Tuning the Aggregates of Thiophene-based Trimers by Methyl Side-chain Engineering for Photocatalytic Hydrogen Evolution.

Organic π-conjugated semiconductors (OCSs) have recently emerged as a promising alternative to traditional inorganic materials for photocatalysis. However, the aggregation of OCSs in photocatalytic aqueous solution caused by self-assembly, which closely relates to the photocatalytic activity, has not yet been studied. Here, the relationship between the aggregation of 4,7-Bis(thiophen-2-yl) benzothiadiazole (TBT) and the photocatalytic activity was systematically investigated by introducing and varying the position of methyl side chains on the two peripheral thiophene units.

Chitosan-Modified Polyethyleneimine Nanoparticles for Enhancing the Carboxylation Reaction and Plants' CO Uptake.

Increasing plants' photosynthetic efficiency is a major challenge that must be addressed in order to cover the food demands of the growing population in the changing climate. Photosynthesis is greatly limited at the initial carboxylation reaction, where CO is converted to the organic acid 3-PGA, catalyzed by the RuBisCO enzyme. RuBisCO has poor affinity for CO, but also the CO concentration at the RuBisCO site is limited by the diffusion of atmospheric CO through the various leaf compartments to the reaction site.

Thiophene-Based Trimers and Their Bioapplications: An Overview.

Certainly, the success of polythiophenes is due in the first place to their outstanding electronic properties and superior processability. Nevertheless, there are additional reasons that contribute to arouse the scientific interest around these materials. Among these, the large variety of chemical modifications that is possible to perform on the thiophene ring is a precious aspect.

Bottom-Up Synthesized MoS Interfacing Polymer Carbon Nanodots with Electrocatalytic Activity for Hydrogen Evolution.

The preparation of an MoS -polymer carbon nanodot (MoS -PCND) hybrid material was accomplished by employing an easy and fast bottom-up synthetic approach. Specifically, MoS -PCND was realized by the thermal decomposition of ammonium tetrathiomolybdate and the in situ complexation of Mo with carboxylic acid units present on the surface of PCNDs. The newly prepared hybrid material was comprehensively characterized by spectroscopy, thermal means, and electron microscopy.

Thiophene-Based Aldehyde Derivatives for Functionalizable and Adhesive Semiconducting Polymers.

The pursuit for novelty in the field of (bio)electronics demands for new and better-performing (semi)conductive materials. Since the discovery of poly(3,4-ethylenedioxythiophene) (PEDOT), the ubiquitous golden standard, many studies have focused on its applications but only few on its structural modification and/or functionalization. This lack of structural variety strongly limits the versatility of PEDOT, thus hampering the development of novel PEDOT-based materials.

Differential properties and effects of fluorescent carbon nanoparticles towards intestinal theranostics.

Given the potential applications of fluorescent carbon nanoparticles in biomedicine, the relationship between their chemical structure, optical properties and biocompatibility has to be investigated in detail. In this work, different types of fluorescent carbon nanoparticles are synthesized by acid treatment, sonochemical treatment, electrochemical cleavage and polycondensation. The particle size ranges from 1 to 6 nm, depending on the synthesis method.

Interfacing Transition Metal Dichalcogenides with Carbon Nanodots for Managing Photoinduced Energy and Charge-Transfer Processes.

Exfoliated semiconducting MoS and WS were covalently functionalized with 1,2-dithiolane-modified carbon nanodots (CNDs). The newly synthesized CND-MoS and CND-WS hybrids were characterized by spectroscopic, thermal, and electron microscopy imaging methods. Based on electronic absorption and fluorescence emission spectroscopy, modulation of the optoelectronic properties of TMDs by interfacing with CNDs was accomplished.

Supramolecular-Enhanced Charge Transfer within Entangled Polyamide Chains as the Origin of the Universal Blue Fluorescence of Polymer Carbon Dots.

The emission of a bright blue fluorescence is a unique feature common to the vast variety of polymer carbon dots (CDs) prepared from carboxylic acid and amine precursors. However, the difficulty to assign a precise chemical structure to this class of CDs yet hampers the comprehension of their underlying luminescence principle. In this work, we show that highly blue fluorescent model types of CDs can be prepared from citric acid and ethylenediamine through low temperature synthesis routes.

Electronic Interactions in Illuminated Carbon Dot/MoS Ensembles and Electrocatalytic Activity towards Hydrogen Evolution.

The preparation, characterization, and photophysical and electrocatalytic properties of carbon dot (CD)/MoS ensembles is reported. Based on electrostatic interactions, ammonium-functionalized MoS , which was prepared upon reaction of 1,2-dithiolane tert-butyl carbamate with MoS followed by acidic deprotection, was coupled with CDs bearing multiple carboxylates on their periphery, as derived upon microwave-assisted polycondensation of citric acid and ethylenediamine followed by alkaline treatment. Insights into electronic interactions between the two species within CD/MoS ensembles emanated from absorption and photoluminescence titration assays.