Origin of the low-energy tail in the photoluminescence spectrum of CsPbBr nanoplatelets: a femtosecond transient absorption spectroscopic study.

CsPbBr nanoplatelets (NPLs), as some of the two-dimensional lead halide perovskites, have been intensively investigated due to their outstanding photophysical and photoelectric properties. However, there remain unclear fundamental issues on their carrier kinetics and the low-energy tail in their photoluminescence (PL) spectrum. In this paper, we synthesized CsPbBr NPLs with five [PbBr] monolayers and performed comprehensive studies by using steady-state absorption, PL, and femtosecond transient absorption (fs-TA) spectroscopic measurements.

Unravelling the doping effect of potassium ions on structural modulation and photocatalytic activity of graphitic carbon nitride.

Graphitic carbon nitride (GCN), as a promising photocatalyst, has been intensely investigated in the photocatalytic fields, but its performance is still unsatisfactory. To date, metal ion doping has been proven to be an effective modification method to improve the photocatalytic activity of GCN. More importantly, comprehensive understanding of the doping mechanism will be of benefit to synthesize efficient GCN based photocatalysts.

A comparison study of sodium ion- and potassium ion-modified graphitic carbon nitride for photocatalytic hydrogen evolution.

It is well known that modifying graphitic carbon nitride (GCN) is an imperative strategy to improve its photocatalytic activity. In this study, Na-doped and K-doped graphitic carbon nitride (GCN-Na and GCN-K) were prepared the simple thermal polymerization of a mixture of melamine and NaCl or KCl, respectively. The structure characterization showed that both Na and K intercalation could reduce the interlayer distance of GCN and introduce cyano defects in GCN, while K apparently had a stronger influence on the structure variation of GCN.

Electrostatic interaction mechanism of visible light absorption broadening in ion-doped graphitic carbon nitride.

Broadening the light response of graphitic carbon nitride (CN) is helpful to improve its solar energy utilization efficiency in photocatalytic reaction. In this work, a facile synthesis method was developed the treatment of potassium-doped CN (CN-K) with HO in isopropanol solvent. Various characterizations indicate the basic structure of CN-K treated with HO (CN-K-OOH) resembles that of CN-K, while it presents light absorption up to 650 nm.

Photon induced quantum yield regeneration of cap-exchanged CdSe/CdS quantum rods for ratiometric biosensing and cellular imaging.

Full water-dispersion of commercial hydrophobic CdSe/CdS core/shell quantum rods (QRs) was achieved by cap-exchange using a dihydrolipoic acid zwitterion ligand at a low ligand:QR molar ratio (LQMR) of 1000. However, this process almost completely quenched the QR fluorescence, greatly limiting its potential in downstream fluorescence based applications. Fortunately, we found that the QR fluorescence could be recovered by exposure to near ultra-violet to blue light radiation (e.

Direct Observation of Surface Polarons in Capped CuInS Quantum Dots by Ultrafast Pump-Probe Spectroscopies.

Semiconductor nanocrystals are mostly prepared by colloid chemistry with organic surfactant molecules, and their surface polarization effect on the carrier relaxations are critical to their optoelectronic applications. Until now, the surface polarization effect and detailed photophysical processes of these capped quantum dots (QDs) are still unclear. Here, we studied the dynamics of the photoinduced carriers and capping molecule  vibrations of capped CuInS quantum dots by using the femtosecond pump-probe system in both visible and IR zones.

Ultrafast Excited-State Intermolecular Proton Transfer in Indigo Oligomer.

It has been a long-lasting debate whether indigo undergoes excited-state proton transfer and how this contributes to its photostability. A prevailing point of view is that a sub-picosecond excited-state intramolecular single proton transfer occurs; however, it has been studied mostly under dilute solution conditions. In this work, excited-state structural dynamics of indigo oligomers formed at millimolar concentration in dimethyl sulfoxide is investigated using femtosecond visible pump spectroscopy, infrared and visible probe spectroscopies, and steady-state infrared and fluorescence spectroscopies.

Photophysics and Photocatalysis of Melem: A Spectroscopic Reinvestigation.

Graphitic carbon nitride (g-CN) is one potential metal-free photocatalyst. The photocatalytic mechanism of g-CN is related to the heptazine ring building unit. Melem is the simplest heptazine-based compound and g-CN is its polymeric product.

Dissecting Multivalent Lectin-Carbohydrate Recognition Using Polyvalent Multifunctional Glycan-Quantum Dots.

Multivalent protein-carbohydrate interactions initiate the first contacts between virus/bacteria and target cells, which ultimately lead to infection. Understanding the structures and binding modes involved is vital to the design of specific, potent multivalent inhibitors. However, the lack of structural information on such flexible, complex, and multimeric cell surface membrane proteins has often hampered such endeavors.

