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The large open circuit voltage ( V OC ) loss and phase segregation are two main obstacles hindering the development of wide-bandgap perovskite solar cells (PSCs). Even though substantial progress has been made through crystallization regulation and surface modification on perovskite, the mechanism of V OC loss and phase segregation has rarely been studied. In this paper, we first investigate the halide ions distribution along the out-of-plane direction and find the initial inhomogeneous distribution of halide ions during the crystallization process is an important reason. It leads to the formation of an unfavorable potential well in PSCs, resulting in V OC loss as well as generation of strong strain exacerbating phase segregation. Through introducing melatonin (MT) into perovskite precursors, a homogeneous distribution of halide anions is realized due to the well-regulated crystallization. Consequently, the treated PSCs exhibit an optimized power conversion efficiency (PCE) of 22.88% with a V OC loss as low as 0.38 V, which are the best values for wide-bandgap PSCs up to now.

Air-processed perovskite solar cells (PSCs) with high photoelectric conversion efficiency (PCE) can not only further reduce the production cost but also promote its industrialization. During the preparation of the PSCs in ambient air, the contact of the buried interface not only affects the crystallization of the perovskite film but also affects the interface carrier transport, which is directly related to the performance of the device. Here, we optimize the buried interface by introducing 3-mercaptopropyltrimethoxysilane (MPTMS, (CH 3 O) 3 Si(CH 2 ) 3 SH) on the nickel oxide (NiO x ) surface. The crystallization of the perovskite film is improved by enhancing surface hydrophobicity; besides, the SH-based functional group of MPTMS passivates the uncoordinated lead at the interface, which effectively reduces the defects at the bottom interface of perovskite and inhibits the nonradiative recombination at the interface. Moreover, the energy level between the NiO x layer and the perovskite layer is better matched. Based on multiple functions of MPTMS modification, the open circuit voltage of the device is obviously improved, and efficient air-processed methylamine-free (MA-free) PSCs are realized with PCE reaching 21.0%. The device still maintains the initial PCE of 85% after 1000 h aging in the glovebox. This work highlights interface modification in air-processed MA-free PSCs to promote the industrialization of PSCs.

Buried interface modification is promising for preparing high-performance perovskite solar cells (PSCs) by improving the film quality and adjusting the interfacial energy level alignment. In this work, multifunctional ethylenediaminetetraacetic acid diammonium (EAD)-modulated ZnO is employed as an effective buried interface to regulate the interplay between SnO 2 and CsPbI 2 Br in carbon-based inorganic PSCs (C-IPSCs). The burying of EAD into the ZnO interlayer not only enhances the photoelectric properties of ZnO by passivating oxygen defects but also adjusts the energy level alignment of the buried interface. More importantly, the perovskite quality is optimized and the buried interface defects are passivated due to the formation of coordination and hydrogen bondings. Benefiting from such a robust and efficient charge transfer configuration, a maximum power conversion efficiency of 14.58% is achieved in the optimized device, which represents the highest performance reported among those of low-temperature CsPbI 2 Br C-IPSCs. In addition, the unencapsulated device demonstrates better long-term and thermal stability.

Nontoxic tin-based perovskite solar cells (Sn-PSCs) as a promising alternative to toxic Pb-PSCs have drawn great attention in recent years for their environmental friendliness and unique optoelectronic properties. However, both the efficiency and long-term stability of Sn-PSCs are considerably inferior to those of Pb-based ones. One of the main reasons is the difficulty in obtaining high-quality Sn-perovskite films due to the rapid crystallization of Sn-perovskites, which also results in poor device reproducibility. Here, we report a novel cation exchange strategy to prepare high-quality formamidinium tin triiodide (FASnI 3 ) perovskite films with a better controlled crystallization process and improved reproducibility, which allows easy access to smooth and pinhole-free perovskite films with oriented crystal growth, enlarged grain size, and reduced trap-state density. The corresponding Sn-PSCs show excellent photovoltaic performance with a champion efficiency of 9.11%, comparable to the best results reported for FASnI 3 -PSCs, and the devices also demonstrate outstanding long-term stability without encapsulation. Our results offer a practical strategy for fabricating Sn-PSCs with superb performance and stability.

In recent years, photodetectors based on organic-inorganic lead halide perovskites have been studied extensively. However, the inclusion of lead in those materials can cause severe human health and environmental problems, which is undesirable for practical applications. Here, we report high-performance photodetectors with a tin-based perovskite/PEDOT:PSS vertical heterojunction. The device demonstrates a broadband photoresponse from NIR to UV. The maximum responsivity and gain are up to 2.6 × 10 6 A/W and 4.7 × 10 6 , respectively. Moreover, a much shorter response time and higher detectivity can be achieved by reducing the thickness of PEDOT:PSS. The outstanding performance is due to the excellent optoelectronic properties of the perovskite and the photogating effect originating from the heterojunction. Furthermore, devices fabricated on flexible substrates can demonstrate not only high sensitivity but also excellent bending stability. This work opens up the opportunity of using lead-free perovskite in highly sensitive photodetectors with vertical heterojunctions.

Three-dimensional branched TiO2 architectures (3D BTA) with controllable morphologies were synthesized via a facile template-free one-pot solvothermal route. The volume ratio of deionized water (DI water) and diethylene glycol in solvothermal process is key to the formation of 3D BTA assembled by nanowire-coated TiO2 dendrites, which combines the advantages of 3D hierarchical structure and 1D nanoscale building blocks. Benefiting from such unique structural features, the BTA in full bloom achieved significantly increased specific surface areas and shortened Li(+) ion/electrons diffusion pathway. The lithium-ion batteries based on BTA in full bloom exhibited remarkably enhanced reversible specific capacity and rate performance, attributing to the high contact area with the electrolyte and the short solid state diffusion pathway for Li(+) ion/electrons promoting lithium insertion and extraction.

Bis(imidazolium) iodides (bis-Im(+)I(-)s) are synthesized with different substituents and used as electrolytes in dye-sensitized solar cells (DSSCs). Three kinds of low-volatility electrolytes are prepared by using 1,1'-methylene bis(3-imidazolium) diiodide (MIDI), 1,1'-methylene bis(3-n-methylimidazolium) diiodide (MMIDI), and 1,1'-methylene-bis(3-n-ethylimidazolium) diiodide (MEIDI) as the iodide sources. The effects of these substituents on the photovoltaic performance of the cells are investigated. It is found that the device shows a lower short-circuit photocurrent (Jsc), higher open-voltage (Voc) and fill factor (FF) with the increased cation size in electrolyte. These results are explained by electrostatic interactions between the solvated Im(+) and the negatively charged species. Meanwhile, the explanation is supported by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), open circuit voltage decay (OCVD), and dark current measurements.