Le He

Prof. Dr. Le He


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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13 December 2019 in Advanced Energy Materials
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Journal Article
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NHNa Han
Na Han
PDPan Ding
Pan Ding
LHLe He
Le He
YLYouyong Li
Youyong Li
YLYanguang Li
Yanguang Li

26 July 2021 in Nature Energy
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Journal Article
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MCMujin Cai
Mujin Cai
ZWZhiyi Wu
Zhiyi Wu
ZLZhao Li
Zhao Li
LWLu Wang
Lu Wang
WSWei Sun
Wei Sun
XZXiaohong Zhang
Xiaohong Zhang

11 May 2012 in Accounts of Chemical Research
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Journal Article
Closed access
LHLe He
Le He
MWMingsheng Wang
Mingsheng Wang
JGJianping Ge
Jianping Ge
YYYadong Yin
Yadong Yin

25 May 2010 in Chemistry – A European Journal
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Journal Article
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MYMiaomiao Ye
Miaomiao Ye
QZQiao Zhang
Qiao Zhang
YHYongxing Hu
Yongxing Hu
JGJianping Ge
Jianping Ge
ZLZhenda Lu
Zhenda Lu
YYYadong Yin
Yadong Yin
Core–shell structured Fe3O4/SiO2/TiO2 nanocomposites with enhanced photocatalytic activity that are capable of fast magnetic separation have been successfully synthesized by combining two steps of a sol–gel process with calcination. The as‐obtained core–shell structure is composed of a central magnetite core with a strong response to external fields, an interlayer of SiO2, and an outer layer of TiO2 nanocrystals with a tunable average size. The convenient control over the size and crystallinity of the TiO2 nanocatalysts makes it possible to achieve higher photocatalytic efficiency than that of commercial photocatalyst Degussa P25. The photocatalytic activity increases as the thickness of the TiO2 nanocrystal shell decreases. The presence of SiO2 interlayer helps to enhance the photocatalytic efficiency of the TiO2 nanocrystal shell as well as the chemical and thermal stability of Fe3O4 core. In addition, the TiO2 nanocrystals strongly adhere to the magnetic supports through covalent bonds. We demonstrate that this photocatalyst can be easily recycled by applying an external magnetic field while maintaining their photocatalytic activity during at least eighteen cycles of use.

24 February 2021 in ACS Nano
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Journal Article
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ZWZhiyi Wu
Zhiyi Wu
CLChaoran Li
Chaoran Li
ZLZhao Li
Zhao Li
KFKai Feng
Kai Feng
MCMujin Cai
Mujin Cai
LHLe He
Le He

24 June 2023 in Nature Communications
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Journal Article
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SZShumin Zhang
Shumin Zhang
FZFeipeng Zhao
Feipeng Zhao
JCJiatang Chen
Jiatang Chen
JFJiamin Fu
Jiamin Fu
JLJing Luo
Jing Luo
Xueliang (Andy) SunXueliang (Andy) Sun
Xueliang (Andy) Sun
Solid electrolyte is vital to ensure all-solid-state batteries with improved safety, long cyclability, and feasibility at different temperatures. Herein, we report a new family of amorphous solid electrolytes, xLi2O-MCly (M = Ta or Hf, 0.8 ≤ x ≤ 2, y = 5 or 4). xLi2O-MCly amorphous solid electrolytes can achieve desirable ionic conductivities up to 6.6 × 10−3 S cm−1 at 25 °C, which is one of the highest values among all the reported amorphous solid electrolytes and comparable to those of the popular crystalline ones. The mixed-anion structural models of xLi2O-MCly amorphous SEs are well established and correlated to the ionic conductivities. It is found that the oxygen-jointed anion networks with abundant terminal chlorines in xLi2O-MCly amorphous solid electrolytes play an important role for the fast Li-ion conduction. More importantly, all-solid-state batteries using the amorphous solid electrolytes show excellent electrochemical performance at both 25 °C and −10 °C. Long cycle life (more than 2400 times of charging and discharging) can be achieved for all-solid-state batteries using the xLi2O-TaCl5 amorphous solid electrolyte at 400 mA g−1, demonstrating vast application prospects of the oxychloride amorphous solid electrolytes.