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Huang, S., Zhang, Q., Xin, P., Zhang, J., Chen, Q., Fu, J., . . . Hu, Z.-J. (2022). Construction of Fe-doped NiS-NiS2 Heterostructured Microspheres Via Etching Prussian Blue Analogues for Efficient Water-Urea Splitting. Small, 18(14), Article ID 2106841.
Open this publication in new window or tab >>Construction of Fe-doped NiS-NiS2 Heterostructured Microspheres Via Etching Prussian Blue Analogues for Efficient Water-Urea Splitting
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2022 (English)In: Small, ISSN 1613-6810, E-ISSN 1613-6829, Vol. 18, no 14, article id 2106841Article in journal (Refereed) Published
Abstract [en]

Developing efficient and robust non-precious-metal-based catalysts to accelerate electrocatalytic reaction kinetics is crucial for electrochemical water-urea splitting. Herein, Fe-doped NiS-NiS2 heterostructured microspheres, an electrocatalyst, are synthesized via etching Prussian blue analogues following a controlled annealing treatment. The resulting microspheres are constructed by mesoporous nanoplates, granting the virtues of large surface areas, high structural void porosity, and accessible inner surface. These advantages not only provide more redox reaction centers but also strengthen structural robustness and effectively facilitate the mass diffusion and charge transport. Density functional theory simulations validate that the Fe-doping improves the conductivity of nickel sulfides, whereas the NiS-NiS2 heterojunctions induce interface charge rearrangement for optimizing the adsorption free energy of intermediates, resulting in a low overpotential and high electrocatalytic activity. Specifically, an ultralow overpotential of 270 mV at 50 mA cm(-2) for the oxygen evolution reaction (OER) is achieved. After adding 0.33 M urea into 1 M KOH, Fe-doped NiS-NiS2 obtains a strikingly reduced urea oxidation reaction potential of 1.36 V to reach 50 mA cm(-2), around 140 mV less than OER. This work provides insights into the synergistic modulation of electrocatalytic activity of non-noble catalysts for applications in energy conversion systems.

Place, publisher, year, edition, pages
Wiley-V C H Verlag GMBH, 2022
Keywords
electrocatalysis; Fe-doping; heterostructures; sulfides; urea electrolysis
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-183408 (URN)10.1002/smll.202106841 (DOI)000757698300001 ()35182017 (PubMedID)
Note

Funding Agencies|Science and Technology Commission of Shanghai MunicipalityScience & Technology Commission of Shanghai Municipality (STCSM) [19ZR1418100]; Science and Technology Program of Shanghai [21010500300]; STINT Joint China-Sweden Mobility Project [CH2017-7243]; Swedish Government strategic faculty grant in material science (SFO, MATLIU) in Advanced Functional Materials (AFM) [VR Dnr. 5.1-2015-5959]; Shanghai Engineering Research Center of Intelligent Computing System [19DZ2252600]

Available from: 2022-03-10 Created: 2022-03-10 Last updated: 2023-04-18Bibliographically approved
Fu, J., Wu, Y., Xin, P., Jin, Z., Zhang, Q., Zhang, J., . . . Huang, S. (2022). Nanoporous CoP nanowire arrays decorated with carbon-coated CoP nanoparticles: the role of interfacial engineering for efficient overall water splitting. International Journal of Energy Research, 46(8), 11359-11370
Open this publication in new window or tab >>Nanoporous CoP nanowire arrays decorated with carbon-coated CoP nanoparticles: the role of interfacial engineering for efficient overall water splitting
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2022 (English)In: International Journal of Energy Research, ISSN 0363-907X, E-ISSN 1099-114X, Vol. 46, no 8, p. 11359-11370Article in journal (Refereed) Published
Abstract [en]

The innovative construction of bifunctional non-noble electrocatalyst for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is imperative for electrochemical water splitting. Herein, we provide a collaborative self-templating method to prepare a hybrid catalyst of nanoporous CoP nanowire (NWs) arrays decorated with carbon-coated CoP nanoparticles (NPs). Its found that the unique structure and morphology of the resultant catalyst can provide abundant available active sites and faciliatate the rapid H-2/O-2 transmission. Additionally, the N-doped carbon improves the conductivity of the catalyst and prevents the aggregation and deactivation of CoP nanoparticles. Forthermore, the strong coupling and synergistic effects by interface engineering are also conducive to the electrochemical performance. Benefiting from these advantages, the CoP NWs/CoP NPs@NC/CC only needs a low overpotential of 103 mV to achieve 10 mA cm(-2) with a small Tafel slope of 87 mV dec(-1) for HER. When employed in an electrolytic cell as an electrocatalyst for overall water splitting, a low voltage of 1.60 V is required to drive 10 mA cm(-2). This study may provide a novel way to fabricate transitionmetal-based catalysts for water splitting.

