陈强
苏州大学特聘教授，博士生导师，国家海外高层次青年人才
2014年硕士毕业于南开大学，师从郑健禺教授；2019年博士毕业于德国马克斯普朗克高分子研究所，师从Klaus Müllen教授（德国科学院院士）；随后在牛津大学化学系从事博士后研究，合作导师为Harry Anderson教授（英国皇家学会院士）；于2023年4月加入苏州大学功能纳米与软物质研究院（FUNSOM）。长期从事于石墨烯纳米结构、分子导线和金属有机配合物的精准合成、光电性能调控及器件应用研究。目前，已在国际著名权威期刊发表研究论文36篇，其中第一作者论文17篇，包括Nat. Chem.（2篇）；J. Am. Chem. Soc.（5篇）；Angew. Chem. Int. Ed.（4篇）等。获欧洲发明专利授权2项。曾获“国家优秀自费留学生奖学金”、德国科学基金会Walter Benjamin奖学金等奖励和荣誉，获国家海外高层次人才项目、国家自然科学基金区域创新发展联合基金重点项目、国家自然科学基金青年项目、江苏省自然科学基金青年项目和姑苏创新创业领军人才计划项目等经费资助。
无
长期从事于纳米尺度有机功能材料化学研究，在新型纳米碳分子的结构设计、可控合成、光电磁性能与应用研究方面取得了原创性成果。主要学术贡献有：1）开发了一系列强荧光性石墨烯分子的设计与合成方法，发现这类材料的受激发射与荧光闪烁性，系统研究了受激发射与边界结构和取代基团的关系，并将此类材料应用于有机激光器件、光传感器以及超高分辨率荧光成像等领域；2）发展了开壳层双自由基石墨烯分子的设计方法，实现了从全苯型闭壳层向非全苯型开壳层电子结构的转变及光电磁性能提升。合成了最大尺寸且具有强磁交换耦合作用的开壳层锯齿型边缘菱形石墨烯分子，并提出了增强磁交换耦合作用的结构设计策略，为能够应用于室温和高温自旋逻辑器件及单分子磁体的纳米石墨烯材料的设计提供了新思路；3）发展了卟啉稠合石墨烯纳米结构的精确合成方法，制备了具有全色谱吸收与强近红外光吸收性质的纳米石墨烯以及具有超高载流子迁移率的金属卟啉稠合石墨烯纳米带，为纳米石墨烯材料光电磁性能调控提供了新途径。
（现有2025年申请-考核制博士招生名额若干，招生广告详见：https://muchong.com/t-16359928-1，欢迎联系咨询）
本课题组长期招聘博士后、博士和硕士研究生。
欢迎具有化学和有机光电材料背景的博士后、研究生和本科生加盟。
课题组将提供优厚的个人待遇并为其创造良好的职业发展机会。
有意者请发邮件至chenqiang@suda.edu.cn咨询。
长期从事于纳米尺度有机功能材料化学研究，在新型纳米碳分子的结构设计、可控合成、光电磁性能与应用研究方面取得了原创性成果。主要学术贡献有：1）开发了一系列强荧光性石墨烯分子的设计与合成方法，发现这类材料的受激发射与荧光闪烁性，系统研究了受激发射与边界结构和取代基团的关系，并将此类材料应用于有机激光器件、光传感器以及超高分辨率荧光成像等领域；2）发展了开壳层双自由基石墨烯分子的设计方法，实现了从全苯型闭壳层向非全苯型开壳层电子结构的转变及光电磁性能提升。合成了最大尺寸且具有强磁交换耦合作用的开壳层锯齿型边缘菱形石墨烯分子，并提出了增强磁交换耦合作用的结构设计策略，为能够应用于室温和高温自旋逻辑器件及单分子磁体的纳米石墨烯材料的设计提供了新思路；3）发展了卟啉稠合石墨烯纳米结构的精确合成方法，制备了具有全色谱吸收与强近红外光吸收性质的纳米石墨烯以及具有超高载流子迁移率的金属卟啉稠合石墨烯纳米带，为纳米石墨烯材料光电磁性能调控提供了新途径。
本课题组依托迟力峰院士团队开展研究工作。
研究组现有助理研究员1名，在读博士生2名，硕士生11名。
每年招收化学方向博士后2-3名，博士生1-2名，硕士生3-4名。
为本科生和研究生讲授《高等有机化学》，2学分/36学时。
After Joining Suda:
(17) Chen Q., Guizzardi M., Méndez F., Cerullo G., Ju C., Scotognella F., M. Paternò G., Müllen K., Narita A., “Synthesis of Circumpyrene Tetracarboxdiimides via Diels-Alder Reaction at Bay Regions of Dibenzo[hi,st]ovalene and Emergence of a Bright Charge-Transfer State”, 2025, under review.
(16) Deniz O.#, Sánchez-Sánchez C.#, Chen Q.#, Shinde P., Pignedoli C. A., Liu J., Feng X., Narita A., Müllen K., Fasel R., Passerone D., Ruffieux P., “Electronic and Magnetic Properties of On-surface Synthesized (4,1,4) Chiral Graphene Nanoribbons”, 2025, in press, DOI: 10.1016/j.carbon.2025.120610. Preprint: 10.2139/ssrn.5235465
(15) Weigold S., Liu Y., Li H., Chen Q., Li X., Zhang H., Xie M., Rominger F., Freudenberg J., Bunz U. H. F., Müllen K., Chi L., “Ring Contraction of Cyclooctatetraenes toward Non‐Benzenoid Polycyclic Aromatic Hydrocarbons by Au(111)‐Catalysis and Bulk Pyrolysis”, Chem. Eur. J., 2025, 0, e202501101.
