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1.
Minna Hou Yuzeng Xu Bo Zhou Ying Tian Yan Wu Dekun Zhang Guangcai Wang Baozhang Li Huizhi Ren Yuelong Li Qian Huang Yi Ding Ying Zhao Xiaodan Zhang Guofu Hou 《Advanced functional materials》2020,30(34)
Surface passivation is increasingly one of the most prominent strategies to promote the efficiency and stability of perovskite solar cells (PSCs). However, most passivation molecules hinder carrier extraction due to poorly conductive aggregation between perovskite surface and carrier transportation layer. Herein, a novel molecule: p‐phenyl dimethylammonium iodide (PDMAI) with ammonium group on both terminals is introduced, and its passivation effect is systematically investigated. It is found that PDMAI can mitigate defects at the surface and promote carrier extraction from perovskite to the hole transporting layer, leading to a lift of open‐circuit voltage of 40 mV. Profiting from superior PDMAI passivation, the average efficiency of PSCs has been elevated from 19.69% to 20.99%. As demonstrated with density functional theory calculations, PDMAI probably tends to anchor onto the perovskite surface with both ? NH3I tails, and enhances the adhesion and contact to perovskite layer. The exposed hydrophobic aryl core protects perovskite against detrimental environmental factors. In addition, the alkyl component between aryl and ammonium groups is demonstrated to be essentially vital in triggering passivation function, which offers the guidance for the design of passivation molecules. 相似文献
2.
Yinghui Wu Qihua Liang Hongwei Zhu Xingyi Dai Bin-Bin Yu Yang Hu Miao Chen Long-Biao Huang Shaik M. Zakeeruddin Zhongjin Shen Junfeng Wang Michael Grätzel 《Advanced functional materials》2023,33(37):2302404
Surface defects cause non-radiative charge recombination and reduce the photovoltaic performance of perovskite solar cells (PSCs), thus effective passivation of defects has become a crucial method for achieving efficient and stable devices. Organic ammonium halides have been widely used for perovskite surface passivation, due to their simple preparation, lattice matching with perovskite, and high defects passivation ability. Herein, a surface passivator 2,4,6-trimethylbenzenaminium iodide (TMBAI) is employed as the interfacial layer between the spiro-OMeTAD and perovskite layer to modify the surface defect states. It is found that TMBAI treatment suppresses the nonradiative charge carrier recombination, resulting in a 60 mV increase of the open-circuit voltage (Voc) (from 1.11 to 1.17 V) and raises the fill factor from 76.3% to 80.3%. As a result, the TMBAI-based PSCs device demonstrates a power conversion efficiency (PCE) of 23.7%. Remarkably, PSCs with an aperture area of 1 square centimeter produce a PCE of 21.7% under standard AM1.5 G sunlight. The unencapsulated TMBAI-modified device retains 92.6% and 90.1% of the initial values after 1000 and 550 h under ambient conditions (humidity 55%–65%) and one-sun continuous illumination, respectively. 相似文献
3.
Yongyu Liao Jianxin Zhang Wenran Wang Zechao Yang Rong Huang Jiage Lin Lei Che Guoying Yang Zhenxiao Pan Huashang Rao Xinhua Zhong 《Advanced functional materials》2023,33(20):2214784
Molecular passivation on perovskite surface is an effective strategy to inhibit surface defect-assisted recombination and reduce nonradiative recombination loss in perovskite solar cells (PSCs). However, the majority of passivating molecules bind to perovskite surface through weak interactions, resulting in weak passivation effects and susceptible to interference from various factors. Especially in carbon-based perovskite solar cells (C-PSCs), the molecular passivation effect is more susceptible to disturbance in subsequent harsh preparation of carbon electrodes via blade-coating route. Herein, bidentate ligand 2,2′-Bipyridine (2Bipy) is explored to passivate surface defects of CsPbI2.6Br0.4 perovskite films. The results indicate that compared with monodentate pyridine (Py), bidentate 2Bipy shows a stronger chelation with uncoordinated Pb(II) defects and exhibits a greater passivation effect on perovskite surface. As a result, 2Bipy-modified perovskite films display a significantly boosted photoluminescence lifetime, accompanied by excellent anchoring stability and anti-dissociation of passivating molecules. Meanwhile, the moisture resistance of the 2Bipy-modified perovskite films is also significantly enhanced. Consequently, the efficiency of C-PSCs is improved to 16.57% (Jsc = 17.16 mA cm−2, Voc = 1.198 V, FF = 80.63%). As far as it is known, this value represents a new record efficiency for hole transport material-free inorganic C-PSCs. 相似文献
4.
