Wang X.,Dalian National Laboratory for Clean Energy |
Jin S.,Dalian National Laboratory for Clean Energy |
Jin S.,University of the Chinese Academy of SciencesBeijing |
An H.,Dalian National Laboratory for Clean Energy |
And 3 more authors.
Journal of Physical Chemistry C | Year: 2015
Although the surface phase junction can efficiently boost photocatalytic (PC) reactions, its role in photoelectrocatalytic (PEC) reactions has not been well-understood yet. In this study, we investigated the effect of the surface phase junction on the PEC performance of photoelectrodes fabricated with Ga2O3 and TiO2 particles. The surface phase junctions beneficial for PC reactions show a negative effect on PEC performance, which is mainly due to the significant influence of charge transportation between semiconductor particles by the surface phase junction. Photogenerated charge separation is promoted by the surface phase junction for both PC and PEC reactions, but the much more severe interfacial recombination occurs in the PEC reaction when charge carriers migrate across semiconductor particles to reach a conducting substrate. The opposite effects of the surface phase junction on PC and PEC performance reported here indicates that the fabrication of a heterojunction or phase junction in the right structure and sequence is vital to PEC systems based on junction, which will be helpful for the development of highly efficient photoconversion systems. © 2015 American Chemical Society.
Ma Y.,Dalian National Laboratory for Clean Energy |
Ma Y.,University of the Chinese Academy of SciencesBeijing |
Du Z.,Dalian National Laboratory for Clean Energy |
Liu J.,Dalian National Laboratory for Clean Energy |
And 4 more authors.
Green Chemistry | Year: 2015
Selective transformation of lignin into value-added aromatics is highly attractive and rather challenging. Catalytic oxidative degradation provides a promising approach to obtain aromatics from lignin while preserving the benzene units. In this study, vanadium-catalyzed aerobic oxidation of 2-phenoxy-1-phenylethanol was studied as a lignin model compound. The solvent played a significant role in the distribution of oxidation products. In the presence of acetic acid, oxidative C-C bond cleavage was preferred, while oxidation products via C-H bond cleavage were rather limited. A one-electron transfer process was involved in the oxidation reaction. The occurrence of vanadium(v) was detected, and the carboxylic group could coordinate to vanadium(v) through exchange with the acetylacetonato ligand during oxidation in the presence of acetic acid. © The Royal Society of Chemistry.
Tao Y.,CAS Changchun Institute of Applied Chemistry |
Tao Y.,University of the Chinese Academy of SciencesBeijing |
Zhang Y.,CAS Changchun Institute of Applied Chemistry |
Zhang Y.,University of the Chinese Academy of SciencesBeijing |
And 4 more authors.
Nanoscale | Year: 2015
We here report a facile one-pot synthesis of fluorescent gold nanoclusters (AuNCs) via the peptide biomineralization method, which can elicit specific immunological responses. The as-prepared peptide-protected AuNCs (peptide-AuNCs) display strong red fluorescence, and more importantly, as compared to the peptide alone, the immune stimulatory ability of the resulting peptide-AuNCs can not only be retained, but can also be efficaciously enhanced. Moreover, through a dual-delivery of antigen peptides and cytosine-phosphate-guanine (CpG) oligodeoxynucleotides (ODNs), the as-prepared peptide-AuNC-CpG conjugates can also act as smart self-vaccines to assist in the generation of high immunostimulatory activity, and be applied as a probe for intracellular imaging. Both in vitro and in vivo studies provide strong evidence that the AuNC-based vaccines may be utilized as safe and efficient immunostimulatory agents that are able to prevent and/or treat a variety of ailments. This journal is © The Royal Society of Chemistry.
Zhang Z.,CAS Lanzhou Institute of Chemical Physics |
Zhang Z.,University of the Chinese Academy of SciencesBeijing |
Wang W.,CAS Lanzhou Institute of Chemical Physics |
Kang Y.,CAS Lanzhou Institute of Chemical Physics |
And 2 more authors.
