Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Dengpeng Wang has a total of 9 co-authors. Here are the top co-authors by number of shared publications:

  • Feng Gao

    Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, MOE Key Laboratory of New Processing Technology for Non-Ferrous Metals and Materials, Guangxi University, Nanning 530004, China

    2 shared publications
  • Xianran Wang

    Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, MOE Key Laboratory of New Processing Technology for Non-Ferrous Metals and Materials, Guangxi University, Nanning 530004, China

    2 shared publications
  • Feng Ren

    Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, MOE Key Laboratory of New Processing Technology for Non-Ferrous Metals and Materials, Guangxi University, Nanning 530004, China

    1 shared publication
  • Jinlei Zhou

    Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, MOE Key Laboratory of New Processing Technology for Non-Ferrous Metals and Materials, Guangxi University, Nanning 530004, China

    1 shared publication
  • Kaituo Wang

    School of Resources, Environment and Materials, Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured Materials, MOE Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, Guangxi University, Nanning, Guangxi, 530004, PR China

    1 shared publication
  • Toyohisa Fujita

    School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China

    1 shared publication

Latest Publications

  • Open Access

    Detection of Cd2+ in Aqueous Solution by the Fluorescent Probe of CdSe/CdS QDs Based on OFF–ON Mode

    by Dengpeng Wang, Feng Gao, Xianran Wang, Xiaomei Ning, Kaituo Wang, Xinpeng Wang, Yuezhou Wei, Toyohisa Fujita

    The detection of heavy metals in aqueous solutions has always attracted much attention from all over the world. A fluorescent probe of CdSe/CdS core-shell quantum dots (QDs) was designed to detect trace Cd2+ in aqueous solutions using the OFF–ON mode rapidly and efficiently, likely based on adsorption and desorption reactions between ethylenediaminetetraacetic acid disodium salt (EDTA) and CdSe/CdS QDs. In the OFF mode, the optical shielding function of EDTA results in fluorescence quenching owing to the strong adsorption ability of EDTA with Cd2+ on the sites of CdSe/CdS QDs surface. In the ON mode, the introduction of Cd2+ promotes the desorption of EDTA from the EDTA-CdSe/CdS QDs and restores the fluorescence intensity. There were two linear response ranges which were 0.1–20 µmol/L and 20–90 µmol/L for the EDTA-CdSe/CdS system to detect Cd2+. The detection limit was 6 nmol/L, and the standard deviation was below 4% for the detection of Cd2+ concentration in tap water.


  • Open Access

    The Effects of Li+ Doping on Structure and Upconversion Luminescent Properties for Bi3.46Ho0.04Yb0.5Ti3O12: xLi Phosphors

    by Feng Ren, Jinlei Zhou, Dengpeng Wang, Xianran Wang, Feng Gao

    A series of novel Li+ doped Bi3.46Ho0.04Yb0.5Ti3O12 (BHYTO: xLi, 0 ≤ x ≤ 0.15) upconversion phosphors were prepared through a sol-gel-sintering method. There exist three emission bands centered at 545 nm, 658 nm, and 756 nm in the upconversion emission spectra at 980 nm excitation, corresponding to energy transitions of 5F4/5S2 → 5I8, 5F5 → 5I8 and 5F4/5S2 → 5I7 of Ho3+, and the upconversion emission intensity of BHYTO: 0.05Li is about 2.2 times stronger than that of BHYTO samples. The luminescent lifetime of the strongest emission (545 nm) is in the range of 45.25 to 65.99 μs for the different BHYTO: xLi phosphors. The energy transfers during the upconversion pumping process from Yb3+ to Ho3+ are mainly responsible for all the emissions, each belonging to a double-photon process. Li+ mainly entered into the interspace sites or occupied Bi3+ sites in Bi4Ti3O12 host during the fabrication process according to its dosage, and the possibility is very low for Li+ to take part in the energy transfer process directly due to its lack of matching levels with 4f of Ho3+ and Yb3+. However, Li+ doping can not only increase the size of crystal grains to improve crystallinity through XRD analysis, but also reduced oxygen vacancies to decrease the number of quenching centers through XPS analysis. The improved crystallinity and reduced quenching centers are proposed to be the main causes for the enhanced upconversion luminescence of the Li+ doped BHYTO phosphor.