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第16届Angewandte Advances前沿交叉论坛暨Angewandte Chemie 新刊发布会邀您见证！

MaterialsViews · 公众号 · · 2025-04-10 08:30

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作为化学领域的顶尖期刊， Angewandte Chemie 及其所属的德国化学学会（GDCh）通过 Angewandte Symposia系列研讨会，持续推动全球化学前沿交流，历届活动反响热烈。 Angewandte Symposia 邀请世界顶尖的化学家作为主讲人，为 Angewandte Chemie 的作者与读者们带来精彩的主题演讲。

为了给 Angewandte Chemie 与化学研究者社群，尤其是年轻科研工作者们提供更多面对面交流的机会以及更好的支持不同事业阶段的化学研究者， Angewandte Chemie 组织了一系列 Angewandte Advances 研讨会。

Angewandte Advances 系列研讨会将作为大型化学学术会议的特别分会场，举行为期半天至一天的学术报告与讨论活动。每期 Angewandte Advances 将邀请来自不同领域、处于不同事业阶段的6-8位优秀学者做学术报告，并由 Angewandte Chemie 的编辑主持以及组织讨论。

本期 Angewandte Advances作为第三届大连催化+国际峰会的特别分会，将邀请到六位主讲人，分别为万颖教授（上海师范大学）、徐铜文教授（中国科学技术大学）、祝艳教授（南京大学）、乔振安教授（吉林大学）、盧怡君教授（香港中文大学）和王训教授（清华大学），敬请期待！

本次研讨会还将隆重举行 Angewandte Chemie Novit 新刊发布会 ，诚邀您共同见证这一重要时刻！

更多关于Novit的创刊宗旨、期刊特色及评审标准，请访问： https://mp.weixin.qq.com/s/P8WozWD-oYzYOGdWC8rU2g

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主讲人及报告简介

万颖

上海师范大学

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Ying Wan, Professor and Ph.D. Supervisor, is a recipient of the National Science Fund for Distinguished Young Scholars and the leader of an innovative research team under the Ministry of Education. Her research focuses on the design and structural regulation of metal catalysts supported on mesoporous materials, as well as their applications in the hydrogenation of nitrogen-containing heterocycles, biomass conversion, and lithium-sulfur batteries. She has published over 90 papers in prestigious journals such as Nat. Catal., Nat. Commun., Chem, JACS, Angew. Chem. and Natl. Sci. Rev. . She holds 15 authorized invention patents and has co-authored three books, including Ordered Mesoporous Materials. Prof. Wan serves as an Associate Editor of Chem. Synth and an editorial board member of Chin. J. Catal. . She has also served as the secretary for the 10 ^th and 11 ^th International Mesostructured Materials Association. Additionally, she is a member of the Catalysis Committee, the Nano Chemistry Committee, and the Committee of Women Chemists of the Chinese Chemical Society.

报告题目：

Designing Carbon Supported Metal Nanocatalysts using the d Charge Descriptor

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Precise catalysis is at the core of breakthroughs in energy and chemical catalysis technologies. It involves precise design and synthesis of catalytic active sites to achieve atomically economical reaction pathways through directional activation of chemical bonds. Our work focuses on the mesoporous carbon supported catalysts tailored for precise catalysis.

Firstly, d/p -electron charge of metal or oxide/sulfide materials which are experimentally measurable are identified as descriptors for catalytic performance. Based on this, principles for designing metal (oxide/sulfide) catalytic materials are proposed, focusing on electronic structure descriptors in catalyst structure-performance relationships. Secondly, utilizing long-range ordered mesoporous structures and local coordination environments, we achieve precise control over electronic structures of active centers, creating mesostructured confined catalysts. Finally, within confined mesospaces, mass transfer and chemical reaction processes can be controlled at the molecular level, and a new mesostructured confined metal precision catalysis system is established with minimal chemical bond transforms, shortest reaction pathways, and lowest carbon emissions.

For example, in the hydrogenation reaction of 2-methyl-3-butyn-2-ol (MBY) to 2-methyl-3-butene-2-ol (MBE), an increase in Pd d -electron charge density changes the adsorption configuration of MBE, breaking the linear scaling relationship. The turn-over frequency (TOF) of Pd/mesoporous carbon catalyst with the highest d charge is 17 times that of Lindlar catalyst, maintaining about 95% MBE selectivity even at close to 100% MBY conversion. A Pd/mesoporous carbon catalyst with increased d charge can simultaneously activate C-H bonds at C2 and C5 positions of pyrrole and thiophene molecules, achieving one-step synthesis of diaryl products with nearly 100% selectivity. This approach shortens reaction steps in traditional homogeneous catalysis.

