Theoretical study of D–A′–π–A/D–π–A′–π–A triphenylamine and quinoline derivatives as sensitizers for dye-sensitized solar cells

We have designed four dyes based on D–A′–π–A/D–π–A′–π–A triphenylamine and quinoline derivatives for dye-sensitized solar cells (DSSCs) and studied their optoelectronic properties as well as the effects of the introduction of alkoxy groups and thiophene group on these properties. The geometries, single point energy, charge population, electrostatic potential (ESP) distribution, dipole moments, frontier molecular orbitals (FMOs) and HOMO–LUMO energy gaps of the dyes were discussed to study the electronic properties of dyes based on density functional theory (DFT). And the absorption spectra, light harvesting efficiency (LHE), hole–electron distribution, charge transfer amount from HOMO to LUMO (Q_CT), D index, H_CT index, S_m index and exciton binding energy (E_coul) were discussed to investigate the optical and charge-transfer properties of dyes by time-dependent density functional theory (TD-DFT). The calculated results show that all the dyes follow the energy level matching principle and have broadened absorption bands at visible region. Besides, the introduction of alkoxy groups into triarylamine donors and thiophene groups into conjugated bridges can obviously improve the stability and optoelectronic properties of dyes. It is shown that the dye D4, which has had alkoxy groups as well as thiophene groups introduced and possesses a D–π–A′–π–A configuration, has the optimal optoelectronic properties and can be used as an ideal dye sensitizer.

We have designed four dyes based on D–A′–π–A/D–π–A′–π–A triphenylamine and quinoline derivatives for DSSCs and studied their optoelectronic properties as well as the effects of the introduction of alkoxy groups and thiophene group on the properties.     

Mechanofluorochromism of (D–π–)2A-type azine-based fluorescent dyes

Bathochromic or hypsochromic shift-type mechanofluorochromism (b-MFC or h-MFC) was found for (D–π–)₂A-type azine-based fluorescent dyes OUY-2, OUK-2, and OUJ-2 possessing intramolecular charge-transfer (ICT) characteristics from two (diphenylamino)carbazole–thiophene units as D (electron-donating group)–π (π-conjugated bridge) moieties to a pyridine, pyrazine, or triazine ring as A (electron-withdrawing group): grinding of the recrystallized dyes induced red or blue shifts of the fluorescent colors, that is, bathochromic or hypsochromic shifts of the fluorescence maximum wavelengths (λ^fl-solid_max). The degrees of MFC evaluated by the absolute value of differences (Δλ^fl-solid_max) in λ^fl-solid_max before and after grinding of the recrystallized dyes increased in the order of OUY-2 (+7 nm) < OUK-2 (−17 nm) < OUJ-2 (+45 nm), so that OUJ-2 exhibits obvious b-MFC, but OUK-2 exhibits h-MFC. X-ray powder diffraction (XRD) and differential scanning calorimetry (DSC) demonstrated that the recrystallized dyes were in the crystalline state but the ground dyes were in the amorphous state. When the ground solids were heated above their crystallization temperatures (T_c), the colors and fluorescent colors recovered to the original ones before grinding or converted to other ones, that is, heating the ground solids in the amorphous state induced the recrystallization to recover the original microcrystals or to form other microcrystals due to polymorph transformation. However, (D–π–)₂Ph-type fluorescent dye OTK-2 having a phenyl group as a substitute for the azine rings exhibited non-obvious MFC. Molecular orbital (MO) calculations indicated that the values of the dipole moments (μ_g) in the ground state were 4.0 debye, 1.4 debye, 3.2 debye, and 2.9 debye for OTK-2, OUY-2, OUK-2, and OUJ-2, respectively. Consequently, on the basis of experimental results and MO calculations, we have demonstrated that the MFC of the (D–π–)₂A-type azine-based fluorescent dyes is attributed to reversible switching between the crystalline state of the recrystallized dyes and the amorphous state of the ground dyes with changes in the intermolecular dipole–dipole and π–π interactions before and after grinding. Moreover, this work reveals that (D–π–)₂A fluorescent dyes possessing dipole moments of ca. 3 debye as well as moderate or intense ICT characteristics make it possible to activate the MFC.

Bathochromic or hypsochromic shift-type mechanofluorochromism (b-MFC of h-MFC) was found for (D–π–)₂A-type azine-based fluorescent dyes: grinding of the recrystallized dyes induced bathochromic or hypsochromic shifts of the fluorescence bands.     