Place, publisher, year, edition, pages
WILEY, 2022
Keywords
electrocatalysis; interface engineering; transition metal phosphides; water splitting
National Category
Energy Engineering
Identifiers
urn:nbn:se:liu:diva-184538 (URN)10.1002/er.7933 (DOI)000780925300001 ()
Note

Funding Agencies|Science and Technology Commission of Shanghai MunicipalityScience & Technology Commission of Shanghai Municipality (STCSM) [19ZR1418100]; Science and Technology Program of Shanghai [21010500300]

Available from: 2022-04-26 Created: 2022-04-26 Last updated: 2023-08-28Bibliographically approved
zhang, x., Chen, J., Hu, J., du Rietz, A., Wu, X., Zhang, R., . . . Hu, Z.-J. (2022). Single-wavelength-excited fluorogenic nanoprobe for accurate real-time ratiometric analysis of broad pH fluctuations in mitophagy. Nano Reseach, 15, 6515-6521
Open this publication in new window or tab >>Single-wavelength-excited fluorogenic nanoprobe for accurate real-time ratiometric analysis of broad pH fluctuations in mitophagy
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2022 (English)In: Nano Reseach, ISSN 1998-0124, E-ISSN 1998-0000, Vol. 15, p. 6515-6521Article in journal (Refereed) Published
Abstract [en]

Mitophagy has a critical role in maintaining cellular homeostasis through acidic lysosomes engulfing excess or impaired mitochondria, thereby pH fluctuation is one of the most significant indicators for tracking mitophagy. Then such precise pH tracking demands the fluorogenic probe that has tailored contemporaneous features, including mitochondrial-specificity, excellent biocompatibility, wide pH-sensitive range of 8.0-4.0, and especially quantitative ability. However, available molecular probes cannot simultaneously meet all the requirements since it is extremely difficult to integrate multiple functionalities into a single molecule. To fully address this issue, we herein integrate two fluorogenic pH sensitive units, a mitochondria-specific block, cell-penetrating facilitator, and biocompatible segments into an elegant silica nano scaffold, which greatly ensures the applicability for real-time tracking of pH fluctuations in mitophagy. Most significantly, at a single wavelength excitation, the integrated pH-sensitive units have spectra-distinguishable fluorescence towards alkaline and acidic pH in a broad range that covers mitochondrial and lysosomal pH, thus enabling a ratiometric analysis of pH variations during the whole mitophagy. This work also provides constructive insights into the fabrication of advanced fluorescent nanoprobes for diverse biomedical applications.

Place, publisher, year, edition, pages
Tsinghua University Press, 2022
Keywords
mitochondrial pH; mitophagy; ratiometric fluorescence; nanoprobe; cell imaging
National Category
Biochemistry and Molecular Biology
Identifiers
urn:nbn:se:liu:diva-185395 (URN)10.1007/s12274-022-4325-3 (DOI)000793658700002 ()
Note

Funding Agencies|Linkoping University

Available from: 2022-06-01 Created: 2022-06-01 Last updated: 2023-05-17Bibliographically approved
Chang, J.-C., Eriksson, F., Sortica, M. A., Greczynski, G., Bakhit, B., Hu, Z.-J., . . . Hsiao, C.-L. (2021). Orthorhombic Ta3-xN5-yOy thin films grown by unbalanced magnetron sputtering: The role of oxygen on structure, composition, and optical properties. Surface & Coatings Technology, 406, Article ID 126665.
Open this publication in new window or tab >>Orthorhombic Ta3-xN5-yOy thin films grown by unbalanced magnetron sputtering: The role of oxygen on structure, composition, and optical properties
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2021 (English)In: Surface & Coatings Technology, ISSN 0257-8972, E-ISSN 1879-3347, Vol. 406, article id 126665Article in journal (Refereed) Published
Abstract [en]

