Tandem solar cells are widely considered the industry’s next step in photovoltaics because of their excellent power conversion efficiency. Since halide perovskite absorber material was developed, it has been feasible to develop tandem solar cells that are more efficient. The European Solar Test Installation has verified a 32.5% efficiency for perovskite/silicon tandem solar cells. There has been an increase in the perovskite/Si tandem devices’ power conversion efficiency, but it is still not as high as it might be. Their instability and difficulties in large-area realization are significant challenges in commercialization. In the first part of this overview, we set the stage by discussing the background of tandem solar cells and their development over time. Subsequently, a concise summary of recent advancements in perovskite tandem solar cells utilizing various device topologies is presented. In addition, we explore the many possible configurations of tandem module technology: the present work addresses the characteristics and efficacy of 2T monolithic and mechanically stacked four-terminal devices. Next, we explore ways to boost perovskite tandem solar cells’ power conversion efficiencies. Recent advancements in the efficiency of tandem cells are described, along with the limitations that are still restricting their efficiency. Stability is also a significant hurdle in commercializing such devices, so we proposed eliminating ion migration as a cornerstone strategy for solving intrinsic instability problems.

A potential field of study for improving the efficiency of next-generation photovoltaic devices hot carriers in perovskite solar cells is investigated in this review paper. Considering their relevance to hot carrier dynamics, the paper thoroughly studies metal halide perovskites’ essential characteristics and topologies. We review important aspects like carrier excitation, exciton binding energy, phonon coupling, carrier excitation, thermalization, and hot hole and hot electron dynamics. We investigate, in particular, the significance of relaxation mechanisms, including thermalization and the Auger heating effect. Moreover, the bottleneck effect and defect management are discussed with an eye on their impact on device performance and carrier behaviour. A review of experimental methods for their use in investigating hot carrier dynamics, primarily transient photovoltage measurements, is included. Utilizing this thorough investigation, we hope to provide an insightful analysis of the difficulties and techniques for reducing the effect of hot carriers in perovskite solar cells and optimizing their performance.

The experimental and theoretical study of photovoltage formation in perovskite solar cells under pulsed laser excitation at 0.53 μm wavelength is presented. Two types of solar cells were fabricated on the base of cesium-containing triple cation perovskite films: (1) Cs_x(FA_0.83MA_0.17)_(1−x)Pb(I_0.83Br_0.17)₃ and (2) Cs_x(FA_0.83MA_0.17)_(1−x)Pb_0.8Sn_0.2(I_0.83Br_0.17)₃. It is found that photovoltage across the solar cells consists of two components, U = U_ph + U_f. The first one, U_ph, is the traditional photovoltage arising due to laser radiation-induced electron-hole pair generation. The second one, U_f, is the fast component following the laser pulse and has a polarity opposite to that of U_ph. It is shown that the fast photovoltage component results from the laser radiation-caused heating of free carriers. The transient photovoltage measurements show that the values of the fast component U_f are nearly the same in both types of perovskite solar cells. The magnitude of the traditional photovoltage of mixed Pb-Sn perovskite solar cells is lower than that of Pb-based cells.