First principles study of electronic and nonlinear optical properties of A–D–π–A and D–A–D–π–A configured compounds containing novel quinoline–carbazole derivatives

Materials with nonlinear optical (NLO) properties have significant applications in different fields, including nuclear science, biophysics, medicine, chemical dynamics, solid physics, materials science and surface interface applications. Quinoline and carbazole, owing to their electron-deficient and electron-rich character respectively, play a role in charge transfer applications in optoelectronics. Therefore, an attempt has been made herein to explore quinoline–carbazole based novel materials with highly nonlinear optical properties. Structural tailoring has been made at the donor and acceptor units of two recently synthesized quinoline–carbazole molecules (Q1, Q2) and acceptor–donor–π–acceptor (A–D–π–A) and donor–acceptor–donor–π–acceptor (D–A–D–π–A) type novel molecules Q1D1–Q1D3 and Q2D2–Q2D3 have been quantum chemically designed, respectively. Density functional theory (DFT) and time-dependent density functional theory (TDDFT) computations are performed to process the impact of acceptor and donor units on photophysical, electronic and NLO properties of selected molecules. The λ_max values (321 and 319 nm) for Q1 and Q2 in DSMO were in good agreement with the experimental values (326 and 323 nm). The largest shift in absorption maximum is displayed by Q1D2 (436 nm). The designed compounds (Q1D3–Q2D3) express absorption spectra with an increased border and with a reduced band gap compared to the parent compounds (Q1 and Q2). Natural bond orbital (NBO) investigations showed that the extended hyper conjugation and strong intramolecular interaction play significant roles in stabilising these systems. All molecules expressed significant NLO responses. A large value of β_tot was elevated in Q1D2 (23 885.90 a.u.). This theoretical framework reveals the NLO response properties of novel quinoline–carbazole derivatives that can be significant for their use in advanced applications.

Materials with nonlinear optical properties have significant applications in nuclear science, biophysics, medicine, chemical dynamics, solid physics & materials science. We show how π bridges, donors & acceptors can be reconfigured to improve optical properties.     

Effect of fluorine substituents on benzothiadiazole-based D–π–A′–π–A photosensitizers for dye-sensitized solar cells

Two D–π–A′–π–A organic dyes with triazatruxene (TAT) as the electron donor, thiophene as the π-spacer, benzoic acid as the anchor group, and benzothiadiazole (BT) or difluorobenzo[c][1,2,5]thiadiazole (DFBT) as the additional acceptor, namely LS101 and LS102, respectively, were applied to dye-sensitized solar cells (DSSCs). As fluorine substituents are usually strong electron-withdrawing groups, introducing two fluorine atoms into BT was expected to strengthen the electron-withdrawing ability of the auxiliary acceptor, resulting in DSSCs with a broader light capture region and further improved power conversion efficiency (PCE). Fluorine is the smallest electron-withdrawing group with an induction effect, but can also act as an electron-donating group owing to its conjugation effect. When the conjugation effect is dominant, the electron-withdrawing ability of additional acceptor DFBT decreases instead. Accordingly, the band gap of LS102 was broadened and the UV-vis absorption spectrum was blue-shifted. In the end, DSSCs based on LS101 achieved a champion PCE of 10.2% (J_sc = 15.1 mA cm⁻², V_oc = 966 mV, FF = 70.1%) while that based on LS102 gave a PCE of only 8.6% (J_sc = 13.4 mA cm⁻², V_oc = 934 mV, FF = 69.1%) under standard AM 1.5G solar irradiation (100 mW cm⁻²) with Co²⁺/Co³⁺ as the electrolyte.

The results and interpretations can clearly explain the reasons for the poor photovoltaic performance of DFBT in DSSCs.     

