Huang Zheng-hong

Dr. Huang Zheng-hong

State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, 100084, PR China
+1
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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15 October 2015 in Advanced Functional Materials
Verified
Journal Article
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QLQinghua Liang
Qinghua Liang
ZLZhi Li
Zhi Li
Huang Zheng-hongHuang Zheng-hong
Huang Zheng-hong
FKFeiyu Kang
Feiyu Kang
QYQuan‐Hong Yang
Quan‐Hong Yang

2 July 2015 in Advanced Materials
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Journal Article
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QLQinghua Liang
Qinghua Liang
ZLZhi Li
Zhi Li
XYXiaoliang Yu
Xiaoliang Yu
Huang Zheng-hongHuang Zheng-hong
Huang Zheng-hong
FKFeiyu Kang
Feiyu Kang
QYQuan‐Hong Yang
Quan‐Hong Yang

16 September 2014 in Nanoscale
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Journal Article
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QLQinghua Liang
Qinghua Liang
LYLing Ye
Ling Ye
Huang Zheng-hongHuang Zheng-hong
Huang Zheng-hong
QXQiang Xu
Qiang Xu
YBYu Bai
Yu Bai
QYQuan-Hong Yang
Quan-Hong Yang
A cost-effective approach to obtain electrode materials with excellent electrochemical performance is critical to the development of supercapacitors (SCs). Here we report the preparation of a three-dimensional (3D) honeycomb-like porous carbon (HLPC) by the simple carbonization of pomelo peel followed by KOH activation. Structural characterization indicates that the as-prepared HLPC with a high specific surface area (SSA) up to 2725 m2 g−1 is made up of interconnected microporous carbon walls. Chemical analysis shows that the HLPC is doped with nitrogen and also has oxygen-containing groups. Electrochemical measurements show that the HLPC not only exhibits a high specific capacitance of 342 F g−1 and 171 F cm−3 at 0.2 A g−1 but also shows considerable rate capability with a retention of 62% at 20 A g−1 as well as good cycling performance with 98% retention over 1000 cycles at 10 A g−1 in 6 M KOH. Furthermore, an as-fabricated HLPC-based symmetric SC device delivers a maximum energy density of ∼9.4 Wh kg−1 in the KOH electrolyte. Moreover, the outstanding cycling stability (only 2% capacitance decay over 1000 cycles at 5 A g−1) of the SC device makes it promising for use in a high-performance electrochemical energy system.

19 May 2011 in Langmuir
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Journal Article
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Huang Zheng-hongHuang Zheng-hong
Huang Zheng-hong
XZXiaoyu Zheng
Xiaoyu Zheng
Wei LvWei Lv
Wei Lv
MWMing Wang
Ming Wang
QYQuan-Hong Yang
Quan-Hong Yang
FKFeiyu Kang
Feiyu Kang

16 November 2016 in Journal of Materials Chemistry A
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Journal Article
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Huang Zheng-hongHuang Zheng-hong
Huang Zheng-hong
ZYZhiyu Yang
Zhiyu Yang
FKFeiyu Kang
Feiyu Kang
MIMichio Inagaki
Michio Inagaki
Carbon materials for electrodes of capacitive deionization (CDI) process are reviewed.

14 October 2011 in Journal of Materials Chemistry
Verified
Journal Article
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LWLei Wang
Lei Wang
MWMing Wang
Ming Wang
Huang Zheng-hongHuang Zheng-hong
Huang Zheng-hong
TCTongxiang Cui
Tongxiang Cui
XGXuchun Gui
Xuchun Gui
DWDehai Wu
Dehai Wu
Capacitive Deionization (CDI) is a promising method for desalination of brackish water because of its energy-efficiency as compared with conventional techniques such as membrane separation and thermal distillation. Carbon nanotube (CNT) sponges, prepared by chemical vapor deposition, are very flexible and have three-dimensional continuous and mesoporous structures, making them promising electrode materials for capacitive deionization. The CDI characteristics of CNT sponges were investigated for the first time by simply compressing them into a CDI cell without any additives. Desalination of NaCl solutions at different concentrations was conducted with a flow-through CDI cell at 1.2V. Experimental data fit well with the Langmuir model, and the deduced maximum desalination capacity was 40 mg g−1, almost 50% higher than the optimal result reported in the literature. By comparing with other carbon-based materials, the excellent CDI performance of CNT sponges was attributed to higher conductivity and larger effective surface area due to their monolithic continuous flexible framework, crystalline microstructure and preferred pore size distribution.