Jianguo Liu

Prof. Jianguo Liu

Key Laboratory of Environmental Optics and Technology, Anhui Institute of Optics and Fine Mechanics, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, China
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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1 December 2017 in Atmospheric Chemistry and Physics
Verified
Journal Article
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CXChengzhi Xing
Chengzhi Xing
WTWei Tan
Wei Tan
SWShanshan Wang
Shanshan Wang
KCKa Lok Chan
Ka Lok Chan
YGYang Gao
Yang Gao
Jianguo LiuJianguo Liu
Jianguo Liu
Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) and lidar measurements were performed in Shanghai, China, during May 2016 to investigate the vertical distribution of summertime atmospheric pollutants. In this study, vertical profiles of aerosol extinction coefficient, nitrogen dioxide (NO2) and formaldehyde (HCHO) concentrations were retrieved from MAX-DOAS measurements using the Heidelberg Profile (HEIPRO) algorithm, while vertical distribution of ozone (O3) was obtained from an ozone lidar. Sensitivity study of the MAX-DOAS aerosol profile retrieval shows that the a priori aerosol profile shape has significant influences on the aerosol profile retrieval. Aerosol profiles retrieved from MAX-DOAS measurements with Gaussian a priori profile demonstrate the best agreements with simultaneous lidar measurements and vehicle-based tethered-balloon observations among all a priori aerosol profiles. Tropospheric NO2 vertical column densities (VCDs) measured with MAX-DOAS show a good agreement with OMI satellite observations with a Pearson correlation coefficient (R) of 0.95. In addition, measurements of the O3 vertical distribution indicate that the ozone productions do not only occur at surface level but also at higher altitudes (about 1.1 km). Planetary boundary layer (PBL) height and horizontal and vertical wind field information were integrated to discuss the ozone formation at upper altitudes. The results reveal that enhanced ozone concentrations at ground level and upper altitudes are not directly related to horizontal and vertical transportation. Similar patterns of O3 and HCHO vertical distributions were observed during this campaign, which implies that the ozone productions near the surface and at higher altitudes are mainly influenced by the abundance of volatile organic compounds (VOCs) in the lower troposphere.

2 February 2007 in Optics Letters
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Journal Article
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YYYue Yang
Yue Yang
GKGuiyun Kai
Guiyun Kai
ZWZhi Wang
Zhi Wang
TSTingting Sun
Tingting Sun
LJLong JIN
Long JIN
XDXiaoyi Dong
Xiaoyi Dong
We propose a novel polarization-maintaining index-guiding photonic crystal fiber (PCF). It is composed of a solid silica core and a cladding with squeezed-hexagonal-lattice elliptical air holes. Using a full-vector finite-element method, we study the modal birefringence of the fundamental modes in such PCFs. Numerical result shows that very high modal birefringence with a magnitude of the order of 10−2 around 1550 nm has been obtained. Furthermore, large normal dispersion appears over a wide range of wavelengths in both orthogonal polarizations.

1 January 2019 in Atmospheric Research
Verified
Journal Article
Closed access
Yan XiangYan Xiang
Yan Xiang
TZTianshu Zhang
Tianshu Zhang
Jianguo LiuJianguo Liu
Jianguo Liu
LLLihui Lv
Lihui Lv
YDYunsheng Dong
Yunsheng Dong
ZCZhenyi Chen
Zhenyi Chen

13 November 2019 in Light: Science & Applications
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Chengxin ZhangChengxin Zhang
Chengxin Zhang
WTWei Tan
Wei Tan
QHQihou Hu
Qihou Hu
ZCZhaonan Cai
Zhaonan Cai
WSWenjing Su
Wenjing Su
Jianguo LiuJianguo Liu
Jianguo Liu
Abundances of a range of air pollutants can be inferred from satellite UV-Vis spectroscopy measurements by using the unique absorption signatures of gas species. Here, we implemented several spectral fitting methods to retrieve tropospheric NO2, SO2, and HCHO from the ozone monitoring instrument (OMI), with radiative simulations providing necessary information on the interactions of scattered solar light within the atmosphere. We analyzed the spatial distribution and temporal trends of satellite-observed air pollutants over eastern China during 2005–2017, especially in heavily polluted regions. We found significant decreasing trends in NO2 and SO2 since 2011 over most regions, despite varying temporal features and turning points. In contrast, an overall increasing trend was identified for tropospheric HCHO over these regions in recent years. Furthermore, generalized additive models were implemented to understand the driving forces of air quality trends in China and assess the effectiveness of emission controls. Our results indicated that although meteorological parameters, such as wind, water vapor, solar radiation and temperature, mainly dominated the day-to-day and seasonal fluctuations in air pollutants, anthropogenic emissions played a unique role in the long-term variation in the ambient concentrations of NO2, SO2, and HCHO in the past 13 years. Generally, recent declines in NO2 and SO2 could be attributed to emission reductions due to effective air quality policies, and the opposite trends in HCHO may urge the need to control anthropogenic volatile organic compound (VOC) emissions.

29 April 2020 in Atmospheric Chemistry and Physics
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FMFanhao Meng
Fanhao Meng
MQMin Qin
Min Qin
KTKe Tang
Ke Tang
JDJun Duan
Jun Duan
WFWu Fang
Wu Fang
WLWenqing Liu
Wenqing Liu
Nitrous acid (HONO), an important precursor of the hydroxyl radical (OH), plays a key role in atmospheric chemistry, but its sources are still debated. The production of HONO on aerosol surfaces or on ground surfaces in nocturnal atmospheres remains controversial. The vertical profile provides vertical information on HONO and NO2 to understand the nocturnal HONO production and loss. In this study, we report the first high-resolution (<2.5 m) nocturnal vertical profiles of HONO and NO2 measured from in situ instruments on a movable container that was lifted on the side wiring of a 325 m meteorological tower in Beijing, China. High-resolution vertical profiles revealed the negative gradients of HONO and NO2 in nocturnal boundary layers, and a shallow inversion layer affected the vertical distribution of HONO. The vertical distribution of HONO was consistent with stratification and layering in the nocturnal urban atmosphere below 250 m. The increase in the HONO ∕ NO2 ratio was observed throughout the column from the clean episode to the haze episode, and relatively constant HONO∕NO2 ratios in the residual layer were observed during the haze episode. Direct HONO emissions from traffic contributed 29.3 % ± 12.4 % to the ambient HONO concentrations at night. The ground surface dominates HONO production by heterogeneous uptake of NO2 during clean episodes. In contrast, the HONO production on aerosol surfaces (30–300 ppt) explained the observed HONO increases (15–368 ppt) in the residual layer, suggesting that the aerosol surface dominates HONO production aloft during haze episodes, while the surface production of HONO and direct emissions into the overlying air are minor contributors. Average dry deposition rates of 0.74±0.31 and 1.55±0.32 ppb h−1 were estimated during the clean and haze episodes, respectively, implying that significant quantities of HONO could be deposited to the ground surface at night. Our results highlight the ever-changing contributions of aerosol and ground surfaces in nocturnal HONO production at different pollution levels and encourage more vertical gradient observations to evaluate the contributions from varied HONO sources.

1 January 2014 in Journal of Environmental Sciences
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Journal Article
Closed access
XZXuliang Zhuang
Xuliang Zhuang
YWYuesi Wang
Yuesi Wang
HHHong He
Hong He
Jianguo LiuJianguo Liu
Jianguo Liu
Xinming WangXinming Wang
Xinming Wang
JMJinzhu Ma
Jinzhu Ma