Fatima Hamie

Bio: Fatima Hamie is an academic researcher from University of Technology of Troyes. The author has contributed to research in topics: Quantum dot & Laser. The author has an hindex of 1, co-authored 1 publications receiving 15 citations.

Functional Materials for Two-Photon Polymerization in Microfabrication

Abstract: Direct laser writing methods based on two-photon polymerization (2PP) are powerful tools for the on-demand printing of precise and complex 3D architectures at the micro and nanometer scale. While much progress was made to increase the resolution and the feature size throughout the years, by carefully designing a material, one can confer specific functional properties to the printed structures thus making them appealing for peculiar and novel applications. This Review summarizes the state-of-the-art of functional resins and photoresists used in 2PP, discussing both the range of material functions available and the methods used to prepare them, highlighting advantages and disadvantages of different classes of materials in achieving certain properties.

Hybrid plasmonic nano-emitters with controlled single quantum emitter positioning on the local excitation field.

Abstract: Hybrid plasmonic nano-emitters based on the combination of quantum dot emitters (QD) and plasmonic nanoantennas open up new perspectives in the control of light. However, precise positioning of any active medium at the nanoscale constitutes a challenge. Here, we report on the optimal overlap of antenna’s near-field and active medium whose spatial distribution is controlled via a plasmon-triggered 2-photon polymerization of a photosensitive formulation containing QDs. Au nanoparticles of various geometries are considered. The response of these hybrid nano-emitters is shown to be highly sensitive to the light polarization. Different light emission states are evidenced by photoluminescence measurements. These states correspond to polarization-sensitive nanoscale overlap between the exciting local field and the active medium distribution. The decrease of the QD concentration within the monomer formulation allows trapping of a single quantum dot in the vicinity of the Au particle. The latter objects show polarization-dependent switching in the single-photon regime. The authors study, on hybrid plasmonic nano-emitters, the spatial overlap between the exciting optical near-field and the nanoscale active medium whose position is controlled via surface plasmon-triggered two-photon polymerization. They also demonstrate such systems down to the single photon level.

3D-Printed Quantum Dot Nanopixels.

Abstract: The pixel is the minimum unit used to represent or record information in photonic devices. The size of the pixel determines the density of the integrated information, such as the resolution of displays or cameras. Most methods used to produce display pixels are based on two-dimensional patterning of light-emitting materials. However, the brightness of the pixels is limited when they are miniaturized to nanoscale dimensions owing to their limited volume. Herein, we demonstrate the production of three-dimensional (3D) pixels with nanoscale dimensions based on the 3D printing of quantum dots embedded in polymer nanowires. In particular, a femtoliter meniscus was used to guide the solidification of liquid inks to form vertically freestanding nanopillar structures. Based on the 3D layout, we show high-density integration of color pixels, with a lateral dimension of 620 nm and a pitch of 3 μm for each of the red, green, and blue colors. The 3D structure enabled a 2-fold increase in brightness without significant effects on the spatial resolution of the pixels. In addition, we demonstrate individual control of the brightness based on a simple adjustment of the height of the 3D pixels. This method can be used to achieve super-high-resolution display devices and various photonic applications across a range of disciplines.

3D nanoprinting of semiconductor quantum dots by photoexcitation-induced chemical bonding

Abstract: Three-dimensional (3D) laser nanoprinting allows maskless manufacturing of diverse nanostructures with nanoscale resolution. However, 3D manufacturing of inorganic nanostructures typically requires nanomaterial-polymer composites and is limited by a photopolymerization mechanism, resulting in a reduction of material purity and degradation of intrinsic properties. We developed a polymerization-independent, laser direct writing technique called photoexcitation-induced chemical bonding. Without any additives, the holes excited inside semiconductor quantum dots are transferred to the nanocrystal surface and improve their chemical reactivity, leading to interparticle chemical bonding. As a proof of concept, we printed arbitrary 3D quantum dot architectures at a resolution beyond the diffraction limit. Our strategy will enable the manufacturing of free-form quantum dot optoelectronic devices such as light-emitting devices or photodetectors. Description Photoprinting nanoparticles Nanoparticle assembly often requires tailored selection of the ligands so that they can selectively bond, as with complementary DNA strands. Alternately, they can be linked together at specified locations using photopolymerization to connect ligands at desired places. However, this process adds to the complexity of making the nanoparticles and is limited by the fidelity of the ligand attachment. Liu et al. show that light can be used to desorb surface thiolate ligands from cadmium selenide/zinc sulfide core shell quantum dots (see the Perspective by Pan and Talapin). The resulting trapped holes drive bonding between the particles through the remaining surface ligands. The authors reveal photoprinting of arbitrary three-dimensional architectures at a resolution beyond the diffraction limit and for a range of nanocrystals. Printing can be optically selected based on the size and/or bandgap of the quantum dots. —MSL Photoexcitation-induced chemical bonding enables high-resolution three-dimensional printing of semiconductor quantum dots.

Polymers for Regenerative Medicine Structures Made via Multiphoton 3D Lithography

Abstract: Multiphoton 3D lithography is becoming a tool of choice in a wide variety of fields. Regenerative medicine is one of them. Its true 3D structuring capabilities beyond diffraction can be exploited to produce structures with diverse functionality. Furthermore, these objects can be produced from unique materials allowing expanded performance. Here, we review current trends in this research area. We pay particular attention to the interplay between the technology and materials used. Thus, we extensively discuss undergoing light-matter interactions and peculiarities of setups needed to induce it. Then, we continue with the most popular resins, photoinitiators, and general material functionalization, with emphasis on their potential usage in regenerative medicine. Furthermore, we provide extensive discussion of current advances in the field as well as prospects showing how the correct choice of the polymer can play a vital role in the structure’s functionality. Overall, this review highlights the interplay between the structure’s architecture and material choice when trying to achieve the maximum result in the field of regenerative medicine.