Spectroscopy, Physical and Theoretical Chemistry, Electronic, Optical and Magnetic Materials, Materials Chemistry
36
Scopus Publications
2148
Scholar Citations
17
Scholar h-index
26
Scholar i10-index
Scopus Publications
Room temperature collective blinking and photon bunching from CsPbBr3 quantum dot superlattice Qiwen Tan, Sudipta Seth, Boris Louis, Xiayan Wu, Nithin Pathoor, Toranosuke Takagi, Shun Omagari, Takumi Sannomiya, Johan Hofkens, Martin Vacha Nature Communications, 2026 Development of quantum systems supporting collective many-body states is crucial for advancement of quantum technologies, and perovskite quantum dots (QDs) have emerged as promising quantum light sources. However, photon bunching, a key signature of collective states, has been observed in perovskites only at cryogenic temperatures. Here, we report collective blinking and photon bunching in perovskite QD superlattices at room temperature. Sub-wavelength-sized CsPbBr3 superlattices exhibit distinct two-level blinking, and demonstrate photon bunching with a degree of up to 3.9. Time-resolved photoluminescence and super-resolution imaging reveal long lifetime components, and emission spatially confined to regions tens of nanometers in size, observations consistent with long-range exciton migration to a localized energy trap within the superlattice. Power-dependent degree of bunching and analysis of the bunching dynamics point to biexciton–exciton cascade emission as the origin of photon bunching. These findings establish perovskite QD superlattices as a promising platform for room-temperature collective optical phenomena. Perovskite quantum dot superlattices have emerged as a promising platform for studying collective optical phenomena. Here the authors report collective photoluminescence blinking and photon bunching in a self-assembled CsPbBr3 quantum dot superlattice, which they attribute to cascade-like biexciton-exciton emission.
Machine learning for microscopy data analytics targeting real-time optical characterization of semiconductor nanocrystals Amitrajit Mukherjee, Robby Reynaerts, Bapi Pradhan, Sudipta Seth, Andreas T. Rösch, Tamali Banerjee, Lata Chouhan, Handong Jin, Christian Sternemann, Michael Paulus, Luca Leoncino, Kunal S. Mali, Steven De Feyter, Maarten B. J. Roeffaers, E. W. Meijer, Johan Hofkens, Elke Debroye Nature Communications, 2026 Semiconductor nanocrystals with uniform morphology and composition are expected to show consistent responses during light-matter interactions. However, microscopy reveals significant variations in their photoluminescence blinking patterns, even under identical experimental conditions. This discrepancy arises from differences in crystal defects and nonradiative trap states. As a result, heterogeneous blinking patterns serve as valuable indicator of material quality, uncovering several concealed features through statistical analysis of large datasets. Nonetheless, efficient segregation and analysis of numerous blinking trajectories remain a challenge due to laborious calculations, computational bottlenecks, and manual intervention. In this study, we introduce a robust unsupervised machine learning (UML) assisted module to cluster high-dimensional blinking patterns in near-real-time, while calculating category-wise power spectral densities (PSD) to investigate active traps. Furthermore, we explore the impact of data preprocessing on clustering performance. The ‘clustering-segregation-analysis’ (UML-PSD) methodology demonstrates versatility, paving a way to advance contemporary (micro)spectroscopy, specifically for rapid and cost-effective optical characterization of semiconductor nanocrystals.
Arm-Length-Controlled CsPbBr3 Nanocrystals for Tunable Optical and Assembly Behavior Irina Skvortsova, Sudipta Seth, Juliette Zito, Robin Girod, Bob Van Hout, Annick De Backer, Tom Stoops, Sergey Abakumov, Evgenii Vlasov, Tejmani Behera, Sandra Van Aert, Elke Debroye, Johan Hofkens, Sara Bals Advanced Materials, 2026 Colloidal cesium lead bromide (CsPbBr 3 ) nanocrystals (NCs) are excellent candidates for various photonic and optoelectronic applications due to their bright and stable green emission. Here, we establish arm length control as a central structural parameter that governs both the optical properties of individual CsPbBr 3 NCs and their self‐assembly behavior. Armed NCs, featuring a cubic core with multiple protruding arms, are synthesized by controlling seed size, concentration, and injection temperature, while arm length is tuned via cesium oleate concentration. Prolonged storage in toluene is shown to lead to a time‐dependent morphological evolution from armed NCs to 26‐faceted rhombicuboctahedra, with short‐armed structures as intermediates. NCs with a longer arm length yield enhanced radiative efficiency, extended photoluminescence (PL) lifetimes, and suppressed blinking, making such NCs suitable for light‐emitting devices and quantum photonic applications. In contrast, short‐armed NCs exhibit faster recombination, stronger PL intermittency, and increased surface accessibility, which are favorable for sensing and high‐speed single‐photon emission. The arm length also governs self‐assembly behavior, hereby opening new possibilities for applications. Armed NCs form densely 3D‐packed assemblies with tunable configurations. This work demonstrates how arm length tuning expands the functional potential of CsPbBr 3 NCs by linking morphological control to both optical response and self‐assembly characteristics.
