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International Journal of Electrochemical Science · 2024 · IF 1.3

Application of Bi/PEDOT composite modified electrode in high-performance Cd (II) detection sensor

Lin Yang,Yijing Ai,Shihui Xu,Lisi Wang,Xiaoping Zhang,Wei Sun

In this paper, Bismuth/poly(3,4-ethylenedioxythiophene) (Bi/PEDOT) modified electrochemical modified electrodes were prepared by electrochemical deposition method, and the electrochemical performance of the electrode was investigated using cyclic voltammetry under the optimal experimental conditions. The PEDOT polymer has high conductivity, and bismuth can form an alloy with cadmium ions. Bi/PEDOT nanocomposite materials have a larger specific surface area and more active sites, which is more conducive to absorbing more cadmium ions (Cd 2+ ). The Differential pulse anodic stripping voltammetry method was used to study the electroanalytical performance of the sensor for Cd 2+ . The data show that the oxidation peak current of cadmium ions in the Bi/PEDOT modified electrode is significantly higher than that of other electrodes, due to the synergistic effect of the composite conductive materials. In the concentration range of 1 nM-40 μM, the concentration of cadmium ions shows a good linear relationship with the peak current, and the lowest detection limit is 0.33 nM. In addition, the sensor also exhibits good stability, reproducibility and very low detection limit, which can be used for rapid determination of trace cadmium ions, with a recovery rate in actual sample analysis of 101.4 %-104.0 %.

研究领域: 电化学 · 材料科学 · 分析化学 · 环境科学
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2024 · IF 4.1

Smartphone-based portable sensor with Bi-MOF nanocomposite for Cd (II) in vegetable samples

Liping Deng,Liangmei Rao,Xinyu Lu,Yutang Wang,Weiming Zhang,Xuemin Duan,Yangping Wen,Zhuohua Kong,Jingkun Xu

The accumulation of heavy metal cadmium (Cd) in the food chain poses a serious threat to human health, necessitating the development of rapid, on-site, and portable detection methods for Cd (II). Herein, we developed a smartphone-based electrochemical sensor for portable determination of Cd (II) in vegetables using a bismuth metal–organic framework (Bi-MOF) nanocomposite. Prismatic rod-like Bi-MOF was hydrothermally synthesized using trimesic acid as organic ligands, and subsequently, carboxyl-functionalized multi-walled carbon nanotubes (COOH-MWCNTs) were incorporated to form Bi-MOF nanocomposite network. The smartphone-based electrochemical sensor enables rapid, sensitive, and portable detection of Cd (II) in vegetable samples using Bi-MOF/COOH-MWCNTs-modified screen-printed carbon electrodes (SPCE). A comparative analysis of traditional electrochemical sensors coupled with desktop computer for linear voltametric responses for Cd (II) in the range of 0.2–500 ng/mL with a limit of detection (LOD) of 0.07 ng/mL using Bi-MOF/COOH-MWCNTs-modified glassy carbon electrodes (GCE), the portable sensor demonstrated good linear range in 0.7–350 ng/mL with a LOD of 0.22 ng/mL. This work introduces a novel approach for on-site and portable detection of Cd (II) in agricultural products.

CAS / MDL: 13746-66-2 2408-70-0
研究领域: 环境科学 · 分析化学 · 材料科学 · 食品安全
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Fe-Bi dual sites regulation of Bi2O2.33 nanosheets to promote photocatalytic nitrogen fixation activity

Chuanyu Zhu,Lulu Zhang,Luyao Cui,Ziqiang Zhang,Rui Li,Yunfang Wang,Yawen Wang,Caimei Fan,Zhuobin Yu,Jianxin Liu

In the process of photocatalytic ammonia synthesis , efficient activation of nitrogen molecules constitutes a fundamental challenge. During the N 2 activation, the close interdependence between the acceptance and donation of electron results in their mutual limitation, leading to high energy barrier for N 2 activation and unsatisfactory photocatalytic performance. This work decoupled the electron acceptance and donation processes by constructing Fe-Bi dual active sites, resulting in enhancing N 2 activation through the high electron trapping ability of Fe 3+ and strong electron donating ability of Bi 2+ . The photocatalytic nitrogen reduction efficiency of 3%Fe/Bi 2 O 2.33 (118.71 μmol g cat −1 h −1 ) is 5.3 times that of Bi 2 O 2.33 (22.41 μmol g cat −1 h −1 ). In-situ Fourier transform infrared (In situ FTIR) spectroscopy and density functional theory (DFT) calculations manifest that Fe 3+ -Bi 2+ dual active sites work together to promote nitrogen adsorption and activation, and the reaction path is more inclined toward alternate hydrogenation path. N 2 adsorption and activation properties are optimized by heteronuclear bimetallic active sites, which offers a new way for the rational design of nitrogen-fixing photocatalysts .