RSC Advances | Year: 2015
As the materials of "green 21st century material worlds", natural silicates have received unprecedented attention by virtue of their abundance, low-cost, stability, and non-toxic and eco-friendly nature compared to other synthetic materials. With the aim to develop a new hybrid silicate adsorbent with improved adsorption properties, the naturally abundant palygorskite (PAL) was functionalized with glycine (GLY) via a simple one-step hydrothermal process and used for capturing Pb(ii) ions from aqueous solution. The main reaction parameters, e.g., the pH values of the reaction medium, solid-to-liquid ratio, reaction time and dosage of GLY, were systematically optimized, and the as-prepared adsorbent was characterized using X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmittance electronic microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR) techniques. The results reveal that the PAL crystal was converted to a hybrid silicate material with the assistance of GLY, and simultaneously the functional groups were introduced during the hydrothermal reaction, which caused an evident enhancement in the adsorption capacity of PAL for Pb(ii) ions from 55.76 mg g-1 to 123.24 mg g-1. Almost 99.60% of Pb(ii) could be captured and removed from a 40 mg L-1 Pb(ii) solution using the as-prepared GLY-PAL silicate adsorbent, which is obviously higher than the 83.85% achieved by raw PAL. The intensified complexation of the functional groups on the silicate with Pb(ii), the electrostatic attraction and the pore adsorption are responsible for the enhancement in the adsorption capability. © The Royal Society of Chemistry.
Zhang T.,CAS Lanzhou Institute of Chemical Physics |
Zhang T.,University of the Chinese Academy of SciencesBeijing |
Cui S.,CAS Lanzhou Institute of Chemical Physics |
Cui S.,University of the Chinese Academy of SciencesBeijing |
And 3 more authors.
Chemical Communications | Year: 2015
A simple method to improve the photoelectrochemical performance of TiO2 nanotube arrays (NTs) by simple air plasma post-treatment is reported. The air plasma treated sample shows higher photocurrent density and incident photo current efficiency with high stability, about 3-4 times that of the pristine TiO2 NTs even after six months. © The Royal Society of Chemistry.
Cao X.-L.,CAS Fujian Institute of Research on the Structure of Matter |
Cao X.-L.,University of the Chinese Academy of SciencesBeijing |
Kong F.,CAS Fujian Institute of Research on the Structure of Matter |
Hu C.-L.,CAS Fujian Institute of Research on the Structure of Matter |
Mao J.-G.,CAS Fujian Institute of Research on the Structure of Matter
Inorganic Chemistry Frontiers | Year: 2014
Using Hg2Cl2, MoO3, and TeO2 (or SeO2) as starting materials, four new mixed-metal tellurites and selenites have been obtained in the unexplored mercury(i)-Mo6+-Se4+/Te4+-O system, namely, Hg2MoSeO6 (1), α-Hg2MoTeO6 (2), β-Hg2MoTeO6 (3), and Hg2Mo2TeO9 (4). They represent the first mercury(i) tellurites and selenites containing octahedrally coordinated d0 transition metal (TM) cations. All four compounds are centrosymmetric. They show three types of 3D structures based on Hg22+ dumbbells, MoO6 octahedra, QO32- (Q = Se, Te) or TeO44- anions. Compounds 1-3 feature similar 1D anionic chains of [MoO3(QO3)]2- (Q = Se or Te), in which the 1D chains of corner-sharing MoO6 octahedra are further decorated by bidentate bridging selenite or tellurite anions. Compounds 1 and 2 are isostructural and their 3D network structures are based on 2D mercury tellurite or selenite layers in the ac plane pillared by MoO6 octahedra, whereas the 3D network of β-Hg2MoTeO6 (3) is composed of 1D mercury tellurite chains along the a axis and 1D chains of [MoO3(TeO3)]2- anions along the b axis. Compound 4 features an unusual 3D network structure composed of novel [Mo2O5(TeO4)]2- double layers interconnected by Hg22+ cations. Within the [Mo2O5(TeO4)]2- double layer, the cyclo-Mo4O20 tetramers are further interconnected via corner sharing into a 2D molybdenum oxide double layer with TeO4 groups capping the walls of the thus-formed eight-membered rings (8-MRs). Thermal stabilities and optical properties as well as theoretical calculations based on density functional theory (DFT) methods were also performed. This journal is © the Partner Organisations.
