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Multifunctional additives for the enhanced performance of the doctor-blading printed perovskite solar modules

Journal of Energy Chemistry 2025年 109卷 368-377页

作者： Linyong Tian Haoyu Cai Zhenyue Wang Yongjun Liu Juan Zhao Guodong Liu Yaqi Cheng Biqi He Hongfei Zhang Long Jiang Bofei Xue Yi-Bing Cheng Jie Zhong State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei 430070 China Nanjing Aolian Light Energy Technology Co. Ltd. Nanjing Jiangsu 320115 China School of Automobile Engineering Wuhan University of Technology Wuhan Hubei 430070 China State Key Laboratory of Oil and Gas Equipment CNPC Tubular Goods Research Institute Xi’an 710077 Shaanxi China Shaanxi Provincial Key Laboratory of Clean Energy Equipment and Materials Xi’an 710077 Shaanxi China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan Guangdong 528216 China

The utilization of self-assembled monolayers (SAMs) has significantly elevated the power conversion efficiency (PCE) of inverted perovskite solar cells (PSCs). However, the inherent hydrophobicity of these SAMs poses challenges in the subsequent printing of perovskite films in PSC upscaling. In this work, we incorporated a multifunctional additive, dimethyl suberimidate dihydrochloride (DMSCl 2 ), into the perovskite precursor to enhance the quality of the blade-coated perovskite film on the SAM interlayer. Characterizations revealed that the function groups of the imino (N–H) and methoxy (CH 3 O–) DMSCl 2 facilitate both bonding between perovskite precursor and SAM molecule (Me-4PACz), which facilitates the large-area printing of perovskite film. These interactions also provide effective passivation within the perovskite films and interface defects of PSCs. As a result, a significantly enhanced PCE from 16.62% to 20.37% was obtained for the printed perovskite solar module (93.10 cm 2 ) and 25.27% for the small device (0.09 cm 2 ). Remarkable stability was achieved with 93.3% of their initial PCE after 1000 h of continuous maximum power point (MPP) tracking. This report suggests that multifunctional additive doping provides a convenient route for the upscaling of perovskite solar cells with SAM interlayers.

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Synergistic Regulation of Texture and Low-Angle Grain Boundaries Enables Mechanically Robust P-Type Bi2Te3- Based Compounds with Superior Thermoelectric Performance

SSRN

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SSRN 2024年

作者： Chen, Shuo Luo, Tingting Li, Junjie Liao, Lin Liu, Yutian Yang, Zhen Zhong, Shenlong Wu, Jinsong Su, Xianli Yan, Yonggao Poudeu, Pierre Ferdinand Poudeu Zhang, Qingjie Tang, Xinfeng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Department of Materials Science and Engineering University of Michigan at Ann Arbo Ann ArborMI48109 United States

Structural material parameters such as grain size, texture, and grain boundary species play crucial roles in anisotropic thermoelectric materials. In this study, the underlying mechanism for rational regulation of grain size, texture, and grain boundary species is uncovered. The variations in the plastic deformation capability and the atomic diffusion rates at different extrusion temperatures lead to a competition between dynamic recrystallization (DRX) and grain growth, which allows for quantitative regulation over grain size, texture, and low-angle grain boundaries (LAGBs) in the material. As a result, grain size can be effectively tuned from the nanometer scale to the micrometer scale, with the orientation factor F(110) adjusting from 0.23 to 0.41, and the concentration of LAGBs varying between 10.9% and 25.2%. The sample extruded at 673 K exhibits an average grain size of 800 nm, which contribute to the observed compressive strength of 226 MPa and bending strength of 126 MPa. Additionally, the high texture and high density of LAGBs ensure a high carrier mobility of 247 cm2 V-1 s-1. The ZT value of 1.2 enables micro-TEC modules and conventional TEC modules to achieve maximum temperature differences (ΔTmax) of 60 K and 78 K, respectively, at the hot-side temperature of 300 K. © 2024, The Authors. All rights reserved.