徐铜文

中国科学技术大学

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Dr. Tongwen Xu is Chair Professor of Chemistry Engineering at University of Science and Technology of China (USTC). He obtained B.E (1989) and M.E. degree (1992) from Hefei University of Technology and Ph.D from Tianjin University (1995). Dr. Xu joined the USTC as an associate professor in 1997 was promoted to a full time professor in 2001. Dr. Xu was a short-term visiting scientist of the University of Tokyo (2000), Tokyo Institute of Technology (2001) and also a Brain-Pool Professor of Korea in Gwangju Institute of Science and Technology (2006-2007). The research interests of Dr. Xu are focused on the development and practical applications of ion exchange membranes. In his lab (http://membrane.ustc.edu.cn), he explores novel types of materials for cation/anion exchange membranes and bipolar membranes. He also investigates green and safe functionalization methods that can convert normal polymers into ion exchange membranes. Dr. Xu is dedicated to the industrial applications of ion exchange membranes, including diffusion dialysis (DD), electrodialysis (ED), bipolar membrane electrodialysis (BMED), water electrolysis and flow batteries. In doing so, he expects to solve the most urgent challenge related to energy conversion and storage, environment and resources. Dr. Xu has authored >600 publications (including Nature, Nature Sustainability, Science Advance, Chem, JACS, Angnew Chem, Adv Mater, AIChE J), 7 Books, 20+ Chapters, and holds >90 issued Patents for ion exchange membranes and related processes. He is named as a highly cited researcher by Thomson Reuters (ISI Web of Knowledge) with over 23000+ citations and H-index of 87. Dr. Xu is the Editor of Journal of Membrane Science, and editorial boards of Advanced Material Technologies, Heliyon, Advanced Membranes, Ind. Eng. Chem. Res.(former), and etc. Dr. Xu ’s contribution to ion exchange membranes and related processes has brought him numerous awards. He received the first class Technical Advance Awards of Chinese Membrane Society (2006, 2009), the first class Technical Advance Awards of Chinese Petroleum and Chemical Engineering Society (2008, 2009, 2021), Outstanding Youth Foundation of China (2010), Fellow of Royal Society of Chemistry(2013), Cheung Kong Scholars (2014), Award for the National Hundred Talent Project (2015), K.C.Wong Talent Award (2016), Hou Debang Chemical Engineering Science and Technology Award of achievements (2016), National Award for Technological Invention (2018), Fellow of Chemical Industry and Engineering Society of China (CIESC) (2020), National Labor Medal(2024), et al.

报告题目：

New Generation Ion Exchange Membranes: Driving the Double Carbon Agenda

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Environmental and energy-related technologies, including redox flow batteries, fuel cells, water electrolysis, electrochemical carbon capture, and electrodialysis-based ion separation, are pivotal in achieving the dual objectives of peak carbon emissions and carbon neutrality. These technologies rely fundamentally on electromembrane processes, where ion exchange membranes (IEMs) play a critical role by enabling selective ion transport and separating anode and cathode reactions. Traditional IEMs, such as those based on perfluorocarbon Nafion and hydrocarbon polyelectrolytes, are well-established and feature microphase-separated structures. However, they are hindered by the well-known conductivity/selectivity tradeoff, which limits their performance in advanced applications. To address this challenge, our research group has pioneered a new paradigm in membrane design: utilizing confined micropores as ion channels. This innovative approach has been realized through membranes fabricated from charged polymers of intrinsic microporosity, hyper-crosslinked polymers, and ultramicroporous polymer frameworks.The rigidly confined micropores in these next-generation membranes offer a unique combination of high size-exclusion-imposed ion selectivity and high free volume-induced permeability. Remarkably, by leveraging rigid pore confinement and multi-interaction mechanisms between ions and the membrane, triazine framework membranes have achieved near-frictionless ion flow, setting a new benchmark for ion transport efficiency. As next-generation IEMs, these micropore-confined membranes have already demonstrated exceptional performance in organic redox flow batteries and water electrolysis systems. We are confident that their potential extends to a wide range of other electromembrane processes, further advancing the development of sustainable energy technologies. In this presentation, we will provide an overview of traditional IEMs developed in our laboratory and highlight the ground breaking applications of next-generation IEMs in flow batteries and water electrolysis. We will also illustrate how these innovations contribute to the realization of the double carbon goals, paving the way for a cleaner, more sustainable future.