研究领域: 材料科学 · 催化 · 光化学 · 环境科学
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Ag@Bi5O7I nanoparticles deposited on Bi(OH)3 nanosheets for boosting photocatalytic antibacterial activity under visible light irradiation

Qinghan Chen,Li Wang,Dehui He,Bo Xiao,Xia Ran,Rong Li,Hong Xu,Jian Feng

A novel [email protected] 5 O 7 I/Bi(OH) 3 (AB) heterojunction was prepared and the enhanced photocatalytic antibacterial activity against Escherichia coli ( E. coli ) under visible light excitation was exhibited. 3 %AB (containing 3 wt% of Ag) presented best photocatalytic performance, and all of E. coli cells were inactivated within 5 min under natural solar light irradiation. The photocatalytic antibacterial mechanism of AB heterojunction was corroborated by SEM, live/dead cell staining and SDS-PAGE assay. The destruction of the cell membrane, the leakage of the intracellular protein and the decomposition of the protein were considered as the events occurred in the antibacterial process. The radical capture experiment confirmed that •O 2 – and e – played the dominant role in the destruction of the cell membrane and the decomposition of the protein. The improvement of the photocatalytic activity can be mainly ascribe to the construction of heterojunction, SPR effect resulted from Ag deposition, enhanced visible light absorption and more surface oxygen vacancies. These factors are advantageous to the generation of the photogenerated electrons and holes, and improve the spatial separation efficiency of the photogenerated charge. This study presented a promising [email protected] 5 O 7 I/Bi(OH) 3 heterojunction as the photocatalyst for the potential application in the treatment of the bacterial contamination.

CAS / MDL: 6104-59-2
研究领域: 材料科学 · 环境科学 · 纳米技术 · 微生物学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Facet-dependent in-situ formation of oxygen vacancy and plasmonic Bi in BiOBr nanosheets and resultant influence on the generation and separation of charge carriers

Mingming Li,Yue Gong,Jiaqiang Wen,Zhengda Li,Yanjie Wang,Tao He

The development of advanced photoactive materials has aroused widespread interest, but is severely plagued by the inherent narrow photo-responsive range and rapid recombination of electrons and holes. In this study, the unconventional BiOBr nanosheets decorated with Bi 0 and oxygen vacancies (OVs) are successfully synthesized through a facial one-pot hydrothermal method, followed by heat treatment. Cetyltrimethylammonium bromide and mannitol contribute to the selective exposure of (001) and (010) facets, respectively. The absence of the outermost Br atoms facilitates the simultaneous generation of OVs and Bi 0 on the surface during heating, forming the Schottky junction. The synergy of SPR in the Bi 0 metal, OVs and Schottky junction can effectively enhance the light absorption and charge separation. This work proposes and verifies a feasible approach to construct defects in-situ by regulating the crystal facets and manipulating the surface atomic arrangement and coordination.

CAS / MDL: 57-09-0
研究领域: 材料科学 · 光化学 · 纳米技术 · 表面科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Construction of covalent organic framework evaporator based on Bi/BiOCl floating layer and its application in solar desalination and clean water production

Xiuling Li,Yanan Pang,Yongle Zhang,Bo Ge,Junchang Liu,Yuling Zhang,Limin Zhao,Guina Ren,Zhaozhu Zhang

Solar interface heating evaporators are widely used and have been able to obtain clean water vapor from sewage. However, the soluble contaminants remaining in the original solution were not removed, and the floating organic pollutants affect the steam production rate. In this paper, the superhydrophobic Bi/BiOCl with low surface tension is synthesized and loaded to the felt to construct the floating layer of the photothermal device. The floating layer collaborated with the filter paper hydrophilic layer and the Pyromellitic dianhydride-Tris (4-aminophenyl) amine covalent organic framework (PMDA-TAPA COF) photothermal layer to treat the sewage containing dissolved pollutants, achieving an interfacial evaporation rate of 1.47 kg⋅m −2 ⋅h −1 . Importantly, the floating layer not only has a contact angle of 161°, which can selectively adsorb the organic solvents floating on the water surface, but also can degrade the pollutants dissolved in the water under the light and solving the problems that hinder device applications. The valence band and conduction band potentials of superhydrophobic Bi/BiOCl are at 3.065 eV and −0.435 eV, respectively, which produce h + and O 2 – under light to degrade dissolved pollutants in water. The introduction of novel superhydrophobic Bi/BiOCl photocatalyst in the floating layer provides a reference for solving the problem of pollutant residues.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
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ACS Catalysis · 2025 · IF 13.1

