共查询到20条相似文献,搜索用时 31 毫秒
1.
Md Ashiqur Rahman Laskar Wenqin Luo Nabin Ghimire Ashraful Haider Chowdhury Behzad Bahrami Ashim Gurung Khan Mamun Reza Rajesh Pathak Raja Sekhar Bobba Buddhi Sagar Lamsal Ke Chen Md Tawabur Rahman Sheikh Ifatur Rahman Khalid Emshadi Tingting Xu Mao Liang Wen‐Hua Zhang Qiquan Qiao 《Advanced functional materials》2020,30(22)
In recent years, hybrid perovskite solar cells (HPSCs) have received considerable research attention due to their impressive photovoltaic performance and low‐temperature solution processing capability. However, there remain challenges related to defect passivation and enhancing the charge carrier dynamics of the perovskites, to further increase the power conversion efficiency of HPSCs. In this work, the use of a novel material, phenylhydrazinium iodide (PHAI), as an additive in MAPbI3 perovskite for defect minimization and enhancement of the charge carrier dynamics of inverted HPSCs is reported. Incorporation of the PHAI in perovskite precursor solution facilitates controlled crystallization, higher carrier lifetime, as well as less recombination. In addition, PHAI additive treated HPSCs exhibit lower density of filled trap states (1010 cm?2) in perovskite grain boundaries, higher charge carrier mobility (≈11 × 10?4 cm2 V?1 s), and enhanced power conversion efficiency (≈18%) that corresponds to a ≈20% improvement in comparison to the pristine devices. 相似文献
2.
Xia Chen Chunyan Deng Jihuai Wu Qi Chen Yitian Du Yuan Xu Ruoshui Li Lina Tan Yuelin Wei Yunfang Huang Zhang Lan 《Advanced functional materials》2024,34(17):2311527
Molecular modulators have been demonstrated to be an effectual strategy for reducing the defect at the interface and in bulk of perovskite and ameliorating the performance and stability of perovskite solar cells (PSCs). Herein, 1-aza-15-crown 5-ether (A15C5), with a unique nitrogen heterocyclic structure as a molecular modulator is introduced at the interface between perovskite layer and hole transport layer of PSCs. Multiple supramolecular synergistic interaction between A15C5 and perovskite dramatically suppress and passivate defects, resulting in a 38% decrease in electron trap-state density in perovskite. The formation of two-dimensional/th3D perovskite heterojunctions induced by planar A15C5 releases residual strain of perovskite film, optimizes the match of energy level array and boosts the stability of devices. Consequently, A15C5-modulated PSC achieves an impressing efficiency of 24.13% along with excellent humidity, light and thermal stability. This work provides a typical strategy to utilize supramolecular crown ether in PSCs. 相似文献
3.
Ding Zheng Gang Wang Wei Huang Binghao Wang Weijun Ke Jenna Leigh Logsdon Hanyu Wang Zhi Wang Weigang Zhu Junsheng Yu Michael R. Wasielewski Mercouri G. Kanatzidis Tobin J. Marks Antonio Facchetti 《Advanced functional materials》2019,29(16)
Perovskite solar cells (PSCs) have advanced rapidly with power conversion efficiencies (PCEs) now exceeding 22%. Due to the long diffusion lengths of charge carriers in the photoactive layer, a PSC device architecture comprising an electron‐ transporting layer (ETL) is essential to optimize charge flow and collection for maximum performance. Here, a novel approach is reported to low temperature, solution‐processed ZnO ETLs for PSCs using combustion synthesis. Due to the intrinsic passivation effects, high crystallinity, matched energy levels, ideal surface topography, and good chemical compatibility with the perovskite layer, this combustion‐derived ZnO enables PCEs approaching 17–20% for three types of perovskite materials systems with no need for ETL doping or surface functionalization. 相似文献
4.
Hobeom Kim Mingyuan Pei Yonghui Lee Albertus A. Sutanto Sanghyun Paek Valentin I. E. Queloz Aron J. Huckaba Kyung Taek Cho Hyung Joong Yun Hoichang Yang Mohammad Khaja Nazeeruddin 《Advanced functional materials》2020,30(19)
Recently, perovskite solar cells (PSC) with high power‐conversion efficiency (PCE) and long‐term stability have been achieved by employing 2D perovskite layers on 3D perovskite light absorbers. However, in‐depth studies on the material and the interface between the two perovskite layers are still required to understand the role of the 2D perovskite in PSCs. Self‐crystallization of 2D perovskite is successfully induced by deposition of benzyl ammonium iodide (BnAI) on top of a 3D perovskite light absorber. The self‐crystallized 2D perovskite can perform a multifunctional role in facilitating hole transfer, owing to its random crystalline orientation and passivating traps in the 3D perovskite. The use of the multifunctional 2D perovskite (M2P) leads to improvement in PCE and long‐term stability of PSCs both with and without organic hole transporting material (HTM), 2,2′,7,7′‐tetrakis‐(N,N‐di‐p‐methoxyphenyl‐amine)‐9,9′‐spirobifluorene (spiro‐OMeTAD) compared to the devices without the M2P. 相似文献
5.
