SiO2 Source Research Articles

Utilizing copper waste to develop silicon-carbon anode materi als for lithium-ion batteries

This study dedicated to a novel method for synthesizing silicon-carbon (Si/C) and silicon dioxide-carbon (SiO2/C) nanocomposite anodes for lithium-ion batteries, utilizing industrial copper slags from the Almalyk Mining and Metallurgical Complex as a cost-effective source of SiO2. The synthesized nanocomposites address key challenges in lithium-ion battery anodes, including the volumetric expansion of silicon and its low conductivity, by leveraging the high lithiation capacity of silicon combined with the structural stability and conductivity of carbon. Amorphous SiO3 was extracted from copper slags via ammonium fluoride (NH4F) treatment and subsequently reduced to metallurgical-grade silicon through carbothermal reduction. The resulting SiO2/C and Si/C composites were thoroughly characterized using SEM, XRD, and electrochemical analyses, demonstrating improved electrochemical performance, favorable particle size distribution, and stability. This approach not only reduces material costs but also promotes environmental sustainability by repurposing industrial waste, offering promising candidates for high-performance lithium-ion battery anodes.

Investigating the dielectric characteristics, electrical conduction mechanisms, morphology, and structural features of mullite via sol-gel synthesis at low temperatures

This research explores the fabrication of mullite precursor powder utilizing the sol-gel process at low temperatures. Silicon tetraethoxide (Si(C2H5O)4) and aluminum nitrate nonahydrate (Al(NO3)3.9H2O) were employed as the sources of SiO2 and Al2O3 oxides, respectively. Various analytical techniques, such as Fourier transform infrared spectroscopy (FTIR), thermogravimetry (TG), dilatometry, differential thermal analysis (DTA), and X-ray powder diffractometer (XRD), were utilized to investigate the formation and crystallization of the amorphous powder. The microstructure of specimens sintered at 1600 °C for 1 h was examined utilizing scanning electron microscopy (SEM). Measurements of hardness (HV) and coefficient of thermal expansion (CTE) were conducted on mullite samples heated to 1600 °C and then cooled, revealing an increase in HV from 888 to 1000 HV as the sintering temperature rose from 1500 to 1600 °C. The CTE of mullite within the temperature range of 50–1300 °C was determined as 5.23 × 10−6/°C. Additionally, the dielectric and electrical characterization of mullite was analyzed utilizing complex impedance spectroscopy at a frequency of 0.1–106 Hz and conductivity measurements over a temperature range of 40–400 °C. The real and imaginary parts of the dielectric permittivity exhibited frequency-dependent and temperature-dependent behaviors. Significantly, the observed variations in the imaginary component of the modulus and impedance maximum frequency point to a relaxation process that is not Debye-type, with calculated activation energies (Ea) consistent across different methods.

Development of 3D-printed magnesium silicate hydrate cement mixes involving metakaolin as a substitute for silica source

ABSTRACT The printability of MgO-SiO2 cement pastes involving the use of microsilica (MS) and metakaolin (MK) as a SiO2 source was thoroughly investigated. Fresh properties, including rheology and early-age strength, mechanical properties and microstructures of pastes incorporating different contents of MK were presented and analyzed. Amongst samples studied, those containing 5% MK as a substitute for MS exhibited the highest static yield stress, and fastest re-flocculation and structuration rates, resulting in the best buildability. Although the inclusion of 10% MK resulted in enhanced paste strength at 7 and 28 days, increased MK content impeded paste printability due to diminished formation of hydrate phases. Use of 5% MK led to higher M-S-H generation compared to other samples at 28 days, contributing to subsequent strength development. Results demonstrated that optimisation of the MK content in MgO-SiO2 pastes can yield satisfactory mechanical strengths without compromising printability.

Sustainable ground improvement of soft clay using eggshell lime and rice husk ash

