Tartaric acid-derived chiral carbon nanodots for catalytic enantioselective ring-opening reactions of styrene oxide.

Chiral carbon nanodots (CNDs) were fabricated through the hydrothermal processing of sulfanilic acid and chiral tartaric acid, exhibiting outstanding catalytic performance for the chiral catalysis of the ring-opening reaction. Furthermore, the catalytic mechanism was proposed to understand the link between the chiral structure and the performance of the catalyst.

Understanding the Visible Absorption of Electron Accepting and Donating CNDs.

Carbon nanodots (CNDs) synthesized from citric acid and formyl derivatives, that is, formamide, urea, or N-methylformamide, stand out through their broad-range visible-light absorbance and extraordinary photostability. Despite their potential, their use has thus far been limited to imaging research. This work has now investigated the link between CNDs' photochemical properties and their chemical structure.

Carbon Nanodots for All-in-One Photocatalytic Hydrogen Generation.

Carbon nanodots (CNDs) were photochemically altered to produce dihydrogen under light irradiation. Within the complex structure of CNDs, photo-oxidation takes place at citrazinic acid molecular fluorophore sites. Important is the fact that the resulting CND materials have a dual function.

The Impact of Aggregation of Quaterthiophenes on the Excited State Dynamics.

Oligothiophenes and their aggregates play a dominant role in optoelectronic and light-harvesting applications. Here, we controlled the degree of aggregation of 2,2':5',2″:5'',2‴-quaterthiophene (QTH) to shed light on the impact of the aggregation on the excited state dynamics. QTH aggregation realized the control over the Intersystem Crossing (ISC) rates and, in turn, the formation of triplet excited states via the simple addition of water to QTH solutions in THF.

Global and target analysis of relaxation processes of the collapsed state of P3HT polymer nanoparticles.

Organic-inorganic heterostructure materials have received significant research interest for designing light harvesting devices because of their efficient charge separation. Here, we design organic and inorganic nano-heterostructures using conjugated polymer nanoparticles (PNPs) [poly(3-hexylthiophene-2,5-diyl), P3HT] and Au nanoparticles. We investigate the carrier relaxation processes of this heterostructure at different time scales by ultrafast transient absorption spectroscopy.

Influence of shape on the carrier relaxation dynamics of CsPbBr perovskite nanocrystals.

Lead halide perovskite nanocrystals (NCs) have recently emerged as a new class of functional materials for designing efficient light harvesting systems because of their unique photophysical properties. Here, we report the influence of different shapes on the relaxation dynamics of perovskite nanocrystals. The structural transformation of CsPbBr NCs from cubic shape to rod shape occurs by changing the solvent from toluene to dichloromethane (DCM).

Ultrafast Relaxation Processes of Conjugated Polymer Nanoparticles in the Presence of Au Nanoparticles.

Considering the importance of conjugated polymer nanoparticles, major emphasis has been given for designing and understanding the energy transfer and charge transfer processes of organic-inorganic hybrids for light harvesting applications. In the present study, we have designed an aqueous solution-based light harvesting system using conjugated polymer nanoparticles (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene], MEH-PPV) and Au nanoparticles. The change in photo-induced processes in the presence of metal nanoparticles are studied by steady-state absorption, time-resolved emission, time-resolved fluorescence up-conversion, ultrafast anisotropy and femtosecond transient absorption spectroscopy.

Role of Structural Distortion in Stabilizing Electrosynthesized Blue-Emitting Phosphorene Quantum Dots.

Luminescent phosphorene quantum dots (PQDs) have emerged as fascinating nanomaterials for potential applications in optoelectronics, catalysis, and sensing. Herein, we investigate the structural distortion of black phosphorus (BP) under an applied electric field to yield blue luminescent PQDs [average diameter 8 ± 1.5 nm ( N = 60)].

Photon Harvesting in Conjugated Polymer-Based Functional Nanoparticles.

The design of new generation light-harvesting systems based on conjugated polymer nanoparticles (PNPs) is an emerging field of research to convert solar energy into renewable energy. In this Perspective, we focus on the understanding of the light harvesting processes like exciton dynamics, energy transfer, antenna effect, charge carrier dynamics, and other related processes of conjugated polymer-based functional nanomaterials. Spectroscopic investigations unveil the rotational dynamics of the dye molecules inside of PNPs and exciton dynamics of the self-assembled structures.

Light Harvesting and Photocurrent Generation in a Conjugated Polymer Nanoparticle-Reduced Graphene Oxide Composite.

Polymer-graphene nanocomposites are promising candidates for light harvesting applications such as photocatalysis and photovoltaics, where significant charge separation occurs due to photoinduced electron transfer. Much attention has been paid to using reduced graphene oxide (r-GO) as template for anchoring various nanomaterials due to its efficient electron accepting and transport properties. Here, poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV) nanoparticles are prepared from MEH-PPV polymer and the change in photophysical properties upon formation of polymer nanoparticles (PNPs) from the molecular state are investigated by using steady-state and time-resolved spectroscopy.

Functionalized dye encapsulated polymer nanoparticles attached with a BSA scaffold as efficient antenna materials for artificial light harvesting.

A potential strategy for a new generation light harvesting system is multi-chromophoric donor-acceptor pairs where light energy is absorbed by an antenna complex and subsequently transfers its energy to the acceptor via energy transfer. Here, we design a system of a functionalized polymer nanoparticle-protein scaffold for efficient light harvesting and white light generation where a dye doped polymer nanoparticle acts as a donor and a dye encapsulated BSA protein acts as an acceptor. Analysis reveals that 91.

Photoswitching and Thermoresponsive Properties of Conjugated Multi-chromophore Nanostructured Materials.

Conjugated multi-chromophore organic nanostructured materials have recently emerged as a new class of functional materials for developing efficient light-harvesting, photosensitization, photocatalysis, and sensor devices because of their unique photophysical and photochemical properties. Here, we demonstrate the formation of various nanostructures (fibers and flakes) related to the molecular arrangement (H-aggregation) of quaterthiophene (QTH) molecules and their influence on the photophysical properties. XRD studies confirm that the fiber structure consists of >95% crystalline material, whereas the flake structure is almost completely amorphous and the microstrain in flake-shaped QTH is significantly higher than that of QTH in solution.

Conjugated polymer P3HT-Au hybrid nanostructures for enhancing photocatalytic activity.

Metal-semiconductor nanostructures have been the subject of great interest, mainly due to their interesting optical properties and their potential applications in light harvesting, photocatalysis and photovoltaic devices. Here, we have designed raspberry type organic-inorganic hybrid nanostructures of the poly-3-hexylthiophene (P3HT)-Au nanoparticle (NP) composite by a simple solution based synthetic method. The electronic interaction of semiconducting P3HT polymer nanoparticles with Au nanoparticles exhibits a bathochromic shift of absorption bands and significant photoluminescence quenching of P3HT nanoparticles in this organic-inorganic hybrid system.

Multichromophoric organic molecules encapsulated in polymer nanoparticles for artificial light harvesting.

We designed a self-assembled multichromophoric organic molecular arrangement inside polymer nanoparticles for light-harvesting antenna materials. The self-assembled molecular arrangement of quaterthiophene molecules was found to be an efficient light-absorbing antenna material, followed by energy transfer to Nile red (NR) dye molecules, which was confined in polymer nanoparticles. The efficiency of the antenna effect was found to be 3.