Anh Ngoc Nguyen
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
Anh Ngoc Nguyen has a total of 42 co-authors. Here are the top co-authors by number of shared publications:
- Hiroaki Benten
Nara Institute of Science and Technology
3 shared publications - Pham Van Trinh
Institute of Materials Science, Vietnam Academy of Science and Technology
3 shared publications - Andrés Gómez
Institut de Ciència de Materials de Barcelona ICMAB, Consejo Superior de Investigaciones Científicas CSIC, Catalonia, Spain
2 shared publications Bui Hung Thang
2 shared publications- Huyen Thi Thanh Nong
LSPM CNRS UPR-3407, University of Sorbonne Paris North (USPN), 99, Av. J. B. Clément, 93430 Villetaneuse, France
2 shared publications - Jeanne Solard
Alice & Bob, Paris, France
2 shared publications
Latest Publications
- Open Access
- 29 August 2026
- Published by Elsevier in SSRN Electronic Journal
Molecular-Scale Visualization of Surfactant Adsorption on Carbon Nanotube Networks Using Frequency-Modulation Atomic Force Microscopy
Surfactants are widely used to disperse and assemble hydrophobic carbon nanotubes (CNTs) in water, yet the nanoscale adsorption structures and roles of surfactants in mesh-like CNT networks remain poorly understood. In this work, we reveal the surface and interfacial structures of a non-ionic surfactant, polyoxyethylene(50) stearyl ether, on single-walled CNTs using high-resolution frequency-modulation atomic force microscopy (FM-AFM) combined with molecular modeling and AFM image simulations. Elongated protrusions spirally wrapping CNT bundles were consistently observed. The height distribution of the protrusions exhibited periodic peaks and mostly exceeded the height expected for a single surfactant molecule, indicating that clustering is necessary for stable adsorption. By comparing the observed topographic images of the adsorbed surfactant clusters with simulated images, we also obtained the true wrapping angles relative to the CNT long axis, with the distribution concentrated within 1–10°. At some CNT/CNT junctions, the apparent heights exceeded the sum of the individual CNT diameters, providing direct evidence of surfactant intercalation at these junctions. These results provide important insights into the adsorption state of the popular surfactant and its direct involvement in charge and heat transport within CNT networks.
- 29 August 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessMolecular-Scale Visualization of Surfactant Adsorption on Carbon Nanotube Networks Using Frequency-Modulation Atomic Force Microscopy
Surfactants are widely used to disperse and assemble hydrophobic carbon nanotubes (CNTs) in water, yet the nanoscale adsorption structures and roles of surfactants in mesh-like CNT networks remain poorly understood. In this work, we reveal the surface and interfacial structures of a non-ionic surfactant, polyoxyethylene(50) stearyl ether, on single-walled CNTs using high-resolution frequency-modulation atomic force microscopy (FM-AFM) combined with molecular modeling and AFM image simulations. Elongated protrusions spirally wrapping CNT bundles were consistently observed. The height distribution of the protrusions exhibited periodic peaks and mostly exceeded the height expected for a single surfactant molecule, indicating that clustering is necessary for stable adsorption. By comparing the observed topographic images of the adsorbed surfactant clusters with simulated images, we also obtained the true wrapping angles relative to the CNT long axis, with the distribution concentrated within 1–10°. At some CNT/CNT junctions, the apparent heights exceeded the sum of the individual CNT diameters, providing direct evidence of surfactant intercalation at these junctions. These results provide important insights into the adsorption state of the popular surfactant and its direct involvement in charge and heat transport within CNT networks.
