INORGANIC CHEMISTRY COMMUNICATIONS
·
2021
·
IF 2.495
Yanan Ding,Feng Wei,Changchang Dong,Jiadong Li,Chang Zhang,Xiaojun Han
Heavy metal ion pollution has been a potential threat to human health. Herein, a sensitive electrochemical sensor for simultaneously detection of Cd(II) and Pb(II) was developed using a metal–organic framework material UiO-66. UiO-66 before and after carbonization was used to modify the GCE electrodes, respectively. The carbonized UiO-66 modified GCE electrode (CUiO-66/Bi/GCE) showed good detection ability with the linear detection range of 10–50 μg/L and detection limit of 1.16 and 1.14 μg/L for Cd(II) and Pb(II), respectively. Compared with UiO-66, carbonized UiO-66 provided more active sites for Bi ions and heavy metal ions to co-deposit and facilitated the electron transfer, leading to better detection performance. The decoration strategy was applied to disposable screen-printed carbon electrodes (SPCEs) to obtain the linear detection range of 20–120 μg/L and detection limit of 4.67 and 1.24 μg/L for Cd(II) and Pb(II) respectively. The prepared electrochemical sensors hold great potential in real water sample detections.
研究领域:
环境科学
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分析化学
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Khak Ho Lim,Yuxuan Xia,Lixiang Xu,Mingjun Zhao,Mingquan Li,Ye Cheng,Jiale Mao,Shuang Wang,Lei Chen,Sai Wing Tsang,Pingwei Liu,Qingyue Wang,Xuan Yang,Wen-Jun Wang,Andreu Cabot,Min Hong,Yu Zhang,Yu Liu
Ag 2 Se has emerged as a promising thermoelectric (TE) material for room-temperature applications. However, its TE performance is limited by the low carrier effective mass ( m* ) of only 0.1 m 0 , where m 0 represents the free electron mass. In this study, we employ a microwave-assisted method to synthesize nanostructured Ag 2-x Se with Pb doping that is found to increase m* to 0.4 m 0 . Accordingly, the Seebeck coefficient is significantly enhanced, which together with the high electrical conductivity, leads to enhanced electronic transport. The increase in m* is systematically investigated by density functional theory calculations and linked to the enhanced electronic by modeling simulations. The calculated band structures reveal that the hybridization of heavy Pb-6p orbitals flattens the conduction band edges, and thereby enhances m* . Furthermore, Pb doping significantly reduces the lattice thermal conductivity due to the high-density point defects, dislocations, and grain boundaries, as revealed by detailed electron microscopy characterizations. The synergy from both enhanced electronic transport and reduced phonon propagation yielded a maximum figure of merit of 1.04 at 376 K, and an average figure of merit of 1.0 for Pb-doped Ag 1.9 Se. The optimized TE performance is further validated in a flexible TE generator, which produced a maximum output power of 0.6 μW at a temperature difference of 45 K. These findings demonstrate that enhancing m* and increasing phonon-scattering using vacancy tuning and aliovalent doping effectively boosts the TE performance of Ag 2 Se, a strategy that can be extended to other TE materials to maximize their potentials for power generation and thermoelectric cooling applications.
研究领域:
材料科学
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凝聚态物理
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产品关联
DOI
高影响因子
Small Methods
·
2023
·
IF 12.4
Shanhong Wan,Shanshan Xiao,Mingquan Li,Xin Wang,Khak Ho Lim,Min Hong,Maria Ibáñez,Andreu Cabot,Yu Liu
Developing cost-effective and high-performance thermoelectric (TE) materials to assemble efficient TE devices presents a multitude of challenges and opportunities. Cu 3 SbSe 4 is a promising p -type TE material based on relatively earth abundant elements. However, the challenge lies in its poor electrical conductivity. Herein, an efficient and scalable solution-based approach is developed to synthesize high-quality Cu 3 SbSe 4 nanocrystals doped with Pb at the Sb site. After ligand displacement and annealing treatments, the dried powders are consolidated into dense pellets, and their TE properties are investigated. Pb doping effectively increases the charge carrier concentration, resulting in a significant increase in electrical conductivity, while the Seebeck coefficients remain consistently high. The calculated band structure shows that Pb doping induces band convergence, thereby increasing the effective mass. Furthermore, the large ionic radius of Pb 2+ results in the generation of additional point and plane defects and interphases, dramatically enhancing phonon scattering, which significantly decreases the lattice thermal conductivity at high temperatures. Overall, a maximum figure of merit ( zT max ) ≈ 0.85 at 653 K is obtained in Cu 3 Sb 0.97 Pb 0.03 Se 4 . This represents a 1.6-fold increase compared to the undoped sample and exceeds most doped Cu 3 SbSe 4 -based materials produced by solid-state, demonstrating advantages of versatility and cost-effectiveness using a solution-based technology.