(14) Liu Y., Weigold S., Yan L., Wei Z., Hanne M., Tverskoy O., You S., Xie M., Zhang Y., Chen Q., Rominger F., Bunz U. H. F., Freudenberg J., Du S., Müllen K., Chi L., “Steering Magnetic Coupling in Diradical Nonbenzenoid Nanographenes”, J. Am. Chem. Soc., 2025, in press, DOI: 10.1021/jacs.5c06416.
(13) Zhang L., Xu Q., Xia L., Jiang W., Wang K., Cao P., Chen Q., Huang M., Arquer F. P. G. de and Zhou Y., “Asymmetrically tailored catalysts towards electrochemical energy conversion with non-precious materials”, Chem. Soc. Rev., 2025, 54, 5108–5145.
(12) Lin Y., Ge Y., Xu C., Zhang H., Cui C., Wu Y., Chi L., and Chen Q., “Unveiling the roles of aromaticity in the optoelectronic and charge-transport properties of dehydrobenzo[n]annulenes”, J. Mater. Chem. C, 2025, in press, DOI: 10.1039/D5TC01951F.
(11) Yang Q., Failla V. A., Turunen P., Mateos-Maroto A., Gai M., Zuschratter W., Westendorf S., Gelléri M., Chen Q., Goudappagouda, Zhao H., Zhu X., Morsbach S., Scheele M., Yan W., Landfester K., Kabe R., Bonn M., Narita A. & Liu X., “Reactivatable stimulated emission depletion microscopy using fluorescence-recoverable nanographene”, Nat. Commun., 2025, 16, 1341.
(10) Gu Y., Xiang F., Liang Y., Bai P., Qiu Z., Chen Q., Narita A., Xie Y., Fasel R., Müllen K., “A Poly(2,7-anthrylene) with peri-Fused Porphyrin Edges”, Angew. Chem. Int. Ed., 2024, 63, e202417129.
(9) Wang L., Liu Y., Xie M., Han Y., Chen L., Xue R., Li H., Zhang X., Zhang D., Zhong Q., Chen Q., Zhang H., Müllen K., and Chi L., “Highly Selective On‐Surface Dehydrogenative Aromatization of n‐Hexyl to Phenyl Substituents”, Angew. Chem. Int. Ed., 2024, 63, e202417070.
(8) Edmondson M., Clarke M., N.O’Shea J.; Chen Q., Anderson H., Saywell A., “On-surface synthesis of Ni-porphyrin doped graphene nanoribbons”, ACS Nano, 2024, 18, 49, 33390–33397.
(7) Garcia-Orrit S., Vega-Mayoral V., Chen Q., Serra G., Guizzardi M., Romano V., Conte Dal S., Cerullo G., Mario Di L., Kot M., Loi Antonietta M., Narita A., Müllen K., Tommasini M., Cabanillas-González J., “Visualizing Thermally Activated Conical Intersections Governing Non-Radiative Triplet Decay in a Ni(II) Porphyrin-Nanographene Conjugate with Variable Temperature Transient Absorption Spectroscopy”, J. Phys. Chem. Lett., 2024, 15, 41, 10366.
(6) Wang L., Han Y., Xie M., Li X., Chen Q., Tang Y., Liu Y., Ge H., Li H., Cai-Liang S., Meerholz K., Zhang H.,* Müllen K.,* Lifeng Chi,“Synthesis of Hexabenzocoronene-cored Graphdiyne Nanosheets through Dehydrogenative Coupling on Au(111) Surface”, Angew. Chem. Int. Ed., 2024, 63, e202411722.
(5) Zhao H., Wang Y., Chen Q., Liu Y., Gao Y., Müllen K., Li S., Narita A., “A Nanographene-Porphyrin Hybrid for Near-Infrared-II Phototheranostics”, Adv. Sci., 2024, 11, 2309131.
(4) Wu M., Mühlinghaus M., Li X., Xu C., Chen Q., Zhang H., Müllen K., Chi L., “On-Surface Synthesis of Chevron-Shaped Conjugated Ladder Polymers Consisting of Benzo[a]azulene Units”, Acta Phys. -Chim. Sin., 2024, 40 (8), 2307024.
(3) Chen Q.,#,* Lodi A.,# Zhang H.,# Gee A., Wang H., Kong F., Clarke M., Edmondson M., Hart J., O’Shea J., Stawski W., Narita A., Saywell A., Bonn M., Müllen K., Bogani L.,* Anderson L. H.,* “Porphyrin-Fused Graphene Nanoribbons”, Nat. Chem., 2024, 16, 1133–1140. | ChemRxiv, 2023, DOI: 10.26434/chemrxiv-2023-ghvdb.
(2) Zhu X.,#Chen Q.,# Zhao H.,# Yang Q., Goudappagouda, Gelléri M., Ritz S., Ng D., Koynov K., Parekh H. S., Chetty Kumar V., Thakur Kumar B., Cremer C., Landfester K., Müllen K., Terenzio M., Bonn M., Narita A., and Liu X., “Intrinsic Burst-Blinking Nanographenes for Super-Resolution Bioimaging”, J. Am. Chem. Soc., 2024, 146, 5195–5203.
(1) Chen Q., Giovannantonio Di M., Eimre K., Urgel I. J., Ruffieux P., Pignedoli A. C., Müllen K., Fasel R., Narita A., “On-Surface Interchain Coupling and Skeletal Rearrangement of Indenofluorene Polymers”, Macromol. Chem. Phys., 2023, 224, 2300345. (invited contribution for Special Issue: 80 Years of MCP: The Next Generation of Polymer Researchers)
-----------------------------------------------------------------------------------------------------------------------------------------------------------------
Before Joining Suda:
(31) Garcia-Orrit S., Vega-Mayoral V., Chen Q., Serra G., Paternò G. M., Cánovas E., Narita A., Müllen K., Tommasini M., Cabanillas-González J., “Nanographene-Based Decoration as a Panchromatic Antenna for Metalloporphyrin Conjugates”, Small, 2023, 19, 2301596. (selected as back cover)
(30) Zhu H., Chen Q., Rončević I., Christensen K. E., Anderson H. L., “Anthracene-Porphyrin Nanoribbons”, Angew. Chem. Int. Ed., 2023, 62, e20230703.| ChemRxiv, 2023, DOI: 10.26434/chemrxiv-2023-zl7ck.
