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ACS Applied Energy Materials · 2024 · IF 5.4

In Situ Structural Self-Optimization and Oxygen Vacancy Creation to Boost the Stability of Bi-MOF Derived Bi2O3@C and BiOCl@C Anodes

Yanting Ma,Yan Tang,Yajuan Xu,Suisui Su,Shuzhen Chen,Shizheng Zheng,Changyuan Hu,Xin Li,Kejie Dai,Rongbin Zhang

Metal oxides are promising alkaline battery electrodes with high theoretical capacity, but the low energy density and poor stability make them far away from actual application. Herein, single Bi-MOF derived ultrastable Bi2O3@C and BiOCl@C anodes are architected via a two-for-one manner. Specifically, optimal Bi2O3@C anode with hierarchical and porous structure delivers high specific capacity (278.3 mAh g–1 at 1 A g–1) owing to the exposed electrochemical active sites, fast charge transfer, and efficient ion diffusion. More importantly, ultrahigh stability (110%, 5000 cycles) is achieved due to the in situ morphological self-optimization and oxygen vacancy creation. Similarly, BiOCl@C anode also displays remarkable capacity and ultralong cycling stability (94%, 15000 cycles) due to the conductive and protective carbon layer, abundant reactive centers, and ion transport channels. Moreover, the in situ phase transition of BiOCl to Bi2O2CO3 also contributes to the outstanding stability. Our work provides rational guidance for architecting high capacitive and ultrastable anodes for aqueous rechargeable alkaline battery.

CAS / MDL: 554-95-0
研究领域: 材料科学 · 电化学
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2023 · IF 10.9

Assembling S-scheme heterojunction between basic bismuth nitrate and bismuth tungstate with promoting charges’ separation for accelerated photocatalytic sulfamethazine degradation

Wenhan Chen,Meng Dai,Li Xiang,Shan Zhao,Shuguang Wang,Zuoli He

The S-scheme heterojunction has garnered increasing attention due to its remarkable oxidation capacity and efficient separation of photogenerated carriers. In this study, a one-pot glycerol-assisted hydrothermal process was utilized to successfully synthesize S-scheme heterojunction photocatalysts comprising basic bismuth nitrate (BBN) and bismuth tungstate (BWO). Interestingly, the BBN/BWO heterogeneous photocatalysts exhibited the highest photocatalytic properties. The optimized product achieved the degradation of sulfamethazine (SMZ) within 1 h, with a kinetic constant ( k ) value of 0.05818 min −1 . The degradation process was influenced significantly by ·O 2 − and h + species. To determine the degradation pathway of SMZ in the presence of BBN/BWO-0.6, liquid chromatography–mass spectrometry (LC–MS) analysis was performed, which revealed a decrease in the toxicity of intermediates and products. The enhanced photocatalytic activity can be attributed to the internal electric field (IEF) of the S-scheme heterojunction between BBN and BWO, effectively promoting the separation of photogenerated carriers. This research presents a viable approach for developing S-scheme heterojunctions in SMZ photodegradation and other environmental applications.

CAS / MDL: 106-51-4 57-68-1
研究领域: 环境科学 · 材料科学
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JOURNAL OF ENVIRONMENTAL MANAGEMENT · 2024 · IF 8

In situ construction of Ag/Bi2O3/Bi5O7I heterojunction with Bi-MOF for enhance the photocatalytic efficiency of bisphenol A by facet-coupling and s-scheme structure

Yong Wang,Shikai Xue,Yuhao Liao,Haiyan Wang,Qiujun Lu,Ningli Tang,Fuyou Du

In this study, Ag/Bi 2 O 3 /Bi 5 O 7 I with s-scheme heterostructures were successfully synthesized in situ by nano-silver modification of CUA-17 and halogenated hydrolysis.The growth rate of Bi 2 O 3 crystals was effectively controlled by adjusting the doping amount of Ag, resulting in the formation of a facet-coupling heterojunctions . Through the investigation of the microstructure and compositional of catalysts, it has been confirmed that an intimate facet coupling between the Bi 2 O 3 (120) facet and the Bi 5 O 7 I (312) facet, which provides robust support for charge transfer. Under visible light irradiation, the AgBOI.3 heterojunction photocatalyst exhibited an outstanding degradation rate of 98.2% for Bisphenol A (BPA) with excellent stability. Further characterization using optical, electrochemical, impedance spectroscopy, and electron spin resonance techniques revealed significantly enhanced efficiency in photogenerated charge separation and transfer, and confirming the s-scheme structure of the photocatalyst. Density functional theory calculations was employed to elucidate the mechanism of BPA degradation and the degradation pathway of BPA was investigated by LC-MS. Finally, the toxicity of the degradation intermediates was evaluated using T.E.S.T software.

