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| 1 | Preparation of MnO2 decorated Co3Fe1Ox powder/monolithic catalyst with improved catalytic activity for toluene oxidation显示文摘In this paper, KMnO4 was used to pre-treat Co3 Fe-layered double hydroxides(LDH) precursor to prepare MnO2 decorated Co3Fe1Ox catalyst. The toluene oxidation performance of the catalyst was investigated systematically. The optimized 0.1 Mn CF-LDO catalyst exhibited the best catalytic performance, and the temperatures of 50% and 90% toluene conversion( T50 and T90) were 218 and 243 ℃, respectively. The apparent activation energy( Ea) was 31.6 k J/mol. The characterization results showed that the pre-redox reaction by KMnO4 could increase the specific surface area, Co^3+ species amount and oxygen defect concentration of the catalyst, which are the main reason of the improved toluene catalytic activity. Besides, this method was also applied to enhance toluene oxidation of iron mesh based monolithic catalyst. The 0.1 Mn CF-LDO/Iron mesh(IM) catalyst showed a 90% toluene conversion at around 316 ℃ which was much lower than that of without MnO2 addition(359 ℃). In addition, the water resistant of all the catalysts was studied as well, all the samples showed relatively good water resistance. The toluene conversion still remained to be over > 80% even in the presence of 10 vol.% water vapor. | Tianshan xue Renna Li Zhang Zhang Yanshan Gao Qiang Wang | 2020 | Journal of Environmental Sciences2020，32，10： | 2 |
| 2 | Sedimentary Facies, Provenance and Geochronology of the Heshangzhen Group: Implications for the Tectonic Evolution of the Eastern Jiangnan Orogen, South China显示文摘The Neoproterozoic Jiangnan orogen plays an important role in the study of the Precambrian tectonic evolution of South China. The tectonic nature of the Neoproterozoic sedimentary basins is still controversial, due to poor understanding of the sedimentary sequences and the lack of geochronological data. Here, we present sedimentological, provenance and geochronological data from the Heshangzhen Group in the eastern Jiangnan orogen. Sedimentological analysis shows that the Luojiamen Formation was deposited in a submarine fan, and the overlying Hongchicun Formation was deposited in front of a fan delta. The youngest detrital zircons constrain the lower Luojiamen and Hongchicun formations with ages of 827.3 ± 8.4 Ma and 825 ± 12 Ma, respectively. The sandstones of the Luojiamen Formation are characterized by a large number of intermediate to felsic volcanic grains, suggesting a volcanic arc source. In contrast, quartz and sedimentary lithic grains increase in the Hongchicun Formation, showing a new input from a collisional orogenic source. Detrital zircon from six sandstone samples in the Luojiamen and Hongchicun formations yield similar age spectra of 930–820 Ma with a peak at ca. 845–860 Ma, with one main cluster at 930–820 Ma. Detrital zircons of 930–845 Ma show a positive value of εHf(t)(+2.4 to +11, mean +7.6), which is similar to the volcanic arc of the nearby Shuangxiwu Group. There are a minor group of zircons with U-Pb ages ranging from 820 Ma to 845 Ma from the middle part of the Luojiamen Formation and Hongchicun Formation, with εHf(t) values between-20 to +2.4, which are consistent with the characteristics of the Shuangqiaoshan Group. within light of the bidirectional paleocurrents in the Luojiamen Formation, it is speculated that the zircons of 820–845 Ma were recycled from the Shuangqiaoshan Group, which is derived from a continental arc to the northwest. Our data suggests that the Luojiamen Formation was formed in an inter-arc basin, while the Hongchicun Formation was formed in an accretionary wedge-top basin. When juxtaposed with the conglomeratic characteristics at the bottom of the Luojiamen Formation, it is believed that the unconformity represented by the ‘Shen Gong Movement' reflects the rapid erosion and accumulation process of island arc volcanic material. The disconformity between the Luojiamen and Hongchicun formations is the imprint of transition from inter-arc basin to accretionary wedge-top basin,which represents the collision between the Shuangxiwu arc and the Yangtze Plate. | ZHOU Xiaohua HU Xiumian JIANG Ren GAO Tianshan MA Xue XING Guangfu SUN Gaoyuan SHU Xujie ZHAO Xilin | 2020 | Acta Geologica Sinica(English Edition)2020，94，4： | 2 |
| 3 | Adsorption of acid red from dye wastewater by Zn2Al NO3 LDHs and the re- source of adsorbent sludge as nanofiller for polypropylene显示文摘 | Xue Tianshan Gao Yanshan Zhang Zhang | 2014 | Alloys and Compounds2014，587，2： | 1 |
| 4 | Recent advances in intermediate-temperature CO_(2) capture: Materials,technologies and applications显示文摘Carbon capture,utilization and storage(CCUS) is widely recognized as a vital strategy for mitigating the impact of human induced climate change.Among various CO_(2) adsorbents,intermediate-temperature solid adsorbents have garnered significant attention due to their potential applications in hydrogen utilization,specifically in the water gas shift,steam reforming and gasification processes.These processes are crucial for achieving carbon neutrality.While laboratory-level studies have showcased the high adsorption capacity of these materials via various synthesis and modification methods,their practical application in complex industrial environments remains challenging,impeding the commercialization process.This review aims to critically summarize the recent research progress made in intermediatetemperature(200-400℃) solid CO_(2) adsorbents,particularly focusing on indicators such as cyclability,gas selectivity,and formability,which play vital roles in industrial application scenarios.Additionally,we provide an overview of laboratory-level advanced technologies specifically tailored for industrial applications.Furthermore,we highlight several industrial-ready advanced technologies that can pave the way for overcoming the challenges associated with large-scale implementation.The insights provided by this review aim to assist researchers in identifying the most relevant research directions for industrial applications.By promoting advances in the application of solid adsorbents,we strive to facilitate the ultimate goal of achieving carbon neutrality. | Chengbo Zhao Leiming Wang Liang Huang Nicholas M.Musyoka Tianshan Xue Jabor Rabeah Qiang Wang | 2024 | Journal of Energy Chemistry2024，90，3： | 0 |
