Jianli Wang

Prof. Dr. Jianli Wang


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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14 February 2019 in ACS Catalysis
Verified
Journal Article
Closed access
HBHazi Ahmad Beejapur
Hazi Ahmad Beejapur
QZQi Zhang
Qi Zhang
KHKecheng Hu
Kecheng Hu
LZLi Zhu
Li Zhu
JWJianli Wang
Jianli Wang
Zhibin YeZhibin Ye
Zhibin Ye

8 April 2019 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
JTJun Tang
Jun Tang
XZXue Zhou
Xue Zhou
SCShixiong Cao
Shixiong Cao
LZLingyu Zhu
Lingyu Zhu
LXLingling Xi
Lingling Xi
JWJianli Wang
Jianli Wang

1 April 2020 in ACS Omega
Verified
Journal Article
Open access
JLJunbin Liao
Junbin Liao
ZLZhen Liu
Zhen Liu
JWJianli Wang
Jianli Wang
Zhibin YeZhibin Ye
Zhibin Ye
Binder, as one of the key components, plays a crucial role in improving the capacity and cycling performance of lithium–sulfur (Li–S) batteries. In this work, commercially available, low-cost, water-soluble polyvinyl alcohol (PVA) has been systematically investigated as a functional polymer binder for high-sulfur-loading cathodes, with the aim of enhancing sulfur utilization, reducing capacity decay, and extending cycling life of the cathodes. In comparison with polyvinylidene fluoride as a conventional binder, PVA shows a valuable polysulfide entrapping ability and a much stronger binding strength. Its superior polysulfide entrapping ability has been verified through theoretical density functional theory calculations and an experimental ex situ adsorption study. In electrochemical Li–S battery performance evaluation, at a sulfur loading density of 3.5 mg cm–2, the sulfur cathode assembled with the PVA binder displays at 0.5 C a very slow capacity decay of only 0.010% per cycle over 250 cycles. Additionally, the strong binding strength of PVA allows the fabrication of thick sulfur cathodes with a high sulfur loading density of 10.5 mg cm–2, which shows a high areal capacity of 4.0 mA h cm–2 and a high cycling stability (capacity decay of 0.1% per cycle). In consideration of the superior capacity retention and cycling performance of its enabled cathodes, the cost-effective PVA is a promising candidate for high-sulfur-loading cathodes in practical applications.

1 July 2019 in Journal of Hazardous Materials
Verified
Journal Article
Closed access
MZMing-Yong Zhou
Ming-Yong Zhou
PZPeng Zhang
Peng Zhang
LFLi-Feng Fang
Li-Feng Fang
BZBaoku Zhu
Baoku Zhu
JWJianli Wang
Jianli Wang
Heba AbdallahHeba Abdallah
Heba Abdallah

8 November 2012 in ChemCatChem
Verified
Journal Article
Closed access
PDF file
ZZZhi Zheng
Zhi Zheng
JWJianli Wang
Jianli Wang
MZMiao Zhang
Miao Zhang
LXLixin Xu
Lixin Xu
JJJianbing Ji
Jianbing Ji

23 December 2020 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
XLXiaobo Liu
Xiaobo Liu
YMYuhua Mao
Yuhua Mao
SYSiyang Yu
Siyang Yu
HZHao Zhang
Hao Zhang
KHKecheng Hu
Kecheng Hu
JWJianli Wang
Jianli Wang
Green and efficient catalysts for the production of biodiesel are highly important. In this study, a Pickering magnetic interface biocatalyst (Fe3O4@PS-NH-lipase) was prepared, which can effectively stabilize the soybean oil-in-methanol emulsion and achieve static transesterification. When the appropriate methanol/soybean oil molar ratio and catalyst loading were chosen, the Pickering interface biocatalyst exhibited outstanding enzymatic activity, reaching a conversion rate of 89.3% after 30 h. Pickering interfacial catalysis (PIC, immobilizing catalytic centers on a carrier and combining it with a Pickering emulsion) shows more significant specific activity, leading to a 1.2-fold improvement in catalytic performance as compared to Pickering assisted catalysis (PAC, relying on the use of nanoparticles for stabilizing Pickering emulsions together with a homogeneous catalyst). Moreover, the recycled catalyst still possesses significant catalytic activity after 5 cycles. This article provides a green and efficient strategy for the effective recovery of biologically active substances and the enhancement of biphasic reactions.