祝艳

南京大学

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Yan Zhu is currently a full-time professor at Nanjing University. Her research focuses on the catalytic application of atomically precise metal clusters with crystallographic structures. She received multiple awards with Distinguished Young Scholar of NSF, The Distinguished Lectureship Award of The Chemical Society of Japan, and Distinguished Woman Young Scientist of Jiangsu Province. She is also selected as editorial board members for Green Energy & Environment and Current Opinion in Green and Sustainable Chemistry.

报告题目：

Catalysis Application of Atomically Precise Metal Clusters

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Heterogeneous catalysts play very important roles in many reactions such as hydrogenation, oxidation and energy production. However, it is still challenging for correlating the catalyst structure with their catalytic properties. Atomically precise metal clusters can solve the difficulty, because their total structures can be solved by single-crystal X-ray crystallography. This report is expected to provide a new scientific vision insight into catalytic mechanisms for some reactions on atomically precise metal cluster catalysts, which is completely different from conversional heterogeneous catalysts. Such metal clusters not only provide new opportunities for unraveling catalysis at an atomic level, but also promote the exploration of new chemical processes with metal clusters as well-defined, highly efficient catalysts. It is expected that metal cluster catalysts can ultimately bring metal catalysis to an exciting, new level.

乔振安

吉林大学

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Zhen-An Qiao got his Ph.D.degree in inorganic chemistry from Jilin University in 2011. He worked as a postdoc at University of Tennessee and Oak Ridge National Laboratory during 2011–2015. He received National Young Talent of China of 2014, and then joined the faculty of Jilin University in 2015, where he is now Professor in the State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Department of Chemistry. In 2024, he received National Outstanding Youth Science Foundation of China. Zhen-An Qiao is committed to the research of synthetic chemistry of mesoporous materials for catalysis, energy storage and bioscience. Focusing on exploring new chemical synthesis methods, the applicant has achieved the directional preparation of new porous materials for well-defined materials with atomically precise surfaces and interfaces, established new methodology by regulating the molecule assembly process as well as the reaction dynamics and thermodynamic equilibrium, thereby gaining a fundamental understanding of how atomic structure affects performance. More than 130 SCI papers have been published by Zhen-An Qiao as corresponding authors, including Angew. Chem. Int. Ed. (12), Adv. Mater. (7), JACS (1), Nat. Commun. (1), ACS Nano. (1) and Nano Lett. (2). The non-self-citations are more than 8000 times. Zhen-An Qiao served as council member of International Mesostructured Materials Association Council and editorial board member for Science Bulletin and Chinese Chemical Letters journals.

报告题目：

Multi-Component Mesoporous Materials: Synthesis, Assembly and Applications

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With the development of synthetic chemistry, mesoporous materials have been designed and gradually expanded from single-component to complicated multicomponent structure with richer functions. Simple component mesoporous materials with high surface and adjustable pore architecture have been widely synthesized and developed. Recently, multicomponent mesoporous materials gradually arouse research interest owing to the high-density redox metal sites, variable electronic structures and excellent thermal stability for fulfilling application requirement. However, the exploration for multicomponent MMOs is at early stage and challenging. Our group is committed to the research of synthetic chemistry of multi-component mesoporous materials. Focusing on exploring new chemical synthesis methods, we have achieved the directional preparation of new mesoporous materials, precise modulation of material microstructure and establishment of new methodology by regulating the molecule assembly process as well as the reaction dynamics and thermodynamic equilibrium. The main innovative results achieved are as follows: 1) An interface confined coordination-self-assembly synthetic method was developed, the principle of energy balance was proposed and a series of mesoporous multiple inorganic materials have been synthesized (including perovskite metal oxides, high-entropy metal oxides, polyanionic materials and so on). 2) Synthesis methods of specific polymerization reactions combined with molecule self-assembly were designed and multi-component doped mesoporous carbon materials have been prepared. 3) By discovering new type of template, the solvent-free synthesis methodology for mesoporous materials has been proposed and established, which realize the universal and efficient synthesis for single component and multi-structured mesoporous materials and some achievements have been transformed.

