APPLIED CATALYSIS B-ENVIRONMENTAL
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2021
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IF 19.503
Lingsong Wang,Huanshun Yin,Suo Wang,Jun Wang,Shiyun Ai
Bi/BiOCl/Bi 2 O 2 CO 3 heterojunction was prepared via one-step hydrothermal process under the synergistic catalysis of Ni 2+ , where Bi(NO 3 ) 3 was employed as Bi source, DMF was used as carbon source and reductant, NiCl 2 was adopted as Cl source and co-catalyst. The content of Bi, BiOCl and Bi 2 O 2 CO 3 can be adjusted by changing the reaction time, temperature, content of DMF and NiCl 2 . The doping of Bi enhanced the photocatalytic activity of BiOCl/Bi 2 O 2 CO 3 under visible-light. Bi/BiOCl/Bi 2 O 2 CO 3 presented photo-degradation activity for environmental pollutants of rhodamine B, sunset yellow and tetracycline, which were 13.01, 9.40, 1.50 times and 168.38, 10.90, 4.75 times higher than BiOCl and Bi 2 O 2 CO 3 , respectively. The improved photocatalytic activity was ascribed to the sensitized effect of Bi and BiOCl, the surface plasmon resonance effect and the heterojunction structure, which inhibited the recombination of photogenerated electron-hole pairs. The degradation mechanism for rhodamine B was discussed, and the decreased toxicity of the degradation products was demonstrated.
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JOURNAL OF CATALYSIS
·
2023
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IF 7.3
Fang Wei,Ting Luo,Yan Wang,Lichun Kong,JiuJu Feng,Zhengquan Li,Ji-Qing Lu,Fa Yang
A novel electrocatalyst for CO 2 -to-formate conversion at low overpotentials with abundant bimetallic interfaces aroused from Pd nanoparticles anchoring in the underlying Bi nanosheet (Pd-BiNS) was developed. This unique synthesis procedure undergoes a continuous reconstruction of Pd-BiOINS to Pd-Bi 2 O 2 CO 3 NS to Pd-BiNS, which was confirmed by in situ Raman spectra combined with quasi- in - situ electron microscopy. The optimized Pd 1 -BiNS exhibits a high Faradaic efficiency of 95 % for formate at only − 0.4 V versus reversible hydrogen electrode over 30 h electrolysis, breaking the limitation that metallic Pd-site is easily poisoned by the generated CO at low overpotentials. The in situ infrared spectroscopy indicates that Pd-BiNS has much suppressed *CO binding and enhanced *OCHO adsorption to inhibit the competing hydrogen evolution reaction by repelling surface water molecules, moreover, a systematic CO 2 RR mechanism with HCO 3 − participating as pre-proton donor for formate generation is unveiled. This work provides new insight into the multisite synergistic regulation at the atomic scale.
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Materials Advances
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2023
·Vol. 4
·期 10
·2365-2371
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IF 5
Shaofan Fang,Jinbo Huang,Huixia Li,Jingheng Nie,Zexiang Liu,Feier Fang,Haizhe Zhong
Luminescent metal halides doped with ns2-metal ions, such as 6s2-metal Bi3+, show excellent optoelectronic properties. However, the origin of the high photoluminescence quantum yield (PLQY) of Cs2SnCl6:Bi remains controversial and unclear. In this study, a series of Cs2SnCl6:Bi were synthesized by adopting different tin precursors of SnCl2/SnCl4. The samples from SnCl2 exhibited much higher PLQY than those from SnCl4, and the doping concentrations of Bi3+ had little effect on the high PLQY. When H3PO2 is added to the precursor of SnCl4 to reduce Sn4+ to Sn2+, the prepared Cs2SnCl6:Bi shows bright emission light and high PLQY. The high PLQY of Cs2SnCl6:Bi is attributed to the co-doping of Bi3+ and Sn2+. [SnCl4]2− and two VCl induce a large extra vibrational energy of the heavy localized excitons from [BiCl5]2− to enhance the efficiency of radiative recombination for high PLQY. This work deepens the understanding of the luminescence mechanism of Cs2SnCl6:Bi and supplies significant references for developing more perovskite materials with outstanding luminescence.