Revealing the Fundamental Origin of the CO-Free Pathway Selectivity in Alkaline Methanol Electrooxidation on Bi-Modified Pt

Lecheng Liang,Hengyu Li,Peng Li,Jinhui Liang,Shao Ye,Binwen Zeng,Mingjia Lu,Yanhong Xie,Yucheng Wang,Taisuke Ozaki,Shengli Chen,Zhiming Cui

A long-standing puzzle for methanol electrooxidation is the fundamental understanding of the origin of electrocatalytic selectivity. Herein, we unequivocally demonstrate that the Bi-modified Pt/C follows a CO-free dominated pathway during alkaline methanol electrooxidation and unveil the formaldehyde (HCHO) intermediate as a critical factor influencing pathway selectivity. These findings are substantiated by kinetic isotope effects, formate Faradaic efficiency, in situ spectroscopy, ab initio molecular dynamics simulations, and density functional theory calculations. Bi modification significantly increases the HCHO dehydrogenation barrier, which facilitates its desorption and subsequent conversion to the H2COOH– anion at the alkaline interface, intrinsically avoiding CO formation. More specifically, the formation of ensemble sites featuring a V-shaped Bi–Pt–Bi configuration inhibits the cleavage of the C–H bond, and the weak OH binding energy at Bi adatoms effectively prevents blockage of oxygenated species, allowing such ensemble sites to fulfill their functional role. This work provides in-depth insights into the origins of pathway selectivity and benefits the theory-guided design of advanced CO-free electrocatalysts.

研究领域: 电化学 · 催化 · 材料科学 · 物理化学 · 计算化学
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Catalysis Science & Technology · 2024 · IF 4.4

Study on graphitic carbon nitride catalysts with Bi and Cu loaded for carbon dioxide photothermal reduction

Bin Guan,Junyan Chen,Zhongqi Zhuang,Lei Zhu,Zeren Ma,Xuehan Hu,Chenyu Zhu,Sikai Zhao,Kaiyou Shu,Hongtao Dang,Zhen Huang

As a significant technology of CO2 utilization, artificial CO2 photoreduction has received more and more attention. Herein, g-C3N4 catalysts modified with Bi and/or Cu for CO2 photothermal reduction were prepared by solvothermal synthesis and impregnation methods. Performance evaluation and physicochemical and photo- and thermochemical characterization indicated that Bi and Cu modification effectively enhanced the photo-absorption properties of g-C3N4 catalysts, improving charge transfer efficiency and catalytic performance. Compared with single-metal modification, Bi and Cu co-modification showed a narrower bandgap and more excellent light and CO2 absorption capacity, suggesting a certain synergistic effect of Bi and Cu co-modification. The alteration of the light absorption properties may be related to the surface plasmon effect of Bi and Cu, and the co-loading of Bi and Cu can exacerbate the effect, which can effectively enhance the photoresponsivity of the catalysts, leading to higher catalytic performance.

研究领域: 催化 · 材料科学 · 环境科学 · 化学工程
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APPLIED CATALYSIS A-GENERAL · 2016 · IF 4.012

Continuously enhanced photoactivity of hierarchical β-Bi2O3/Bi2S3 heterostructure derived from novel BiO2CH3 octagonal nanoplates

Yangyang Zhang,Yiping Guo,Bijun Fang,Yujie Chen,Huanan Duan,Hua Li,Hezhou Liu

BiO 2 CH 3 nanoplate, a new organometallic crystal, with octagonal morphology is successfully prepared using methanol solvothermal method and further employed as template to fabricate porous β-Bi 2 O 3 octagonal nanoplates with a thickness of less than 50   nm. Then a series of hierarchical octagonal haystack-like β-Bi 2 O 3 /Bi 2 S 3 hybrids with large heterointerface and small bandgaps (1.36–1.44   eV) are constructed. It is found that, different from many regular photocatalysts that suffer from shrink of photocatalytic efficiency, the photoactivities of all β-Bi 2 O 3 /Bi 2 S 3 heterostructures are continuously enhanced with growing test cycles, owing to the formation of Bi 2 O 3− x S x solid solution, in which the built-in electric filed induced by lattice distortion can brings about higher e − /h + separation efficiency. The gradually increasing photocatalytic activity can reach to an up limit in about 5 photocatalytic cycles and maintain at this level. β-Bi 2 O 3 /Bi 2 S 3 heterostructure loaded with 20   mol% of Bi 2 S 3 is demonstrated to be the best photocatalyst and capable of fully decomposing Rh B in 30   min. Our work provides deep insights into the nature of the inversed photocatalytic behavior and facilitates the advanced design of photocatalysts with unabated photoactivities.

