Dr Junke Wang

Abstract:

Vacuum-based deposition is a scalable, solvent-free industrial method ideal for uniform coatings on complex substrates. However, all vacuum-deposited perovskite solar cells fabricated by thermal evaporation trail solution-processed counterparts in efficiency and stability due to film quality challenges, necessitating advancement and improved understanding. Here, we report a co-evaporation route for 1.67-eV wide-bandgap perovskites by introducing a PbCl2 co-source to optimize film quality. We promote perovskite formation with pronounced (100) “face-up” orientation and deliver a certified all vacuum-deposited solar cell with 18.35% efficiency (19.3% in the lab) for 0.25-cm2 devices (18.5% for 1-cm2 cells). These cells retain 80% of peak efficiency after 1,080 hours under the ISOS-L-2 protocol. Leveraging operando hyperspectral imaging, we provide spatiotemporal spectral insight into halide segregation and trap-mediated recombination, correlating microscopic luminescence features with macroscopic device performance while distinguishing radiative from non-ideal recombination channels. We further demonstrate 27.2%-efficient 1-cm2 evaporated perovskite-on-silicon tandems and outdoor stability of all vacuum-deposited tandems in Italy, retaining ~80% initial performance after 8 months.

Abstract:

Raw data for 'Homogenized optoelectronic properties in perovskites: achieving high-efficiency solar cells with common chloride additives'

Abstract:

Perovskite inks play critical roles in determining film quality and device performance, and ink stability is desired to ensure high device reproducibility. Here, we reveal the instability issue of current cesium-formamidinium lead triiodide (CsxFA1-xPbI3) inks whose aggregation and precipitation tendencies are induced by excessively strong solvent-lead-halide coordination. By modulating coordination strength between precursor salts and solvents, we identify solvent coordination-dispersion equilibrium as the governing factor for ink stability and develop a stable ink that exhibits a remarkable increase in the shelf life. It effectively tunes ink drying and film crystallization, resulting in blade-coated perovskite films with excellent uniformity and low defect density. This enhancement led to increased aperture efficiency of ambient-fabricated p-i-n perovskite modules to 23.5%. The resultant devices also exhibit high durability, and 99% of the initial PCE was retained after 1700 hours of maximum power point tracking following the ISOS-L-2 standard protocol.

Abstract:

Additive engineering is among the most commonly used strategies to enhance the performance and stability of perovskite solar cells. Prior research often focused on optimizing device performance by using additives in the perovskite precursor solution to influence the rate of crystallization and film formation, but a fundamental understanding of the effect of additives on the stoichiometry of the absorber remains elusive. In this study, we reveal how additives affect the ABX3 stoichiometry of the perovskite absorber and its photovoltaic properties. We find that the solar cell performance of a wide-bandgap (1.77 eV) Cs0.2FA0.8Pb-(I0.6Br0.4)3 perovskite decreases when processed with either of two common additives, lead thiocyanate and lead chloride, because the additive disturbs the stoichiometry. Interestingly, the addition of excess formamidinium iodide (FAI) to the precursor solution can restore the initial ABX3 stoichiometry and fully recover the device performance. The excess of FAI that is required depends on whether the halide or pseudohalide additive is incorporated into the crystal lattice. Finally, we alter the stoichiometry of an additive-free perovskite absorber by inducing either an excess or a deficiency of FAI or lead iodide in the precursor and show that slight deviations from the ideal stoichiometry rapidly degrade the device performance. This work provides fundamental insights into the importance of bulk stoichiometry in perovskite absorbers and can serve as a basis for future rational additive engineering.

Abstract:

Improved understanding of heterojunction interfaces has enabled multijunction photovoltaic devices to achieve power conversion efficiencies that exceed the detailed-balance limit for single-junctions. For wide-bandgap perovskites, however, the pronounced energy loss across the heterojunctions of the active and charge transport layers impedes multijunction devices from reaching their full efficiency potential. Here we find that for polycrystalline perovskite films with mixed-halide compositions, the crystal termination—a factor influencing the reactivity and density of surface sites—plays a crucial role in interfacial passivation for wide-bandgap perovskites. We demonstrate that by templating the growth of polycrystalline perovskite films toward a preferred (100) facet, we can reduce the density of deep-level trap states and enhance the binding of modification ligands. This leads to a much-improved heterojunction interface, resulting in open-circuit voltages of 1.38 V for 1.77-eV single-junction perovskite solar cells. In addition, monolithic all-perovskite double-junction solar cells achieve open-circuit voltage values of up to 2.22 V, with maximum power point tracking efficiencies reaching 28.6% and 27.7% at 0.25 and 1.0 cm2 cell areas, respectively, along with improved operational and thermal stability at 85 °C. This work provides universally applicable insights into the crystalline facet-favourable surface modification of perovskite films, advancing their performance in optoelectronic applications.