研究领域:
材料科学
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能源技术
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产品关联
DOI
PubMed
高影响因子
Journal of the Taiwan Institute of Chemical Engineers
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2016
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IF 2.848
Ruiqi Fu,Yu Liu,Zimo Lou,Zhuoxing Wang,Shams Ali Baig,Xinhua Xu
A novel adsorbent (AC/Fe 3 O 4 @SiO 2 –NH 2 ) was synthesized via a co-condensation process for the enhanced removal of Pb(II) from aqueous solutions. Characterization analyses including SEM, TEM, BET and XRD confirmed the successful integration of magnetic nanoparticles and amino groups with carbon matrix. Results demonstrated that AC/Fe 3 O 4 @SiO 2 –NH 2 (mass ratio of AC to Fe 3 O 4 was 1:0.25) with specific surface area (48.9 m 2 /g) showed higher adsorption capacity for Pb(II) as compared to other mass ratios. Kinetics study revealed that the adsorption reach equilibrium within 20 h and the maximum adsorption capacity of 104.2 mg/g was achieved with increasing the initial concentration from 20 to 250 mg/L using AC/Fe 3 O 4 @SiO 2 –NH 2 . Maximum removal efficiency was recorded at pH 5.2 and the removal capacities toward four divalent metal ions calculated by the Langmuir model were found to be in the order of Pb(II) > Cu(II) > Ni(II) > Cd(II). Furthermore, Δ G 0 decreased from –1.6 to −3.1 kJ/mol with increase in temperature from 293 to 333 K illustrating that the adsorption was spontaneous and an endothermic process. Complexation adsorption mechanism was found prominent in FTIR and XPS analyses between Pb(II) and AC/Fe 3 O 4 @SiO 2 –NH 2 due to the presence of amino groups.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
RSC Advances
·
2014
·Vol. 4
·期 56
·29715-29723
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IF 3.708
Shoulian Wei,Yong Liu,Mingdong Shao,Ling Liu,Hongwu Wang,Yanqing Liu
A novel magnetic ion-imprinted polymer (MIIP) was prepared by inverse microemulsion polymerization using ethylene glycol dimethacrylate (EGDMA) as the cross-linker, and 2,2-azo-bis-isobutyronitrile (AIBN) as the initiator. Fe3O4 particles were incorporated into the imprinted polymer matrix containing 4-vinyl pyridine and acrylate-modified Spirulina platensis as the functional monomers, Pb(II) and Cd(II) as double-templates. The MIIP product was characterized by Fourier-transform infrared spectroscopy, thermal gravimetric analysis and scanning electron microscopy and then evaluated for the magnetic solid-phase extraction of Pb(II) and Cd(II) from environmental and food samples. Inductively coupled plasma-optical emission spectrometry detection was also performed. The obtained MIIP showed the magnetic property, agglomerates of globular particles and rough surface morphologies. The maximum static adsorption capacities of MIIP for Pb(II) and Cd(II) were 108 and 56 mg g−1, respectively. The factors affecting the adsorption and separation of Pb(II) and Cd(II), namely, solution pH, adsorbent dosage, eluting solvent, and elution time, were investigated. Under the optimized conditions, the detection limits (S/N = 3) of the method were 0.1 and 0.08 μg kg−1 for Pb(II) and Cd(II), respectively. The relative standard deviations (RSDs) for 10-replicate detections of a soil sample were 3.3% and 3.7% for Pb(II) and Cd(II), respectively. Standard solutions containing Pb(II) and Cd(II) in the concentration range of 0.8 to 5000 μg kg−1 were analyzed by the proposed procedure and it was found that the calibration curve was linear in this range (R2 ≥ 0.999). The proposed method was successfully used to determine the Pb(II) and Cd(II) contents of cinnamon, lotus root and sweet potato with recovery rates ranging from 87.5% to 106%.