CAS / MDL: 80-05-7 64-75-5
研究领域: 环境科学 · 材料科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Converting commercial Bi2O3 particles into Bi2O2Se@Bi4O8Se nanosheets for “rocking chair” zinc-ion batteries

Haonan Yue,Mengwei Han,Xinni Li,Ting Song,Yong Pei,Xianyou Wang,Xiongwei Wu,Tengfei Duan,Bei Long

The development of a low-cost, high-capacity, and insertion-type anode is key for promoting “rocking chair” zinc-ion batteries. Herein, commercial Bi 2 O 3 (BiO) particles are transformed into Bi 2 O 2 Se@Bi 4 O 8 Se (BiOSe) nanosheets through a simple selenylation process. The change in morphology from commercial BiO particle to BiOSe nanosheet leads to an increased specific surface area of the material. The enhanced electronic/ionic conductivity results in its excellent electrochemical kinetics. Ex situ XRD and XPS tests prove the intercalation-type mechanism of BiO and BiOSe as well as the superior electrochemical reversibility of BiOSe compared to BiO. Furthermore, the H + /Zn 2+ co-insertion mechanism of BiOSe is revealed. This makes BiOSe to have low discharge plateaus of 0.38/0.68 V, a high reversible capacity of 182 mA h g −1 at 0.1 A g −1 , and a long cyclic life of 500 cycles at 1 A g −1 . Besides, the BiOSe//MnO 2 “rocking chair” zinc-ion battery offers a high capacity of ≈90 mA h g −1 at 0.2 A g −1 . This work provides a reference for turning commercial material into high-performance anode for “rocking chair” zinc-ion batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 电池技术
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Science Bulletin · 2025 · IF 21.1

Adsorption configuration control on Pt-Bi2O3 for the oriented conversion of glycerol to glyceric acid via terminal hydroxyl oxidation

Han-Yue Yang,Bin Sun,Xue Xiao,Xuan Ai,Rui-Bin Jiang,Pei Chen,Yu Chen

Glycerol, a byproduct of biodiesel production, can be efficiently converted into valuable chemicals through electrocatalytic reaction. In this study, platinum (Pt) nanocrystals decorated on bismuth oxide (Bi 2 O 3 ) nanosheets (PtBi DONS) with an optimal Pt:Bi ratio of 1:1 were successfully synthesized using a galvanic replacement method. Pt 1 Bi 1 DONS exhibit remarkable electrocatalytic performance for glycerol electrooxidation, achieving an excellent catalytic activity (current of 0.82 A mg Pt –1 at 0.67 V vs. reversible hydrogen electrode (RHE)) and an exceptional selectivity of 96.6% for C 3 products, particularly glyceric acid. The superior performance stems from two key factors: (1) electron transfer from Bi 2 O 3 to Pt creates electron-rich Pt sites that suppress C–C bond cleavage and (2) Bi 2 O 3 facilitates favorable glycerol adsorption configurations through multiple hydroxyl group interactions. Mechanistic studies using operando spectroscopy and electrochemical impedance spectroscopy revealed that the synergistic effect between Pt and Bi 2 O 3 promotes rapid charge transfer and stable intermediate formation. Moreover, PtBi DONS showed excellent versatility in oxidizing other polyols compared with monoalcohols.

研究领域: 化学工程 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Facile synthesis of three-dimensional WO3-x/Bi/BiOCl hierarchical heterostructures with broad spectrum driven photocatalytic activity

Yunfang Huang,Hui Xu,Dan Luo,Yuezhu Zhao,Yu Fang,Qiyao Guo,Yuelin Wei,Leqing Fan,Jihuai Wu

To improve the utilization efficiency of solar energy and separation of photogenerated carries, a novel three-dimensional (3D) WO 3-x /Bi/BiOCl hierarchical heterostructures with broad spectrum responsive photocatalytic activity have been fabricated through a facile solvothermal technique. The influences of varying loading of WO 3-x on the physical performances of the as-obtained composites were systematically characterized by X-ray diffraction, scanning electron microscope, transmission electron microscopy , X-ray photoelectron spectroscopy, optical absorbance, photoluminescence and specific surface areas. The WO 3-x /Bi/BiOCl displayed a strong optical absorption from 250 to 2500 nm, and showed the superior photocatalytic performance in degradation of rhodamine B (RhB) than that of individual components. Among the as-prepared samples, the sample S24 with the appropriate content of WO 3-x displayed the best photocatalytic performance, which can photodegrade RhB with the efficiency of 100%, 100% and 96% under the UV light within 8 min, visible light within 3 min and near-infrared light within 120 min exposure, respectively. Furthermore, a plausible mechanism of the RhB degradation on WO 3-x /Bi/BiOCl photocatalysts under the near-infrared light irradiation was proposed according to the photocatalytic activity and radical species trapping experiments.