Direct growth of orthorhombic Ta3N5-type Ta-O-N compound thin films, specifically Ta3-xN5-yOy, on Si and sapphire substrates with various atomic fractions is realized by unbalanced magnetron sputtering. Low-degree fiber-textural Ta3-xN5-yOy films were grown through reactive sputtering of Ta in a gas mixture of N-2, Ar, and O-2 with keeping a partial pressure ratio of 3:2:0.1 in a total working pressure range of 5-30 mTorr. With increasing total pressure from 5 to 30 mTorr, the atomic fraction of O in the as-grown Ta3-xN5-yOy films was found to increase from 0.02 to 0.15 while that of N and Ta decrease from 0.66 to 0.54 and 0.33 to 0.31, respectively, leading to a decrease in b lattice constant up to around 1.3%. Metallic TaNx phases were formed without oxygen. For a working pressure of 40 mTorr, an amorphous, O-rich Ta-N-O compound film with a high O fraction of similar to 0.48, was formed, mixed with non-stoichiometric TaON and Ta2O5. By analyzing the plasma discharge, the increasing O incorporation is associated with oxide formation on top of the Ta target due to a higher reactivity of Ta with O than with N. The increase of O incorporation in the films also leads to a optical bandgap widening from similar to 2.22 to similar to 2.96 eV, which is in agreement with the compositional and structural changes from a crystalline Ta3-xN5-yOy to an amorphous O-rich Ta-O-N compound.

Place, publisher, year, edition, pages
ELSEVIER SCIENCE SA, 2021
Keywords
Ta3N5; Magnetron sputtering; XRD; XPS; ERDA; Optical absorption spectroscopy
National Category
Inorganic Chemistry
Identifiers
urn:nbn:se:liu:diva-173006 (URN)10.1016/j.surfcoat.2020.126665 (DOI)000604750600025 ()
Note

Funding Agencies|Vetenskapseddet [2018-04198]; Energimyndigheten [46658-1]; Stiftelsen 011e Engkvist Byggmastare [197-0210]; Linkoping University Library; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [SFO-Mat-LiU 2009-00971]; VR-RFI [821-2012-5144, 2017-00646_9]; Swedish Foundation for Strategic Research (SSF)Swedish Foundation for Strategic Research [RIF14-0053, 5E13-0333]

Available from: 2021-01-27 Created: 2021-01-27 Last updated: 2023-12-21
Xu, W., Hu, Q., Bai, S., Bao, C., Miao, Y., Yuan, Z., . . . Gao, F. (2019). Rational molecular passivation for high-performance perovskite light-emitting diodes. Nature Photonics, 13(6), 418-424
Open this publication in new window or tab >>Rational molecular passivation for high-performance perovskite light-emitting diodes
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2019 (English)In: Nature Photonics, ISSN 1749-4885, E-ISSN 1749-4893, Vol. 13, no 6, p. 418-424Article in journal (Refereed) Published
Abstract [en]

A major efficiency limit for solution-processed perovskite optoelectronic devices, for example light-emitting diodes, is trap-mediated non-radiative losses. Defect passivation using organic molecules has been identified as an attractive approach to tackle this issue. However, implementation of this approach has been hindered by a lack of deep understanding of how the molecular structures influence the effectiveness of passivation. We show that the so far largely ignored hydrogen bonds play a critical role in affecting the passivation. By weakening the hydrogen bonding between the passivating functional moieties and the organic cation featuring in the perovskite, we significantly enhance the interaction with defect sites and minimize non-radiative recombination losses. Consequently, we achieve exceptionally high-performance near-infrared perovskite light-emitting diodes with a record external quantum efficiency of 21.6%. In addition, our passivated perovskite light-emitting diodes maintain a high external quantum efficiency of 20.1% and a wall-plug efficiency of 11.0% at a high current density of 200 mA cm−2, making them more attractive than the most efficient organic and quantum-dot light-emitting diodes at high excitations.

