Electronic Structure of Colloidal 2H-MoS Mono and Bilayers Determined by Spectroelectrochemistry.

The electronic structure of mono and bilayers of colloidal 2H-MoS nanosheets synthesized by wet-chemistry using potential-modulated absorption spectroscopy (EMAS), differential pulse voltammetry, and electrochemical gating measurements is investigated. The energetic positions of the conduction and valence band edges of the direct and indirect bandgap are reported and observe strong bandgap renormalization effects, charge screening of the exciton, as well as intrinsic n-doping of the as-synthesized material. Two distinct transitions in the spectral regime associated with the C exciton are found, which overlap into a broad signal upon filling the conduction band.

Substrate Effects on the Bandwidth of CdSe Quantum Dot Photodetectors.

We investigate the time-resolved photocurrent response of CdSe quantum dot (QD) thin films sensitized with zinc β-tetraaminophthalocyanine (Zn4APc) (Kumar , , 2019, 11, 48271-48280) on three different substrates, namely, silicon with 230 nm SiO dielectric, glass, and polyimide. While Si/SiO (230 nm) is not suitable for any transient photocurrent characterization due to an interfering photocurrent response of the buried silicon, we find that polyimide substrates invoke the larger optical bandwidth with 85 kHz vs 67 kHz for the same quantum dot thin film on glass. Upon evaluation of the transient photocurrent, we find that the photoresponse of the CdSe quantum dot films can be described as a combination of carrier recombination and fast trapping within 2.

Heteroatom Cycloaddition at the (BN) Bay Region of Dibenzoperylene.

Cycloaddition-dehydration involving a BNBN-butadiene analogue at the bay region of a dibenzoperylene and a non-enolizable aldehyde provides a novel strategy for incorporation of the oxadiazadiborinane (B N CO) ring into the scaffold of a polycyclic aromatic hydrocarbon resulting in highly emissive compounds.

Electron-Conducting PbS Nanocrystal Superlattices with Long-Range Order Enabled by Terthiophene Molecular Linkers.

PbS nanocrystals are surface-functionalized with the organic semiconductor 5,5″-dithiol-[2,2':5,2″-terthiophene] and assembled to afford hybrid nanostructured thin films with a large structural coherence and an electron mobility of 0.2 cm/(V s). Electrochemistry, optical spectroscopy, and quantum mechanical calculations are applied to elucidate the electronic structure at the inorganic/organic interface, and it is established that electron injection into the molecule alters its (electronic) structure, which greatly facilitates coupling of the neighboring PbS 1S states.

Correlated, Dual-Beam Optical Gating in Coupled Organic-Inorganic Nanostructures.

An optical switch with two distinct resonances is formed by combining PbS nanocrystals and the conductive polymer poly[sodium 2-(2-ethynyl-4-methoxyphenoxy)acetate] (PAE) into a hybrid thin film. Infrared excitation of the nanocrystals invokes charge transfer and consecutive polaron formation in the PAE, which activates the switch for excited-state absorption at visible frequencies. The optical modulation of the photocurrent response of the switch exhibits highly wavelength-selective ON/OFF ratios.