Nadia Gholampour
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Nadia Gholampour has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
Capucine Sassoye
Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP) UMR 7574 CNRS -Sorbonne Université, Campus Pierre et Marie Curie 4 Place Jussieu F-75005 Paris France
1 shared publication- Damien P. Debecker
Université Catholique de Louvain (UCLouvain), Institute of Condensed Matter and Nanosciences (IMCN), Place Louis Pasteur 1, Louvain-la-Neuve, 1348, Belgium
1 shared publication - Dominikus Brian
Division of Arts and Sciences, NYU Shanghai, 1555 Century Avenue, Shanghai 200122, China
1 shared publication François Devred
Institute of Condensed Matter and Nanosciences (IMCN) Université catholique de Louvain (UCLouvain) Place Louis Pasteur1, Box L4.01. Ottignies-Louvain-la-Neuve, 09 1348 Louvain-la-Neuve Belgium
1 shared publicationMohammad-Reza Ahmadian-Yazdi
University of Michigan–Shanghai Jiao Tong University Joint Institute, Shanghai, People’s Republic of China
1 shared publication- Morteza Eslamian
University of Michigan-Shanghai Jiao Tong University, Shanghai 200240, China
1 shared publication
Latest Publications
- 10 February 2023
- Published by Wiley in ChemCatChem
- Vol. 15 (5)
CO2 Methanation over Cobalt Nanoparticles Embedded in ZIF‐L–Derived Porous Carbon
Catalytic hydrogenation of CO2 into CH4 is an effective method to convert waste CO2 and green hydrogen into clean fuel on a large scale. However, the viability of such process largely relies on the development of highly active heterogeneous catalysts. Here, a tailored methanation catalyst, Co nanoparticles immobilized into a highly porous N‐doped carbon matrix, is prepared by the carbonization of a cobalt‐based layered zeolitic imidazolate framework (ZIF−L) material under an argon atmosphere. This catalyst displays a specific activity of 22.3 molCH4/gcat.min at 350 °C, significantly outperforming a similar catalyst derived from the more conventional ZIF‐67 (11.7 molCH4/gcat.min). This is explained by the stabilization of small Co nanoparticles (∼20 nm) and by the presence of abundant medium‐strength basic sites related to the nitrogen doping in the catalyst prepared from ZIF−L. Notably, the new catalyst shows high stability; no deactivation is observed up to 60 hours on stream.
- 10 February 2023
- Published by Wiley in ChemCatChem
- Vol. 15 (5)
CO2 Methanation over Cobalt Nanoparticles Embedded in ZIF‐L–Derived Porous Carbon
Catalytic hydrogenation of CO2 into CH4 is an effective method to convert waste CO2 and green hydrogen into clean fuel on a large scale. However, the viability of such process largely relies on the development of highly active heterogeneous catalysts. Here, a tailored methanation catalyst, Co nanoparticles immobilized into a highly porous N‐doped carbon matrix, is prepared by the carbonization of a cobalt‐based layered zeolitic imidazolate framework (ZIF−L) material under an argon atmosphere. This catalyst displays a specific activity of 22.3 molCH4/gcat.min at 350 °C, significantly outperforming a similar catalyst derived from the more conventional ZIF‐67 (11.7 molCH4/gcat.min). This is explained by the stabilization of small Co nanoparticles (∼20 nm) and by the presence of abundant medium‐strength basic sites related to the nitrogen doping in the catalyst prepared from ZIF−L. Notably, the new catalyst shows high stability; no deactivation is observed up to 60 hours on stream.
- 19 March 2021
- Published by Springer Nature in Journal of Porous Materials
- Vol. 28 (4) , 1105-1113
Investigation of zeolitic imidazolate frameworks–derived carbon nanotubes thin film in solar vapor generation
- 19 March 2021
- Published by Springer Nature in Journal of Porous Materials
- Vol. 28 (4) , 1105-1113
Investigation of zeolitic imidazolate frameworks–derived carbon nanotubes thin film in solar vapor generation
- Open Access
Tailoring Characteristics of PEDOT:PSS Coated on Glass and Plastics by Ultrasonic Substrate Vibration Post Treatment
In this work, we excited as-spun wet films of PEDOT:PSS by ultrasonic vibration with varying frequency and power. This is a low-cost and facile technique for tailoring the structural and surface characteristics of solution-processed thin films and coatings. We deposited the coatings on both rigid and flexible substrates and performed various characterization techniques, such as atomic force microscopy (AFM), scanning electronic microscopy (SEM), X-ray photoelectron spectroscopy (XPS), attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), transmittance, electrical conductivity, and contact angle measurements, to understand how the ultrasonic vibration affects the coating properties. We found that as a result of ultrasonic vibration, PEDOT:PSS sheet conductivity increases up to five-fold, contact angle of water on PEDOT:PSS increases up to three-fold, and PEDOT:PSS roughness on glass substrates substantially decreases. Our results affirm that ultrasonic vibration can favor phase separation of PEDOT and PSS and rearrangement of PEDOT-rich charge transferring grains. In addition to providing a systematic study on the effect of ultrasonic frequency and power on the film properties, this work also proves that the ultrasonic vibration is a novel method to manipulate and tailor a wide range of properties of solution-processed thin films, such as compactness, chain length and arrangement of polymer molecules, conductivity, and surface wettability. This ultrasonication method can serve organic, printed and flexible electronics.
Open AccessTailoring Characteristics of PEDOT:PSS Coated on Glass and Plastics by Ultrasonic Substrate Vibration Post Treatment
In this work, we excited as-spun wet films of PEDOT:PSS by ultrasonic vibration with varying frequency and power. This is a low-cost and facile technique for tailoring the structural and surface characteristics of solution-processed thin films and coatings. We deposited the coatings on both rigid and flexible substrates and performed various characterization techniques, such as atomic force microscopy (AFM), scanning electronic microscopy (SEM), X-ray photoelectron spectroscopy (XPS), attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), transmittance, electrical conductivity, and contact angle measurements, to understand how the ultrasonic vibration affects the coating properties. We found that as a result of ultrasonic vibration, PEDOT:PSS sheet conductivity increases up to five-fold, contact angle of water on PEDOT:PSS increases up to three-fold, and PEDOT:PSS roughness on glass substrates substantially decreases. Our results affirm that ultrasonic vibration can favor phase separation of PEDOT and PSS and rearrangement of PEDOT-rich charge transferring grains. In addition to providing a systematic study on the effect of ultrasonic frequency and power on the film properties, this work also proves that the ultrasonic vibration is a novel method to manipulate and tailor a wide range of properties of solution-processed thin films, such as compactness, chain length and arrangement of polymer molecules, conductivity, and surface wettability. This ultrasonication method can serve organic, printed and flexible electronics.