(29) Chen Q., Thompson A. L., Christensen K. E., Horton P. N., Coles S. J., Anderson H. L., “β,β-Directly Linked Porphyrin Rings: Synthesis, Photophysical Properties, and Fullerene Binding”, J. Am. Chem. Soc., 2023, 145, 11859−11865.
(28) Biswas K.,# Soler D.,# Mishra S.,#Chen Q.,# Yao X.,# Sánchez-Grande A., Eimre K., Mutombo P., Martín C., Lauwaet K., Gallego M. J., Ruffieux P., Pignedoli A. C., Müllen K., Miranda R., Urgel I. José, Narita A., Fasel R., Jelínek P., Écija D., “Steering Large Magnetic Exchange Coupling in Nanographenes near the Closed-Shell to Open-Shell Transition”, J. Am. Chem. Soc., 2023, 145, 2968–2974. (# equal contribution.)
(27) Björk J.,# Sánchez‐Sánchez C.,#Chen Q.,# Pignedoli A C., Rosen J., Ruffieux P., Feng X., Narita A., Müllen K., Fasel R., “The Role of Metal Adatoms in a Surface‐Assisted Cyclodehydrogenation Reaction on a Gold Surface”, Angew. Chem. Int. Ed., 2022, 61, e2022123. (# equal contribution.)
(26) Jin E., Fu S., Hanayama H., Addicoat A. M., Wei W., Chen Q., Graf R., Landfester K., Bonn M., Zhang I. K., Wang I. H., Müllen K., Narita A., “A Nanographene-Based Two-Dimensional Covalent Organic Framework as a Stable and Efficient Photocatalyst”, Angew. Chem. Int. Ed., 2022, 61, e20211405.
(25) Paternò G. M.,#Chen Q.,# Mármol R. M.,# Guizzardi M., Bonal V., Kabe R., Barker A. J., Boj P. G., Chatterjee S., Ie Y., Villalvilla J. M., Quintana J. A., Scotognella F., Müllen K., Díaz-García M. A., Narita A., Lanzani G., “Excited States Engineering Enables Efficient Near-Infrared Lasing in Nanographenes”, Mater. Horiz., 2022, 9, 393–402. (# equal contribution. Collected in special issue in honour of Seth Marder)
(24) Paternò G. M.,Goudappagouda, Chen Q., Lanzani G., Scotognella F., Narita A., “Large Polycyclic Aromatic Hydrocarbons as Graphene Quantum Dots: from Synthesis to Spectroscopy and Photonics”, Adv. Optical Mater., 2021, 9, 2100508. (selected as Inside Front Cover. collected in Special Issue: Optical Properties and Applications of Crystalline Materials)
(23) Jin E., Yang Q., Ju C.,Chen Q., Landfester K., Bonn M., Müllen K., Liu X., Narita A., “A Highly Luminescent Nitrogen-Doped Nanographene as an Acid- and Metal-Sensitive Fluorophore for Optical Imaging”, J. Am. Chem. Soc., 2021, 143, 10403–10412. (Highlighted by Synfacts 2021, 17, 1093)
(22) Mishra S.,# Yao X.,# Chen Q.,# Eimre Kristjan, Gröning O., Ortiz R., Di Giovannantonio M., Sancho-García J. C., Fernández-Rossier J., Pignedoli C. A., Müllen K., Ruffieux P., Narita A., Fasel R., “Large magnetic exchange coupling in rhombus-shaped nanographenes with zigzag periphery”, Nat. Chem., 2021, 13, 581–586. (# equal contribution.) | ChemRxiv, 2020, DOI: 10.48550/arXiv.2003.03577.
(21) Chen Q., Baumgarten M., Wagner M., Hu Y., Hou I, Narita A., Müllen K., “Dicyclopentaannelated Hexa-peri-hexabenzocoronenes with a Singlet Biradical Ground State”, Angew. Chem. Int. Ed., 2021, 60, 11300–11304.
(20) Chang H., Liu H, Dmitrieva E.,Chen Q., Ma J., He P., Liu P., Popov A. A., Cao X-Y, Wang X-Y, Zou Y., Narita A., Müllen K., Peng H., Hu Y., “Furan-Containing Double Tetraoxa[7]helicene and Its Radical Cation”, Chem. Commun., 2020, 56, 15181–15184.
(19) Xu X., Chen Q., Narita A., “Synthesis and Characterization of Dibenzo[hi,st]ovalene as a Highly Fluorescent Polycyclic Aromatic Hydrocarbon and Its π-Extension to Circumpyrene”, J. Syn. Org. Chem. Jpn., 2020, 78, 1094–1104.
(18) Di Giovannantonio M., Chen Q., Urgel I. J., Ruffieux P., Pignedoli C. A., Müllen K., Narita A., Fasel R., “On-Surface Synthesis of Oligo(indenoindene)”, J. Am. Chem. Soc., 2020, 142, 12925–12929.
