Methanolysis of ammonia borane catalyzed by NiO–CuO heterostructured nanosheets: cooperation of visible light and oxygen vacancy

IF 9.6 1区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
You-Xiang Shao, Yuan-Zhong Li, Xue-Qi Lian, Xiao-Ting Che, Qian-Yi Li, Yu-Fa Feng, Hui-Ze Wang, Jin-Yun Liao, Quan-Bing Liu, Hao Li
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Abstract

Developing cost-effective and high-activity catalysts for the methanolysis of ammonia borane (AB) has attracted great attention in the field of hydrogen energy recently. Besides the modification of the electronic structure of the catalysts, external factors such as visible light irradiation can improve the efficiency of hydrogen production as well. In the present study, a Z-scheme heterostructured VO–Cu0.5Ni0.5O catalysts were constructed by introducing a plenteous phase interface and oxygen vacancy (Vo). The catalytic activity of as-prepared VO–Cu0.5Ni0.5O toward AB methanolysis has been improved dramatically with the assistance of visible light irradiation. The turnover frequency (TOF) under visible light irradiation was measured to be 29 molH2·molcat.−1·min−1, which is 1.4 times larger than the TOF in the absence of visible light. Systematic characterization experiments and density functional theory (DFT) calculations were conducted to unveil the causation of enhanced catalytic activity. The results demonstrated that the enhancement of the catalytic activity of VO–Cu0.5Ni0.5O originated from the electronic structure modification induced by the formation of heterojunctions, the introduction of oxygen vacancies, and the assistance of visible light cooperatively. The formation of heterojunction and the introduction of oxygen vacancies provoked the upshift of the d-band center; while the visible light irradiation induced the photogenerated electrons to transfer from Cu to Ni sites at the interface. Such electron structure modulation is beneficial for the construction of abundant active sites, thereby enhancing the adsorption of methanol on the Ni sites, which is considered as the rate-determine step for the methanolysis of AB. The strong interaction between Ni and O weakened the O–H bond of methanol, accelerating the methanolysis of AB. These results demonstrate the utilization of combined heterojunction, oxygen vacancy, and visible light to explore highly active AB methanolysis catalysts, which should shed light on the exploration of more effective catalysts for AB methanolysis.

Graphical Abstract

Abstract Image

NiO-CuO异质结构纳米片催化的氨硼烷甲醇分解:可见光和氧空位的协同作用
近年来,开发具有成本效益和高活性的硼烷氨甲烷化催化剂在氢能领域引起了极大关注。除了改变催化剂的电子结构外,可见光照射等外部因素也能提高制氢效率。本研究通过引入丰满相界面和氧空位(Vo)构建了 Z 型异质结构 VO-Cu0.5Ni0.5O 催化剂。在可见光照射的帮助下,制备的 VO-Cu0.5Ni0.5O 对 AB 甲醇分解的催化活性显著提高。在可见光照射下测得的翻转频率(TOF)为 29 molH2-molcat.-1-min-1,是无可见光时的 1.4 倍。为了揭示催化活性增强的原因,研究人员进行了系统的表征实验和密度泛函理论(DFT)计算。结果表明,VO-Cu0.5Ni0.5O 催化活性的增强源于异质结的形成、氧空位的引入和可见光的辅助作用所诱导的电子结构修饰。异质结的形成和氧空位的引入引起了 d 波段中心的上移;而可见光的照射则促使光生电子从界面上的铜位点转移到镍位点。这种电子结构调整有利于构建丰富的活性位点,从而提高甲醇在镍位点上的吸附力,这被认为是 AB 甲醇分解的决定性步骤。Ni 和 O 之间的强相互作用削弱了甲醇的 O-H 键,加速了 AB 的甲醇分解。这些结果表明了利用异质结、氧空位和可见光的组合来探索高活性 AB 甲醇分解催化剂的方法,为探索更有效的 AB 甲醇分解催化剂提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Rare Metals
Rare Metals 工程技术-材料科学:综合
CiteScore
12.10
自引率
12.50%
发文量
2919
审稿时长
2.7 months
期刊介绍: Rare Metals is a monthly peer-reviewed journal published by the Nonferrous Metals Society of China. It serves as a platform for engineers and scientists to communicate and disseminate original research articles in the field of rare metals. The journal focuses on a wide range of topics including metallurgy, processing, and determination of rare metals. Additionally, it showcases the application of rare metals in advanced materials such as superconductors, semiconductors, composites, and ceramics.
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