Fahimeh Shahvaranfard Marco Altomare Yi Hou Seyedsina Hejazi Wei Meng Benedict Osuagwu Ning Li Christoph J. Brabec Patrik Schmuki 《Advanced functional materials》2020,30(10)
The engineering of the electron transport layer (ETL)/light absorber interface is explored in perovskite solar cells. Single‐crystalline TiO2 nanorod (NR) arrays are used as ETL and methylammonium lead iodide (MAPI) as light absorber. A dual ETL surface modification is investigated, namely by a TiCl4 treatment combined with a subsequent PC61BM monolayer deposition, and the effects on the device photovoltaic performance were evaluated with respect to single modifications. Under optimized conditions, for the combined treatment synergistic effects are observed that lead to remarkable enhancements in cell efficiency, from 14.2% to 19.5%, and to suppression of hysteresis. The devices show JSC, VOC, and fill factor as high as 23.2 mA cm?2, 1.1 V, and 77%, respectively. These results are ascribed to a more efficient charge transfer across the ETL/perovskite interface, which originates from the passivation of defects and trap states at the ETL surface. To the best of our knowledge, this is the highest cell performance ever reported for TiO2 NR‐based solar cells fabricated with conventional MAPI light absorber. Perspective wise, this ETL surface functionalization approach combined with more recently developed and better performing light absorbers, such as mixed cation/anion hybrid perovskite materials, is expected to provide further performance enhancements. 相似文献
5.
The performance of perovskite solar cells (PSCs) is extremely dependent on morphology and crystallinity of perovskite film. One of the most effective methods to achieve high performance perovskite solar cells has been to introduce additives that serve as dopants, crystallization or passivation agents. Herein a facile strategy by introducing methylammonium chloride (MACl) and polar solvent N,N-Dimethylformamide (DMF) as co-additives in two-step sequential method is proposed to realize high quality perovskite film. It is demonstrated that DMF facilitates methylammonium iodide (MAI) penetrating easily into PbI2 layer to form highly crystalized perovskite film with uniform morphology which is essential to achieve high VOC. While MACl induces MAPbI3 to crystallize in a pure α-phase and suppress non-photovoltaic phase, which guarantees high FF. Pure α-phase perovskite film with uniform morphology can be achieved by adopting MACl and DMF together and the corresponding solar cell illustrates a power conversion efficiency (PCE) of 19.02% with substantially promoted durability. Moreover, A VOC as high as 1.181 V is succeeded for MAPbI3 based solar cell benefiting from the synergistic effect. 相似文献
6.
Yoo Min Shin Ji Hyeon Lee Geon Yeong Kim Hae Mee Ju Yeon Sik Jung Jea Woong Jo Min-Jae Choi 《Advanced functional materials》2023,33(4):2210155
1D perovskite materials are of significant interest to build a new class of nanostructures for electronic and optoelectronic applications. However, the study of colloidal perovskite nanowires (PNWs) lags far behind those of other established perovskite materials such as perovskite quantum dots and perovskite thin films. Herein, a dual-phase passivation strategy to synthesize all-inorganic PNWs with minimized surface defects is reported. The local phase transition from CsPbBr3 to CsPb2Br5 in PNWs increases the photoluminescence quantum yield, carrier lifetime, and water-resistivity, owing to the energetic and chemical passivation effect. In addition, these dual-phase PNWs are employed as an interfacial layer in perovskite solar cells (PSCs). The enhanced surface passivation results in an efficient carrier transfer in PSCs, which is a critical enabler to increase the power conversion efficiency (PCE) to 22.87%, while the device without PNWs exhibits a PCE of 20.74%. The proposed strategy provides a surface passivation platform in 1D perovskites, which can lead to the development of novel nanostructures for future optoelectronic devices. 相似文献
7.
