Weiping Gong

Prof. Weiping Gong

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 July 2020 in Materials
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Journal Article
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Sergey UshakovSergey Ushakov
Sergey Ushakov
Shmuel HayunShmuel Hayun
Shmuel Hayun
WGWeiping Gong
Weiping Gong
ANAlexandra Navrotsky
Alexandra Navrotsky
Phase transformations in multicomponent rare earth sesquioxides were studied by splat quenching from the melt, high temperature differential thermal analysis and synchrotron X-ray diffraction on laser-heated samples. Three compositions were prepared by the solution combustion method: (La,Sm,Dy,Er,RE)2O3, where all oxides are in equimolar ratios and RE is Nd or Gd or Y. After annealing at 800 °C, all powders contained mainly a phase of C-type bixbyite structure. After laser melting, all samples were quenched in a single-phase monoclinic B-type structure. Thermal analysis indicated three reversible phase transitions in the range 1900–2400 °C, assigned as transformations into A, H, and X rare earth sesquioxides structure types. Unit cell volumes and volume changes on C-B, B-A, and H-X transformations were measured by X-ray diffraction and consistent with the trend in pure rare earth sesquioxides. The formation of single-phase solid solutions was predicted by Calphad calculations. The melting point was determined for the (La,Sm,Dy,Er,Nd)2O3 sample as 2456 ± 12 °C, which is higher than for any of constituent oxides. An increase in melting temperature is probably related to nonideal mixing in the solid and/or the melt and prompts future investigation of the liquidus surface in Sm2O3-Dy2O3, Sm2O3-Er2O3, and Dy2O3-Er2O3 systems.

7 September 2023 in Journal of the European Ceramic Society
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Journal Article
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MXMingjun Xie
Mingjun Xie
XLXiao Li
Xiao Li
YLYuanming Lai
Yuanming Lai
CQCong Qi
Cong Qi
JYJun Yin
Jun Yin
CWChongsheng Wu
Chongsheng Wu

5 March 2023 in Scripta Materialia
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Journal Article
Closed access
XNXiang Niu
Xiang Niu
WLWei Liang
Wei Liang
Xiaodong JianXiaodong Jian
Xiaodong Jian
HTHui Tang
Hui Tang
TWTing Wang
Ting Wang
SLSheng-Guo Lu
Sheng-Guo Lu

17 September 2018 in Journal of Materials Science
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Journal Article
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RGR. Grote
R. Grote
MZM. Zhao
M. Zhao
LSLindsay Shuller-Nickles
Lindsay Shuller-Nickles
JAJ. Amoroso
J. Amoroso
WGWeiping Gong
Weiping Gong
KBKyle S. Brinkman
Kyle S. Brinkman

18 October 2021 in Advanced Optical Materials
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QLQiuguo Li
Qiuguo Li
HRHao Rao
Hao Rao
XMXinzhou Ma
Xinzhou Ma
HMHaijuan Mei
Haijuan Mei
ZZZhengting Zhao
Zhengting Zhao
Xianguang YangXianguang Yang
Xianguang Yang
Physical characteristics of Cu2Te are poorly investigated due to limited Te sources available and unclear atomic positions of crystal structure. Herein, hexagonal Cu2Te microdisks are successfully prepared via chemical vapor deposition procedure using GaTe as Te source. The epitaxial growth mechanism of the Cu2Te hexagonal structures with the orthorhombic phase is rationalized by proposed layer‐over‐layer growth model. The photoluminescence (PL) spectrum of Cu2Te microdisks shows a new red emission band in addition to usual infrared light emission due to Cu deficiency. Single Cu2Te microdisk operates as an optical microcavity supporting whispering gallery modes for red lasing around 627.5 nm. This Cu2Te microdisk microcavity exhibits a high quality factor of 1568 and a low lasing threshold of 125 kW cm−2 at room temperature. Meanwhile, Cu2Te microdisks have been exhibited as an ideal platform for surface enhanced Raman scattering (SERS) eliminating drawbacks of noble metal substrates with detection limitation to nanomolar level and an enhancement factor of ≈1.95 × 105. Hexagonal Cu2Te microdisks turn out to be an efficient microcavity for red lasing and low‐cost nonmetallic SERS substrates, opening potential applications in photonics and biological detection of aromatic molecules.

15 October 2017 in Journal of the American Ceramic Society
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Journal Article
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WGWeiping Gong
Weiping Gong
LWLili Wu
Lili Wu
ANAlexandra Navrotsky
Alexandra Navrotsky