Photophysical properties and fluorosolvatochromism of D–π–A thiophene based derivatives

Solvation-dependent photophysical properties of two push–pull thiophene-based compounds with donor–π–acceptor (D–π–A) structures were investigated using absorption, fluorescence emission and time resolved spectroscopy, and supported by different solvation models. Intramolecular charge transfer characteristics of the structurally similar 2-fluoro-4-(5-(4-methoxyphenyl)thiophen-2-yl)benzonitrile (MOT) and 4-(5-(4-(dimethylamino)phenyl)thiophen-2-yl)-2-fluorobenzonitrile (DMAT) were investigated. Significant enhancement of intramolecular charge transfer strength has been observed through molecular structure modification of the electron donating group from a methoxy to dimethylamine group. Ground state absorption spectra show a small red shift of about 10 nm and 18 nm while the fluorescence emission spectra show a large red shift of about 66 nm and 162 nm on changing from the nonpolar cyclohexane to the aprotic polar DMSO for MOT and DMAT, respectively. Dipole moment change from the ground state to the charge transfer excited state is calculated to be 6.6 D in MOT and 9.0 D in DMAT. The fluorescence quantum yield, fluorescence lifetime and the derived radiative and non-radiative rate constants were found to be better correlated to the emission energy rather than any of the solvent properties. Three multi-parametric relationships were used in the interpretation of the specific versus non-specific solute–solvent interactions, namely, Kamlet–Taft, Catalán and Laurence et al. models. The findings of these approaches are used to extract useful information about different aspects of solvent effects on the photophysical properties of the two studied compounds. Kamlet–Taft solvatochromic model indicates that non-specific interactions are dominant in controlling the photophysical properties. Catalán''s solvent dipolarity/polarizability parameter is found to play a significant role in solvatochromic behaviour which is also designated by the Laurence model.

Solvation-dependent photophysical properties of two push–pull thiophene-based compounds with donor–π–acceptor (D–π–A) structures were investigated using absorption, fluorescence emission and time resolved spectroscopy, and supported by different solvation models.     

Impact of various heterocyclic π-linkers and their substitution position on the opto-electronic attributes of the A–π–D–π–A type IECIO-4F molecule: a comparative analysis

To investigate the consequence of different substitution positions of various π-linkers on the photovoltaic properties of an organic solar cell molecule, we have introduced two series of six three-donor molecules, by the substitution of some effective π-linkers on the A–π–D–π–A type reference molecule IECIO-4F (taken as IOR). In series “a” the thienyl or furyl bridge is directly linked between the donor and acceptor moieties, while in series “b” the phenyl ring of the same bridge is working as the direct point of attachment. The frontier molecular orbitals, density of states, transition density matrix, molecular electrostatic potential surfaces, exciton binding energy, excitation energy, wavelength of maximum absorption, open-circuit voltage, fill factor, and some other photovoltaic attributes of the proposed molecules were analyzed through density functional theory (DFT) and its time-dependent (TD) approach; the TD-DFT method. Though both series of newly derived molecules were a step up from the reference molecule in almost all of the studied characteristics, the “a” series (IO1_a to IO3_a) seemed to be better due to their desirable properties such as the highest maximum absorption wavelength (λ_max), open-circuit voltage, and fill factor, along with the lowest excitation and exciton dissociation energy, etc. of its molecules. Also, the studied morphology, optical characteristics, and electronic attributes of this series of proposed molecules signified the fact that the molecules with thienyl or furyl ring working as the direct link between the acceptor and donor molecules showed enhanced charge transfer abilities, and could provide a maximum quantum yield of the solar energy supplied.

We have introduced two series of six three-donor molecules, by the substitution of some effective π-linkers on the A–π–D–π–A type reference molecule IECIO-4F (taken as IOR) for efficient organic solar cells.     

D–π–A azine based AIEgen with solvent dependent response towards a nerve agent

We developed a D–π–A based unsymmetrical azine molecule 4-((E)-((E)-(4-(dipropylamino)benzylidene)hydrazono)methyl)benzonitrile [DPBN] and studied its optical and aggregation induced emission properties. The DPBN molecule shows good aggregation induced emission (AIE) behaviour with 1157-fold fluorescence enhancement in the aggregated state. In addition to that, both colorimetric as well as fluorometric sensing studies revealed that DPBN selectively detects diethylchlorophosphate (DCP), a potent nerve agent. Interestingly, DPBN shows solvent dependent optical output in the presence of DCPvia two different mechanisms. In the monomer state, it shows red shifted fluorescence enhancement along with color change from colorless to orange color via the formation of a new intramolecular charge transfer state in pure tetrahydrofuran (THF). In the aggregated state, DPBN shows blue shifted emission with fluorescence enhancement in THF–water mixture by protonation at the amine nitrogen centre. Thus, DPBN can be used as a diagnostic measure to selectively detect nerve agents like DCP. This study also paves the way for further development of molecular probes for nerve agents that would represent immense implications in various fields of chemistry and biology.

