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用于光催化CO还原的镍基层状双氢氧化物中三价/四价金属元素的调控

Modulation of Trivalent/Tetravalent Metallic Elements in Ni-Based Layered Double Hydroxides for Photocatalytic CO Reduction.

作者信息

Wang Ruonan, Wang Xinyi, Xiong Yongheng, Hou Yuyan, Wang Yaxuan, Ding Jie, Zhong Qin

机构信息

School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu 210094, P. R. China.

School of Nursing, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, Shandong 271016, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2022 Aug 10;14(31):35654-35662. doi: 10.1021/acsami.2c07940. Epub 2022 Jul 30.

Abstract

Herein, by modulating trivalent/tetravalent metallic elements, NiMLDHs (M = Al, Co, Fe, Mn, and Ti) were successfully prepared and evaluated in photocatalytic CO reduction reaction (PCRR). Photocatalytic results declared that the electronic yields followed the order of NiTiLDH > NiCoLDH > NiFeLDH > NiMnLDH > NiAlLDH. Multiple characterizations affirmed that the introduction of various trivalent/tetravalent metallic elements could visibly affect the three critical aspects: (i) light harvesting; (ii) charge separation and transfer; and (iii) surface reactions, thus governing PCRR performance. Importantly, an in-depth mechanistic investigation was conducted by in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) experiments. These layered double hydroxides (LDHs) exhibited different adsorption/activation behaviors toward CO molecule: NiAlLDH primarily converted CO into b-CO species; NiCoLDH, NiFeLDH, and NiMnLDH could induce c-CO intermediate; NiTiLDH could generate a higher proportion of CO species, which was an important intermediate to produce CO. More favorable carries separation and adsorption/activation process was presented upon NiTiLDH, thus more markedly enhancing photoactivity.

摘要

在此,通过调节三价/四价金属元素,成功制备了镍基层状双氢氧化物(NiMLDHs,M = Al、Co、Fe、Mn和Ti),并对其在光催化CO还原反应(PCRR)中的性能进行了评估。光催化结果表明,电子产率顺序为NiTiLDH > NiCoLDH > NiFeLDH > NiMnLDH > NiAlLDH。多种表征证实,引入各种三价/四价金属元素会显著影响三个关键方面:(i)光捕获;(ii)电荷分离与转移;(iii)表面反应,从而决定PCRR性能。重要的是,通过原位漫反射红外傅里叶变换光谱(DRIFTS)实验进行了深入的机理研究。这些层状双氢氧化物(LDHs)对CO分子表现出不同的吸附/活化行为:NiAlLDH主要将CO转化为b-CO物种;NiCoLDH、NiFeLDH和NiMnLDH可诱导生成c-CO中间体;NiTiLDH能产生更高比例的CO物种,这是生成CO的重要中间体。NiTiLDH具有更有利的载流子分离和吸附/活化过程,从而更显著地提高了光活性。

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