonradiative energy losses,and provides atomistic insights into unusual defect properties of metal halide perovskites needed for rational design of high-performance perovskite solar cells and optoelectronic devices.展开更多
基金the Beijing Science Foundation(No.2212031)the National Natural Science Foundation of China(Nos.51861135101,21973006,21573022,21688102 and 21590801)R.L.acknowledges the Recruitment Program of Global Youth Experts of China and the Beijing Normal University Startup.O.V.P.acknowledges funding from the U.S.Department of Energy(No.DE SC0014429).
文摘MAPbBr_(3)(MA=CH_(3)NH_(3)^(+))doping with bismuth increases electric conductivity,charge carrier density and photostability,reduces toxicity,and expands light absorption.However,Bi doping shortens excited-state lifetimes due to formation of DY−charge recombination centers.Using nonadiabatic molecular dynamics and time-domain density functional theory,we demonstrate that the DY−center forms a deep,highly localized hole trap,which accelerates nonradiative relaxation ten-fold and is responsible for 90%of carrier losses.Hole trapping occurs by coupling between the valence band and the trap state,facilitated by the Br atoms surrounding the Bi dopant.Passivation of the DY−center with chlorines heals the local geometry distortion,eliminates the trap state,and makes the carrier lifetimes longer than even in pristine MAPbBr_(3).The decreased charge recombination arises from reduced nonadiabatic coupling and shortened coherence time,due to diminished electron–hole overlap around the passivated defect.Our study demonstrates accelerated nonradiative recombination in Bi-doped MAPbBr_(3),suggests a strategy for defect passivation and reduction of nonradiative energy losses,and provides atomistic insights into unusual defect properties of metal halide perovskites needed for rational design of high-performance perovskite solar cells and optoelectronic devices.