Selective detection of diethylchlorophosphate using a D–π–A based AIEgen in aqueous as well as non-aqueous environment via different sensing mechanisms.     

Characterization and simulation study of organic solar cells based on donor–acceptor (D–π–A) molecular materials

In this study, the analysis of microelectronic and photonic structure in a one dimension program [AMPS-1D] has been successfully used to study organic solar cells. The program was used to optimize the performance of organic solar cells based on (carbazole-methylthiophene), benzothiadiazole and thiophene [(Cbz-Mth)-B-T]2 as electron donors, and [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) as an electron acceptor. The optoelectronic properties of these dyes were investigated by using the Density Functional Theory DFT/B3LYP/6-31G(d,p) method. We studied the influence of the variation of the thickness of the active layer, the temperature, and the density of the effective states of the electrons and the holes in the conduction and valence bands respectively on the performance of the solar cells based on [(Cbz-Mth)-BT]2–PCBM as a photoactive material, sandwiched between a transparent indium tin oxide (ITO) and an aluminum (Al) electrode. The addition of other thiophene units in the copolymer or the deposition of a layer of PEDOT between the anode (ITO) and the active layer, improves the performances of the cell, especially resulting in a remarkable increase in the value of the power conversion efficiency (PCE).

The solar cell ITO/PEDOT/[(Cbz-Mth)-B-DT]2-A:PCBM/Al under study and the results obtained, including a power conversion efficiency of 11%. The impact of several parameters on the performance has been studied to obtain the optimal device architecture.     

First theoretical probe for efficient enhancement of optical nonlinearity via structural modifications into phenylene based D–π–A configured molecules

The design of nonlinear optical (NLO) materials using conjugated molecules via different techniques is reported in the literature to boost the use of these systems in NLO. Therefore, in the current study, designed phenylene based non-fullerene organic compounds with a D–π–A framework were selected for NLO investigation. The initial compound (PMD-1) was taken as a reference and its seven derivatives (PMDC2–PMDC8) were made by introducing different acceptor moieties into the chemical structure of PMD-1. To explain the NLO findings, frontier molecular orbital (FMO), transition density matrix (TDM), density of states (DOS), natural bond orbital (NBO) and UV-Vis study of the title compounds was executed by applying the PBE1PBE functional with the 6-311G(d,p) basis set. The descending order of band gaps (E_gap) was reported as PMDC7 (2.656) > PMDC8 (2.485) > PMD-1 (2.131) > PMDC3 (2.103) > PMDC2 (2.079) > PMDC4 (2.065) > PMDC5 (2.059) > PMDC6 (2.004), in eV. Global reactivity parameters (GRPs) were associated with E_gap values as PMDC6 with the lowest band gap showed less hardness (0.0368 E_h) and high softness (13.5785 E_h). The UV-Vis investigation revealed that the maximum λ_max (739.542 nm) was exhibited by PMDC6 in dichloromethane (DCM) as compared to other derivatives. Additionally, natural bond orbital (NBO) based findings revealed that PMDC6 exhibited the highest stability value (34.98 kcal mol⁻¹) because of prolonged hyper-conjugation. The dipole moment (μ), average linear polarizability 〈α〉, first hyperpolarizability (β_tot) and second hyperpolarizability (γ_tot) were evaluated for the reference and its derivatives. Consequently, among the designed compounds, the highest β_tot (4.469 × 10⁻²⁷ esu) and γ_tot (5.600 × 10⁻³² esu) values were shown by PMDC6. Hence, it''s concluded from said results that these structural modifications proved PMDC6 as the best second and third order NLO candidate for various applications like fiber optics, signal processing and data storage.

The design of nonlinear optical (NLO) materials using conjugated molecules via different techniques is reported in the literature to boost the use of these systems in NLO.     

