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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Thiourea with sulfur-donor as an effective additive for enhanced performance of lead-free double perovskite photovoltaic cells

Xiaoqing Yang,Huimin Xiang,Jianying Huang,Chuan Zhou,Ran Ran,Wei Wang,Wei Zhou,Zongping Shao

Lead-free inorganic Cs 2 AgBiBr 6 double perovskites have emerged as promising materials in perovskite solar cells (PSCs) to tackle the inferior stability and toxicity issues of organic–inorganic hybrid PSCs. However, the power conversion efficiencies (PCEs) of Cs 2 AgBiBr 6 solar cells are remarkably restricted by the intrinsic and extrinsic defects of Cs 2 AgBiBr 6 films. More specifically, the fast crystallization process in the formation of Cs 2 AgBiBr 6 films strongly prevents the homogeneous growth of perovskite crystals, leading to inferior Cs 2 AgBiBr 6 film quality. This work introduces a facile strategy to retard the crystallization of Cs 2 AgBiBr 6 perovskites by introducing Lewis base additives into the precursor solution. The incorporation of a strongly coordinated thiourea additive with a sulfur donor leads to the generation of a Lewis acid base adduct, which retards the crystallization process for Cs 2 AgBiBr 6 crystals, improves the quality of the Cs 2 AgBiBr 6 film, decreases the defect density and inhibits charge carrier recombination. After optimization, the cell delivers a superior PCE of 3.07%, surpassing that reported for most Cs 2 AgBiBr 6 -based solar cells in the literature, and exhibits outstanding stability with a PCE retention rate of 95% after 20 days of storage in air. This work provides an effective strategy for further improvements in the performance of inorganic lead-free Cs 2 AgBiBr 6 -based photovoltaic cells .

研究领域: 材料科学 · 能源科学
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2020 ·Vol. 20 ·期 2 ·1008-1012 · IF 1.134

Cesium-Containing Methylammonium Lead Iodide Light Absorber for Planar Perovskite Solar Cells

Zhao Xiao-Chong,Wu Dong-Xue,Yang Li-Jun,Tang Jun,Yue Guo-Zong,Yang Pan

Institute of Materials, Chinese Academy of Engineering Physics, Jiangyou 621908, P. R. China To improve the stability of organic–inorganic hybrid perovskite, cesium-containing methylammonium lead iodide perovskite have been synthesized by one-step solution deposition. With the increasing of Cs+ doping concentration, direct optical band gap of perovskite was increases, while defects and roughness of perovskite thin films were gradually augmented. A certain amount of Cs+ incorporated in perovskite absorb layer could improve power conversion efficiency through the enhancing of open circuit voltage and fill factor. However, excessive Cs+ doping concentration results in the reduced of short-circuit current and fill factor, which reduced power conversion efficiency. The optimized ratio 10% Cs+ doping achieved the highest power conversion efficiency (16.84%).

研究领域: 材料科学 · 能源工程
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ACS Nano · 2021 · IF 15.881

Efficiently Passivated PbSe Quantum Dot Solids for Infrared Photovoltaics

Sisi Liu,Kao Xiong,Kang Wang,Guijie Liang,Ming-Yu Li,Haodong Tang,Xiaokun Yang,Zhen Huang,Linyuan Lian,Manlin Tan,Kai Wang,Liang Gao,Haisheng Song,Daoli Zhang,Jianbo Gao,Xinzheng Lan,Jiang Tang,Jianbing Zhang

Infrared (IR) solar cells are promising devices for significantly improving the power conversion efficiency of common solar cells by harvesting the low-energy IR photons. PbSe quantum dots (QDs) are superior IR photon absorbing materials due to their strong quantum confinement and thus strong interdot electronic coupling. However, the high chemical activity of PbSe QDs leads to etching and poor passivation in ligand exchange, resulting in a high trap-state density and a high open circuit voltage (VOC) deficit. Here we develop a hybrid ligand co-passivation strategy to simultaneously passivate the Pb and Se sites; that is, halide anions passivate the Pb sites and Cd cations passivate the Se sites. The cation and anion hybrid passivation substantially improves the quality of PbSe QD solids, giving rise to an excellent trap-state control and prolonged carrier lifetime. A high VOC and a high short circuit current density (JSC) are achieved simultaneously in the IR QD solar cells based on this hybrid ligand treatment. Finally, a IR-PCE of 1.31% under the 1100-nm-filtered solar illumination is achieved in the PbSe QD solar cells, which is the highest IR-PCE for PbSe QD IR solar cells at present. Additionally, the PbSe QD devices show a high external quantum efficiency of 80% at ∼1295 nm.

