JOURNAL OF POWER SOURCES
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2022
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IF 9.794
Liang Liu,Baocang Liu,Xuan Xu,Peng Jing,Jun Zhang
The electrochemical oxidation of glycerol is considered as a promising route to generate high value-added products. Rationally tuning the electronic structure of Pt catalysts by supporter and modifier is desirable for promoting the activity and stability of glycerol electrooxidation reaction (GEOR). In this work, we report Pt–Bi hybrid nanoparticles anchored hollow titanium nitride nanowires grew on carbon cloth (Pt 1-x -Bi x /TiN HNWs/CC (0≤ x ≤ 1)) as a self-supported monolithic electrode for efficient GEOR. Contributed by 3D porous nanotube structure, high corrosion resistance and conductivity of TiN, and strong electronic coupling effect of Pt, Bi, and TiN, the optimized Pt 0.95 -Bi 0.05 /TiN HNWs/CC electrode exhibits good catalytic activity and stability for GEOR. It shows a high peak current density of 88.4 mA cm −2 or 306.7 mA mg Pt −1 in 0.05 M glycerol +1.0 M KOH solution. After continuous electrolysis for 8 h in 0.05 M glycerol +1.0 M KOH solution at a constant potential of 0.85 V versus reversible hydrogen electrode (vs. RHE), a high glycerol conversion of 87.0%, a moderate selectivity of 36.6% for glyceric acid , and a good stability were achieved, which is superior to other compared electrodes and most of the reported Pt–Bi catalysts.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 30
·期 1
·1399-1412
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IF 5.19
Chen Jun,Zhang Boding,Wang Bingxing,Zhang Wenlong,Wang Jichao,Cui Chengxing,Wang Songlin
Wastewater containing quinoline has become a common pollutant in water and soil environments, which poses a threat to human health due to its carcinogenicity, teratogenicity, and mutagenicity. Quinoline’s stability and toxicity hinders its degradation by conventional physicochemical and biological methods. In this contribution, Fe-Co-Bi/kaolin particle electrodes were prepared for the efficient degradation of quinoline in wastewater, and characterized by using scanning electron microscope, X-ray diffraction, pyridine-IR, Brunauer–Emmett–Teller, X-ray photoelectron spectroscopy, and four-probe resistivity test. Parameters affecting the degradation efficiency were optimized to be the particle electrode dosage of 40 g/L, pH 3.5, H 2 O 2 addition of 67.6 mmol/L, electrical conductivity of 12.7 ms/cm, and voltage of 20 V. The constructed three-dimensional catalytic particle electrode system (3D-CPE) achieved 92.1% removal rate of chemical oxygen demand (COD) under the optimal conditions. Hydroxyl radicals (•OH) generated in the 3D-CPE process were identified by radical scavenging tests and electron spin response analysis. To unravel the degradation mechanism, the intermediate products were identified by using high performance liquid chromatography-mass spectrometry. The degradation mechanism was discussed with the help of theoretical calculation.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
·
IF 5.518
Qi Wang,Yu Mei,Ruoxue Zhou,Sridhar Komarneni,Jianfeng Ma
The Ti 3 C 2 -based MXene with unique lamellar nanostructure and high conductivity is expected to effectively improve photocatalytic ability of composites as a cocatalyst. Herein, two dimensional Ti 3 C 2 -based MXene nanosheets decorated with copper sulfide particles (CuS@MXene) were synthesized by hydrothermal treatment to boost catalytic persulfate (PS) activation under light, exhibiting remarkable reactivity and stability for the rapid removal of Orange II. The phase composition of CuS@MXene was detected by X-ray diffraction (XRD), the morphology of CuS@MXene was characterized by scanning electron microscope (SEM), and the results of X-ray photoelectron spectroscopy (XPS) proved the elemental composition and valence state of elements in the CuS@MXene. The dosage of PS and initial pH of solution were the main factors affecting the removal rate of Orange II, and the quenching experiment showed that 1 O 2 was the primary reactive species for the removal of Orange II in CuS@MXene -PS system. In addition, this study showed that CuS@MXene provided bi-active centers for PS activation, which was mainly attributed to the rapid charge transfer between dual electron-rich active centers of Cu and Ti. This system may be applicable to the degradation of other challenging organic pollutants .
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2022
·
IF 24.319
Chunxiao Zhang,Yingjie Li,Zirui He,Jianli Zhao,Dong Wang
Herein, a hollow microtubular Fe/Mn-promoted CaO-Ca 12 Al 14 O 33 bi-functional material was prepared by the bio-template method and used for H 2 production from sorption enhanced water gas shift (SEWGS). The microtubular Fe/Mn-promoted CaO-Ca 12 Al 14 O 33 exhibits excellent CO 2 capture and H 2 production performance in SEWGS/regeneration cycles. The stable hollow microtubular structure improves available adsorption and catalytic sites in Fe/Mn-promoted CaO-Ca 12 Al 14 O 33 for CO 2 capture and H 2 production. Mn addition improves CO 2 affinity capacity of the microtubular material. The Fe-Mn interaction increases redox ability of Fe 3+ /Fe 3+, 2+ , which promotes CO conversion. Moreover, the formed Ca 2 Fe 2 O 5 and Ca 2 MnO 4 both increase oxygen vacancies to promote catalytic activity of the microtubular material for WGS and its CO 2 capture capacity. The CO conversions for the microtubular material with the Fe/Mn/Al/Ca molar ratio= 10/2/10/100 are 98.7% and 94.0% after 20 cycles under the mild and severe calcination conditions, respectively. The hollow microtubular bi-functional material shows good prospect for efficient H 2 production from SEWGS.
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APPLIED ENERGY
·
2022
·
IF 11.446
Xianyao Yan,Yingjie Li,Chaoying Sun,Chunxiao Zhang,Liguo Yang,Xiaoxu Fan,Leizhe Chu
The sorption-enhanced steam gasification of biomass (SESGB) using CaO-based materials is considered as a promising method for H 2 production. Ca-Al-Ce material has been reported as a good bi-functional material in SESGB process. Red mud is a solid waste in aluminium industry with large yield, which is rich in Fe 2 O 3 . In this work, a red mud-doped Ca-Al-Ce bi-functional material was prepared by wet-mechanical mixing method for H 2 production from SESGB. The CO 2 capture, H 2 production, and tar reduction performances during SESGB process using the red mud-doped Ca-Al-Ce bi-functional material were studied. The results show that the optimum addition amount of red mud in the bi-functional material is 5 wt%. After 20 SESGB cycles, the H 2 concentration using the red mud-doped Ca-Al-Ce material achieves 65.1 vol%, which is 82.4% higher than that using Ca-Al-Ce material. Besides, with the addition of red mud in the bi-functional material, the tar, residue char yields and CO 2 concentration decrease by 25.2%, 8.6% and 52.2%, respectively. Fe 2 O 3 in the red mud reacts with CaO to form Ca 2 Fe 2 O 5 in the 1st cycle, and Ca 2 Fe 2 O 5 is stable during 20 cycles, which is beneficial for the generation of oxygen vacancy. The oxidation states of Fe species in the material increase with the number of SESGB cycles, thus the catalytic effects on water gas shift reaction and tar reduction are promoted. The red mud addition is the key factor that results in high H 2 production, CO 2 capture and tar reduction performances, so the red mud-doped Ca-Al-Ce material appears promising for SESGB.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2021
·
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
·
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
·
2023
·Vol. 4
·期 10
·2365-2371
·
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
·
2021
·
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
·
2026
·
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
·
2023
·
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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危险品化学品经营许可证（带存储）