Fabrication of BP2T functionalized graphene via non-covalent π–π stacking interactions for enhanced ammonia detection

Graphene has stimulated great enthusiasm in a variety of fields, while its chemically inert surface still remains challenging for functionalization towards various applications. Herein, we report an approach to fabricate non-covalently functionalized graphene by employing π–π stacking interactions, which has potentialities for enhanced ammonia detection. 5,5′-Di(4-biphenylyl)-2,2′-bithiophene (BP2T) molecules are used in our work for the non-covalent functionalization through strong π–π interactions of aromatic structures with graphene, and systematic investigations by employing various spectroscopic and microscopic characterization methods confirm the successful non-covalent attachment of the BP2T on the top of graphene. From our gas sensing experiments, the BP2T functionalized graphene is promising for ammonia sensing with a 3-fold higher sensitivity comparing to that of the pristine graphene, which is mainly attributed to the enhanced binding energy between the ammonia and BP2T molecules derived by employing the Langmuir isotherm model. This work provides essential evidence of the π–π stacking interactions between graphene and aromatic molecules, and the reported approach also has the potential to be widely employed in a variety of graphene functionalizations for chemical detection.

Non-covalent functionalization of graphene has been achieved by employing π–π stacking interactions, and it is promising for ammonia detection with greatly enhanced sensitivity.     

Synthesis and characterization of ethyl benzotriazolyl acrylate-based D–π–A fluorophores for live cell-based imaging applications

A series of eight new ethyl (Z)-benzotriazolyl acrylates 6a–d and 7a–d have been synthesized by conventional heating and microwave irradiation from ethyl benzotriazolyl acetates 3 and 4 with the corresponding aromatic aldehydes. This work reports the synthetic approach and spectroscopic characterization (¹H, ¹³C-NMR, HRMS) of all the synthesized compounds. X-ray diffraction analyses were performed for molecules 6a, 7a and 7d. Photophysical properties of compounds were evaluated. Finally, compound 6a was tested in a human cell line and showed low to no cytotoxicity at relevant concentrations. Initial testing demonstrates its potential use as a fluid-phase fluorescent marker for live cell imaging.

Synthesis of eight new benzotriazolyl derivatives, characterization, X-ray diffraction analyses, photophysical properties and their application as safe-fluorophores in mammalian cells.     

Efficiency difference between furan- and thiophene-based D–π–A dyes in DSSCs explained by theoretical calculations

The performance of two donor–π-bridge–acceptor type phenothiazine dyes bearing different π-bridges (furan and thiophene) was investigated by density functional theory and time-dependent density functional theory to explore the reasons for the differences in DSSC efficiency. It was revealed that dye1 with furan showed higher short-circuit photocurrent density due to its larger driving force and better light harvesting efficiency compared with dye2. Moreover, a larger number of photo-injected electrons into TiO₂ for dye1 leads to higher open-circuit photovoltage. Our results indicate that furan could be used as a promising π-bridge to improve the efficiency of PTZ dyes. We hope that our work can provide a theoretical basis and view for designing efficient dyes in dye-sensitized solar cells (DSSCs).

The performance of two D–π–A type phenothiazine dyes bearing different π-bridges (furan and thiophene) was investigated by DFT and TDDFT to explore the reasons for the differences in DSSC efficiency.     

D–π–A type conjugated indandione derivatives: ultrafast broadband nonlinear absorption responses and transient dynamics

The ultrafast nonlinear optical response of two 1,3-indandione derivatives (INB3 and INT3) was systematically investigated by the femtosecond Z-scan and pump-probe technique at multiple visible and near infrared wavelengths. Both compounds show strong broadband nonlinear absorption (NLA) and different wavelength-dependent two-photon absorption (TPA) characteristics in the range of 650–1100 nm. The TPA cross section of trithiophene-based compound INT3 was found to be larger than that of triphenylamine-based compound INB3 in the red region (650–800 nm), which is attributed to its longer π-conjugated structure and better molecular planarity. Interestingly, the effective NLA of INB3 was found to be larger than INT3 in the NIR region (800–1100 nm), which is related to the excited state absorption (ESA) induced by TPA. The ultrafast dynamics of both compounds were investigated by femtosecond transient absorption spectroscopy, which revealed a broadband ESA including several relaxation processes. This work extends nonlinear optical research on indandione derivatives, and the results suggest that these derivatives are promising candidates for optical limiting applications.

In the red region (650–800 nm), the nonlinear absorption of trithiophene-based compound INT3 is greater than that of triphenylamine-based compound INB3, while in the NIR region (800–1100 nm), the strength of nonlinear absorption is the opposite.     

