Jin-Song Hu

Prof. Dr. Jin-Song Hu

Institute of Chemistry, Chinese Academy of Science, Beijing 100190, China

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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4 August 2008 in Advanced Materials
Verified
Journal Article
Open access
PDF file
YGYu‐Guo Guo
Yu‐Guo Guo
Jin-Song HuJin-Song Hu
Jin-Song Hu
LWLi‐Jun Wan
Li‐Jun Wan
One of the greatest challenges for our society is providing powerful electrochemical energy conversion and storage devices. Rechargeable lithium‐ion batteries and fuel cells are amongst the most promising candidates in terms of energy densities and power densities. Nanostructured materials are currently of interest for such devices because of their high surface area, novel size effects, significantly enhanced kinetics, and so on. This Progress Report describes some recent developments in nanostructured anode and cathode materials for lithium‐ion batteries, addressing the benefits of nanometer‐size effects, the disadvantages of ‘nano’, and strategies to solve these issues such as nano/micro hierarchical structures and surface coatings, as well as developments in the discovery of nanostructured Pt‐based electrocatalysts for direct methanol fuel cells (DMFCs). Approaches to lowering the cost of Pt catalysts include the use of i) novel nanostructures of Pt, ii)new cost‐effective synthesis routes, iii) binary or multiple catalysts, and iv) new catalyst supports. magnified image

4 March 2016 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
Wenjie JiangWenjie Jiang
Wenjie Jiang
Lin GuoLin Guo
Lin Guo
LLLi Li
Li Li
YZYun Zhang
Yun Zhang
XZXing Zhang
Xing Zhang
LWLi-Jun Wan
Li-Jun Wan

12 September 2006 in Advanced Materials
Verified
Journal Article
Closed access
PDF file
LZL.‐S. Zhong
L.‐S. Zhong
Jin-Song HuJin-Song Hu
Jin-Song Hu
HLH.‐P. Liang
H.‐P. Liang
ACA.‐M. Cao
A.‐M. Cao
WSWeiguo Song
Weiguo Song
LWL.‐J. Wan
L.‐J. Wan

15 December 2008 in Advanced Functional Materials
Verified
Journal Article
Closed access
PDF file
WZWei‐Ming Zhang
Wei‐Ming Zhang
XWXing‐Long Wu
Xing‐Long Wu
Jin-Song HuJin-Song Hu
Jin-Song Hu
YGYu‐Guo Guo
Yu‐Guo Guo
LWLi‐Jun Wan
Li‐Jun Wan

18 March 2008 in Advanced Materials
Verified
Journal Article
Closed access
PDF file
WZWei‐Ming Zhang
Wei‐Ming Zhang
Jin-Song HuJin-Song Hu
Jin-Song Hu
YGYu‐Guo Guo
Yu‐Guo Guo
SZShu‐Fa Zheng
Shu‐Fa Zheng
LZLiang‐Shu Zhong
Liang‐Shu Zhong
LWLi‐Jun Wan
Li‐Jun Wan

19 March 2021 in Nature Communications
Verified
Journal Article
Open access
PDF file
GYGege Yang
Gege Yang
JZJiawei Zhu
Jiawei Zhu
PYPengfei Yuan
Pengfei Yuan
YHYongfeng Hu
Yongfeng Hu
GQGan Qu
Gan Qu
JZJia-Nan Zhang
Jia-Nan Zhang
As low-cost electrocatalysts for oxygen reduction reaction applied to fuel cells and metal-air batteries, atomic-dispersed transition metal-nitrogen-carbon materials are emerging, but the genuine mechanism thereof is still arguable. Herein, by rational design and synthesis of dual-metal atomically dispersed Fe,Mn/N-C catalyst as model object, we unravel that the O2 reduction preferentially takes place on FeIII in the FeN4 /C system with intermediate spin state which possesses one eg electron (t2g4eg1) readily penetrating the antibonding π-orbital of oxygen. Both magnetic measurements and theoretical calculation reveal that the adjacent atomically dispersed Mn-N moieties can effectively activate the FeIII sites by both spin-state transition and electronic modulation, rendering the excellent ORR performances of Fe,Mn/N-C in both alkaline and acidic media (halfwave positionals are 0.928 V in 0.1 M KOH, and 0.804 V in 0.1 M HClO4), and good durability, which outperforms and has almost the same activity of commercial Pt/C, respectively. In addition, it presents a superior power density of 160.8 mW cm−2 and long-term durability in reversible zinc–air batteries. The work brings new insight into the oxygen reduction reaction process on the metal-nitrogen-carbon active sites, undoubtedly leading the exploration towards high effective low-cost non-precious catalysts.