研究领域: 材料科学 · 环境科学
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Materials Research Express · 2021 ·Vol. 8 ·期 3 ·035507 · IF 1.62

Thermal behavior and combustion performance of Al/Bi2O3 nano thermites with the effect of potassium perchlorate

Shi Li,Tao Guo,Miao Yao,Wen Ding,Jialin Chen,Jiaxing Song,Sheng Zhang,Rui Zhu

To study the effect of the addition of potassium perchlorate (KClO4) on the performance of nano thermites, Al/Bi2O3 nano thermites with different mass fraction (wt%) of KClO4 was made by ultrasonic dispersion method. Then, all samples were tested by SEM, DSC and rapid excitation ignition. DSC results showed Al/Bi2O3/10 wt%KClO4 had the highest heat release. Compared with Al/Bi2O3, the heat release increased by 28.32%. The results of activation energy calculations showed Al/Bi2O3/30 wt%KClO4 had the lowest activation energy (Ea). Its activation energy was reduced by 30%, mere about 149.17 KJ mol−1. Finally, it can be seen from the combustion situation that the addition of KClO4 reduced the intensity of burning. This work found a way to increase the heat release or reduce the activation energy of nano thermites by controlling the amount of KClO4 added.

研究领域: 材料科学 · 燃烧学 · 化学工程
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2024 · IF 5.8

Formation kinetics and equilibrium thermodynamics study on the Bi2O3-TiO2 system for synthesis of the bismuth titanate ceramics

Lang Xiao,Weiping Gong,Zhao-hui Long,Jiahui Zhao,Duoduo Zhang,Ting Wang,Kai Li,Alexandra Navrotsky

Formation kinetics and equilibrium thermodynamics are fundamental knowledge for predicting microstructure and properties during materials processing and utilization. This work prepared high purity Bi 12 TiO 20 , Bi 4 Ti 3 O 12 and Bi 2 Ti 4 O 11 compounds and characterized these compounds by in-suit X-ray diffraction, scanning electron microscope, energy dispersive spectrometer as well as calorimetry. Based on the experimental data obtained in this work and the literature, a thermodynamic description of the Bi 2 O 3 –TiO 2 system was carried out, a thermodynamic database as well as the calculated phase diagram of the system was provided. The discrepancy between the present calculation with the experimental data were discussed, the formation kinetics of the compounds was explained and the bismuth titanate ceramics with tailored structure and specific physical properties were sintered.

CAS / MDL: 13463-67-7 1304-76-3
研究领域: 材料科学 · 物理化学
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CRYSTENGCOMM · 2014 ·Vol. 17 ·期 3 ·671-677 · IF 3.858

Synthesis of monodisperse Bi2O3-modified CeO2 nanospheres with excellent photocatalytic activity under visible light

Qinghua Wang,Shiyong Yu,Zhibing Tan,Renfei Zhang,Zhao Li,Xuechuan Gao,Beibei Shen,Haiquan Su

In this work, monodisperse CeO2/Bi2O3 nanospheres were successfully synthesized via the three-step method, which is a traditional hydrothermal dip-coating–anneal method, and subsequent facile calcination at 600 °C for 4 h. The structure of obtained products was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). The results showed that highly uniform CeO2 microspheres and monodisperse CeO2/Bi2O3 nanospheres were obtained, the sizes of CeO2 microspheres and CeO2/Bi2O3 nanospheres were ~100 nm and ~125 nm. Besides that, the photocatalytic activities of CeO2/Bi2O3 nanocomposites were evaluated by photodegradation of Rhodamine B (RhB) under visible light. CeO2/Bi2O3 nanospheres exhibited a wide visible-light absorption with an edge at ca. 800 nm, which indicated a wide red shift compared to that of individual CeO2 microspheres (ca. 450 nm) and individual Bi2O3 nanoparticles (ca. 450 nm). Furthermore, the obtained CeO2/Bi2O3 nanospheres had remarkable photocatalytic degradation activities of dye under visible light compared with the activities of two individual photocatalysts of CeO2 microspheres and Bi2O3 NPs with the same concentration. The higher photocatalytic degradation activities of the photocatalysts could be ascribed to the following factors: (1) a large specific surface area of CeO2/Bi2O3 nanospheres with small size, (2) the efficient separation of photogenerated electrons and holes of the photocatalysts, and (3) a wide visible-light photoabsorption range (700 nm > λ > 400 nm). Therefore, small monodisperse CeO2/Bi2O3 nanospheres were designed by a simple route with efficient photocatalytic activity.

