Pub Date : 2024-06-12DOI: 10.3390/inorganics12060164
S. Vinothini, Arjunan Karthi Keyan, S. Sakthinathan, Te-Wei Chiu, N. Vittayakorn
The demand for regenerative energy and electric automotive applications has grown in recent decades. Supercapacitors have multiple applications in consumer alternative electronic products due to their excellent energy density, rapid charge/discharge time, and safety. CuFe2O4-incorporated three-dimensional graphene sheet (3DGS) nanocomposites were studied by different characterization studies such as X-ray diffraction, transmission electron microscopy, and scanning electron microscopy. The electrochemical studies were based on cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS) measurements. As prepared, 3DGS/CuFe2O4 nanocomposites exhibited an excellent surface area, high energy storage with appreciable durability, and excellent electrocatalysis properties. A supercapacitor with 3DGS/CuFe2O4-coated nickel foam (NF) electrodes exhibited an excellent specific capacitance of 488.98 Fg−1, a higher current density, as well as a higher power density. After charge–discharge cycles in a 2.0 M KOH aqueous electrolyte solution, the 3DGS/CuFe2O4/NF electrodes exhibited an outstanding cyclic stability of roughly 95% at 10 Ag−1, indicating that the prepared nanocomposites could have the potential for energy storage applications. Moreover, the 3DGS/CuFe2O4 electrode exhibited an excellent electrochemical detection of chloramphenicol with a detection limit of 0.5 µM, linear range of 5–400 µM, and electrode sensitivity of 3.7478 µA µM−1 cm−2.
{"title":"CuFe2O4 Nanofiber Incorporated with a Three-Dimensional Graphene Sheet Composite Electrode for Supercapacitor and Electrochemical Sensor Application","authors":"S. Vinothini, Arjunan Karthi Keyan, S. Sakthinathan, Te-Wei Chiu, N. Vittayakorn","doi":"10.3390/inorganics12060164","DOIUrl":"https://doi.org/10.3390/inorganics12060164","url":null,"abstract":"The demand for regenerative energy and electric automotive applications has grown in recent decades. Supercapacitors have multiple applications in consumer alternative electronic products due to their excellent energy density, rapid charge/discharge time, and safety. CuFe2O4-incorporated three-dimensional graphene sheet (3DGS) nanocomposites were studied by different characterization studies such as X-ray diffraction, transmission electron microscopy, and scanning electron microscopy. The electrochemical studies were based on cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS) measurements. As prepared, 3DGS/CuFe2O4 nanocomposites exhibited an excellent surface area, high energy storage with appreciable durability, and excellent electrocatalysis properties. A supercapacitor with 3DGS/CuFe2O4-coated nickel foam (NF) electrodes exhibited an excellent specific capacitance of 488.98 Fg−1, a higher current density, as well as a higher power density. After charge–discharge cycles in a 2.0 M KOH aqueous electrolyte solution, the 3DGS/CuFe2O4/NF electrodes exhibited an outstanding cyclic stability of roughly 95% at 10 Ag−1, indicating that the prepared nanocomposites could have the potential for energy storage applications. Moreover, the 3DGS/CuFe2O4 electrode exhibited an excellent electrochemical detection of chloramphenicol with a detection limit of 0.5 µM, linear range of 5–400 µM, and electrode sensitivity of 3.7478 µA µM−1 cm−2.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141353700","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Binary transition metal selenides (BTMSs) are more promising than single transition metal selenides (TMS) as anode materials of sodium-ion batteries (SIBs). However, it is still very challenging to prepare high-performance BTMSs in the pure phase, instead of a mixture of two TMSs. In this study, a binary metal center-based MOF derived selenization strategy was developed to prepare iron–cobalt selenide (Fe2CoSe4@NC) and iron–nickel selenide (Fe2NiSe4@NC) nanocomposites in the single phase and when wrapped with carbon layers. As the anode material of SIBs, Fe2CoSe4@NC exhibits higher long-term cycling performance than Fe2NiSe4@NC, maintaining a capacity of 352 mAh g−1 after 2100 cycles at 1.0 A g−1, which is ascribed to the higher percentage of the nanopores, larger lattice spacing, and faster Na+ diffusion rate in the electrode materials of the former rather than the latter.