关键词： Compressive strength

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Adsorptive Behavior of Methyl Blue on Graphene Aerogel:A Mechanism Study

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Journal of Wuhan University of technology(materials Science) 2021年第2期36卷 239-242页

作者： SONG Xuyan HE Yunlu PAN Xi WEI Min LI Ran ZHOU Xiaoyu ZHENG Ying LI Junsheng TANG Haolin Technology Centre of Hubei China Tobacco Industry Co. Ltd.Wuhan 430051China College of Urban Construction Wuchang Shouyi UniversityWuhan 430064China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Graphene aerogel was synthesized and used for the removal of methyl blue from aqueous *** effect of solution pH,temperature and adsorption time on the adsorption performance of the graphene aerogel was studied *** addition,investigations were also performed to determine the nature of *** experimental results show that graphene aerogel is a highly efficient adsorbent for the treatment of methyl blue in aqueous *** addition,the adsorption of methyl blue proceeds through a single layer physical adsorption on the graphene *** findings herein are useful for the future development of adsorbent for in water.

关键词： graphene aerogel adsorption methyl blue mechanism

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Groups-dependent phosphines as the organic redox for point defects elimination in hybrid perovskite solar cells

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Journal of Energy Chemistry 2021年第3期30卷 23-29页

作者： Zhengli Wu Miao Zhang Yifan Liu Yuxi Dou Yinjie Kong Lin Gao Weitao Han Guijie Liang Xiao Li Zhang Fuzhi Huang Yi-Bing Cheng Jie Zhong State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan 528200GuangdongChina Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices Hubei University of Arts and ScienceXiangyang 441053HubeiChina School of Materiale Science and Engineering Zhengzhou UniversityZhengzhou 450001HenanChina Department of Materials Science and Engineering Monash UniversityVIC 3800Australia

Lead(Pb)^(0) and iodine(I)^(0) point defects generated during perovskite solar cell(PSC)fabrication and photoconversion form deep band energy levels as the carriers’recombination *** defects not only deteriorate device efficiency,but also facilitate chemical degradation with ion migration,resulting in restricted device ***,we present a novel type of phosphines as the point defects stabilizer for hybrid perovskite solar cells with enhanced *** phosphines with varied side groups of tributyl,trioctyl and triphenyl are exampled as the dopants in perovskite *** group dependent redox properties were observed in the perovskite film,dependent on their molecular weights and steric hinderances of *** partially oxidized tributyl phosphine(TBUP)with additional tributyl phosphine oxides(TBPO)is efficient in reduction of lead(Pb)^(0) and iodine(I)^(0) concentrations during the device fabrication and *** device with TBUP-TBPO pair showed enhanced power conversion efficiency(PCE)to 20.48% and maintain 91.7% of their initial PCEs after 500 h at 65℃ thermal ***,this work presents an efficient route of utilize the phosphine species to reduce point defects in the perovskite film,which promoting further development of novel phosphorous additives with defects stabilization,interface passivation and encapsulation for low-cost solution processed PSCs.

关键词： Redox Perovskite solar cells Phosphine organics Lead defect Stability

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Layered manganese phosphorus trisulfides for high-performance lithium-ion batteries and the storage mechanism

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Carbon Energy 2023年第3期5卷 160-169,170,171页

作者： Hailin Shen Yueling Cai Zhongtao Ma Peng Wang Bingkun Guo Jipeng Cheng Qianqian Li Hongtao Wang Zhongyuan Liu Anmin Nie Jinsong Wu Materials Genome Institute Shanghai UniversityShanghaiChina Shanghai Key Laboratory of Mechanics in Energy Engineering School of Mechanics and Engineering ScienceShanghai Institute of Applied Mathematics and MechanicsShanghai UniversityShanghaiChina State Key Laboratory of Silicon Materials School of Materials Science and EngineeringZhejiang UniversityHangzhouChina Center for X‐mechanics Zhejiang UniversityHangzhouChina State Key Laboratory of Metastable Materials Science and Technology Center for High Pressure ScienceYanshan UniversityQinhuangdaoChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanChina Nanostructure Research Center Wuhan University of TechnologyWuhanChina