Donor moieties with D–π–a framing modulated electronic and nonlinear optical properties for non-fullerene-based chromophores

Herein, a series of non-fullerene-based substantial chromophores (FHD1–FHD6) with a D–π–A framework was designed from a synthesized non-fullerene compound (FH) via structural tailoring with various donor moieties. The FH and its designed derivatives were optimized with frequency analysis at the M06/6-311G (d,p) level to confirm their true minima on potential energy surfaces. These optimized geometries were utilized to perform further analyses, such as absorption, natural bonding orbital (NBO), frontier molecular orbital (FMO), and nonlinear orbital (NLO) analyses at the aforesaid level. Quantum chemical study revealed that all the designed chromophores exhibited a lower band gap than that of the parent molecule with the exception of FHD3. Furthermore, density of states (DOS) analysis supported the findings from the FMO study, and this agreement revealed that the efficient charge was transferred from the HOMO to the LUMO. The NBO investigations disclosed that all the compounds comprised donor moieties with positive charges and acceptors having negative charges. Interestingly, π-conjugated linkers were also found with positive charges, showing an effective donating property. These NBO findings explicated that FHD1–FHD6 exhibited an efficient push–pull mechanism. The λ_max values of the designed chromophores were observed to be greater than the reference compound. The average polarizability 〈α〉, first hyperpolarizability (β_tot), and second hyperpolarizability 〈γ〉 values of FHD2 were found to be 2.170 × 10⁻²², 3.150 × 10⁻²⁷, and 4.275 × 10⁻³² esu, respectively, while all the other derivatives had been reported in the relevant range. Efficient NLO data revealed that FH-based derivatives may contribute significantly toward NLO technology.

Herein, a series of non-fullerene-based substantial chromophores (FHD1–FHD6) with a D–π–A framework was designed from a synthesized non-fullerene compound (FH) via structural tailoring with various donor moieties.     

Tuning the fluorescence based on the combination of TICT and AIE emission of a tetraphenylethylene with D–π–A structure

A simple D–π–A structured tetraphenylethylene with two electron-rich methyloxy groups and two electron withdrawing cyano groups, which features both twisted intramolecular charge-transfer (TICT) and aggregation-induced emission (AIE) properties, namely TPEOMeCN has been prepared. The emission of TPEOMeCN examined in various solvents is dependent on the polarities of solvents, which indicates the TICT character. The emission intensity of the compound also enhances with the increasing water fraction in H₂O–DMSO mixtures, demonstrating the typical AIE property. Excitingly, the TICT and AIE emission could be observed separately or simultaneously by adjusting the water fraction or viscosity of the solvent. Encouragingly, the combined emission of the TPEOMeCN derived from this single molecule could be readily tuned via regulating the viscosity of the system, resulting in a broad emission peak which covers the visible spectrum (400–700 nm). This work provides a general strategy for designing molecules combining TICT emission and AIE for application as full-color emitters.

The combination of the TICT and AIE properties in a tetraphenylethylene based molecule with D–π–A structure is observed by simply adjusting the viscosity of the solvent.     

Correction: D–π–A type conjugated indandione derivatives: ultrafast broadband nonlinear absorption responses and transient dynamics

Correction for ‘D–π–A type conjugated indandione derivatives: ultrafast broadband nonlinear absorption responses and transient dynamics’ by Lu Chen et al., RSC Adv., 2022, 12, 8624–8631, DOI: 10.1039/D2RA00349J.

The authors regret that contact details for the corresponding authors were not provided. The corrected contact details for the corresponding authors are provided below.* Corresponding author. E-mail addresses: nc.ude.stsu@ihzgnixuw (Xingzhi Wu), nc.ude.adus@0102yjy (Junyi Yang), nc.ude.tih@gnosly (Yinglin Song).The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.     

Visible light-induced oxidative α-hydroxylation of β-dicarbonyl compounds catalyzed by ethylenediamine–copper(ii)

We have developed an efficient oxidative α-hydroxylation of β-keto esters with firstly using the structurally simple ethylenediamine–copper(ii) as a catalyst for β-keto esters activation and using visible light as the driving force for generating more active singlet oxygen (¹O₂) from triplet state oxygen (³O₂) in the air, providing a series of α-hydroxy β-keto esters in excellent yields (up to 99%) under extremely low photosensitizer loading (0.01 mol%) and catalyst loading (1 mol%) within a short time. Moreover, the gram-scale synthesis showed the practical utility of this protocol.

An efficient visible light-induced oxidative α-hydroxylation of β-dicarbonyl compounds has been developed using structurally simple ethylenediamine–copper(ii) as a catalyst.     