(17) Liu X., Chen S., Chen Q., Gelleri S., Ritz S., Kumar S., Cremer C., Landfester K., Müllen K., Parekh S., Narita A., Bonn M., “Nanographene-Based Dyes as Stable, High-Brightness Probes for Super-Resolution Microscopy”, Angew. Chem. Int. Ed., 2020, 59, 496–502. (Selected as back cover)
(16) Chen Q., Schollmeyer D., Müllen K., Narita A., “Synthesis of Circumpyrene by Alkyne Benzannulation of Dibrominated Dibenzo[hi,st]ovalene”, J. Am. Chem. Soc., 2019, 141, 19994–19999.
(15) Fantuzzi P., Candini A., Chen Q., Dumslaff T., Müllen K., Narita A., Affronte M., “Color Sensitive Response of Graphene-Graphene Quantum Dot Photo-Transistor”, J. Phys. Chem. C, 2019, 123, 26490–26497.
(14) Chen Q.,# Thoms S.,# Stöttinger S., Schollmeyer D., Müllen K., Narita A., Basché T., “Dibenzo[hi,st]ovalene as Highly Luminescent Nanographene: Efficient Synthesis via Photochemical Cyclodehydroiodination, Opto-electronic Properties and Single Molecule Spectroscopy”, J. Am. Chem. Soc., 2019, 141, 16439–16449. (# equal contribution. Highlighted by Synfacts 2019, 15, 1371)
(13) Chen Q.,# Zajaczkowski W.,# Seibel J.,# Stöttinger S., Feyter S., Pisula W., Müllen K., Narita A., “Synthesis and Supramolecular Organization of Discotic Liquid Crystalline Dibenzo[hi,st]ovalene with Long-Range Helical Packing”, J. Mater. Chem. C, 2019, 7, 12898–12906. (# equal contribution. Invited article for 2019 Emerging Investigators Themed Issue and selected as inside Front Cover.)
(12) Urgel I. J., Di Giovannantonio M., Gandus G., Chen Q., Liu X., Hayashi H., Ruffieux P., Decurtins S., Narita A., Passerone D., Yamada H., Liu S.-X., Müllen K., Pignedoli A. C., Fasel R., “Overcoming Steric Hindrance in Aryl-Aryl Homocoupling via On-Surface Copolymerization”, ChemPhysChem, 2019, 20, 2360–2366.
(11) Hu Y., Paternò G. M., Wang X.-Y., Wang X.-C., Guizzardi M., Chen Q., Schollmeyer D., Cao X.-Y., Cerullo G., Scotognella F., Müllen K., Narita A., “π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon”, J. Am. Chem. Soc., 2019, 141, 12797–12803.
(10) Giovannantonio M., Eimre K., Yakutovich A., Chen Q., Mishra S., Urgel J., Pignedoli C., Ruffieux C., Müllen K., Narita A., Fasel R., “On-Surface Synthesis of Indeno[2,1-b]fluorene Polymers with Antiaromatic and Open-Shell Characters”, J. Am. Chem. Soc., 2019, 141, 12346–12354.
(9) Chen Q., Wang D., Baumgarten M., Schollmeyer D., Müllen K., Narita A., “Regioselective Bromination of Dibenzo[hi,st]ovalene and Its Post-Synthetic Functionalization”, Chem. Asian J., 2019, 14, 1703–1707. (Invited article for Special Issue: π-Conjugated Compounds for Molecular Materials and highlighted in ChemistryViews, 23, MAR, 2019).
(8) Narita A., Chen Z. P., #Chen Q.,# Müllen K., “Solution and On-Surface Synthesis of Structurally Defined Graphene Nanoribbons as a New Family of Semiconductors”, Chem. Sci., 2019, 10, 964–975. (# equal contribution)
(7) Paternò G. M., Moretti L., Barker J. A., Chen Q., Müllen K., Narita A., Cerullo G., Scotognella F., Lanzani G., “Pump–Push–Probe for Ultrafast All-Optical Switching: The Case of a Nanographene Molecule”, Adv. Funct. Mater., 2019, 29, 1805249.
(6) Paternò G. M., Nicoli L., Chen Q., Müllen K., Narita A., Lanzani G., Scotognella F., “Modulation of the Nonlinear Optical Properties of Dibenzo[hi,st]ovalene by Peripheral Substituents”, J. Phys. Chem. C, 2018, 122, 25007–25013.
(5) Chen Q., Brambilla L., Daukiya L., Mali K. S., De Feyter S., Tommasini M., Müllen K., Narita A. “Synthesis of Triply Fused Porphyrin-Nanographene Conjugates”, Angew. Chem. Int. Ed., 2018, 57, 11233–11237. (Highlighted by Synfacts 2018, 14, 1032)
(4) Coles D. M.#, Chen Q.,# Flatten L. C., Smith J. M., Müllen K., Narita A., Lidzey D. G., “Strong Exciton-Photon Coupling in a Nanographene Filled Microcavity”, Nano Lett., 2017, 17, 5521–5525. (# equal contribution)
(3) Liu Z., Wang H. I., Narita A., Chen Q., Mics Z., Turchinovich D., Kläui M., Bonn M., Müllen K., “Photoswitchable Micro-Supercapacitor Based on a Diarylethene-Graphene Composite Film”, J. Am. Chem. Soc., 2017, 139, 9443–9446.
(2) Paternò G. M.,# Chen Q.,# Wang X. Y., Liu J., Motti S. G., Petrozza A., Feng X., Lanzani G., Müllen K, Narita A., Scotognella F., “Synthesis of Dibenzo[hi,st]ovalene and Its Amplified Spontaneous Emission in a Polystyrene Matrix”, Angew. Chem. Int. Ed., 2017, 56, 6753–6757. (# equal contribution)
(1)Chen Q., Zhu Y. Z., Fan Q. J., Zhang S. C., Zheng J. Y., “Simple and Catalyst-Free Synthesis of meso-O-, -S-, and -C-Substituted Porphyrins”, Org. Lett., 2014, 16, 1590–1593.