{"title":"MOF-Derived Fe2CoSe4@NC and Fe2NiSe4@NC Composite Anode Materials towards High-Performance Na-Ion Storage","authors":"Hangxuan Xie, Wei Zhang, Chao Wang, Shangcheng Zhao, Zhentao Hao, Xiaolian Huang, Kanghua Miao, Xiongwu Kang","doi":"10.3390/inorganics12060165","DOIUrl":"https://doi.org/10.3390/inorganics12060165","url":null,"abstract":"Binary transition metal selenides (BTMSs) are more promising than single transition metal selenides (TMS) as anode materials of sodium-ion batteries (SIBs). However, it is still very challenging to prepare high-performance BTMSs in the pure phase, instead of a mixture of two TMSs. In this study, a binary metal center-based MOF derived selenization strategy was developed to prepare iron–cobalt selenide (Fe2CoSe4@NC) and iron–nickel selenide (Fe2NiSe4@NC) nanocomposites in the single phase and when wrapped with carbon layers. As the anode material of SIBs, Fe2CoSe4@NC exhibits higher long-term cycling performance than Fe2NiSe4@NC, maintaining a capacity of 352 mAh g−1 after 2100 cycles at 1.0 A g−1, which is ascribed to the higher percentage of the nanopores, larger lattice spacing, and faster Na+ diffusion rate in the electrode materials of the former rather than the latter.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141351099","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-06-10DOI: 10.3390/inorganics12060163
Yuchen Qiao, Enting Xu, Yameng Hao, Xuemei Yang, Ming Ni
Hydrogen has the potential to serve as a new energy resource, reducing greenhouse gas emissions that contribute to climate change. Natural hydrogenases exhibit impressive catalytic abilities for hydrogen production, but they often lack oxygen tolerance. Oxygen-tolerant hydrogenases can work under oxygen by reacting with oxygen to form inactive states, which can be reactivated to catalytic states by oxygen atom removal. Herein, we synthesized three NiFeSe complexes: (NiSe(CH3)FeCp, NiSe(CH3)FeCp* and NiSe(PhNMe2)FeCp) with features of active sites of [NiFeSe]-H2ases, which are the oxygen-tolerant hydrogenases, and we investigated the influence of electronic and steric factors on the oxygen reaction of these “biomimetic” complexes. In our research, we found that they react with oxygen, forming 1-oxygen species, which is related to the O2-damaged [NiFeSe] active site. Through a comparative analysis of oxygen reactions, we have discovered that electronic factors and steric hindrance on Se play a significant role in determining the oxygen reactivity of NiFe complexes related to hydrogenases’ active sites.
氢有可能成为一种新能源，减少导致气候变化的温室气体排放。天然氢酶在催化制氢方面表现出惊人的能力，但它们通常缺乏耐氧性。耐氧氢化酶可在氧气环境下工作，与氧反应形成非活性状态，通过去除氧原子可重新激活为催化状态。在此，我们合成了三种具有耐氧氢化酶[NiFeSe]-H2ase活性位点特征的NiFeSe配合物：（NiSe(CH3)FeCp、NiSe(CH3)FeCp*和NiSe(PhNMe2)FeCp），并研究了电子和立体因素对这些 "仿生物 "配合物氧反应的影响。在研究中，我们发现它们会与氧气发生反应，形成 1-氧物种，这与被氧气破坏的 [NiFeSe] 活性位点有关。通过对氧反应的比较分析，我们发现 Se 上的电子因素和立体阻碍在决定与氢化酶活性位点有关的 NiFe 复合物的氧反应性方面起着重要作用。
{"title":"Electronic and Steric Effects on Oxygen Reactivities of NiFeSe Complexes Related to O2-Damaged [NiFeSe]-Hydrogenases’ Active Site","authors":"Yuchen Qiao, Enting Xu, Yameng Hao, Xuemei Yang, Ming Ni","doi":"10.3390/inorganics12060163","DOIUrl":"https://doi.org/10.3390/inorganics12060163","url":null,"abstract":"Hydrogen has the potential to serve as a new energy resource, reducing greenhouse gas emissions that contribute to climate change. Natural hydrogenases exhibit impressive catalytic abilities for hydrogen production, but they often lack oxygen tolerance. Oxygen-tolerant hydrogenases can work under oxygen by reacting with oxygen to form inactive states, which can be reactivated to catalytic states by oxygen atom removal. Herein, we synthesized three NiFeSe complexes: (NiSe(CH3)FeCp, NiSe(CH3)FeCp* and NiSe(PhNMe2)FeCp) with features of active sites of [NiFeSe]-H2ases, which are the oxygen-tolerant hydrogenases, and we investigated the influence of electronic and steric factors on the oxygen reaction of these “biomimetic” complexes. In our research, we found that they react with oxygen, forming 1-oxygen species, which is related to the O2-damaged [NiFeSe] active site. Through a comparative analysis of oxygen reactions, we have discovered that electronic factors and steric hindrance on Se play a significant role in determining the oxygen reactivity of NiFe complexes related to hydrogenases’ active sites.