Xingzhong Guo

Dr. Xingzhong Guo

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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6 January 2016 in Journal of Sol-Gel Science and Technology
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Journal Article
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Xingzhong GuoXingzhong Guo
Xingzhong Guo
QZQilong Zhang
Qilong Zhang
XDXingeng Ding
Xingeng Ding
QSQianhong Shen
Qianhong Shen
CWChunchun Wu
Chunchun Wu
HYHui Yang
Hui Yang

12 February 2020 in Small
Verified
Journal Article
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HLHuanyun Liao
Huanyun Liao
Xingzhong GuoXingzhong Guo
Xingzhong Guo
YHYang Hou
Yang Hou
HLHao Liang
Hao Liang
ZZZheng Zhou
Zheng Zhou
HYHui Yang
Hui Yang

1 July 2019 in Applied Surface Science
Verified
Journal Article
Closed access
HYHui Yang
Hui Yang
SBShengchi Bai
Shengchi Bai
Xingzhong GuoXingzhong Guo
Xingzhong Guo
HWHaifeng Wang
Haifeng Wang

21 January 2025 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
ZXZhou Xu
Zhou Xu
Xingzhong GuoXingzhong Guo
Xingzhong Guo
XZXuemei Zeng
Xuemei Zeng
JLJunxiang Liu
Junxiang Liu
JYJingran Yin
Jingran Yin
TLTongchao Liu
Tongchao Liu

28 January 2021 in Sustainable Energy & Fuels
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Journal Article
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FLFu Liu
Fu Liu
Xingzhong GuoXingzhong Guo
Xingzhong Guo
YHYang Hou
Yang Hou
FWFan Wang
Fan Wang
CZChang Zou
Chang Zou
HYHui Yang
Hui Yang
Electrochemical water splitting provides a prominent route towards clean energy conversion and storage, while unsuitable catalysts restrict its application. Core–shell hierarchical heterostructure materials with strong synergistic effects based on non-noble metal elements have been developed to compensate for inadequacy. In this work, a core–shell hierarchical heterostructure Co9S8/Ni3S2@NiFe-LDH electrocatalyst was prepared via hydrothermal and electrodeposition methods. The resultant Co9S8/Ni3S2@NiFe-120 electrocatalyst consists of Co9S8 substrates as the core and NiFe-LDHs as the shell, and exhibits excellent overall water splitting electrocatalytic activity with a low overpotential of 229 mV for the oxygen evolution reaction (OER), and 151 mV for the hydrogen evolution reaction (HER) and a full cell voltage of 1.62 V at 10 mA cm−2 current density. The core–shell heterostructure constructed by electrodeposition endows the catalyst with outstanding stability and low degradation in long-term catalytic processes as shown by continuous chronopotentiometry tests at current densities of 50, 100 and 200 mA cm−2 for 72 h. The as-prepared core–shell hierarchically heterostructural Co9S8/Ni3S2@NiFe-120 with high-efficiency and good-durability is a promising bifunctional electrocatalyst towards practical applications in overall water splitting.

30 January 2017 in RSC Advances
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Journal Article
Open access
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Xingzhong GuoXingzhong Guo
Xingzhong Guo
ZWZichen Wang
Zichen Wang
WZWenjun Zhu
Wenjun Zhu
HYHui Yang
Hui Yang
Multilayer molybdenum disulfide (MoS2) was facilely prepared by a chelation-assisted sol–gel method with ammonium molybdate tetrahydrate ((NH4)6Mo7O24·4H2O) as the molybdenum source, thioacetamide (CH3CSNH2) as the sulfur source and diethylenetriamine pentaacetic acid (Dtpa) as the chelating agent, subsequently followed by high-temperature calcination. The chelating agent Dtpa ingeniously mediated the chelation reaction of the system and promoted the formation of a monolithic gel. The hexagonal MoS2 crystal (2H-MoS2) with good crystallinity precipitated after calcination at 1000 °C with the Mo and S mass ratio of 1 : 3. The adjustable MoS2 layers stacked together to form MoS2 flakes, and these flakes aggregated to construct crystalline MoS2 particles. The electrochemical tests showed the possibility of as-prepared MoS2 crystals applied as a negative electrode for lithium ion batteries.