研究领域:
材料科学
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分析化学
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环境科学
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产品关联
DOI
高影响因子
Science China-Chemistry
·
2017
·Vol. 61
·期 2
·164-171
·
IF 4.132
Huang Xueqiong,Kong Long,Huang Shouqiang,Liu Min,Li Liang
In this work, we report the synthesis of magnetic sulfur-doped Fe 3 O 4 nanoparticles (Fe 3 O 4 :S NPs) with a novel simple strategy, which includes low temperature multicomponent mixing and high temperature sintering. The prepared Fe 3 O 4 :S NPs exhibit a much better adsorption performance towards Pb(II) than bare Fe 3 O 4 nanoparticles. FTIR, XPS, and XRD analyses suggested that the removal mechanisms of Pb(II) by Fe 3 O 4 :S NPs were associated with the process of precipitation (formation of PbS), hydrolysis, and surface adsorption. The kinetic studies showed that the adsorption data were described well by a pseudo second-order kinetic model, and the adsorption isotherms could be presented by Freundlich isotherm model. Moreover, the adsorption was not significantly affected by the coexisting ions, and the adsorbent could be easily separated from water by an external magnetic field after Pb(II) adsorption. Thus, Fe 3 O 4 :S NPs are supposed to be a good adsorbents for Pb(II) ions in environmental remediation.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
Journal of Materials Chemistry A
·
2015
·Vol. 3
·期 30
·15755-15763
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IF 7.443
Long Kong,Lili Yan,Zan Qu,Naiqiang Yan,Liang Li
In this study, magnetic β-cyclodextrin stabilized Fe3S4 nanoparticles (CD-Fe3S4) were fabricated via a facile one-step route. The as-prepared CD-Fe3S4 exhibited a high Pb(II) adsorption capacity of 256 mg g−1, and it also showed a surprisingly efficient adsorption toward Zn(II), Cd(II), and Cu(II). XRD, FTIR and XPS analyses suggested that the mechanisms governing Pb(II) removal by CD-Fe3S4 were precipitation (formation of galena) and surface adsorption. Additionally, the magnetic properties of the synthesized Fe3S4 nanoparticles allow fast separation of sorbents from water. The sorption kinetic data were well-described by a pseudo-second-order model, whereas the adsorption isotherms followed a Langmuir isotherm model. Our experimental results proved that the β-cyclodextrin stabilized Fe3S4 could be a promising candidate for the removal of Pb(II) from water via simultaneously taking advantage of its magnetic properties and high affinity for heavy metals.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
ACS Applied Materials & Interfaces
·
2021
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IF 9.229
Hao Dong,Shefiu Kareem,Xiao Gong,Jian Ruan,Peng Gao,Xuedong Zhou,Xiaoqing Liu,Xiujian Zhao,Yi Xie
Lead halide perovskite (LHP) nanomaterials have attracted tremendous attention owing to their remarkable optoelectronic properties. However, they are extremely unstable under moist environments, high temperatures, and light illumination due to their intrinsic structural lability, which has been the critical unsolved problem for practical applications. To address this issue, we propose a facile and environmentally friendly ligand-free approach to design and synthesize rod-like CsPb2Br5-embedded Pb(OH)Br with excellent stability under various harsh environments such as soaking in water, heating, and ultraviolet (UV) illumination. Plate-like CsPbBr3- and Cs4PbBr6-embedded Pb(OH)Br powders are first formed by evaporating the solvent in a dispersion of ethanol (or methanol, isopropanol), Cs2CO3, and PbBr2. Upon soaking in water, the plate-like sample undergoes phase transformation from CsPbBr3 and Cs4PbBr6 to CsPb2Br5 and shape conversion from nanoplate to a microrod, leading to the formation of rod-like CsPb2Br5-embedded Pb(OH)Br. The stable Pb(OH)Br coating effectively prevents the luminescent CsPb2Br5 nanocrystals from reacting with water, leading to extremely high aqueous stability of the CsPb2Br5-embedded Pb(OH)Br. The photoluminescence (PL) intensity of the representative CsPb2Br5-embedded Pb(OH)Br sample can maintain 92.2% of the initial PL intensity value even after soaking in room-temperature water for 165 days; in the meantime, the phase and shape are preserved. The typical sample also shows outstanding stability under hot water, UV illumination, and annealing conditions. The ultrahigh aqueous stability, thermal stability, and photostability of the CsPb2Br5-embedded Pb(OH)Br nanomaterials suggest an effective, facile, and environmentally friendly technique to grow perovskite-based nanomaterials for promising practical applications in the optoelectronic field.
研究领域:
材料科学
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光学
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DOI
高影响因子
ELECTROANALYSIS
·
2020
·Vol. 33
·期 4
·947-955
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IF 2.544
Yanqiu Fu,Jinrui Li,Wei Jin,Zhonggang Liu
In this work, a dual-functional electrochemical sensor has been proposed based on Sn-doped defective Bi 2 S 3 (TDDB) microspheres, which exhibited the excellent electrochemical performance on Pb(II) and H 2 O 2 detection. The TDDB offered a satisfied detection limit of 8.0 nM towards Pb(II) with a sensitivity of 96.7 μA ⋅ μM −1 . As a H 2 O 2 sensor, a high sensitivity of 3540 μA mM −1 cm −2 was obtained in a linear range from 0.45 mM to 10 mM with a detection limit of 10 nM. Moreover, the electrochemical detection of Pb(II) in Taihu Lake and H 2 O 2 in human serum was achieved with high reliability and good recovery.