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141362454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Anode materials have a vital influence on the performance of sodium ion batteries. In this paper, SnSb nanoparticles were distributed uniformly in N-doped three-dimensional porous carbon (SnSb@N-PC), which effectively avoided the agglomeration of alloy nanoparticles and greatly improved the capacity retention rate of SnSb@N-PC. At the same time, the porous carbon substrate brings higher conductivity, larger specific surface area, and more sodium storage sites, which makes the material obtain excellent sodium storage properties. The first discharge-specific capacity of SnSb@N-PC was 846.3 mAh g−1 at the current density of 0.1 A g−1, and the specific capacity remained at 483 mAh g−1 after 100 cycles. Meanwhile, the specific capacity of SnSb@N-PC was kept at 323 mAh g−1 after 400 cycles at a high current density of 1.5 A g−1, which indicated that the recombination of SnSb with porous carbon played a key role in the electrochemical performance of SnSb. The contribution of capacitance contrast capacity was able to reach more than 90% by the cyclic voltammetry (CV) test at high sweep speed, and larger Na+ diffusivity was obtained by the constant current intermittent titration technique (GITT) test, which explains the good rate performance of SnSb@N-PC.
负极材料对钠离子电池的性能有着至关重要的影响。本文将SnSb纳米颗粒均匀分布在掺杂N的三维多孔碳（SnSb@N-PC）中，有效避免了合金纳米颗粒的团聚，大大提高了SnSb@N-PC的容量保持率。同时，多孔碳基底带来了更高的电导率、更大的比表面积和更多的储钠位点，使材料获得了优异的储钠性能。在电流密度为 0.1 A g-1 时，SnSb@N-PC 的首次放电比容量为 846.3 mAh g-1，循环 100 次后比容量仍为 483 mAh g-1。同时，在 1.5 A g-1 的高电流密度下，SnSb@N-PC 的比容量在循环 400 次后保持在 323 mAh g-1 的水平，这表明 SnSb 与多孔碳的重组对 SnSb 的电化学性能起着关键作用。通过高扫描速度下的循环伏安法（CV）测试，电容对比容量的贡献率达到了 90% 以上，通过恒流间歇滴定技术（GITT）测试，获得了更大的 Na+ 扩散率，这说明 SnSb@N-PC 具有良好的速率性能。
{"title":"Limited Domain SnSb@N-PC Composite Material as a High-Performance Anode for Sodium Ion Batteries","authors":"Zhaomeng Liu, Hailong Ren, Shizheng Fu, Wentao Yang, Yihua Li, Yang Jiao, Botao Zhang","doi":"10.3390/inorganics12060162","DOIUrl":"https://doi.org/10.3390/inorganics12060162","url":null,"abstract":"Anode materials have a vital influence on the performance of sodium ion batteries. In this paper, SnSb nanoparticles were distributed uniformly in N-doped three-dimensional porous carbon (SnSb@N-PC), which effectively avoided the agglomeration of alloy nanoparticles and greatly improved the capacity retention rate of SnSb@N-PC. At the same time, the porous carbon substrate brings higher conductivity, larger specific surface area, and more sodium storage sites, which makes the material obtain excellent sodium storage properties. The first discharge-specific capacity of SnSb@N-PC was 846.3 mAh g−1 at the current density of 0.1 A g−1, and the specific capacity remained at 483 mAh g−1 after 100 cycles. Meanwhile, the specific capacity of SnSb@N-PC was kept at 323 mAh g−1 after 400 cycles at a high current density of 1.5 A g−1, which indicated that the recombination of SnSb with porous carbon played a key role in the electrochemical performance of SnSb. The contribution of capacitance contrast capacity was able to reach more than 90% by the cyclic voltammetry (CV) test at high sweep speed, and larger Na+ diffusivity was obtained by the constant current intermittent titration technique (GITT) test, which explains the good rate performance of SnSb@N-PC.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141375036","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-06-06DOI: 10.3390/inorganics12060161
Rubén D. Parra
