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CHEMOSPHERE · 2023 · IF 8.8

Preparation of Ti/SnO2–Sb/La-βPbO2 electrode and its application in the degradation of some pollutants including prednisolone and 8-Hydroxyquinoline

Hoang Nguyen Tien,Fredrick M. Mwazighe

In this work, a novel La-doped βPbO 2 (Ti/SnO 2 –Sb/La-βPbO 2 ) was prepared using electrodeposition method and applied to the degradation of prednisolone (PRD), 8-Hydroxyquinoline (8-HQ), and other typical organic pollutants. Compared with the conventional electrode Ti/SnO 2 –Sb/βPbO 2 , La 2 O 3 doping enhanced oxygen evolution potential (OEP), reactive surface area, stability and repeatability of the electrode. The 10 g L −1 of La 2 O 3 doping exhibited the highest electrochemical oxidation capability of the electrode with [•OH]ss being determined at 5.6 × 10 −13  M. The quenching experiments were conducted to confirm the main oxidizing species (here: •OH) in the electrochemical process. The study showed that the pollutants were removed in the electrochemical (EC) process with different degradation rates and indicated that the second-order rate constant of organic pollutants towards •OH ( k OP,•OH ) has a linear relationship with the degradation rate of organic pollutants ( k OP ) in the electrochemical process. Another new finding in this work is that a regression line of k OP,•OH and k OP can be used to estimate k OP,•OH of an organic chemical, which cannot be determined using the competition method. k PRD,•OH and k 8-HQ,•OH were determined to be 7.4 × 10 9  M −1  s −1 and (4.6–5.5) × 10 9  M −1  s −1 , respectively. Compared with conventional supporting electrolyte (like SO 4 2− ), H 2 PO 4 − and HPO 4 2− improved k PRD and k 8-HQ by 1.3–1.6-fold, while SO 3 2− and HCO 3 − inhibited k PRD and k 8-HQ significantly, down to 80%. Additionally, the degradation pathway of 8-HQ was proposed based on the detection of intermediates from GC-MS.

CAS / MDL: 10025-91-9 10026-06-9
研究领域: 环境科学 · 电化学工程 · 污染控制
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SENSORS AND ACTUATORS B-CHEMICAL · 2020 · IF 7.1

Microhotplate gas sensors incorporated with Al electrodes and 3D hierarchical structured PdO/PdO2-SnO2:Sb materials for sensitive VOC detection

Hao Wu,Jun Yu,Zhongzhou Li,Guanyu Yao,Rui Cao,Xiaogan Li,Huichao Zhu,Aixiang He,Zhenan Tang

High-performance, low-power microhotplate (MHP) gas sensors loaded with 3D hierarchical structured PdO/PdO 2 -SnO 2 :Sb materials on a pair of Al gas sensing electrodes were fabricated through advanced high-accuracy electrohydrodynamic printing method. The PdO/PdO 2 -SnO 2 :Sb materials with various PdO/PdO 2 concentrations were initially synthesized via a mild and simple hydrothermal reaction. Their micromorphology and chemical composition were characterized by SEM, XRD, TEM, and XPS, which proved the successful synthesis. The gas sensing performance of the sensors to benzene, ethanol, acetone, formaldehyde, and ethanol-acetone mixed gas (volume ratio 1:1) was tested. The sensing property of the materials is regulated with different content of PdO/PdO 2 . The identification of the VOCs is realized by two-step principal component analysis (PCA). Simulation calculations on the I–V characteristic of the MHP gas sensors reveal that carriers have to get through Al 2 O 3 barriers by Poole-Frenkel emission, which significantly affects the carrier conduction as well as the gas sensing properties. The gas sensing mechanism is analyzed from the aspects of gas sensing material and electrodes.