研究领域: 材料科学 · 纳米技术 · 环境化学 · 光催化 · 无机合成
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Reinforced BiOBr for visible-light-driven nitrogen fixation: A synergistic effect of cocatalyst and oxygen vacancies

Jianxing Liu,Zhe Li,Lin Nie,Xiangxin Xue,Mao Liu

Photocatalytic nitrogen fixation is a promising long-term strategy for NH 3 synthesis, with the development of effective and durable photocatalysts being crucial for achieving high-efficiency N 2 to NH 3 conversion. In this study, we employed vacancy and interface engineering to create bismuth (Bi) nanoparticles on hierarchical oxygen-deficient BiOBr microspheres using a one-step solvothermal approach. These Bi-decorated BiOBr microspheres, featuring oxygen vacancies, achieved a high photocatalytic ammonia synthesis rate of 222.3 μmol·g −1 ·h −1 in pure water under visible light irradiation, which is 3.25 times higher than that of the original BiOBr. Atomic-scale images of the interface between the defective regions of BiOBr and the Bi cocatalyst and several other material characterizations confirmed that the enhanced photoreduction activity of Bi/BiOBr is due to the synergistic effects of the metal Bi and the oxygen vacancies. These results present a straightforward and practical method for designing efficient photocatalysts for nitrogen fixation.

CAS / MDL: 10035-06-0 7758-02-3
研究领域: 材料科学 · 环境科学 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Transformation of amorphous Bi2O3 to crystal Bi2O2CO3 on Bi nanospheres surface for photocatalytic NOx oxidation: Intensified hot-electron transfer and reactive oxygen species generation

Peng Zhang,Yongfang Rao,Yu Huang,Meijuan Chen,Tingting Huang,Wingkei Ho,Shuncheng Lee,Junbo Zhong,Junji Cao

The inevitable amorphous Bi 2 O 3 on the surface of plasmonic Bi nanospheres serving as the recombination center of hot electron-hole pairs, hindered the transfer of photo-generated hot electrons and production of reactive oxygen species (ROS) seriously. In this study, Bi@amorphous Bi 2 O 3 was transformed to Bi@crystal Bi 2 O 2 CO 3 by secondary hydrothermal reaction. Bi@Bi 2 O 2 CO 3 core–shell photocatalyst exhibited higher visible-light catalytic activity (34.1%) than Bi@Bi 2 O 3 did (12.3%) in terms of NO x removal. Photoelectrochemical, surface photovoltage spectroscopy spectra and Kelvin probe force microscopy measurement results indicate that Bi 2 O 2 CO 3 shell reduced the transmission resistance of hot electrons excited from Bi core. O 2 -TPD, trapping experiments and density functional theory further confirmed that the transferred hot electrons were a help for ROS generation and •O 2 − radicals were the major contributor. This study not only addresses the unsettled issue of surface amorphous Bi 2 O 3 , but also provides a facile method to transform the amorphous shell to crystal phase of core–shell photocatalyst and new insights into the hot electrons separation and the formation of main ROS over the surface crystal transition of plasmonic Bi.

研究领域: 材料科学 · 环境科学 · 化学
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GREEN CHEMISTRY · 2013 ·Vol. 15 ·期 8 ·2215-2221 · IF 6.828

Aerobic oxidation of primary aliphatic alcohols over bismuth oxide supported platinum catalysts in water

Tianliang Lu,Zhongtian Du,Junxia Liu,Hong Ma,Jie Xu

Catalytic oxidation of non-activated aliphatic alcohols with molecular oxygen is rather challenging, especially in an aqueous medium in the absence of an additional base. Bismuth is usually used as a promoter of platinum-based catalysts. In this work, bismuth oxide was explored as a support, and Pt0 nanoparticles supported on bismuth oxide (Pt/Bi2O3) exhibited high activity for aerobic oxidation of n-butanol using water as a solvent in the absence of an additional base under optimized conditions. Besides n-butanol, liquid primary aliphatic alcohols with low solubility in water could also be smoothly oxidized into the corresponding carbonyl compounds with molecular oxygen. Pt/Bi2O3 reduced by H2 at about 200 °C showed the highest activity for aerobic oxidation of n-butanol. At this temperature, platinum oxide was reduced to Pt0 and bismuth oxide could be reduced partially which might change the surface property of bismuth oxide.

研究领域: 催化化学 · 环境科学
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