The complexation of an alkali metal ion by a model macrocycle is examined using the M05-2X/DGDZVP DFT method. The macrocycle is built by connecting three cyclopenta[b]pyrrole motifs with alternating acetylene and ethylene linkages. Replacing one of the C-H bonds in each motif with a C-I bond allows for the formation of three intramolecular C-I···N halogen bonds. Two distinct binding modes were found for the complexation of each metal ion. In one mode, the binding of the ion occurs solely by the iodine atoms, via I···M+ interactions, while maintaining the integrity of the halogen bonds. The complexation energies are in the range −66 to −35 kcal/mol. In the other mode, the binding of the ion includes one nitrogen atom as well, with binding energies in the range of −71 to −38 kcal/mol. In this binding mode, the halogen bond network is weakened. The presence and strength of the interactions are further examined using AIM and NBO calculations. Lastly, the geometries for the transition state structures linking the less stable to the more stable metal ion complexes were obtained, and their calculated Gibbs free energy barriers were found in the range of 1.6 to 1.9 kcal/mol.
{"title":"Alkali Metal-Ion Binding by a Model Macrocycle Containing a C-I···N Halogen Bonded Network: A DFT Study of C-I···M+ and N···M+ Binding Interactions, M+ = Li+, Na+, K+, and Rb+","authors":"Rubén D. Parra","doi":"10.3390/inorganics12060161","DOIUrl":"https://doi.org/10.3390/inorganics12060161","url":null,"abstract":"The complexation of an alkali metal ion by a model macrocycle is examined using the M05-2X/DGDZVP DFT method. The macrocycle is built by connecting three cyclopenta[b]pyrrole motifs with alternating acetylene and ethylene linkages. Replacing one of the C-H bonds in each motif with a C-I bond allows for the formation of three intramolecular C-I···N halogen bonds. Two distinct binding modes were found for the complexation of each metal ion. In one mode, the binding of the ion occurs solely by the iodine atoms, via I···M+ interactions, while maintaining the integrity of the halogen bonds. The complexation energies are in the range −66 to −35 kcal/mol. In the other mode, the binding of the ion includes one nitrogen atom as well, with binding energies in the range of −71 to −38 kcal/mol. In this binding mode, the halogen bond network is weakened. The presence and strength of the interactions are further examined using AIM and NBO calculations. Lastly, the geometries for the transition state structures linking the less stable to the more stable metal ion complexes were obtained, and their calculated Gibbs free energy barriers were found in the range of 1.6 to 1.9 kcal/mol.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141380864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lanthanide elements such as europium exhibit distinctive emissions due to the transitions of inner-shell 4f electrons. Inorganic materials containing lanthanide elements have been widely used as phosphors in conventional displays. The hybridization of lanthanide ions with organic components enables to control of the material’s shapes and properties and broadens the possibility of lanthanide compounds as inorganic–organic materials. Lanthanide ion-containing polyoxometalate anions (Ln-POM) are a promising category as an inorganic component to design and synthesize inorganic–organic hybrids. Several inorganic–organic Ln-POM systems have been reported by hybridizing with cationic surfactants as luminescent materials. However, single-crystalline ordering has not been achieved in most cases. Here, we report syntheses and structures of inorganic–organic hybrid crystals of lanthanide-based POM and bolaamphiphile surfactants with two hydrophilic heads in one molecule. An emissive decatungstoeuropate ([EuW10O36]9−, EuW10) anion was employed as a lanthanide source. The bolaamphiphile counterparts are 1,8-octamethylenediammonium ([H3N(CH2)8NH3]2+, C8N2) and 1,10-decamethylenediammonium ([H3N(CH2)10NH3]2+, C10N2). Both hybrid crystals of C8N2-EuW10 and C10N2-EuW10 were successfully obtained as single crystals, and their crystal structures were unambiguously determined using X-ray diffraction measurements. The photoluminescence properties of C8N2-EuW10 and C10N2-EuW10 were investigated by means of steady-state and time-resolved spectroscopy. The characteristic emission derived from the EuW10 anion was retained after the hybridization process.