- Open Access
- 1 May 2024
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 7 (9) , 9880-9886
Carbon Nanotube Yarns Tailored Using Dispersants and Surfactants for Flexible and Wearable Thermoelectric Generators
- 1 May 2024
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 7 (9) , 9880-9886
Open AccessCarbon Nanotube Yarns Tailored Using Dispersants and Surfactants for Flexible and Wearable Thermoelectric Generators
- 8 September 2023
- Published by Japan Society of Applied Physics
Enhancement of Thermoelectric Properties in Carbon-Nanotube Yarns by an Improved Dispersion Method
2023 International Conference on Solid State Devices and Materials ,Enhancement of Thermoelectric Properties in Carbon-Nanotube Yarns by an Improved Dispersion Method
- 8 September 2023
- Published by Japan Society of Applied Physics
Enhancement of Thermoelectric Properties in Carbon-Nanotube Yarns by an Improved Dispersion Method
2023 International Conference on Solid State Devices and Materials ,Enhancement of Thermoelectric Properties in Carbon-Nanotube Yarns by an Improved Dispersion Method
- Open Access
- 2 February 2022
- Published by MDPI AG in Applied Sciences
- Vol. 12 (3) , 1589
Robust Piezoelectric Coefficient Recovery by Nano-Inclusions Dispersion in Un-Poled PVDF–Ni0.5Zn0.5Fe2O4 Ultra-Thin Films
This work aimed to study the influence of the hybrid interface in polyvinylidene fluoride (PVDF)-based composite thin films on the local piezoelectric response. Our results provide evidence of a surprising contradiction: the optimization process of the β-phase content using nano-inclusions did not correspond to the expected nanoscale piezoelectric optimization. A large piezoelectric loss was observed at the nanoscale level, which contrasts with the macroscopic polarization measurement observations. Our main goal was to show that the dispersion of metallic ferromagnetic nano-inclusions inside the PVDF films allows for the partial recovery of the local piezoelectric properties. From a dielectric point of view, it is not trivial to expect that keeping the same amount of the metallic volume inside the dielectric PVDF matrix would bring a better piezoelectric response by simply dispersing this phase. On the local resonance measured by PFM, this should be the worst due to the homogeneous distribution of the nano-inclusions. Both neat PVDF films and hybrid ones (0.5% in wt of nanoparticles included into the polymer matrix) showed, as-deposited (un-poled), a similar β-phase content. Although the piezoelectric coefficient in the case of the hybrid films was one order of magnitude lower than that for the neat PVDF films, the robustness of the polarized areas was reported 24 h after the polarization process and after several images scanning. We thus succeeded in demonstrating that un-poled polymer thin films can show the same piezoelectric coefficient as the poled one (i.e., 10 pm/V). In addition, low electric field switching (50 MV/m) was used here compared to the typical values reported in the literature (100–150 MV/m).
- 2 February 2022
- Published by MDPI AG in Applied Sciences
- Vol. 12 (3) , 1589
Open AccessRobust Piezoelectric Coefficient Recovery by Nano-Inclusions Dispersion in Un-Poled PVDF–Ni0.5Zn0.5Fe2O4 Ultra-Thin Films
This work aimed to study the influence of the hybrid interface in polyvinylidene fluoride (PVDF)-based composite thin films on the local piezoelectric response. Our results provide evidence of a surprising contradiction: the optimization process of the β-phase content using nano-inclusions did not correspond to the expected nanoscale piezoelectric optimization. A large piezoelectric loss was observed at the nanoscale level, which contrasts with the macroscopic polarization measurement observations. Our main goal was to show that the dispersion of metallic ferromagnetic nano-inclusions inside the PVDF films allows for the partial recovery of the local piezoelectric properties. From a dielectric point of view, it is not trivial to expect that keeping the same amount of the metallic volume inside the dielectric PVDF matrix would bring a better piezoelectric response by simply dispersing this phase. On the local resonance measured by PFM, this should be the worst due to the homogeneous distribution of the nano-inclusions. Both neat PVDF films and hybrid ones (0.5% in wt of nanoparticles included into the polymer matrix) showed, as-deposited (un-poled), a similar β-phase content. Although the piezoelectric coefficient in the case of the hybrid films was one order of magnitude lower than that for the neat PVDF films, the robustness of the polarized areas was reported 24 h after the polarization process and after several images scanning. We thus succeeded in demonstrating that un-poled polymer thin films can show the same piezoelectric coefficient as the poled one (i.e., 10 pm/V). In addition, low electric field switching (50 MV/m) was used here compared to the typical values reported in the literature (100–150 MV/m).
- Open Access
- 17 May 2020
- Published by Wiley in Global Challenges
- Vol. 4 (9)
Solar Cell Based on Hybrid Structural SiNW/Poly(3,4 ethylenedioxythiophene): Poly(styrenesulfonate)/Graphene
Solar energy is considered as a potential alternative energy source. The solar cell is classified into three main types: i) solar cells based on bulk silicon materials (monocrystalline, polycrystalline), ii) thin‐film solar cells (CIGS, CdTe, DSSC, etc.), and iii) solar cells based on nanostructures and nanomaterials. Nowadays, commercial solar cells are usually made by bulk silicon material, which requires not only high fabrication costs but also limited performance. In this study, the fabrication of high‐performance solar cells based on hybrid structure of silicon nanowires/poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)/graphene (SiNW/PEDOT:PSS/Gr) is focused upon. SiNWs with different lengths of 125, 400, 800 nm, and 2 µm are fabricated by a metal‐assisted chemical etching method, and their influence on the performance of the hybrid solar cells is studied and investigated. The experimental results indicate that the suitable SiNW length for the fabrication of the hybrid solar cells is about 400 nm and the best power conversion efficiency obtained is about 9.05%, which is about 2.1 times higher than that of the planar Si solar cell.