陈强
苏州大学特聘教授，博士生导师，国家海外高层次青年人才
2014年硕士毕业于南开大学，师从郑健禺教授；2019年博士毕业于德国马克斯普朗克高分子研究所，师从Klaus Müllen教授（德国科学院院士）；随后在牛津大学化学系从事博士后研究，合作导师为Harry Anderson教授（英国皇家学会院士）；于2023年4月加入苏州大学功能纳米与软物质研究院（FUNSOM）。长期从事于石墨烯纳米结构、分子导线和金属有机配合物的精准合成、光电性能调控及器件应用研究。目前，已在国际著名权威期刊发表研究论文36篇，其中第一作者论文17篇，包括Nat. Chem.（2篇）；J. Am. Chem. Soc.（5篇）；Angew. Chem. Int. Ed.（4篇）等。获欧洲发明专利授权2项。曾获“国家优秀自费留学生奖学金”、德国科学基金会Walter Benjamin奖学金等奖励和荣誉，获国家海外高层次人才项目、国家自然科学基金区域创新发展联合基金重点项目、国家自然科学基金青年项目、江苏省自然科学基金青年项目和姑苏创新创业领军人才计划项目等经费资助。
无
长期从事于纳米尺度有机功能材料化学研究，在新型纳米碳分子的结构设计、可控合成、光电磁性能与应用研究方面取得了原创性成果。主要学术贡献有：1）开发了一系列强荧光性石墨烯分子的设计与合成方法，发现这类材料的受激发射与荧光闪烁性，系统研究了受激发射与边界结构和取代基团的关系，并将此类材料应用于有机激光器件、光传感器以及超高分辨率荧光成像等领域；2）发展了开壳层双自由基石墨烯分子的设计方法，实现了从全苯型闭壳层向非全苯型开壳层电子结构的转变及光电磁性能提升。合成了最大尺寸且具有强磁交换耦合作用的开壳层锯齿型边缘菱形石墨烯分子，并提出了增强磁交换耦合作用的结构设计策略，为能够应用于室温和高温自旋逻辑器件及单分子磁体的纳米石墨烯材料的设计提供了新思路；3）发展了卟啉稠合石墨烯纳米结构的精确合成方法，制备了具有全色谱吸收与强近红外光吸收性质的纳米石墨烯以及具有超高载流子迁移率的金属卟啉稠合石墨烯纳米带，为纳米石墨烯材料光电磁性能调控提供了新途径。
（现有2025年申请-考核制博士招生名额若干，招生广告详见：https://muchong.com/t-16359928-1，欢迎联系咨询）
本课题组长期招聘博士后、博士和硕士研究生。
欢迎具有化学和有机光电材料背景的博士后、研究生和本科生加盟。
课题组将提供优厚的个人待遇并为其创造良好的职业发展机会。
有意者请发邮件至chenqiang@suda.edu.cn咨询。
长期从事于纳米尺度有机功能材料化学研究，在新型纳米碳分子的结构设计、可控合成、光电磁性能与应用研究方面取得了原创性成果。主要学术贡献有：1）开发了一系列强荧光性石墨烯分子的设计与合成方法，发现这类材料的受激发射与荧光闪烁性，系统研究了受激发射与边界结构和取代基团的关系，并将此类材料应用于有机激光器件、光传感器以及超高分辨率荧光成像等领域；2）发展了开壳层双自由基石墨烯分子的设计方法，实现了从全苯型闭壳层向非全苯型开壳层电子结构的转变及光电磁性能提升。合成了最大尺寸且具有强磁交换耦合作用的开壳层锯齿型边缘菱形石墨烯分子，并提出了增强磁交换耦合作用的结构设计策略，为能够应用于室温和高温自旋逻辑器件及单分子磁体的纳米石墨烯材料的设计提供了新思路；3）发展了卟啉稠合石墨烯纳米结构的精确合成方法，制备了具有全色谱吸收与强近红外光吸收性质的纳米石墨烯以及具有超高载流子迁移率的金属卟啉稠合石墨烯纳米带，为纳米石墨烯材料光电磁性能调控提供了新途径。
本课题组依托迟力峰院士团队开展研究工作。
研究组现有助理研究员1名，在读博士生2名，硕士生11名。
每年招收化学方向博士后2-3名，博士生1-2名，硕士生3-4名。
为本科生和研究生讲授《高等有机化学》，2学分/36学时。
After Joining Suda:
(17) Chen Q., Guizzardi M., Méndez F., Cerullo G., Ju C., Scotognella F., M. Paternò G., Müllen K., Narita A., “Synthesis of Circumpyrene Tetracarboxdiimides via Diels-Alder Reaction at Bay Regions of Dibenzo[hi,st]ovalene and Emergence of a Bright Charge-Transfer State”, 2025, under review.
(16) Deniz O.#, Sánchez-Sánchez C.#, Chen Q.#, Shinde P., Pignedoli C. A., Liu J., Feng X., Narita A., Müllen K., Fasel R., Passerone D., Ruffieux P., “Electronic and Magnetic Properties of On-surface Synthesized (4,1,4) Chiral Graphene Nanoribbons”, 2025, in press, DOI: 10.1016/j.carbon.2025.120610. Preprint: 10.2139/ssrn.5235465
(15) Weigold S., Liu Y., Li H., Chen Q., Li X., Zhang H., Xie M., Rominger F., Freudenberg J., Bunz U. H. F., Müllen K., Chi L., “Ring Contraction of Cyclooctatetraenes toward Non‐Benzenoid Polycyclic Aromatic Hydrocarbons by Au(111)‐Catalysis and Bulk Pyrolysis”, Chem. Eur. J., 2025, 0, e202501101.
