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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Ionic Liquids Modulating CsPbI3 Colloidal Quantum Dots Enable Improved Mobility for High-Performance Solar Cells

Rui Han,Qian Zhao,Abhijit Hazarika,Juan Li,Hongkun Cai,Jian Ni,Jianjun Zhang

Colloidal all-inorganic CsPbI3 perovskite quantum dots (PQDs) have shown tremendous potential in photovoltaic applications in recent years due to their outstanding optoelectronic properties that general metal halide perovskites offer, along with the added advantages that originates from size reduction and the quantum confinement effect. However, the issue of low carrier mobility in PQD films caused by insulating organic ligands capped on the PQD surface still remains to be addressed while aiming for high-efficiency PQD solar cells. Herein, we propose a novel strategy that takes benefits of ionic liquids, which can offer the high polarity and the electron donating ability to boost the mobility of PQD films in photovoltaic devices. Specifically, 1-propyl-3-methylimidazolium iodide to modulate the colloidal CsPbI3 PQD surface and couple QDs is demonstrated for the first time. The lone pair electrons on the nitrogen of the imidazole ring within the ionic liquid binds to the empty nonbonding surface orbitals of CsPbI3 PQDs while the long-chain insulating ligands are replaced, which enables not only efficient charge transport but also reduced defect density in the assembled PQD solid films. The resulting CsPbI3 PQD solar cell shows a significant increase in efficiency with suppressed hysteresis, indicating the impressive potential of this strategy for developing highly efficient PQD solar cells.

研究领域: 材料科学 · 能源科学 · 纳米技术
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CHEMISTRY OF MATERIALS · 2022 · IF 10.508

Selectively Fluorinated Benzylammonium-Based Spacer Cation Enables Graded Quasi-2D Perovskites for Efficient and Stable Solar Cells

Guijun Yan,Guomin Sui,Wentao Chen,Kuo Su,Yaqing Feng,Bao Zhang

It is an effective strategy to improve the performance of quasi-two-dimensional (Q-2D) perovskite solar cells (PSCs) by introducing fluoro-substituted aromatic alkylammonium spacer cations into the active layer. Herein, the influence of the benzylammonium (BA) and the x-fluorobenzylammonium (xFBA) cation, in which x stands for the substitution position of the benzene ring (o, ortho; m, meta; p, para), on the crystal orientation, phase distribution, film morphology of the Q-2D (n = 5) perovskite films, and the corresponding device performance is systematically evaluated. The result suggests that compared with BA and oFBA, mFBA and pFBA have a larger dipole moment, forming a dense perovskite film with gradient structures where the n = 1 2D perovskite mainly exists at the top of the film and the large n-phase perovskite exists at the bottom of the film. Encouragingly, the (pFBA)2MA4Pb5I16 (MA = CH3NH3+)-based perovskite solar cells achieve the highest efficiency of 17.12%, with an open-circuit voltage of 1.175 V, a short-circuit current density of 18.50 mA cm–2, and a fill factor of 78.78%, which is significantly higher than those of BA (14.07%)-, oFBA (12.89%)-, and mFBA (14.67%)-based PSCs. Furthermore, pFBA-based devices also exhibit the best stability compared to the other three devices.

研究领域: 材料科学 · 能源技术
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Small · 2024 ·Vol. 20 ·期 35 ·2401330 · IF 13

Suppressing Deep-Level Trap Toward Over 13% Efficient Solution-Processed Kesterite Solar Cell

Yingfen Li,Yue Jian,Fang Huang,Nian Zhou,Wanqiu Chai,Juguang Hu,Jun Zhao,Zhenghua Su,Shuo Chen,Guangxing Liang

Cu 2 ZnSn (S,Se) 4 (CZTSSe), a promising absorption material for thin-film solar cells, still falls short of reaching the balance limit efficiency due to the presence of various defects and high defect concentration in the thin film. During the high-temperature selenization process of CZTSSe, the diffusion of various elements and chemical reactions significantly influence defect formation. In this study, a NaOH-Se intermediate layer introduced at the back interface can optimize Cu 2 ZnSnS 4 (CZTS)precursor films and subsequently adjust the Se and alkali metal content to favor grain growth during selenization. Through this back interface engineering, issues such as non-uniform grain arrangement on the surface, voids in bulk regions, and poor contact at the back interface of absorber layers are effectively addressed. This method not only optimizes morphology but also suppresses deep-level defect formation, thereby promoting carrier transport at both interfaces and bulk regions of the absorber layer. Consequently, CZTSSe devices with a NaOH-Se intermediate layer improved fill factor, open-circuit voltage, and efficiency by 13.3%. This work initiates from precursor thin films via back interface engineering to fabricate high-quality absorber layers while advancing the understanding regarding the role played by intermediate layers at the back interface of kesterite solar cells.

