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Green N1 Additive Modified Perovskite Precursor Enables Effective Manufacturing of Large-Area Solar Cell Modules with High Efficiency and Stability

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SSRN 2023年

作者： Zang, Yue Shao, Tianxiang Jiao, Chuanjia Zhou, Peng Li, Wangnan Cheng, Jiahao Yang, Gaoyuan Tu, Yibo Ye, Jingchuan Li, Guodong Chu, Liang Lu, Shaojian Liang, Guijie Liang, Ying Wang, Jingyang Zhong, Zhicheng Hu, Run Yan, Wensheng Institute of Carbon Neutrality and New Energy School of Electronics and Information Hangzhou Dianzi University Hangzhou310018 China Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices Hubei University of Arts and Science Xiangyang441053 China Hubei Longzhong laboratory Xiangyang441000 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Hubei Institute of Aerospace Chemotechnology Xiangyang441003 China School of Energy and Power Engineering Huazhong University of Science and Technology Wuhan430074 China

Perovskite solar cells (PSCs) have been continuously breaking the solar photoelectric power conversion efficiency (PCE) record, while two long-standing challenges remain formidable on the practical commercialization path of PSCs, i.e. effective large-area manufacturing and high device operational stability. Here, we report a green additive of N-methyl-2-piperidone (N1) to modify the perovskite precursor, enabling the one-step mass manufacturing of high-quality large-area perovskite films with enhanced PCE and operational stability. The results show that due to the stronger complexation ability of N1 additive with PbI2, the generated PbI2-N1 complex can effectively prevent the preferential nucleation and realize lead halide-framework template-assistant crystallization reaction with organic cation in the one-step solution preparation of perovskite (FAPbI3)0.95(MAPbBr3)0.05 thin films, which result in the uniform grain size and smooth, dense film quality. Therefore, the PSCs device with small active area of 0.09 cm2 exhibits an efficiency of 22.2%, which is further improved to 23.2% by passivating the perovskite interface using PEAI. Moreover, highly-efficient slot-die printed 5×5 cm2 PSC module has been obtained with a champion PCE of 21% and improved operational stability over 1000 h. This work demonstrated a new strategy to realize high-quality large-scale perovskite films for solution-processed PSC modules, and may be further improved and extended to other kinds of PSCs and perovskite light-emitting diodes and detectors. © 2023, The Authors. All rights reserved.

关键词： Nucleation

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Emerging heterostructured C3N4 photocatalysts for photocatalytic environmental pollutant elimination and sterilization

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Inorganic Chemistry Frontiers 2023年第13期10卷 3756-3780页

作者： Yang Ding Chunhua Wang Lang Pei Soumyajit Maitra Qinan Mao Runtian Zheng Meijiao Liu Yun Hau Ng Jiasong Zhong Li-Hua Chen Bao-Lian Su Center of Advanced Optoelectronic Materials College of Materials and Environmental Engineering Hangzhou Dianzi University Hangzhou 310018 China School of Energy and Environment City University of Hong Kong Tat Chee Avenue Kowloon Hong Kong China Department of Materials University of Oxford Oxford UK Laboratory of Inorganic Materials Chemistry (CMI) University of Namur 61 rue de Bruxelles Namur Belgium Department of Chemistry Zhejiang Sci-Tech University Hangzhou 310018 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology 122 Luoshi Road 430070 Wuhan Hubei China

Photocatalysis is deemed a highly prominent technology to solve environmental problems such as pollution, CO2 emission and bacterial contamination. As an important photocatalyst, g-C3N4 has attracted a great amount of...