Although advanced anode materials for the lithium-ion battery have been investigated for decades,a reliable,high-capacity,and durable material that can enable a fast charge remains ***,we report that a metal phosphorous trichalcogenide of MnPS_(3)(manganese phosphorus trisulfide),endowed with a unique and layered van der Waals structure,is highly beneficial for the fast insertion/extraction of alkali metal ions and can facilitate changes in the buffer volume during cycles with robust structural *** few-layered MnPS_(3)anodes displayed the desirable specific capacity and excellent rate chargeability owing to their good electronic and ionic *** assembled as a half-cell lithium-ion battery,a high reversible capacity of 380 mA h g^(−1)was maintained by the MnPS_(3)after 3000 cycles at a high current density of 4 A g^(−1),with a capacity retention of close to or above 100%.In full-cell testing,a reversible capacity of 450 mA h g^(−1)after 200 cycles was maintained as *** results of in-situ TEM revealed that MnPS_(3)nanoflakes maintained a high structural integrity without exhibiting any pulverization after undergoing large volumetric expansion for the insertion of a large number of lithium *** kinetics of lithium-ion diffusion,stable structure,and high pseudocapacitance contributed to their comprehensive performance,for example,a high specific capacity,rapid charge-discharge,and long ***_(3)is thus an efficient anode for the next generation of batteries with a fast charge/discharge capability.

关键词： cyclic stability in‐situ TEM MnPS3 pseudocapacitance rate performance

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Step-scheme CdS/TiO_(2) nanocomposite hollow microsphere with enhanced photocatalytic CO_(2) reduction activity

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Journal of materials Science & technology 2020年第21期56卷 143-150页

作者： Zhongliao Wang Yifan Chen Liuyang Zhang Bei Cheng Jiaguo Yu Jiajie Fan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China School of Materials Science and Engineering Zhengzhou UniversityZhengzhou450001China

Converting solar energy into chemical energy by artificial photosynthesis is promising in addressing the issues of the greenhouse effect and fossil fuel ***,a novel photocatalyst,***/TiO_(2) hollow microspheres(HS),were dedicatedly designed to boost overall photocatalytic ***_(2) nanoparticles were in-situ decorated on the inside and outside the shell of Cd S HS,ensuring close contact between TiO_(2) and *** CdS/TiO2 HS with abundant mesopores inside of the shell boost the light absorption via multiscattering effect as well as accessible to reactions in all *** heterojunction was scrutinized and the charge transfer across it was revealed by in-situ irradiated X-ray photoelectron spectroscopy(ISI-XPS).Ultimately,the charge transfer in this composite was determined to follow stepscheme mechanism,which not only facilitates the separation of charge carriers but also preserves strong redox *** from the intimate linkage between Cd S and TiO_(2) and the favorable step-scheme heterojunction,enhanced photocatalytic CO_(2) reduction activity was *** CH4 yield rate of CdS/TiO_(2) reaches 27.85μmol g^(–1) h^(–1),which is 145.6 and 3.8 times higher than those of pristine CdS and TiO_(2),*** work presents a novel insight into constructing step-scheme photocatalytic system with desirable performance.

关键词： Step-scheme heterojunction CdS TiO_(2) Hollow microspheres Photocatalytic CO2 reduction

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Achieving better aqueous rechargeable zinc ion batteries with heterostructure electrodes

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Nano Research 2021年第9期14卷 3174-3187页

作者： Buke Wu Wen Luo Ming Li Lin Zeng Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Mechanical and Energy Engineering Southern University of Science and TechnologyShenzhen 518055China Department of Physics School of ScienceWuhan University of TechnologyWuhan 430070China Guangdong Provincial Key Laboratory of Energy Materials for Electric Power Southern University of Science and TechnologyShenzhen 518055China Key Laboratory of Energy Conversion and Storage Technologies(Southern University of Science and Technology) Ministry of EducationShenzhen 518055China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu hydrogen ValleyFoshan 528200China

Aqueous rechargeable zinc ion batteries(ARZIBs)have received unprecedented attention owing to the low cost and high-safety ***,their further development and application are hindered by the issues of electrodes such as cathode dissolution,zinc anode dendrite,passivation,as well as sluggish reaction *** heterostructure electrodes is a powerful method to improve the electrochemical performance of electrodes by grafting the advantages of functional materials onto the active *** this review,various modified heterostructure electrodes with optimized electrochemical performance and wider applications are ***,the synergistic effect between active materials and functional materials are also in-depth *** specific modification methods are divided into interphase modification(electrode-electrolyte interphase and electrode-current collector interphase)and structure ***,the conclusion and future perspective on the optimization mechanism of functional materials,and the cost issue of practical heterostructure electrodes in ARZIBs are also *** is expected that this review can promote the further development of ARZIBs towards practical utility.