Fengyou Wang Yuhong Zhang Meifang Yang Donglai Han Lili Yang Lin Fan Yingrui Sui Yunfei Sun Xiaoyan Liu Xiangwei Meng Jinghai Yang 《Advanced functional materials》2021,31(5):2008052
Organolead halide hybrid perovskite solar cells (PSCs) have become a shining star in the renewable devices field due to the sharp growth of power conversion efficiency; however, interfacial recombination and carrier-extraction losses at heterointerfaces between the perovskite active layer and the carrier transport layers remain the two main obstacles to further improve the power conversion efficiency. Here, novel field-effect passivation has been successfully induced to effectively suppress the interfacial recombination and improve interfacial charge transfer by incorporating interfacial polarization via inserting a high work function interlayer between perovskite and holes transport layer. The charge dynamics within the device and the mechanism of the field-effect passivation are elucidated in detail. The unique interfacial dipoles reinforce the built-in field and prevent the photogenerated charges from recombining, resulting in power conversion efficiency up to 21.7% with negligible hysteresis. Furthermore, the hydrophobic interlayer also suppresses the perovskite decomposition by preventing the moisture penetration, thereby improving the humidity stability of the PSCs (>91% of the initial power conversion efficiency (PCE) after 30 d in 65 ± 5% humidity). Finally, several promising research perspectives based on field-effect passivation are also suggested for further conversion efficiency improvements and photovoltaic applications. 相似文献
6.
You Gao Hasan Raza Zhengping Zhang Wei Chen Zonghao Liu 《Advanced functional materials》2023,33(26):2215171
It is widely believed that excess/residual lead iodide (PbI2) can affect the performance of perovskite solar cells . Moderate PbI2 can enhance efficiency by passivating defects, while extremely active PbI2 leads to non-negligible hysteresis effects and reduces device stability. Although several efforts are made to investigate the role of excess PbI2, its impact is still underestimated. Recent advances further demonstrate the extraordinary potential of modifying excess PbI2; however, a comprehensive study is required to obtain a deeper understanding. Herein, the important breakthroughs regarding excess PbI2 are reviewed and the mechanism of excess PbI2 in terms of efficiency and stability is rethought. In addition, the origins, verification, and regulation of residual PbI2 are summarized. 相似文献
7.
Jiajia Suo Bowen Yang Edoardo Mosconi Hyeon-Seo Choi YeonJu Kim Shaik M. Zakeeruddin Filippo De Angelis Michael Grätzel Hui-Seon Kim Anders Hagfeldt 《Advanced functional materials》2021,31(34):2102902
Surface passivation treatment is a widely used strategy to resolve trap-mediated nonradiative recombination toward high-efficiency metal-halide perovskite photovoltaics. However, a lack of passivation with mixture treatment has been investigated, as well as an in-depth understanding of its passivation mechanism. Here, a systematic study on a mixed-salt passivation strategy of formamidinium bromide (FABr) coupled with different F-substituted alkyl lengths of ammonium iodide is demonstrated. It is obtained better device performance with decreasing chain length of the F-substituted alkyl ammonium iodide in the presence of FABr. Moreover, they unraveled a synergistic passivation mechanism of the mixed-salt treatment through surface reconstruction engineering, where FABr dominates the reformation of the perovskite surface via reacting with the excess PbI2. Meanwhile, ammonium iodide passivates the perovskite grain boundaries both on the surface and top perovskite bulk through penetration. This synergistic passivation engineer results in a high-quality perovskite surface with fewer defects and suppressed ion migration, leading to a champion efficiency of 23.5% with mixed-salt treatment. In addition, the introduction of the moisture resisted F-substituted groups presents a more hydrophobic perovskite surface, thus enabling the decorated devices with excellent long-term stability under a high humid atmosphere as well as operational conditions. 相似文献
8.
