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1.
J Phys Chem B ; 118(4): 1088-96, 2014 Jan 30.
Article in English | MEDLINE | ID: mdl-24401127

ABSTRACT

In recent years, the effect of molecular charge on the rotational dynamics of probe solutes in room-temperature ionic liquids (RTILs) has been a subject of growing interest. For the purpose of extending our understanding of charged solute behavior within RTILs, we have studied the rotational dynamics of three illustrative xanthene fluorescent probes within a series of N-alkylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([Cnmpyr][Tf2N]) RTILs with different n-alkyl chain lengths (n = 3, 4, 6, 8, or 10) using time-resolved fluorescence anisotropy decay. The rotational dynamics of the neutral probe rhodamine B (RhB) dye lies between the stick and slip boundary conditions due to the influence of specific hydrogen bonding interactions. The rotation of the negatively charged sulforhodamine 640 (SR640) is slower than that of its positively charged counterpart rhodamine 6G (R6G). An analysis based upon Stokes-Einstein-Debye hydrodynamics indicates that SR640 adheres to stick boundary conditions due to specific interactions, whereas the faster rotation of R6G is attributed to weaker electrostatic interactions. No significant dependence of the rotational dynamics on the solvent alkyl chain length was observed for any of the three dyes, suggesting that the specific interactions between dyes and RTILs are relatively independent of this solvent parameter.

2.
J Phys Chem B ; 116(27): 7883-90, 2012 Jul 12.
Article in English | MEDLINE | ID: mdl-22690897

ABSTRACT

NMR spectroscopy and time-resolved fluorescence anisotropy decay (TRFAD) are two of the most commonly used methods to study solute-solvent interactions. However, only a few studies have been reported to date using a combined NMR and TRFAD approach to systematically investigate the overall picture of diffusional and rotational dynamics of both the solute and solvent. In this paper, we combined NMR and TRFAD to probe fluorescent rhodamine dye in a pyrrolidinium-based room temperature ionic liquid (RTIL), an emergent environmentally friendly solvent type used in several energy-related applications. A specific interaction of the R6G cation and [Tf2N] anion was identified, resulting in near-stick boundary condition rotation of R6G in this RTIL. The diffusional rates of the R6G solute and [C4mpyr][Tf2N] solvent derived from (1)H NMR suggest the rates are proportional to their corresponding hydrodynamic radii. The (1)H and (13)C NMR studies of self-rotational dynamics of [C4mpyr][Tf2N] showed that the self-rotational correlation time of [C4mpyr](+) is 47 ± 2 ps at 300 K. At the same temperature, we find that the correlation time for N-CH3 rotation in [C4mpyr](+) is 77 ± 2 ps, comparable to overall molecular reorientation. This slow motion is attributed to properties of the cation structure.


Subject(s)
Ionic Liquids/chemistry , Pyrrolidines/chemistry , Rhodamines/chemistry , Fluorescence Polarization , Magnetic Resonance Spectroscopy , Molecular Structure , Rotation , Time Factors
3.
Nano Rev ; 22011.
Article in English | MEDLINE | ID: mdl-22110870

ABSTRACT

Photovoltaic functions in organic materials are intimately connected to interfacial morphologies of molecular packing in films on the nanometer scale and molecular levels. This review will focus on current studies on correlations of nanoscale morphologies in organic photovoltaic (OPV) materials with fundamental processes relevant to photovoltaic functions, such as light harvesting, exciton splitting, exciton diffusion, and charge separation (CS) and diffusion. Small molecule photovoltaic materials will be discussed here. The donor and acceptor materials in small molecule OPV devices can be fabricated in vacuum-deposited, multilayer, crystalline thin films, or spin-coated together to form blended bulk heterojunction (BHJ) films. These two methods result in very different morphologies of the solar cell active layers. There is still a formidable debate regarding which morphology is favored for OPV optimization. The morphology of the conducting films has been systematically altered; using variations of the techniques above, the whole spectrum of film qualities can be fabricated. It is possible to form a highly crystalline material, one which is completely amorphous, or an intermediate morphology. In this review, we will summarize the past key findings that have driven organic solar cell research and the current state-of-the-art of small molecule and conducting oligomer materials. We will also discuss the merits and drawbacks of these devices. Finally, we will highlight some works that directly compare the spectra and morphology of systematically elongated oligothiophene derivatives and compare these oligomers to their polymer counterparts. We hope this review will shed some new light on the morphology differences of these two systems.