Photocatalysis is deemed a highly prominent technology to solve environmental problems such as pollution, CO₂ emission and bacterial contamination. As an important photocatalyst, g-C3N4 has attracted a great amount of attention in environmental remediation owing to its good stability, excellent light response, low cost and environmentally friendly properties. However, the pristine g-C3N4 photocatalyst generally suffers from serious photoinduced charge carrier recombination, poor surface active sites, and insufficient visible light harvesting, thereby leading to unsatisfactory photocatalytic performance. Heterostructured C₃N₄ photocatalysts have recently become a research focus in environmental fields thanks to their fast photoexcited electron–hole pair dissociation, broadened visible light response range, and sufficient photoredox capability. Herein, we critically review the up-to-date developments of heterostructured C₃N₄ photocatalysts in organic pollutant elimination, heavy metal ion reduction, CO₂ conversion and bacterial inactivation. Meanwhile, the strategies for constructing efficient C₃N₄ based heterostructures with enhanced environmental photocatalytic capability are thoroughly described, which should help readers to quickly acquire in-depth knowledge and to inspire new concepts in heterostructure engineering. Finally, the challenges and opportunities in fabricating heterostructured C₃N₄ photocatalysts for large-scale and commercial applications are discussed to give a clear study direction in this field.

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Weaving 3D highly conductive hierarchically interconnected nanoporous web by threading MOF crystals onto multi walled carbon nanotubes for high performance Li-Se battery

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能源化学 2021年第8期59卷 396-404页

作者： Chao Li Yingying Wang Hongyan Li Jing Liu Jianping Song Luca Fusaro Zhi-Yi Hu Yanxin Chen Yu Li Bao-Lian Su Laboratory of Inorganic Materials Chemistry (CMI) University of Namur B-5000 Namur Belgium Namur Institute of Structured Matter (NISM) University of Namur 61 Rue de Bruxelles B-5000 Namur Belgium Institute of Microscale Optoelectronics College of Physics and Optoelectronic Engineering Collaborative Innovation Centre for Optoelectronic Science & Technology Shenzhen University Shenzhen 518060 Guangdong China Laboratory of Inorganic Materials Chemistry (CMI) University of Namur B-5000 Namur Belgium Namur Institute of Structured Matter (NISM) University of Namur 61 Rue de Bruxelles B-5000 Namur Belgium Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 Hubei China Namur Institute of Structured Matter (NISM) University of Namur 61 Rue de Bruxelles B-5000 Namur Belgium Laboratory of Inorganic Materials Chemistry (CMI) University of Namur B-5000 Namur Belgium Namur Institute of Structured Matter (NISM) University of Namur 61 Rue de Bruxelles B-5000 Namur Belgium Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 Hubei China

Lithium-selenium (Li-Se) battery has attracted growing ***,its practical application is still impeded by the shuttle effect of the formed ***,we report in-situ hydrothermal weaving the three-dimensional (3D) highly conductive hierarchically interconnected nanoporous web by threading microporous metal organic framework MIL-68(Al) crystals onto multi-walled carbon nanotubes (MWCNTs).Such 3D hierarchically nanoporous web (3D MIL-68 (Al)@MWCNTs web) with a very high surface area,a large amount of micropores,electrical conductivity and elasticity strongly traps the soluble polyselenides during the electrochemical reaction and significantly facilitates lithium ion diffusion and electron *** dynamic calculation confirmed the strong affinity of MIL-68 (Al) for the adsorption of polyselenides,quite suitable for Li-Se *** hexahedral channels (1.56 nm) are more efficient for the confinement of polyselenides and for the diffusion of electrolytes compared to their smaller triangular channels (0.63 nm).All these excellent characteristics of 3D MIL-68 (Al)@MWCNTs web with suitable confinement of a large amount of selenium and the conductive linkage between MIL-68(Al) host by MWCNTs result in a high capacity of 453 mAh/g at 0.2C with 99.5％ coulombic efficiency after 200 cycles with significantly improved cycle stability and rate *** 3D MIL-68 (Al)@MWCNTs web presents a good performance in Li-Se battery in term of the specific capacity and cycling stability and also in terms of rate performance compared with all the metal-organic framework (MOF) based or MOF derived porous carbons used in Li-Se battery.