Li L.,CAS Fujian Institute of Research on the Structure of Matter |
Zhang S.,CAS Fujian Institute of Research on the Structure of Matter |
Xu Y.,CAS Fujian Institute of Research on the Structure of Matter |
Xu Y.,University of the Chinese Academy of SciencesBeijing |
And 3 more authors.
Inorganic Chemistry | Year: 2015
A new entangled metal-organic framework shows reversible structural dynamics and luminescence changing in response to the loss of guest H2O molecules. Furthermore, an intense and sensitive luminescence turn-on sensing was observed by the naked eye for 1 upon detection of the volatile organic solvent molecule CH3CN, accompanied by reversible structural transformation. © 2015 American Chemical Society.
Sun H.,CAS Changchun Institute of Applied Chemistry |
Sun H.,University of the Chinese Academy of SciencesBeijing |
Gao N.,CAS Changchun Institute of Applied Chemistry |
Ren J.,CAS Changchun Institute of Applied Chemistry |
Qu X.,CAS Changchun Institute of Applied Chemistry
Chemistry of Materials | Year: 2015
An effective and economic rewritable paper (RPs) based on the reversible discoloration reactions of polyoxometalates (POMs) was designed. Polyethylene glycol was utilized not only to passivate efficiently the hydroxyl groups of paper but also possess excellent swellability and assisted the penetration of H2O2 molecules. Consequently, this increased the opportunity of triggering the redox reaction of POMs, which made the characters and patterns clearer on RP. For control, the PRPs without PEG20000 were also prepared. After characters were written, the H2O2 ink diffused rapidly on the surface of paper without PEG20000, resulting in the unclear written records; whereas for the PEG20000 passivated RP, the written characters were clear and neat, which demonstrated the necessity of PEG in construction of PRPs. Because a household UV disinfector can be used as the UV light source and H2O2 and isopropyl alcohol are domestic disinfectant, detergents and flavoring agent, the designed PRPs show promising potential for use as a long lasting rewritable paper.
Kang X.,CAS Changchun Institute of Applied Chemistry |
Yang Y.,CAS Changchun Institute of Applied Chemistry |
Yang Y.,University of the Chinese Academy of SciencesBeijing |
Huang L.,CAS Changchun Institute of Applied Chemistry |
And 5 more authors.
Green Chemistry | Year: 2015
Water-soluble CuInSe2/ZnS (CISe/ZnS) and AgInSe2/ZnS (AISe/ZnS) core/shell quantum dots (QDs) on a multigram scale have been synthesized by using gelatin and thioglycolic acid as dual stabilizers in an electric pressure cooker. The core/shell QDs present composition-tunable emission in the range of 582 nm to 686 nm with a maximum PLQY of 23.3%. The core/shell QDs also exhibit good water/buffer stability. The red-emitting CISe/ZnS QDs are applied as wavelength converters to achieve warm white light-emitting diodes. This journal is © The Royal Society of Chemistry.
Bi Y.,Chinese Academy of Sciences |
Bi Y.,University of the Chinese Academy of SciencesBeijing |
Ren Y.,Chinese Academy of Sciences |
Bi F.,Chinese Academy of Sciences |
And 2 more authors.
Journal of Alloys and Compounds | Year: 2015
Abstract With ethylene glycol as the solvent, monodispersed cobalt ferrite nanospheres were prepared via a solvothermal method assisted by water. The samples were mainly characterized by X-ray diffraction, scanning electron microscope, and transmission electron microscope. The size of as-prepared products ranges from 10 nm to 200 nm. Size distribution and chemical composition were controlled by the amount of water and pH value in the reaction system. More important, suitable amount of water can avoid the use of surfactant. © 2015 Elsevier B.V.