Ultrathin Nanosheets Research Articles

The study of electron mobility on ultra-scaled silicon nanosheet FET

The nanosheet FET (NSFET) is the successor to FinFET, and its mobility significantly affects device performance. In this paper, we investigate the impact of phonon (ph) and surface roughness (SR) scattering on the electron mobility of n-type silicon NSFETs. The effects of channel width, thickness, and doping concentrations on NSFETs' mobility are also analyzed. Non-Equilibrium Green’s Function (NEGF) solver which incorporates scattering mechanisms using the self-energy formulation is employed. The mobility behavior in NSFETs is strongly affected by ph scattering and SR scattering. As for ultrathin nanosheets, severe mobility degradation is dominated by SR scattering. The mobility is slightly affected by the doping concentrations. Simulation results provide guidance to researchers and industry in understanding and predicting the variation of mobility under the trend of continuous scaling.

Hierarchical NiCo2Se4 Arrays Composed of Atomically Thin Nanosheets: Simultaneous Improvements in Thermodynamics and Kinetics for Electrocatalytic Water Splitting in Neutral Media.

The inefficiency of electrocatalysts for water splitting in neutral media stems from a comprehensive impact of poor intrinsic activity, a limited number of active sites, and inadequate mass transport. Herein, hierarchical ultrathin NiCo2Se4 nanosheets are synthesized by the selenization of NiCo2O4 porous nanoneedles. Theoretical and experimental investigations reveal that the intrinsic hydrogen evolution reaction (HER) activity primarily originate from the NiCo2Se4, whereas the high oxygen evolution reaction (OER) performance is related to the NiCoOOH due to the structural reconstruction. The abundant Se and O vacancies introduced by atomically thin nanostructure modulate the electronic structure of NiCo2Se4 and NiCoOOH, thereby improving the intrinsic HER and OER activities, respectively. COMSOL simulation demonstrate the edges of extended nanosheets from the main body significantly promote the charge aggregation, boosting the reduction and oxidation current during HER/OER process. This charge aggregation effect notably exceeds the tip effect for the nanoneedle, highlighting the unique advantage of the hierarchical nanosheet structure. Benefiting from abundant vacancies and unique nanostructure, the hierarchical ultrathin nanosheet simultaneously improve the thermodynamics and kinetics of the electrocatalyst. The optimized samples display an overpotential of 92mV for HER and 214mV for OER at 100mA cm-2, significantly surpassing the performance of currently reported HER/OER catalysts in neutral media.

Multi-Responsive Peptide-Based Ultrathin Nanosheets Prepared by a Horizontal Monolayer Assembly.

In this study, peptide-based self-assembled nanosheets with a thickness of approximately 1 nm were prepared using a hierarchical covalent physical fabrication strategy. The covalent alternating polymerization of helical peptide E3 with an azobenzene (AZO) structure yielded copolymers CoP(E3-AZO), which physically self-assembled into ultrathin nanosheets in an unanticipated two-dimensional horizontal monolayer arrangement. This special monolayer arrangement enabled the thickness of the nanosheets to be equal to the cross-sectional diameter of a single linear copolymer, which is a rare phenomenon. Molecular dynamics simulations suggested that the synergistic effect of multiple molecular interactions drives the self-assembly of CoP(E3-AZO) into nanosheets and that various methods, including phototreatment, pH adjustment, the addition of additives, and introduction of cosolvents, can alter the molecular interactions and modulate the self-assembly of CoP(E3-AZO), yielding diverse nanostructures. Remarkably, the ultrathin nanosheets selectively inhibited cancer cells at certain concentrations.

Multi‐Responsive Peptide‐Based Ultrathin Nanosheets Prepared by a Horizontal Monolayer Assembly

AbstractIn this study, peptide‐based self‐assembled nanosheets with a thickness of approximately 1 nm were prepared using a hierarchical covalent physical fabrication strategy. The covalent alternating polymerization of helical peptide E3 with an azobenzene (AZO) structure yielded copolymers CoP(E3‐AZO), which physically self‐assembled into ultrathin nanosheets in an unanticipated two‐dimensional horizontal monolayer arrangement. This special monolayer arrangement enabled the thickness of the nanosheets to be equal to the cross‐sectional diameter of a single linear copolymer, which is a rare phenomenon. Molecular dynamics simulations suggested that the synergistic effect of multiple molecular interactions drives the self‐assembly of CoP(E3‐AZO) into nanosheets and that various methods, including phototreatment, pH adjustment, the addition of additives, and introduction of cosolvents, can alter the molecular interactions and modulate the self‐assembly of CoP(E3‐AZO), yielding diverse nanostructures. Remarkably, the ultrathin nanosheets selectively inhibited cancer cells at certain concentrations.