(14) Liu Y., Weigold S., Yan L., Wei Z., Hanne M., Tverskoy O., You S., Xie M., Zhang Y., Chen Q., Rominger F., Bunz U. H. F., Freudenberg J., Du S., Müllen K., Chi L., “Steering Magnetic Coupling in Diradical Nonbenzenoid Nanographenes”, J. Am. Chem. Soc., 2025, in press, DOI: 10.1021/jacs.5c06416.
(13) Zhang L., Xu Q., Xia L., Jiang W., Wang K., Cao P., Chen Q., Huang M., Arquer F. P. G. de and Zhou Y., “Asymmetrically tailored catalysts towards electrochemical energy conversion with non-precious materials”, Chem. Soc. Rev., 2025, 54, 5108–5145.
(12) Lin Y., Ge Y., Xu C., Zhang H., Cui C., Wu Y., Chi L., and Chen Q., “Unveiling the roles of aromaticity in the optoelectronic and charge-transport properties of dehydrobenzo[n]annulenes”, J. Mater. Chem. C, 2025, in press, DOI: 10.1039/D5TC01951F.
(11) Yang Q., Failla V. A., Turunen P., Mateos-Maroto A., Gai M., Zuschratter W., Westendorf S., Gelléri M., Chen Q., Goudappagouda, Zhao H., Zhu X., Morsbach S., Scheele M., Yan W., Landfester K., Kabe R., Bonn M., Narita A. & Liu X., “Reactivatable stimulated emission depletion microscopy using fluorescence-recoverable nanographene”, Nat. Commun., 2025, 16, 1341.
(10) Gu Y., Xiang F., Liang Y., Bai P., Qiu Z., Chen Q., Narita A., Xie Y., Fasel R., Müllen K., “A Poly(2,7-anthrylene) with peri-Fused Porphyrin Edges”, Angew. Chem. Int. Ed., 2024, 63, e202417129.
(9) Wang L., Liu Y., Xie M., Han Y., Chen L., Xue R., Li H., Zhang X., Zhang D., Zhong Q., Chen Q., Zhang H., Müllen K., and Chi L., “Highly Selective On‐Surface Dehydrogenative Aromatization of n‐Hexyl to Phenyl Substituents”, Angew. Chem. Int. Ed., 2024, 63, e202417070.
(8) Edmondson M., Clarke M., N.O’Shea J.; Chen Q., Anderson H., Saywell A., “On-surface synthesis of Ni-porphyrin doped graphene nanoribbons”, ACS Nano, 2024, 18, 49, 33390–33397.
(7) Garcia-Orrit S., Vega-Mayoral V., Chen Q., Serra G., Guizzardi M., Romano V., Conte Dal S., Cerullo G., Mario Di L., Kot M., Loi Antonietta M., Narita A., Müllen K., Tommasini M., Cabanillas-González J., “Visualizing Thermally Activated Conical Intersections Governing Non-Radiative Triplet Decay in a Ni(II) Porphyrin-Nanographene Conjugate with Variable Temperature Transient Absorption Spectroscopy”, J. Phys. Chem. Lett., 2024, 15, 41, 10366.
(6) Wang L., Han Y., Xie M., Li X., Chen Q., Tang Y., Liu Y., Ge H., Li H., Cai-Liang S., Meerholz K., Zhang H.,* Müllen K.,* Lifeng Chi,“Synthesis of Hexabenzocoronene-cored Graphdiyne Nanosheets through Dehydrogenative Coupling on Au(111) Surface”, Angew. Chem. Int. Ed., 2024, 63, e202411722.
(5) Zhao H., Wang Y., Chen Q., Liu Y., Gao Y., Müllen K., Li S., Narita A., “A Nanographene-Porphyrin Hybrid for Near-Infrared-II Phototheranostics”, Adv. Sci., 2024, 11, 2309131.
(4) Wu M., Mühlinghaus M., Li X., Xu C., Chen Q., Zhang H., Müllen K., Chi L., “On-Surface Synthesis of Chevron-Shaped Conjugated Ladder Polymers Consisting of Benzo[a]azulene Units”, Acta Phys. -Chim. Sin., 2024, 40 (8), 2307024.
(3) Chen Q.,#,* Lodi A.,# Zhang H.,# Gee A., Wang H., Kong F., Clarke M., Edmondson M., Hart J., O’Shea J., Stawski W., Narita A., Saywell A., Bonn M., Müllen K., Bogani L.,* Anderson L. H.,* “Porphyrin-Fused Graphene Nanoribbons”, Nat. Chem., 2024, 16, 1133–1140. | ChemRxiv, 2023, DOI: 10.26434/chemrxiv-2023-ghvdb.
(2) Zhu X.,#Chen Q.,# Zhao H.,# Yang Q., Goudappagouda, Gelléri M., Ritz S., Ng D., Koynov K., Parekh H. S., Chetty Kumar V., Thakur Kumar B., Cremer C., Landfester K., Müllen K., Terenzio M., Bonn M., Narita A., and Liu X., “Intrinsic Burst-Blinking Nanographenes for Super-Resolution Bioimaging”, J. Am. Chem. Soc., 2024, 146, 5195–5203.
(1) Chen Q., Giovannantonio Di M., Eimre K., Urgel I. J., Ruffieux P., Pignedoli A. C., Müllen K., Fasel R., Narita A., “On-Surface Interchain Coupling and Skeletal Rearrangement of Indenofluorene Polymers”, Macromol. Chem. Phys., 2023, 224, 2300345. (invited contribution for Special Issue: 80 Years of MCP: The Next Generation of Polymer Researchers)
-----------------------------------------------------------------------------------------------------------------------------------------------------------------
Before Joining Suda:
(31) Garcia-Orrit S., Vega-Mayoral V., Chen Q., Serra G., Paternò G. M., Cánovas E., Narita A., Müllen K., Tommasini M., Cabanillas-González J., “Nanographene-Based Decoration as a Panchromatic Antenna for Metalloporphyrin Conjugates”, Small, 2023, 19, 2301596. (selected as back cover)
(30) Zhu H., Chen Q., Rončević I., Christensen K. E., Anderson H. L., “Anthracene-Porphyrin Nanoribbons”, Angew. Chem. Int. Ed., 2023, 62, e20230703.| ChemRxiv, 2023, DOI: 10.26434/chemrxiv-2023-zl7ck.
