JIE XING

Dr. JIE XING


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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15 February 2022 in Coatings
Verified
Journal Article
Open access
PDF file
SHShindume Lomboleni Hamukwaya
Shindume Lomboleni Hamukwaya
HHHuiying Hao
Huiying Hao
ZZZengying Zhao
Zengying Zhao
Jingjing DongJingjing Dong
Jingjing Dong
TZTingting Zhong
Tingting Zhong
MMMelvin M. Mashingaidze
Melvin M. Mashingaidze
The recent rapid development in perovskite solar cells (PSCs) has led to significant research interest due to their notable photovoltaic performance, currently exceeding 25% power conversion efficiency for small-area PSCs. The materials used to fabricate PSCs dominate the current photovoltaic market, especially with the rapid increase in efficiency and performance. The present work reviews recent developments in PSCs’ preparation and fabrication methods, the associated advantages and disadvantages, and methods for improving the efficiency of large-area perovskite films for commercial application. The work is structured in three parts. First is a brief overview of large-area PSCs, followed by a discussion of the preparation methods and methods to improve PSC efficiency, quality, and stability. Envisioned future perspectives on the synthesis and commercialization of large-area PSCs are discussed last. Most of the growth in commercial PSC applications is likely to be in building integrated photovoltaics and electric vehicle battery charging solutions. This review concludes that blade coating, slot-die coating, and ink-jet printing carry the highest potential for the scalable manufacture of large-area PSCs with moderate-to-high PCEs. More research and development are key to improving PSC stability and, in the long-term, closing the chasm in lifespan between PSCs and conventional photovoltaic cells.

19 January 2015 in Applied Physics Letters
Verified
Journal Article
Closed access
PDF file
JXJIE XING
JIE XING
EGEr-Jia Guo
Er-Jia Guo
JDJingjing Dong
Jingjing Dong
HHHuiying Hao
Huiying Hao
ZZZhiyuan Zheng
Zhiyuan Zheng
CZChangchun Zhao
Changchun Zhao
A high-sensitive and fast-response photodetector based on BiFeO3 (BFO) ferroelectric thin film is fabricated using coplanar electrode configuration. A large photocurrent/dark current ratio is found up to two orders of magnitude at 1 V bias. Enhanced photocurrent and rectification behavior of the photodetector are observed after applying high voltage pulses to the BFO film. The short-circuit current varies systematically with the poling process and increases linearly with the light density. On the contrary, the open-circuit voltage keeps as a constant during the measurements. We attribute these behaviors to the depolarization field and the interfacial fields at the film-electrode interfaces. The BFO device presents a peak response of 0.15 mA/W at 365 nm and the response speed is on the order of tens of nanoseconds. Our work highlights the potential application of photodetector based on the ferroelectric materials.

3 October 2017 in Discover Nano
Verified
Journal Article
Open access
PDF file
PLPengyu Liu
Pengyu Liu
TLTao Luo
Tao Luo
JXJIE XING
JIE XING
HXHong Xu
Hong Xu
HHHuiying Hao
Huiying Hao
JDJingjing Dong
Jingjing Dong
High-quality WS2 film with the single domain size up to 400 μm was grown on Si/SiO2 wafer by atmospheric pressure chemical vapor deposition. The effects of some important fabrication parameters on the controlled growth of WS2 film have been investigated in detail, including the choice of precursors, tube pressure, growing temperature, holding time, the amount of sulfur powder, and gas flow rate. By optimizing the growth conditions at one atmospheric pressure, we obtained tungsten disulfide single domains with an average size over 100 μm. Raman spectra, atomic force microscopy, and transmission electron microscopy provided direct evidence that the WS2 film had an atomic layer thickness and a single-domain hexagonal structure with a high crystal quality. And the photoluminescence spectra indicated that the tungsten disulfide films showed an evident layer-number-dependent fluorescence efficiency, depending on their energy band structure. Our study provides an important experimental basis for large-area, controllable preparation of atom-thick tungsten disulfide thin film and can also expedite the development of scalable high-performance optoelectronic devices based on WS2 film.