{"title":"Lanthanide-Containing Polyoxometalate Crystallized with Bolaamphiphile Surfactants as Inorganic–Organic Hybrid Phosphors","authors":"Rieko Ishibashi, Ruka Koike, Yoriko Suda, Tatsuhiro Kojima, Toshiyuki Sumi, Toshiyuki Misawa, Kotaro Kizu, Yosuke Okamura, Takeru Ito","doi":"10.3390/inorganics12060146","DOIUrl":"https://doi.org/10.3390/inorganics12060146","url":null,"abstract":"Lanthanide elements such as europium exhibit distinctive emissions due to the transitions of inner-shell 4f electrons. Inorganic materials containing lanthanide elements have been widely used as phosphors in conventional displays. The hybridization of lanthanide ions with organic components enables to control of the material’s shapes and properties and broadens the possibility of lanthanide compounds as inorganic–organic materials. Lanthanide ion-containing polyoxometalate anions (Ln-POM) are a promising category as an inorganic component to design and synthesize inorganic–organic hybrids. Several inorganic–organic Ln-POM systems have been reported by hybridizing with cationic surfactants as luminescent materials. However, single-crystalline ordering has not been achieved in most cases. Here, we report syntheses and structures of inorganic–organic hybrid crystals of lanthanide-based POM and bolaamphiphile surfactants with two hydrophilic heads in one molecule. An emissive decatungstoeuropate ([EuW10O36]9−, EuW10) anion was employed as a lanthanide source. The bolaamphiphile counterparts are 1,8-octamethylenediammonium ([H3N(CH2)8NH3]2+, C8N2) and 1,10-decamethylenediammonium ([H3N(CH2)10NH3]2+, C10N2). Both hybrid crystals of C8N2-EuW10 and C10N2-EuW10 were successfully obtained as single crystals, and their crystal structures were unambiguously determined using X-ray diffraction measurements. The photoluminescence properties of C8N2-EuW10 and C10N2-EuW10 were investigated by means of steady-state and time-resolved spectroscopy. The characteristic emission derived from the EuW10 anion was retained after the hybridization process.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141106839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-22DOI: 10.3390/inorganics12060144
Zijing Wang, Yuze Tang, Limei Ai, Minghui Liu, Yurong Wang
FePMo12O40@PVP composite materials were synthesized with the regulation of polyvinylpyrrolidone (PVP) to control the structure. The samples were characterized by FT-IR, XRD, XPS, SEM, TEM and UV-Vis DRS. The composite retains the Keggin-type polyoxometalates structure, exhibiting a high specific surface area that enhances photon capture efficiency. Analysis of UV-Vis DRS absorption band edge and band gap indicated that the composite was responsive to visible light. Photocatalytic degradation of Rhodamine B (RhB) by FePMo12O40@PVP was investigated under commonly used LED light source, demonstrating excellent photocatalytic performance as 2.5 g-FePMo12O40@PVP (0.015 g) can remove 83% of RhB (10 mg/L) in 40 min. The FePMo12O40@PVP composite material demonstrated sustained moderate degradation efficiency even after undergoing three cycles of repeated use. The non-covalent interaction and strong interfacial coupling between PVP and FePMo12O40 promoted the transfer of h+, and e−, ∙O2−, ·OH, and h+ served as the primary active species in this photocatalytic system. This environmentally friendly material has the potential to significantly reduce energy consumption and offers valuable insights for the future treatment of dye wastewater.