Rational Construction of Bi2CuO12Se4 and VGCFs@Fe2O3 Composite Electrodes for High-Performance Semi-Solid-State Asymmetric Supercapacitors.

Recently, supercapacitors (SCs) are extensively explored as effective energy storage devices. Specifically, asymmetric SCs are being developed to enhance energy density using suitable materials with favorable nanostructures. This study describes the construction of a bismuth copper selenite (BCS-200) working electrode with an ultrathin nanosheet(UTNS) architecture. This morphology is achieved using a low-cost electrodeposition (ED) method, followed by annealing. The impact of ED time on the development of morphology is studied by synthesizing comparative electrodes simultaneously. The optimized BCS-200 electrode prepared with a deposition time of 200 s shows higher specific capacity/capacitance (Cs/Csc) values of 330.9 mAh g-1/2206.6 F g-1 than the other synthesized electrodes (BCS-100, BCS-150, BCS-250, and BCS-300). Besides, a vapor-grown carbon fiber (VGCF)-added Fe2O3 composite coated on nickel foam (NF) is developed as a negative electrode. The VGCFs@Fe2O3/NF electrode exhibits the (Cs/Csc) values of 183.5 mAh g-1/734.4 F g-1, which is associated with ultra-high cycling stability. In addition, the fabricated BCS-200 and VGCFs@Fe2O3/NF electrodes are combined to construct a wearable semi-solid-state asymmetric SC (SSASC) with an energy density (Ed) of 20.5Wh kg-1 and a cycling stability of 91.7% over 40000 charge/discharge cycles. Furthermore, the real-time applicability of the SSASC is verified by powering it in practical applications.

Mild formation of Ni(OH)2 dense nanosheets array for ultra-efficient electrocatalytic hydrogen evolution

Synthesizing high performance and affordable nickel-based electrocatalysts has been one of the research hotspots in the field of clean energy conversion. Herein, facile electroless plating accompanied with mild impregnation method is explored to synthesize petal-like Ni(OH)2 flakes on carbon cloth (CC) for electrocatalytic alkaline hydrogen evolution reaction (HER). Notably, the optimal Ni(OH)2/CC electrode has outstanding HER activity requiring only 24.6 mV vs. RHE of overpotential to reach 25 mA cm−2 of current density, and only 101.5 mV vs. RHE of overpotential to reach 100 mA cm−2. Meanwhile, the 25-h stability test results performed well. This is primarily due to its plentiful interfacial contact, favorable surface morphology of ultrathin and dense nanosheets array, and rapid electron transport. Overall, this study provides a viable approach for the development of efficient, low-cost, hydrophilic nickel-based catalysts for electrocatalytic water splitting applications.

Rapid fluorescent nucleic acid sensing with ultra-thin gold nanosheets

Fluorescently labeled DNA oligonucleotides and gold nanospheres have been frequently utilized in biosensors, providing efficient nucleic acid detection. Nevertheless, the restricted loading capacity of gold nanospheres undermines overall sensitivity. In this study, we employed four-atom-thick ultrathin gold nanosheets (AuNSs), utilizing a “pre-mix model” for rapid target nucleic acid detection. In this approach, fluorescently labeled DNA probes were pre-incubated with the target nucleic acid, followed by the addition of AuNSs for probe adsorption and fluorescence quenching. With the developed method, we efficiently and rapidly detected the SARS-CoV-2 N gene sequence within 30 min, involving a brief 15-min target pre-incubation and a subsequent 15-min adsorption of free probes and fluorescence quenching by AuNSs. This method exhibited heightened sensitivity compared to gold nanospheres, boasting a limit of detection (LOD) of 0.808 nM. Furthermore, exceptional recovery was achieved in simulated biological samples. The study introduces an effective strategy for nucleic acid sensing characterized by rapidity, heightened sensitivity, ease of operation, and robustness. These findings encourage further development of rapid biomarker sensing methods employing 2D nanomaterials.

Ultrathin Ni-Fe MOF Nanosheets: Efficient and Durable Water Oxidation at High Current Densities.