研究领域: 材料科学 · 太阳能技术 · 纳米技术
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ACS Applied Energy Materials · 2021 · IF 6.024

CsPbI3 Perovskite Quantum Dot Solar Cells with Both High Efficiency and Phase Stability Enabled by Br Doping

Yueli Liu,Qitao Li,Wenchao Zhang,Zifan Yang,Sijie Zhao,Wen Chen

All-inorganic CsPbI3 perovskite quantum dots (QDs) have attracted great attention since emerging as a new class of materials with superior light-harvesting properties and enhanced thermal stability compared to organic–inorganic hybrid perovskites. However, poor phase stability remains a bottleneck for practical applications. In the present work, CsPb(I1–xBrx)3 perovskite QDs are synthesized by Br doping to increase the tolerance factor for the improvement of phase stability, and the balance between the stability of solar cells and the power conversion efficiency (PCE) is considered by adjusting the Br doping content. It is found that the phase stability of CsPb(I1–xBrx)3 QDs is much improved, while their band gap increases from 1.77 to 1.89 eV when the Br doping content increases from 0 to 30%. CsPbI2.4Br0.6 QD-based perovskite solar cells (PSCs) achieve a proper balance between high PCE and stability; the PCE is 12.31%, approaching that of the CsPbI3-based PSCs (14.13%), and may retain 87% of the initial efficiency after 15 days of storage in ambient air.

研究领域: 材料科学 · 光伏技术
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JOURNAL OF MATERIALS SCIENCE · 2017 ·Vol. 52 ·期 22 ·13203-13211 · IF 2.599

Large enhanced conversion efficiency of perovskite solar cells by CsBr doping

Zhang Li-Ying,Zhang Yong,Guan Wei-Bao,Wang Ke-Fan,Cheng Zhen-Xiang,Wang Yuan-Xu

Perovskite solar cells single-doped with Br − or Cs + ions have been proved to be an effective approach to improve their efficiency and stability. In our work, we took advantage of co-doping with Br − and Cs + . At our studied doping levels from CH 3 NH 3 I:PbI 2 :CsBr = 1:1:0 ( x  = 0) to 0.85:1:0.15 ( x  = 0.15), CsBr doping does not introduce any detectable impurity, and the crystal grains grow larger with increasing CsBr doping level. Furthermore, when the CsBr doping level is less than x  = 0.1, it can progressively enhance the optical absorption of the perovskite film, although the absorption begins to decrease when the doping level rises above x  = 0.1. X-ray photoelectron spectroscopy measurements show that Br − has successfully replaced I − and bonds with Pb 2+ after CsBr doping. At the optimized doping level of x  = 0.1, the incorporation of CsBr in the reaction system can improve the morphology of perovskite films and greatly enhance the efficiency from 9.8% for undoped sample to 13.6%, better than single Br − or Cs + doping. Our result shows that CsBr doping is an effective method to enhance the efficiency of perovskite solar cells.

CAS / MDL: 68-12-2
研究领域: 材料科学 · 能源技术
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ACS Applied Materials & Interfaces · 2025 · IF 8.2

Influence of SrBr2 Doping on 4T CsPbBr3/Cs0.05(FA0.83MA0.17)0.95Pb(I0.83Br0.17)3 Tandem Device for Underwater Photovoltaic Applications

Huiren Zheng,Jize Wang,Junye Pan,Chunyang Zheng,Yuxin Zhang,Ankang Shu,Bin Li,Shaowen Cao,Yong Peng

Underwater photovoltaics plays a pivotal role in photovoltaic applications. However, the underwater solar spectrum differs significantly from that in air, and as water depth increases, solar spectra across various wavebands exhibit distinct attenuation rates. Specifically, the attenuation rate of the red component of sunlight is considerably higher than that of green and blue light (400–600 nm). Thus, under these unique spectral conditions, there is an urgent need to develop stable devices that minimize power conversion efficiency (PCE) loss with increasing water depth. The 4-terminal (4T) structure tandem cell, designed with 2.35 eV CsPbBr3 and 1.63 eV Cs0.05(FA0.83MA0.17)0.95Pb(I0.83Br0.17)3, is prioritized due to its suitable optical response range and low PCE loss with increasing water depth. As CsPbBr3 utilized blue and green light in tandem, which has the highest light intensity underneath water, this study employed doping of SrBr2 into the CsPbBr3 film. This approach reduced the defect density of the film, enhanced carrier transport efficiency, and improved the photoelectric responsivity of the device in the 425–500 nm band. The CsPbBr3 perovskite solar cells that were fabricated demonstrated a high open-circuit voltage of 1.46 V and an exceptional PCE of 7.62%. Additionally, these devices exhibited excellent stability. Consequently, the 4T tandem device achieved PCEs of 15.28, 11.79, and 10.33% at 0, 0.5, and 0.7 m underwater depths respectively, with a variation rate of only 32%. Furthermore, the device demonstrated remarkable stability under working conditions, with an efficiency decay of less than 13% after continuous irradiation for 30 days. These findings suggest that the 4T tandem solar cell holds considerable potential for application in underwater photovoltaics.