27 September 2016 in Journal of Physics D: Applied Physics
Verified
Journal Article
Closed access
PDF file
JDJianyu Du
Jianyu Du
JXJIE XING
JIE XING
CGChen Ge
Chen Ge
HLHao Liu
Hao Liu
PLPengyu Liu
Pengyu Liu
HGHua Gao
Hua Gao
We investigated a high-performance deep ultraviolet photodetector based on a β -gallium oxide ( β -Ga 2 O 3 ) nanowire network. β -Ga 2 O 3 nanowires were grown at different temperatures by a chemical vapor deposition method. X-ray diffraction, scanning electron microscopy, transmission electron microscopy and energy dispersive spectrum analysis were utilized to characterize the structure and morphology. With increasing the temperature, the nanowires became thicker and their surface appeared more rough with many kinks and branch-like shapes. It is proposed that the growth mechanism is dominated by a combination of vapor–liquid–solid and vapor–solid growth. A photodetector based on the best quality β -Ga 2 O 3 nanowire network was fabricated by a simple and cheap mask method, which exhibited excellent photoelectric performance. The responsive spectrum presented a peak response located at 231 nm with a sharp cutoff at 270 nm. The response rejection ratio of I 231 nm / I 290 nm is more than three orders of magnitude, demonstrating an intrinsic solar-blindness. The full width at half maximum of the response curve is only 1.2 ns under pulsed laser irradiation. The high sensitivity, superior selectivity, ultrafast response speed and simple fabrication technology show that the β -Ga 2 O 3 nanowire network has promising application in solar-blind photodetectors.

25 October 2022 in Nanomaterials
Verified
Journal Article
Open access
PDF file
SHShindume Lomboleni Hamukwaya
Shindume Lomboleni Hamukwaya
HHHuiying Hao
Huiying Hao
MMMelvin M. Mashingaidze
Melvin M. Mashingaidze
TZTingting Zhong
Tingting Zhong
STShu Tang
Shu Tang
HLHao Liu
Hao Liu
Lead-free, bismuth-based perovskite solar cells (PSCs) are promising, non-toxic, and stable alternatives to lead-based PSCs, which are environmentally harmful and highly unstable under deprived air conditions. However, bismuth-based PSCs still suffer from low-power-conversion efficiency (PCE) due to their large bandgap and poor film morphology. Their poor film-forming ability is the greatest obstacle to Cs₃Bi₂I₉ progress in thin-film solar cell technology. This study synthesizes novel, lead-free perovskites with a small bandgap, excellent stability, and highly improved photovoltaic performance by integrating different amounts of potassium iodide (KI) into a perovskite precursor solution. KI incorporation improves the crystallinity of the perovskite, increases the grain size, and decreases the potential contact distribution, which is demonstrated by X-ray diffraction, electronic scanning microscopy, atomic force microscopy, and ultraviolet-visible spectroscopy. The Cs₃Bi₂I₉ PSC device with 2 vol. % incorporation of KI shows the highest PCE of 2.81% and Voc of 1.01 V as far as all the Bi-based cells fabricated for this study are concerned. The study demonstrates that incorporating KI in the Cs₃Bi₂I₉ perovskite layer highly stabilizes the resultant PSC device against humidity to the extent that it maintains 98% of the initial PCE after 90 days, which is suitable for solar cell applications. The devices also demonstrate greater resistance to airborne contaminants and high temperatures without encapsulation, opening up new possibilities for lead-free Cs₃Bi₂I₉ PSCs in future commercialization.

6 April 2023 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
ZGZihao Guo
Zihao Guo
JLJinhui Liu
Jinhui Liu
XHXu Han
Xu Han
FMFangyuan Ma
Fangyuan Ma
DRDongke Rong
Dongke Rong
JXJIE XING
JIE XING