Yong Hui Yan-Yan Tan Liang Chen Zi-Ang Nan Jian-Zhang Zhou Jia-Wei Yan Bing-Wei Mao 《Advanced functional materials》2021,31(36):2103894
Witnessed by the rapid increase of power conversion efficiency to 25.5%, organic–inorganic hybrid perovskite solar cells (PSCs) are becoming promising candidates of next-generation photovoltaics. However, PSCs can be unstable under the influence of light and bias. Especially, grain boundaries (GBs) are vulnerable to attack by light and bias in perovskite films, leading to degradation of photovoltaic properties of PSCs. Herein, photocurrent atomic force microscopy and Kelvin probe force microscopy are employed to systematically investigate the bias-dependent charge transport behaviors and stability of (FAPbI3)0.85(MAPbBr3)0.15 perovskite under working condition. Bias-dependent morphology and photocurrent images show irreversible decomposition of the perovskite at a bias of 0.1 V or below, which is accelerated by light illumination, leading to formation of an interfacial layer that restricts carrier transport. Meanwhile, GBs appear to enhance carrier transport at larger bias, but serve as breakthrough sites for perovskite decomposition at smaller bias. Introducing excess methylammonium iodide promotes decomposition, while potassium iodide passivation greatly relieves the decomposition. These results support the ion migration mechanism of decomposition through interfaces and GBs. This work provides a deeper understanding of bias-induced degradation of PSCs as well as bias-dependent double-edged roles of GBs, and forms valuable guidance for appropriate operation of PSCs. 相似文献
8.
Shuangjie Wang Zhen Li Yuanyuan Zhang Xingrui Liu Jian Han Xuanhua Li Zhike Liu Shengzhong Liu Wallace C. H. Choy 《Advanced functional materials》2019,29(15)
Despite being a promising candidate for next‐generation photovoltaics, perovskite solar cells (PSCs) exhibit limited stability that hinders their practical application. In order to improve the humidity stability of PSCs, herein, a series of ionic liquids (ILs) “1‐alkyl‐4‐amino‐1,2,4‐triazolium” (termed as RATZ; R represents alkyl chain, and ATZ represents 4‐amino‐1,2,4‐triazolium) as cations are designed and used as additives in methylammonium lead iodide (MAPbI3) perovskite precursor solution, obtaining triazolium ILs‐modified PSCs for the first time (termed as MA/RATZ PSCs). As opposed to from traditional methods that seek to improve the stability of PSCs by functionalizing perovskite film with hydrophobic molecules, humidity‐stable perovskite films are prepared by exploiting the self‐assembled monolayer (SAM) formation of water‐soluble triazolium ILs on a hydrophilic perovskite surface. The mechanism is validated by experimental and theoretical calculation. This strategy means that the MA/RATZ devices exhibit good humidity stability, maintaining around 80% initial efficiency for 3500 h under 40 ± 5% relative humidity. Meanwhile, the MA/RATZ PSCs exhibit enhanced thermal stability and photostability. Tuning the molecule structure of the ILs additives achieves a maximum power conversion efficiency (PCE) of 20.03%. This work demonstrates the potential of using triazolium ILs as additives and SAM and molecular design to achieve high performance PSCs. 相似文献
9.
Yuhong Zhang Lin Xu Yanjie Wu Huan Zhang Fancong Zeng Jiahe Xing Bin Liu Yu Qi Biao Dong Xue Bai Hongwei Song 《Advanced functional materials》2023,33(17):2214102
Introducing excess PbI2 has proven to be an effective in situ passivation strategy for enhancing efficiency of perovskite solar cells (PSCs). Nevertheless, the photoinstability and hysteresis are still tough issues owing to the photolysis nature of PbI2. Moreover, the humidity-related degradation of perovskite films is also a difficult territory to cover in such an in situ passivation strategy. Herein, a synergistic strategy is reported via initiatively inducing vertical graded PbI2 distribution (GPD) in the whole perovskite film and capping a cis-Ru(H2dcbpy)(dnbpy)(NCS)2 (Z907) internal encapsulation (IE) layer on the surface to ameliorate the above issues. The GPD design can enhance luminescence, prolong carrier lifetimes, ascertaining the improvement of efficiency and elimination of photoinstability in the PSCs. Besides, the introduced IE layer not only can promote the moisture and thermal resistance, but also inhibit Pb leakage and ion migration in the PSCs. Through the synergetic regulations, the resultant PSCs exhibit an impressive open circuit voltage (VOC) of 1.253 V, fill factor of 81.25%, and power conversion efficiency (PCE) of 24.28%. Moreover, the PSCs maintain 91% of its initial PCE at relative humidity of 85% after 500 h aging and 94% under continuous heating at 85 °C after 750 h aging. 相似文献
10.