研究领域: 材料科学 · 光催化
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2022 · IF 10.319

Multiple anti-counterfeiting strategy by integrating up-conversion, down-shifting luminescence, phosphorescence and photochromism into NaYTiO4: Bi/Er phosphors

Yuzhen Wang,Xuanyi Yuan,Yongge Cao,Chaoyang Ma

With the rapid development of science and technology, the high-security-level anti-counterfeiting technique is essential for ensuring property or information security. In this work, we prepared micron NaYTiO 4 : Bi/Er (NYT: Bi/Er) phosphors with integrating up-conversion (UC) photoluminescence, down-shifting (DS) emission, phosphorescence and photochromism (PC) performances for advanced multiple anti-counterfeiting application. Owing to the abundant energy levels of Er 3+ ions, the UC and DS luminescence behaviors are anticipated. Specifically, the yellow-green emission of Er 3+ ions can be observed upon 980 nm excitation, and the bright green emission is demonstrated under 281 or 254 nm excitation due to the energy transitions of Er 3+ ions and the energy transfer process from Bi 3+ to Er 3+ ions. Besides, the introduction of Bi 3+ ions generates defect levels in the matrix and thus leads to phosphorescence. Furthermore, the repeatable PC performance could be triggered by the 365 nm irradiation and vanished with 450 nm illumination or thermal stimulation. To verify the practical usability of NYT: Bi/Er phosphors on anti-counterfeiting applications, some experiments are designed and successfully executed. It is believed that the NYT: Bi/Er phosphors can be a promising candidate for high-security-level multiple anti-counterfeiting.

研究领域: 材料科学 · 光学材料 · 安全技术
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2022 ·Vol. 30 ·期 11 ·28874-28888 · IF 5.19

Dual modification based on electrostatic repulsion of bentonite and SPR effect of Bi facilitate charge transfer of Bi2WO6 for antibiotics degradation

Zhu Tingting,Hou Yanping,Huang Guofu,Fu Tian,Yang Jinhang,Wang Yutong,Zhang Hanbing

Development of efficient photocatalysts is vital for light-driven removal of refractory antibiotics. Herein, Bi 2 WO 6 microspheres were successfully anchored on the surface of bentonite, and metallic Bi was reduced in-situ by a one-step solvothermal method. Notably, the Bi/Bi 2 WO 6 /BT with a mass ratio of 0.15:1:0.1 exhibited the best photocatalytic activity toward degradation of tetracycline (TC) and ciprofloxacin (CIP) after 120 min of visible light irradiation, and their reaction rate constants were 8.0 and 5.5 folds higher than that of pristine Bi 2 WO 6 , respectively. The boosted photocatalytic activity over Bi/Bi 2 WO 6 /BT was ascribed to the establishment of electrostatic repulsion and SPR effect, which synergistically promoted charges transfer, thus achieving more h + and ·O 2 − radical generation. Moreover, possible TC and CIP degradation pathways over Bi/Bi 2 WO 6 /BT were proposed based on the identified intermediates, and most of the intermediates were less toxic than TC and CIP. The study provides options to develop high-efficiency photocatalytic composites for contaminants elimination using semiconductors and readily available bentonite.

研究领域: 环境科学 · 材料科学 · 化学
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CERAMICS INTERNATIONAL · 2021 · IF 4.527

Bi and Al co-doped anatase titania for photosensitized degradation of Rhodamine B under visible-light irradiation

Shunhang Wei,Jian Gao,Pingru Wu,Bo Yao,Haitao Xu,Yongsheng Tan,Shiyan Liu,Rong Wu,Yawei Wang,Lei Wang,Zebo Fang,Qifeng Liang

Although TiO 2 is a wide band gap semiconductor , it demonstrates photodegradation activity under visible light irradiation after dye sensitization. Compared with esterification between the surface hydroxyl group of TiO 2 and the carboxylic group of dyes, electrostatic interaction between TiO 2 and dye shows better photosensitized performance. In this work, Bi/Al co-doping anatase titania (Ti 1-x Bi 2x/3 Al 2x/3 O 2 (0 ≤ x ≤ 0.3)) is designed to enhance the electrostatic interaction. The effect of Al ions is to enhance the solubility of Bi 3+ into titania nanocrystals . A new band gap is generated after high concentration of Bi element doping , which not only promotes the absorption of visible light, but also improves the utilization of photogenerated carriers. Based on the results of transmission electron microscopy , light absorption, photodegradation activity and density functional theory calculations, it is found that bismuth dopant is the electron capture site. It first accumulates electrons through photocatalytic degradation reaction to enhance electrostatic adsorption between the catalyst and the positively charged dye molecules, and finally realizes high-efficiency photosensitization degradation of Rhodamine B. In addition, the sensitized titania has excellent photodegradation recyclability.

研究领域: 材料科学 · 光化学 · 环境科学
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