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徐翔

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  • 教师姓名:徐翔

  • 职称:讲师

  • 教师拼音名称:xuxiang

  • 所在单位:能源科学与工程学院

  • 学历:博士研究生毕业

  • 学位:工学博士学位

  • 毕业院校:中南大学

  • 在职信息:在职

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Synergistic Dual Heteroatom-Engineered Superactivated Carbon Unlocks Record-High Hydrogen Storage via Mg─F Orbital Hybridization

发布时间:2025-10-21
点击次数:

DOI码:
10.1002/adma.202509511
发表刊物:
Advanced Materials
关键字:
biochar, hydrogen storage, orbital-level modulation, surface modification, superactivated carbon
摘要:
Hydrogen storage remains a critical challenge for sustainable energy systems. Here, a surface functionalization strategy is reported through C-Mg─F ternary coordination to engineer biomass-derived porous carbons with exceptional hydrogen storage performance. Using tobacco stems as precursors, the synthesized Mg-F@C material achieves record hydrogen uptake capacities under 77 K of 4.2 wt% at 1 bar and 9.7 wt% at 50 bar, doubling pristine carbon performance. Multiscale analyses reveal adsorption mechanisms dominated by orbital interactions at Mg-active sites, where H2 electron transfer arises from hybridization of Mg 2p and unsaturated 3s orbitals, inducing directional polarization of H2 electron clouds which synergizes with hierarchical porosity (3500 m2 g−1 surface area) to enhance adsorption. Combined photophysical analysis establishes a mechanistic framework linking static electronic configurations to dynamic adsorption processes. The material retains structural integrity under pressure cycling and demonstrates universal applicability across diverse biomass. This work provides a generalizable paradigm for designing high-capacity hydrogen storage materials via orbital-level modulation of porous carbons.
论文类型:
期刊论文
论文编号:
e09511
是否译文:
发表时间:
2025-10-21
收录刊物:
SCI
发布期刊链接:
https://advanced.onlinelibrary.wiley.com/doi/10.1002/adma.202509511