{"title":"Polymer-Based Immobilized FePMo12O40@PVP Composite Materials for Photocatalytic RhB Degradation","authors":"Zijing Wang, Yuze Tang, Limei Ai, Minghui Liu, Yurong Wang","doi":"10.3390/inorganics12060144","DOIUrl":"https://doi.org/10.3390/inorganics12060144","url":null,"abstract":"FePMo12O40@PVP composite materials were synthesized with the regulation of polyvinylpyrrolidone (PVP) to control the structure. The samples were characterized by FT-IR, XRD, XPS, SEM, TEM and UV-Vis DRS. The composite retains the Keggin-type polyoxometalates structure, exhibiting a high specific surface area that enhances photon capture efficiency. Analysis of UV-Vis DRS absorption band edge and band gap indicated that the composite was responsive to visible light. Photocatalytic degradation of Rhodamine B (RhB) by FePMo12O40@PVP was investigated under commonly used LED light source, demonstrating excellent photocatalytic performance as 2.5 g-FePMo12O40@PVP (0.015 g) can remove 83% of RhB (10 mg/L) in 40 min. The FePMo12O40@PVP composite material demonstrated sustained moderate degradation efficiency even after undergoing three cycles of repeated use. The non-covalent interaction and strong interfacial coupling between PVP and FePMo12O40 promoted the transfer of h+, and e−, ∙O2−, ·OH, and h+ served as the primary active species in this photocatalytic system. This environmentally friendly material has the potential to significantly reduce energy consumption and offers valuable insights for the future treatment of dye wastewater.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141110171","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Supercapacitors are prospective energy storage devices for electronic devices due to their high power density, rapid charging and discharging, and extended cycle life. Materials with limited conductivity could have low charge-transfer ions, low rate capability, and low cycle stability, resulting in poor electrochemical performance. Enhancement of the device’s functionality can be achieved by controlling and designing the electrode materials. Graphene oxide (GO) has emerged as a promising material for the fabrication of supercapacitor devices on account of its remarkable physiochemical characteristics. The mechanical strength, surface area, and conductivity of GO are all quite excellent. These characteristics make it a promising material for use as electrodes, as they allow for the rapid storage and release of charges. To enhance the overall electrochemical performance, including conductivity, specific capacitance (Cs), cyclic stability, and capacitance retention, researchers concentrated their efforts on composite materials containing GO. Therefore, this review discusses the structural, morphological, and surface area characteristics of GO in composites with metal oxides, metal sulfides, metal chalcogenides, layered double hydroxides, metal–organic frameworks, and MXene for supercapacitor application. Furthermore, the organic and bacterial functionalization of GO is discussed. The electrochemical properties of GO and its composite structures are discussed according to the performance of three- and two-electrode systems. Finally, this review compares the performance of several composite types of GO to identify which is ideal. The development of these composite devices holds potential for use in energy storage applications. Because GO-modified materials embrace both electric double-layer capacitive and pseudocapacitive mechanisms, they often perform better than pristine by offering increased surface area, conductivity, and high rate capability. Additionally, the density functional theory (DFT) of GO-based electrode materials with geometrical structures and their characteristics for supercapacitors are addressed.
超级电容器具有功率密度高、充放电速度快、循环寿命长等优点，是电子设备的理想储能设备。电导率有限的材料可能会产生低电荷转移离子、低速率能力和低循环稳定性，从而导致电化学性能低下。通过控制和设计电极材料可以增强设备的功能。氧化石墨烯（GO）因其显著的理化特性，已成为制造超级电容器器件的一种前景广阔的材料。GO 的机械强度、表面积和导电性都相当出色。这些特性使其成为一种很有前途的电极材料，因为它们可以快速存储和释放电荷。为了提高整体电化学性能，包括电导率、比电容（Cs）、循环稳定性和电容保持率，研究人员集中精力研究含有 GO 的复合材料。因此，本综述讨论了在超级电容器应用中，GO 与金属氧化物、金属硫化物、金属瑀、层状双氢氧化物、金属有机框架和 MXene 复合材料的结构、形态和表面积特征。此外，还讨论了 GO 的有机功能化和细菌功能化。根据三电极和双电极系统的性能，讨论了 GO 及其复合结构的电化学特性。最后，本综述比较了几种 GO 复合类型的性能，以确定哪种类型最理想。这些复合装置的开发具有在储能应用中使用的潜力。由于 GO 改性材料同时具有双电层电容和伪电容机制，因此它们的性能往往优于原始材料，因为它们具有更大的表面积、导电性和更高的速率能力。此外，还探讨了具有几何结构的 GO 基电极材料的密度泛函理论（DFT）及其在超级电容器中的特性。