An Interdiffusion Method for Highly Performing Cesium/Formamidinium Double Cation Perovskites 下载免费PDF全文
Weiming Qiu Aniruddha Ray Manoj Jaysankar Tamara Merckx Joao P. Bastos David Cheyns Robert Gehlhaar Jef Poortmans Paul Heremans 《Advanced functional materials》2017,27(28)
The fabrication of high‐quality cesium (Cs)/formamidinium (FA) double‐cation perovskite films through a two‐step interdiffusion method is reported. Csx FA1‐x PbI3‐y(1‐x )Bry(1‐x ) films with different compositions are achieved by controlling the amount of CsI and formamidinium bromide (FABr) in the respective precursor solutions. The effects of incorporating Cs+ and Br? on the properties of the resulting perovskite films and on the performance of the corresponding perovskite solar cells are systematically studied. Small area perovskite solar cells with a power conversion efficiency (PCE) of 19.3% and a perovskite module (4 cm2) with an aperture PCE of 16.4%, using the Cs/FA double cation perovskite made with 10 mol% CsI and 15 mol% FABr (Cs0.1FA0.9PbI2.865Br0.135) are achieved. The Cs/FA double cation perovskites show negligible degradation after annealing at 85 °C for 336 h, outperforming the perovskite materials containing methylammonium (MA). 相似文献
11.
Erpeng Li Enbing Bi Yongzhen Wu Weiwei Zhang Linchang Li Han Chen Liyuan Han He Tian Wei‐Hong Zhu 《Advanced functional materials》2020,30(7)
All organic charge‐transporting layer (CTL)‐featured perovskite solar cells (PSCs) exhibit distinct advantages, but their scaling‐up remains a great challenge because the organic CTLs underneath the perovskite are too thin to achieve large‐area homogeneous layers by spin‐coating, and their hydrophobic nature further hinders the solution‐based fabrication of perovskite layer. Here, an unprecedented anchoring‐based coassembly (ACA) strategy is reported that involves a synergistic coadsorption of a hydrophilic ammonium salt CA‐Br with hole‐transporting triphenylamine derivatives to acquire scalable and wettable organic hole‐extraction monolayers for p–i–n structured PSCs. The ACA route not only enables ultrathin organic CTLs with high uniformity but also eliminates the nonwetting problem to facilitate large‐area perovskite films with 100% coverage. Moreover, incorporation of CA‐Br in the ACA strategy can distinctly guarantee a high quality of electronic connection via the cations' vacancy passivation. Consequently, a high power‐conversion‐efficiency (PCE) of 17.49% is achieved for p–i–n structured PSCs (1.02 cm2), and a module with an aperture area of 36 cm2 shows PCE of 12.67%, one of the best scaling‐up results among all‐organic CTL‐based PSCs. This work demonstrates that the ACA strategy can be a promising route to large‐area uniform interfacial layers as well as scaling‐up of perovskite solar cells. 相似文献
12.