Interaction between triethanolamine and singlet or triplet excited state of xanthene dyes in aqueous solution.

Triethanolamine (TEOA) has been often used as a hole-scavenger in dye-sensitized semiconductor photocatalytic systems. However, the femtosecond time-resolved kinetics of the interaction between a sensitized dye and TEOA has not been reported in literatures. Herein, we selected four commonly used xanthene dyes, such as fluorescein, dibromofluorescein, eosin Y, and erythrosine B, and studied their ultrafast fluorescence quenching dynamics in the presence of TEOA in aqueous solution, respectively, by using both femtosecond transient absorption and time-resolved fluorescence measurements.

Charge carrier kinetics of carbon nitride colloid: a femtosecond transient absorption spectroscopy study.

Carbon nitrides (CN) have been widely used in photocatalytic applications. However, the charge carrier kinetics of CN after light excitation remains unclear. Herein, we prepared a stable and transparent CN colloid in an aqueous tetraethylammonium hydroxide solution and investigated its carrier kinetics using both femtosecond transient absorption and picosecond time-resolved fluorescence spectroscopy.

Fluorescence quenching of coumarin 153 by hydroxyl-functionalized room temperature ionic liquids.

Steady-state absorption and fluorescence as well as time-resolved fluorescence of coumarin 151 (C151) and coumarin 153 (C153) were measured in hydroxyl-functionalized ionic liquids ([HOEmim][BF4] and [HOEmim][N(CN)2]) and in nonhydroxyl-functionalized ionic liquids ([Emim][BF4] and [Emim][N(CN)2]). Both the steady-state fluorescence and time-resolved fluorescence observations reveal that hydroxyl-functionalized ionic liquid quenches the fluorescence of C153 while the nonhydroxyl-functionalized ionic liquid does not. We also measured the time-resolved fluorescence anisotropy of C151 and C153 in both [HOEmim][BF4] and [Emim][BF4].

Time-Resolved Study on Xanthene Dye-Sensitized Carbon Nitride Photocatalytic Systems.

Dye sensitization is a promising strategy to extend the visible light absorption of carbon nitride (C3N4) and increase the photocatalytic hydrogen evolution efficiency of C3N4 under visible light irradiation. However, the interaction dynamics between C3N4 and a sensitized dye has not been reported in the literature. Herein, we selected four commonly used xanthene dyes such as fluorescein, dibromofluorescein, eosin Y, and erythrosine B and prepared their corresponding dye-sensitized-C3N4 composites.

A sensitive fluorescence anisotropy method for detection of lead (II) ion by a G-quadruplex-inducible DNA aptamer.

Sensitive and selective detection of Pb(2+) is of great importance to both human health and environmental protection. Here we propose a novel fluorescence anisotropy (FA) approach for sensing Pb(2+) in homogeneous solution by a G-rich thrombin binding aptamer (TBA). The TBA labeled with 6-carboxytetramethylrhodamine (TMR) at the seventh thymine nucleotide was used as a fluorescent probe for signaling Pb(2+).

Ultrafast fluorescence quenching dynamics of Atto655 in the presence of N-acetyltyrosine and N-acetyltryptophan in aqueous solution: proton-coupled electron transfer versus electron transfer.

We studied the ultrafast fluorescence quenching dynamics of Atto655 in the presence of N-acetyltyrosine (AcTyr) and N-acetyltryptophan (AcTrp) in aqueous solution with femtosecond transient absorption spectroscopy. We found that the charge-transfer rate between Atto655 and AcTyr is about 240 times smaller than that between Atto655 and AcTrp. The pH value and D2O dependences of the excited-state decay kinetics of Atto655 in the presence of AcTyr and AcTrp reveal that the quenching of Atto655 fluorescence by AcTyr in aqueous solution is via a proton-coupled electron-transfer (PCET) process and that the quenching of Atto655 fluorescence by AcTrp in aqueous solution is via an electron-transfer process.

Specific and sensitive fluorescence anisotropy sensing of guanine-quadruplex structures via a photoinduced electron transfer mechanism.

Fluorescence anisotropy (FA) is a homogeneous, ratiometric, and real-time analytical technology. By selective labeling of a guanine (G)-quadruplex motif with tetramethylrhodamine (TMR), here, it is established that a large reduction in FA response can be specifically associated with the unfolding → folding transition of G-quadruplex structures. On the basis of fluorescence intensity, polarization and lifetime analysis, and molecular docking simulation, the mechanism was found to be that the labeled fluorophore (TMR) can intramolecularly interact with adjacent G bases in an unfolded G-quadruplex motif, which allows for the photoinduced electron transfer (PET) occurring between the fluorophore and G bases, leading to a short fluorescence lifetime.