关键词： Lithium selenium battery Selenium confinement 3D hierarchically nanoporous web Metal–organic framework (MOF) Multi walled carbon nanotubes

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Post-annealing tailored 3D cross-linked TiNb2O7 nanorod electrode: towards superior lithium storage for flexible lithium-ion capacitors

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Science China materials 2020年第4期63卷 492-504页

作者： Bohua Deng Haoyang Dong Tianyu Lei Ning Yue Liang Xiao Jinping Liu School of Chemistry Chemical Engineering and Life SciencesWuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

TiNb2O7 anode materials(TNO)have unique potential for applications in Li-ion capacitors(LICs)due to their high specific capacity of ca.280 mA h g^-1 over a wide anodic Li-insertion potential ***,their highrate capability is limited by their poor electronic and ionic *** particular,studies on TNO for LICs are lacking and that for flexible LICs have not yet been ***,a unique TNO porous electrode with cross-linked nanorods tailored by post-annealing and its application in flexible LICs are *** binder-free TNO anode exhibits superior rate performance(~66.3%capacity retention as the rate increases from 1 to 40 C),which is ascribed to the greatly shortened ion-diffusion length in TNO nanorods,facile electrolyte penetration and fast electron transport along the continuous single-crystalline nanorod ***,the TNO anode shows an excellent cycling stability up to 2000 cycles and good flexibility(no capacity loss after continuous bending for 500 times).Model flexible LIC assembled with the TNO anode and activated carbon cathode exhibits increased gravimetric and volumetric energy/power densities(~100.6 W h kg^-1/4108.8 W kg^-1;10.7 mW h cm^-3/419.3 mW cm^-3),more superior to previously reported hybrid *** device also efficiently powers an LED light upon 180°bending.

关键词： post-annealing cross-linked nanorods facile electron transport superior rate performance flexible Li-ion capacitors

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Sandwiching Sulfur into the Dents Between N,O Co-Doped Graphene Layered Blocks with Strong Physicochemical Confinements for Stable and High-Rate Li-S Batteries

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Nano-Micro Letters 2020年第11期12卷 13-24页

作者： Mengjiao Shi Su Zhang Yuting Jiang Zimu Jiang Longhai Zhang Jin Chang Tong Wei Zhuangjun Fan Key Laboratory of Superlight Materials and Surface Technology Ministry of EducationCollege of Material Science and Chemical EngineeringHarbin Engineering UniversityHarbin 150001People’s Republic of China Key Laboratory of Energy Materials Chemistry Ministry of EducationKey Laboratory of Advanced Functional MaterialsAutonomous RegionInstitute of Applied ChemistryXinjiang UniversityUrumqi 830046People’s Republic of China State Key Laboratory of Heavy Oil Processing School of Materials Science and EngineeringChina University of PetroleumQingdao 266580People’s Republic of China

The development of lithium-sulfur batteries(LSBs)is restricted by their poor cycle stability and rate performance due to the low conductivity of sulfur and severe shuttle ***,an N,O co-doped graphene layered block(NOGB)with many dents on the graphene sheets is designed as effective sulfur host for high-performance LSB *** sulfur platelets are physically confined into the dents and closely contacted with the graphene scaffold,ensuring structural stability and high *** highly doped N and O atoms can prevent the shuttle effect of sulfur species by strong chemical ***,the micropores on the graphene sheets enable fast Li^+transport through the *** a result,the obtained NOGB/S composite with 76 wt%sulfur content shows a high capacity of 1413 mAh g^-1 at 0.1 C,good rate performance of 433 mAh g^-1 at 10 C,and remarkable stability with 526 mAh g^-1 at after 1000 cycles at 1 C(average decay rate:0.038%per cycle).Our design provides a comprehensive route for simultaneously improving the conductivity,ion transport kinetics,and preventing the shuttle effect in LSBs.

