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Metal halide perovskites are considered as game changers for future solar cell technology due to their rapidly increasing device efficiencies and potential for manufacturing at low cost. In view of their promising commercial potential, increasing research efforts are now dedicated to the development of large‐area perovskite solar modules. Herein, the motivation for developing perovskite solar modules and the challenges to fabricate large‐area perovskite solar cells with high efficiency are discussed. The important thin‐film processing methods including solution‐based and vacuum‐based deposition technologies for scaling up the fabrication of perovskites are reviewed. In addition, other key challenges that need to be overcome to bring perovskite solar modules into photovoltaic (PV) markets are also discussed, including module stability, potential lead leakage issue, and outdoor field testing of the perovskite modules. Finally, opinions on the future development of perovskite PV modules are shared. [ABSTRACT FROM AUTHOR]

Energy production of perovskite‐based photovoltaic (PV) technology can be increased not only by improving device efficiency of perovskite solar cells (PVSCs) but also by innovative concepts such as bifacial and tandem configurations which require low‐damage and highly transparent top electrodes. Herein, an amorphous CdO‐In2O3 alloy film with high transparency and low resistivity and its application in a bifacial PVSC and a perovskite/Si 4T tandem solar cell are reported. Due to the high optical transmittance, the CdO‐In2O3‐based PVSC shows a high bifaciality factor of 84.0%, and the CdO‐In2O3‐based perovskite/Si 4T tandem solar cell achieves a champion power conversion efficiency of 25.12%, much higher than the indium tin oxide based tandem cell. Finally, a yearly energy yield calculation and levelized cost of energy (LCOE) analysis for these PV technologies (together with Si single‐junction solar cells as a reference) in Singapore, Australia, and Germany are conducted. The results demonstrate the potential of CdO‐In2O3‐based perovskite PV technologies, yet more efforts are still required to further reduce the manufacturing cost to achieve competitive LCOE values in countries with relatively low PV installation cost. [ABSTRACT FROM AUTHOR]

The lattice defects in the bulk and on the surface of the halide perovskite layer serve as trap sites and recombination centers to annihilate photogenerated carriers, determining the performance and stability of perovskite optoelectronic devices. Herein, the previously reported surface defects passivation engineering is extended to a full defects passivation strategy through stereoscopically introducing the cysteamine hydrochloride (CSA‐Cl) in the bulk and on the surface of perovskites. First‐principle density functional theory (DFT) calculations are employed to theoretically verify the multiple defects passivation effect of the CAS‐Cl on the perovskite. The perovskite layer with full defects passivation exhibits superior carrier dynamics as revealed by femtosecond transient absorption due to the reduced defect density determined by a highly sensitive photothermal deflection spectroscopy technique. Consequently, a high efficiency approaching 21% is achieved for the inverted planar perovskite solar cells (PVSCs). More importantly, the CAS‐Cl passivated PVSCs exhibit operation in air, which will be beneficial for the in situ device test for understanding the photophysics involved. This work provides a promising strategy to reduce the defects in both the perovskite bulk and surface for superior optoelectronic properties, facilitating the development of highly efficient and stable PVSCs and other optoelectronic devices. [ABSTRACT FROM AUTHOR]

Non-wetting hole transport materials (HTMs) have great potential in facilitating large-sized perovskite crystal growth and enhancing device stability by opposing moisture ingress, However, the severe non-wetting issue limits the wide application of these materials in low-temperature solution-processed inverted planar perovskite solar cells (PVSCs), and corresponding devices are rarely reported. Here, a facile ultraviolet-ozone (UVO) modification method is demonstrated to overcome this issue. By carefully controlling the UVO modification time, the surface wettability of poly-TPD can be tuned without affecting the bulk properties of the film, hence perovskite films with desired grain size and excellent coverage can be deposited via a one-step spin-coating method. Benefiting from the high-quality perovskite, well-matched energy level alignment and hydrophobic property of poly-TPD, the resulting PVSCs show a champion power conversion efficiency of 18.19% with significantly enhanced stability as compared to the PEDOT:PSS counterparts. Moreover, the UVO modification approach also demonstrates its validity when being extended to other hydrophobic HTMs. This work not only provides a general strategy to broaden the selection pool of HTMs for solution-processed inverted planar PVSCs, but also may triggers the exploration of more advanced strategies to make non-wetting HTMs applicable in solution-processed inverted planar PVSCs. [ABSTRACT FROM AUTHOR]

[Display omitted] The power conversion efficiency for single-junction solar cells is limited by the Shockley-Quiesser limit. An effective approach to realize high efficiency is to develop multi-junction cells. These years have witnessed the rapid development of organic–inorganic perovskite solar cells. The excellent optoelectronic properties and tunable bandgaps of perovskite materials make them potential candidates for developing tandem solar cells, by combining with silicon, Cu(In,Ga)Se 2 and organic solar cells. In this review, we present the recent progress of perovskite-based tandem solar cells, including perovskite/silicon, perovskite/perovskite, perovskite/Cu(In,Ga)Se 2 , and perovskite/organic cells. Finally, the challenges and opportunities for perovskite-based tandem solar cells are discussed. [ABSTRACT FROM AUTHOR]