- 17 May 2020
- Published by Wiley in Global Challenges
- Vol. 4 (9)
Open AccessSolar Cell Based on Hybrid Structural SiNW/Poly(3,4 ethylenedioxythiophene): Poly(styrenesulfonate)/Graphene
Solar energy is considered as a potential alternative energy source. The solar cell is classified into three main types: i) solar cells based on bulk silicon materials (monocrystalline, polycrystalline), ii) thin‐film solar cells (CIGS, CdTe, DSSC, etc.), and iii) solar cells based on nanostructures and nanomaterials. Nowadays, commercial solar cells are usually made by bulk silicon material, which requires not only high fabrication costs but also limited performance. In this study, the fabrication of high‐performance solar cells based on hybrid structure of silicon nanowires/poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)/graphene (SiNW/PEDOT:PSS/Gr) is focused upon. SiNWs with different lengths of 125, 400, 800 nm, and 2 µm are fabricated by a metal‐assisted chemical etching method, and their influence on the performance of the hybrid solar cells is studied and investigated. The experimental results indicate that the suitable SiNW length for the fabrication of the hybrid solar cells is about 400 nm and the best power conversion efficiency obtained is about 9.05%, which is about 2.1 times higher than that of the planar Si solar cell.
- Open Access
Spin Coating and Micro-Patterning Optimization of Composite Thin Films Based on PVDF
We optimize the elaboration of very thin film of poly(vinylidene fluoride) (PVDF) polymer presenting a well-controlled thickness, roughness, and nano-inclusions amount. We focused our effort on the spin coating elaboration technique which is easy to transfer to an industrial process. We show that it is possible to obtain continuous and smooth thin films with mean thicknesses of 90 nm by properly adjusting the concentration and the viscosity of the PVDF solution as well as the spin rate and the substrate temperature of the elaboration process. The electro-active phase content versus the magnetic and structural properties of the composite films is reported and fully discussed. Last but not least, micro-patterning optical lithography combined with plasma etching has been used to obtain well-defined one-dimensional micro-stripes as well as squared-rings, demonstrating the easy-to-transfer silicon technology to polymer-based devices.
Open AccessSpin Coating and Micro-Patterning Optimization of Composite Thin Films Based on PVDF
We optimize the elaboration of very thin film of poly(vinylidene fluoride) (PVDF) polymer presenting a well-controlled thickness, roughness, and nano-inclusions amount. We focused our effort on the spin coating elaboration technique which is easy to transfer to an industrial process. We show that it is possible to obtain continuous and smooth thin films with mean thicknesses of 90 nm by properly adjusting the concentration and the viscosity of the PVDF solution as well as the spin rate and the substrate temperature of the elaboration process. The electro-active phase content versus the magnetic and structural properties of the composite films is reported and fully discussed. Last but not least, micro-patterning optical lithography combined with plasma etching has been used to obtain well-defined one-dimensional micro-stripes as well as squared-rings, demonstrating the easy-to-transfer silicon technology to polymer-based devices.
- Open Access
Microstructure and Mechanical Properties of Ti6Al4V Alloy Consolidated by Different Sintering Techniques
In this paper, we investigated the effect of the different sintering techniques including vacuum sintering, capsule-free hot isostatic pressing (HIP), and capsule HIP on the microstructure and mechanical properties of Ti6Al4V alloy. The obtained results indicated that full density Ti6Al4V alloy could be obtained by using capsule HIP technique. The alloy sintered by capsule HIP had the highest hardness (~405 HV) and compressive yield strength (~1056 MPa). It is interesting that the geometry has a significant influence on the relative density and mechanical properties of the alloy sintered by the capsule-free HIP. The relative density, hardness, and compressive yield strength rise from center to periphery of the specimen. This is attributed to the heating and pressing in the capsule-free, which are external, leading to the densification processes starting from the outside to the inner parts of the pressed specimen. Using theoretical prediction with Gibson and Ashby power law found that the yield strength of the alloy sintered by capsule-HIP technique is much lower than that of the calculated value due to the formation of the coarse lamellar microstructure of α-Ti grains.
Open AccessMicrostructure and Mechanical Properties of Ti6Al4V Alloy Consolidated by Different Sintering Techniques
In this paper, we investigated the effect of the different sintering techniques including vacuum sintering, capsule-free hot isostatic pressing (HIP), and capsule HIP on the microstructure and mechanical properties of Ti6Al4V alloy. The obtained results indicated that full density Ti6Al4V alloy could be obtained by using capsule HIP technique. The alloy sintered by capsule HIP had the highest hardness (~405 HV) and compressive yield strength (~1056 MPa). It is interesting that the geometry has a significant influence on the relative density and mechanical properties of the alloy sintered by the capsule-free HIP. The relative density, hardness, and compressive yield strength rise from center to periphery of the specimen. This is attributed to the heating and pressing in the capsule-free, which are external, leading to the densification processes starting from the outside to the inner parts of the pressed specimen. Using theoretical prediction with Gibson and Ashby power law found that the yield strength of the alloy sintered by capsule-HIP technique is much lower than that of the calculated value due to the formation of the coarse lamellar microstructure of α-Ti grains.