Stabilization of clay using lime or cement is conventionally accepted practice. Although it is effective, they impose several implications on the environment. Hence, it is high time that an alternate sustainable binder needs to be investigated. Eggshell, a waste from food industry, is an alternate source for calcite and can be considered to produce eggshell lime (EL). Also, rice husk ash (RHA), an agricultural waste product, is a silica rich source which is a pozzolanic material. In the current study, the efficiency of both the materials in stabilizing the soft soil is investigated and the results suggests that the plasticity and the strength characteristics of soft clay can be significantly improved by the addition of EL. After adding optimum concentration of 3 % EL, the liquid limit decreased from 74 % to 53 %, plastic limit increased from 27 % to 46 % and shrinkage limit increased from 8 % to 44 %. On increasing the EL content, the swelling got reduced from 88 % of virgin clay to 17 % in case of 3 % EL and finally to zero with 5 % of EL. Also, the addition of combination of EL and RHA to the soft clay has improved the strength characteristics significantly. As the curing days increased, slight variation was only seen in the plasticity characteristics which may be due to rapidity of cation exchange. But strength characteristics increased suggesting the occurrence of pozzolanic reactions and formation of gel. The 28th day strength of the clay treated with 3 % EL increased to as high as 757 kPa. The strength characteristics showed that as we increase the percentages of EL and RHA combination, the strength would increase tremendously much better than the treatment with eggshell lime alone. This is because of the supply of CaO and SiO2 sources. For 5 % of EL and 15 % of RHA, the 1 day curing strength was near to 500 kPa. With less concentration of eggshell lime and RHA, the treated soil was appearing to be more porous in SEM while when the binder concentration was increased, the pores were filled and presence of C-S-H gel was also detected. XRD test results also showed the presence of C-S-H gel.

Utilizing silica fume and synthetically produced mesoporous silicas for simulated flue gas CO2 adsorption

ABSTRACT Carbon capture and storage (CCS) is crucial in mitigating greenhouse gas emissions. Solid adsorbents, notable for their reusability and corrosion resistance, are gaining attention in CO2 gas separation. This study uses Silica fume as an adsorbent and silica source for SiO2 and MCM-41 silica-based adsorbents. Silica was extracted via an alkaline dissolution method, and adsorbents were synthesized using a CO2-induced precipitation method, chosen for its shorter synthesis time and CO2 utilization. The effects of pore volume, average pore diameter, and specific surface area on amine loading and CO2 adsorption capacity were investigated using CTAB surfactant in SiO2 synthesis, resulting in MCM-41. The synthesized adsorbents were modified with TEPA and DEA amines due to their high affinity for CO2. After determining optimal amine loading, the impact of combining TEPA with DEA was examined. The highest CO2 adsorption capacity under simulated flue gas conditions (15% volume CO2 and 85% volume N2) was 198 milligrams per gram of adsorbent for the SiO2 adsorbent functionalized with 50% by weight amine (28% TEPA and 22% DEA). Variations in CO2 adsorption over time, the influence of adsorbent quantity on adsorption capacity, the affinity of the adsorbent for N2 adsorption, and the adsorption–desorption cycle were investigated. The 28%TEPA-22%DEA-SiO2 adsorbent emerged as the optimal choice due to its large total volume and average pore diameter, absence of a template in its structure, excellent performance in CO2 adsorption, lack of affinity for N2, and robust adsorption–desorption stability.

The Potential Perspective of Processing Rice Husk as SiO<sub>2</sub> Source to Tetraalkoxysilane in Indonesia

Tetra-alkoxysilane (TROS) is one of the useful chemicals and it can be processed to produce semiconductor and photovoltaic devices. Now, the transformation of silica (SiO2) to TROS is garnering interest due to the potential of extracting it from biomass. As the 14th largest country, Indonesia possesses an abundant source of SiO2 from mining activities and agricultural waste, notably rice husk (RH). However, only a little concrete action is planned for leveraging RH into a more valuable industrial substance. This review will explain two routes for TROS—conventional and direct—comparing their respective benefits and drawbacks. Additionally, it presents a simulation of various scenarios for scaling TROS production to an industrial level, considering technoeconomic and environmental assessment aspects. The focus then shifts to Indonesia’s strategic trajectory for 2045, offering recommendations to enhance resource utilization for economic and national development.

Li4SiO4-Based Heat Carrier Derived from Different Silica Sources for Thermochemical Energy Storage