Zhuowei Li Junlin Wang Yanyu Deng Jianing Xi Yi Zhang Chunyu Liu Wenbin Guo 《Advanced functional materials》2023,33(18):2214562
Numerous strategies have been practiced to improve the power conversion efficiency of CsPbI2Br-based perovskite solar cells (PSCs), which definitely makes efficiency gradually approach the theoretical efficiency limit. However, sufficient device stability is still in urgent demand for commercialization, pushing to overcome some instability sources induced by hygroscopicity of spiro-OMeTAD and residual strain of perovskite layer. To address these issues, p-type semiconductor of PCPDTBT is used to replace spiro-OMeTAD, enabling dual functions of hole transport and strain regulation. On the one hand, undoped PCPDTBT performs excellent hole extraction and transport, while avoiding the perovskite degradation caused by the hygroscopicity of common additives. On the other hand, PCPDTBT assisted by a thermally spin-coating method compensates for the thermally-induced residual strain in perovskite layer owing to its high thermal expansion coefficient. Consequently, CsPbI2Br-based PSCs with PCPDTBT layer achieve improved efficiency of 16.5% as well as enhanced stability. This study provides a simple and facile strategy to achieve efficient and stable CsPbI2Br-based PSCs. 相似文献
9.
Yong-Chun Ye Li Chen Xian-Min Chen Chun-Ying Ma Bing-Hao Lv Jiang-Ying Wang Wei-Dong Dou Chu Zhang Ting-Li Ma Jian-Xin Tang 《Advanced functional materials》2024,34(8):2310136
Tin oxide (SnO2) is currently the dominating electron transport material (ETL) used in state-of-the-art perovskite solar cells (PSCs). However, there are amounts of defects distributed at the interface between ETL and perovskite to deteriorate PSC performance. Herein, a molecule bridging layer is built by incorporating 2,5-dichloroterephthalic acid (DCTPA) into the interface between the SnO2 and perovskites to achieve better energy level alignment and superior interfacial contact. The multifunctional molecular bridging layer not only can passivate the trap states of Sn dangling bonds and oxygen vacancies resulting in improved conductivity and the electron extraction of SnO2 but also can regulate the perovskite crystal growth and reduce defect-assisted nonradiative recombination due to its strong interaction with undercoordinated lead ions. As a result, the DCTPA-modified PSCs achieve champion power conversion efficiencies (PCEs) of 23.25% and 20.23% for an active area of 0.15 cm2 device and 17.52 cm2 mini-module, respectively. Moreover, the perovskite films and PSCs based on DCTPA modification show excellent long-term stability. The unencapsulated target device can maintain over 90% of the initial PCE after 1000 h under ambient air. This strategy guides design methods of molecule bridging layer at the interface between SnO2 and perovskite to improve the performance of PSCs . 相似文献
10.
Efficient and Stable Perovskite Solar Cells via Dual Functionalization of Dopamine Semiquinone Radical with Improved Trap Passivation Capabilities
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Qifan Xue Meiyue Liu Zhenchao Li Lei Yan Zhicheng Hu Jiawen Zhou Wenqiang Li Xiao‐Fang Jiang Baomin Xu Fei Huang Yuan Li Hin‐Lap Yip Yong Cao 《Advanced functional materials》2018,28(18)
Highly efficient planar heterojunction perovskite solar cells (PVSCs) with dopamine (DA) semiquinone radical modified poly(3,4‐ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) (DA‐PEDOT:PSS) as a hole transporting layer (HTL) were fabricated. A combination of characterization techniques were employed to investigate the effects of DA doping on the electron donating capability of DA‐PEDOT:PSS, perovskite film quality and charge recombination kinetics in the solar cells. Our study shows that DA doping endows the DA‐PEDOT:PSS‐modified PVSCs with a higher radical content and greater perovskite to HTL charge extraction capability. In addition, the DA doping also improves work function of the HTL, increases perovskite film crystallinity, and the amino and hydroxyl groups in DA can interact with the undercoordinated Pb atoms on the perovskite crystal, reducing charge‐recombination rate and increasing charge‐extraction efficiency. Therefore, the DA‐PEDOT:PSS‐modified solar cells outperform those based on PEDOT:PSS, increasing open‐circuit voltage (V oc) and power conversion efficiency (PCE) to 1.08 V and 18.5%, respectively. Even more importantly, the efficiency of the unencapsulated DA‐PEDOT:PSS‐based PVSCs are well retained with only 20% PCE loss after exposure to air for 250 hours. These in‐depth insights into structure and performance provide clear and novel guidelines for the design of effective HTLs to facilitate the practical application of inverted planar heterojunction PVSCs. 相似文献
11.
