| 1. |
- Zhu, Haibo, et al.
(författare)
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Insight into Benzothiadiazole Acceptor in D-A-pi-A Configuration on Photovoltaic Performances of Dye-Sensitized Solar Cells
- 2014
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Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 2:4, s. 1026-1034
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Tidskriftsartikel (refereegranskat)abstract
- The option of conjugated pi-linkers is critical for molecular engineering toward the energy-level strategy of donor-pi-acceptor (D-pi-A) sensitizers. There is always a balance in the optimization of a it-linker. The pi-conjugation should be enlarged to expand the light-harvesting capability of sensitizers for an increase in photocurrent; however, the oversized it-linker also would affect seriously the photovoltage and photostability. Two sensitizers, WS-22 and WS-23, are constructed without or with benzothiadiazole (BTD) in a molecular skeleton, aiming to gain insight into the effect of an auxiliary acceptor in D-A-pi-A sensitizers on the photophysical and photovoltaic performances, especially focusing on the exploitation of the short circuit current density (J(sc)) and open circuit voltage (V-oc). Compared with the typical D-pi-A sensitizer WS-22, the incorporation of an auxiliary acceptor of BTD in WS-23 can improve the light-harvesting ability both in red-shifting the absorption peaks and the increment of absorption coefficient. The predominant increase by 15.6% in light-harvesting efficiency (LHE) of WS-23 results in a relatively higher J(sc) from 13.77 (WS-22) to 16.91 mA cm(-2) (WS-23). Moreover, the improvement of the V-oc in WS-23 is originated by a synergy contribution of the uplifting of E-CB and inhibition of charge recombination. The stepped light-induced transient (SLIT) measurements indicate that the introduction of BTD can negatively shift the conduction band of the TiO2 film. For WS-23, the higher molecular dipole moment can bring forth a more effective charge separation between donor and acceptor units, also resulting in an increase in V-oc. The incorporated BTD unit can increase V-oc by 57 mV, arising from the CB edge shift of TiO2 (accounting for 40%, 23 mV) and the retarding charge recombination (accounting for 60%, 34 mV). As a consequence, WS-23 realizes an optimizing photovoltaic efficiency (eta = 8.15%), with an improvement of 36.5% with respect to WS-22.
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| 2. |
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| 3. |
- Ding, Yubin, et al.
(författare)
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Acid/Base Switching of the Tautomerism and Conformation of a Dioxoporphyrin for Integrated Binary Subtraction
- 2014
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Ingår i: Chemistry - A European Journal. - : Wiley. - 0947-6539 .- 1521-3765. ; 20:40, s. 12910-12916
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Tidskriftsartikel (refereegranskat)abstract
- Compared with most of the reported logic devices based on the supramolecular approach, systems based on individual molecules can avoid challenging construction requirements. Herein, a novel dioxoporphyrin DPH22 was synthesized and two of its tautomers were characterized by single-crystal X-ray diffraction studies. Compound DPH22 exhibits multichannel controllable stepwise tautomerization, protonation, and deprotonation processes through interactions with H and F- ions. By using the addition of H+ and F- ions as inputs and UVNis absorption values at.1=412, 510, 562, and 603 nm as outputs, the controlled tautomerism of DPH22 has been successfully used for the construction of an integrated molecular level half-subtractor and comparator. In addition, this acid/base-switched tautomerism is reversible, thus endowing the system with ease of reset and recycling; consequently, there is no need to modulate complicated intermolecular interactions and electron-/chargetransfer processes.
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| 4. |
- Ding, Yubin, et al.