Thermochemical energy storage (TCES) is one of the key technologies facilitating the integration of renewable energy sources and mitigating the climate crisis. Recently, Li4SiO4 has been reported to be a promising heat carrier material for TCES applications, owing to its moderate operation temperature and stability. During the synthetic processes, the properties of the Si source used directly influence the performance of derived Li4SiO4 materials; however, the internal relations and effects are not yet clear. Hence, in this work, six kinds of SiO2 sources with different phases, morphology, particle size, and surface area were selected to synthesize a Li4SiO4-based TCES heat carrier. The physicochemical properties of the SiO2 and the corresponding derived Li4SiO4 were characterized, and the comprehensive performance (e.g., heat storage/releasing capacity, rate, and cyclic stability) of the Li4SiO4 samples was systematically tested. It was found that the silica microspheres (SPs), which possess an amorphous phase, uniform micro-scale structure, and small particle size, could generate Li4SiO4 TCES materials with a highest initial capacity of 777.7 kJ/kg at 720 °C/900 °C under pure CO2. As a result, the SP-L showed an excellent cumulative heat storage amount of 5.84 MJ/kg within 10 heat-releasing/storage cycles, which was nearly 1.5 times greater than the value of Li4SiO4 derived from commonly used silicon dioxide. Furthermore, the effects of the utilized Si source on the performance of as-prepared Li4SiO4 and corresponding mechanisms were discussed, which offers guidance for the future selection of Si sources to produce high-performance Li4SiO4-based TCES heat carriers.

High-temperature CO2 sorption over Li4SiO4 synthesized from diatomite: study of sorption heat and isotherm modeling.

The Li4SiO4 seems to be an excellent sorbent for CO2 capture at post-combustion. Our work contributes to understanding the effect of the natural Algerian diatomite as a source of SiO2 in the synthesis of Li4SiO4 for CO2 capture at high temperature. For this purpose, we use various molar % (stoichiometric and excess) of calcined natural diatomite and pure SiO2. To select the best composition, CO2 sorption isotherms at 500°C on the prepared Li4SiO4 are obtained using TGA measurements under various flows of CO2 in N2. The sorbent having 10% molar SiO2 in diatomite (10%ND-LS) exhibits the best CO2 uptake, probably due to various factors such as the content of the different secondary phases. A comparative study was performed at 400 to 500°C on this selected 10%ND-LS and those with stoichiometric composition obtained with diatomite and pure SiO2. The obtained isotherms show the endothermic character of CO2 sorption. In addition, the evolution of isosteric heat highlights the nature of the involved CO2/Li4SiO4 interactions, by considering the double-shell mechanism. Finally, the experimental sorption isotherms are confronted with some well-known adsorption models to explain the phenomenon occurring over our prepared sorbents. Freundlich and Jensen-Seaton models present a better correlation with the experimental results.

Fabrication of Porous Anorthite Ceramic Insulation Using Solid Wastes.

Porous anorthite (CaAl2Si2O8) ceramics, suitable for thermal insulation in buildings, were obtained using waste seashells as a source of CaO, kaolin as a source of Al2O3 and SiO2 and banana peel as a pore former. Changing the volume of banana peel as well as the processing temperature was found to be an effective approach to control the thermo-mechanical properties of the obtained anorthite ceramics. The sintering of powder compacts containing up to 30 wt% banana peel at temperatures ranging from 1100 to 1200 °C resulted in anorthite ceramics possessing up to 45% open porosity, a compressive strength between 13 and 92 MPa, a bulk density between 1.87 and 2.62 g/cm3 and thermal conductivity between 0.097 and 3.5 W/mK. It was shown that waste materials such as seashells and banana peel can be used to obtain cost-effective thermal insulation in buildings.

Precipitation synthesis of Zn2-xCoxSiO4 blue ceramic pigments: Color performance and application

A simplified precipitation route based on using silica hydrogel derived from serpentine minerals as a source of silica SiO2 has been first applied for producing blue cobalt-doped willemite pigments. The relevant variations of cobalt ions concentrations in SiO2–NaOH–ZnCl2–CoCl2–H2O system adequate with Zn2-xCoxSiO4 compositions where 0<x ≤ 0.92 and heat-treatment at 900 °C have yielded the pigments demonstrating a wide spectrum of blue tints. The optical characteristics of these pigments have revealed that Zn1·5Co0·5SiO4 pigment is distinguished by the highest absorption responsible for deepest blue hue similar to ultramarine. The comparison of their chromatic parameters with those of the identical ones produced by sol-gel routes has shown that the synthesized pigments with the compositions where x = 0.2 ÷ 0.5 manifest competitive color performances. The synthesis optimization has reduced calcination temperature up to 800 °C and stirring time up to 60 min. The homogeneity achieved in the intermediates by the suggested synthesis has yielded the pigments having uniform crystalline structure with controlled particle size. 120-minutes stirring has reduced the pigment particle size to dimensions less than 66 nm. Zn1.5Co0.5SiO4 pigment exhibits excellent color performances and tinting on heating up to 1200 °C and in wall tile glaze.