研究领域:
分析化学
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环境科学
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生物医学工程
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产品关联
DOI
高影响因子
RSC Advances
·
2020
·Vol. 10
·期 13
·7619-7627
·
IF 3.119
Chunmei Xiao,Jianming Lin
The existence of Pb(II) ions in water systems poses significant potential hazards to public health and the environment. In the present study, poly(2-acrylamido-2-methylpropanesulfonic acid) (PAMPS) brush-modified Ni3Si2O5(OH)4 nanotubes were prepared, and their adsorption efficiency against the Pb(II) ions was investigated. The characterization results of FTIR spectroscopy, TGA, TEM, and XPS indicated the successful grafting of PAMPS on the surface of free Ni3Si2O5(OH)4 NTs, and the prepared PAMPS-g-Ni3Si2O5(OH)4 NTs exhibited a 6–8 nm grafting layer, which could provide abundant binding sites for metal adsorption. During the Pb(II) removal process, a pH-dependent adsorption behavior was observed, and the adsorption processes fitted well with the pseudo-second-order kinetic model and the Langmuir isotherm model. Compared with unmodified Ni3Si2O5(OH)4, the PAMPS-g-Ni3Si2O5(OH)4 NTs exhibited obviously faster adsorption of Pb(II) and higher equilibrium adsorption capacity for the removal of Pb(II). The maximum adsorption capacity calculated via the Langmuir isotherm model was 0.653 mmol g−1 (135.3 mg g−1) at 298 K. In a metal coexisting system, the total adsorption capacity of the NTs was increased; this indicated the potential of the proposed NTs in the removal of Pb(II) from metal coexisting wastewater. This study showed the significant potential of PAMPS-g-Ni3Si2O5(OH)4 NTs in the effective removal of Pb(II).
研究领域:
环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
CLEAN-Soil Air Water
·
2016
·Vol. 44
·期 9
·1146-1153
·
IF 1.716
Hongmei Jiang,Menglan Sun,Jiangyan Xu,Aimin Lu,Ying Shi
Preparation of polyethyleneimine functionalized magnetic Fe 3 O 4 by using a one-step solvothermal method is reported in this paper. The effect of the amount of polyethyleneimine on the properties of the prepared materials including the shape, size, and adsorption performance was investigated in detail. The magnetic adsorbent with the best adsorption capacity was prepared and used for the removal of Pb(II) in an aqueous medium. Adsorption experiments were performed to evaluate the effect of different sorption parameters, such as pH, initial concentration of Pb 2+ , and contact time. Langmuir and pseudo-second-order models were used for isotherm and kinetic studies, through which a maximum adsorption capacity of 143 mg g −1 could be calculated. Pb(II) could be desorbed from magnetic Fe 3 O 4 nanoparticles modified with polyethyleneimine by 0.5 mol L −1 HCl and used for five cycles without any adsorption performance loss, indicating that the polymeric magnetic adsorbent used in this work had good reusability and great potential for practical application.
研究领域:
材料科学
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环境科学
·
化学工程
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DOI
高影响因子
ChemSusChem
·
2024
·
IF 7.5
Dong Li,Kaixuan Wang,Ying Chen,Renyi Li,Jiahong Tang,Yizhou Zhao,Wei Guo,Qi Chen,Yujing Li
Graphical A 0D/1D CPB@TCN heterojunction photocatalyst for CO 2 reduction is synthesized by immobilizing CsPbBr 3 (CPB) quantum dots on one-dimensional porous tubular g-C 3 N 4 (TCN). The strong Pb−N chemical bonding between CPB quantum dots and TCN provides a fast charge transfer channel for the CPB@TCN, which promotes the efficient separation and transfer of photogenerated carriers, resulting in excellent photocatalytic activity. Halide perovskite CsPbBr 3 (CPB) quantum dots (QDs) are considered as a promising candidate for solar-driven CO 2 conversion for their unique optoelectronic properties and suitable band structures. However, the CO 2 conversion efficiency of pristine CsPbBr 3 quantum dots is severely limited due to their rapid electron-hole pair recombination and insufficient active sites. In this study, by immobilizing CPB QDs onto one-dimensional (1D) porous tubular g-C 3 N 4 (TCN), an effective 0D/1D CPB@TCN heterojunction photocatalyst for CO 2 reduction is fabricated. Density functional theory (DFT) calculations combined with experimental studies demonstrate that CPB QDs are uniformly anchored on the surface of TCN through Pb−N chemical bonding, resulting in efficient separation and transfer of photogenerated carriers in CPB@TCN photocatalysts. The resultant CPB@TCN photocatalysts exhibit significantly enhanced photocatalytic activity for CO 2 reduction with the highest conversion rate of 22.62 μmol g −1 h −1 , which is 5.33-times higher than that of pristine CPB QDs. This work unveils the interfacial bonding mechanism of CPB@TCN heterojunction through Pb−N chemical bond, which provides new insights for the development perovskite-based heterojunction photocatalysts.
研究领域:
材料科学
·
环境科学
·
化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子