Efficient, durable, and economical electrocatalysts are crucial for advancing energy technology by facilitating the oxygen evolution reaction (OER). Here, ultrathin Ni-Fe metal-organic skeleton (MOF) nanosheets were created in situ on nickel foam (NiFe-UMNs/NF). The catalyst exhibited excellent OER catalytical abilities, with only 269 mV overpotentials at 250 mA cm-2. Besides, when integrated with Pt/C/NF, NiFe-UMNs/NF held the potential for application in industrial alkaline water electrolysis with an initial voltage retention of approximately 86% following a continuous operation of 100 h at a current density of 250 mA cm-2. The super performance of the NiFe-UMNs/NF catalyst was attributed to ultrathin morphology, super hydrophilicity, and synergistic effects between Ni and Fe within the MOF. In situ Raman showed that NiFe-UMNs were converted to NiFeOOH as the active species in the OER process. Density functional theory revealed that iron doping accelerated the rate-determining step and reduced the OER reaction energy barrier. This work elucidated a promising electrocatalyst for OER and enriched the practical implementation of MOF materials.

Enhanced Photobiocatalytic Cascades at Pickering Droplet Interfaces.

Developing new methods to engineer photobiocatalytic reactions is of utmost significance for artificial photosynthesis, but it remains a grand challenge due to the intrinsic incompatibility of biocatalysts with photocatalysts. In this work, photocatalysts and enzymes were spatially colocalized at Pickering droplet interfaces, where the reaction microenvironment and the spatial distance between two distinct catalysts were exquisitely regulated to achieve unprecedented photobiocatalytic cascade reactions. As proof of the concept, ultrathin graphitic carbon nitride nanosheets loaded with Au nanoparticles were precisely positioned in the outer interfacial layer of Pickering oil droplets to produce H2O2 under light irradiation, while enzymes were exactly placed in the inner interfacial layer to catalyze the subsequent biocatalytic oxidation reactions using in situ formed H2O2 as an oxidant. In the alkene epoxidation and thioether oxidation, our interfacial photobiocatalytic cascades showed a 2.0-5.8-fold higher overall reaction efficiency than the photobiocatalytic cascades in the bulk water phase. It was demonstrated that spatial localization of the photocatalyst and the enzyme at Pickering oil droplet interfaces not only provided their respective preferable reaction environments and intimate proximity for rapid H2O2 transport but also protected the enzyme from oxidative inactivation caused by the photogenerated species. These remarkable interfacial effects contributed to the significantly enhanced photobiocatalytic cascading efficiency. Our work presents an innovative photobiocatalytic reaction system with manifold benefits, providing a cutting-edge platform for solar-driven chemical transformations via photobiocatalysis.

Reduced graphene oxide decorated CuO@NiO nanocomposite and their improved photosensitive activity for photodetection applications

In our proposed work, pure rGO and CuO@NiO/rGO (CNR) nanocomposites (NCs) with different ratios of CuO@NiO:rGO (90:10, 75:25 and 50:50) were synthesized and explored by XRD, SEM with EDX, TEM, XPS, UV–visible, PL and utilized to measure the current – voltage characteristics under dark and illumination conditions. TEM analysis indicates ultra-thin nanosheets of rGO with lengths of several tens of micrometer and CuO@NiO particle sizes is ∼50 nm. XPS analysis showed the presence of element and chemical states for Cu, Ni, O, and C in CNR-(50:50) sample. The energy gap (Eg) of pure rGO is 3.99eV whereas the CNR for 90:10, 75:25 and 50:50 NCs energy gap (Eg) values are viz., 1.43eV, 1.41eV and 1.39eV. The diode characteristic of CNR-(50:50)/n-Si exhibit lower ideality factor (n = 1.96), higher barrier height (ΦB = 0.80eV) under illumination condition. The CNR-(50:50)/n-Si photodiode exhibits higher photosensitivity (PS), responsivity (R), External Quantum Efficiency (EQE) and detectivity (D*) values of 956.45 %, 656.29 mA/W, 367.6/1 % and 5.72 × 1012 (Jones) respectively.