研究领域: 材料科学 · 能源科学
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JOURNAL OF MATERIALS SCIENCE · 2021 ·Vol. 56 ·期 10 ·6374-6384 · IF 4.22

Self-passivated hybrid perovskite films for improved photovoltaic performance of solar cells

Qi Xingnan,Zhang Tingting,Tan Furui,Mei Yantao,Huang Junyi,Yue Gentian,Gao Yueyue,Liu Rong,Dong Chen,Zhang Lisheng,Zhang Weifeng

Abstract Defect passivation management of perovskite films is of great importance in improving the performance of perovskite solar cells. Various in situ or post-passivation strategies were adopted to modify the optoelectric properties of perovskite films. However, these modifications increased the fabrication complexity and cost of the devices. Here, we developed a facile self-passivation strategy to effectively decrease charge trap states and suppress the non-radiative recombination loss in perovskite films. By simply aging the precursor solution, we found that the fabricated perovskite films possess residual PbI 2 phase that could decrease trap density, enhance the radiative recombination intensity, and facilitate charge transfer and collection. Therefore, the solar cells with this self-passivated perovskite film generated an increased efficiency of 21.1% compared to that of 19.9% for the control devices from fresh precursor solution. Graphical abstract

研究领域: 材料科学 · 光伏技术
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APPLIED SURFACE SCIENCE · 2025 · IF 6.9

In-situ growth of perovskite-type LaBO3 (B = Ni, Co, Fe, Mn) films by metal oleate route

Xin Liu,Liping Yang,Li Chen,Shuxia Li,Peng Li,Yongrong Sun,Ning Kang,Chenglong Wang

It is still challenged to propose a straightforward and in-situ growth method of fabricating perovskite-type metal oxide films with dense and uniform surface coverage. This paper presents a simple strategy to prepare LaBO 3 (where B = Ni, Co, Fe, Mn) films by metal oleate (MO) route, in which metal oleates (La(OA) 3 and (B(OA) x , x  = 2 or 3) serve as effective ligands to inhibit the self-aggregation among crystal grains. The as-prepared LaNiO 3 film with uniform and dense surface shows a reduced contact angle (31.5° vs 51.2°) and surface roughness (Ra = 14.2 vs 23.9 nm) compared with film prepared by Sol-gel (SG) method. Finally, the LaNiO 3 film by MO route is successfully employed as hole transport layer (HTL) in perovskite solar cells (PSCs) to obtain a power conversion efficiency (PCE) up to 15.62 %, which is 1.54 times that of PSCs by SG method. This work opens an avenue for fabricating LaBO 3 films with dense and uniform surface coverage by MO route.

CAS / MDL: 67-68-5 109-86-4 68-12-2
研究领域: 材料科学 · 能源科学
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Joule · 2022 · IF 46.048

Tailoring solvent-mediated ligand exchange for CsPbI3 perovskite quantum dot solar cells with efficiency exceeding 16.5%

Donglin Jia,Jingxuan Chen,Junming Qiu,Huili Ma,Mei Yu,Jianhua Liu,Xiaoliang Zhang

Inorganic CsPbI 3 perovskite quantum dot (PQD) shows high potential for new-generation photovoltaics due to its outstanding optoelectronic properties. However, the binding-energy-driven ligand exchange of PQDs limits the construction of conductive and stable PQD solids for efficient PQD solar cells (PQDSCs). Herein, protic 2-pentanol with superior ligand solubility is delicately screened from massive solvents to mediate the ligand exchange of PQDs due to its appropriate dielectric constant and acidity, which could maximize the removal of pristine insulating oleylamine ligands from the PQD surface without introducing halogen vacancy defects. Employing tailored short choline ligands and 2-pentanol solvent for the post-treatment of PQD solids, PQDSC yields an efficiency of 16.53%, which is the highest among inorganic PQDSCs. This outstanding performance is attributed to the improved charge carrier transport and surface defect passivation of PQDs. This work provides a feasible platform for tuning the surface properties of PQDs and paves the way for realizing high-performing optoelectronics.

