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| 2. |
- Chen, X, et al.
(författare)
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Negative thermal quenching of below-bandgap photoluminescence in InPBi
- 2017
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 110:5
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Tidskriftsartikel (refereegranskat)abstract
- This paper reports a temperature-dependent (10-280 K) photoluminescence (PL) study of below-bandgap electron-hole recombinations and anomalous negative thermal quenching of PL intensity in InP1- xBix (x = 0.019 and 0.023). Four PL features are well resolved by curve-fitting of the PL spectra, of which the energies exhibit different temperature dependence. The integral intensities of the two high-energy features diminish monotonically as temperature rises up, while those of the two low-energy features decrease below but increase anomalously above 180 K. A phenomenological model is established that the residual electrons in the final state of the PL transition transfer into nonradiative state via thermal hopping, and the thermal hopping produces in parallel holes in the final state and hence enhances the radiative recombination significantly. A reasonable interpretation of the PL processes in InPBi is achieved, and the activation energies of the PL quenching and thermal hopping are deduced. © 2017 Author(s).
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| 3. |
- Liu, Chenjuan, 1988-, et al.
(författare)
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A free standing Ru–TiC nanowire array/carbon textile cathode with enhanced stability for Li–O2 batteries
- 2018
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 6, s. 23659-23668
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Tidskriftsartikel (refereegranskat)abstract
- The instability of carbon cathode materials is one of the key problems that hinder the development of lithium–air/lithium–oxygen (Li–O2) batteries. In this contribution, a type of TiC-based cathode is developed as a suitable alternative to carbon based cathodes, and its stability with respect to its surface properties is investigated. Here, a free-standing TiC nanowire array cathode was in situ grown on a carbon textile, covering its exposed surface. The TiC nanowire array, via deposition with Ru nanoparticles, showed enhanced oxygen reduction/evolution activity and cyclability, compared to the one without Ru modification. The battery performance of the Li–O2cells with Ru–TiC was investigated by using in operando synchrotron radiation powder X-ray diffraction (SR-PXD) during a full cycle. With the aid of surface analysis, the role of the cathode substrate and surface modification is demonstrated. The presented results are a further step toward a wise design of stable cathodes for Li–O2 batteries.
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| 5. |
- Meng, Jingxiang, et al.
(författare)
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Adaptive Differentiation in Seedling Traits in a Hybrid Pine Species Complex, Pinus densata and Its Parental Species, on the Tibetan Plateau
- 2015
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Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 10:3
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Tidskriftsartikel (refereegranskat)abstract
- Evidence from molecular genetics demonstrates that Pinus densata is a natural homoploid hybrid originating from the parent species Pinus tabuliformis and Pinus yunnanensis, and ecological selection may have played a role in the speciation of Pinus densata. However, data on differentiation in adaptive traits in the species complex are scarce. In this study, we performed a common garden test on 16 seedling traits to examine the differences between Pinus densata and its parental species in a high altitude environment. We found that among the 16 analyzed traits, 15 were significantly different among the species. Pinus tabuliformis had much earlier bud set and a relatively higher bud set ratio but poorer seedling growth, and Pinus yunnanensis had opposite responses for the same traits. Pinus densata had the greatest fitness with higher viability and growth rates than the parents. The relatively high genetic contribution of seedling traits among populations suggested that within each species the evolutionary background is complex. The correlations between the seedling traits of a population within a species and the environmental factors indicated different impacts of the environment on species evolution. The winter temperature is among the most important climate factors that affected the fitness of the three pine species. Our investigation provides empirical evidence on adaptive differentiation among this pine species complex at seedling stages.
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| 6. |
- Qiu, Zhen, et al.
(författare)
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Controlled crystal growth orientation and surface charge effects in self-assembled nickel oxide nanoflakes and their activity for the oxygen evolution reaction
- 2017
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Ingår i: International journal of hydrogen energy. - : Elsevier. - 0360-3199 .- 1879-3487. ; 42:47, s. 28397-28407
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Tidskriftsartikel (refereegranskat)abstract
- Although sustainable hydrogen production from solar energy is a promising route for the future, the cost of the necessary photovoltaic and photoelectrochemical devices as well as a lack of detailed understanding and control of catalyst interfaces in nanomaterials with high catalytic activity are the largest impediments to commercial implementation. Here, we report how a higher catalytic efficiency can be achieved by utilizing an earth-abundant Nickel oxide (NiO) catalyst via an improved control of the crystalline growth orientation and self-assembly. The relationship between the surface charge and the morphology of the nano-catalysts is investigated using a hydrothermal method where the pH is utilized to control both the crystal growth direction and crystallization of Ni(OH)2 and eventually in NiO, where the self-assembly properties of nanoflakes (NFs) into hierarchical flower-like nickel oxide NFs depend on balancing of forces during synthesis. The surface charge ofthe NiO at different pH values was measured with electrophoretic dynamic light scattering (EDLS) and is known to be closely related to that of Ni(OH)2 and is here utilized to control the relative change in the surface charge in the precursor solution. By preparing NiO NFs under variation of the pH conditions of the precursor Ni(OH)2 system, the surface energies of exposed lattice planes of the growing nanostructures can be altered and an enhanced crystal growth orientation in a different direction can be controlled. Specifically, the [111] and [220] growth orientation in cubic NiO can be favored or suppressed with respect to the [200] direction. Benefiting from the large surface area provided by the mesoporous NiO NFs, the catalyst electrode exhibits high activity toward the oxygen evolution reactions in alkaline electrolyte. The NiO nanostructure synthesized at pH 10 displays oxygen evolution reaction (OER) overpotential of 0.29 V and 0.35 V versus the reversible hydrogen electrode (RHE) at 1 mA cm2 and 10 mA cm2 current density, respectively. This is compared to commercial NiO with more than 0.15 V additional overpotential and the same or lower overpotential compared to RuO2 and IrO2 at alkaline conditions. The results show that the OER catalytic activity can be drastically increased by a detailed control of the crystal growth orientation and the self-assembly behavior where the active surface charge around the point of zero charge during synthesis of the metal hydroxides/oxides is introduced as an important design principle for producing efficient electrocatalysts.