关键词： Graphene Physicochemical confinement Cycle stability Shuttle effect Li-S batteries

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Significantly enhanced energy storage performance of BaTiO3-based amorphous thin films through the synergistic function of variable valence ions

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Ceramics International 2025年

作者： Yao, Yiming Tao, Cheng Huang, Rui Zhang, Jian Zhang, Tianyu Hao, Hua Yao, Zhonghua Liu, Hanxing Cao, Minghe State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China International School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China

Amorphous thin films have been widely studied due to the excellent breakdown strength in recent years. However, their practical application faces significant challenges primarily caused by low polarization and energy density. Herein, we propose a multi-variable valence ions doping strategy to enhance the energy storage performance of BaTiO3-based amorphous thin films. The Ba0.92Bi0.08Ti1-x(Ni0.5Mn0.5)xO3(BBTNM) amorphous thin films were fabricated by chemical solution deposition method. In addition, the synergistic effects of variable valence ions (Ni, Mn) on the microstructure, dielectric and energy storage properties of the films were systematically studied. Compared with the undoped Ba0.92Bi0.08TiO3(BBT) film, the polarization and energy storage performance of the BBTNM film have been significantly improved owing to the defect dipoles generated by the incorporation of variable valence ions. Notably, a high discharge energy density of 93.3 J/cm3 together with an energy efficiency of 83 % could be achieved in the x = 0.08 film at 7.05 MV/cm. Simultaneously, the film exhibits excellent thermal stability within the range of 20 °C–160 °C, and still maintains favorable performance after 105 cycles. Overall, this work introduces a new approach for designing BaTiO3-based thin film materials. © 2025

关键词： Amorphous films

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Cu catalysts detour hydrogen evolution reaction

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Matter 2022年第8期5卷 2537-2540页

作者： Ying Dong Jing Li Xiao-Yu Yang Department of Forensic Medicine Huazhong University of Science and Technology 13 Hangkong Road Wuhan 430030 China Hubei Province Key Laboratory of Coal Conversion and New Carbon Materials School of Chemistry and Chemical Engineering Wuhan University of Science and Technology Wuhan 430081 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & Shenzhen Research Institute & Joint Laboratory for Marine Advanced Materials in Pilot National Laboratory for Marine Science and Technology (Qingdao) Wuhan University of Technology 122 Luoshi Road Wuhan 430070 China School of Engineering and Applied Sciences Harvard University Cambridge MA 02138 USA

The use of electrocatalytic reactions in aqueous solution to produce high-value chemicals is severely restricted by the occurrence of the electrochemical reaction of water. In a recent study published in Nature Nanotechnology by Haotian Wang and colleagues, hydrophilic-hydrophobic Cu catalysts, which suppress the undesirable hydrogen evolution reaction, have been discovered to promote conversion of 99% nitrate at an industrial wastewater level into ammonia using an industrial-relevant reduction current of 1 A/cm 2 .

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Optical phonon dominated heat transport: A first-principles thermal conductivity study of BaSnS2

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Physical Review B 2021年第24期104卷 245209-245209页

作者： Zhi Li Hongyao Xie Shiqiang Hao Yi Xia Xianli Su Mercouri G. Kanatzidis Christopher Wolverton Xinfeng Tang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Department of Chemistry Northwestern University Evanston Illinois 60201 USA Department of Materials Science and Engineering Northwestern University Evanston Illinois 60208 USA

Acoustic phonons with long mean free paths have long been believed to control the lattice thermal conductivity κL in solids dominantly. In this study, however, we demonstrate an optical phonon dominated κL in BaSnS2. By solving the Peierls-Boltzmann transport equation, we predict a low diagonal lattice thermal conductivity κL(D) of 0.34Wm−1K−1 at 850 K, which is less than half the κL(D) of SnS at the same temperature. Further calculations following the Allen-Feldman model suggest the additional off-diagonal lattice thermal conductivity κL(OD) contributed by wavelike tunneling phonons. The κL(OD) becomes pronounced at the high temperature (0.17Wm−1K−1 at 850 K) and leads to a deviation of the temperature dependence of κL from T–1 to T–0.76, suggesting the potential lattice anharmonicity in BaSnS2. Further analyses indicate BaSnS2 has over 68% of κL contributed by optical phonons. We show this uncommon optical phonon dominated κL is due to the relatively high group velocities of optical phonons in BaSnS2. The phonon mode visualization suggests these relatively high-velocity optical phonons correspond to the antiphase vibrations in BaSnS2 monolayers, which is originated from the unique permutation of SnS3 tetrahedra. Finally, by investigating the mode-resolved group velocity, relaxation time, and Grüneisen parameter, we attribute the intrinsic low κL of BaSnS2 to the soft lattice and the relatively high lattice anharmonicity induced by the Ba-S weak bonding and Sn(II) lone-pair electrons. Our study explicitly analyzes the microscopic mechanism of optical phonon dominated heat transport in BaSnS2 and suggests it worthy of further experimental studies as an intrinsic low-κL material.

