| 1. |
- Hu, Peiji, et al.
(författare)
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In-situ exsolution of FeCo nanoparticles over perovskite oxides for efficient electrocatalytic nitrate reduction to ammonia via localized electrons
- 2024
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Ingår i: Applied Catalysis B: Environmental. - 0926-3373. ; 357
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Tidskriftsartikel (refereegranskat)abstract
- FeCo nanoparticles exsolved from Co-doped Sm0.9FeO3 nanofibers with abundant oxygen vacancies (Vos) are proposed as an efficient electrocatalyst to promote nitrate reduction reaction (NITRR). Such catalyst achieves a maximum Faradaic efficiency (FE) of 90.3 % and a large NH3 yield of 17.2 mg h−1 mg−1cat. at a negatively shifted potential of −0.9 V in 0.1 M PBS with 0.1 M NaNO3, and the alloy nanoparticles socketed into nanofibers remain extremely stable during long-term electrolysis. The reaction pathway favoring the formation of NH2OH is uncovered by in situ electrochemical tests and theoretical calculations reveal the exsolution of FeCo alloy combined with the generation of Vos enhances nitrate adsorption and lowers energy increase of the potential determining step. Finite-element simulations unveil the applied current and charges are localized on the alloys along the nanofiber, which confirms the exsolved FeCo nanoparticles are the main active sites for NITRR.
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| 2. |
- Li, Xuping, et al.
(författare)
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A three-dimensional ratiometric sensing strategy on unimolecular fluorescence-thermally activated delayed fluorescence dual emission
- 2019
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Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 10
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Tidskriftsartikel (refereegranskat)abstract
- Visualized sensing through fluorescence signals is a powerful method for chemical and physical detection. However, the utilization of fluorescent molecular probes still suffers from lack of precise signal self-calibration in practical use. Here we show that fluorescence and thermally activated delayed fluorescence can be simultaneously produced at the single-molecular level. The thermally activated delayed fluorescence serves as a sensing signal with its wavelength and lifetime both altered correlating to polarity, whereas the fluorescence always remains unchanged as an internal reference. Upon the establishment of a three-dimensional working curve upon the ratiometric wavelength and photoluminescence lifetime vs. polarity, disturbance factors during a relevant sensing process can be largely minimized by such a multiple self-calibration. This strategy was further applied into a precise detection of the microenvironmental polarity variation in complex phospholipid systems, towards providing new insights for convenient and accurate diagnosis of membrane lesions.
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| 3. |
- Wang, Rui, et al.
(författare)
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Environmentally friendly Mn-alloyed core/shell quantum dots for high-efficiency photoelectrochemical cells
- 2020
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 8:21, s. 10736-10741
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Tidskriftsartikel (refereegranskat)abstract
- Colloidal quantum dot (QD)-based photoelectrochemical (PEC) cells are cost-effective devices showing remarkable solar-to-fuel conversion efficiency. However, the extensive use of highly toxic elements (e.g. Pb and Cd) in QDs' synthesis and device fabrication is still a major challenge towards their practical development. Herein, we fabricate a solar-driven PEC cell based on environmentally friendly Mn-alloyed CuInS2 (MnCIS)/ZnS core/shell QDs, showing more favorable band alignment, efficient charge transfer, reduced charge recombination and lower charge transfer resistance with respect to the control device fabricated using unalloyed CuInS2 (CIS)/ZnS core/shell QDs. An unprecedented photocurrent density of ∼5.7 mA cm−2 with excellent stability was obtained for the as-fabricated MnCIS/ZnS core/shell QD-based PEC device when operated under standard one sun irradiation (AM 1.5G, 100 mW cm−2). These results indicate that the transition metal-alloyed environmentally friendly core/shell QDs are promising for next-generation solar technologies.
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| 4. |
- Zhao, Pei, et al.
