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第六届新型太阳能电池材料科学与技术学术研讨会

作者： Jiang He Zhiliang Ku Yong Peng State key lab of advanced technology for materials synthesis and processing Wuhan University of Technology

Organi/Inorganic perovskite materials behavior differently under a testing condition of IEC61215. In this research, the behavior of series of perovskite materials with varied A cations under the thermal cycling testing standards were studied. We analyzed the defeating mechanisms of those materials through temperature depended XRD, SEM and AFM ***. Finally, we draw a conclusion that FACsPb（I/Br） perovskite materials could the most stable one under thermal cycling testing condition. This perovskite materials can be stable because the phase change related materials decomposition under frequent temperature change does not happen in this material, however other perovskite materials will decompose. A device with an architecture of FTO/TiO/FACsPbI/graphite electrode was then encapsulated and tested under a condition of -30℃-85℃ for 200 times. After testing, the device finally kept about 83% of its initial power conversion efficiency.

关键词： Standard stability tests Perovskite solar cells thermal cycling tests

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Emerging semiconductors and metal-organic-compounds-related photocatalysts for sustainable hydrogen peroxide production

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Matter 2022年第7期5卷 2119-2167页

作者： Yang Ding Soumyajit Maitra Somoprova Halder Chunhua Wang Runtian Zheng Tarek Barakat Subhasis Roy Li-Hua Chen Bao-Lian Su Laboratory of Inorganic Materials Chemistry (CMI) University of Namur 61 rue de Bruxelles 5000 Namur Belgium Namur Institute of Structured Matter (NISM) University of Namur 61 rue de Bruxelles 5000 Namur Belgium Department of Chemical Engineering University of Calcutta 92 APC Road Kolkata West Bengal 700009 India Department of Chemistry KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology 122 Luoshi Road Wuhan Hubei 430070 China Clare Hall University of Cambridge CB2 1EW Cambridge UK

As a versatile raw material, hydrogen peroxide (H 2 O 2 ) is extensively employed in chemicals synthesis, medical disinfection, textile industry, and environmental remediation fields. H 2 O 2 generation through a photocatalytic route has attracted increasing interest. Tremendous progress and achievements have been made over the past decades in photocatalytic H 2 O 2 production. Herein, we critically review the state-of-the art developments on various photocatalysts, including carbon nitride, titania, bismuth, sulfide, carbon, and metal-organic-compound-related materials, for the highly efficient light-driven H 2 O 2 synthesis. Significantly, these materials show tunable morphology, micro-nanostructure, surface chemistry, and electronic band-gap structure characters for sufficient light harvesting, rapid hole-electron pairs separation and transfer, and favorable reactants adsorption as well as facilitated products desorption, thus delivering great activity for efficient light-driven H 2 O 2 production. The specific challenges and opportunities related to photocatalytic materials discovery and development that will emerge from this important field are discussed.

关键词： hydrogen peroxide photocatalysts design carbon nitride titania metal-organic materials

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Crystallization Thermodynamics Regulation of 1.85 eV Wide-Bandgap Perovskite for Efficient and Stable Perovskite-Organic Tandem Photovoltaics

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Angewandte Chemie 2025年

作者： Guanshui Xie Dr. Huan Li Jun Fang Xin Wang Haichen Peng Dr. Dongxu Lin Nuanshan Huang Lin Gan Prof. Wenjia Li Ruixuan Jiang Prof. Tongle Bu Prof. Fuzhi Huang Prof. Sisi He Prof. Longbin Qiu Department of Mechanical and Energy Engineering SUSTech Energy Institute for Carbon Neutrality Southern University of Science and Technology Shenzhen 518055 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P. R. China Shenzhen Key Laboratory of Flexible Printed Electronics Technology School of Science Harbin Institute of Technology (Shenzhen) University Town Shenzhen Guangdong 518055 China