Binbin Luo Sara Bonabi Naghadeh A'Lester Allen Xueming Li Jin Z. Zhang 《Advanced functional materials》2017,27(6)
A new strategy has been developed using peptides with amino and carboxylic functional groups as passivating ligands to produce methyl ammonium lead bromide (CH3NH3PbBr3) perovskite nanocrystals (PNCs) with excellent optical properties. The well‐passivated PNCs can only be obtained when both amino and carboxylic groups are involved, and this is attributed to the protonation reaction between ? NH2 and ? COOH that is essential for successful passivation of the PNCs. To better understand this synergistic effect, peptides with different lengths have been studied and compared. Due to the polar nature of peptides, peptide‐passivated PNCs (denoted as PNCspeptide) aggregate and precipitate from nonpolar toluene solvent, resulting in a high product yield (≈44%). Furthermore, the size of PNCspeptide can be varied from ≈3.9 to 8.6 nm by adjusting the concentration of the peptide, resulting in tunable optical properties due to the quantum confinement effect. In addition, CsPbBr3 PNCs are also synthesized with peptides as capping ligands, further demonstrating the generality and versatility of this strategy, which is important for generating high quality PNCs for photonics applications including light‐emitting diodes, optical sensing, and imaging. 相似文献
13.
Kaicheng Zhang Andrej Vincze Ezzeldin Metwalli Jiyun Zhang Chao Liu Wei Meng Boxue Zhang Jingjing Tian Thomas Heumueller Zhiqiang Xie Junsheng Luo Andres Osvet Tobias Unruh Larry Lüer Ning Li Christoph J. Brabec 《Advanced functional materials》2023,33(42):2303455
Mixed lead and tin (Pb/Sn) hybrid perovskites exhibit a great potential in fabricating all-perovskite tandem devices due to their easily tunable bandgaps. However, the energy deficit and instability in Pb/Sn perovskite solar cells (PSCs) constrain their practical applications, which renders defect passivation engineering indispensable to develop highly efficient and long-term stable PSCs. Herein, the mechanisms of strain tailoring and defect passivation in Pb/Sn PSCs by 2D ligands are investigated. The 2D ligands include electroneutral cations with long alkyl chain (LAC), iodates with relatively short alkyl chain (SAC) and their mixtures. This study reveals that LAC ligands facilitate the relaxation of tensile strain in perovskite films while SAC ligands cause strain buildup. By mixing LAC/SAC ligands, tensile strain in perovskite films can be balanced which improves solar cell performance. PSCs with admixed β-guanidinopropionic acid (GUA)/phenethylammonium iodide (PEAI) exhibit enhanced open circuit voltage and fill factor, which is attributed to reduced nonradiative recombination losses in the bulk and at the interfaces. Furthermore, the operational stability of PSCs is slightly improved by the mixed 2D ligands. This work reveals the mechanisms of 2D ligands in strain tailoring and defect passivation toward efficient and stable narrow-bandgap PSCs. 相似文献
14.
Yong‐Heng Jia Stefanie Neutzner Yang Zhou Ming Yang Jetsabel Maria Figueroa Tapia Nan Li Hui Yu Jie Cao Jian‐Pu Wang Annamaria Petrozza Ching‐Ping Wong Ni Zhao 《Advanced functional materials》2020,30(1)
Introducing extensively excess ammonium halides when forming perovskites has recently been demonstrated as an effective approach to improve the performance of perovskite light‐emitting diodes (PeLEDs). Here, Cs0.17FA0.83PbI2.5Br0.5 is used as a model system to elucidate the impact of introducing excess formamidinium iodide (FAI) on the crystallization process of the perovskite film and operation of the corresponding PeLED. The excess FAI ratio is varied from 0 to 120 mol% and the crystallization process of the perovskite through in situ absorbance, in situ photoluminescence, and ex situ X‐ray diffraction measurements is systematically monitored. The results suggest that excess FAI triggers formation of a compact wide‐bandgap intermediate phase in the as‐deposited film, which then transforms to isolated and highly crystalline perovskite grains upon annealing. Using excitation correlation photoluminescence spectroscopy it is found that excess FAI results in a lower density of deep trap states and therefore a reduction of nonradiative losses in the material. This leads to a greatly enhanced maximum external quantum efficiency (EQE) from 0.25% (stoichiometric) to 12.7% (90 mol% excess). Furthermore, the FAI‐excess perovskite film is optimized with Pb(SCN)2 and 5‐ammonium valeric acid iodide additives and achieve a record radiance of 965 W Sr?1 m?2 for near‐infrared PeLEDs and a high EQE of 17.4%. 相似文献
15.