Origin of quartz and its implications for different phase fluids in lacustrine shales from the Qingshankou Formation, southern Songliao Basin, China

Quartz, an important mineral that occurs in lacustrine shales, can be of different types and origins. Yet, only few studies have investigated how quartz from different sources contribute to phase fluids, such as adsorbed and free fluids present within shale matrix pores. This study integrates various experimental techniques, including X-ray diffraction analysis, geochemical analysis, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and high-frequency two-dimensional nuclear magnetic resonance analysis to quantitatively characterize the different phase fluids associated with various types of quartz occurring in the Qingshankou Formation shale. The characterization results indicated four distinct quartz types: silt-sized quartz, microcrystalline quartz linked with clay minerals, organism-skeletal quartz, and quartz aggregates comprising multiple crystals. The Fe–Al–Mn ternary diagram and SiO2 versus Zr scatter plot indicate that terrigenous clastic material is the primary source of SiO2 in shale quartz. Smectite-to-illite transition plays a pivotal role in authigenic quartz formation. Based on quartz concentration data obtained using major element analysis, we estimated the ranges of terrigenous clastic quartz, diagenetic quartz formed by the smectite-to-illite transition, and biogenic quartz concentrations to be from 55.49% to 92.03% (average 84.70%), 6.67%–20.30% (average 13.12%), and 0%–24.21% (average 2.17%), respectively. The solid organic matter in shale is affected by both terrigenous detrital quartz and authigenic quartz transformed from the clay in the basin. Authigenic quartz, formed by the smectite-to-illite transition, considerably enhances the development of solid organic matter in the Qingshankou Formation. By contrast, an abundance of terrigenous detrital quartz can lead to a dilution of the solid organic matter. Thus, this study provides the first direct evidence that along with a high value of bio-organic matter yield factor, the source of quartz plays a significant role in controlling organic matter abundance.

Carbon Capture Performance Enhancement of Solid State Synthesized Li4SiO4 Powders by Using Different Kind Steel Slags as SiO2 Source

The potential of lithium orthosilicate (Li4SiO4) as a material to capture carbon dioxide (CO2) is being explored due to its excellent capture capability and thermal stability. Currently, a significant portion of the world's energy needs are met through the burning of fossil fuels, which leads to an increase in atmospheric CO2 and contributes to global warming. While fossil fuels will remain the primary source of energy for several more years, it is crucial to develop cost-effective and environmentally friendly technology for large-scale CO2 capture and storage before its release into the atmosphere in order to mitigate the associated greenhouse effect. This study focuses on optimizing the synthesis of lithium orthosilicate using a solid-state method to enhance CO2 capture. The research involves assessing the key characteristics of the synthesized material that improve CO2 capture efficiency. The starting materials used for comparison include lithium carbonate (Li2CO3), BF (blast furnace), BOF (blast oxygen furnace) and EAF (electric arc furnace) slags, and pure reagents of silicon dioxide (SiO2). The effect of process conditions, such as synthesis temperatures ranging from 850 to 950°C and varying holding times of 4, 6, 8, and 10 hours in a muffle furnace, were studied and compared. X-ray diffraction (XRD) analysis was performed to characterize the samples and slags. CO2 capture performance of the samples were evaluated in thermobalance test under 92 vol% CO2 (N2 balance) gas concentration at 600°C. As to conclude, carbon dioxide capturing sorbent material was produced by utilizing the slags generated as a by-product in steel production. Thus, considering the principles of circular economy, a material defined as waste was used as raw material for the production of another product used for lowering atmospheric CO2 levels.

Key developments in magnesiothermic reduction of silica: insights into reactivity and future prospects.

Porous Si (p-Si) nanomaterials are an exciting class of inexpensive and abundant materials within the field of energy storage. Specifically, p-Si has been explored in battery anodes to improve charge storage capacity, to generate clean fuels through photocatalysis and photoelectrochemical processes, for the stoichiometric conversion of CO2 to value added chemicals, and as a chemical H2 storage material. p-Si can be made from synthetic, natural, and waste SiO2 sources through a facile and inexpensive method called magnesiothermic reduction (MgTR). This yields a material with tunable properties and excellent energy storage capabilities. In order to tune the physical properties that affect performance metrics of p-Si, a deeper understanding of the mechanism of the MgTR and factors affecting it is required. In this perspective, we review the key developments in MgTR and discuss the thermal management strategies used to control the properties of p-Si. Additionally, we explore future research directions and approaches to bridge the gap between laboratory-scale experiments and industrial applications.