The role of the donor group and electron-accepting substitutions inserted in π-linkers in tuning the optoelectronic properties of D–π–A dye-sensitized solar cells: a DFT/TDDFT study

The design of low-cost and high-efficiency sensitizers is one of the most important factors in the expansion of dye-sensitized solar cells (DSSCs). To obtain effective sensitizer dyes for applications in dye-sensitized solar cells, a series of metal-free organic dyes with the D–π–A–A arrangement and with different donor and acceptor groups have been designed by using computational methodologies based on density functional theory (DFT) and time-dependent density functional theory (TD-DFT). We have designed JK-POZ(1–3) and JK-PTZ(1–3) D–π–A–A organic dyes by modifying the donor and π-linker units of the JK-201 reference dye. Computational calculations of the structural, photochemical properties and electrochemical properties, as well as the key parameters related to the short-circuit current density and open-circuit voltage, including light-harvesting efficiency (LHE), singlet excited state lifetime (τ), reorganization energies (λ_total), electronic injection-free energy (ΔG^inject) and regeneration driving forces (ΔG^reg) of dyes were calculated and analyzed. Moreover, charge transfer parameters, such as the amount of charge transfer (q^CT), the charge transfer distance (D^CT), and dipole moment changes (μ^CT), were investigated. The results show that ΔG^reg, λ_max, λ_total and τ of JK-POZ-3 and JK-PTZ-3 dyes are superior to those of JK-201, indicating that novel JK-POZ-3 and JK-PTZ-3 dyes could be promising candidates for improving the efficiency of the DSSCs devices.

A series of metal-free organic dyes with the D–π–A–A arrangement and with different donor and acceptor groups have been designed theoretically.     

New organic dye-sensitized solar cells based on the D–A–π–A structure for efficient DSSCs: DFT/TD-DFT investigations

Global energy consumption has increased due to population growth and economic development. Solar energy is one of the most important renewable energy sources for human consumption. In this research, four novel organic dyes (D2–D5) of the D–A–π–A structure based on triphenylamine (TPA) were studied theoretically using DFT and TD-DFT techniques for future usage as dye-sensitized solar cells (DSSCs). The effects of modifying the π-spacer of the reference molecule D1 on the structural, electronic, photovoltaic, and optical characteristics of the D2–D5 dyes were studied in detail. D2–D5 exhibited band gaps (E_gap) in the range from 1.89 to 2.10 eV with λ_abs in the range of 508 to 563 nm. The results obtained show that modifying the π-spacer of the dye D1 increased its hole injection and reinforced the intramolecular charge-transfer (ICT) impact, which resulted in a red-shifted ICT absorption with a greater molar extinction coefficient. The theoretically calculated open-circuit voltage (V_oc) values ranged from 0.69 to 1.06 eV, while the light-harvesting efficiency (LHE) values varied from 0.95 to 0.99. Indeed, this theoretical research could guide chemists to synthesize effective dyes for DSSCs.

Global energy consumption has increased due to population growth and economic development.     

Ultrahigh permeance of a chemical cross-linked graphene oxide nanofiltration membrane enhanced by cation–π interaction

Cross-linking with large flexible molecules is a common method to improve the stability and control the interlayer spacing of graphene oxide (GO) membranes, but it still suffers from the limitation of low water flux. Herein, a novel high flux GO membrane was fabricated using a pressure-assisted filtration method, which involved a synergistic chemical cross-linking of divalent magnesium ions and 1,6-hexanediamine (HDA) on a polyethersulfone (PES) support. The membrane cross-linked with magnesium ions and HDA (GO_{HDA–Mg²⁺}) exhibited a high water flux up to 144 L m⁻² h⁻¹ bar⁻¹, about 7 times more than that of cross-linked GO membranes without adding magnesium ions (GO_HDA), while keeping excellent rejection performance. The GO_{HDA–Mg²⁺} membrane also showed an outstanding stability in water for a long time. The effects of magnesium ions on the GO_{HDA–Mg²⁺} membrane were analyzed using several characterization methods, including Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The results indicated that magnesium ions not only promoted reasonable cross-linking, but also improved the stacking of GO sheets to give lower mass transfer resistance channels for water transport in the membranes, resulting in the ultrahigh permeance of the GO membranes.

Chemical cross-linking together with magnesium ions, potentially promoting reasonable cross-linking and improving the water channels of membrane in terms of flatness and surface with low mass transfer resistance.