研究领域: 材料科学 · 传感器技术 · 化学
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ACS Nano · 2021 · IF 15.881

Ultrafast Study of Exciton Transfer in Sb(III)-Doped Two-Dimensional [NH3(CH2)4NH3]CdBr4 Perovskite

Jingjie Wu,Xianli Li,Xin Lian,Binbin Su,Junhong Pang,Ming-De Li,Zhiguo Xia,Jin Z. Zhang,Binbin Luo,Xiao-Chun Huang

Antimony-based metal halide hybrids have attracted enormous attention due to the stereoactive 5s2 electron pair that drives intense triplet broadband emission. However, energy/charge transfer has been rarely achieved for Sb3+-doped materials. Herein, Sb3+ ions are homogeneously doped into 2D [NH3(CH2)4NH3]CdBr4 perovskite (Cd-PVK) using a wet-chemical method. Compared to the weak singlet exciton emission of Cd-PVK at 380 nm, 0.01% Sb3+-doped Cd-PVK exhibits intense triplet emission located at 640 nm with a near-unity quantum yield. Further increasing the doping concentration of Sb3+ completely quenches singlet exciton emission of Cd-PVK, concurrently with enhanced Sb3+ triplet emission. Delayed luminescence and femtosecond-transient absorption studies suggest that Sb3+ emission originates from exciton transfer (ET) from Cd-PVK host to Sb3+ dopant, while such ET cannot occur with Pb2+-doped Cd-PVK because of the mismatch of energy levels. In addition, density function theory calculations indicate that the introduced Sb3+ likely replace the Cd2+ ions along with the deprotonation of butanediammonium for charge balance, instead of generating Cd2+ vacancies. This work provides a deeper understanding of the ET of Sb3+-doped Cd-PVK and suggests an effective strategy to achieve efficient triplet Sb3+ emission beyond 0D Cl-based hybrids.

CAS / MDL: 110-60-1
研究领域: 材料科学 · 光电学 · 化学 · 物理学
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CHEMOSPHERE · 2020 · IF 5.778

Degradation of aqueous cefotaxime in electro-oxidation — electro-Fenton —persulfate system with Ti/CNT/SnO2–Sb–Er anode and Ni@NCNT cathode

Jiawei Lei,Pingzhou Duan,Weijun Liu,Zhirong Sun,Xiang Hu

Due to the potential threatening of antibiotics in aqueous environment, a novel electro-oxidation (EO) — electro-Fenton (EF) —persulfate (PS) system with the addition of peroxydisulfate and Fe 2+ was installed for the degradation of cefotaxime. Ti/CNT/SnO 2 –Sb–Er with an ultra-high oxygen evolution potential (2.15 V) and enhanced electrocatalytic surface area was adopted as anode. The OH production and electrode stability test demonstrated great improvement in the electrochemical performances. Ni@NCNT cathode was tested with higher H 2 O 2 generation by the presence of nitrogen functionalities due to the acceleration of electron transfer of O 2 reduction. Experiment results indicated CNT and ErO 2 modification increased the molecular and TOC removal of cefotaxime. Coupling processes of EO-EF and EO-PS both resulted in shorter electrolysis time for complete cefotaxime removal, however, the mineralization ability of EO-PS process was lower than EO-EF, which might result from the immediate vanishing of PS. Thus, a further improved treatment EO-EF-PS system achieved an 81.6% TOC removal towards 50 mg L −1 cefotaxime after 4 h electrolysis, under the optimal working condition Fe 2+  = PS = 1 mM. The influence of current density and initial concentration on the performance of all processes was assessed. Methanol and tert-butanol were added in the system as OH and SO 4 − scavengers, which illustrating the mechanism of EO-EF-PS oxidizing process was the result of the two free radicals. Major intermediates were deduced and the degradation pathway of cefotaxime was analyzed. This research provides a potential coupling process with high antibiotic removal efficiency and effective materials for practical uses.