Synthesis of double-shell carbonyl iron powder @SiO2 @C for enhanced electromagnetic wave absorption

Enhancing the electromagnetic wave absorption bandwidth and reflection loss depth of carbonyl iron powder (CIP) is a known challenge. Building a core-shell structure for electromagnetic wave absorbing materials is one of the most effective methods available. In this paper, tetraethyl orthosilicate was used as the SiO2 source and glucose-coated as the carbon source, and then the capsules were carbonized at 300 °C for 5 h to obtain CIP@SiO2 @C capsules with a bilayer shell structure. The minimum RL was − 62.2 dB at 11.9 GHz with a thickness of 1.73 mm, and the effective absorption bandwidth (RL < −10 dB) was up to 8.6 GHz at 1.64 mm coating thickness, covering almost the whole X and Ku bands(8–18 GHz). The results showed that the microwave absorption performance significantly improved after introducing SiO2 and carbon shell layer structure. The excellent absorption performance can be attributed to the enhanced eddy current loss., impedance matching characteristics, and the synergistic effect of dielectric and magnetic losses after the introduction of the coating. We believed that this work would provide a valuable reference for structural design and optimization of high-performance absorbing materials.

Sustainable Harnessing of SiO2 Nanoparticles from Rice Husks: A Review of the Best Synthesis and Applications

The extraction of silica particles from rice husks has been extensively studied. This review aims to present the most efficient approach to harnessing rice husk biomass and converting silica into high-value-added materials for direct applications to address current challenges like water purification. Rice husks, as a residue from agriculture, had been largely used as a source of power through direct incineration in major rice-producing countries. However, rice husks present an intriguing opportunity as a renewable source of SiO2, offering a low-cost adsorbent with a high surface area and ease of functionalization that can be transformed into diverse mesoporous silica structures or composites, enabling applications in catalysis, drug delivery, water treatment, etc. This dual potential of rice husks can be harnessed by combining bio-oil and syngas production through pyrolysis with the efficient extraction of SiO2, ensuring the comprehensive utilization of the biomass. This review not only highlights the immense potential of silica nanoparticles but also serves as a roadmap for future investigations, with the ultimate aim of harnessing the full capabilities of this renewable and sustainable resource, contributing to the circular economy by yielding valuable by-products.

Synthesis and characterization of Fe3O4/SiO2/Alginate photocatalyst from tin tailings for batik cual waste degradation

Fe3O4/SiO2/Alginate as photocatalyst for degradation of Batik Cual Waste has been synthesized. This study aimed to determine the degradation of cual batik waste using Fe3O4/SiO2/Alginate photocatalyst assisted by UV-C light. In this research, Fe3O4 was synthesized through the coprecipitation method, then coated with SiO2 and sodium alginate The source of SiO2 used comes from tin tailings sand. SiO2 content in tin tailings is 87.45%. UV DRS analysis showed that the band gap energies of SiO2, Fe3O4, Fe3O4/SiO2, Fe3O4/SiO2/Alginate were 1.76 eV, 1.61 eV, 2.04 eV and 1.59 eV, respectively. XRD analysis showed that the Fe3O4/SiO2 composite was successfully formed in the presence of typical diffraction peaks for silica quartz and magnetite on the composite diffractogram. Based on the percent degradation data, it was obtained that the optimal degradation time using the Fe3O4/SiO2/Alginate composite was 96.73% at 30 minutes.

Improvement of Phase Transformation and Densification of SiO2-ZrO2 Ceramics by Using Desert Sand as a SiO2 Source

Improvement of Phase Transformation and Densification of SiO2-ZrO2 Ceramics by Using Desert Sand as a SiO2 Source

Source of quartz cement and its impact on reservoir quality in Jurassic Shaximiao Formation in central Sichuan Basin, China