关键词： zinc ion battery heterostructure electrodes interphase modification structure optimization

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Tuning the Oxygen Vacancies and Mass Transfer of Porous Conductive Ceramic Supported Irox Catalyst Via Polyether Derived Composite Oxide Pyrolysis: Toward a Highly Efficient Oxygen Evolution Reaction Catalyst for Water Electrolysis

SSRN

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SSRN 2023年

作者： Zhang, Hao Zhu, Liyan Shen, Yuhan Wu, Mingjuan Tian, Tian Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China Hubei Key Laboratory of Fuel Cell Wuhan430070 China

Slow oxygen evolution reaction (OER) and material transport impedance in catalyst coated membrane (CCM) are major challenges for the practical proton exchange membrane water electrolyzer (PEMWE). Herein, we present a novel OER catalyst with a multilevel porous support and abundant oxygen vacancies to boost efficiency and durability in water electrolysis. The formation of a heterointerface with abundant oxygen vacancies in IrOx improves the catalytic activity and prevents IrOx from peroxidation. Furthermore, the unique pore structure of the support facilitates the mass transport of the anode catalyst layer during water electrolysis at high current density, and the material transport resistance of the water electrolyzer is only 0.0154 Ω cm2 at 1.5 A cm-2. When used in a PEMWE, the prepared electrocatalysts have an impressive electrochemical performance of 1.87 V at 3·A cm-2 with an Ir loading of only 0.91 mg cm-2. This approach highlights the importance of oxygen vacancies and transportation in the catalyst-support interface, providing a promising solution for high-rate practical water electrolysis. © 2023, The Authors. All rights reserved.

关键词： Mass transfer

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Boosting oxygen evolution of LiCoO2 electrocatalysts via lithium defect

Materials Today Catalysis

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materials Today Catalysis 2025年 8卷

作者： Li, Huamei Li, Mengyuan Liao, Lingling Yang, Han Xiang, Kun Luo, Guoqiang Xie, Mingjiang School of Chemistry and Environmental Engineering Engineering Research Center of Phosphorus Resources Development and Utilization of Ministry of Education Wuhan Institute of Technology Wuhan430205 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Hubei Key Lab for Processing and Application of Catalytic Materials College of Chemical Engineering Huanggang Normal University Huanggang438000 China

The challenge of the complex oxygen evolution reaction (OER) currently impedes the efficient production of hydrogen via electrolytic water splitting. To address this issue, the development and improvement of effective electrocatalysts are required. LiCoO2, a key material in lithium-ion batteries, has shown promising potential as an electrocatalyst for electrochemical energy conversion. However, OER catalysts derived from LiCoO2 have faced obstacles such as high overpotential and a complicated preparation process. In this study, the preparation method is adjusted to optimize the synthesis of Li1-xCoO2 with a defective structure, resulting in an impressive overpotential of only 290 mV at a current density of 100 mA cm−2 and a remarkable Tafel slope of 15.2 mV dec−1. The exceptional catalytic activity of Li1-xCoO2 can be attributed to the absence of Li, which triggers oxidative alterations in the electronic structure of Co. Density functional theory (DFT) calculations reveal that Li defects can influence the d-band center of active Co sites, enhancing the adsorption capabilities of Co sites towards *OOH intermediates and increasing the conductivity of the electrocatalyst during the OER process. These alterations improve the velocity of the crucial step in the reaction, ultimately boosting the catalyst's overall performance and efficiency. © 2024 The Authors

关键词： Lithium-ion batteries

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Change in elastic properties during room-temperature aging in body-centered cubic Mg-Li and Mg-Li-Al single crystals

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Journal of materials Science & technology 2022年第14期109卷 49-53页

作者： Ruxia Liu Shota Higashino Koji Hagihara Lianmeng Zhang Tohru Sekino Masakazu Tane SANKEN(The Institute of Scientific and Industrial Research) Osaka University8-1 MihogaokaIbarakiOsaka 567-0047Japan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Graduate School of Engineering Osaka City University3-3-138 SugimotoOsaka558-8585Japan Department of Physical Science and Engineering Nagoya Institute of TechnologyNagoya 466-8555Japan

Biodegradable materials,with many advantages over conventionally used non-biodegradable materials,have received much attention owing to the elimination of the need for a secondary surgery for the removal of implants after *** with other biodegradable ceramics and/or polymers,Mg alloys are considered to be the most promising biodegradable orthopedic materials because they feature not only high specific strength and compressive yield strength but also a low Young’s modulus,which is comparable to that of human bones(10-30 GPa)[1,2].

关键词： strength aging alloys

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