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| 1 | Nitrogen-doped hierarchically porous carbon spheres for low concentration CO_(2) capture显示文摘Synthesis of spherical carbon beads with effective CO_2 capture capability is highly desirable for large scale application of CO2 sorption, but remains challenging. Herein, a facile and efficient strategy to prepare nitrogen-doped hierarchically porous carbon spheres was developed via co-pyrolyzation of poly(vinylidene chloride) and melamine in alginate gel beads. In this approach, melamine not only serves as the nitrogen precursor, but also acts as a template for the macropores structures. The nitrogen contents in the hierarchically porous carbon spheres reach a high level, ranging from 11.8 wt% to 14.7 wt%, as the melamine amount increases. Owing to the enriched nitrogen functionalities and the special hierarchical porous structure, the carbon spheres exhibit an outstanding CO_2 capture performance, with the dynamic capacity of as much as about 7 wt% and a separation factor about 49 at 25 °C in a gas mixture of CO_2/N_2(0.5:99.5, v/v). | Yang Li Jing Wang Sisi Fan Fanan Wang Zheng Shen Hongmin Duan Jinming Xu Yanqiang Huang | 2021 | Journal of Energy Chemistry2021，30，2： | 3 |
| 2 | In-situ carbonization approach for the binder-free Ir-dispersed ordered mesoporous carbon hydrogen evolution electrode显示文摘A binder-free Ir-dispersed ordered mesoporous carbon(Ir-OMC) catalytic electrode has been prepared through a designed in-situ carbonization method, which involves coating resorcinol and formaldehyde mixtures with iridium precursors onto the three-dimensional nickel foam framework, followed by insitu calcination in N_2 atmosphere at 800 ℃ for 3 h. This electrode shows a large surface area, ordered mesoporous structure and homogeneous distribution of metal nanoparticles. It presents good activity and stability towards hydrogen evolution reaction, which is attributed to the efficient mass and electron transport from the intimate contact among Ir nanoparticles, ordered mesoporous carbon matrix and 3 D conductive substrate. We hope that this in-situ carbonization synthetic route can also be applied to design more high-performance catalysts for water splitting, fuel cells and other clean energy devices. | Yanghua He Jinming Xu Fanan Wang Xiaochen Zhao Guangzhao Yin Qing Mao Yanqiang Huang Tao Zhang | 2017 | Journal of Energy Chemistry2017，26，6： | 1 |
| 3 | Facet effect on the reconstructed Cu-catalyzed electrochemical hydrogenation of 5-hydroxymethylfurfural(HMF) towards 2,5-bis(hydroxymethy)furan (BHMF)显示文摘The electrochemical hydrogenation of HMF to BHMF is an elegant alternative to the conventio nal thermocatalytic route for the production of high-value-added chemicals from biomass resources.In virtue of the wide potential window with promising Faradic efficiency(FE) towards BHMF,Cu-based electrode has been in the center of investigation.However,its structure-activity relationship remains ambiguous and its intrinsic catalytic activity is still unsatisfactory.In this work,we develop a two-step oxidation-reduction strategy to reconstruct the surface atom arrangement of the Cu foam(CF).By combination of multiple quasi-situ/in-situ techniques and density functional theory(DFT) calculation,the critical factor that governs the reaction is demonstrated to be facet effect of the metallic Cu crystal:Cu(110) facet accounts for the most favorable surface with enhanced chemisorption with reactants and selective production of BHMF,while Cu(100) facet might trigger the accumulation of the by-product 5,5'-bis(hydroxy methy)hydrofurion(BHH).With the optimized composition of the facets on the reconstructed Cu(OH)_(2)-ER/CF,the performance could be noticeably enhanced with a BHMF FE of 92.3% and HMF conversion of 98.5% at a potential of -0.15 V versus reversible hydrogen electrode(vs.RHE) in 0.1 M KOH solution.This work sheds light on the incomplete mechanistic puzzle for Cu-catalyzed electrochemical hydrogenation of HMF to BHMF,and provides a theoretical foundation for further precise design of highly efficient catalytic electrodes. | Mengxia Li Tianxi Zheng Dongfei Lu Shiwei Dai Xin Chen Xinchen Pan Dibo Dong Rengui Weng Gang Xu Fanan Wang | 2023 | Journal of Energy Chemistry2023，，9： | 1 |
| 4 | Into the “secret” double layer: Alkali cation mediates the hydrogen evolution reaction in basic medium显示文摘The hydrogen evolution reaction(HER) – as an essential half reaction in water electrolysis and chlor-alkali process has been well studied in acidic electrolyte, but much less has been known in basic medium. In this study, by combining kinetic modeling and electrochemical measurements, we show that hydrated alkali cation clusters can adsorb on the surface of HER catalyst in basic electrolyte. The bound H2 O molecules in the 'clusters' can thus be in-situ activated through the hydration effect, which dissociate on the catalyst surface as the reactant of HER. The effective concentration and hydration energy of alkali cation can influence the H2 O dissociation rate, and hence the kinetics of HER. Our work demonstrates a new understanding of the HER mechanism in basic reaction electrolyte. | Fanan Wang Gang Xu Yanghua He Zhipeng Liu Zhigang Zhang Qing Mao Yanqiang Huang | 2020 | Journal of Energy Chemistry2020，29，12： | 0 |
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