(29) Chen Q., Thompson A. L., Christensen K. E., Horton P. N., Coles S. J., Anderson H. L., “β,β-Directly Linked Porphyrin Rings: Synthesis, Photophysical Properties, and Fullerene Binding”, J. Am. Chem. Soc., 2023, 145, 11859−11865.
(28) Biswas K.,# Soler D.,# Mishra S.,#Chen Q.,# Yao X.,# Sánchez-Grande A., Eimre K., Mutombo P., Martín C., Lauwaet K., Gallego M. J., Ruffieux P., Pignedoli A. C., Müllen K., Miranda R., Urgel I. José, Narita A., Fasel R., Jelínek P., Écija D., “Steering Large Magnetic Exchange Coupling in Nanographenes near the Closed-Shell to Open-Shell Transition”, J. Am. Chem. Soc., 2023, 145, 2968–2974. (# equal contribution.)
(27) Björk J.,# Sánchez‐Sánchez C.,#Chen Q.,# Pignedoli A C., Rosen J., Ruffieux P., Feng X., Narita A., Müllen K., Fasel R., “The Role of Metal Adatoms in a Surface‐Assisted Cyclodehydrogenation Reaction on a Gold Surface”, Angew. Chem. Int. Ed., 2022, 61, e2022123. (# equal contribution.)
(26) Jin E., Fu S., Hanayama H., Addicoat A. M., Wei W., Chen Q., Graf R., Landfester K., Bonn M., Zhang I. K., Wang I. H., Müllen K., Narita A., “A Nanographene-Based Two-Dimensional Covalent Organic Framework as a Stable and Efficient Photocatalyst”, Angew. Chem. Int. Ed., 2022, 61, e20211405.
(25) Paternò G. M.,#Chen Q.,# Mármol R. M.,# Guizzardi M., Bonal V., Kabe R., Barker A. J., Boj P. G., Chatterjee S., Ie Y., Villalvilla J. M., Quintana J. A., Scotognella F., Müllen K., Díaz-García M. A., Narita A., Lanzani G., “Excited States Engineering Enables Efficient Near-Infrared Lasing in Nanographenes”, Mater. Horiz., 2022, 9, 393–402. (# equal contribution. Collected in special issue in honour of Seth Marder)
(24) Paternò G. M.,Goudappagouda, Chen Q., Lanzani G., Scotognella F., Narita A., “Large Polycyclic Aromatic Hydrocarbons as Graphene Quantum Dots: from Synthesis to Spectroscopy and Photonics”, Adv. Optical Mater., 2021, 9, 2100508. (selected as Inside Front Cover. collected in Special Issue: Optical Properties and Applications of Crystalline Materials)
(23) Jin E., Yang Q., Ju C.,Chen Q., Landfester K., Bonn M., Müllen K., Liu X., Narita A., “A Highly Luminescent Nitrogen-Doped Nanographene as an Acid- and Metal-Sensitive Fluorophore for Optical Imaging”, J. Am. Chem. Soc., 2021, 143, 10403–10412. (Highlighted by Synfacts 2021, 17, 1093)
(22) Mishra S.,# Yao X.,# Chen Q.,# Eimre Kristjan, Gröning O., Ortiz R., Di Giovannantonio M., Sancho-García J. C., Fernández-Rossier J., Pignedoli C. A., Müllen K., Ruffieux P., Narita A., Fasel R., “Large magnetic exchange coupling in rhombus-shaped nanographenes with zigzag periphery”, Nat. Chem., 2021, 13, 581–586. (# equal contribution.) | ChemRxiv, 2020, DOI: 10.48550/arXiv.2003.03577.
(21) Chen Q., Baumgarten M., Wagner M., Hu Y., Hou I, Narita A., Müllen K., “Dicyclopentaannelated Hexa-peri-hexabenzocoronenes with a Singlet Biradical Ground State”, Angew. Chem. Int. Ed., 2021, 60, 11300–11304.
(20) Chang H., Liu H, Dmitrieva E.,Chen Q., Ma J., He P., Liu P., Popov A. A., Cao X-Y, Wang X-Y, Zou Y., Narita A., Müllen K., Peng H., Hu Y., “Furan-Containing Double Tetraoxa[7]helicene and Its Radical Cation”, Chem. Commun., 2020, 56, 15181–15184.
(19) Xu X., Chen Q., Narita A., “Synthesis and Characterization of Dibenzo[hi,st]ovalene as a Highly Fluorescent Polycyclic Aromatic Hydrocarbon and Its π-Extension to Circumpyrene”, J. Syn. Org. Chem. Jpn., 2020, 78, 1094–1104.
(18) Di Giovannantonio M., Chen Q., Urgel I. J., Ruffieux P., Pignedoli C. A., Müllen K., Narita A., Fasel R., “On-Surface Synthesis of Oligo(indenoindene)”, J. Am. Chem. Soc., 2020, 142, 12925–12929.
