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512 results on '"Wang, Rongming"'

16. A Mini Review: Phase Regulation for Molybdenum Dichalcogenide Nanomaterials.

Author

Han, Xiaosong, Zhang, Zhihong, and Wang, Rongming

Subjects
ELECTRONIC band structure, MOLYBDENUM, NANOSTRUCTURED materials, TRANSITION metals, ELECTRONIC structure, CHEMICAL properties
Abstract

Atomically thin two-dimensional transition metal dichalcogenides (TMDCs) have been regarded as ideal and promising nanomaterials that bring broad application prospects in extensive fields due to their ultrathin layered structure, unique electronic band structure, and multiple spatial phase configurations. TMDCs with different phase structures exhibit great diversities in physical and chemical properties. By regulating the phase structure, their properties would be modified to broaden the application fields. In this mini review, focusing on the most widely concerned molybdenum dichalcogenides (MoX2: X = S, Se, Te), we summarized their phase structures and corresponding electronic properties. Particularly, the mechanisms of phase transformation are explained, and the common methods of phase regulation or phase stabilization strategies are systematically reviewed and discussed. We hope the review could provide guidance for the phase regulation of molybdenum dichalcogenides nanomaterials, and further promote their real industrial applications. [ABSTRACT FROM AUTHOR]

Published
2024
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18. Assembling ionic liquid into porous molecular filler of mixed matrix membrane to trigger high gas permeability, selectivity, and stability for CO2/CH4 separation.

Author

Yu, Liting, Hao, Liqin, Feng, Yang, Pang, Jia, Guo, Mengwei, Li, Liangjun, Fan, Weidong, Fan, Lili, Wang, Rongming, Kang, Zixi, and Sun, Daofeng

Subjects
IONIC liquids, PERMEABILITY, POROSITY, SEPARATION of gases, POROUS materials
Abstract

As an emerging zero-dimensional nano crystalline porous material, porous organic cages (POCs) with soluble properties in organic solvents, are promising candidates as molecular fillers in mixed matrix membranes (MMMs). The pore structure of POCs should be adjusted to trigger efficient gas separation performance, and the interaction between filler and matrix should be optimized. In this work, ionic liquid (IL) was introduced into the molecular fillers of CC3, to construct the IL@CC3/PIM-1 membrane to effectively separate CO2 from CH4. The advantages of doping IL include: (1) narrowing the cavity size of POCs from 4.4 to 3.9 Å to enhance the diffusion selectivity, (2) strengthening the CO2 solubility to heighten the gas permeability, and (3) improving the compatibility between filler and matrix to upgrade membrane stability. After the optimization of the membrane composite, the IL@CC3/PIM-1-10% membrane possesses the CO2 permeability of 7868 Barrer and the CO2/CH4 selectivity of 73.4, which compared to the CC3/PIM-1-10% membrane, improved by 15.9% and 106.2%, respectively. Furthermore, the membrane has maintained a stable separation performance at varied temperatures and pressures during the long-term test. The proposed method offers an efficient way to improve the performance of POCs-based MMMs in gas separation. [ABSTRACT FROM AUTHOR]

Published
2024
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42. Pseudocapacitance of Bimetallic Solid‐Solution MXene for Supercapacitors with Enhanced Electrochemical Energy Storage.

Author

He, Zhiquan, Yao, Li, Guo, Wei, Sun, Nana, Wang, Fadi, Wang, Yuhang, Wang, Rongming, and Wang, Fengping

Subjects
SUPERCAPACITORS, ENERGY storage, TRANSITION metal carbides, POTASSIUM fluoride, TRANSITION metals, METALLIC surfaces
Abstract

MXenes, a family of 2D transition metal carbides, are considered promising high‐rate pseudocapacitive materials because of their metallic‐like conductivity and transition metal oxide‐like surfaces. Currently, nearly 50 stoichiometric MXenes have been synthesized. However, only a few MXenes, such as Ti3C2, have shown stable pseudocapacitive charge storage so far. Further improving the inherent pseudocapacitance of MXenes without losing their cyclability remains a challenge. Herein, a mild method is reported to produce highly stable bimetallic solid‐solution MXene Ti2VC2 using a solution of potassium fluoride and hydrochloric acid. The electrochemical properties of resulting multilayered clay‐like and delaminated Ti2VC2 films are investigated, exceeding the performance of typical Ti3C2 in acidic electrolytes. These electrodes deliver up to 2000 F cm−3 and retain more than 90% of their initial capacitance after 20 000 cycles, surpassing most state‐of‐the‐art supercapacitor materials known. The pseudocapacitive charge storage of Ti2VC2 is deeply investigated through in situ and ex situ experimental studies, confirmed the pseudocapacitive mechanism is a combination of hydrated H+ intercalation and surface redox. This work provides a practical route toward future rational design on the atomic scale for high‐performance pseudocapacitive materials. [ABSTRACT FROM AUTHOR]

Published
2023
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45. Interfacial Mediation by Sn And S Vacancies of p‐SnS/n‐ZnIn2S4 for Enhancing Photocatalytic Hydrogen Evolution with New Scheme of Type‐I Heterojunction.

Author

Jia, Xiaofang, Lu, Yue, Du, Kunrong, Zheng, Huibin, Mao, Liang, Li, Hao, Ma, Zhaoyu, Wang, Rongming, and Zhang, Junying

Subjects
HETEROJUNCTIONS, HYDROGEN evolution reactions, SURFACE photovoltage, HYDROGEN, DENSITY functional theory, TIN, FERMI level
Abstract

The construction of interfacial electric field (IEF) in semiconductor heterojunction is of great significance in boosting photocatalytic hydrogen evolution through efficient separation of photogenerated charge‐carriers. However, the exploitation of IEF in type‐I heterojunction has not been proposed for designing photocatalysts. Herein, based on the density functional theory prediction, p‐SnS with different work functions modulated by Sn‐vacancy are compounded with n‐ZnIn2S4 containing S‐vacancy to form type‐I heterojunction. The optimized SnS/ZnIn2S4 photocatalyst without co‐catalysts exhibits an impressive hydrogen evolution rate of 22.75 mmol g−1 h−1, 6.23 times of ZnIn2S4. Systematic investigations reveal that the interfacial Sn‐S bond acts as a transport channel that accelerates the interface charge‐carriers transfer under the promotion of IEF originating from the significant Fermi level difference. A large difference in the surface photovoltage signal of SnS/ZnIn2S4 and ZnIn2S4 is achieved from effective photogenerated charge‐carriers separation by IEF. The new p‐n type‐I scheme of SnS/ZnIn2S4 induced by the interfacial mediation can separate the photogenerated charge‐carriers, and retain the highly reductive electrons of ZnIn2S4 for hydrogen evolution, overcoming the disadvantage of reduction potential decline in the typical type‐I scheme. This study will afford a new theoretical basis for the achievement of high‐efficiency photocatalytic hydrogen evolution through interface modulation. [ABSTRACT FROM AUTHOR]

Published
2023
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