Susanne T. Birkhold Eugen Zimmermann Tom Kollek Daniel Wurmbrand Sebastian Polarz Lukas Schmidt‐Mende 《Advanced functional materials》2017,27(6)
Despite their outstanding photovoltaic performance, organic–inorganic perovskite solar cells still face severe stability issues and limitations in their device dimension. Further development of perovskite solar cells therefore requires a deeper understanding of loss mechanisms, in particular, concerning the origin and impact of trap states. Here, different surface properties of submicrometer sized CH3NH3PbI3 particles are studied as a model system by photoluminescence spectroscopy to investigate the impact of the perovskite crystal surface on photoexcited states. Comparison of single crystals with either isolating or electron‐rich surface passivation indicates the presence of positively charged surface trap states that can be passivated in case of the latter. These surface trap states cause enhanced nonradiative recombination at room temperature, which is a loss mechanism for solar cell performance. In the orthorhombic phase, the origin of multiple emission peaks is identified as the recombination of free and bound excitons, whose population ratio critically depends on trap state properties. The dynamics of exciton trapping at 50 K are observed on a time‐scale of tens of picoseconds by a simultaneous population decrease and increase of free and bound excitons, respectively. These results emphasize the potential of surface passivation to further improve the performance of perovskite solar cells. 相似文献
16.
A Universal Strategy to Utilize Polymeric Semiconductors for Perovskite Solar Cells with Enhanced Efficiency and Longevity 下载免费PDF全文
Fangchao Li Jianyu Yuan Xufeng Ling Yannan Zhang Yingguo Yang Sin Hang Cheung Carr Hoi Yi Ho Xingyu Gao Wanli Ma 《Advanced functional materials》2018,28(15)
In this contribution, a facile and universal method is successfully reported to fabricate perovskite solar cells (PSCs) with enhanced efficiency and stability. Through dissolving functional conjugated polymers in antisolvent chlorobenzene to treat the spinning CH3NH3PbI3 perovskite film, the resultant devices exhibit significantly enhanced efficiency and longevity simultaneously. In‐depth characterizations demonstrate that thin polymer layer well covers the top surface of perovskite film, resulting in certain surface passivation and morphology modification. More importantly, it is shown that through rational chemical modification, namely molecular fluorination, the air stability and photostability of the perovskite solar cells are remarkably enhanced. Considering the vast selection of conjugated polymer materials and easy functional design, promising new results are expected in further enhancement of device performance. It is believed that the findings provide exciting insights into the role of conjugated polymer in improving the current perovskite‐based solar cells. 相似文献
17.
Shiheng Wang Huaiqing Luo Zhenkun Gu Rudai Zhao Lutong Guo Na Wang Yunjie Lou Qun Xu Shou Peng Yiqiang Zhang Yanlin Song 《Advanced functional materials》2023,33(26):2214834
The two-step sequentially deposition strategy has been widely used to produce high-performance FAPbI3-based solar cells. However, due to the rapid reaction between PbI2 and FAI, a dense perovskite film forms on top of the PbI2 layer immediately and blocks the FAI diffusion into the bottom of the PbI2 film for a complete reaction, which results in a low-efficiency and limited reproducibility of perovskite solar cells (PSCs). Here, high-quality α-FAPbI3 perovskite films by crystal growth regulation with 4-fluorobenzamide additives is fabricated. The additives can interact with FAI to suppress the fast reaction between the FAI and PbI2 and effectively passivate the under-coordinated Pb2+ or I- defects. As a result, α-FAPbI3 perovskite films with low trap density and large grain size are prepared. The modified PSCs present a high-power conversion efficiency of 24.08%, maintaining 90% of their initial efficiency after 1400 h in high humidity. This study provides an efficient strategy of synergistic crystallization and passivation to form high-quality α-FAPbI3 films for high-performance PSCs. 相似文献
18.