(författare)
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alpha-Monoacylated and alpha,alpha '- and alpha,beta '-Diacylated Dipyrrins as Highly Sensitive Fluorescence "Turn-on" Zn2+ Probes
- 2013
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Ingår i: Journal of Organic Chemistry. - : American Chemical Society (ACS). - 0022-3263 .- 1520-6904. ; 78:11, s. 5328-5338
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Tidskriftsartikel (refereegranskat)abstract
- With the purpose of developing readily synthesized CHEF (chelation-enhanced fluorescence) type Zn2+ probes with relatively simple molecular structures and excellent sensing behavior, p-anisoyl chloride was used for the acylation of 5-(pentafluorophenyl)dipyrromethane. Interestingly, the alpha,beta'-diacylated product PS2 with a unique substitution mode was obtained in high yield in addition to the normal a-substituted mono- and diacylated products PSI and PS3. Further oxidation of PS1-PS3 afforded dipyrrins S1-S3. Crystal structure and H-1 NMR measurements of S2 demonstrate the existence of a pure tautomer, which is consistent with DFT calculations. S1-S3 show highly Zn2+ selective "turn-on" fluorescence based on a CHEF mechanism by the formation of 2:1 (probe:metal) Zn2+ complexes. The emission colors can be easily tuned from green to red by changing the dipyrrin substitution modes. Furthermore, these probes demonstrate fast responses and wide applicable pH ranges. Among them, S2 shows the highest Zn2+ sensitivity, with a detection limit of 4.4 x 10(-8) M.
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| 5. |
- Ding, Yubin, et al.
(författare)
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From nonconjugation to conjugation : novel meso-OH substituted dipyrromethanes as fluorescence turn-on Zn2+ probes
- 2013
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Ingår i: Organic and biomolecular chemistry. - : Royal Society of Chemistry (RSC). - 1477-0520 .- 1477-0539. ; 11:16, s. 2685-2692
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Tidskriftsartikel (refereegranskat)abstract
- Most reported Zn2+ probes suffer from the interference of background fluorescence originated from the conjugated structures of commonly utilized fluorophores. In this work, three novel meso-hydroxyl group substituted dipyrromethanes DPMOH1-DPMOH3 were synthesized and found to be colourless and nonfluorescent due to the interruption of the conjugated p system by an sp(3) carbon between the two pyrrolic units. Interestingly, only the addition of Zn2+ to the solutions of DPMOH1-DPMOH3 promoted their oxidation to dipyrrin forms, and bright fluorescence "turn on" was observed due to the formation of corresponding dipyrrin complexes with the dipyrrin : zinc stoichiometry of 2 :1. Zn2+ detection mechanism was investigated by UV-Vis, fluorescence, H-1 NMR and HRMS analyses, which can be ascribed to the CHEF type fluorescence enhancement, resulting from good rigidity of the dipyrrin complexes. Hence, DPMOH1-DPMOH3 can be used as fluorescence turn-on Zn2+ probes with the advantage of no background fluorescence.
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| 6. |
- Li, Xin, et al.
(författare)
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Theoretical insight into the enhanced hindrance, thermal stability and optical properties of diarylethene with a benzobis(thiadiazole) bridge and benzothiophene rings
- 2016
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Ingår i: Dyes and pigments. - : ELSEVIER SCI LTD. - 0143-7208 .- 1873-3743. ; 125, s. 348-355
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Tidskriftsartikel (refereegranskat)abstract
- To rationalize the effects of intramolecular steric hindrance on the performance of diarylethene photoswitches, we here present a density functional theory study on the thermal bistability and optical properties of a photochromic diarylethene BBTE consisting of a benzobis(thiadiazole) bridge and benzothiophene rings, in which prominent steric hindrance exists owing to the extended structures of is-conjugated groups. Our calculations not only provide rational explanations for the isolation of enantiopure anti-parallel conformers of the open-ring isomer, but also elucidate the detailed pathway of a two-step ground-state ring-opening process, where the thermal stability of the closed-ring isomer is guaranteed by an overall free energy barrier of around 113 kJ mol(-1) (27 kcal mol(-1)). In addition, the tunable intramolecular charge transfer of the donor acceptor structure formed by the benzobis(thiadiazole) bridge and the bulky benzothiophene rings is also addressed within time-dependent density functional theory. Charge transfer excitations in the open- and the closed-ring isomers are characterized as long-range and medium-range, respectively. We show that the diarylethene derivative under investigation can serve as a promising platform for future development of optoelectronic materials.
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| 7. |
- Lu, Kaifeng, et al.