{"title":"Recent Progress Using Graphene Oxide and Its Composites for Supercapacitor Applications: A Review","authors":"Ganesan Sriram, Muthuraj Arunpandian, Karmegam Dhanabalan, Vishwanath Rudregowda Sarojamma, Selvaraj David, Mahaveer D. Kurkuri, Tae Hwan Oh","doi":"10.3390/inorganics12060145","DOIUrl":"https://doi.org/10.3390/inorganics12060145","url":null,"abstract":"Supercapacitors are prospective energy storage devices for electronic devices due to their high power density, rapid charging and discharging, and extended cycle life. Materials with limited conductivity could have low charge-transfer ions, low rate capability, and low cycle stability, resulting in poor electrochemical performance. Enhancement of the device’s functionality can be achieved by controlling and designing the electrode materials. Graphene oxide (GO) has emerged as a promising material for the fabrication of supercapacitor devices on account of its remarkable physiochemical characteristics. The mechanical strength, surface area, and conductivity of GO are all quite excellent. These characteristics make it a promising material for use as electrodes, as they allow for the rapid storage and release of charges. To enhance the overall electrochemical performance, including conductivity, specific capacitance (Cs), cyclic stability, and capacitance retention, researchers concentrated their efforts on composite materials containing GO. Therefore, this review discusses the structural, morphological, and surface area characteristics of GO in composites with metal oxides, metal sulfides, metal chalcogenides, layered double hydroxides, metal–organic frameworks, and MXene for supercapacitor application. Furthermore, the organic and bacterial functionalization of GO is discussed. The electrochemical properties of GO and its composite structures are discussed according to the performance of three- and two-electrode systems. Finally, this review compares the performance of several composite types of GO to identify which is ideal. The development of these composite devices holds potential for use in energy storage applications. Because GO-modified materials embrace both electric double-layer capacitive and pseudocapacitive mechanisms, they often perform better than pristine by offering increased surface area, conductivity, and high rate capability. Additionally, the density functional theory (DFT) of GO-based electrode materials with geometrical structures and their characteristics for supercapacitors are addressed.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141113318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-22DOI: 10.3390/inorganics12060143
A. Al-Wasidi, Reem K. Shah, Ehab A. Abdelrahman, El-Sayed M. Mabrouk
This work studies the synthesis, characterization, and application of CuFe2O4 nanoparticles for the removal of acid blue 113 and malachite green dyes from aqueous media. Utilizing the combustion procedure, CuFe2O4 nanoparticles were synthesized using two different fuels: L-alanine (CFA) and L-valine (CFV). Besides, the synthesized CuFe2O4 nanoparticles were characterized through some tools, including Fourier transform infrared (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray (EDX), and field emission scanning electron microscope (FE-SEM). XRD analysis verified the creation of a CuFe2O4 cubic spinel structure without any contaminants, revealing average crystallite sizes of 26.37 and 17.65 nm for the CFA and CFV samples, respectively. The FTIR spectra exhibited peaks indicative of metal-oxygen bond stretching, verifying the presence of a spinel formation. Elemental analysis via EDX confirmed the stoichiometric composition typical of copper ferrite. In addition, FE-SEM displayed that the CFA and CFV samples are composed of particles with spherical and irregular shapes, measuring average diameters of 188.35 and 132.78 nm, respectively. The maximum adsorption capabilities of the CFA and CFV samples towards acid blue 113 dyes are 281.69 and 297.62 mg/g, respectively. Also, the maximum adsorption capabilities of the CFA and CFV products towards malachite green dye are 280.11 and 294.99 mg/g, respectively. Kinetic and equilibrium studies revealed that the adsorption process of acid blue 113 and malachite green dyes onto the CFA and CFV samples followed the pseudo-second-order model and Langmuir isotherm. Thermodynamic analysis indicated that the adsorption process was physical, spontaneous, and exothermic.