CAS / MDL: 10476-81-0 57-13-6
研究领域: 材料科学 · 能源技术 · 光电子学
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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2024 · IF 6.3

Enhancing the performance of CZTSSe solar cells via an alternate spin-coating process with DMSO and DMF

Yunjie Bai,Yiming Wang,Ruijian Liu,Yu He,Yuhao Zhang,Chu Liu,Hongmei Luan,Yanchun Yang,Chengjun Zhu

The CZTSSe absorber layer prepared with DMSO exhibits extensive cavities at its bottom, and a prominent double-layer structure is frequently observed within the CZTSSe absorber synthesized using DMF , both of which have a detrimental impact on the device performance. In this paper, an alternate spin-coating process using DMSO and DMF solvent systems is proposed, which eliminates the double-layer structure of CZTSSe and reduces the number of cavities at the bottom of the absorber layer, thereby enhancing its overall quality. This method outperforms the traditional single-solution spin-coating technique by combining the advantages of two solvent systems, allowing for the preparation of an ideal CZTSSe film without disturbing the elemental ratio, ultimately resulting in a single-layer absorber composed of large grains. After three repetitions of an identical alternate spin-coating process, the average grain size of the absorber layer increased from 0.83 to 1.21 μm. This innovative process leads to a reduction in carrier recombination and an improvement in the short-circuit current density, ultimately raising the photoelectric conversion efficiency from 7.40% to 8.88%.

研究领域: 材料科学 · 能源技术
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ACS Applied Materials & Interfaces · 2019 · IF 8.456

Lead Oxalate-Induced Nucleation Retardation for High-Performance Indoor and Outdoor Perovskite Photovoltaics

Chong Dong,Meng Li,Yue Zhang,Kai-Li Wang,Shuai Yuan,Femi Igbari,Yingguo Yang,Xingyu Gao,Zhao-Kui Wang,Liang-Sheng Liao

Perovskite solar cells have attracted worldwide attention as one of the key research areas in the field of thin-film photovoltaics. Although they exhibit easy solution processability, it is important to effectively control the crystallization of the light-absorbing layer, which affects the performance and stability of devices. Here, we present lead oxalate (PbC2O4) as a nonhalide lead constituent of the perovskite precursor solution, which contributes to anion replacement during thin film annealing. This strategy limits the perovskite nucleation rate and retards crystallization. As a result, we achieved excellent perovskite films with larger grains and fewer defects. The open-circuit voltage of the optimal device under 1 sun illumination rose to 1.12 V with a power conversion efficiency (PCE) of 20.20%. In addition, the indoor PCE at 1000 lux can reach 34.86%. This nonhalide lead compound dopant provides a guide for the crystallization of perovskite materials and paves a way for the fabrication of nonhalide perovskite solar cells.

CAS / MDL: 814-94-8
研究领域: 材料科学 · 能源科学
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CHEMISTRY OF MATERIALS · 2016 · IF 9.407

Improving the Performance of Solution-Processed Cu2ZnSn(S,Se)4 Photovoltaic Materials by Cd2+ Substitution

Jie Fu,Qingwen Tian,Zhengji Zhou,Dongxing Kou,Yuena Meng,Wenhui Zhou,Sixin Wu

Additional elements in the Cu2ZnSn(S,Se)4 (CZTSSe) absorber layers can play a crucial role in improving the performance of thin film solar cells. In this paper, a significant performance enhancement of CZTSSe thin film solar cells was achieved by the partial substitution of the Zn2+ cation with Cd2+. A small amount of Cd2+ can be successfully incorporated into the host lattice of CZTSSe to form a homogeneous Cu2Zn1–xCdxSn(S,Se)4 (CZCTSSe) alloy material. We demonstrated that the crystal growth and the band gap of CZCTSSe thin films are affected by the Cd doping level. Additionally, the impact of Cd content on the space-charge density (Nc-v) and the depletion width (Wd) of CZCTSSe solar cells was systematically investigated. By this cation substitution approach, the power conversion efficiency of the solar cells based on the CZCTSSe absorber was successfully increased from 5.41 to 8.11% for the optimal composition (x = 5%).