Structure-modulation of flower-like VS2 via ammonium ion intercalation for high performance potassium-ion batteries

Transition vanadium sulfide is a promising anode material for potassium-ion batteries (PIBs), but the volume variation during charge-discharge cycling and low electric conductivity seriously hinder its applications. Herein, we designed a multilayer lamellar self-assembled flower-like vanadium sulfide with ammonium ion intercalation (VS2–NF) by a facile and inexpensive hydrothermal method to improve its electrochemical potassium ion storage performance. By introducing ammonia during the hydrothermal synthesis process, the structures of vanadium sulfide transformed to nanoflowers composed by ultrathin nanosheets from the initial nanosphere structures. The intercalation of ammonium ion enlarges the lattice fringes and induces anisotropic growth of vanadium sulfide, resulting in a large number of mesopores and increased specific surface area as well as the reactive sites of vanadium sulfide, which contribute to the enhanced potassium ion storage performance. Consequently, the structure-modulated VS2–NF exhibits a high specific capacity of 507 mAh g−1 after 50 cycles at a current density of 100 mA g−1. This approach provides a new routine for the modification of other transition metal disulfides as anode materials for PIBs.

One-step electrodeposition synthesis of NiFePS on carbon cloth as self-supported electrodes for electrochemical overall water splitting

Electrocatalytic water splitting (EWS) for hydrogen production is considered an ideal strategy for utilizing renewable energy, reducing fossil fuel consumption, and addressing environmental pollution issues. Traditional noble metal electrocatalysts have excellent performance, but their cost is high. Developing efficient, stable, and relatively inexpensive dual functional electrocatalysts is crucial for promoting large-scale EWS hydrogen production processes. Herein, a simple one-step electrodeposition method was used to grow nickel–iron phosphorus-sulfides (NiFePS) on the surface of hydrophilic treated carbon cloth (CC). The resultant NiFePS/CC with a phosphorus to sulfur ratio of 1:4 exhibited the best electrocatalytic performance, requiring only −91 mV and 216 mV overpotentials to generate the current densities of 10 mA·cm−2 in hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. When it was used as a bifunctional electrocatalyst to overall water splitting (OWS), a voltage of 1.536 V can generate a current density of 10 mA·cm−2. The excellent electrocatalytic performance can be ascribed to two factors: 1) the CC with excellent conductivity serves as a growth substrate, reducing the impedance of charge transfer from the electrode to the electrolyte and accelerating the electron transfer rate; 2) The large number of ultra-thin nanosheets formed on the surface of the catalyst increase the electrochemical specific surface area, expose more reaction sites, and thus improve the electrocatalytic reaction performance. This work provides a new approach for designing efficient non-noble metal electrocatalysts for water splitting.

Multihole Ce-doped NiSe2/CoP hybrid nanosheets for improved electrocatalytic alkaline water and simulative seawater oxidation

The investigation of cost-effective and highly efficient electrocatalysts for alkaline water and simulative seawater oxidation is essential to the conversion and storage of renewable energy. In this paper, the Ce–NiSe2/CoP catalyst with multihole and ultrathin nanosheet structure is generated. The unique structural characteristics of Ce–NiSe2/CoP heterojunction nanosheets contribute the excellent OER performance under different alkaline 1 M KOH and simulated seawater (1 M KOH + 0.5 M NaCl) electrolytes. Specifically, this catalyst exhucture is generated. The unique structural characteristics of Ce–NiSe2/CoP heterojunction nanosheets conibits the low overpotentials of 287 and 304 mV at the current density of 10 mA cm−2, along with the Tafel slopes of 87.1 and 78.8 mV dec−1 in two solutions, respectively. Moreover, the Ce–NiSe2/CoP target product also displays good stability. The present study introduces a promising strategy for the advancement of high-performance electrocatalysts in green energy field.

A ZSM-5 zeolite nanosheet with single-unit-cell thickness templated by bi-ammonium surfactants with large-diameter hydrophobic groups

Ultra-thin zeolite nanosheets have received widespread attention due to their superior catalytic performance compared to bulk zeolites. Here, we have designed a new structure-directing agent with a tert-butyl benzene group as the large-diameter hydrophobic end of a bi-ammonium surfactant molecule. Using this novel structure-directing agent, zeolite nanosheets with a thickness of ∼ 2.5 nm were synthesized, which exhibit better catalytic performance than bulky zeolites in the Friedel-Crafts alkylation reaction of trimethylbenzene and benzyl alcohol.