Hongrui Sun Sanlong Wang Shanshan Qi Pengyang Wang Renjie Li Biao Shi Qixing Zhang Qian Huang Shengzhi Xu Ying Zhao Xiaodan Zhang 《Advanced functional materials》2023,33(23):2213913
Inorganic perovskite solar cells (IPSCs) have developed rapidly due to their good thermal stability and the bandgap suitable for perovskite/silicon tandem solar cells. However, the large open-circuit voltage (VOC) deficit derived from the surface defects and the energy level structure mismatch impede the development of device performance, especially in the P-I-N structure IPSCs. Herein, an innovative in situ etching (ISE) treatment method is proposed to reduce surface defects through methanol without additional passivator. It is found that the perovskite films treated with methanol result in a slight excess of PbI2 on the surface and inserted into the grain boundaries. Therefore, the successful decrease of surface defects by methanol and the passivation of grain boundary defects by PbI2 greatly reduce the trap density of perovskite films. And the larger work function of PbI2 contributes to the energy band of perovskite surface bending downward and forms gradient energy level alignment at the I/N interface, which accelerates extraction of charge carriers. As a result, the efficiency of CsPbI2.85Br0.15 inverted IPSC is enhanced from 16.00% to 19.34%, which is one of the mostly efficient IPSCs. This work provides an original idea without additional passivator to manage the defects of inorganic perovskite. 相似文献
19.
Efficient 4,4′,4″‐tris(3‐methylphenylphenylamino)triphenylamine (m‐MTDATA) Hole Transport Layer in Perovskite Solar Cells Enabled by Using the Nonstoichiometric Precursors 下载免费PDF全文
《Advanced functional materials》2018,28(36)
To overcome the drawbacks of the acidic and hygroscopic nature of the poly(3,4‐ethylenedio‐xythiophene):poly(styrenesulfonate) hole transport layer (HTL), the p‐type polymeric hole transport materials have attracted great attention and have been applied into perovskite solar cells. Here, a starburst amine molecule 4,4′,4″‐tris(3‐methylphenylphenylamino)triphenylamine (m‐MTDATA) without any additive is demonstrated as an effective hole transport material in perovskite solar cells. Meanwhile, considering the different surface affinity of precursor's composition on m‐MTDATA, the influence of the molar ratios between lead iodine (PbI2) and methylammonium iodide in precursor solution on the perovskite characteristics and device performance is investigated in‐depth. Ultimately, an enhanced efficiency of 17.73% and a high fill factor of 79.6% are achieved, which attribute to the strong passivation effect of traps and small resistance loss from appropriate unreacted PbI2 left in the perovskite layer. This work not only provides a remarkable HTL, but also reveals that the adjustment of precursor ratio is necessary for the one‐step solution approach, because the affinities of precursor's composition may be different with the underlying transport layers. 相似文献
20.
Anurag Krishna Mohammad Ali Akhavan Kazemi Michel Sliwa G. N. Manjunatha Reddy Laurent Delevoye Olivier Lafon Alexandre Felten Mai Trang Do Sbastien Gottis Frdric Sauvage 《Advanced functional materials》2020,30(13)
Improving the performances of photovoltaic (PV) devices by suppressing nonradiative energy losses through surface defect passivation and enhancing the stability to the level of standard PV represents one critical challenge for perovskite solar cells. Here, reported are the advantages of introducing a tetrapropylammonium (TPA+) cation that combines two key functionalities, namely surface passivation of CH3NH3PbI3 nanocrystals through strong ionic interaction with the surface and bulk passivation via formation of a type I heterostructure that acts as a recombination barrier. As a result, nonencapsulated perovskite devices with only 2 mol% of TPA+ achieve power conversion efficiencies over 18.5% with higher VOC under air mass 1.5G conditions. The devices fabricated retain more than 85% of their initial performances for over 1500 h under ambient conditions (55% RH ± 5%). Furthermore, devices with TPA+ also exhibit excellent operational stability by retaining over 85% of the initial performance after 250 h at maximum power point under 1 sun illumination. The effect of incorporation of TPA+ on the structural and optoelectronic properties is studied by X‐ray diffraction, ultraviolet–visible absorption spectroscopy, ultraviolet photon–electron spectroscopy, time‐resolved photoluminescence, and scanning electron microscopy imaging. Atomic‐level passivation upon addition of TPA+ is elucidated employing 2D solid‐state NMR spectroscopy. 相似文献