NH2-MIL-125 双缺陷工程的便捷途径:通过加速电子迁移率提高光催化氢气进化和氮氧化物去除能力

IF 6.7 1区 工程技术 Q2 ENERGY & FUELS
Fuel Pub Date : 2024-11-26 DOI:10.1016/j.fuel.2024.133860
Xingyan Liu , Tianrong Xiong , Yonggang Xu , Kunhe Yang , Youzhou He , Haifeng Yang , Hong Wu , Jiajia Jing , Siqi Li , Siping Wei
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引用次数: 0

摘要

MOFs缺陷工程是加速电荷转移以进一步提高光催化性能的一种可行方法。目前,MOFs 的缺陷工程策略主要集中在单一调整模式上,存在明显的天花板效应,能否通过两种或多种调整模式的组合进一步突破天花板效应仍处于起步阶段。在这项工作中,首先通过乙醇溶热法中的单一调整模式对原始 NH2-MIL-125 进行调整,得到部分链接缺陷的 NM-125-X(其中 X 表示溶热处理中使用的不同温度,在 X = 120 时观察到最佳结果)。随后,NM-125-120 在水加热搅拌中通过另一种调节模式对配体缺陷进行了进一步调节,最终得到了有缺陷的 NM-125-120-65。通过双缺陷工程途径获得的 NM-125-120-65 具有优异的光催化性能,制氢率为 11585.23 μmol-g-1,分别是部分缺陷 NM-125-120 (9427.65 μmol-g-1)和原始 NH2-MIL-125 (824.85 μmol-g-1)的 1.23 倍和 14.05 倍。此外,NM-125-120-65 对 NO 的去除率为 64.8%,也高于 NM-125-120(37.8%)和 NH2-MIL-125(23.6%)。通过一系列的对比实验,特别是 TGA 和 XPS,可以发现乙醇溶热法可以形成配体缺陷的 NH2-MIL-125,而且通过在水加热搅拌中进一步重新调节配体缺陷,还可以进一步扩大连接体缺陷。PL发射光谱、IT图和EIS测量结果表明,与NM-125-120和NH2-MIL-125相比,NM-125-120-65具有优异的导电性和电子迁移率。这项工作为在现有缺陷MOFs的基础上,通过双连接子缺陷工程调整模式进行另一种调整模式的后续缺陷工程提供了一种新的方法,从而进一步获得更好的光催化性能,以解决环境和能源危机。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A convenient double defect engineering avenue for NH2-MIL-125 to enhance photocatalytic hydrogen evolution and NO removal via accelerating the electron mobility

A convenient double defect engineering avenue for NH2-MIL-125 to enhance photocatalytic hydrogen evolution and NO removal via accelerating the electron mobility
Defect engineering for MOFs is a promising approach to accelerate the charge transfer to further enhance the photocatalytic performance. Up to now, the current defect engineering strategy for MOFs mainly focuses on a single adjustment mode with the apparent ceiling effect, whether the further break out of the ceiling effect could be achieved through the combination of two or more adjustment modes is still in its infancy. In this work, the original NH2-MIL-125 was firstly adjusted by a single adjustment mode in ethanol solvothermal method to obtain partially linker defective NM-125-X (where X signifies the distinct temperatures used in the solvothermal treatment, with optimal results observed at X = 120). Subsequently, the NM-125-120 was further re-regulated by adjusting the ligand defects through another adjustment mode in water heating agitation, resulting in the ultimate defective NM-125-120-65. The NM-125-120-65 obtained through double defect engineering avenue showed superior photocatalytic performance with the hydrogen production rate of 11585.23 μmol·g−1, which was 1.23 and 14.05 times as those of partially defective NM-125-120 (9427.65 μmol·g−1) and original NH2-MIL-125 (824.85 μmol·g−1), respectively. In addition, the NO removal rate of NM-125-120-65 was 64.8 % also higher than that of NM-125-120 (37.8 %) and NH2-MIL-125 (23.6 %). Through a series of comparative experiments, especially TGA and XPS, it was noted that the ligand defective NH2-MIL-125 can be formed by ethanol solvothermal method, and it was also confirmed that through further re-regulating the ligand defects in water heating agitation, the linker defects could also be further expanded. The PL emission spectra, IT diagrams, and EIS measurements displayed that the NM-125-120-65 had outstanding conductivity and excellent electron mobility compared to NM-125-120 and NH2-MIL-125. This work provided a novel approach for the subsequent defect engineering by another adjustment mode based on the existing defective MOFs via double linker defect engineering adjustment modes, so as to further obtain better photocatalytic performance for solving the environmental and energy crisis.
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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