Xiayan Wu Yue Jiang Cong Chen Jiali Guo Xiangyu Kong Yancong Feng Sujuan Wu Xingsen Gao Xubing Lu Qianming Wang Guofu Zhou Yiwang Chen Jun‐Ming Liu Krzysztof Kempa Jinwei Gao 《Advanced functional materials》2020,30(6)
Triple cation perovskites (Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3) have received lots of attention owing to the excellent stability and photovoltaic performance. However, the development toward efficient solar cells has been significantly impeded by its intrinsic precursor instability, as well as defective crystal surface. Herein, a strategy for introducing the additive of 1,4,7,10,13,16‐hexaoxacyclooctadecane (18C6) in the precursor solution, rendering an excellent stability of more than one month, and the defect passivation effect on the crystal surface are demonstrated. In those perovskite solar cells, a power conversion efficiency of 20.73% has been achieved with a substantially improved open‐circuit voltage and fill factor. As evidenced by the density functional theory calculations, the fundamental reason relating to the enhanced performance is found to be the interaction effect between the 18C6 and cations, and in particular the formation of the 18C6/Pb complex. This finding represents an alternative strategy for achieving a stable precursor solution and efficient perovskite solar cells. 相似文献
12.
Two critical limitations of organic–inorganic lead halide perovskite materials for solar cells are their poor stability in humid environments and inclusion of toxic lead. In this study, high‐throughput density functional theory (DFT) methods are used to computationally model and screen 1845 halide perovskites in search of new materials without these limitations that are promising for solar cell applications. This study focuses on finding materials that are comprised of nontoxic elements, stable in a humid operating environment, and have an optimal bandgap for one of single junction, tandem Si‐perovskite, or quantum dot–based solar cells. Single junction materials are also screened on predicted single junction photovoltaic (PV) efficiencies exceeding 22.7%, which is the current highest reported PV efficiency for halide perovskites. Generally, these methods qualitatively reproduce the properties of known promising nontoxic halide perovskites that are either experimentally evaluated or predicted from theory. From a set of 1845 materials, 15 materials pass all screening criteria for single junction cell applications, 13 of which are not previously investigated, such as (CH3NH3)0.75Cs0.25SnI3, ((NH2)2CH)Ag0.5Sb0.5Br3, CsMn0.875Fe0.125I3, ((CH3)2NH2)Ag0.5Bi0.5I3, and ((NH2)2CH)0.5Rb0.5SnI3. These materials, together with others predicted in this study, may be promising candidate materials for stable, highly efficient, and nontoxic perovskite‐based solar cells. 相似文献
13.
Kai Wang Jiang Liu Jun Yin Erkan Aydin George T. Harrison Wenzhu Liu Shanyong Chen Omar F. Mohammed Stefaan De Wolf 《Advanced functional materials》2020,30(35)
Defects at the surface and grain boundaries of metal–halide perovskite films lead to performance losses of perovskite solar cells (PSCs). Here, organic cyano‐based π‐conjugated molecules composed of indacenodithieno[3,2‐b]thiophene (IDTT) are reported and it is found that their cyano group can effectively passivate such defects. To achieve a homogeneous distribution, these molecules are dissolved in the antisolvent, used to initiate the perovskite crystallization. It is found that these molecules are self‐anchored at the grain boundaries due to their strong binding to undercoordinated Pb2+. On a device level, this passivation scheme enhances the charge separation and transport at the grain boundaries due to the well‐matched energetic levels between the passivant and the perovskite. Consequently, these benefits contribute directly to the achievement of power conversion efficiencies as high as 21.2%, as well as the improved environmental and thermal stability of the PSCs. The surface treatment provides a new strategy to simultaneously passivate defects and enhance charge extraction/transport at the device interface by manipulating the anchoring groups of the molecules. 相似文献
14.