4.
Phys Chem Chem Phys ; 13(27): 12395-8, 2011 Jul 21.
Article in English | MEDLINE | ID: mdl-21660316

ABSTRACT

In this work, we provide new experimental evidence for chain length-dependent self-aggregation in room temperature ionic liquids (RTILs) using fluorescence correlation spectroscopy (FCS). In studying a homologous series of N-alkyl-N-methylpyrrolidinium bis(trifluoromethylsulfonyl) imide, [C(n)MPy][Tf(2)N] RTILs of varying alkyl chain length (n = 3, 4, 6, 8, and 10), biphasic rhodamine 6G solute diffusion dynamics were observed; both the fast and slow diffusion coefficients decreased with increasing alkyl chain length, with the relative contribution from slower diffusion increasing for longer-chain [C(n)MPy][Tf(2)N]. We propose that the biphasic diffusion dynamics originate from self-aggregation of the nonpolar alkyl chains in the cationic [C(n)MPy](+).

6.
J Phys Chem B ; 114(45): 14505-13, 2010 Nov 18.
Article in English | MEDLINE | ID: mdl-20491461

ABSTRACT

Conjugated oligomers containing a common central thienothiophene unit symmetrically connected to two identical thiophene oligomers were studied as model systems for a series of low bandgap organic diblock copolymers. The oligothiophene side chain fragments were varied in length as a means to tune the electronic coupling between the thienothiophene and oligothiophene moieties. The fragment length dependence of both the ground- and excited-state electronic and structural properties of a series of diblock oligomers were investigated in detail. The charge transfer character in these diblock oligomers, revealed by their optical absorption and fluorescence spectra, is responsible for their low band gap and energy gap tunability compared with their homooligomer counterparts. The electronic spectra and theoretical analysis indicate a partially localized central charge in the first excited state. Using experimental results and comparing them with theoretical calculations, we estimate that the electronic effects from a single thienothiophene unit spreads over seven to nine adjacent units through π-conjugation along the oligomers.

7.
J Phys Chem B ; 114(2): 742-8, 2010 Jan 21.
Article in English | MEDLINE | ID: mdl-20038154

ABSTRACT

Molecular packing structures and photoinduced charge separation dynamics have been investigated in a recently developed bulk heterojunction (BHJ) organic photovoltaic (OPV) material based on poly(thienothiophene-benzodithiophene) (PTB1) with a power conversion efficiency (PCE) of >5% in solar cell devices. Grazing incidence X-ray scattering (GIXS) measurements of the PTB1:PCBM ([6,6]-phenyl-C(61)-butyric acid methyl ester) films revealed pi-stacked polymer backbone planes oriented parallel to the substrate surface, in contrast to the pi-stacked polymer backbone planes oriented perpendicular to the substrate surface in regioregular P3HT [poly(3-hexylthiophene)]:PCBM films. A approximately 1.7 times higher charge mobility in the PTB1:PCBM film relative to that in P3HT:PCBM films is attributed to this difference in stacking orientation. The photoinduced charge separation (CS) rate in the pristine PTB1:PCBM film is more than twice as fast as that in the annealed P3HT:PCBM film. The combination of a small optical gap, fast CS rate, and high carrier mobility in the PTB1:PCBM film contributes to its relatively high PCE in the solar cells. Contrary to P3HT:PCBM solar cells, annealing PTB1:PCBM films reduced the device PCE from 5.24% in the pristine film to 1.92% due to reduced interfacial area between the electron donor and the acceptor. Consequently, quantum yields of exciton generation and charge separation in the annealed film are significantly reduced compared to those in the pristine film.