研究领域: 材料科学 · 光伏技术 · 半导体物理
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JOURNAL OF MOLECULAR STRUCTURE · 2025 · IF 4.7

Electron-withdrawing effect of carboxyl-functionalized CNT on the triiodide reduction of ZnIn2S4 in dye-sensitized solar cells

Qing Wang,Changcheng Lin,Xinyi He,Hui Zhang,DongMeng Chen,Shaowei Jin,Xueqin Zuo

This study presents a straightforward yet effective one-step hydrothermal method for the homogeneous deposition of ZnIn 2 S 4 (ZIS) onto carbon nanotubes (CNT), resulting in the formation of a unique plum-blossom ZIS@CNT heterostructure composite. The heterostructure formed between ZIS and CNT not only constructs an efficient electron transfer channel, but also provides an appropriate driving force for the transfer of electrons to active sites through the electron-withdrawing effect of carboxyl groups. When the ZIS@CNT composite was utilized as the counter electrode (CE) in a dye-sensitized solar cell (DSSC), the resulting DSSC exhibited an extremely high photoelectric conversion efficiency (PCE) of 9.35 %, which is 27.73 % higher than that of based on the traditional Pt CE (7.32 %). This study provides a new idea for the application of carbon nanomaterials and ZIS in DSSCs, and reveals the reasons for the excellent PCE of ZIS@CNT from the perspective of interface charge distribution.

CAS / MDL: 10196-18-6 22519-64-8
研究领域: 材料科学 · 纳米技术 · 太阳能电池
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Small · 2025 · IF 12.1

Dual-Source Evaporation Processed Novel NaBiS2 Absorber Material for Eco-Friendly and Stable Photovoltaics

Zijun Yi,Long Zhang,Wenguang Zhang,Yihuai Huang,Yuchen Xiong,Changkai Huang,Guibin Shen,Abdul Basit,Xuehong Ren,Yubo Luo,Xin Li,Junyou Yang

Exploring and developing novel, low-cost, and environmentally friendly photovoltaic materials is a vital trend in the evolution of solar cell technology. The distinctive properties of alkali bismuth ternary sulfides have spurred increased research and application in optoelectronic devices. In this study, a novel method is reported for preparing NaBiS 2 film by sequential thermal evaporation of Na 2 S and Bi 2 S 3 layers followed by heating post-treatment for the first time, as well as the preparation of solar cells with NaBiS 2 as the light-absorbing layer. Based on X-ray diffraction and Raman analysis, the prepared NaBiS 2 film is confirmed to be a single-phase material, without the presence of any secondary phases. Additionally, the photoelectric characteristics of NaBiS 2 are investigated and incorporated this material into solar cell devices. By optimizing the device architecture, the solar cell utilizing NaBiS 2 as the light-absorbing layer achieved a photoelectric conversion efficiency of 2.91%, which is the highest efficiency reported for NaBiS 2 solar cells up to now. The research has provided a valuable perspective and path for the development of novel photovoltaic materials in the solar cell field.

CAS / MDL: 1345-07-9 1313-82-2
研究领域: 材料科学 · 光伏技术 · 能源研究
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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2024 · IF 6.3

Synthesized Cs-rich Cs0.7FA0.3PbI2Br perovskite film by two-dimensional to three-dimensional phase transition

Xueting Zhang,Jicheng Zhang,Nan Tian,Zhaoxuan Huang,Shiyu Duan,Jilin Wang,Disheng Yao,Guoyuan Zheng,Yanhan Yang,Bing Zhou,Fei Long

Stability of perovskite is the main limitation of the commercialization of perovskite solar cells . Recent studies have shown that FA-Cs perovskites are expected to achieve ideal crystal structures with outstanding stability when FA content is 30 %. And its bandgap can be adjusted to 1.8 eV, making it suitable for a top battery in the tandem cell. However, when the content of Cs ions in the component exceeds 30 %, phase separation occurs. In this study, a Cs-rich Cs 0.7 FA 0.3 PbI 2 Br perovskite film was synthesized by using a 2D to 3D phase transition method. Through the high orientation of the 2D CsPbI 3 -FAI alloy-like phase and the anisotropic volatilization of FA, a well-oriented α-Cs 0.7 FA 0.3 PbI 2 Br perovskite phase is obtained. The α-Cs 0.7 FA 0.3 PbI 2 Br shows excellent thermal and UV stability and improved humidity stability. Meanwhile, the fabricated Cs 0.7 FA 0.3 PbI 2 Br perovskite solar cell achieved a competitive power conversion efficiency of 14.87 % successfully breaking the world record for this perovskite system. This further advances the research progress of Cs-rich perovskites in highly efficient and stable solar cells.

CAS / MDL: 7550-45-0
研究领域: 材料科学 · 能源研究
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