High Resolution Imaging of Nonequilibrium Colloidal Self-Assembly via Photofixation Jagannath Satpathy, Jim Jui-Kai Chen, Gang Wen, Hiroshi Masuhara, Sudipta Seth, Volker Leen, Susana Rocha, Johan Hofkens, Boris Louis, Roger Bresolí-Obach ACS Nano, 2026 The self-organization of colloidal nanoparticles into complex structures, both in equilibrium and out-of-equilibrium, is a growing area in colloidal science with potential for creating functional materials. While equilibrium assemblies form stable and periodic structures, out-of-equilibrium (or active) assemblies exhibit dynamic, reconfigurable behavior under external stimuli. Therefore, understanding the structure-function relationships in these assemblies remains challenging due to their transient nature and limitations of current characterization methods. In this work, we present a methodology termed Fixation and Resolving of Colloidal Active Matter Ensembles (FRAME). FRAME combines UV photopolymerization to fix nonequilibrium colloidal assemblies with high-resolution imaging techniques, including 3D confocal microscopy, SEM and 3D STED super-resolution imaging, for subsequent structural characterization. We applied this method to Optical Matter (OM) structures formed within an optical trap at the glass/water interface. Using FRAME, we conducted a detailed analysis of OM structures composed of colloidal nanoparticles ranging from 200 nm to 1 μm. We demonstrate the robustness of this method by validating that the fixation process does not alter structural properties, allowing for accurate structural analysis. FRAME offers a distinct approach for investigating nonequilibrium colloidal assemblies, enabling the way for their rational design and application across a broad range of colloidal systems.
Programmable Shape-Directed Optical Binding of Plasmonic Nanoparticles Jim Jui‐Kai Chen, Ashish Kar, Pengfei Yu, Ana Sánchez Iglesias, Chih‐Hao Huang, Jagannath Satpathy, Jianfang Wang, Luis M. Liz‐Marzán, Hiroshi Masuhara, Roger Bresolí‐Obach, Sudipta Seth, Susana Rocha, Boris Louis, Johan Hofkens Advanced Optical Materials, 2025 Controlling the organization of plasmonic nanoparticles with optical forces is essential for designing reconfigurable light‐responsive materials. However, the role of particle shape in determining optical binding geometries remains unresolved. Here, it is demonstrated that the interplay between gold nanoparticle (Au NP) morphology and optical scattering governs distinct near‐field and far‐field configurations under optical trapping at a water‐glass interface. Au spheres, rods, plates, and decahedra exhibit characteristic orientations and binding behaviors that directly correlate with their shape‐dependent scattering responses to linearly polarized near‐infrared lasers. By tuning the trapping wavelength, transitions in interparticle spacing, orientation, and collective arrangement are induced across two‐, three‐, and five‐particle systems. These results establish NP shape as a versatile design parameter for programming optical matter, offering new opportunities for dynamic nanoscale assembly, tunable plasmonic interactions, and light‐driven metamaterials.
From mapping to manipulation: 3D insights into dielectrophoresis and electrokinetics for advanced sorting for Colloidal memory applications Flip De Jong, Pablo Diez-Silva, Jui-kai Chen, Sudipta Seth, Harishankar Balakrishnan, Bing-Yang Shih, Maarten Rosmeulen, Susana Rocha, Andrey Klymchenko, Luis Liz-Marzan, Roger Bresoli-Obach, Manuel I. Marques, Rafael Delgado Buscalioni, Johan Hofkens, Boris Louis Proceedings of SPIE the International Society for Optical Engineering, 2025 The precise manipulation of nanoscale particles is essential for advancing applications in colloidal selfassembly, targeted sorting, and emerging paradigms such as colloidal memory. Here, we present a high-speed multiplane 3D imaging platform that enables direct visualization and quantification of dielectrophoretic (DEP) forces and electrokinetic flows acting on individual nanoparticles in real time. Using 200 nm dye-doped polystyrene particles, we map both positive and negative DEP regimes, capturing spatial force distributions with sub-50 nm axial resolution and frame rates exceeding 100 fps. Our approach reveals distinct particle behaviors across frequency regimes, including trapping near electrodes under positive DEP and levitation above the surface under negative DEP. In addition, we characterize electrokinetic flow fields in 3D, which play a critical role at higher voltages. This methodology provides a robust experimental framework for investigating DEP manipulation schemes, validating theoretical models, and selectively addressing particle mixtures, a key requirement for future molecular machines and frequency-controlled colloidal memory systems.