CAS / MDL: 9002-84-0
研究领域: 环境科学 · 生物医学工程
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ENVIRONMENTAL POLLUTION · 2023 · IF 8.9

Impact of coexisting components in acid mine drainage on Sb(Ⅲ) oxidation by biosynthesized iron nanoparticles

Xiaoying Jin,Lu Yang,Heng Li,Zhiqiang Chen,Zuliang Chen

Despite the oxidation mechanism of antimonite (Sb(Ⅲ)) by biosynthesized iron nanoparticles (Fe NPs) has been reported, the impact of coexisting components in acid mine drainage (AMD) on the Sb(III) oxidation by Fe NPs is unknown. Herein, how the coexisting components in AMD affect Sb(Ⅲ) oxidation by Fe NPs was investigated. Firstly, Fe NPs achieved complete oxidation of Sb(Ⅲ) (100%), while only 65.0% of Sb(Ⅲ) was oxidized when As(Ⅲ) was added, due to competitive oxidation between As(Ⅲ) and Sb(Ⅲ), which was verified by characterization analysis. Secondly, the decline in solution pH improved Sb(Ⅲ) oxidation from 69.5% (pH 4) to 100% (pH 2), which could be attributed to the rise of Fe 3+ in solution promoting the electron transfer between Sb(Ⅲ) and Fe NPs. Thirdly, the oxidation efficiencies of Sb(Ⅲ) fell by 14.9 and 44.2% following the addition of oxalic and citric acid , respectively, resulting from the fact that these two acids reduced the redox potential of Fe NPs, thereby inhibiting Sb(Ⅲ) oxidation by Fe NPs. Finally, the interference effect of coexisting ions was studied, where PO 4 3− significantly reduced Sb(Ⅲ) oxidation efficiency due to the occupation of the surface-active sites on Fe NPs. Overall, this study has significant implications for the prevention of Sb contamination in AMD.

研究领域: 环境化学 · 纳米技术 · 水处理
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Fabrication of aligned carbon nanofiber doped with SnO2-Sb for efficient electrochemical removal of tetracycline

Chengdong Shi,Shuyan Yu,Congju Li

In recent years, tetracycline (TC) has become an emerging refractory antibiotic pollutant due to excessive use and abuse. The aim of this work is to prepare aligned carbon nanofibrous (ACFs) membrane by electrospinning technology and then dope with SnO 2 -Sb to electrocatalytic degrade TC. The in-situ growth of SnO 2 -Sb on the carbon nanofiber surface to fabricate SnO 2 -Sb/ACFs membrane can increase the oxygen evolution reaction potential and improve conductivity. And the SnO 2 -Sb/ACFs membrane was used as the anodic membrane of a flow-through mode electrochemical membrane reactor to remove TC in aqueous solutions. The outstanding degradation performance of SnO 2 -Sb/ACFs membrane on TC was investigated systematically. The results show that the 3-layer SnO 2 -Sb/ACFs-3 membranes can effectively degrade 20 mg/L TC at an applied potential of 2.5 V. Moreover, SnO 2 -Sb/ACFs-3 membrane shows excellent degradation stability after 10 cycles of degradation experiments. For exploring the possible TC degradation pathways, HPLC-MS was used to identify the main intermediates during the electrochemical oxidation process. The anodic membrane electrode prepared in this work puts forward a new idea for the safe and efficient degradation of TC.

研究领域: 环境科学 · 材料科学 · 电化学 · 水处理
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RSC Advances · 2015 ·Vol. 5 ·期 25 ·19601-19612 · IF 3.84

Different mechanisms and electrocatalytic activities of Ce ion or CeO2 modified Ti/Sb–SnO2 electrodes fabricated by one-step pulse electro-codeposition

Tigang Duan,Ye Chen,Qing Wen,Ying Duan

Sb-doped SnO2 electrode was fabricated by the one-step pulse electro-codeposition method, and was modified through either cerium dioxide nanoparticle (nano-CeO2) or cerium ion doping. The results showed that the effects of nano-CeO2 doping and cerium ion doping are quite different. Nano-CeO2 doping shrinks the unit cell volume, improves the degree of crystallinity and refines crystalline grains, while cerium ion doping expands the volume and deteriorates the crystallinity. Nano-CeO2 doping mitigates the surface antimony enrichment and promotes the complete oxidation of antimony so that the majority of antimony oxidation states exist as the Sb5+ state, but cerium ion doping aggravates the enrichment and increases the Sb3+ content. Electrochemical phenol degradation showed that the Ti/Sb–SnO2–CeO2 electrode has a higher degradation efficiency and its kinetic rate constant is 1.46 times as much as that of Ti/Ce–Sb–SnO2. Besides, due to the compact active layer of Ti/Sb–SnO2–CeO2 protecting the titanium substrate from passivation, the accelerated service lifetime of Ti/Sb–SnO2–CeO2 is prolonged, which is 1.28 times as long as that of Ti/Ce–Sb–SnO2.

