MOF-Derived Hollow C, N-Doped Co3O4 Dodecahedral Nanostructure Enwrapped with MgIn2S4 Nanosheets for Enhanced Photocatalytic N2 Reduction

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Pub Date : 2024-12-25 DOI:10.1021/acs.inorgchem.4c04746
Ranjit Bariki, Sudhir K. Sahoo, Aditya Ranjan Pati, Sibun Kumar Pradhan, Saumyaranjan Panda, Swagat Kumar Nayak, Braja Gopal Mishra
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Abstract

Design of hierarchical hollow nanoheterostructure materials through interfacial and defect engineering is an innovative approach for achieving optimal charge separation dynamics and photon harvesting efficiency. Herein, we have described a facile technique to fabricate hollow MOF-derived C, N-doped-Co3O4 (C, N-Co3O4) dodecahedral particles enwrapped with MgIn2S4 nanosheets for enhanced N2 reduction performance. ZIF-67 was initially used as a sacrificial template to prepare hollow C, N-Co3O4 using a carbonization route followed by low-temperature calcination treatment. The controlled synthetic protocol not only led to nonmetal doping but also produced an interwoven carbon matrix that improved the photoelectron mobility. Density functional theory calculations further substantiated the creation of atomic defects through substitution of C at tetrahedral Co2+ sites and N at lattice O2– sites of the Co3O4 structure. C, N-Co3O4 was subsequently coupled with MgIn2S4 nanosheets to prepare the C, N-Co3O4/MgIn2S4 [C, N-CM (X)] p–n heterojunctions. The photocatalytic study revealed that the NH4+ ion production activity of the optimal C, N-CM (1:1) material (334 μmol g–1 h–1) was significantly higher (4–10 times) than that of pure components. The enhanced activity of the composite was ascribed to its distinct topological features, superior charge carrier dynamics, and creation of atomic defects that afforded a large number of surface-active sites.

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mof衍生的MgIn2S4纳米片包裹的空心C, n掺杂Co3O4十二面体纳米结构增强光催化N2还原
通过界面和缺陷工程设计分层中空纳米异质结构材料是实现最佳电荷分离动力学和光子捕获效率的创新途径。在此,我们描述了一种简单的技术来制备空心mof衍生的C, n掺杂co3o4 (C, N-Co3O4)十二面体粒子,这些粒子被MgIn2S4纳米片包裹,以增强N2还原性能。以ZIF-67为牺牲模板,采用炭化后低温煅烧的方法制备了空心C, N-Co3O4。控制合成方案不仅导致非金属掺杂,而且产生了一个交织的碳基质,提高了光电子迁移率。密度泛函理论计算进一步证实了通过在Co3O4结构的四面体Co2+位上取代C和在晶格O2 -位上取代N来产生原子缺陷。C, N-Co3O4随后与MgIn2S4纳米片偶联,制备了C, N-Co3O4/MgIn2S4 [C, N-CM (X)] p-n异质结。光催化研究表明,最佳C, N-CM(1:1)材料(334 μmol g-1 h-1)的NH4+离子生成活性显著高于纯组分(4-10倍)。复合材料的活性增强归因于其独特的拓扑特征,优越的载流子动力学,以及提供大量表面活性位点的原子缺陷的产生。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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