研究领域: 材料科学 · 光伏技术 · 纳米科技
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Journal of Materials Chemistry A · 2021 ·Vol. 10 ·期 2 ·779-788 · IF 12.732

A high-efficiency (12.5%) kesterite solar cell realized by crystallization growth kinetics control over aqueous solution based Cu2ZnSn(S,Se)4

Kang Yin,Xiao Xu,Muyu Wang,Jiazheng Zhou,Biwen Duan,Jiangjian Shi,Dongmei Li,Huijue Wu,Yanhong Luo,Qingbo Meng

Crystallization growth plays a crucial role in influencing the film quality and final photoelectric conversion performance of a kesterite Cu2ZnSn(S,Se)4 (CZTSSe) solar cell. Herein, an exploration of a two-step selenization strategy to control the growth kinetics of an aqueous solution derived CZTSSe film for high solar cell efficiency is reported. By synergistically exploiting the benefits of high and low temperature selenization in facilitating the CZTSSe phase formation, introducing beneficial point defect states, configuring the interfacial energy band structure, and sustaining excellent surface microstructure, a total-area cell efficiency of 12.5% has been achieved. These results demonstrate the significance of controlling the crystallization growth of CZTSSe to improve the device performance. The high cell performance achieved here is comparable to that of hydrazine or dimethyl sulfoxide solution-based cells and thus would help facilitate the development of CZTSSe solar cells toward more diversified film fabrication technologies.

研究领域: 材料科学 · 可再生能源
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Frontiers in Chemistry · 2020 · IF 3.693

Trap-Filling of ZnO Buffer Layer for Improved Efficiencies of Organic Solar Cells

Li Mingguang,Li Jing,Yu Longsheng,Zhang Ying,Dai Yizhong,Chen Runfeng,Huang Wei

Trap-assisted recombination loss in the cathode buffer layers (CBLs) is detrimental to the electron extraction process and severely restricts the power conversion efficiencies (PCEs) of organic solar cells (OSCs). Herein, a novel organic–inorganic hybrid film composed of zinc oxide (ZnO) and 2,3,5,6-tetrafluoro-7,7,8, 8-tetracyanoquinodimethane (F4TCNQ) is designed to fill the intrinsic charge traps of ZnO-based CBLs by doping F4TCNQ for high-performance inverted OSCs. Thus, constructed ZnO:F4TCNQ hybrid film exhibits enhanced surface hydrophobicity and adjustable energy levels, providing favorable interfacial condition for electron extraction process. Consequently, trap-assisted recombination loss in the CBLs was efficiently suppressed, leading to the significantly improved fill factor and PCEs of both fullerene- and non-fullerene-based OSCs using the ZnO:F4TCNQ hybrid CBLs. This work illustrates a convenient organic acceptor doping approach to suppress the internal charge traps of traditional inorganic CBLs, which will shed new light on the fabrication of high-performance CBLs with facile electron extraction processes in inverted OSC devices.

研究领域: 材料科学 · 能源科学 · 光电转换
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ACS Applied Materials & Interfaces · 2016 · IF 7.145

High-Quality Perovskite Films Grown with a Fast Solvent-Assisted Molecule Inserting Strategy for Highly Efficient and Stable Solar Cells

Shuai Yuan,Zhiwen Qiu,Chaomin Gao,Hailiang Zhang,Yanan Jiang,Cuncheng Li,Jinghua Yu,Bingqiang Cao

The performance of organolead halide perovskites based solar cells has been enhanced dramatically due to the morphology control of the perovskite films. In this paper, we present a fast solvent-assisted molecule inserting (S-AMI) strategy to grow high-quality perovskite film, in which the methylammonium iodide/2-propanol (MAI/IPA) solution is spin-coated onto a dimethylformamide (DMF) wetted mixed lead halide (PbX2) precursor film. The DMF can help the inserting of MAI molecules into the PbX2 precursor film and provide a solvent environment to help the grain growth of the perovskite film. The perovskite film grown by the S-AMI approach shows large and well-oriented grains and long carrier lifetime due to the reduced grain boundary. Solar cells constructed with these perovskite films yield an average efficiency over 17% along with a high average fill factor of 80%. Moreover, these unsealed solar cell devices exhibit good stability in an ambient atmosphere.

CAS / MDL: 4733-39-5
研究领域: 材料科学 · 光伏技术 · 物理化学
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Nature Communications · 2021 ·Vol. 12 ·期 1 ·1-11 · IF 14.919

Implementing an intermittent spin-coating strategy to enable bottom-up crystallization in layered halide perovskites

Yan Yajie,Yang Yingguo,Liang Mingli,Abdellah Mohamed,Pullerits Tõnu,Zheng Kaibo,Liang Ziqi