Place, publisher, year, edition, pages
Springer Nature Publishing AG, 2019
National Category
Physical Sciences
Identifiers
urn:nbn:se:liu:diva-157707 (URN)10.1038/s41566-019-0390-x (DOI)000468752300019 ()
Note

Funding agencies:  ERC Starting Grant [717026]; National Basic Research Program of China (973 Program) [2015CB932200]; National Natural Science Foundation of China [61704077, 51572016, 51721001, 61634001, 61725502, 91733302, U1530401]; Natural Science Foundation of Jiangsu 

Available from: 2019-06-19 Created: 2019-06-19 Last updated: 2021-12-28Bibliographically approved
Hu, J., Liu, T., Gao, H.-W., Lu, S., Uvdal, K. & Hu, Z.-J. (2018). Selective detections of Hg2+ and F- by using tailor-made fluorogenic probes. Sensors and actuators. B, Chemical, 269, 368-376
Open this publication in new window or tab >>Selective detections of Hg2+ and F- by using tailor-made fluorogenic probes
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2018 (English)In: Sensors and actuators. B, Chemical, ISSN 0925-4005, E-ISSN 1873-3077, Vol. 269, p. 368-376Article in journal (Refereed) Published
Abstract [en]

By ingeniously using a (imino)coumarin-precursor, three reactive fluorogenic probes of MP, FP, and FMP have been fabricated in a single facile synthetic route. MP and FP are able to respectively act as selective "turn-on" fluorescent probes for detecting Hg2+ and F- in buffer solution via specific analyte-induced reactions. Linear ranges for the detection of Hg2+ and F- are 0-10 mu M and 0-100 mu M with the limits of detection (LODs) of 4.0 x 10(-8) M and 1.14 x 10(-6) M (3 delta/slope), respectively. FMP is able to work as a molecular "AND" logic gate-based fluorogenic probe for monitoring the coexistence of Hg2+ and F- via a multistep reaction cascade. The analytes-induced sensing mechanisms have been determined by using high-performance liquid chromatography analysis (HPLC). In addition, three probes show negligible toxicity under the experimental conditions, and are successfully used for monitoring Hg2+ and F- in living cells with good cell permeability. The success of the work demonstrates that ingenious utility of specific analyte-induced reactions and conventional concepts on the appropriate molecular scaffold can definitely deliver tailor-made probes for various intended sensing purposes. (C) 2018 Published by Elsevier B.V.

Place, publisher, year, edition, pages
Elsevier, 2018
Keywords
Coumarin; Chemosensor; Mercury; Fluoride; "AND" logic gate
National Category
Analytical Chemistry
Identifiers
urn:nbn:se:liu:diva-149331 (URN)10.1016/j.snb.2018.04.164 (DOI)000433211100044 ()
Note

Funding Agencies|Natural Science Foundation of Shanghai [17ZR1410500]; National Natural Science Foundation of China [21577098, 21477073]; Swedish Research Council (VR) [621-2013-5357]; Swedish Government strategic faculty grant in material science (SFO, MATLIU) in Advanced Functional Materials (AFM) (VR) [5.1-2015-5959]

Available from: 2018-07-02 Created: 2018-07-02 Last updated: 2021-10-13
Hu, J., Hu, Z.-J., Chen, Z., Gao, H.-W. & Uvdal, K. (2016). A logic gate-based fluorogenic probe for Hg2+ detection and its applications in cellular imaging. Analytica Chimica Acta, 919, 85-93
Open this publication in new window or tab >>A logic gate-based fluorogenic probe for Hg2+ detection and its applications in cellular imaging
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2016 (English)In: Analytica Chimica Acta, ISSN 0003-2670, E-ISSN 1873-4324, Vol. 919, p. 85-93Article in journal (Refereed) Published
Abstract [en]

A new colorimetric and fluorogenic probe (RN3) based on rhodamine-B has been successfully designed and synthesized. It displays a selective response to Hg2+ in the aqueous buffer solution over the other competing metals. Upon addition of Hg2+, the solution of RN3 exhibits a naked eye observable color change from colorless to red and an intensive fluorescence with about 105-fold enhancement. The changes in the color and fluorescence are ascribed to the ring-opening of spirolactam in rhodamine fluorophore, which is induced by a binding of the constructed receptor to Hg2+ with the association and dissociation constants of 0.22 x 10(5) M-1 and 25.2 mM, respectively. The Jobs plot experiment determines a 1: 1 binding stoichiometry between RN3 and Hg2+. The resultant "turn-on" fluorescence in buffer solution, allows the application of a method to determine Hg2+ levels in the range of 4.0-15.0 mu M, with the limit of detection (LOD) calculated at 60.7 nM (3 sigma/slope). In addition, the fluorescence turn-off and color fading-out happen to the mixture of RN3-Hg2+ by further addition of I- or S2-. The reversible switching cycles of fluorescence intensity upon alternate additions of Hg2+ and S2- demonstrate that RN3 can perform as an INHIBIT logic gate. Furthermore, the potential of RN3 as a fluorescent probe has been demonstrated for cellular imaging. (C) 2016 Elsevier B.V. All rights reserved.