Photothermal catalysis enhances cellulose oxidation kinetics to promote the hydrogen evolution in alkaline solution over Pt/ZnIn2S4

The slow oxidation kinetics of cellulose severely limits photocatalytic cellulose reforming for hydrogen production. Herein, ZIS photocatalysts with different morphologies were prepared and Pt nanoparticles were deposited on their surfaces. The cellulose oxidation kinetics were enhanced through the strategy of photothermal catalysis and pH optimization, which led to efficient hydrogen generation. The ultrathin nanosheet structure endows 1 % Pt/ZIS-300 with a stronger photogenerated carrier separation ability than 1 % Pt/ZIS-0 (nanoflower) and facilitates ·OH generation. Heat can induce the production of ·OH from 1 % Pt/ZIS-300 and enhance the adsorption of 1 % Pt/ZIS-300 to cellulose by changing the surface potential of 1 % Pt/ZIS-300, which promotes the oxidation kinetics of cellulose. As a result, the hydrogen yield of 1 % Pt/ZIS-300 under photothermal catalytic condition (80 ℃) reached 1218 μmol/gcat after 4 h of reaction. Appropriate NaOH concentration contributes to cellulose solubilization and ·OH production, but too high OH− concentration causes a negative shift of the potential on the 1 % Pt/ZIS-300 and cellulose surface, which hinders the mass transfer process and reduces the oxidation kinetics of cellulose.

Bio-synthesized copper nanoparticle anchored ultrathin petal-shaped black phosphorous nanosheets and 3D graphene decorated nanocomposite for electrochemical sensing of methotrexate and paracetamol in diverse matrices

Creating a sensor that can concurrently monitor multiple therapeutic drugs in complex media is a challenging yet essential endeavor. This study presents a novel biomolecule-free electrochemical platform for simultaneous and highly selective detection of methotrexate (MTR) and paracetamol (PRC) in various matrices, including pharmaceutical formulations, simulated blood samples, and water samples. The platform utilizes a multi-layered petal-shaped black phosphorous structure supported on 3D graphene, along with bio-synthesized copper nanoparticles (BP-3DGp@BCuN). Prior to the sensing study, the as-prepared BP-3DGp@BCuN nanocomposite was characterized using FESEM, EDX, FTIR, UV, XPS, Raman spectroscopy, BET, and XRD. Electrochemical studies of BP-3DGp@BCuN nanocomposite reveal a considerable enhancement of the current compared to pure BP or 3DGp. The petal-shaped black phosphorous comprising of 3DGp and BCuN provides a larger surface area, effective mass transport, and more active sites for the attachment of the target analytes that amplified the current signals and detection sensitivity. Furthermore, computational analysis proves that the BP-3DGp@BCuN nanocomposite has strong interaction with the target MTR and PRC compared to other modifiers. Under optimized conditions, the proposed sensing method shows a linear detection range of 0.05–70 µM and 0.5–210 µM with limit of detection (LOD) values of 0.045 nM and 0.36 nM, with high sensitivity of 37.40 and 14.94 μA μM−1 cm−2 for PRC and MTR respectively. The real-life application of the present sensor was examined in pharmaceutical formulations, simulated blood, and water samples.

Ultrafast and Parts-per-Billion-Level MEMS Gas Sensors by Hetero-Interface Engineering of 2D/2D Cu-TCPP@ZnIn2S4 with Enriched Surface Sulfur Vacancies.

The primary challenge for resonant-gravimetric gas sensors is the synchronous improvement of the sensitivity and response time, which is restricted by low adsorption capacity and slow mass transfer in the sensing process and remains a great challenge. In this study, a novel 2D/2D Cu-TCPP@ZnIn2S4 composite is successfully constructed, in which Cu-TCPP MOF is used as a core substrate for the growth of 2D ultrathin ZnIn2S4 nanosheets with well-defined {0001} crystalline facets. The Cu-TCPP@ZnIn2S4 sensor exhibited high sensitivity (1.5 Hz@50 and 2.3 Hz@100 ppb), limit of detection (LOD: 50 ppb), and ultrafast (9 s @500 ppb) detection of triethylamine (TEA), which is the lowest LOD and the fastest sensor among the reported TEA sensors at room temperature, tackling the bottleneck for the ultrafast detection of the resonant-gravimetric sensor. These above results provide an innovative and easily achievable pathway for the synthesis of heterogeneous structure sensing materials.