Wide-band gap perovskite with adjustable band gaps can be integrated with organic solar cells to form tandem solar cells (TSCs), thereby surpassing the Shockley–Queisser limit. However, increasing Br content to elevate the band gap above 1.8 eV complicates crystallization, leading to inferior film quality and defects due to the unmanageable evolution of intermediate phases. Surface passivation improves crystallization but hard to moderate the inhomogeneous component distributions and defects in the bulk phase. Here, we introduce a diammonium salt as an additive to regulate the homogeneity and crystallization of perovskite film, eliminating the low-dimensional intermediate phase for orientated crystallization of 1.85 eV perovskite, resulting in efficient wide-band gap perovskite solar cells with an impressive open-circuit voltage ( V oc ) of 1.379 V and operational stability remaining 85 % of their initial efficiency after illumination for 1200 h. Furthermore, perovskite-organic TSCs achieve a champion power conversion efficiency of 24.03 % and a high V oc of 2.108 V, one of the highest V oc for perovskite-organic TSCs.

关键词： Wide-band gap perovskite Low-dimensional intermediate phase Suppressed phase segregation Reduced voltage loss Perovskite-organic tandem solar cells

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Ammonium Ion Batteries: Material, Electrochemistry and Strategy

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Angewandte Chemie 2023年第23期135卷

作者： Runtian Zheng Yuhang Li Dr. Haoxiang Yu Xikun Zhang Dr. Ding Yang Dr. Lei Yan Prof. Yu Li Prof. Jie Shu Prof. Bao-Lian Su School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 Zhejiang China Laboratory of Inorganic Materials Chemistry (CMI) University of Namur 61 rue de Bruxelles 5000 Namur Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 Hubei China

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Excipient-free porphyrin/SN-38 based nanotheranostics for drug delivery and cell imaging

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Nano Research 2020年第2期13卷 503-510页

作者： Ye Yuan Ruonan Bo Di Jing Zhao Ma Zhongling Wang Tzu-yin Lin Lijie Dong Xiangdong Xue Yuanpei Li Center for Smart Materials and Devices State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070China Department of Biochemistry and Molecular Medicine UC Davis Comprehensive Cancer CenterUniversity of California DavisSacramento 95817USA School of Veterinary Medicine Yangzhou UniversityYangzhou 225009Chino Department of Oncolog) Xiangya HospitalCentral South UniversityChangsha 410008China Department of Radiology Shanghai General HospitalShanghai jiao Tong University School of MedicineShanghai 200080China Division of Hematology/Oncology Department of Internal MedicineUniversity of California DavisSacramento 95817USA College of Life Sciences Northwest UniversityXian 710069China

Nanotheranostics with comprehensive diagnostic and therapeutic capabilities show exciting cancer treatment ***,we develop an excipient-free drug delivery system for cancer diagnosis as well as therapy,in which a near infra-red photosensitizer and a chemotherapeutic drug can be self-delivered without any *** building block of the drug delivery system was synthesized by covalently conjugating four anticancer drugs(7-ethyl-10-hydroxy-camptothecin,SN-38)with a photosensitizer(porphyrin)via hydrolyzable ester linkage,which endows the drug delivery system with 100%active pharmaceutical ingredients,excellent imaging,and therapeutic *** conjugates can readily self-assemble into nanosheets(PS NSs)and remain stable for at least 20 days in aqueous *** PS NSs,fluorescence resonance energy transfer(FRET)dominates the fluorescence of SN-38 and enables to monitor the drug release *** PS NSs also show excellent anticancer activity in vitro,due to the increased cell uptake with the synergistic effect of photodynamic therapy and chemotherapy.

关键词： porphyrin 7-ethyl-10-hydroxy-camptothecin(SN-38) drug delivery self-indication nanotheranostics photodynamic therapy

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Symmetry-Broken Ru Nanoparticles with Parasitic Ru-Co Dual-Single Atoms Overcome the Volmer Step of Alkaline Hydrogen Oxidation

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Angewandte Chemie 2024年第12期136卷

作者： Xueqin Q. Mu Prof. Suli L. Liu Mengyang Y. Zhang Zechao C. Zhuang Ding Chen Yuru R. Liao Hongyu Y. Zhao Prof. Shichun C. Mu Dingsheng S. Wang Prof. Zhihui H. Dai School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing 211816 P. R. China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P. R. China Engineering Research Center of Advanced Rare Earth Materials Department of Chemistry Tsinghua University Beijing 100084 P. R. China

