Scalable integration of MOFs, COFs, and MXenes with g-C3N4 for solar H2 generation: A review of energy conversion strategies

IF 8.3 2区 工程技术 Q1 CHEMISTRY, PHYSICAL
Ahmad Husain , Dong-Eun Lee , Qamar Tabrez Siddiqui , Prem Gunnasegaran , Mohtaram Danish , Wan-Kuen Jo
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引用次数: 0

Abstract

Motivated by the transformative potential of photocatalytic water splitting for hydrogen (H2) production, researchers are placing greater focus on this approach due to the increasing demand for sustainable and clean energy alternatives. As a corollary, recent strides in coupling metal-organic frameworks (MOFs), covalent organic frameworks (COFs), and MXenes with graphitic carbon nitride (g-C3N4) for solar-induced H2 generation have been brought to light in this review. MOFs, with their tunable structures and high surface areas, enhance charge separation and interfacial transport, making them ideal for constructing efficient heterojunctions with g-C3N4. COFs, featuring light elements and modular synthesis, contribute extended light absorption and abundant catalytic sites, synergizing effectively with g-C3N4 to achieve superior H2 evolution rates. Additionally, MXenes, exemplified by Ti3C2, introduce exceptional conductivity and broaden the absorption spectrum of g–C3N4–based heterojunctions, reinforcing their role in photocatalysis. Besides, this work critically examines the structural, electronic, and catalytic properties of these hybrid materials, emphasizing their impact on photocatalytic performance. The synthesis strategies for MOF/g-C3N4, COF/g-C3N4, and Ti3C2/g-C3N4 heterostructures are thoroughly reviewed, highlighting chemical compatibility and heterojunction engineering. Key approaches include precise fabrication techniques such as thermal, chemical, and physical etching for MXenes preparation and interfacial optimization for MOF and COF heterojunctions. Additionally, the recyclability and stability of these heterostructures are evaluated to assess their potential for sustainable H2 generation. Benchmark results and scaling-up strategies are discussed to provide a comprehensive roadmap for achieving solar H2 generation at practical scales. By integrating fundamental insights with cutting-edge developments, this review aims to guide future research in designing hybrid photocatalysts for a scalable and efficient H2 economy.

Abstract Image

mof、COFs和MXenes与g-C3N4太阳能制氢的可扩展集成:能源转换策略综述
由于对可持续和清洁能源替代品的需求不断增加,研究人员越来越关注光催化水裂解制氢(H2)的变革潜力。因此,本文综述了近年来在金属有机框架(mof)、共价有机框架(COFs)和MXenes与石墨氮化碳(g-C3N4)耦合用于太阳能诱导制氢方面取得的进展。mof具有可调的结构和高表面积,增强了电荷分离和界面输运,是与g-C3N4构建高效异质结的理想材料。COFs具有轻元素和模块化合成的特点,具有较强的光吸收能力和丰富的催化位点,与g-C3N4有效协同作用,达到较高的析氢速率。此外,以Ti3C2为例,MXenes引入了优异的导电性,拓宽了g - c3n4基异质结的吸收光谱,增强了它们在光催化中的作用。此外,本研究批判性地考察了这些杂化材料的结构、电子和催化性能,强调了它们对光催化性能的影响。综述了MOF/g-C3N4、COF/g-C3N4和Ti3C2/g-C3N4异质结构的合成策略,重点介绍了化学相容性和异质结工程。关键方法包括精确制造技术,如MXenes制备的热、化学和物理蚀刻,以及MOF和COF异质结的界面优化。此外,对这些异质结构的可回收性和稳定性进行了评估,以评估其可持续制氢的潜力。讨论了基准结果和扩大战略,为实现实际规模的太阳能氢气发电提供了全面的路线图。通过将基本见解与前沿发展相结合,本文旨在指导未来设计可扩展和高效H2经济的混合光催化剂的研究。
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来源期刊
International Journal of Hydrogen Energy
International Journal of Hydrogen Energy 工程技术-环境科学
CiteScore
13.50
自引率
25.00%
发文量
3502
审稿时长
60 days
期刊介绍: The objective of the International Journal of Hydrogen Energy is to facilitate the exchange of new ideas, technological advancements, and research findings in the field of Hydrogen Energy among scientists and engineers worldwide. This journal showcases original research, both analytical and experimental, covering various aspects of Hydrogen Energy. These include production, storage, transmission, utilization, enabling technologies, environmental impact, economic considerations, and global perspectives on hydrogen and its carriers such as NH3, CH4, alcohols, etc. The utilization aspect encompasses various methods such as thermochemical (combustion), photochemical, electrochemical (fuel cells), and nuclear conversion of hydrogen, hydrogen isotopes, and hydrogen carriers into thermal, mechanical, and electrical energies. The applications of these energies can be found in transportation (including aerospace), industrial, commercial, and residential sectors.
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