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Author

H.-Y. Chen

Other affiliations: Wilmington University
Bio: H.-Y. Chen is an academic researcher from DuPont. The author has contributed to research in topics: Ionic conductivity & Crystal structure. The author has an hindex of 8, co-authored 9 publications receiving 609 citations. Previous affiliations of H.-Y. Chen include Wilmington University.

Papers
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Journal ArticleDOI
TL;DR: The structure of BiVO 4 was refined at 4.5, 295 and 566k from powder neutron diffraction data and at 295K from powder X-ray diffraction by the Rietveld profile technique as mentioned in this paper.

358 citations

Journal ArticleDOI
L.H. Brixner1, H.-Y. Chen1, C.M. Foris1
TL;DR: LaWO 4 Cl as mentioned in this paper is representative of a series of Ln WO 4Cl compounds in which Ln can be La to Sm, Tb, and Eu, and their excitation and emission spectra are reported.

38 citations

Journal ArticleDOI
R.D. Shannon1, H.-Y. Chen1, T. Berzins1
TL;DR: The structure of isotypic Na 5 YSi 4 O 12 is characterized by Si 12 O 36 rings stacked to form columns held apart by MO 6 octahedra.

37 citations

Journal ArticleDOI
L.H. Brixner1, L.H. Brixner2, H.-Y. Chen1, H.-Y. Chen2, C.M. Foris1, C.M. Foris2 
TL;DR: In this paper, the structure of rare earth chlorotung states was determined and refined to an R value of 3.5% and the space group is P6/sub 3/m with La in 10-coordination and W in an unusual trigonally prismatic 6-coordinate.

36 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, highly crystalline monoclinic and tetragonal BiVO4 photocatalysts were obtained by the reaction of layered potassium vanadate powder (KV3O8 and K3V5O14) with Bi(NO3)3 for 3 days in aqueous media at room temperature.
Abstract: BiVO4 photocatalysts for O2 evolution, which work under visible light irradiation, were prepared by an aqueous process. The BiVO4 photocatalysts were obtained by the reaction of layered potassium vanadate powder (KV3O8 and K3V5O14) with Bi(NO3)3 for 3 days in aqueous media at room temperature. Highly crystalline monoclinic and tetragonal BiVO4 were selectively synthesized by changing the ratio of vanadium to bismuth in the starting materials. X-ray diffraction and scanning electron microscopy measurements showed that the monoclinic BiVO4 was formed via a tetragonal BiVO4 intermediate. Tetragonal BiVO4 with a 2.9 eV band gap mainly possessed an ultraviolet absorption band while monoclinic BiVO4 with a 2.4 eV band gap had a characteristic visible light absorption band in addition to the UV band. The UV bands observed in the tetragonal and monoclinic BiVO4 were assigned to the band transition from O2p to V3d whereas the visible light absorption was due to the transition from a valence band formed by Bi6s or ...

1,761 citations

Journal ArticleDOI
TL;DR: This review describes the crystal and electronic structures that are closely related to the photoelectrochemical properties of BiVO(4) and the latest efforts toward addressing these limitations in order to improve the performances of Bi VO(4)-based photoanodes are discussed.
Abstract: Harvesting energy directly from sunlight as nature accomplishes through photosynthesis is a very attractive and desirable way to solve the energy challenge. Many efforts have been made to find appropriate materials and systems that can utilize solar energy to produce chemical fuels. One of the most viable options is the construction of a photoelectrochemical cell that can reduce water to H2 or CO2 to carbon-based molecules. Bismuth vanadate (BiVO4) has recently emerged as a promising material for use as a photoanode that oxidizes water to O2 in these cells. Significant advancement in the understanding and construction of efficient BiVO4-based photoanode systems has been made within a short period of time owing to various newly developed ideas and approaches. In this review, the crystal and electronic structures that are closely related to the photoelectrochemical properties of BiVO4 are described first, and the photoelectrochemical properties and limitations of BiVO4 are examined. Subsequently, the latest efforts toward addressing these limitations in order to improve the performances of BiVO4-based photoanodes are discussed. These efforts include morphology control, formation of composite structures, composition tuning, and coupling oxygen evolution catalysts. The discussions and insights provided in this review reflect the most recent approaches and directions for general photoelectrode developments and they will be directly applicable for the understanding and improvement of other photoelectrode systems.

1,146 citations

Journal ArticleDOI
TL;DR: In this article, the photocatalytic activity of tetragonal BiVO4 for O2 evolution from an aqueous AgNO3 solution under visible light irradiation was negligible.
Abstract: BiVO4 powder with scheelite structure was obtained by hydrolyzing a nitric acid solution of Bi(NO3)3 and Na3VO4 with bases (Na2CO3 and NaHCO3) at room temperature. Tetragonal BiVO4 of a high-temperature form was obtained after 4.5 h of preparation time while monoclinic BiVO4 was done after 46 h. Although the structure and the band gap of tetragonal BiVO4 with scheelite structure were similar to those of monoclinic BiVO4, the photocatalytic activity of the tetragonal BiVO4 for O2 evolution from an aqueous AgNO3 solution under visible light irradiation was negligible. In contrast, the monoclinic BiVO4 showed high photocatalytic activity. Distortion of a Bi−O polyhedron by a 6s2 lone pair of Bi3+ plays an important role for high photocatalytic activity of the monoclinic BiVO4 under visible light irradiation.

947 citations

Journal ArticleDOI
TL;DR: In this paper, high-crystalline monoclinic scheelite BiVO4 powders are synthesized from aqueous Bi(NO3)3 and NH4VO3 solutions over a wide range of pH by a hydrothermal process.
Abstract: Highly crystalline monoclinic scheelite BiVO4 powders are synthesized from aqueous Bi(NO3)3 and NH4VO3 solutions over a wide range of pH by a hydrothermal process BiVO4 powders with various morphologies, surface textures, and grain shapes are selectively synthesized by adjusting the pH The dependence of the Raman peak position and intensity on the synthesis conditions indicates that the symmetry distortions in the local structure of the synthesized BiVO4 are affected by the preparation conditions These variations in the local structure result in the modification of the electronic structure of BiVO4, which results in a blue-shift in the UV-vis absorption spectrum of hydrothermally synthesized BiVO4 in comparison with a well-crystallized sample prepared by homogeneous coprecipitation The photocatalytic activities for O2 evolution from an aqueous AgNO3 solution under visible-light irradiation are strongly dependent on the pH used in the synthesis The differences in the photocatalytic activities between BiVO4 samples prepared under various conditions is attributed to the degree of structural distortion, leading to differences in the mobility of photogenerated holes formed in the valence band, which consists of Bi 6s and O 2p orbitals

810 citations

Journal ArticleDOI
TL;DR: In this article, the authors comprehensively review the structures, thermal expansion, phase transitions, electrical conductivity and stability of bismuth oxide and doped Bismuth Oxide systems and show that they exhibit a complex array of structures and properties depending upon the dopant concentration, temperature and atmosphere.
Abstract: Bismuth oxide systems exhibit high oxide ion conductivity and have been proposed as good electrolyte materials for applications such as solid oxide fuel cells and oxygen sensors. However, due to their instability under conditions of low oxygen partial pressures there has been difficulty in developing these materials as alternative electrolyte materials compared to the state-of-the-art cubic stabilised zirconia electrolyte. Bismuth oxide and doped bismuth oxide systems exhibit a complex array of structures and properties depending upon the dopant concentration, temperature and atmosphere. In this paper we comprehensively review the structures, thermal expansion, phase transitions, electrical conductivity and stability of bismuth oxide and doped bismuth oxide systems. ©

614 citations