Jinli Qiao

Jinli Qiao


Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

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

Representative Publications

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1 January 2014 in Chemical Society Reviews
Verified
Journal Article
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PDF file
JQJinli Qiao
Jinli Qiao
YLYuyu Liu
Yuyu Liu
FHFeng Hong
Feng Hong
JZJiujun Zhang
Jiujun Zhang
This paper reviews recent progress made in identifying electrocatalysts for carbon dioxide (CO2) reduction to produce low-carbon fuels, including CO, HCOOH/HCOO−, CH2O, CH4, H2C2O4/HC2O4 −, C2H4, CH3OH, CH3CH2OH and others. The electrocatalysts are classified into several categories, including metals, metal alloys, metal oxides, metal complexes, polymers/clusters, enzymes and organic molecules. The catalyts' activity, product selectivity, Faradaic efficiency, catalytic stability and reduction mechanisms during CO2 electroreduction have received detailed treatment. In particular, we review the effects of electrode potential, solution–electrolyte type and composition, temperature, pressure, and other conditions on these catalyst properties. The challenges in achieving highly active and stable CO2 reduction electrocatalysts are analyzed, and several research directions for practical applications are proposed, with the aim of mitigating performance degradation, overcoming additional challenges, and facilitating research and development in this area.

6 February 2017 in Chemical Society Reviews
Verified
Journal Article
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YZYun Zheng
Yun Zheng
JWJianchen Wang
Jianchen Wang
BYBo Yu
Bo Yu
WZWenqiang Zhang
Wenqiang Zhang
JCJing Chen
Jing Chen
JZJiujun Zhang
Jiujun Zhang
High-temperature solid oxide electrolysis cells (SOECs) are advanced electrochemical energy storage and conversion devices with high conversion/energy efficiencies. They offer attractive high-temperature co-electrolysis routes that reduce extra CO2 emissions, enable large-scale energy storage/conversion and facilitate the integration of renewable energies into the electric grid. Exciting new research has focused on CO2 electrochemical activation/conversion through a co-electrolysis process based on the assumption that difficult CO double bonds can be activated effectively through this electrochemical method. Based on existing investigations, this paper puts forth a comprehensive overview of recent and past developments in co-electrolysis with SOECs for CO2 conversion and utilization. Here, we discuss in detail the approaches of CO2 conversion, the developmental history, the basic principles, the economic feasibility of CO2/H2O co-electrolysis, and the diverse range of fuel electrodes as well as oxygen electrode materials. SOEC performance measurements, characterization and simulations are classified and presented in this paper. SOEC cell and stack designs, fabrications and scale-ups are also summarized and described. In particular, insights into CO2 electrochemical conversions, solid oxide cell material behaviors and degradation mechanisms are highlighted to obtain a better understanding of the high temperature electrolysis process in SOECs. Proposed research directions are also outlined to provide guidelines for future research.

2 May 2013 in Chemical Society Reviews
Verified
Journal Article
Closed access
PDF file
YWYan-Jie Wang
Yan-Jie Wang
JQJinli Qiao
Jinli Qiao
RBRyan Baker
Ryan Baker
JZJiujun Zhang
Jiujun Zhang
In this review, we examine the most recent progress and research trends in the area of alkaline polymer electrolyte membrane (PEM) development in terms of material selection, synthesis, characterization, and theoretical approach, as well as their fabrication into alkaline PEM-based membrane electrode assemblies (MEAs) and the corresponding performance/durability in alkaline polymer electrolyte membrane fuel cells (PEMFCs). Respective advantages and challenges are also reviewed. To overcome challenges hindering alkaline PEM technology advancement and commercialization, several research directions are then proposed.

1 February 2014 in Advanced Energy Materials
Verified
Journal Article
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XZXuejun Zhou
Xuejun Zhou
JQJinli Qiao
Jinli Qiao
LYLin Yang
Lin Yang
JZJiujun Zhang
Jiujun Zhang

1 December 2009 in International Journal of Hydrogen Energy
Verified
Journal Article
Closed access
WDWei Dai
Wei Dai
HWHaijiang Wang
Haijiang Wang
XYXiao-Zi Yuan
Xiao-Zi Yuan
JMJonathan J. Martin
Jonathan J. Martin
DYDaijun Yang
Daijun Yang
JMJianxin Ma
Jianxin Ma

16 December 2021 in Nano-Micro Letters
Verified
Journal Article
Open access
PDF file
FDFang Dong
Fang Dong
MWMingjie Wu
Mingjie Wu
ZCZhangsen Chen
Zhangsen Chen
Xianhu LiuXianhu Liu
Xianhu Liu
GZGaixia Zhang
Gaixia Zhang
Shuhui SunShuhui Sun
Shuhui Sun
Rechargeable zinc-air batteries (ZABs) are currently receiving extensive attention because of their extremely high theoretical specific energy density, low manufacturing costs, and environmental friendliness. Exploring bifunctional catalysts with high activity and stability to overcome sluggish kinetics of oxygen reduction reaction and oxygen evolution reaction is critical for the development of rechargeable ZABs. Atomically dispersed metal-nitrogen-carbon (M-N-C) catalysts possessing prominent advantages of high metal atom utilization and electrocatalytic activity are promising candidates to promote oxygen electrocatalysis. In this work, general principles for designing atomically dispersed M-N-C are reviewed. Then, strategies aiming at enhancing the bifunctional catalytic activity and stability are presented. Finally, the challenges and perspectives of M-N-C bifunctional oxygen catalysts for ZABs are outlined. It is expected that this review will provide insights into the targeted optimization of atomically dispersed M-N-C catalysts in rechargeable ZABs.