Unveiling the Local Fate of Charge Carriers in Halide Perovskite Thin Films via Correlation Clustering Imaging Sudipta Seth, Boris Louis, Koki Asano, Toon Van Roy, Maarten B. J. Roeffaers, Elke Debroye, Ivan G. Scheblykin, Martin Vacha, Johan Hofkens Chemical and Biomedical Imaging, 2025 High Resolution Image Download MS PowerPoint Slide As the field of metal halide perovskites matures, a range of compositionally different perovskite films has found a place in efficient optoelectronic devices. These films feature variable local structural stability, carrier diffusion, and recombination, while there is still a lack of easy-to-implement generic protocols for high-throughput characterization of these variable properties. Correlation clustering imaging (CLIM) is a recently developed tool that resolves peculiarities of local photophysics by assessing the dynamics of photoluminescence detected by wide-field optical microscopy. We demonstrate the capability of CLIM as a high-throughput characterization tool of perovskite films using MAPbI 3 (MAPI) and triple cation mixed halide (TCMH) perovskites as examples where it resolves the interplay of carrier diffusion, recombination, and defect dynamics. We found significant differences in the appearance of metastable defect states in these two films. Despite a better surface quality and larger grain size, MAPI films showed more pronounced effects of fluctuating defect states than did TCMH films. As CLIM shows a significant difference between materials known to lead to different solar cell efficiencies, it can be considered a tool for quality control of thin films for perovskite optoelectronic devices.
In Operando Locally-Resolved Photophysics in Perovskite Solar Cells by Correlation Clustering Imaging Boris Louis, Sudipta Seth, Qingzhi An, Ran Ji, Yana Vaynzof, Johan Hofkens, Ivan G. Scheblykin Advanced Materials, 2025 The instability of metal halide perovskites limits the commercialization of solar cells despite their impressive efficiencies. This instability, driven by photo‐induced ion migration, leads to material restructuring, defect formation, degradation, and defect healing. However, these same “unwanted” properties enable to propose Correlation Clustering Imaging (CLIM), a technique that detects local photoluminescence (PL) fluctuations through wide‐field fluorescence microscopy. It is shown that such fluctuations are present in high‐quality perovskites and their corresponding solar cells. CLIM successfully visualizes the polycrystalline grain structure in perovskite films, closely matching electron microscopy images. The analysis of fluctuations reveals a dominant metastable defect responsible for the fluctuations. In solar cells in short‐circuit conditions, these fluctuations are significantly larger, and corresponding correlated regions extend up to 10 micrometers, compared to 2 micrometers in films. It is proposed that the regions resolved by CLIM in solar cells possess a common pool of charge extraction channels, which fluctuate and cause PL to vary. Since PL fluctuations reflect non‐radiative recombination processes, CLIM provides valuable insights into the structural and functional dynamics of carrier transport, ion migration, defect behavior, and recombination losses. CLIM offers a non‐invasive approach to understanding luminescent materials and devices in operando, utilizing contrasts based on previously untapped properties.
From halide perovskite nanocrystals to supercrystals: fundamentals and applications S. L. Aneesha, Yifei Xia, Takuya Okamoto, Deepika Gaur, Sudipta Seth, Johan Hofkens, Lakshminarayana Polavarapu, Vasudevanpillai Biju Chemical Society Reviews, 2025 Halide perovskite supercrystals (or superlattices) are electronically coupled nanomaterials, such as nanocrystals, quantum dots, or nanoplatelets that offer collective optical and electronic properties distinct from those of their constituents.
