Single Ensemble Non-exponential Photoluminescent Population Decays from a Broadband White-Light-Emitting Perovskite.
Journal of the American Chemical Society
The mechanism of white-light emission from layered Pb-X (X = Cl or Br) perovskites following UV excitation has generated considerable interest. Prior time-dependent studies indicated that the broadband photoluminescence (PL) from (110) perovskites arises from a distribution of self-trapped excitonic sites emitting in different regions of the visible spectrum with different decay dynamics. Here, using time-correlated single photon counting to study single crystals, we show that the white-light emission decay from the (110) perovskite (EDBE)PbBr4 (EDBE = 2,2'-(ethylenedioxy)bis(ethylammonium)) behaves as a single ensemble. Following the rapid decay (0.6 ns) of a small spectral side band, the broad emission line shape is constant to 100 ns. We propose that rapid local structural fluctuations cause the self-trapped excitons (STEs) to experience a wide range of energies, resulting in the very broad PL. The STEs sample fluctuating local environments on time scales fast compared to the PL, which averages the PL decay at all emission wavelengths, yielding single ensemble PL dynamics. Although emission occurs from a very wide, inhomogeneously broadened spectral line with time-averaged single ensemble luminescence dynamics, the decay is tri-exponential. Two heuristic models for the tri-exponential decay involving defects are discussed. Spin-coated films show faster non-exponential decays with the slowest component of the crystal PL absent. Like the crystals, the film PL decays as a single ensemble. These results demonstrate that the broadband emission decay of (EDBE)PbBr4 arises from a time-averaged single ensemble and not from a set of excited states emitting with distinct luminescence decays at different wavelengths.
View details for DOI 10.1021/jacs.0c05636
View details for PubMedID 32909430
Understanding and controlling white-light emission from halide perovskites
AMER CHEMICAL SOC. 2019
View details for Web of Science ID 000525061503723
Tuning the bandgap of Cs2AgBiBr6 through dilute tin alloying.
2019; 10 (45): 10620–28
The promise of lead halide hybrid perovskites for optoelectronic applications makes finding less-toxic alternatives a priority. The double perovskite Cs2AgBiBr6 (1) represents one such alternative, offering long carrier lifetimes and greater stability under ambient conditions. However, the large and indirect 1.95 eV bandgap hinders its potential as a solar absorber. Here we report that alloying crystals of 1 with up to 1 atom% Sn results in a bandgap reduction of up to ca. 0.5 eV while maintaining low toxicity. Crystals can be alloyed with up to 1 atom% Sn and the predominant substitution pathway appears to be a ∼2 : 1 substitution of Sn2+ and Sn4+ for Ag+ and Bi3+, respectively, with Ag+ vacancies providing charge compensation. Spincoated films of 1 accommodate a higher Sn loading, up to 4 atom% Sn, where we see mostly Sn2+ substitution for both Ag+ and Bi3+. Density functional theory (DFT) calculations ascribe the bandgap redshift to the introduction of Sn impurity bands below the conduction band minimum of the host lattice. Using optical absorption spectroscopy, photothermal deflection spectroscopy, X-ray absorption spectroscopy, 119Sn NMR, redox titration, single-crystal and powder X-ray diffraction, multiple elemental analysis and imaging techniques, and DFT calculations, we provide a detailed analysis of the Sn content and oxidation state, dominant substitution sites, and charge-compensating defects in Sn-alloyed Cs2AgBiBr6 (1:Sn) crystals and films. An understanding of heterovalent alloying in halide double perovskites opens the door to a wider breadth of potential alloying agents for manipulating their band structures in a predictable manner.
View details for DOI 10.1039/c9sc02581b
View details for PubMedID 32110348
View details for PubMedCentralID PMC7020786
Dynamically Disordered Lattice in a Layered Pb-I-SCN Perovskite Thin Film Probed by Two-Dimensional Infrared Spectroscopy.
Journal of the American Chemical Society
The dynamically flexible lattices in lead halide perovskites may play important roles in extending carrier recombination lifetime in 3D perovskite solar-cell absorbers and in exciton self-trapping in 2D perovskite white-light phosphors. Two-dimensional infrared (2D IR) spectroscopy was applied to study a recently reported Pb-I-SCN layered perovskite. The Pb-I-SCN perovskite was spin-coated on a SiO2 surface as a thin film, with a thickness of 100 nm, where the S12CN- anions were isotopically diluted with the ratio of S12CN:S13CN = 5:95 to avoid vibrational coupling and excitation transfer between adjacent SCN- anions. The 12CN stretch mode of the minor S12CN- component was the principal vibrational probe that reported on the structural evolution through 2D IR spectroscopy. Spectral diffusion was observed with a time constant of 4.1 ± 0.3 ps. Spectral diffusion arises from small structural changes that result in sampling of frequencies within the distribution of frequencies comprising the inhomogeneously broadened infrared absorption band. These transitions among discrete local structures are distinct from oscillatory phonon motions of the lattice. To accurately evaluate the structural dynamics through measurement of spectral diffusion, the vibrational coupling between adjacent SCN- anions had to be carefully treated. Although the inorganic layers of typical 2D perovskites are structurally isolated from each other, the 2D IR data demonstrated that the layers of the Pb-I-SCN perovskite are vibrationally coupled. When both S12CN- and S13CN- were pumped simultaneously, cross-peaks between S12CN and S13CN vibrations and an oscillating 2D band shape of the S12CN- vibration were observed. Both observables demonstrate vibrational coupling between the closest SCN- anions, which reside in different inorganic layers. The thin films and the isotopic dilution produced exceedingly small vibrational echo signal fields; measurements were made possible using the near-Brewster's angle reflection pump-probe geometry.
View details for PubMedID 30024160