| 5 | Synergy of phosphorus vacancies and build-in electric field into NiCo/NiCoP Mott-Schottky integrated electrode for enhanced water splitting performance显示文摘Vacancy engineering and Mott-Schottky heterostructure can accelerate charge transfer,regulate adsorption energy of reaction intermediates,and provide additional active sites,which are regarded as valid means for improving catalytic activity.However,the underlying mechanism of synergistic regulation of interfacial charge transfer and optimization of electrocatalytic activity by combining vacancy and Mott-Schottky junction remains unclear.Herein,the growth of a bifunctional NiCo/NiCoP Mott-Schottky electrode with abundant phosphorus vacancies on foam nickel(NF)has been synthesized through continuous phosphating and reduction processes.The obtained NiCo/NiCoP heterojunctions show remarkable OER and HER activities,and the overpotentials for OER and HER are as low as 117 and 60 mV at 10 mA/cm^(2) in 1 mol/L KOH,respectively.Moreover,as both the cathode and anode of overall water splitting,the voltage of the bifunctional NiCo/NiCoP electrocatalyst is 1.44 V at 10 mA/cm^(2),which are far exceeding the benchmark commercial electrodes.DFT theoretical calculation results confirm that the phosphorus vacancies and build-in electric field can effectively accelerate ion and electron transfer between NiCo alloy and NiCoP semiconductor,tailor the electronic structure of the metal centers and lower the Gibbs free energy of the intermediates.Furthermore,the unique self-supported integrated structure is beneficial to facilitate the exposure of the active site,avoid catalyst shedding,thus improving the activity and structural stability of NiCo/NiCoP.This study provides an avenue for the controllable synthesis and performance optimization of Mott-Schottky electrocatalysts. | Xiaochen Zhang Hui Xue Jing Sun Niankun Guo Tianshan Song Jiawen Sun Yi-Ru Hao Qin Wang | 2024 | Chinese Chemical Letters2024，35，2： | 0 |
| 6 | Interfacial charge redistribution to promote the catalytic activity of Vs-CoP-CoS_(2)/C n-n heterojunction for oxygen evolution显示文摘Modulating surface charge redistribution based on interface and defect engineering has been considered as a resultful means to boost electrocatalytic activity.However,the mechanism of synergistic regulation of heterojunction and vacancy defects remains unclear.Herein,a Vs-CoP-CoS_(2)/C n-n heterojunction with sulfur vacancies is successfully constructed,which manifests superior electrocatalytic activity for oxygen evolution,as demonstrated by a low overpotential of 170 mV to reach 10 mA/cm^(2).The experimental results and density functional theory calculations testify that the outstanding OER performance of Vs-CoP-CoS_(2)/C heterojunction is owed to the synergistic effect of sulfur vacancies and built-in electric field at n-n heterogeneous interface,which accelerates the electron transfer,induces the charge redistribution,and regulates the adsorption energy of active intermediates during the reaction.This study affords a promising means to regulate the electrocatalytic performance by the construction of heterogeneous interfaces and defects,and in-depth explores the synergistic mechanisms of n-n heterojunction and vacancies. | Jiawen Sun Hui Xue Jing Sun Niankun Guo Tianshan Song Yi-Ru Hao Qin Wang | 2024 | Chinese Chemical Letters2024，35，2： | 0 |
| 7 | Co-Construction of Sulfur Vacancies and Heterogeneous Interface into Ni_(3)S_(2)/MoS_(2) Catalysts to Achieve Highly Efficient Overall Water Splitting显示文摘Integrating the advantages of anion vacancies and heterostructures into the catalytic materials may increase the binding affinities to intermediates, provide more active sites, and significantly promote the activity of overall water splitting. However, the successful assembly of anion vacancies and heterostructures for high-efficiency water splitting performance is still challenging. In this work, we ingeniously present the co-construction of sulfur vacancies and heterogeneous interface into Ni_(3)S_(2)/MoS_(2) catalysts on nickel foam(NF). The introduction of sulfur vacancies and Ni_(3)S_(2)/MoS_(2) heterostructures can significantly improve electron and ion transport, effectively improve structural stability, and enhance overall water splitting activity. The obtained VSNi_(3)S_(2)/MoS_(2) catalysts(VS stands for sulfur vacancies) exhibit superior OER and HER activities,and the overpotentials for OER and HER are 180 and 71 mV at 10 mA·cm^(-2), respectively. Furthermore, a low water splitting voltage of 1.46 V is required at 10 mA·cm^(-2) for the VS-Ni_(3)S_(2)/MoS_(2) catalysts, which is considerably lower than most that of water splitting electrocatalysts currently reported. This work offers an effective mean for the preparation of catalysts with both anion vacancies and heterostructures for achieving high-performance alkaline overall water splitting. | Zhaoyang An Hui Xue Jing Sun Niankun Guo Tianshan Song Jiawen Sun Yi-Ru Hao Qin Wang | 2022 | Chinese Journal of Structural Chemistry2022，41，8： | 0 |
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