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| 7. |
- Qiu, Zhen, 1988-, et al.
(författare)
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In operando Raman investigation of Fe doping influence on catalytic NiO intermediates for enhanced overall water splitting
- 2019
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Ingår i: Nano Energy. - : Elsevier BV. - 2211-2855 .- 2211-3282. ; 66
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Tidskriftsartikel (refereegranskat)abstract
- Transition metal iron (Fe)-incorporated Ni oxide and oxyhydroxide compounds generally show an enhanced activity for alkaline water splitting. However, the role of Fe for this enhanced activity is not fully elucidated, especially under hydrogen evolution reaction (HER). Herein, we combine electrochemical and spectroscopic techniques to investigate the Fe doping effect on self-standing NiO nanosheets for enhanced activities for both HER and oxygen evolution reaction (OER) in overall water splitting. The results show that the presence of Fe suppresses Ni self-oxidation and adjusts the Ni–O local environment and its ability to form surface phases. In operando Raman spectroscopy is utilized to explore the active intermediates present under catalytic conditions. Apart from a slight suppression of grain size, our results show that Fe incorporation into NiO enhances in-situ formation of active layered intermediates NixFe1-xOOH with a phase transformation of FeOOH layers into γ-NiOOH layers containing Ni4+ at potentials approaching OER in contrast to undoped NiO electrodes with a dominating conversion of NiO to β-NiOOH, with persisting Ni3+. In addition, the work function on the electrode surface is reduced by 90 meV upon Fe doping, revealing a higher intrinsic Fermi-level and thus a lower requirement for added bias during HER. Together with the lower resistance for electron transport beneficial for both HER and OER, this leads to improved OER and HER efficiency upon Fe-doping. The study shows how Fe doping influences the active catalytic NiO intermediates for both HER and OER. Specifically, in operando vibrational spectroscopy utilized in parallel with electrochemical characterization can shed light on enhancement mechanisms and influence of doping for catalytic intermediates under any chosen bias at the respective electrode under full water splitting.
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| 8. |
- Song, Xiu-Neng, et al.
(författare)
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Theoretical Identification of Three C-66 Fullerene Isomers and Related Chlorinated Derivatives by X-ray Photoelectron Spectroscopy and Near-edge X-ray Absorption Fine Structure Spectroscopy
- 2016
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Ingår i: JOURNAL OF PHYSICAL CHEMISTRY A. - : American Chemical Society (ACS). - 1089-5639 .- 1520-5215. ; 120:50, s. 9932-9940
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Tidskriftsartikel (refereegranskat)abstract
- C is X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectra for three C-66 fullerene isomers and related chlorinated species have been calculated by density functional theory (DFT) method. The XPS spectra show isomer dependence for the three, pristine C-66 isomers but not for the chlorinated species. The NEXAFS spectra exhibit strong dependence on the structures of all the investigated molecules and thus can be well employed to identify the three C-66 fullerene isomers and related chlorinated species. Both XPS and NEXAFS spectra of the chlorinated species present significant variations compared with the pristine fullerenes. The spectral components for carbon atoms of different local environments have been explored as well. The spectra for the carbon atoms connecting to chlorine atoms exhibit a significant blue shift compared to the others.
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| 9. |
- Wang, Guang-Wei, et al.
(författare)
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Theoretical Isomer Identification of Three C-56 Fullerenes and Their Chlorinated Derivatives by XPS and NEXAFS Spectra
- 2016
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 120:25, s. 13779-13786
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Tidskriftsartikel (refereegranskat)abstract
- The C Is X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy for three C-56 fullerene isomers and their chlorinated derivatives have been theoretically simulated by means of density functional theory (DFT). Compared with XPS, the NEXAFS spectra present remarkable dependence on the structures of all the studied molecules and thus can be used to identify the three C-56 isomers and chlorinated species. The spectra of the chlorinated species present significant variations compared with the pristine fullerenes. The spectral components of carbon atoms of different local environment have been investigated as well. The spectra of carbons saturated by chlorine atoms exhibit a shift toward higher energies compared with the others.
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