(17) Liu X., Chen S., Chen Q., Gelleri S., Ritz S., Kumar S., Cremer C., Landfester K., Müllen K., Parekh S., Narita A., Bonn M., “Nanographene-Based Dyes as Stable, High-Brightness Probes for Super-Resolution Microscopy”, Angew. Chem. Int. Ed., 2020, 59, 496–502. (Selected as back cover)
(16) Chen Q., Schollmeyer D., Müllen K., Narita A., “Synthesis of Circumpyrene by Alkyne Benzannulation of Dibrominated Dibenzo[hi,st]ovalene”, J. Am. Chem. Soc., 2019, 141, 19994–19999.
(15) Fantuzzi P., Candini A., Chen Q., Dumslaff T., Müllen K., Narita A., Affronte M., “Color Sensitive Response of Graphene-Graphene Quantum Dot Photo-Transistor”, J. Phys. Chem. C, 2019, 123, 26490–26497.
(14) Chen Q.,# Thoms S.,# Stöttinger S., Schollmeyer D., Müllen K., Narita A., Basché T., “Dibenzo[hi,st]ovalene as Highly Luminescent Nanographene: Efficient Synthesis via Photochemical Cyclodehydroiodination, Opto-electronic Properties and Single Molecule Spectroscopy”, J. Am. Chem. Soc., 2019, 141, 16439–16449. (# equal contribution. Highlighted by Synfacts 2019, 15, 1371)
(13) Chen Q.,# Zajaczkowski W.,# Seibel J.,# Stöttinger S., Feyter S., Pisula W., Müllen K., Narita A., “Synthesis and Supramolecular Organization of Discotic Liquid Crystalline Dibenzo[hi,st]ovalene with Long-Range Helical Packing”, J. Mater. Chem. C, 2019, 7, 12898–12906. (# equal contribution. Invited article for 2019 Emerging Investigators Themed Issue and selected as inside Front Cover.)
(12) Urgel I. J., Di Giovannantonio M., Gandus G., Chen Q., Liu X., Hayashi H., Ruffieux P., Decurtins S., Narita A., Passerone D., Yamada H., Liu S.-X., Müllen K., Pignedoli A. C., Fasel R., “Overcoming Steric Hindrance in Aryl-Aryl Homocoupling via On-Surface Copolymerization”, ChemPhysChem, 2019, 20, 2360–2366.
(11) Hu Y., Paternò G. M., Wang X.-Y., Wang X.-C., Guizzardi M., Chen Q., Schollmeyer D., Cao X.-Y., Cerullo G., Scotognella F., Müllen K., Narita A., “π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon”, J. Am. Chem. Soc., 2019, 141, 12797–12803.
(10) Giovannantonio M., Eimre K., Yakutovich A., Chen Q., Mishra S., Urgel J., Pignedoli C., Ruffieux C., Müllen K., Narita A., Fasel R., “On-Surface Synthesis of Indeno[2,1-b]fluorene Polymers with Antiaromatic and Open-Shell Characters”, J. Am. Chem. Soc., 2019, 141, 12346–12354.
(9) Chen Q., Wang D., Baumgarten M., Schollmeyer D., Müllen K., Narita A., “Regioselective Bromination of Dibenzo[hi,st]ovalene and Its Post-Synthetic Functionalization”, Chem. Asian J., 2019, 14, 1703–1707. (Invited article for Special Issue: π-Conjugated Compounds for Molecular Materials and highlighted in ChemistryViews, 23, MAR, 2019).
(8) Narita A., Chen Z. P., #Chen Q.,# Müllen K., “Solution and On-Surface Synthesis of Structurally Defined Graphene Nanoribbons as a New Family of Semiconductors”, Chem. Sci., 2019, 10, 964–975. (# equal contribution)
(7) Paternò G. M., Moretti L., Barker J. A., Chen Q., Müllen K., Narita A., Cerullo G., Scotognella F., Lanzani G., “Pump–Push–Probe for Ultrafast All-Optical Switching: The Case of a Nanographene Molecule”, Adv. Funct. Mater., 2019, 29, 1805249.
(6) Paternò G. M., Nicoli L., Chen Q., Müllen K., Narita A., Lanzani G., Scotognella F., “Modulation of the Nonlinear Optical Properties of Dibenzo[hi,st]ovalene by Peripheral Substituents”, J. Phys. Chem. C, 2018, 122, 25007–25013.
(5) Chen Q., Brambilla L., Daukiya L., Mali K. S., De Feyter S., Tommasini M., Müllen K., Narita A. “Synthesis of Triply Fused Porphyrin-Nanographene Conjugates”, Angew. Chem. Int. Ed., 2018, 57, 11233–11237. (Highlighted by Synfacts 2018, 14, 1032)
(4) Coles D. M.#, Chen Q.,# Flatten L. C., Smith J. M., Müllen K., Narita A., Lidzey D. G., “Strong Exciton-Photon Coupling in a Nanographene Filled Microcavity”, Nano Lett., 2017, 17, 5521–5525. (# equal contribution)
(3) Liu Z., Wang H. I., Narita A., Chen Q., Mics Z., Turchinovich D., Kläui M., Bonn M., Müllen K., “Photoswitchable Micro-Supercapacitor Based on a Diarylethene-Graphene Composite Film”, J. Am. Chem. Soc., 2017, 139, 9443–9446.
(2) Paternò G. M.,# Chen Q.,# Wang X. Y., Liu J., Motti S. G., Petrozza A., Feng X., Lanzani G., Müllen K, Narita A., Scotognella F., “Synthesis of Dibenzo[hi,st]ovalene and Its Amplified Spontaneous Emission in a Polystyrene Matrix”, Angew. Chem. Int. Ed., 2017, 56, 6753–6757. (# equal contribution)
(1)Chen Q., Zhu Y. Z., Fan Q. J., Zhang S. C., Zheng J. Y., “Simple and Catalyst-Free Synthesis of meso-O-, -S-, and -C-Substituted Porphyrins”, Org. Lett., 2014, 16, 1590–1593.