Quartz cement is an essential authigenic mineral in the tight sandstones of the Shaximiao Formation in the Sichuan Basin, China. Accurately identifying its sources and investigating its impact on reservoir quality is important for understanding diagenetic fluid evolution and pore development in these reservoirs. To address this, we conducted a systematic analysis of the silicon sources in quartz cement employing mineralogical, fluid inclusion, and geochemical data. Quartz cement is characterized by two phases of quartz overgrowth and pore-filling authigenic quartz. Homogenization temperatures of fluid inclusions range from 60 to 150 °C, indicating that quartz cementation occurred from the early diagenetic phase (B stage) to the late mesodiagenetic phase. During the early diagenetic stage, volcanic material was dissolved by meteoric water, resulting in the formation of the earliest quartz cement and smectite. At temperatures of approximately 70–100 °C, smectite illitization, accompanied by K-feldspar consumption and SiO2 precipitation. In the mesodiagenetic stage (temperature approximately 100–130 °C), organic acids led to the dissolution of minerals like feldspar and laumontite, releasing SiO2. In the deep burial stage, clastic quartz grains experienced dissolution due to high stress, providing a limited source of SiO2. Smectite alteration and the dissolution of aluminosilicate minerals represent the primary sources of silicon for quartz cementation, while contributions from volcanic material hydrolysis and pressure solution are relatively minor. The presence of chlorite films inhibits the development of quartz overgrowths, and the limited precipitation of authigenic quartz within the primary porosity has a minimal impact on reservoir quality. Consequently, sandstones rich in chlorite films represent a favorable lithology for the development of high-quality reservoirs.

Propylamine Silica-Titania Hybrid Material Modified with Ni(II) as the Catalyst for Benzyl Alcohol to Benzaldehyde Conversion

SiO2-TiO2@propylamine-Ni(II) as the catalyst for the benzyl alcohol oxidation has been synthesized by utilizing rice husk ash as the SiO2 source. This research was started by extracting SiO2 from rice husk ash and continued by synthesizing the SiO2-TiO2 composite using titanium(IV) tetraisopropoxide (TTIP) as TiO2 precursor and PEG-40 as template. The composite functionalization and metal modification were carried out by adding (3-aminopropyl)triethoxysilane (APTES) as the source of propylamine linker and impregnating NiCl2·6H2O as the nickel precursor, respectively. The catalysts were synthesized by varying the ratios between each component within the material. The prepared materials were then characterized using ATR-IR, XRD, XRF, PSA, SAA, AAS, SEM-EDX, HR-TEM, and TGA. The catalyst activity was investigated by applying it to the oxidation reaction of benzyl alcohol to benzaldehyde with H2O2 as the oxidizing agent under sonication system. The obtained products were then analyzed by using GC-MS to quantify the success of the reaction. All characterizations performed in this research generally indicate the success in the synthesis of SiO2-TiO2@propylamine-Ni(II) materials. Under the same condition including at room temperature, 1 h reaction time, and sonication system, the optimal oxidation reaction of benzyl alcohol was reached when SiO2-TiO2@propylamine-Ni(II)5 was used as the catalyst in 98.52% yield.

Two New Members of the Lanthanoid Bismuth Oxide Oxidosilicates LnBiO[SiO4] with Ln=La and Gd

AbstractThe isostructural lanthanoid bismuth oxide oxidosilicates with the formula LnBiO[SiO4] (Ln=La and Gd) crystallize in the triclinic space group with the lattice parameters a=571.04(3) pm, b=681.13(4) pm, c=697.98(4) pm and α=105.805(2)°, β=110.456(2)°, γ=99.871(2)°, Vuc=0.23380(2) nm3 for Ln=La and a=554.12(3) pm, b=670.68(4) pm, c=689.57(4) pm and α=104.619(2)°, β=110.793(2)°, γ=99.560(2)°, Vuc=0.22237(2) nm3 for Ln=Gd with Z=2 for both. Colorless single crystals were serendipitously obtained from the reaction of bismuth sesquioxide, bismuth trifluoride and the lanthanoid sesquioxides at 850 °C in unprotected torch‐sealed silica ampoules as SiO2 source. Their crystal structure features Ln3+ cations surrounded by eight oxygen atoms as distorted square antiprisms [LnO8]13−, which are linked via edges with three further polyhedra of this kind to form layers {[LnO O ]7−} within the (010) plane. The oxygen environment of the Bi3+ cations has to be described as ψ1‐octahedral (square pyramids [BiO5]7−) with five oxide ligands and the stereochemically active lone pair. Two of them are edge‐linked to form ψ1‐bioctahedra [Bi2O8]10−. Four out of five oxygen atoms belong to discrete [SiO4]4− tetrahedra, which separate {[OLn Bi ]4+} chains of trans‐edge connected [OLn2Bi4]10+ tetrahedral, centered by the fifth oxygen atom propagating along [100] for charge compensation. Furthermore, the magnetic properties of GdBiO[SiO4] were investigated, showing Curie‐Weiss behavior without any magnetic ordering phenomena down to lowest temperatures.