Place, publisher, year, edition, pages
ELSEVIER SCIENCE BV, 2016
Keywords
Mercury; Rhodamine; Fluorogenic probe; Fluorescent imaging; Logical gate
National Category
Analytical Chemistry
Identifiers
urn:nbn:se:liu:diva-128135 (URN)10.1016/j.aca.2016.03.017 (DOI)000374642400011 ()27086103 (PubMedID)
Note

Funding Agencies|National Natural Science Foundation of China [21577098]; Knut and Alice Wallenberg Foundation (KAW) [2012.0083]; Swedish Government Strategic Faculty Grant in Material Science 11 (SFO, MATLIU) in Advanced Functional Materials (AFM) (VR) [5.1-2015-5959]; Centre in Nano Science and Nanotechnology (CeNano) Grant in LiTH

Available from: 2016-05-19 Created: 2016-05-19 Last updated: 2021-10-13
Hu, J., Hu, Z.-J., Liu, S., Zhang, Q., Gao, H.-W. & Uvdal, K. (2016). A new ratiometric fluorescent chemodosimeter based on an ICT modulation for the detection of Hg2+. Sensors and actuators. B, Chemical, 230, 639-644
Open this publication in new window or tab >>A new ratiometric fluorescent chemodosimeter based on an ICT modulation for the detection of Hg2+
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2016 (English)In: Sensors and actuators. B, Chemical, ISSN 0925-4005, E-ISSN 1873-3077, Vol. 230, p. 639-644Article in journal (Refereed) Published
Abstract [en]

We design and synthesize a new ratiometric fluorescent chemodosimeter (S1) for the selective and sensitive detection of Hg2+. Upon addition of Hg2+, the emission of the S1 exhibits a large bathochromic shift from 393 to 515 nm (up to 122 nm) which is ascribed to an intramolecular charge transfer process in the resultant. The Hg2+-induced dethioacetalization for sensing mechanism has been demonstrated by using high-performance liquid chromatography analysis of the sensing process. The interference experiments further demonstrate that S1 exhibits very high selectivity towards Hg2+ over other coexisting cations/anions. Subsequently, a good linearity of the concentrations of Hg2+ (0-15 mu M) vs the ratiometric signals (I-515/I-393) allows a fluorogenic method for the quantitative detection of Hg2+, with the limitation of detection determined to be 5.22 x 10(-7) M. (C) 2016 Elsevier B.V. All rights reserved.

Place, publisher, year, edition, pages
ELSEVIER SCIENCE SA, 2016
Keywords
Chemodosimeter; Ratiometric fluorescence; Mercury detection; Intramolecular charge transfer; Phenanthroimidazole
National Category
Physical Sciences
Identifiers
urn:nbn:se:liu:diva-128714 (URN)10.1016/j.snb.2016.02.125 (DOI)000374329300081 ()
Note

Funding Agencies|National Natural Science Foundation of China [21577098]; Foundation of State Key Laboratory of Pollution Control and Resource Reuse, China [PCRRK13024]; Knut and Alice Wallenberg Foundation (KAW) [2012.0083]; Swedish Government strategic faculty grant in material science (SFO, MATLIU) in Advanced Functional Materials (AFM) (VR) [5.1-2015-5959]; International Exchange Program for Graduate Students of Tongji University [201502013]

Available from: 2016-06-07 Created: 2016-05-30 Last updated: 2021-10-13
Yu, Y., Hu, Z.-J., Zhang, Y. & Gao, H. (2016). CTAB@BiOCl: a highly adsorptive photocatalyst for eliminating dye contamination. RSC Advances, 6(22), 18577-18582
Open this publication in new window or tab >>CTAB@BiOCl: a highly adsorptive photocatalyst for eliminating dye contamination
2016 (English)In: RSC Advances, E-ISSN 2046-2069, Vol. 6, no 22, p. 18577-18582Article in journal (Refereed) Published
Abstract [en]