9.
J Phys Chem A ; 111(29): 6832-42, 2007 Jul 26.
Article in English | MEDLINE | ID: mdl-17518452

ABSTRACT

The effects of anchoring groups on electron injection from adsorbate to nanocrystalline thin films were investigated by comparing injection kinetics through carboxylate versus phosphonate groups to TiO2 and SnO2. In the first pair of molecules, Re(LA)(CO)3Cl (ReC1A) and Re(Lp)(CO)3Cl (ReC1P), [LA=2,2'-bipyridine-4,4'-bis-CH2-COOH, Lp=2,2'-bipyridine-4,4'-bis-CH2-PO3H2], the anchoring groups were insulated from the bipyridine ligand by a CH2 group. In the second pair of molecules, Ru(dcbpyH2)2(NCS)2 (RuN3) and Ru(bpbpyH2)2(NCS)2 (RuN3P), [dcbpy=2,2'-bipyridine-4,4'-biscarboxylic acid, bpbpy=2,2'-bipyridine-4,4'-bisphosphonic acid], the anchoring groups were directly connected to the bipyridine ligands. The injection kinetics, as measured by subpicosecond IR absorption spectroscopy, showed that electron injection rates from ReC1P to both TiO2 and SnO2 were faster than those from ReC1A. The injection rates from RuN3 and RuN3P to SnO2 films were similar. On TiO2, the injection kinetics from RuN3 and RuN3P were biphasic: carboxylate group enhances the rate of the <100 fs component, but reduces the rate of the slower components. To provide insight into the effect of the anchoring groups, the electronic structures of Re-bipyridyl-Ti model clusters containing carboxylate and phosphonate anchoring groups and with and without a CH2 spacer were computed using density functional theory. With the CH2 spacer, the phosphonate group led to a stronger electronic coupling between bpy and Ti center than the carboxylate group, which accounted for the faster injection from ReC1P than ReC1A. When the anchoring groups were directly connected to the bpy ligand without the CH2 spacer, such as in RuN3 and RuN3P, their effects were 2-fold: the carboxylate group enhanced the electronic coupling of bpy pi* with TiO2 and lowered the energy of the bpy orbital. How these competing factors led to different effects on TiO2 and SnO2 and on different components of the biphasic injection kinetics were discussed.

10.
J Phys Chem B ; 111(24): 6903-12, 2007 Jun 21.
Article in English | MEDLINE | ID: mdl-17518489

ABSTRACT

Factors that control photoinduced interfacial electron transfer (ET) between molecular adsorbates and semiconductor nanoparticles have been intensely investigated in recent years. In this work, the solvent dependence of interfacial ET was studied by comparing ET rates in dye sensitized TiO2 nanocrystalline films in different solvent environments. Photoinduced ET rates from Re(LA)(CO)3Cl [LA=dcbpy=4,4'-dicarboxy-2,2'-bipyridine] (ReC1A) to TiO2 nanocrystalline thin films in air, pH buffer, MeOH, EtOH, and DMF were measured by femtosecond transient IR spectroscopy. The ET rates in these solvent environments were noticeably different. However, differences between the rates in pH buffer and nonaqueous solvents (MeOH, EtOH, and DMF) were much smaller than the values expected from much more negative TiO2 conduction band-edge positions in the latter solvents under anhydrous conditions. It was suggested that the presence of adsorbed water, which was evident in FTIR spectra, lowered the band edge of TiO2 in these solvents and reduced the rate differences. The important effect of adsorbed water was verified by comparing two samples of Re(LP)(CO)3Cl [LP=2,2'-bipyridine-4,4'-bis-CH2PO(OH)2] sensitized TiO2 in DMF, in which the presence of a trace amount of water was found to significantly increase the injection rate.

11.
J Phys Chem B ; 110(50): 25496-503, 2006 Dec 21.
Article in English | MEDLINE | ID: mdl-17165998

ABSTRACT

We present a study of photoinduced interfacial electron transfer (ET) dynamics of SnO2 nanocrystalline thin films sensitized by polythiophene derivatives (regioregular poly(3-hexylthiophene) (P3HT) and regiorandom poly(3-undecyl-2,2'-bithiophene) (P3UBT)). ET dynamics were measured by following the dynamics of injected electrons in SnO2 and polarons in the conjugated polymer using ultrafast mid-IR transient absorption spectroscopy. The rate of electron transfer from P3HT and P3UBT to SnO2 films was determined to occur on sub-picosecond time scale (120 +/- 20 fs). In P3HT/SnO2 composite, interchain charge transfer was found to compete with and reduce the quantum efficiency of interfacial electron transfer at high polymer loading. This interchain charge separation processes can be reduced in non-regioregular polymer or at low polymer loading levels.