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
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IF 8.128
Jialu Huang,Chengwei Deng,Yue Liu,Tingting Han,Feng Ji,Yuehua Zhang,Hongbin Lu,Ping Hua,Bowei Zhang,Tao Qian,Xiaolei Yuan,Yaoyue Yang,Yong Yao
Palladium (Pd) is supposed to be one of the most promising catalytic metals towards ethanol (C 2 H 5 OH) oxidation reaction (EOR). However, Pd electrocatalysts easily suffer from the poisoning of the intermediates (especially CO), resulting in the quick decay of EOR catalysis. Herein, inspired by the Brønsted-Lowry acid-base theory, a “attraction–repulsion” concept is proposed to guide the surface structure engineering toward EOR catalysts. Specifically, we induce Bi(OH) 3 species as Brønsted base onto PdBi nanoplates to effectively repel the adsorption of CO intermediates. The PdBi-Bi(OH) 3 nanoplates show an impressive mass activity of 4.46 A mg Pd -1 during the EOR catalysis and keep excellent stability. Both the stability and enhanced performance are attributed by the interfacial Brønsted base Bi(OH) 3 which can selectively attract and repel reactants and intermediates, as evidenced from in situ measurements and theoretical views.
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RESEARCH ON CHEMICAL INTERMEDIATES
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2026
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IF 3.3
Ma Yong-hu,Ma Fu,Zhao Tiao-bin,Gao Zi-yi,La Ying-hong,Zhao Hong-jian
Limited interfacial charge separation efficiency and insufficient redox capacity severely hinder the practical application of conventional Bi 2 WO 6 -based photocatalysts. To address these issues, a novel Bi(C 2 O 4 )OH/Bi 2 WO 6 heterojunction was constructed via a facile room-temperature one-pot liquid-phase deposition method. Multiple characterizations confirm the intimate interfacial contact between Bi(C 2 O 4 )OH nanorods and uniformly anchored Bi 2 WO 6 nanoparticles, accompanied by the introduction of abundant oxygen vacancies. On the basis of radical trapping experiments, EPR measurements, and electrochemical tests, an S-scheme charge-transfer model is proposed. This model retains the strong redox potentials of both semiconductors, while oxygen vacancies are speculated to act as efficient interfacial charge-trapping and transfer sites to synergistically promote the migration and separation of photogenerated carriers. The optimized 7%Bi(C 2 O 4 )OH/Bi 2 WO 6 composite achieves an RhB removal efficiency of 97.6% within 60 min for 50 mL of RhB solution (30 mg·L -1 ) under 5-W LED lamp irradiation. Radical trapping and EPR tests confirm that ·O 2 - , h⁺, and ·OH are the dominant active species. This work presents a facile and efficient room-temperature fabrication strategy for Bi-based heterojunctions and systematically elucidates the synergistic promotion mechanism between oxygen vacancies and the proposed S-scheme charge-transfer pathway, offering new insights for designing high-performance photocatalysts for organic wastewater remediation.
