Exploring advanced nanostructures and functional materials for efficient hydrogen storage: a theoretical investigation on mechanisms, adsorption process, and future directions.

IF 4.2 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Frontiers in Chemistry Pub Date : 2025-02-11 eCollection Date: 2025-01-01 DOI:10.3389/fchem.2025.1525140
Gourhari Jana, Pratim Kumar Chattaraj
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Abstract

Hydrogen is a promising candidate for renewable energy storage and transportation due to its high energy density and zero carbon emissions. Its practical applications face challenges related to safe, efficient storage and release systems. This review article investigates advanced nanostructured materials for hydrogen storage, including metal acetylide and cyanide complexes, B,N-doped γ-graphyne nanotubes (γ-GNT), lithium-phosphide double helices, and Ni-decorated carbon-based clusters. Density Functional Theory (DFT) based computations are used to analyze binding energies, thermodynamic stability, and adsorption mechanisms. Ni-decorated C12N12 nanoclusters demonstrate enhanced storage capacities, binding up to eight H2 molecules with a favorable N-(μ-Ni)-N configuration. Lithium-phosphide double helices show potential for 9.6 wt% hydrogen storage within a stable, semiconducting framework. Functionalization of γ-GNT with OLi2 at boron-doped sites significantly enhances storage potential, achieving optimal hydrogen binding energies for practical applications. Additionally, metal acetylide and cyanide complexes, stabilized by noble gas insertion, display thermodynamically favorable hydrogen adsorption. These results highlight the potential of these functionalized nanostructures for achieving high-capacity, reversible hydrogen storage. The nanostructures in this study, such as γ-graphyne nanotubes (γ-GNT), lithium-phosphide double helices, metal acetylide and cyanide complexes, and Ni-decorated carbon-based clusters, are selected based on their ability to exhibit complementary hydrogen adsorption mechanisms, including physisorption and chemisorption. γ-GNT offers high surface area and tunable electronic properties, ideal for physisorption enhanced by heteroatom doping. Lithium-phosphide double helices facilitate Kubas-like chemisorption through unsaturated lithium centers. Metal acetylide and cyanide complexes stabilize hydrogen adsorption via charge transfer and conjugated frameworks, while Ni-decorated clusters combine polarization-induced physisorption. These materials represent a strategic approach to addressing the challenges of hydrogen storage through diverse and synergistic mechanisms. The review also addresses challenges and outlines future directions to advance hydrogen's role as a sustainable fuel.

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探索高效储氢的先进纳米结构和功能材料:机理、吸附过程和未来发展方向的理论研究。
氢因其高能量密度和零碳排放而成为可再生能源储存和运输的有前途的候选者。其实际应用面临着与安全、高效的存储和释放系统相关的挑战。本文综述了用于储氢的先进纳米结构材料,包括金属乙酰基和氰化物配合物、B、n掺杂γ-石墨烯纳米管(γ-GNT)、磷化锂双螺旋和ni修饰碳基簇。基于密度泛函理论(DFT)的计算用于分析结合能、热力学稳定性和吸附机理。ni修饰的C12N12纳米簇具有增强的存储能力,可以结合多达8个H2分子,具有良好的N-(μ-Ni)-N结构。在稳定的半导体框架内,磷化锂双螺旋结构显示出9.6 wt%的储氢潜力。γ-GNT在硼掺杂位点与OLi2的功能化显著提高了存储潜力,为实际应用获得了最佳的氢结合能。此外,通过惰性气体插入稳定的金属乙酰醚和氰化物配合物在热力学上表现出有利的氢吸附。这些结果突出了这些功能化纳米结构在实现高容量、可逆储氢方面的潜力。本研究中选择的纳米结构,如γ-石墨烯纳米管(γ-GNT)、磷化锂双螺旋、金属乙酰醚和氰化物配合物以及ni修饰的碳基簇,是基于它们具有互补的氢吸附机制,包括物理吸附和化学吸附的能力。γ-GNT具有高表面积和可调谐的电子特性,是通过杂原子掺杂增强物理吸附的理想选择。磷化锂双螺旋通过不饱和锂中心促进库巴斯类化学吸附。金属乙酰醚和氰化物配合物通过电荷转移和共轭框架稳定氢吸附,而ni修饰团簇结合极化诱导的物理吸附。这些材料代表了通过多种协同机制解决储氢挑战的战略方法。该报告还提出了挑战,并概述了氢作为可持续燃料的未来发展方向。
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来源期刊
Frontiers in Chemistry
Frontiers in Chemistry Chemistry-General Chemistry
CiteScore
8.50
自引率
3.60%
发文量
1540
审稿时长
12 weeks
期刊介绍: Frontiers in Chemistry is a high visiblity and quality journal, publishing rigorously peer-reviewed research across the chemical sciences. Field Chief Editor Steve Suib at the University of Connecticut is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to academics, industry leaders and the public worldwide. Chemistry is a branch of science that is linked to all other main fields of research. The omnipresence of Chemistry is apparent in our everyday lives from the electronic devices that we all use to communicate, to foods we eat, to our health and well-being, to the different forms of energy that we use. While there are many subtopics and specialties of Chemistry, the fundamental link in all these areas is how atoms, ions, and molecules come together and come apart in what some have come to call the “dance of life”. All specialty sections of Frontiers in Chemistry are open-access with the goal of publishing outstanding research publications, review articles, commentaries, and ideas about various aspects of Chemistry. The past forms of publication often have specific subdisciplines, most commonly of analytical, inorganic, organic and physical chemistries, but these days those lines and boxes are quite blurry and the silos of those disciplines appear to be eroding. Chemistry is important to both fundamental and applied areas of research and manufacturing, and indeed the outlines of academic versus industrial research are also often artificial. Collaborative research across all specialty areas of Chemistry is highly encouraged and supported as we move forward. These are exciting times and the field of Chemistry is an important and significant contributor to our collective knowledge.
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