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HighlightsRecent progress of efficiency and long-term stability for perovskite solar cells, and the development of perovskite-based tandem solar cells are described.The progress of lead-free perovskite solar cells and their potential for industrial production are discussed in detail.The current status, ongoing challenges, and the future outlooks of perovskite solar cells are highlighted.Perovskite solar cells (PSCs) emerging as a promising photovoltaic technology with high efficiency and low manufacturing cost have attracted the attention from all over the world. Both the efficiency and stability of PSCs have increased steadily in recent years, and the research on reducing lead leakage and developing eco-friendly lead-free perovskites pushes forward the commercialization of PSCs step by step. This review summarizes the main progress of PSCs in 2020 and 2021 from the aspects of efficiency, stability, perovskite-based tandem devices, and lead-free PSCs. Moreover, a brief discussion on the development of PSC modules and its challenges toward practical application is provided.

The world record device efficiency of single‐junction solar cells based on organic–inorganic hybrid perovskites has reached 25.5%. Further improvement in device power conversion efficiency (PCE) can be achieved by either optimizing perovskite films or designing novel device structures such as perovskite/Si tandem solar cells. With the marriage of perovskite and Si solar cells, a tandem device configuration is able to achieve a PCE exceeding the Shockley–Queisser limit of single‐junction solar cells by enhancing the usage of solar spectrum. After several years of development, the highest PCE of the perovskite/Si tandem cell has reached 29.5%, which is higher than that of perovskite‐ and Si‐based single‐junction cells. Here, in this review, we will (1) first discuss the device structure and fundamental working principle of both two‐terminal (2T) and four‐terminal (4T) perovskite/Si tandem solar cells; (2) second, provide a brief overview of the advances of perovskite/Si tandem solar cells regarding the development of interconnection layer, perovskite active layer, tandem device structure, and light management strategies; (3) third, discuss the challenges and opportunities for further developing perovskite/Si tandem solar cells. This review article, on the one hand, provides a comprehensive understanding to readers on the development of perovskite/Si tandems. On the other hand, it proposes various novel applications that may bring such tandems into the market in a near future. Perovskite/Si tandem solar cells are considered as a game‐changer in future solar technology. It has attracted tremendous attention in photovoltaic (PV) field due to its potential to achieve over 30% efficiency. Here, we provide an overview on the development of perovskite/Si tandem solar cells, including the device architecture, interconnection layer, perovskite active layer, and light management. Finally, the integration of perovskite/Si tandem cells and electrochemical cells for some novel applications, such as water splitting or energy storage, is reviewed and discussed. Such new applications may bring perovskite‐based PV technology into market in the near future.

The manipulation of crystal orientation from the thermodynamic equilibrium states is desired in layered hybrid perovskite films to direct charge transport and enhance the perovskite devices performance. Here we report a templated growth mechanism of layered perovskites from 3D-like perovskites which can be a general design rule to align layered perovskites along the out-of-plane direction in films made by both spin-coating and scalable blading process. The method involves suppressing the nucleation of both layered and 3D perovskites inside the perovskite solution using additional ammonium halide salts, which forces the film formation starts from solution surface. The fast drying of solvent at liquid surface leaves 3D-like perovskites which surprisingly templates the growth of layered perovskites, enabled by the periodic corner-sharing octahedra networks on the surface of 3D-like perovskites. This discovery provides deep insights into the nucleation behavior of octahedra-array-based perovskite materials, representing a general strategy to manipulate the orientation of layered perovskites. The orientation of layered perovskites plays a crucial role in their charge transport behavior and hence, the efficiency of related solar cells. Here, the authors find that preformed 3D-like perovskites can efficiently template the growth of layered perovskites and determine their orientation.

HighlightsPolarization is an exceptional physical property of light that carries and differentiates a significant amount of optical information. Perovskite materials are utilized in polarization-sensitive photodetectors owing to their crystal structure anisotropy and controllable orientation growth, in addition to their excellent photovoltaic performance.This paper presents an overview of the structural characteristics and photovoltaic performance of different optical structures and low-dimensional perovskite polarization photodetectors. This summary will contribute to the future development of perovskite-based photodetectors that are sensitive to polarization.

The incompatibility of the high sensitivity and wide linear range still restricts the further development of active sensors. Here we report a triboelectric pressure sensor based on water-containing triboelectric elastomer with gradient-based microchannels. Tiny amount of liquid is injected into the triboelectric elastomer and the pressure-induced water bridges can modulate the built-in electric field of the sensor, which enhance the signal linearity near the compression limit. Moreover, it has been found that liquid-solid contact electrification can be enhanced by triggering selective ionic transfer, while the prepared ion-rich interface in the microchannels boosts the sensitivity of the sensor. Hence, an ultra-wide linear range (5 kPa–1240 kPa) with a sensitivity of 0.023 V kPa −1 can be achieved, which is so far the widest linear range of active sensors to our knowledge. Our work can promote the practical application of triboelectric sensors and provide new insights for other sensory devices. The incompatibility between high sensitivity and a wide linear range has hindered the development of sensors. Here, the authors propose a pressure sensor that combines a water-containing triboelectric elastomer with gradient-based microchannels, achieving an ultra-wide linear range and high sensitivity simultaneously.

