Chenshan Gao

Dr. Chenshan Gao

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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17 October 2023 in Nanomaterials
Verified
Journal Article
Open access
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HCHongyuan Cui
Hongyuan Cui
CGChenshan Gao
Chenshan Gao
PWPengwei Wang
Pengwei Wang
LLLijie Li
Lijie Li
HYHuaiyu Ye
Huaiyu Ye
YLYufei Liu
Yufei Liu
The adsorption properties of Cu, Ag, Zn, and Cd-modified SnP3 monolayers for H2S have been studied using density functional theory (DFT). Based on phonon spectrum calculations, a structurally stable intrinsic SnP3 monolayer was obtained, based on which four metal-modified SnP3 monolayers were constructed, and the band gaps of the modified SnP3 monolayers were significantly reduced. The adsorption capacity of Cu, Zn-modified SnP3 was better than that of Ag, Cd-modified SnP3. The adsorption energies of Cu-modified SnP3 and Zn-modified SnP3 for H2S were −0.749 eV and −0.639 eV, respectively. In addition, Cu-modified SnP3 exhibited chemisorption for H2S, while Zn-modified SnP3 exhibited strong physisorption, indicating that it can be used as a sensor substrate. Co-adsorption studies showed that ambient gases such as N2, O2, and H2O had little effect on H2S. The band gap change rate of Zn-modified SnP3 after adsorption of H2S was as high as −28.52%. Recovery time studies based on Zn-modified SnP3 showed that the desorption time of H2S was 0.064 s at 298 K. Therefore, Zn-modified SnP3 can be used as a promising sensor substrate for H2S due to its good selectivity, sensitivity, and fast recovery time.

15 January 2022 in Journal of Materials Research and Technology
Verified
Journal Article
Open access
XLXu Liu
Xu Liu
SLShizhen Li
Shizhen Li
CTChunjian Tan
Chunjian Tan
CGChenshan Gao
Chenshan Gao
YLYang Liu
Yang Liu
GZGuoqi Zhang
Guoqi Zhang

28 July 2021 in 2D Materials
Verified
Journal Article
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HTHongyu Tang
Hongyu Tang
CGChenshan Gao
Chenshan Gao
HYHuiru Yang
Huiru Yang
LSLeandro Nicolás Sacco
Leandro Nicolás Sacco
RSRobert Sokolovskij
Robert Sokolovskij
GZGuoqi Zhang
Guoqi Zhang
In this paper, tin oxidation (SnO x )/tin-sulfide (SnS) heterostructures are synthesized by the post-oxidation of liquid-phase exfoliated SnS nanosheets in air. We comparatively analyzed the NO2 gas response of samples with different oxidation levels to study the gas sensing mechanisms. The results show that the samples oxidized at 325 °C are the most sensitive to NO2 gas molecules, followed by the samples oxidated at 350 °C, 400 °C and 450 °C. The repeatabilities of 350 °C samples are better than that of 325 °C, and there is almost no shift in the baseline. Thus this work systematically analyzed the gas sensing performance of SnO x /SnS-based sensor oxidized at 350 °C. It exhibits a high response of 171% towards 1 ppb NO2, a wide detecting range (from 1 ppb to 1 ppm), and an ultra-low theoretical detection limit of 5 ppt, and excellent repeatability at room temperature. The sensor also shows superior gas selectivity to NO2 in comparison to several other gas molecules, such as NO, H2, SO2, CO, NH3, and H2O. After x-ray diffraction, x-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscope, and electron paramagnetic resonance characterizations combining first principle analysis, it is found that the outstanding NO2 sensing behavior may be attributed to three factors: the Schottky contact between electrodes and SnO x /SnS; active charge transfer in the surface and the interface layer of SnO x /SnS heterostructures; and numerous oxygen vacancies generated during the post-oxidation process, which provides more adsorption sites and superior bandgap modulation. Such a heterostructure-based room-temperature sensor can be fabricated in miniaturized size with low cost, making it possible for large-scale applications.

30 July 2022 in Physica E: Low-dimensional Systems and Nanostructures
Verified
Journal Article
Closed access
SHShuhan Hou
Shuhan Hou
ZWZhaokun Wang
Zhaokun Wang
HYHuiru Yang
Huiru Yang
JJJing Jiang
Jing Jiang
CGChenshan Gao
Chenshan Gao
HYHuaiyu Ye
Huaiyu Ye

1 December 2020 in Vacuum
Verified
Journal Article
Closed access
CGChenshan Gao
Chenshan Gao
XLXu Liu
Xu Liu
HYHuiru Yang
Huiru Yang
QZQuan Zhou
Quan Zhou
YZYingying Zhang
Yingying Zhang
GZGuoqi Zhang
Guoqi Zhang

8 September 2021 in Nanotechnology
Verified
Journal Article
Closed access
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QLQipeng Liu
Qipeng Liu
QZQuan Zhou
Quan Zhou
CGChenshan Gao
Chenshan Gao
LLLian Liu
Lian Liu
HYHuaiyu Ye
Huaiyu Ye
Hybrid supercapacitors have attracted considerable attention for the use in the energy storage systems due to the simultaneous possession of high power and energy. Herein, Co 3 O 4 array with amorphous carbon on Ni foam has been derived from the Co-MOF. The electrochemical dynamics and energy storage mechanism of the prepared electrode have been investigated, which reveals the enhancement of the capacitive behavior with the scan rate. The electrochemically active specific surface area (ECSA) of our sample is calculated as 1416 cm 2 for per square centimeter of electrode. The prepared material exhibits an excellent electrochemical performance (3.17 F · cm −2 at 1 mA · cm −2 and 2.076 F · cm −2 at 30 mA · cm −2 ). Further, the long-term life shows 96.7% capacity retention at 50 mV · s −1 after 20 000 cycles in KOH aqueous electrolyte. The Coulomb efficiency is noted to range from 95% to 100% even after 20 000 cycles. Further, the symmetrical solid-state supercapacitor represents a wide operating voltage range and high scan rate for practical applications. Three charged solid-state supercapacitors are observed to lit 160 parallel green LEDs (20 mA, 2.2V) for approximately 50 s. These findings from this study confirm the potential of Co 3 O 4 array with carbon hybridization as an effective supercapacitor electrode material.