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Nano Research
·
2023
·
IF 9.9
Dou Tong,Song Dian,Wang Yiping,Zhao Xuhui,Zhang Fazhi,Lei Xiaodong
Electrocatalytic CO 2 reduction reaction (ECO 2 RR) converts CO 2 to high-value chemical products and promotes the carbon cycle. Sulfur (S)-modified copper (Cu) and bismuth (Bi)-based catalysts have been recognized as promising catalysts for ECO 2 RR. Both of them are highly active for selective formate generation, however, their poor stability and severe competing hydrogen evolution reaction (HER) remain challenging. Herein, S-doped Cu coated with Bi (Bi/Cu-S) is developed to improve ECO 2 RR selectivity to formate. Bi/Cu-S/brass mesh (BM) electrode material for ECO 2 RR was prepared by electrodepositing Bi on the surface of Cu-S/BM nanowires obtained from CuS/BM after the electroreduction. The Faradaic efficiency (FE) of the formate reaches the maximum of 94.3% at −0.9 V vs. reversible hydrogen electrode (RHE) with a partial current density as high as −50.7 mAcm −2 and a yield of 30.7 mmolh −1 cm −2 under 0.5 M KHCO 3 electrolyte. Meanwhile, the FE of formate is higher than 90% in the voltage range of −0.8 to −1.0 V vs. RHE. It also shows good stability at −0.9 V vs. RHE with the FE of formate remaining above 93% after a 10 h reaction. Density functional theory (DFT) calculations demonstrate that the Bi/Cu-S structure promotes the adsorption of CO 2 and effectively inhibits HER by enhancing the adsorption of *H to a great extent, improving the selective conversion of CO 2 to formate. This work deepens the understanding of the mechanism of Cu-Bi-based catalysts and S-modified Cu-based catalysts in selective ECO 2 RR to formate, and also provides a new strategy for catalyst design.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2023
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IF 7.2
Ning Lv,Huitao Li,Jinjuan Dong,Xianrui Liu,Tianbao Li,Jujie Luo
Bi nanoflakes on Ni foam (NF) for supercapacitors (SCs) are prepared by simple one-step microwave irradiation without further calcination. XRD and XPS results reveal the successful synthesis of Bi crystal. SEM and EDS results uncover the growth of Bi and the constituent elements of the complexes. The Bi anode on NF (Bi/NF) not only enables an ultra-large specific capacity of 4651 F g −1 (1 A g −1 ) and a capacity maintenance rate of 75% (after 1000 cycles), but it also exhibits outstanding catalytic hydrogen precipitation reaction, reaching an overpotential of −136 mV versus the reversible hydrogen electrode at −10 mA cm −2 and Tafel slope of 114.4 mV dec −1 . The Bi anode is gathered into the asymmetric SC, which demonstrates an ultra-high energy density of 125 Wh kg −1 (power density of 640 W kg −1 ) in an alkaline electrolyte.
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DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 38
·13732-13736
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IF 4
Ziyan Lv,Rukang Li
Much effort has been devoted to synthesizing nonlinear optical crystals with efficient second harmonic responses. Herein, a tantalum phosphate crystal Na11Ta8P7O43 with a moderate second harmonic response was obtained using self-fluxes of NaH2PO4 and Na2HPO4. Na11Ta8P7O43 belongs to the Cc space group of monoclinic systems with cell parameters of a = 8.5710(2) Å, b = 15.1144(4) Å, c = 28.7712(7) Å, β = 92.304(2)°, Z = 4. Its structural features were unique (Ta8O33) bi-capped triangular prisms uniformly oriented with a PO4 connection in the ab plane, which were further joined through additional PO4 groups in the c direction, resulting in moderate nonlinear effects. In addition, this crystal has the characteristics of phase-matchable second harmonic generation, a shorter cutoff edge than the known materials LiTaO3 and KTiOPO4, and high transmittance from the visible to the near infrared band, and may serve as a potential nonlinear optical crystal.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
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IF 8.128
Xingchi Li,Huaming You,Cheng Wang,Dongmei Liu,Rui Yu,Siyu Guo,Yuan Wang,Yukou Du
Modifying the electronic structure and optimizing the geometric structure can expeditiously tune the electrocatalytic properties of catalysts, resulting in considerably enhanced electrocatalytic performance towards electrocatalytic oxidation of liquid fuels . We herein report a simple synthetic strategy to prepare Bi-doped 3D taraxacum-like Pd nanocages (NCs) composed of porous nanosheets , which possess high surface areas and strong synergistic effects. Notably, a trace of Bi diffuses into the lattice of Pd and increases the electronic effects of the surface of Pd, endowing PdBi-0.5 NCs/C with superior electrocatalytic performance towards ethanol oxidation reaction (EOR). The mass activity and specific activity of PdBi-0.5 NCs/C were 3494.8 mA mg Pd −1 and 10.37 mA cm −2 , being 4.08- and 4.82- fold enhancements as compared with commercial Pd/C, respectively. Moreover, the highly open porous 3D nanocages structure with rich active sites and defects can also facilitate the mass/electron transfer to favor the EOR kinetics.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2020
·
IF 4.65
Mingliang Ma,Yuying Yang,Yan Chen,Yong Ma,Ping Lyu,Aiqi Cui,Weibo Huang,Zhe Zhang,Yanzheng Li,Feiyan Si
The flower-like Fe 3 O 4 /SiO 2 /MnO 2 /BiOBr-Bi magnetic composite photocatalyst was prepared in this work. The combination of BiOBr and Bi metal with flower-like MnO 2 constituted a heterojunction structure, which increased the specific surface area of the photocatalyst and promoted the separation of photo-generated carriers, resulting in the enhanced catalytic performance. The morphologies and the compositions of the photocatalyst were characterized in detail. Under simulated light, the degradation of organic dye methylene blue (MB) was used to research the photocatalytic activity. In the case of 15 mg photocatalyst, it was found that the photocatalytic degradation efficiency to the MB solution was 95.23% within 150 min. Moreover, the degradation rate of MB could still reach 81.11% after four cycles. The design of flower-like composites with magnetic core-shell structure provided a new method for fabricating photocatalysts having excellent catalytic performance and cyclic stability.