Tandem solar cells can boost efficiency by using a wider range of the solar spectrum. The bandgap of organic semiconductors can be tuned over a wide range, but, for a two-terminal device that directly connects the cells, the currents produced must be nearly equal. Meng et al. used a semiempirical analysis to choose well-matched top- and bottom-cell active layers. They used solution processing to fabricate an inverted tandem device that has a power conversion efficiency as high as 17.4%. Science , this issue p. 1094 A semi-empirical analysis helped to optimize materials for a tandem organic solar cell with high power conversion efficiency. Although organic photovoltaic (OPV) cells have many advantages, their performance still lags far behind that of other photovoltaic platforms. A fundamental reason for their low performance is the low charge mobility of organic materials, leading to a limit on the active-layer thickness and efficient light absorption. In this work, guided by a semi-empirical model analysis and using the tandem cell strategy to overcome such issues, and taking advantage of the high diversity and easily tunable band structure of organic materials, a record and certified 17.29% power conversion efficiency for a two-terminal monolithic solution-processed tandem OPV is achieved.

Although lead‐based perovskite solar cells (PSCs) are highly efficient, the toxicity of lead (Pb) limits its large‐scale commercialization. As such, there is an urgent need to find alternatives. Many studies have examined tin‐based PSCs. However, pure tin‐based perovskites are easily oxidized in the air or just in glovebox with an ultrasmall amount of oxygen. Such a characteristic makes their performance and stability less ideal compared with those of lead‐based perovskites. Herein, how to address the instability of tin‐based perovskites is introduced in detail. First, the crystalline structure, optical properties, and sources of instability of tin‐based perovskites are summarized. Next, the preparation methods of tin‐based perovskite are discussed. Then, various measures for solving the instability problem are explained using four strategies: additive engineering, deoxidizer, partial substitution, and reduced dimensions. Finally, the challenges and prospects are laid out to help researchers develop highly efficient and stable tin‐based perovskites in the future. Nontoxic tin‐based perovskite solar cells (PSCs) have attracted attention, but are easily oxidized, which causes their performance and stability to be far behind lead‐based PSCs. Here, strategies to improve the stability of tin‐based PSCs (additive engineering, deoxidizer, partial substitution, and reduced dimensions) are reviewed. Outlooks are also proposed to avoid the shortcoming for fabricating highly efficient and stable PSCs.

This article explores the dissipative control for a class of nonlinear DP-CPS (distributed parameter cyber physical system) within a finite-time interval. By utilizing a Takagi-Sugeno (T-S) fuzzy model to represent the system’s nonlinear aspects, the studied system is formulated as a class of fuzzy parabolic partial differential equation (PDE). In order to optimize network resources, both the system state and input signal are subjected to quantization using dynamic quantizers. Subsequently, a dynamic state control strategy is proposed, taking into account potential DoS attack. The finite-time boundedness of the fuzzy parabolic PDE is analyzed, with respect to the influence of quantization, through the construction of an appropriate Lyapunov functional. The article then presents the conditions for finite-time dissipative control design, alongside the adjustment parameters for the dynamic quantizers within the fuzzy closed-loop system. Furthermore, the decoupling of interlinked nonlinear terms in the control design conditions is achieved by using an arbitrary matrix. Finally, an example is provided and the simulation results indicate the effectiveness of the dissipative control method proposed.

HighlightsThe partial substitution of Br− on I-sites, and the restricted motion of MA+ cations in correlation with suppressed electron-phonon coupling promote charge transport.The perovskite parent lattice of 2FEABr-treated perovskites was firmed, and the difficulty degree for A-site MA+ cations running out of the inorganic framework was thus enhanced.The efficiency was enhanced from 19.44% to 21.06%, accompanied with excellent stability.Surface passivation via post-treatment is an important strategy for improving power conversion efficiency and operational stability of perovskite solar cells. However, so far the interaction mechanisms between passivating additive and perovskite are not well understood. Here, we report the atomic-scale interaction of surface passivating additive 2,2-difluoroethylammonium bromine (2FEABr) on the MAPbI3. It is found that the bulky 2FEA+ cations tend to distribute at film surface, while the Br− anions diffuse from surface into bulk. A combination of 19F, 207Pb, and 2H solid-state NMR further reveal the Br− anions’ partial substitution for the I− sites, the restricted motion of partial MA+ cations, and the firmed perovskite lattices, which would improve charge transport and stability of the perovskite films. Optical spectroscopy and ultraviolet photoelectron spectroscopy demonstrate that the 2FEABr induced surface passivation and energetic modification suppress the nonradiative recombination loss. These findings enable the efficiency of the p-i-n structured PSC significantly increasing from 19.44 to 21.06%, accompanied by excellent stability. Our work further establishes more knowledge link between passivating additive and PSC performance.