(författare)
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One-step solvothermal synthesis of high-emissive amphiphilic carbon dots via rigidity derivation
- 2018
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Ingår i: Chemical Science. - : Royal Society of Chemistry. - 2041-6520 .- 2041-6539. ; 9:5, s. 1323-1329
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Tidskriftsartikel (refereegranskat)abstract
- In nanoscience, amphiphilic carbon dots (ACDs) are of great importance due to their excellent transferability for application in biological sensing, imaging and labelling. However, facile synthetic strategies are still limited, especially for obtaining high-emissive ACDs. Since the development of a high-emissive feature is strongly desired for improving the practical resolution in vivo, here we report a chemical strategy that uses rigid molecules to straightforwardly construct amphiphilic carbon dots (ACDs) with high luminescence quantum yields (QYs). By using 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate (HATU), a typical coplanar compound, as the only precursor, well-defined ACDs were prepared via a one-step solvothermal process which exhibited a superior QY of up to 29%, largely superior to those prepared from precursors with less rigid structures. The effect can be mainly attributed to a significant suppression of the competition of non-radiative decay through rigidity derivation. Metal ionic doping during the synthesis resulted in a further improvement of the crystallinity and monodispersity of the materials, with retention of the high-emissive ability. This high-emissive photoluminescence behavior of the ACDs is accompanied with an excitation-wavelength dependence, a high biocompatibility and a low toxicity, which together make the ACDs advantageous for application in multi-channel bioimaging.
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| 5. |
- Zheng, Wei, et al.
(författare)
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Bright Free-Radical Emission in Ionic Liquids
- 2023
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773.
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Tidskriftsartikel (refereegranskat)abstract
- It is challenging to achieve stable and efficient radical emissions under ambient conditions. Herein, we present a rational design strategy to protect photoinduced carbonyl free radical emission through electrostatic interaction and spin delocalization effects. The host-guest system is constructed from tricarbonyl-substituted benzene molecules and a series of imidazolium ionic liquids as the guest and host, respectively, whereby the carbonyl anion radical emission can be in situ generated under the light irradiation and further stabilized by electrostatic interaction. More importantly, the anion species and the alkyl chain length of imidazolium ionic liquids show a noticeable effect on luminescence efficiency, with the highest radical emission efficiency is as high as 53.3 % after optimizing the imidazole ionic liquids structure, which is about four times higher than the polymer-protected radical system. Theoretical calculations confirm the synergistic effect of strong electrostatic interactions and that the spin delocalization effect significantly stabilizes the radical emission. Moreover, such a radical emission system also could be integrated with a fluorescent dye to induce multi-color or even white light emission with reversible temperature-responsive characteristics. The radical emission system can also be used to detect different amine compounds on the basis of the emission changes and photoactivation time.
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| 6. |
- Zhou, Yunyun, et al.
(författare)
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Anti-Kasha's Rule Emissive Switching Induced by Intermolecular H-Bonding
- 2018
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Ingår i: Chemistry of Materials. - : AMER CHEMICAL SOC. - 0897-4756 .- 1520-5002. ; 30:21, s. 8008-8016
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Tidskriftsartikel (refereegranskat)abstract
- The exploration of emission pathways from high-excited states in organic luminogens has recently become prosperous owing to improved possibilities to study so-called anti-Kasha's rule emission with the potential of improving the luminescent quantum efficiency. However, emission pathway switching among different high-excited states has rarely been addressed through external control. We here present a rational design and synthesis of a novel azulene-based emitter to achieve a responsive control of its anti-Kasha's rule emissive switching. The emitter initially gives rise to an S-3-to-S-0 dominant emission as indicated by our experimental and theoretical studies. On this basis, it can be toggled into an S-2-to-S-0 dominant emission upon the H-bond formation between the triformyl groups and water molecules. Such a process, which originates from the H-bonding regulated distribution of excited state energy, is accompanied by a remarkable fluorescent color conversion and a significant improvement of the fluorescent quantum yield in the azulene family. Moreover, a reversible emissive switching in doped films was observed to depend on a solid-state H-bond tuning process with moisture sensitivity. These results may provide new insight for building advanced chemical systems for visualized sensing with high distinguishability.
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