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Institution

China University of Petroleum

EducationBeijing, China
About: China University of Petroleum is a education organization based out in Beijing, China. It is known for research contribution in the topics: Catalysis & Oil shale. The organization has 39802 authors who have published 39151 publications receiving 483760 citations. The organization is also known as: Zhōngguó Shíyóu Dàxué & China University of Petroleum (Beijing).


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TL;DR: An asymmetric supercapacitor with high energy density has been developed successfully using graphene/MnO2 composite as positive electrode and activated carbon nanofibers (ACN) as negative electrode in a neutral aqueous Na2SO4 electrolyte as mentioned in this paper.
Abstract: Asymmetric supercapacitor with high energy density has been developed successfully using graphene/MnO2 composite as positive electrode and activated carbon nanofibers (ACN) as negative electrode in a neutral aqueous Na2SO4 electrolyte. Due to the high capacitances and excellent rate performances of graphene/MnO2 and ACN, as well as the synergistic effects of the two electrodes, such asymmetric cell exhibits superior electrochemical performances. An optimized asymmetric supercapacitor can be cycled reversibly in the voltage range of 0–1.8 V, and exhibits maximum energy density of 51.1 Wh kg−1, which is much higher than that of MnO2//DWNT cell (29.1 Wh kg−1). Additionally, graphene/MnO2//ACN asymmetric supercapacitor exhibits excellent cycling durability, with 97% specific capacitance retained even after 1000 cycles. These encouraging results show great potential in developing energy storage devices with high energy and power densities for practical applications.

1,768 citations

Journal ArticleDOI

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TL;DR: In this paper, a high-voltage asymmetric supercapacitor is successfully fabricated using Ni(OH)2/graphene and porous graphene as the positive and negative electrodes, respectively.
Abstract: Hierarchical flowerlike nickel hydroxide decorated on graphene sheets has been prepared by a facile and cost-effective microwave-assisted method. In order to achieve high energy and power densities, a high-voltage asymmetric supercapacitor is successfully fabricated using Ni(OH)2/graphene and porous graphene as the positive and negative electrodes, respectively. Because of their unique structure, both of these materials exhibit excellent electrochemical performances. The optimized asymmetric supercapacitor could be cycled reversibly in the high-voltage region of 0–1.6 V and displays intriguing performances with a maximum specific capacitance of 218.4 F g−1 and high energy density of 77.8 Wh kg−1. Furthermore, the Ni(OH)2/graphene//porous graphene supercapacitor device exhibits an excellent long cycle life along with 94.3% specific capacitance retained after 3000 cycles. These fascinating performances can be attributed to the high capacitance and the positive synergistic effects of the two electrodes. The impressive results presented here may pave the way for promising applications in high energy density storage systems.

1,629 citations

Journal ArticleDOI

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TL;DR: A novel hybrid nanostructure with CoP nanoparticles embedded in a N-doped carbon nanotube hollow polyhedron (NCNHP) through a pyrolysis-oxidation-phosphidation strategy derived from core-shell ZIF-8@ZIF-67 is reported, benefiting from the synergistic effects between highly active CoP NPs and NCNHP.
Abstract: The construction of highly active and stable non-noble-metal electrocatalysts for hydrogen and oxygen evolution reactions is a major challenge for overall water splitting. Herein, we report a novel hybrid nanostructure with CoP nanoparticles (NPs) embedded in a N-doped carbon nanotube hollow polyhedron (NCNHP) through a pyrolysis–oxidation–phosphidation strategy derived from core–shell ZIF-8@ZIF-67. Benefiting from the synergistic effects between highly active CoP NPs and NCNHP, the CoP/NCNHP hybrid exhibited outstanding bifunctional electrocatalytic performances. When the CoP/NCNHP was employed as both the anode and cathode for overall water splitting, a potential as low as 1.64 V was needed to achieve the current density of 10 mA·cm–2, and it still exhibited superior activity after continuously working for 36 h with nearly negligible decay in potential. Density functional theory calculations indicated that the electron transfer from NCNHP to CoP could increase the electronic states of the Co d-orbital a...

921 citations

Journal ArticleDOI

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TL;DR: This article reviewed the connection between these two issues and concluded that limits to availability of fossil fuels will set a limit for mankind's ability to affect the climate, however, this limit is unclear as various studies have reached quite different conclusions regarding future atmospheric CO2 concentrations caused by fossil fuel limitations.
Abstract: Future scenarios with significant anthropogenic climate change also display large increases in world production of fossil fuels, the principal CO2 emission source. Meanwhile, fossil fuel depletion has also been identified as a future challenge. This chapter reviews the connection between these two issues and concludes that limits to availability of fossil fuels will set a limit for mankind’s ability to affect the climate. However, this limit is unclear as various studies have reached quite different conclusions regarding future atmospheric CO2 concentrations caused by fossil fuel limitations.It is concluded that the current set of emission scenarios used by the IPCC and others is perforated by optimistic expectations on future fossil fuel production that are improbable or even unrealistic. The current situation, where climate models largely rely on emission scenarios detached from the reality of supply and its inherent problems is problematic. In fact, it may even mislead planners and politicians into making decisions that mitigate one problem but make the other one worse. It is important to understand that the fossil energy problem and the anthropogenic climate change problem are tightly connected and need to be treated as two interwoven challenges necessitating a holistic solution.

800 citations

Journal ArticleDOI

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TL;DR: The fundamental engineering principles used to design RCA nanotechnologies are introduced, the recently developed RCA-based diagnostics and bioanalytical tools are discussed, and the use of RCA to construct multivalent molecular scaffolds and nanostructures for applications in biology, diagnostic and therapeutics is summarized.
Abstract: Rolling circle amplification (RCA) is an isothermal enzymatic process where a short DNA or RNA primer is amplified to form a long single stranded DNA or RNA using a circular DNA template and special DNA or RNA polymerases. The RCA product is a concatemer containing tens to hundreds of tandem repeats that are complementary to the circular template. The power, simplicity, and versatility of the DNA amplification technique have made it an attractive tool for biomedical research and nanobiotechnology. Traditionally, RCA has been used to develop sensitive diagnostic methods for a variety of targets including nucleic acids (DNA, RNA), small molecules, proteins, and cells. RCA has also attracted significant attention in the field of nanotechnology and nanobiotechnology. The RCA-produced long, single-stranded DNA with repeating units has been used as template for the periodic assembly of nanospecies. Moreover, since RCA products can be tailor-designed by manipulating the circular template, RCA has been employed to generate complex DNA nanostructures such as DNA origami, nanotubes, nanoribbons and DNA based metamaterials. These functional RCA based nanotechnologies have been utilized for biodetection, drug delivery, designing bioelectronic circuits and bioseparation. In this review, we introduce the fundamental engineering principles used to design RCA nanotechnologies, discuss recently developed RCA-based diagnostics and bioanalytical tools, and summarize the use of RCA to construct multivalent molecular scaffolds and nanostructures for applications in biology, diagnostics and therapeutics.

788 citations


Authors

Showing all 39802 results

NameH-indexPapersCitations
Lei Jiang1702244135205
Shi-Zhang Qiao14252380888
Jian Zhou128300791402
Tao Zhang123277283866
Jian Liu117209073156
Qiang Yang112111771540
Jianjun Liu112104071032
Ju Li10962346004
Peng Wang108167254529
Alan R. Fersht10840033895
Jian Zhang107306469715
Wei Liu102292765228
Xiaoming Sun9638247153
Haibo Zeng9460439226
Chao Wang9156132854
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2022374
20214,950
20204,419
20194,424
20183,709
20173,282