Efficient dual-single-atom catalysts are crucial for enhancing atomic efficiency and promoting the commercialization of fuel cells, but addressing the sluggish kinetics of hydrogen oxidation reaction (HOR) in alkaline media and the facile dual-single-atom site generation remains formidable challenges. Here, we break the local symmetry of ultra-small ruthenium (Ru) nanoparticles by embedding cobalt (Co) single atoms, which results in the release of Ru single atoms from Ru nanoparticles on reduced graphene oxide (Co 1 Ru 1,n /rGO). In situ operando spectroscopy and theoretical calculations reveal that the oxygen-affine Co atom disrupts the symmetry of ultra-small Ru nanoparticles, resulting in parasitic Ru and Co dual-single-atom within Ru nanoparticles. The interaction between Ru single atoms and nanoparticles forms effective active centers. The parasitism of Co atoms modulates the adsorption of OH intermediates on Ru active sites, accelerating HOR kinetics through faster formation of *H 2 O. As anticipated, Co 1 Ru 1,n /rGO exhibits ultrahigh mass activity (7.68 A mg Ru −1 ) at 50 mV and exchange current density (0.68 mA cm −2 ), which are 6 and 7 times higher than those of Ru/rGO, respectively. Notably, it also displays exceptional durability surpassing that of commercial Pt catalysts. This investigation provides valuable insights into hybrid multi-single-atom and metal nanoparticle catalysis.

关键词： dual-single-atom catalysts hydrogen oxidation reaction symmetry-breaking parasitic Ru nanoparticles

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Designing Zn atomic coordination sites within TpBpy COFs for efficient photocatalytic CO2 reduction under visible light irradiation

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Chemical Engineering Journal 2025年 516卷

作者： Zhou, Min Ding, Lingling Chen, Keqiang Bao, Yunan Liu, Yueli Chen, Wen State Key Laboratory of Silicate Materials for Architectures School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China Shenzhen Research Institute of Wuhan University of Technology Shenzhen518000 China Hubei Key Laboratory of Energy Storage and Power Battery School of Optoelectronic Engineering School of New Energy Hubei University of Automotive Technology Shiyan442002 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China Faculty of Materials Science and Chemistry China University of Geosciences Wuhan430074 China Wuhan Brilliant Tech Co. Ltd. Wuhan430205 China

Optimizing coordination microenvironments and achieving high single-atom loads for single-atoms catalysts (SACs) are crucial for enhancing photocatalytic CO2 reduction. Driven by the abundant coordination site in covalent organic frameworks (COFs), the designing with different metal coordination modes is considered to be efficient route for the high-performance CO2 photoreduction, while it still suffers great challenge. Here, Zn-NO3 coordination mode in Zn SACs/TpBpy is synthesized via a one-step solvothermal strategy, achieving an exceptional Zn loading of 11.4 wt%. In-situ characterization and theoretical calculation reveal that the Zn-NO3 coordination mode optimizes the electronic structure, facilitating photogenerated charge separation, prolonging carrier lifetimes, and reducing energy barriers for key intermediates *COOH during CO2RR. Furthermore, the high content of Zn sites provides more active sites for the adsorption and activation of CO2 molecule, facilitating the transfer of the photogenerated electrons from TpBpy COFs to the Zn active sites under the visible light irradiation. As a result, Zn/TpBpy COFs with Zn-NO3 coordination mode exhibit a high CO production rate of 281.75 μmol g−1h−1, along with a remarkable selectivity of 99.96 % under visible light irradiation. This work offers insights for the design of efficient SACs through the optimization of the coordination microenvironment and metal loading content. © 2025 Elsevier B.V.

关键词： Photocatalytic activity

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TiO 2 nanofluid infused nanocoating for long-term anti-corrosion

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Chemical Physics Letters 2023年 830卷

作者： Zi-Yan Xu Jing-jing Xie Hao Yu Yang Ge Wei Geng Xiao-Yu Yang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & Shenzhen Research Institute & Laoshan Laboratory Wuhan University of Technology Wuhan 430070 PR China School of Chemical Engineering and Technology Sun Yat-Sen University 2 Daxue Road Zhuhai 519082 PR China

Marine corrosion has been a global problem with the damage on environment, and economy. With the development, traditional coating technology is difficult to meet the current demands of applications. In this study, TiO 2 nanoparticles were modified and dispersed in silicone oil to form TiO 2 nanofluid. And, the nanofluid was infused into hierarchical structure to produce the SLIPS which is obtained by spraying with the solution of Al 2 O 3 , which significantly reduce the lubricant leaching. As synthesized coating shows the good performance in corrosion resistance. The coating prepared by this novel method show the great potential applications in different marine environments.