关键词： Chemical bonding Heat transfer Lattice dynamics Optical phonons Thermal conductivity

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One-Pot K+ and Po43- Co-Doping Enhances Electrochemical Performance of Li-Rich Li1.2ni0.13co0.13mn0.54o2 Cathode for Li-Ion Battery

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SSRN 2022年

作者： Peng, Yan Wu, Liang Li, Chao-Fan Luo, Bi-Cheng Hu, Zhi-Yi Li, Yu Su, Bao-Lian State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology 122 Luoshi Road Hubei Wuhan430070 China Wuhan University of Technology 122 Luoshi Road Hubei Wuhan430070 China University of Namur 61 Rue de Bruxelles NamurB-5000 Belgium

The high specific capacity of Li-rich Mn-based oxides make them promising cathodes for high-energy-density lithium-ion batteries (LIBs). However, the problems such as low initial coulombic efficiency, fast capacity and voltage fading, poor kinetics, large voltage hysteresis, and poor safety hamper their fast commercialization. Herein, we report one-pot K + and PO 4 3- co-doping Li-rich Mn-based oxides Li 1.2 Ni 0.13 Co 0.13 Mn 0.54 O 2 cathode material to improve the electrochemical performance for LIBs. On the one hand, K + doping can stabilize the bulk structure and enlarge the Li slabs to facilitate the diffusion of Li + , resulting in enhanced cycling and rate performance. On the other hand, PO 4 3- doping changes the electronic structure of the material and weakens the covalency of TM-O, decreasing the irreversible loss of lattice oxygen and stabilizing the structure. As a result, the K + and PO 4 3- co-doping can effectively alleviate the capacity and voltage decay and the modified sample shows better cycling stability (88.6%@0.5 C@250 cycles) and rate performance (155.5 mAh g −1 @5 C) compared to the pristine material. Our strategy here provides a facile one-pot method to modifying Li-rich cathode material for high-performance LIBs. © 2022, The Authors. All rights reserved.

关键词： Lithium-ion batteries

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Strongly enhancing the energy storage properties and stability of amorphous BaTiO3 thin films via ions doping

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Scripta materialia 2025年 265卷

作者： Chang, Ruiling Yao, Zhonghua Xing, Yutong Wang, Jun Hao, Hua Cao, Minghe Liu, Hanxing State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China International School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China Sanya Science and Education Innovation Park of Wuhan University of Technology Sanya572000 China

Amorphous thin films with high power density and breakdown strength satisfy the needs of advanced power electronic systems. Nonetheless, improving the energy storage density of amorphous films is critical for addressing the growing demand for electricity. We apply high spontaneous polarization BaTiO3 as the main component to make (1-x)Ba(Ti0.99Mn0.02)O3-xBiFeO3((1-x)BTM-xBF) thin films. Doping BiFeO3 (BF) synergistically boosts polarization. The introduction of amorphous phases and Mn ions enhances the breakdown strength. The results demonstrate that, at x = 0.10, the film can achieve both a high efficiency of 80.3 % and an excellent energy storage density of 111.3 J cm-3. Moreover, the film has a strong thermal stability within a broad range of 20 to 160 °C, as well as the cycling reliability is as high as 105 times. The present study offers a practical approach to develop film capacitors with outstanding energy storage capabilities. © 2025 Acta materialia Inc.

关键词： Amorphous films

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