CAS / MDL: 1306-38-3
研究领域: 电化学 · 材料科学 · 环境工程
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OPTICAL MATERIALS · 2024 · IF 3.8

Optimization of transparent conductive properties of magnetron sputtered Sb-doped SnO2 films by RF power: Towards application in polymer-dispersed liquid crystal (PDLC) films

B.L. Zhu,X.J. Cai,C.C. Wang,J. Wu,J.L. Yao,W.Q. Sun

Sb-doped SnO 2 (ATO) films were prepared with different RF powers ( P RF ) under two O 2 flow rates ( F O 2 ) by magnetron sputtering , and then subjected to rapid thermal annealing (RTA) treatment. The effects of P RF , F O 2 , and RTA on the crystallinity, stress, surface morphology , conductive properties, transmittance in visible-light range ( T Vis ), and energy gap ( E g ) of the films were investigated. As the P RF increases, the film crystallinity improves or first improves and then slightly degrades, and the compressive stress decreases. With increasing P RF , the surface changes from textured to granular morphology and from granular to honeycomb-like morphology under two F O 2 , respectively. Meanwhile, the conductive properties first enhance and then degrade, and the T Vis and E g tend to decrease, especially at higher P RF . Basically, the films prepared with higher F O 2 have lower compressive stress, inferior conductive properties, and larger T Vis and E g compared with the films prepared with lower F O 2 . After RTA, the film crystallinity obviously improves, the compressive stress transforms into tensile stress , and the surface morphology has not undergone significant changes. Meanwhile, the conductive properties significantly enhance and E g obviously increases. The T Vis of the films prepared with lower F O 2 can be increased by RTA. The influence mechanisms of the above factors on the structure and optoelectronic properties of the ATO films were explored, and ultimately, the ATO films have the T Vis of 76.35–80.86%, sheet resistance of 51.7–91.9 Ω/sq., and quality factor of 1.03–1.67 × 10 −3  Ω −1 within the optimized P RF range. Polymer-dispersed liquid crystal (PDLC) films were fabricated using optimized performance ATO films as electrodes, and their on-state transmittance, off-state transmittance, threshold electric field, and saturation electric field were 2.08–4.61%, 61.69–68.56%, 0.656–0.796 V/μm, and 1.68–2.108 V/μm, respectively. The current results indicate the potential application of ATO films in PDLC films as electrode.

CAS / MDL: 75980-60-8
研究领域: 材料科学 · 光学工程
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Frontiers in Chemistry · 2022 · IF 5.545

Doping of Sb into Cu2ZnSn(S,Se)4 absorber layer via Se&Sb2Se3 co-selenization strategy for enhancing open-circuit voltage of kesterite solar cells

Zhao Benhui,Deng Yueqing,Cao Lei,Zhu Jichun,Zhou Zhengji

Kesterite-structured Cu2ZnSn(S,Se)4 (CZTSSe) thin film photovoltaics have attracted considerable attention in recent years because of its low-cost and eco-friendly raw material, as well as high theoretical conversion efficiency. However, its photovoltaic performance is hindered by large open-circuit voltage (VOC) deficiency due to the presence of intrinsic defects and defect clusters in the bulk of CZTSSe absorber films. The doping of extrinsic cation to the CZTSSe matrix was adopted as an effective strategy to ameliorate defect properties of the solar cell absorbers. Herein, a novel Se&Sb2Se3 co-selenization process was employed to introduce Sb into CZTSSe crystal lattice. The results reveal that Sb-doping plays an active role in the crystallization and grain growth of CZTSSe absorber layer. More importantly, one of the most seriously detrimental SnZn deep defect is effectively passivated, resulting in significantly reduced deep-level traps and band-tail states compared to Sb free devices. As a result, the power conversion efficiency of CZTSSe solar cell is increased significantly from 9.17% to 11.75%, with a VOC especially enlarged to 505 mV from 449 mV. This insight provides a deeper understanding for engineering the harmful Sn-related deep defects for future high-efficiency CZTSSe photovoltaic devices.