Unconventional Optical Matter of Hybrid Metal-Dielectric Nanoparticles at Interfaces Boris Louis, Chih-Hao Huang, Marc Melendez, Ana Sánchez-Iglesias, Jorge Olmos-Trigo, Sudipta Seth, Susana Rocha, Rafael Delgado-Buscalioni, Luis M. Liz-Marzán, Manuel I. Marqués, Hiroshi Masuhara, Johan Hofkens, Roger Bresolí-Obach ACS Nano, 2024 Optical matter, a transient arrangement formed by the interaction of light with micro/nanoscale objects, provides responsive and highly tunable materials that allow for controlling and manipulating light and/or matter. A combined experimental and theoretical exploration of optical matter is essential to advance our understanding of the phenomenon and potentially design applications. Most studies have focused on nanoparticles composed of a single material (either metallic or dielectric), representing two extreme regimes, one where the gradient force (dielectric) and one where the scattering force (metallic) dominates. To understand their role, it is important to investigate hybrid materials with different metallic-to-dielectric ratios. Here, we combine numerical calculations and experiments on hybrid metal-dielectric core-shell particles (200 nm gold spheres coated with silica shells with thicknesses ranging from 0 to 100 nm). We reveal how silica shell thickness critically influences the essential properties of optical binding, such as interparticle distance, reducing it below the anticipated optical binding length. Notably, for silica shells thicker than 50 nm, we observed a transition from a linear arrangement perpendicular to polarization to a hexagonal arrangement accompanied by a circular motion. Further, the dynamic swarming assembly changes from the conventional dumbbell-shaped to lobe-like morphologies. These phenomena, confirmed by both experimental observations and dynamic numerical calculations, demonstrate the complex dynamics of optical matter and underscore the potential for tuning its properties for applications.
Arm‐Length‐Controlled CsPbBr 3 Nanocrystals for Tunable Optical and Assembly Behavior I Skvortsova, S Seth, J Zito, R Girod, B Van Hout, A De Backer, T Stoops, ... Advanced Materials 38 (23), e19211 , 2026 2026 Citations: 1
Room temperature collective blinking and photon bunching from CsPbBr 3 quantum dot superlattice Q Tan, S Seth, B Louis, X Wu, N Pathoor, T Takagi, S Omagari, ... Nature Communications , 2026 2026
High Resolution Imaging of Nonequilibrium Colloidal Self-Assembly via Photofixation J Satpathy, JJK Chen, G Wen, H Masuhara, S Seth, V Leen, S Rocha, ... ACS nano 20 (7), 6287-6299 , 2026 2026
Machine learning for microscopy data analytics targeting real-time optical characterization of semiconductor nanocrystals A Mukherjee, R Reynaerts, B Pradhan, S Seth, AT Rösch, T Banerjee, ... Nature Communications , 2026 2026
Programmable Shape‐Directed Optical Binding of Plasmonic Nanoparticles JJK Chen, A Kar, P Yu, AS Iglesias, CH Huang, J Satpathy, J Wang, ... Advanced Optical Materials 13 (34), e03071 , 2025 2025 Citations: 1
M3Scope a 3D multimode multiplane microscope for imaging nanoscale dynamics in soft matter S Huysecom, F Bevilacqua, RB Obach, S Seth, LM Liz-Marzan, J Hofkens, ... arXiv preprint arXiv:2511.10174 , 2025 2025
Microscopic Intricacies of Self-Healing in Halide Perovskite-Charge Transport Layer Heterostructures T Behera, B Louis, L Paesen, RV Brande, K Asano, M Vacha, M Roeffaers, ... arXiv preprint arXiv:2510.11948 , 2025 2025
From mapping to manipulation: 3D insights into dielectrophoresis and electrokinetics for advanced sorting toward colloidal memory applications F de Jong, P Diez-Silva, JK Chen, S Seth, H Balakrishnan, BY Shih, ... Molecular and Nanophotonic Machines, Devices, and Applications VIII 13592, 53-59 , 2025 2025