Md Arafat Mahmud The Duong Yanting Yin Huyen T. Pham Daniel Walter Jun Peng Yiliang Wu Li Li Heping Shen Nandi Wu Naeimeh Mozaffari Gunther Andersson Kylie R. Catchpole Klaus J. Weber Thomas P. White 《Advanced functional materials》2020,30(7)
Defect‐mediated carrier recombination at the interfaces between perovskite and neighboring charge transport layers limits the efficiency of most state‐of‐the‐art perovskite solar cells. Passivation of interfacial defects is thus essential for attaining cell efficiencies close to the theoretical limit. In this work, a novel double‐sided passivation of 3D perovskite films is demonstrated with thin surface layers of bulky organic cation–based halide compound forming 2D layered perovskite. Highly efficient (22.77%) mixed‐dimensional perovskite devices with a remarkable open‐circuit voltage of 1.2 V are reported for a perovskite film having an optical bandgap of ≈1.6 eV. Using a combination of experimental and numerical analyses, it is shown that the double‐sided surface layers provide effective defect passivation at both the electron and hole transport layer interfaces, suppressing surface recombination on both sides of the active layer. Despite the semi‐insulating nature of the passivation layers, an increase in the fill factor of optimized cells is observed. The efficient carrier extraction is explained by incomplete surface coverage of the 2D perovskite layer, allowing charge transport through localized unpassivated regions, similar to tunnel‐oxide passivation layers used in silicon photovoltaics. Optimization of the defect passivation properties of these films has the potential to further increase cell efficiencies. 相似文献
15.
In Situ Growth of 2D Perovskite Capping Layer for Stable and Efficient Perovskite Solar Cells
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《Advanced functional materials》2018,28(17)
2D halide perovskites have recently been recognized as a promising avenue in perovskite solar cells (PSCs) in terms of encouraging stability and defect passivation effect. However, the efficiency (less than 15%) of ultrastable 2D Ruddlesden–Popper PSCs still lag far behind their traditional 3D perovskite counterparts. Here, a rationally designed 2D‐3D perovskite stacking‐layered architecture by in situ growing 2D PEA2PbI4 capping layers on top of 3D perovskite film, which drastically improves the stability of PSCs without compromising their high performance, is reported. Such a 2D perovskite capping layer induces larger Fermi‐level splitting in the 2D‐3D perovskite film under light illumination, resulting in an enhanced open‐circuit voltage (Voc) and thus a higher efficiency of 18.51% in the 2D‐3D PSCs. Time‐resolved photoluminescence decay measurements indicate the facilitated hole extraction in the 2D‐3D stacking‐layered perovskite films, which is ascribed to the optimized energy band alignment and reduced nonradiative recombination at the subgap states. Benefiting from the high moisture resistivity as well as suppressed ion migration of the 2D perovskite, the 2D‐3D PSCs show significantly improved long‐term stability, retaining nearly 90% of the initial power conversion efficiency after 1000 h exposure in the ambient conditions with a high relative humidity level of 60 ± 10%. 相似文献
16.
Lu‐Lu Jiang Zhao‐Kui Wang Meng Li Cong‐Cong Zhang Qing‐Qing Ye Ke‐Hao Hu Ding‐Ze Lu Peng‐Fei Fang Liang‐Sheng Liao 《Advanced functional materials》2018,28(7)
Organometallic halide perovskite films with good surface morphology and large grain size are desirable for obtaining high‐performance photovoltaic devices. However, defects and related trap sites are generated inevitably at grain boundaries and on surfaces of solution‐processed polycrystalline perovskite films. Seeking facial and efficient methods to passivate the perovskite film for minimizing defect density is necessary for further improving the photovoltaic performance. Here, a convenient strategy is developed to improve perovskite crystallization by incorporating a 2D polymeric material of graphitic carbon nitride (g‐C3N4) into the perovskite layer. The addition of g‐C3N4 results in improved crystalline quality of perovskite film with large grain size by retarding the crystallization rate, and reduced intrinsic defect density by passivating charge recombination centers around the grain boundaries. In addition, g‐C3N4 doping increases the film conductivity of perovskite layer, which is beneficial for charge transport in perovskite light‐absorption layer. Consequently, a champion device with a maximum power conversion efficiency of 19.49% is approached owing to a remarkable improvement in fill factor from 0.65 to 0.74. This finding demonstrates a simple method to passivate the perovskite film by controlling the crystallization and reducing the defect density. 相似文献
17.
Perovskite Solar Cells: Passivated Perovskite Crystallization via g‐C3N4 for High‐Performance Solar Cells (Adv. Funct. Mater. 7/2018)
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Lu‐Lu Jiang Zhao‐Kui Wang Meng Li Cong‐Cong Zhang Qing‐Qing Ye Ke‐Hao Hu Ding‐Ze Lu Peng‐Fei Fang Liang‐Sheng Liao 《Advanced functional materials》2018,28(7)
18.