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Sustainable Energy & Fuels
·
2020
·Vol. 4
·期 7
·3334-3339
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IF 5.503
You Xu,Tianlun Ren,Shanshan Yu,Hongjie Yu,Shuli Yin,Ziqiang Wang,Xiaonian Li,Liang Wang,Hongjing Wang
The electrocatalytic nitrogen reduction reaction (NRR) for ammonia (NH3) synthesis is highly desirable yet still challenging. Catalysts, as the core component of electrocatalytic NRR systems, are a specific focus of research. In this work, we demonstrate that NRR active semimetal bismuth (Bi) ultrathin nanosheets (Bi NSs) could be prepared by means of the in situ electrochemical reduction-assisted exfoliation of BiOCl nanoplates (BiOCl NPs). Such a conversion, from semiconductive BiOCl NPs to semimetal Bi NSs, could create enlarged surface areas and bring about abundant under-coordinated Bi sites and accelerated electron transport capability. With these advantageous properties, the as-converted Bi NSs exhibit efficient NRR electrocatalytic activity in 0.1 M Na2SO4, achieving a high faradaic efficiency (14.14%) and NH3 yield (11.11 μg h−1 mgcat.−1) at −0.5 V (vs. reversible hydrogen electrode), as well as high NH3 selectivity.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2020
·
IF 4.65
Junli Wang,Lei Jin,Tingting Wang,Lijun Zhao,Fan Guan,Shaopeng Li,Dan Wang,Junhao Zhang
We report the ethylene glycol-mediated solvothermal synthesis of the continuous solid solution (Sb 1-x Bi x ) 2 S 3 (0 < x < 1) with 1D nanostructures (nanowires and nanorods). The ternary products show a broad variation in Bi:Sb composition ratios (53:47–7:93), length-to-diameter aspect ratios (2.7–66.2), and optical bandgap energies (1.36–1.55 eV) as well as an enhanced photocurrent (e.g., (Sb 1-x Bi x ) 2 S 3 with x = 0.22 is three times higher than pure Sb 2 S 3 ). The gradual shift of peak positions in the XRD patterns and the uniform distributions of Bi, Sb and S elements in EDS mapping prove the formation of single-phase (Sb 1-x Bi x ) 2 S 3 solid solution. Its formation is due to an isostructure-favored alloying mechanism, since Sb 2 S 3 and Bi 2 S 3 possess the same orthorhombic structure (space group: Pnma) and the similar lattice constants . The substitution of Bi for Sb isovalent cations can shorten the lengths of ternary alloyed Sb–Bi–S nanowires and transfer them to low aspect-ratio nanorods at high Bi/Sb precursor ratios. The dependence of the lengths on Bi/Sb ratios is reasonably interpreted considering the differences in the number of nuclei at different amounts of Bi ions and the covalency of Bi–S and Sb–S bonds during the alloying process.
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