Three-dimensional optical reconstruction of colloidal electrokinetics via multiplane imaging F de Jong, P Diez-Silva, JK Chen, R Pérez-Peláez, S Seth, ... arXiv preprint arXiv:2503.23839 , 2025 2025 Citations: 2
INTERMITTENCY OF THE NEAR-INFRARED LUMINESCENCE FROM CsPbBr3 MICROCRYSTALS J Vandenwijngaerden, D Santantonio, H Balakrishnan, R Bresoli-Obach, ... Near-Infrared Luminescence from Deep Defects in CsPbBr3 Perovskite, 177 , 2025 2025
Unveiling the local fate of charge carriers in halide perovskite thin films via correlation clustering imaging S Seth, B Louis, K Asano, T Van Roy, MBJ Roeffaers, E Debroye, ... Chemical & Biomedical Imaging 3 (4), 244-252 , 2025 2025 Citations: 7
In Operando Locally‐Resolved Photophysics in Perovskite Solar Cells by Correlation Clustering Imaging B Louis, S Seth, Q An, R Ji, Y Vaynzof, J Hofkens, IG Scheblykin Advanced Materials 37 (7), 2413126 , 2025 2025 Citations: 16
From halide perovskite nanocrystals to supercrystals: fundamentals and applications SL Aneesha, Y Xia, T Okamoto, D Gaur, S Seth, J Hofkens, L Polavarapu, ... Chemical Society Reviews 54, 9585-9611 , 2025 2025 Citations: 10
Unconventional Optical Matter of Hybrid Metal–Dielectric Nanoparticles at Interfaces B Louis, CH Huang, M Melendez, A Sánchez-Iglesias, J Olmos-Trigo, ... ACS nano 18 (47), 32746-32758 , 2024 2024 Citations: 11
Enhancing the X-ray Sensitivity of Cs 2 AgBiBr 6 Double Perovskite Single Crystals through Cation Engineering D Valli, H Zhang, M Betušiak, G Romolini, A Meulemans, D Escudero, ... ACS Applied Optical Materials 2 (10), 2075-2084 , 2024 2024 Citations: 17
High resolution imaging of non-equilibrium colloidal self-assembly enabled by photopolymerization J Satpathy, JK Chen, G Wen, H Masuhara, S Seth, V Leen, S Rocha, ... ChemRxiv 2024 (0920) , 2024 2024 Citations: 1
Amine‐Free Multi‐Faceted CsPbBr 3 Nanocrystals for Complete Suppression of Long‐Lived Dark States NVS Praneeth, S Akhil, A Mukherjee, S Seth, S Khatua, N Mishra Advanced Optical Materials 12 (16), 2303222 , 2024 2024 Citations: 17
Correlation Clustering Imaging: A method for Functional Mapping of Semiconductor materials and photovoltaic devices in operando B Louis, S Seth, Q An, R Ji, Y Vaynzof, J Hofkens, I Scheblykin ChemRxiv 2024 (0308) , 2024 2024 Citations: 1
Photoluminescence Polarization of MAPbBr 3 Perovskite Nanostructures. Can the Dielectric Contrast Effect Explain It? J Shi, I Ryabov, S Seth, PA Frantsuzov, S Rafie-Zinedine, A Walther, ... Acs Photonics 9 (12), 3888-3898 , 2022 2022 Citations: 3
Presence of Maximal Characteristic Time in Photoluminescence Blinking of MAPbI 3 Perovskite S Seth, EA Podshivaylov, J Li, M Gerhard, A Kiligaridis, PA Frantsuzov, ... Advanced Energy Materials 11 (44), 2102449 , 2021 2021 Citations: 26
MOST CITED SCHOLAR PUBLICATIONS
Tackling the Defects, Stability, and Photoluminescence of CsPbX 3 Perovskite Nanocrystals S Seth, T Ahmed, A De, A Samanta ACS Energy Letters 4 (7), 1610-1618 , 2019 2019 Citations: 335
Boosting the Photoluminescence of CsPbX 3 (X = Cl, Br, I) Perovskite Nanocrystals Covering a Wide Wavelength Range by Postsynthetic Treatment with … T Ahmed, S Seth, A Samanta Chemistry of Materials 30 (11), 3633-3637 , 2018 2018 Citations: 323
A Facile Methodology for Engineering the Morphology of CsPbX 3 Perovskite Nanocrystals under Ambient Condition S Seth, A Samanta Scientific reports 6 (1), 37693 , 2016 2016 Citations: 196
Fluorescence Blinking and Photoactivation of All-Inorganic Perovskite Nanocrystals CsPbBr 3 and CsPbBr 2 I S Seth, N Mondal, S Patra, A Samanta The journal of physical chemistry letters 7 (2), 266-271 , 2016 2016 Citations: 193