The title composite was synthesized under facile conditions by hydrolysis and co-precipitation. Through comparative studies, it was found that the morphology, structure and properties were affected by hexadecyl trimethylammonium bromide (CTAB) doping. Although the surface area decreases from 53.5 to 7.5 m(2) g(-1), it was found that CTAB@BiOCl exhibits higher adsorption capacity than the isolated BiOCl, and still maintains good photocatalytic activity, which is a little worse than the isolated BiOCl has. This was caused by the lower content of BiOCl in CTAB@BiOCl, which is less than 70%. The studies show that, in high concentrations of dye-contaminated water, the composite exhibits strong adsorption capacities of 901 mg g(-1) to Congo Red (CR) and 699 mg g(-1) to Reactive Red 3 (X3B). In the low-concentration case, it is able to process photocatalysis of those dyes. In the recycling experiment, the CTAB@BiOCl composite was regenerated in situ. And CTAB in the composite was almost completely degraded after five cycles, resulting in the regenerated BiOCl. Subsequently, the surface area of the composite increases from 7.5 to 22.62 m(2) g(-1), and along with this the adsorption capacities to CR and X3B decrease obviously due to the absence of the CTAB component. In addition, the photocatalysis activity of the generated composite has been promoted to be similar to the isolated BiOCl.

Place, publisher, year, edition, pages
ROYAL SOC CHEMISTRY, 2016
National Category
Physical Sciences
Identifiers
urn:nbn:se:liu:diva-126147 (URN)10.1039/c5ra27714k (DOI)000370717900083 ()
Note

Funding Agencies|National Key Technologies R&D Program of China [2012BAJ25B02]

Available from: 2016-03-15 Created: 2016-03-15 Last updated: 2022-09-15
Zhang, Q., Luo, L., Xu, H., Hu, Z.-J., Brommesson, C., Wu, J., . . . Uvdal, K. (2016). Design, synthesis, linear and nonlinear photophysical properties of novel pyrimidine-based imidazole derivatives. New Journal of Chemistry, 40(4), 3456-3463
Open this publication in new window or tab >>Design, synthesis, linear and nonlinear photophysical properties of novel pyrimidine-based imidazole derivatives
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2016 (English)In: New Journal of Chemistry, ISSN 1144-0546, E-ISSN 1369-9261, Vol. 40, no 4, p. 3456-3463Article in journal (Refereed) Published
Abstract [en]

Novel donor-pi-acceptor (D-pi-A) and donor-pi-acceptor-pi-donor (D-pi-A-pi-D) type pyrimidine imidazole derivatives with flexible ether chains (L1 and L2) have been efficiently synthesized through improved Knoevenagel condensation and Ullmann reactions with high yields. Based on systematic photophysical investigations and theoretical calculations, the structure-property relationships can be described as follows: (1) the linear and nonlinear optical properties of the target chromophores change regularly with increasing the number of branches and the polarity of the solvents. (2) The single-substituted chromophore L2 exhibited a remarkable negative solvato-kinetic effect, while the double-substituted chromophore L1 showed a positive solvato-kinetic effect. Significant bathochromic shifting of the emission spectra and larger Stokes shifts were observed in polar solvents. (3) The two-photon absorption (TPA) cross-section results further demonstrated that their TPA cross section values (delta) increase notably with increasing branch number, and the presence of high pi-delocalization could induce large size-scalable TPA enhancements. (4) By comprehensively considering the optical performance, cytotoxicity and solubility, L1 was identified as the better candidate for living cell (HepG2) imaging.

Place, publisher, year, edition, pages
ROYAL SOC CHEMISTRY, 2016
National Category
Physical Sciences
Identifiers
urn:nbn:se:liu:diva-127760 (URN)10.1039/c5nj02874d (DOI)000373993600060 ()
Note

Funding Agencies|National Natural Science Foundation of China [21501001, 21271004, 51372003, 51432001, 21271003, 51072001, 81503009, 51272001]; National Key Basic Research Program 973 [2013CB632705]; Ministry of Education; Program for New Century Excellent Talents in University (China); Doctoral Program Foundation of Ministry of Education of China [20113401110004]; China Postdoctoral Science Foundation [2015M571912]; Swedish Research Council (VR) [621-2013-5357]; Swedish Government (SFO, MATLIU) in Advanced Functional Materials (AFM); Wenner-Gren Foundation

Available from: 2016-05-12 Created: 2016-05-12 Last updated: 2022-02-07
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ORCID iD: ORCID iD iconorcid.org/0000-0001-9905-0881

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