(författare)
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Novel Approach on Developing TiO2-Supported Heteropolyacids Catalyst for the Efficient Conversion of Xylose to Furfural
- 2022
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Ingår i: Energy & Fuels. - : American Chemical Society (ACS). - 0887-0624 .- 1520-5029. ; 36:14, s. 7599-7607
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Tidskriftsartikel (refereegranskat)abstract
- The conversion of biomass-derived monosaccharides to value-added platform compounds, regarded as the alternative biofuels precursors, has attracted increasing attention. This work provides a novel approach on developing efficient and recyclable catalyst for biorefining. Herein, a titania-supported tungstophosphoric acid (TPA-TiO2) nanocomposite catalyst with advantages in acidity flexibility and catalytic stability was proposed for the efficient dehydration of xylose to furfural. The loading of the active component of TPA played an important role in the acidity and Lewis/Brønsted acids distribution of the catalyst. The structure characterization of the catalyst showed that the TPA particles were distributed well in TiO2 support. After the optimization of catalytic reaction conditions, the xylose conversion could approach to 96.12% while the furfural yield of 76.71% was obtained at 190 °C for 60 min catalyzed by TiO2-TPA-3 in a methyl isobutyl ketone (MIBK)–water biphasic solvent system. It was still about 80% of the initial yield after the fifth recycling of the TiO2-supported heteropolyacids catalyst. Furthermore, the reaction kinetics of xylose dehydration to furfural was investigated. The catalytic system in this work had a lower activation energy for xylose dehydration, and the decrease in furfural yield was mainly caused by the side reaction of furfural with intermediates. This work provides a novel approach on developing efficient and recyclable catalyst for biorefining.
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| 8. |
- Meng, Xianle, et al.
(författare)
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Novel Bisthienylethenes Containing Naphthalimide as the Center Ethene Bridge : Photochromism and Solvatochromism for Combined NOR and INHIBIT Logic Gates
- 2008
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 112:49, s. 15636-15645
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Tidskriftsartikel (refereegranskat)abstract
- Two novel photochromic bisthienylethene derivatives BTE-NA1 and BTE-NA2 with a six-membered aryl ring of naphthalimide fluorescent moiety as the center ethene bridging unit were synthesized and fully characterized by H-1 NMR, C-13 NMR, and HRMS. They exhibit considerably high cyclization quantum yield and good fatigue resistance. Interestingly, the fluorescence of BTE-NA1 arising from the naphthalimide unit could be well modulated by photochromism and solvatochromism. Quantum chemical calculations were carried out to study their geometrical, electronic, and optical properties, which were in good accordance with the experimental data. Furthermore, a combined NOR and INHIBIT logic operation based on BTE-NA1 has been successfully mimicked with fluorescence changes as outputs.
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| 9. |
- Song, Liwen, et al.
(författare)
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Synthesis and Photochromism of Naphthopyrans Bearing Naphthalimide Chromophore : Predominant Thermal Reversibility in Color-Fading and Fluorescence Switch
- 2011
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 115:49, s. 14648-14658
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Tidskriftsartikel (refereegranskat)abstract
- Two novel photochromic naphthopyrans containing naphthalimide moieties (Nip1 and Nip2) were studied in solution under flash photolysis conditions, exhibiting highly photochromic response, rapid thermal bleaching rate and good fatigue-resistance. Owing to the different N-substituted imide groups at the naphthalimide units, the thermal bleaching rate of Nip2 bearing phenyl on the naphthalimide unit is found to be approximately 2 times that of Nip1 bearing n-butyl, indicating that the photochromic properties can be modulated with introduction of different functional groups on the naphthalimide unit. In Nip1 and Nip2, the strong electron-withdrawing effect of the imide group incorporated at the naphthalimide moiety maintains several merits: (i) shifting absorption bands to longer wavelength, (ii) beneficial to an enhancement in the ratio of transoid-cis (TC) isomer and an increase in the transformation rate from transoid-trans (TT) to TC with respect to reference compound NP, and (iii) resulting in a preferable color bleaching rate and fading absolutely to their colorless state with thermal reversibility. As demonstrated in the system of NP, the slow transformation process from TT to TC might be the predominant dynamic step in thermal back process, leading to the residual color of NP being only faded to its original colorless state by visible light irradiation. The optical densities of colored forms for Nip1 and Nip2 are dependent upon the intensity of incident light, ensuring a possible application in the manufacture of ophthalmic lenses and smart windows. Moreover, the fluorescence of Nip1 and Nip2 can be switched on and off by photoinduced conversion between the closed and open forms.
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| 10. |
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