盧怡君

香港中文大学

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Prof. Yi-Chun Lu received her Ph.D. degree from MIT in 2012. She is a Professor at The Chinese University of Hong Kong (CUHK). She serves as the Associate Editor of Journal of Materials Chemistry A and Materials Advances from Royal Society of Chemistry. She is Fellow of Royal Society of Chemistry, Founding Member of Young Academy of Science of Hong Kong and was the recipient of ISE Tajima Prize, Hong Kong Engineering Science and Technology Award 2023, Xplorer Prize 2021, IBA Early Career Award 2021 etc. Dr. Lu's research interest centers on developing fundamental understandings and material design principles for clean energy storage and conversion. Specifically, her research group is studying: Electrode and electrolyte design for high-energy metal-air and metal sulfur batteries; Redox-active components and solution chemistry for redox-flow batteries; Electrode and electrolyte design for high-voltage aqueous batteries; Mechanistic understanding of interfacial phenomena governing electrochemical energy conversion and storage processes.

报告题目：

Material Designs for High-Performance Aqueous Redox Flow Batteries

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Energy storage systems play a crucial role in the integration of renewable energy sources, which are often unstable and intermittent, such as solar and wind power. These systems ensure a reliable and consistent energy supply by storing excess energy generated during peak production times and releasing it when production is low. Non-aqueous lithium-ion batteries dominate the battery market due to their high energy density, which allows them to store a large amount of energy in a relatively small volume. However, these batteries have a significant drawback: they are flammable. This flammability poses a risk of catastrophic damage, especially in large-scale applications where safety is paramount. Aqueous redox flow batteries (RFBs) offer a promising alternative for scalable, safe, and long-duration energy storage. One of the key advantages of RFBs is their design flexibility, which allows for independent scaling of power and energy capacity. This makes them highly adaptable to various energy storage needs. However, the widespread adoption of all-vanadium redox flow battery is limited by the low abundance and high cost of vanadium, making them less economically viable for large-scale deployment. In this presentation, we will discuss the development of emerging flow battery systems offering low-cost and high-capacity energy storage. We will discuss innovative approaches to mitigate crossover and improve reaction kinetics, thereby making these batteries more efficient and reliable.

王训

清华大学

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Xun Wang received his PhD degree from the Department of Chemistry, Tsinghua University in 2004. He then joined the faculty of the Department of Chemistry, Tsinghua University in 2004, and was promoted to associate professor and full professor in 2005 and 2007, respectively. His current research interests include the synthetic methodology, formation mechanism, and properties of monodisperse nanocrystals. His main awards include National Natural Science Award (2nd grade, 2023, 2008) Xplorer Prize (2019), ISHA Roy-Somiya Award (2018), Science and Technology Award for Chinese Youth (2009), National Fund for Outstanding Young Scientists (2007) and IUPAC Prize for Young Chemists (2005).

报告题目：

Sub-1nm Materials Chemistry

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Subnanometer materials (SNMs) refer to nanomaterials with a feature size close to 1 nm, similar with the diameter of a single polymer, DNA strand and a single cluster/unit cell. The growth and assembly of sub-nanometer building blocks can be controlled by interactions at atomic levels, representing the limit for the precise manipulation of materials. The size, geometry and flexibility of 1D SNMs inorganic backbones is similar with the polymer chains, bringing excellent gelability, adhesiveness and processability different from inorganic nanocrystals. The ultrahigh surface atom ratio of SNMs results in significantly increased surface energy, leading to the significant rearrangement of surface atoms. Unconventional phases, immiscible metal alloys and high entropy materials with few atomic layers can be stabilized, and the spontaneously twisting of SNMs may induce the intrinsic structural chirality. Electron delocalization may also emerge at the sub-nanoscale, giving rise to the significantly enhanced catalytic activity. In this talk, I will summarize recent progress on SNMs, including their synthesis, polymer-like properties, structural chirality and catalytic properties toward energy conversion. As a critical size region in nanoscience, the development of functional SNMs may fuse the boundary of inorganic materials and polymers, and conduce to the precise manufacturing of materials at atomic levels.

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