Ultrathin metal-organic framework nanosheets (Cu-TCPP) assembled micro flower combined with endonuclease signal amplification for ultrasensitive detection

Metal-organic framework play an important role in developing novel detection techniques. Herein, an ultrathin two-dimensional (2D) metal-organic framework nanosheet (Cu-TCPP) assembled microflower was successfully synthesized and applied for ultrasensitive detection. The high detection performance of Cu-TCPP microflower was attributed to high-capacity aptamer adsorption and specific desorption resulting from numerous approachable active sites, and its ultrathin nanosheets microflower-like structure. Moreover, the Cu-TCPP microflower had overcame the disadvantages of 2D MOF nanosheets which tended to agglomerate. Moreover, it exhibited excellent fluorescence quenching performance as a donor for fluorescence resonance energy transfer. Acetamiprid, a new chloronicotinic neurotoxic insecticide was used as the model analyte. The ultrasensitive sensor was developed by combining the Cu-TCPP microflower with deoxyribonuclease Ⅰ signal enhanced fluorescence. When acetamiprid was present, the fluorescent labeled aptamer probe was selectively bound to acetamiprid and desorbed from the Cu-TCPP microflower, resulting in fluorescence recovery. Subsequently, DNase Ⅰ was used to cleave the DNA strands of the aptamer probe, and acetamiprid was released to participate in a new cycle. The detection limit of the assay was as low as 5.56 pg/mL with a linear range 50.00 pg/mL∼5.00 μg/mL, and it was a universal platform to detect other analytes.

Electrocatalytic and Selective Oxidation of Glycerol to Formate on 2D 3d-Metal Phosphate Nanosheets and Carbon-Negative Hydrogen Generation.

In the landscape of green hydrogen production, alkaline water electrolysis is a well-established, yet not-so-cost-effective, technique due to the high overpotential requirement for the oxygen evolution reaction (OER). A low-voltage approach is proposed to overcome not only the OER challenge by favorably oxidizing abundant feedstock molecules with an earth-abundant catalyst but also to reduce the energy input required for hydrogen production. This alternative process not only generates carbon-negative green H2 but also yields concurrent value-added products (VAPs), thereby maximizing economic advantages and transforming waste into valuable resources. The essence of this study lies in a novel electrocatalyst material. In the present study, unique and two-dimensional (2D) ultrathin nanosheet phosphates featuring first-row transition metals are synthesized by a one-step solvothermal method, and evaluated for the electrocatalytic glycerol oxidation reaction (GLYOR) in an alkaline medium and simultaneous H2 production. Co3(PO4)2 (CoP), Cu3(PO4)2 (CuP), and Ni3(PO4)2 (NiP) exhibit 2D sheet morphologies, while FePO4 (FeP) displays an entirely different snowflake-like morphology. The 2D nanosheet morphology provides a large surface area and a high density of active sites. As a GLYOR catalyst, CoP ultrathin (∼5 nm) nanosheets exhibit remarkably low onset potential at 1.12 V (vs RHE), outperforming that of NiP, FeP, and CuP around 1.25 V (vs RHE). CoP displays 82% selective formate production, indicating a superior capacity for C-C cleavage and concurrent oxidation; this property could be utilized to valorize larger molecules. CoP also exhibits highly sustainable electrochemical stability for a continuous 200 h GLYOR operation, yielding 6.5 L of H2 production with a 4 cm2 electrode and 98 ± 0.5% Faradaic efficiency. The present study advances our understanding of efficient GLYOR catalysts and underscores the potential of sustainable and economically viable green hydrogen production methodologies.

A novel highly dispersed calcium silicate hydrate nanosheets for efficient high-concentration Cu2+ adsorption

Currently, the low cost and effective purification toward heavy metal ions in wastewater has garnered global attention. Herein, we used hydrothermal method to prepare highly dispersed calcium silicate hydrate in fluorite tailings. And the stacking thickness of calcium silicate hydrate layered morphology was less than 5 nm. For high concentration Cu2+ purification investigation in wastewater, we found that the equilibrium adsorption capacity reached 797.92 mg/g via the CSH with 3:2 Ca/Si molar ratio, be 1.43–21.8 times than that of reported data. Therein, the metal-metal exchange and deposition are the primary pathways for Cu2+ adsorption, and electrostatic attraction is the secondary pathway. And the relative ∼100 % removal rate of high-concentration Ni2+ and Cr3+ ions were confirmed via CSH prepared from different tailings. This method offers a cost-effective way to utilize tailings for preparing highly efficient adsorbents toward HMIs removal in wastewater.