Unique Seamlessly Bonded CNT@Graphene Hybrid Nanostructure Introduced in an Interlayer for Efficient and Stable Perovskite Solar Cells
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Xuanhua Li Tengteng Tong Qinjiang Wu Shaohui Guo Qiang Song Jian Han Zhixiang Huang 《Advanced functional materials》2018,28(32)
Carbon nanomaterials have been widely used as an interlayer for realizing efficient and stable perovskite solar cells (PSCs). Theoretically, the design of a carbon composite interlayer that combines excellent conductivity with a high specific surface area is a better strategy than the application of pure nanocarbons. Here, an unusual seamlessly bonded carbon nanotube@graphene (CNT@G) hybrid nanomaterial was strategically synthesized and demonstrated to behave as an efficient interlayer for realizing efficient and stable PSCs. Due to the advantage of the seamless bond, the as‐proposed hybrid nanostructure showed an apparent improvement compared to the use of CNTs only, graphene only, or a simple mixture of CNTs and graphene. The power conversion efficiency improved from 15.67% to 19.56% after introduction of the hybrid nanomaterial due to efficient carrier extraction, faster charge transport, and restrained carrier recombination. More importantly, PSCs with a CNT@G hybrid‐decorated hole transport layer (HTL) showed good thermal stability during a 50 h heat‐aging test at 100 °C and water stability under ambient humidity (30–50% relative humidity) for 500 h because the hybrid nanostructure exhibited an increased capability to block ion/molecule diffusion. Our results provide an alternative approach for fully exploring the potential application of nanocarbons in the development of high‐performance PSCs. 相似文献
19.
Shan Tan Jiangjian Shi Bingcheng Yu Wenyan Zhao Yusheng Li Yiming Li Huijue Wu Yanhong Luo Dongmei Li Qingbo Meng 《Advanced functional materials》2021,31(21):2010813
All-inorganic perovskite cesium lead iodide (CsPbI3) exhibits excellent prospects for commercial application as a light absorber in single-junction or tandem solar cells due to its outstanding thermal stability and proper bandgap. However, the device performance of CsPbI3-based perovskite solar cells (PSCs) is still restricted by the unsatisfactory crystal quality and severe non-radiative recombination. Herein, inorganic additive ammonium halides are introduced into the precursor solution to regulate the nucleation and crystallization of the CsPbI3 film by exploiting the atomic interaction between the ammonium group and the Pb–I framework. The grain boundaries and interfacial contact of the CsPbI3 film have been improved, which leads to significant suppression in the non-radiative recombination and an enhancement in the charge transport ability. With these benefits, a high efficiency of 18.7% together with an extraordinarily high fill factor of 0.83–0.84 has been achieved, comparable to the highest records reported so far. Moreover, the cell exhibits ultra-high photoelectrical stability under continuous light illumination and high bias voltage with 96% of its initial power-conversion efficiency being sustained after 2000 h operation, even superior to the world-champion CsPbI3 solar cell. The findings are promising for the development and application of all-inorganic PSCs using a simple inorganic additive strategy. 相似文献
20.
In‐Hyeok Park Leiqiang Chu Kai Leng Yu Fong Choy Wei Liu Ibrahim Abdelwahab Ziyu Zhu Zhirui Ma Wei Chen Qing‐Hua Xu Goki Eda Kian Ping Loh 《Advanced functional materials》2019,29(39)
Hybrid organic–inorganic perovskites have recently emerged as potential disruptive photovoltaic technology. However, the toxicity of lead used in state‐of‐the‐art hybrid perovskites solar cell prevents large‐scale commercialization, which calls for lead‐free alternatives. Sn‐based perovskites have been considered as alternatives but they are limited by rapid oxidation and decomposition in ambient air. Here, an Sn‐based two‐dimensional hybrid organic–inorganic perovskites [A2B(n‐1)SnnI(3n+1)] (n = 1 and 2) are reported with improved air stability, using bulky stilbene derivatives as the organic cations (2‐(4‐(3‐fluoro)stilbenyl)ethanammonium iodide (FSAI)). The moisture stability of the [(FSA)2SnI4] perovskites is attributed to the hydrophobic properties of fluorine‐functionalized organic chains (FSA), as well as the strong cohesive bonding in the organic chains provided by H bonds, CH···X type H bonds, weak interlayer F···F interaction, and weak face‐to‐face type π‐π interactions. The photodetector device fabricated on exfoliated single crystal flake of [(FSA)2SnI4] exhibits fast and stable photoconductor response. 相似文献