Two-dimensional halide perovskites (2D PVSKs) have drawn tremendous attentions owing to their outstanding ambient stability. However, the random orientation of layered crystals severely impedes the out-of-plane carrier transport and limits the solar cell performance. An in-depth understanding coupled with an effective control of the crystallization in 2D PVSKs is the crux for highly efficient and durable devices. In this contribution, we accidentally discovered that the crystallization of 2D PVSKs can be effectively regulated by so-called ′intermittent spin-coating (ISC)′ process. Combined analyses of in(ex)-situ grazing-incidence wide-angle X-ray scattering with time-of-flight secondary ion mass spectrometry distinguish the interface initialized bottom-up crystallization upon ISC treatment from the bi-directional one in the conventional spin-coating process, which results in significantly enhanced crystal orientation and thus facilitated carrier transport as confirmed by both electrical measurements and ultrafast spectroscopies. As a result, the p-i-n architecture planar solar cells based on ISC fabricated paradigm PEA 2 MA 3 Pb 4 I 13 deliver a respectable efficiency of 11.2% without any treatment, which is three-fold improvement over their spin-coated counterparts and can be further boosted up to 14.0% by NH 4 Cl addition, demonstrating the compatibility of ISC method with other film optimization strategies.

研究领域: 材料科学 · 能源技术
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GREEN CHEMISTRY · 2020 ·Vol. 22 ·期 11 ·3597-3607 · IF 9.48

Boosting the efficiency of solution-based CZTSSe solar cells by supercritical carbon dioxide treatment

Hai-Qin Xiao,Wen-Hui Zhou,Dong-Xing Kou,Zheng-Ji Zhou,Yue-Na Meng,Ya-Fang Qi,Sheng-Jie Yuan,Qing-Wen Tian,Si-Xin Wu

Cu2ZnSn(S,Se)4 (CZTSSe) solar cells have been receiving considerable attention in recent years, owing to their low cost and toxicity as well as a high abundance of their constituent elements. Solution-based (mainly precursor solution) methods have been widely used in the fabrication of CZTSSe-based thin film solar cells. Though most record solar cells since 2009 have been achieved using solution-based methods, carbonaceous residues are always formed during post deposition treatment (PDT). These carbonaceous residues are detrimental to grain growth of CZTSSe to form large grains. The presence of unwanted small grain layers will increase the series resistance and reduce the fill factor of the solar cell, thus consequently decreasing the efficiency of CZTSSe solar cells. Herein, we propose “green” supercritical carbon dioxide (SCCO2) treatment to overcome the challenge of carbonaceous residues. FT-IR, SEM, XRD and Raman characterization studies were used to confirm the reduction of carbonaceous residues in CZTSSe films. The solar cell fabricated from a selenized CZTSSe precursor film with SCCO2 treatment under optimal conditions showed the best conversion efficiency of 11.23% (VOC = 0.456 V, JSC = 36.6 mA cm−2, FF = 67.1%). To the best of our knowledge, this is the first report on boosting the efficiency of solution-based CZTSSe solar cells by using SCCO2 treatment. In addition, this unique SCCO2 treatment may also bring forth new ideas for other solution-based optoelectronic devices.

研究领域: 材料科学 · 太阳能 · 纳米技术
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Laser & Photonics Reviews · 2025 · IF 10

Complete Reaction to Remove PbI2 Residue in Photovoltaic Perovskites

Namatullah Nizamani,Xin Chen,Yan-Hui Lou,Run-Jun Jin,Kai-Li Wang,Chun-Hao Chen,Jing Chen,Yu Xia,Lei Huang,Zhao-Kui Wang

In the pursuit of high-performance FAPbI 3 -based perovskite solar cells, the two-step sequential deposition method has garnered significant attention due to its superior control over film crystallization dynamics, critical for achieving uniform, and compact perovskite layers. However, the rapid reaction between PbI 2 and FAI often results in residual PbI 2 clusters, which accelerate the degradation of perovskite solar cells (PSCs). Herein, the dual-site molecular additive 1-aminonaphthalene-6-sulfonic acid (ANSA) is introduced to achieve fast nucleation and slow crystallization, thereby enabling the formation of high-quality FAPbI 3 perovskite films. ANSA coordinates with both PbI 2 and DMSO, facilitating the formation of an improved PbI 2 (DMSO) intermediate phase, enabling a more uniform and complete conversion of PbI 2 into the perovskite phase. Additionally, the amino and sulfonic acid functional groups of ANSA contribute to the passivation of undercoordinated Pb 2+ ions, thereby perovskite films with lower trap densities and larger grain sizes are achieved. Consequently, the power conversion efficiency (PCE) increases from 23.27% in the pristine device to 25.79% for the ANSA-treated device. Furthermore, device stability is significantly improved with the modified device retaining 95% of its original PCE after 1500 h of storage.

CAS / MDL: 119-79-9
研究领域: 材料科学 · 光伏技术 · 纳米材料 · 表面化学 · 能源材料
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