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Long-term Durability of Seawater Electrolysis for Hydrogen: From Catalysts to Systems

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Angewandte Chemie 2024年第47期136卷

作者： Yu Liu Yong Wang Prof. Paolo Fornasiero Prof. Ge Tian Prof. Peter Strasser Prof. Xiao-Yu Yang State Key Laboratory of Silicate Materials for Architectures & State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & School of Chemistry Chemical Engineering and Life Sciences & Foshan Xianhu Laboratory & Laoshan Laboratory & School of Materials Science and Engineering & International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China Department of Chemical and Pharmaceutical Sciences University of Trieste and ICCOM-CNR and INSTM Trieste Research Units 34127 Trieste Italy Technical University Berlin Department of Chemistry 10623 Berlin Germany

Direct electrochemical seawater splitting is a renewable, scalab.e, and potentially economic approach for green hydrogen production in environments where ultra-pure water is not readily availab.e. However, issues related to low durability caused by complex ions in seawater pose great challenges for its industrialization. In this review, a mechanistic analysis of durability issues of electrolytic seawater splitting is discussed. We critically analyze the development of seawater electrolysis and identify the durability challenges at both the anode and cathode. Particular emphasis is given to elucidating rational strategies for designing electrocatalysts/electrodes/interfaces with long lifetimes in realistic seawater including inducing passivating anion layers, preferential OH − adsorption, employing anti-corrosion materials, fabricating protective layers, immobilizing Cl − on the surface of electrocatalysts, tailoring Cl − adsorption sites, inhibition of OH − binding to Mg 2+ and Ca 2+ , inhibition of Mg and Ca hydroxide precipitation adherence, and co-electrosynthesis of nano-sized Mg hydroxides. synthesis methods of electrocatalysts/electrodes and innovations in electrolyzer are also discussed. Furthermore, the prospects for developing seawater splitting technologies for clean hydrogen generation are summarized. We found that researchers have rethought the role of Cl − ions, as well as more attention to cathodic reaction and electrolyzers, which is conducive to accelerate the commercialization of seawater electrolysis.

关键词： direct electrochemical seawater splitting hydrogen production durability electrocatalysts/electrodes/interfaces design electrolyzer innovation

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Rapid fabrication and thermoelectric performance of SnTe via non-equilibrium laser 3D printing

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Rare Metals 2018年第4期37卷 300-307页

作者： Tian-Le Chen Chuang Luo Yong-Gao Yan Ji-Hui Yang Qing-Jie Zhang Ctirad Uher Xin-Feng Tang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Department of Materials Science and Engineering University of Washington Department of Physics University of Michigan

Thermoelectric technologies based on Seebeck and Peltier effects, as energy techniques able to directly convert heat into electricity and vice versa, hold promise for addressing the global energy and environmental problems. The development of efficient and low-cost thermo- electric modules is the key to their large-scale commercial applications. In this paper, using a non-equilibrium laser 3D printing technique, we focus an attention on the fabrication of mid-temperature p-type SnTe thermoelectric materials. The influence of laser power, scanning speed and layer thickness on the macro-defects, chemical and phase composition, microstructure and thermoelectric performance was systematically investigated. First and foremost, the processing parameter window for printing a highquality layer is determined. This is followed by the finite element method used to simulate and verify the influence of the laser-induced molten pool temperature distribution on the final composition and microstructure. Finally, the high-performance SnTe layer with 10 mm × 10 mm in area is produced within seconds with room temperature Seebeck coefficient close to that of SnTe manufactured by the traditional methods. Consequently, this work lays a solid foundation for the future fabrication of thermoelectric modules using laser non-equilibrium printing techniques.

关键词： Selective laser melting Laser non-equilibriumheating SnTe compound Thermoelectric performance

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