Structural heterogeneity in the collision complex between organic dyes and tryptophan in aqueous solution.

The heterogeneity on photoinduced electron transfer (PET) kinetics between a labeled fluorophore and an amino acid residue has been extensively studied in biopolymers. However in aqueous solutions, the heterogeneity on PET kinetics between a fluorophore and a quencher has rarely been reported. Herein, we selected four commonly used fluorophores, such as tetramethylrhodamine (TMR), Rhodamine B (RhB), Alexa fluor 546 (Alexa546), and Atto655, and studied their respective PET kinetics in 50 mM tryptophan solutions with femtosecond transient absorption spectroscopy to explore the structural heterogeneity in their corresponding collision complexes.

Photophysics and locations of IR125 and C152 in AOT reverse micelles.

Many fluorescent chromophores have been employed to investigate the nature and dynamics of the water confined in reverse micelles (RMs). However, some questions remain as to the location of a probe in a RM and the diameter of the RM at which the physical characteristic of the water inside RMs becomes similar to that of bulk water. In this work, we systematically studied the photophysics of IR125 and C152 in AOT RMs at different w(0) by means of static absorption and fluorescence spectroscopy as well as time-resolved fluorescence spectroscopy.

Ultrafast photoinduced electron transfer between tetramethylrhodamine and guanosine in aqueous solution.

Photoinduced electron transfer based fluorescence correlation spectroscopy (PET-FCS) is a powerful tool to study biomolecular processes. However, some questions remain as to how to correctly interpret the PET-FCS data. In this work, we studied the PET process between tetramethylrhodamine and guanosine by means of femtosecond transient absorption spectroscopy.

Photophysical properties of Atto655 dye in the presence of guanosine and tryptophan in aqueous solution.

Atto655 has been widely used as an excellent probing dye through photoinduced electron transfer (PET) for biochemical processes in oligonucleotides or polypeptides. However, its photophysical properties in the presence of the quenchers guanosine and tryptophan have not been carefully studied. In this work, we investigated the dynamics of PET between Atto655 and the two quenchers in aqueous solution with femtosecond transient absorption experiments.

Measurements of heme relaxation and ligand recombination in strong magnetic fields.

Heme cooling signals and diatomic ligand recombination kinetics are measured in strong magnetic fields (up to 10 T). We examined diatomic ligand recombination to heme model compounds (NO and CO), myoglobin (NO and O(2)), and horseradish peroxidase (NO). No magnetic field induced rate changes in any of the samples were observed within the experimental detection limit.

Temperature-dependent heme kinetics with nonexponential binding and barrier relaxation in the absence of protein conformational substates.

We present temperature-dependent kinetic measurements of ultrafast diatomic ligand binding to the "bare" protoheme (L(1)-FePPIX-L(2), where L(1) = H(2)O or 2-methyl imidazole and L(2) = CO or NO). We found that the binding of CO is temperature-dependent and nonexponential over many decades in time, whereas the binding of NO is exponential and temperature-independent. The nonexponential nature of CO binding to protoheme, as well as its relaxation above the solvent glass transition, mimics the kinetics of CO binding to myoglobin (Mb) but on faster time scales.

Dynamics of nitric oxide rebinding and escape in horseradish peroxidase.

Ultrafast kinetic measurements of NO rebinding to horseradish peroxidase (HRP) are reported for the first time. The geminate kinetics are found to be exponential for all HRP samples studied. The ferric forms of HRP have NO geminate recombination time constants in the range of 15-30 ps, while the ferrous form has a time constant of approximately 7 ps.

Temperature-dependent studies of NO recombination to heme and heme proteins.

The rebinding kinetics of NO to the heme iron of myoglobin (Mb) is investigated as a function of temperature. Below 200 K, the transition-state enthalpy barrier associated with the fastest (approximately 10 ps) recombination phase is found to be zero and a slower geminate phase (approximately 200 ps) reveals a small enthalpic barrier (approximately 3 +/- 1 kJ/mol). Both of the kinetic rates slow slightly in the myoglobin (Mb) samples above 200 K, suggesting that a small amount of protein relaxation takes place above the solvent glass transition.

CO rebinding to protoheme: investigations of the proximal and distal contributions to the geminate rebinding barrier.

The rebinding kinetics of CO to protoheme (FePPIX) in the presence and absence of a proximal imidazole ligand reveals the magnitude of the rebinding barrier associated with proximal histidine ligation. The ligation states of the heme under different solvent conditions are also investigated using both equilibrium and transient spectroscopy. In the absence of imidazole, a weak ligand (probably water) is bound on the proximal side of the FePPIX-CO adduct.