Fluorescent Phase-Pure Zero-Dimensional Perovskite-Related Cs 4 PbBr 6 Microdisks: Synthesis and Single-Particle Imaging Study S Seth, A Samanta The Journal of Physical Chemistry Letters 8 (18), 4461-4467 , 2017 2017 Citations: 163
Photoluminescence of zero-dimensional perovskites and perovskite-related materials S Seth, A Samanta The Journal of Physical Chemistry Letters 9 (1), 176-183 , 2018 2018 Citations: 126
Are Shockley-Read-Hall and ABC models valid for lead halide perovskites? A Kiligaridis, PA Frantsuzov, A Yangui, S Seth, J Li, Q An, Y Vaynzof, ... Nature communications 12 (1), 3329 , 2021 2021 Citations: 120
Broadband ultrafast nonlinear optical studies revealing exciting multi-photon absorption coefficients in phase pure zero-dimensional Cs 4 PbBr 6 perovskite films KN Krishnakanth, S Seth, A Samanta, SV Rao Nanoscale 11 (3), 945-954 , 2019 2019 Citations: 102
Broadband femtosecond nonlinear optical properties of CsPbBr 3 perovskite nanocrystals KN Krishnakanth, S Seth, A Samanta, SV Rao Optics letters 43 (3), 603-606 , 2018 2018 Citations: 97
Photoluminescence Flickering and Blinking of Single CsPbBr 3 Perovskite Nanocrystals: Revealing Explicit Carrier Recombination Dynamics S Seth, T Ahmed, A Samanta The Journal of Physical Chemistry Letters 9 (24), 7007-7014 , 2018 2018 Citations: 93
Mechanistic Investigation of the Defect Activity Contributing to the Photoluminescence Blinking of CsPbBr 3 Perovskite Nanocrystals T Ahmed, S Seth, A Samanta ACS nano 13 (11), 13537-13544 , 2019 2019 Citations: 91
Dark excitons of the perovskites and sensitization of molecular triplets N Mondal, A De, S Seth, T Ahmed, S Das, S Paul, RK Gautam, A Samanta ACS Energy Letters 6 (2), 588-597 , 2021 2021 Citations: 33
Differences in the behavior of dicationic and monocationic ionic liquids as revealed by time resolved-fluorescence, NMR and fluorescence correlation spectroscopy D Majhi, S Seth, M Sarkar Physical Chemistry Chemical Physics 20 (11), 7844-7856 , 2018 2018 Citations: 29
Presence of Maximal Characteristic Time in Photoluminescence Blinking of MAPbI 3 Perovskite S Seth, EA Podshivaylov, J Li, M Gerhard, A Kiligaridis, PA Frantsuzov, ... Advanced Energy Materials 11 (44), 2102449 , 2021 2021 Citations: 26
ACS Energy Lett. 2019, 4, 1610; c) H. Huang, MI Bodnarchuk, S. V. Kershaw, MV Kovalenko, AL Rogach S Seth, T Ahmed, A De, A Samanta ACS Energy Lett 2, 2071 , 2017 2017 Citations: 21
Enhancing the X-ray Sensitivity of Cs 2 AgBiBr 6 Double Perovskite Single Crystals through Cation Engineering D Valli, H Zhang, M Betušiak, G Romolini, A Meulemans, D Escudero, ... ACS Applied Optical Materials 2 (10), 2075-2084 , 2024 2024 Citations: 17
Amine‐Free Multi‐Faceted CsPbBr 3 Nanocrystals for Complete Suppression of Long‐Lived Dark States NVS Praneeth, S Akhil, A Mukherjee, S Seth, S Khatua, N Mishra Advanced Optical Materials 12 (16), 2303222 , 2024 2024 Citations: 17
Highly efficient energy transfer from fluorescent gold nanoclusters to organic j-aggregates S Banerjee, N Preeyanka, H Dey, S Seth, A Rahaman, M Sarkar The Journal of Physical Chemistry C 124 (9), 5009-5020 , 2020 2020 Citations: 17
Electrostatically Driven Förster Resonance Energy Transfer between a Fluorescent Metal Nanoparticle and J-Aggregate in an Inorganic–Organic Nanohybrid Material AK Agrawal, PK Sahu, S Seth, M Sarkar The Journal of Physical Chemistry C 123 (6), 3836-3847 , 2019 2019 Citations: 17
In Operando Locally‐Resolved Photophysics in Perovskite Solar Cells by Correlation Clustering Imaging B Louis, S Seth, Q An, R Ji, Y Vaynzof, J Hofkens, IG Scheblykin Advanced Materials 37 (7), 2413126 , 2025 2025 Citations: 16