12.
J Phys Chem B ; 110(11): 5238-44, 2006 Mar 23.
Article in English | MEDLINE | ID: mdl-16539453

ABSTRACT

Photoinduced electron injection dynamics from Ru(dcbpy)(2)(X)(2) (dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; X(2) = 2SCN(-), 2CN(-), and dcbpy; referenced as RuN3, Ru505, and Ru470) to In(2)O(3) nanocrystalline thin films were studied using ultrafast transient IR absorption spectroscopy. After 532 nm excitation of the adsorbates, the dynamics of electron injection from their excited states to In(2)O(3) were studied by monitoring the IR absorption of the injected electrons in the semiconductor. The injection kinetics were non-single-exponential. For samples exposed to air, the half rise times, defined as the time of 50% injection yield, were 5 +/- 0.8, 85 +/- 20, and >200 ps for RuN3, Ru505, and Ru470, respectively. For samples in pH 2 buffer, the corresponding half time for injection from these complexes became 6 +/- 1, 105 +/- 20, and 18 +/- 5 ps. The injection kinetics from RuN3 to In(2)O(3) was found to be similar to that to SnO(2). These kinetics traces showed a negligible <100 fs injection component and were very different from those to TiO(2). The dependences of the injection kinetics on adsorbate energetics and the nature of the semiconductors are discussed.

13.
J Phys Chem B ; 109(15): 7088-94, 2005 Apr 21.
Article in English | MEDLINE | ID: mdl-16851807

ABSTRACT

Ultrafast infrared spectroscopy was utilized to investigate the electron-transfer dynamics from Ru(dcbpy)(2)(X)(2) complexes (dcbpy = 4,4'-dicarboxy-2,2'-bipyridine; X(2) = SCN(-), 2CN(-), and dcbpy; referenced as RuN3, Ru505, and Ru470, respectively) to nanocrystalline SnO(2) films. For both films exposed to air (dry) and submerged in a pH 2 buffer solution, all traces show biphasic dynamics with a small ultrafast component (less than 10%) and nonexponential slow component, indicating that most injection occurs from thermalized excited state of the dye. In the dry film, the injection rate becomes slower, comparing RuN3, Ru505, and Ru470, correlating with decreasing excited-state oxidation potentials in these dyes. However, the variation of injection rate with dye potential is less noticeable at pH 2. The possible reason for the different injection dynamics in these dyes and under different environments are discussed. These injection dynamics are also compared with those on TiO(2) and ZnO.

14.
J Phys Chem B ; 109(15): 7095-102, 2005 Apr 21.
Article in English | MEDLINE | ID: mdl-16851808

ABSTRACT

Ultrafast transient IR spectroscopy has been used to examine the effect of doping on interfacial electron transfer (ET) dynamics in Re(dpbpy)(CO)(3)Cl (dpbpy = 4,4'-(CH(2)PO(OH)(2))2-2,2'-bipyridine) (ReC1PO(3)) sensitized ATO (Sb:SnO(2)) nanocrystalline thin films. In films consisting of particles with 0%, 2% and 10% Sb dopant, the rates of electron injection from the adsorbate excited state to ATO were independent of and the rates of the recombination increased with the doping level. The observed similar forward electron injection rates were attributed to negligible changes of available accepting states in the conduction band at the doping levels studied. The dependence of the recombination rate on conduction band electron density and a possible mechanism for the recombination process were discussed.

15.
J Phys Chem B ; 109(41): 19345-55, 2005 Oct 20.
Article in English | MEDLINE | ID: mdl-16853498

ABSTRACT

Photoinduced interfacial electron transfer (ET) from molecular adsorbates to semiconductor nanoparticles has been a subject of intense recent interest. Unlike intramolecular ET, the existence of a quasicontinuum of electronic states in the solid leads to a dependence of ET rate on the density of accepting states in the semiconductor, which varies with the position of the adsorbate excited-state oxidation potential relative to the conduction band edge. For metal oxide semiconductors, their conduction band edge position varies with the pH of the solution, leading to pH-dependent interfacial ET rates in these materials. In this work we examine this dependence in Re(L(P))(CO)3Cl (or ReC1P) [L(P) = 2,2'-bipyridine-4,4'-bis-CH2PO(OH)2] and Re(L(A))(CO)3Cl (or ReC1A) [L(A) = 2,2'-bipyridine-4,4'-bis-CH2COOH] sensitized TiO2 and ReC1P sensitized SnO2 nanocrystalline thin films using femtosecond transient IR spectroscopy. ET rates are measured as a function of pH by monitoring the CO stretching modes of the adsorbates and mid-IR absorption of the injected electrons. The injection rate to TiO2 was found to decrease by 1000-fold from pH 0-9, while it reduced by only a factor of a few to SnO2 over a similar pH range. Comparison with the theoretical predictions based on Marcus' theory of nonadiabatic interfacial ET suggests that the observed pH-dependent ET rate can be qualitatively accounted for by considering the change of density of electron-accepting states caused by the pH-dependent conduction band edge position.

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