研究领域: 材料科学 · 光伏技术 · 半导体物理
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MATERIALS RESEARCH BULLETIN · 2018 · IF 2.873

Sb nanoparticles encapsulated in 3D porous carbon as anode material for lithium-ion and potassium-ion batteries

Hong Wang,Xuan Wu,Xiujun Qi,Wei Zhao,Zhicheng Ju

In the current research project, we have synthesized a novel Sb/Carbon nanocomposite with 3D porous structure which is successfully applied to the Li/K-ion batteries as anode materials. The unique structure shows the homogeneous Sb nanoparticles embedded into a 3D porous carbon (Sb@PC), relieving the intense volume expansion of inner Sb alloying and contributing to the integrity of the structure. As anode materials of Li-ion and K-ion batteries, they both showed an excellent electrochemical performance.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 电池技术
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APPLIED ORGANOMETALLIC CHEMISTRY · 2020 ·Vol. 34 ·期 6 ·e5612 · IF 3.14

Degradation of p-aminophenol wastewater using Ti-Si-Sn-Sb/GAC particle electrodes in a three-dimensional electrochemical oxidation reactor

Na Zhang,Jiaqi Bu,Yong Meng,Jia Wan,Lu Yuan,Xin Peng

In this study, Ti-Si-Sn-Sb/GAC particle electrodes were prepared by sol–gel method. The particle electrodes were characterized by SEM, XRD, EDX, and BET then used to carry out three-dimensional (3D) electrocatalytic oxidation degradation on simulated refractory p-aminophenol (PAP) wastewater. The effects of initial pH, cell voltage, aeration flow rate and initial PAP concentration on degradation experiments were investigated. Under the optimal conditions, the PAP and COD removal rates were 89.45% and 75.17% respectively. In addition, the possible degradation mechanism of PAP was further investigated by UV–Vis and HPLC. Finally, it was found that the Ti-Si-Sn-Sb/GAC particle electrodes with high catalytic activity and excellent stability could significantly improve the PAP wastewater removal efficiency.

CAS / MDL: 123-30-8
研究领域: 环境科学 · 电化学工程
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Amplifying photoreduction efficacy of Bi-Sb bimetallic nanocrystals: Manipulating carrier dynamics to boost CO2-to-CO conversion

Jie Tian,Zhijian Wang,Yaqin Hou,Yatao Yang,Haijun Chen,Zhanggen Huang

Inorganic Bi-based halide perovskites have attracted significant attention in the field of CO 2 photoreduction due to their excellent optoelectronic conversion performance and low toxicity. However, the inherent strong localization of electron-hole pairs remains the main factors limiting charge carrier transport and CRR performance. In this work, CBSB-x NCs with different Bi/Sb ratios were synthesized assisted by ultrasound methods to manipulate carrier behavior and assess CRR performance. The photoelectrochemical properties revealed that incorporation of Sb effectively suppressed nonradiative recombination and improved transport efficiency of charge carriers. Among the bimetallic variants, CBSB-1 NCs exhibited enhanced catalytic performance in CO production, with a yield of 38.77 μmol·g −1 and a high selectivity of 96.53 %. In-situ DRIFTS and DFT calculations indicated that Sb as co-catalytic sites promote charge transfer at the Bi-Br-Sb interface, accelerate the rapid evolution of b-CO 3 2- to HCOO - and significantly reduce the reaction energy barrier of CO.

研究领域: 材料科学 · 化学工程 · 环境科学 · 纳米技术 · 光化学
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