Modulation of Trivalent/Tetravalent Metallic Elements in Ni-Based Layered Double Hydroxides for Photocatalytic CO2 Reduction

被引:16
|
作者
Wang, Ruonan [1 ]
Wang, Xinyi [2 ,3 ]
Xiong, Yongheng [1 ]
Hou, Yuyan [1 ]
Wang, Yaxuan [1 ]
Ding, Jie [1 ]
Zhong, Qin [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Shandong First Med Univ, Sch Nursing, Tai An 271016, Shandong, Peoples R China
[3] Shandong Acad Med Sci, Tai An 271016, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalysis; CO2; layered double hydroxides; in situ DRIFTS; CHARGE-TRANSFER; ACTIVE-SITES; TIO2; H2O; HETEROJUNCTION; PHOTOREDUCTION; IDENTIFICATION; PERFORMANCE; INTERFACE; EVOLUTION;
D O I
10.1021/acsami.2c07940
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Herein, by modulating trivalent/tetravalent metallic elements, NiMLDHs (M = Al, Co, Fe, Mn, and Ti) were successfully prepared and evaluated in photocatalytic CO(2 )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 CO2 molecule: NiAlLDH primarily converted CO2 into b-CO32- species; NiCoLDH, NiFeLDH, and NiMnLDH could induce c-CO32- intermediate; NiTiLDH could generate a higher proportion of (CO2)-C-center dot- 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.
引用
收藏
页码:35654 / 35662
页数:9
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