{"title":"Facile Synthesis of CuFe2O4 Nanoparticles for Efficient Removal of Acid Blue 113 and Malachite Green Dyes from Aqueous Media","authors":"A. Al-Wasidi, Reem K. Shah, Ehab A. Abdelrahman, El-Sayed M. Mabrouk","doi":"10.3390/inorganics12060143","DOIUrl":"https://doi.org/10.3390/inorganics12060143","url":null,"abstract":"This work studies the synthesis, characterization, and application of CuFe2O4 nanoparticles for the removal of acid blue 113 and malachite green dyes from aqueous media. Utilizing the combustion procedure, CuFe2O4 nanoparticles were synthesized using two different fuels: L-alanine (CFA) and L-valine (CFV). Besides, the synthesized CuFe2O4 nanoparticles were characterized through some tools, including Fourier transform infrared (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray (EDX), and field emission scanning electron microscope (FE-SEM). XRD analysis verified the creation of a CuFe2O4 cubic spinel structure without any contaminants, revealing average crystallite sizes of 26.37 and 17.65 nm for the CFA and CFV samples, respectively. The FTIR spectra exhibited peaks indicative of metal-oxygen bond stretching, verifying the presence of a spinel formation. Elemental analysis via EDX confirmed the stoichiometric composition typical of copper ferrite. In addition, FE-SEM displayed that the CFA and CFV samples are composed of particles with spherical and irregular shapes, measuring average diameters of 188.35 and 132.78 nm, respectively. The maximum adsorption capabilities of the CFA and CFV samples towards acid blue 113 dyes are 281.69 and 297.62 mg/g, respectively. Also, the maximum adsorption capabilities of the CFA and CFV products towards malachite green dye are 280.11 and 294.99 mg/g, respectively. Kinetic and equilibrium studies revealed that the adsorption process of acid blue 113 and malachite green dyes onto the CFA and CFV samples followed the pseudo-second-order model and Langmuir isotherm. Thermodynamic analysis indicated that the adsorption process was physical, spontaneous, and exothermic.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141109106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-21DOI: 10.3390/inorganics12060142
V. Thirumal, B. Babu, P. Rajkumar, Jinho Kim, Kisoo Yoo
The development of advanced tin and niobium bimetallic composite electrode materials is crucial for enhancing the performance of supercapacitors. In this paper, we present a novel bimetallic composite material consisting of zero-dimensional spherical-like SnNb2O6 nanocomposites synthesized through the reaction of tin oxide (SnO2) and niobium pentoxide (Nb2O5) precursors, alongside comparative materials. The morphology of the spherical agglomerates comprising Sn/Nb oxide particles that were nucleated on the SnNb2O6 surface was characterized using field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM). The as-prepared heterostructures of the SnNb2O6 composites were analyzed for elemental composition, including Sn3d, Nb3d, and O1s; moreover, chemical oxidative state analysis was performed through X-ray photoelectron spectroscopy (XPS). Additionally, cyclic voltammetry curves exhibited pseudocapacitive redox behavior for the SnNb2O6 composites, while the galvanostatic charge-discharge (GCD) performance demonstrated a maximum specific capacitance of 294.8 F/g at 1 A/g. Moreover, SnNb2O6 composite electrodes demonstrated rapid charge–discharge kinetics and excellent cycling stability, with a capacitance retention of 95.7% over 10,000 cycles. This study elucidated the synthesis of tin–niobium oxide-based composites, demonstrating their potential for high-performance supercapacitors.
{"title":"Enhancing Supercapacitor Performance with Zero-Dimensional Tin–Niobium Oxide Heterostructure Composite Spheres: Electrochemical Insights","authors":"V. Thirumal, B. Babu, P. Rajkumar, Jinho Kim, Kisoo Yoo","doi":"10.3390/inorganics12060142","DOIUrl":"https://doi.org/10.3390/inorganics12060142","url":null,"abstract":"The development of advanced tin and niobium bimetallic composite electrode materials is crucial for enhancing the performance of supercapacitors. In this paper, we present a novel bimetallic composite material consisting of zero-dimensional spherical-like SnNb2O6 nanocomposites synthesized through the reaction of tin oxide (SnO2) and niobium pentoxide (Nb2O5) precursors, alongside comparative materials. The morphology of the spherical agglomerates comprising Sn/Nb oxide particles that were nucleated on the SnNb2O6 surface was characterized using field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM). The as-prepared heterostructures of the SnNb2O6 composites were analyzed for elemental composition, including Sn3d, Nb3d, and O1s; moreover, chemical oxidative state analysis was performed through X-ray photoelectron spectroscopy (XPS). Additionally, cyclic voltammetry curves exhibited pseudocapacitive redox behavior for the SnNb2O6 composites, while the galvanostatic charge-discharge (GCD) performance demonstrated a maximum specific capacitance of 294.8 F/g at 1 A/g. Moreover, SnNb2O6 composite electrodes demonstrated rapid charge–discharge kinetics and excellent cycling stability, with a capacitance retention of 95.7% over 10,000 cycles. This study elucidated the synthesis of tin–niobium oxide-based composites, demonstrating their potential for high-performance supercapacitors.","PeriodicalId":13572,"journal":{"name":"Inorganics","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141113586","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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