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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).


Papers
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Journal ArticleDOI
TL;DR: In this article, the predictability of economic policy uncertainty (EPU) to stock market volatility was investigated and in-sample evidence suggests that higher EPU leads to significant increases in market volatility.

351 citations

Journal ArticleDOI
TL;DR: This state-of-the-art review will provide a platform for understanding the intricate details of heteroatom-doped CDs, a summary of the latest progress in the field, and related applications in biology and is expected to inspire further developments in this exciting class of materials.
Abstract: Heteroatom-doped carbon dots (CDs), due to their excellent photoluminescence (PL) properties, attracted widespread attention recently and demonstrated immense promise for diverse applications, particularly for biological applications. The objective of this feature article is to provide a comprehensive overview of the recent progress in the research and development of heteroatom-doped CDs and a detailed description of the influence of single or co-doping heteroatoms on their PL behavior. The most recent understanding and critical insights into the PL mechanism of heteroatom-doped CDs are also highlighted. Moreover, potential bio-related applications of heteroatom-doped CDs in biosensing, bioimaging, and theranostics are also reviewed. This state-of-the-art review will provide a platform for understanding the intricate details of heteroatom-doped CDs, a summary of the latest progress in the field, and related applications in biology and is expected to inspire further developments in this exciting class of materials.

350 citations

Journal ArticleDOI
TL;DR: In this article, the authors investigated the effect of thermochemical sulfate reduction (TSR) on the isotope compositions of different hydrocarbon gas components at different TSR stages.
Abstract: The Puguang gas field is the largest gas field found in marine carbonates in China. Marine carbonate reservoirs in this field were buried to a depth of about 7000 m (22,966 ft) and experienced maximum temperature up to 220C before uplift to the present-day depth of 5000–5500 m (16,404–18,045 ft), with present-day thermal maturity between 2.0 and 3.0% equivalent vitrinite reflectance (Ro). Sulfur-rich pyrobitumens with reflectance up to 3.5% are widespread in the reservoirs and resulted from thermal cracking of crude oils most likely generated from Upper Permian source rocks and thermochemical sulfate reduction (TSR). Natural gases in the Puguang gas field have wide variations in nonhydrocarbon gas contents, with H2S contents between 5.1 and 58.3% and CO2 contents between 7.9 and 18.0%. The hydrocarbon gases originated mainly from thermal cracking of accumulated oil but were altered by TSR. Thermochemical sulfate reduction in the study area exerted different effects on the isotope compositions of different hydrocarbon gas components at different TSR stages. The differential increase of 13C values for different gas components reflects transformation from a heavy-hydrocarbon-gas–dominated TSR stage to a methane-dominated TSR stage. This caused a decrease of 13Cmethane13Cethane values and a corresponding conversion from reversed to normal isotope distributions. Thermochemical sulfate reduction in the study area appears to have been limited by sulfate concentrations in the reservoirs. A successive, three-stage TSR series, namely, liquid-hydrocarbon–involved TSR, heavy-hydrocarbon-gas–dominated TSR, and methane-dominated TSR, occurred in reservoirs with sufficient sulfate concentration. Methane can be the dominant organic reactant for TSR, but only at elevated temperature and after most C2+ hydrocarbons are exhausted.

336 citations

Journal ArticleDOI
TL;DR: In this article, a new visible-light-induced Co 3 O 4 -g-C 3 N 4 heterojunction photocatalysts were synthesized via a facile mixing-and-heating method.
Abstract: Novel visible-light-induced Co 3 O 4 -g-C 3 N 4 heterojunction photocatalysts were synthesized via a facile mixing-and-heating method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), ultraviolet–visible diffuse reflection spectroscopy (DRS), electron spin resonance (ESR) and photoluminescence spectroscopy (PL). The heterojunction photocatalysts exhibit a significantly enhanced photocatalytic activity in degrading methyl orange (MO). The optimal Co 3 O 4 content with the highest photocatalytic activity was determined to be 0.2 wt%. The synergetic effect between Co 3 O 4 and g-C 3 N 4 plays an important role in promoting photo-generated carrier separation. The ESR and PL results reveals that the enhanced photocatalytic activity of Co 3 O 4 -g-C 3 N 4 was mainly due to the superior amount and longer lifetime of oxidative radicals ( O 2 − ), as well as the efficient separation of charge carriers. Possible mechanism is proposed for the high photocatalytic activity of heterojunction structures, to guide the design of photocatalysts.

336 citations

Journal ArticleDOI
TL;DR: In this paper, a 3D-networked heterogeneous nickel phosphide/sulfide electrocatalyst consisting of Ni2P strongly coupled with Ni3S2 in situ grown on Ni foam is presented.

335 citations


Authors

Showing all 40138 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
2023163
20221,053
20214,986
20204,421
20194,425
20183,709