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CATALYSIS TODAY · 2024 · IF 5.2

Efficient photocatalytic CO2 N-formylation of amines over Pd/Bi-ZnOx without extra reductant

Peng Bai,Yicheng Zhao,Yongdan Li

Photocatalytic N -formylation of amines with CO 2 is a promising strategy to convert CO 2 into value-added chemicals sustainably. In this work, Pd-Bi bimetallic modified ZnO enriched in oxygen vacancies is constructed for photocatalytic CO 2 formylation of benzylamine at room temperature without any reductants. The Pd and Bi sites reduce the band gap energy of ZnO, promote the separation of the photogenerated charge carriers and enhance the adsorption capacity of CO 2 . The yield of N -benzylformamide reaches 31.7 mmol g −1 with a selectivity of 85.3 % after 3-hour radiation in N , N -dimethylformamide (DMF) solvent. The aldehyde group involved in the formylation of benzylamine is derived from the decomposition of DMF, which is regenerated with the aldehyde group coming from the reduction of CO 2 . The decomposition-regeneration cycle of DMF solvent enlarges the reaction region, which is beneficial to the activity and selectivity of the formylation process. The synergistic photocatalytic system shows a good universality. This study provides a new approach to high-efficiency CO 2 utilization and formamide production.

研究领域: 材料科学 · 环境科学 · 化学工程
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ACS Sustainable Chemistry & Engineering · 2024 · IF 7.1

Efficient CO2 Reduction to Formate with Nano-Roughened Cu–Bi Alloy Hollow Fiber Electrodes

Zhibin Zhang,Lei Wang,Xixian Yang,Mengyuan Chu,Liyun Huang,Jiayi Fan,Wucheng Xie,Defei Liu,Wenbing Yuan,Yue Situ

The electroreduction of CO2 to formate is of significant interest due to its potential for sustainable fuel and chemical production. Hollow fiber electrodes, which integrate gas diffusion and catalytic layers, offer structural advantages. These advantages enhance gas–solid–liquid-phase reactions, making them particularly beneficial for CO2 electroreduction. This work reports a copper–bismuth alloy hollow fiber with a nanostructured surface, designed with specific metal ratios and transformed into a sulfur surface-modified copper–bismuth alloy hollow fiber (Cu7S4–CuBi HF) electrode with nanoflower structures. CO2-penetration mode enhances formate current density and Faradaic Efficiency (FE) while suppressing the hydrogen evolution reaction (HER), due to the fiber’s unique gas transport. The nanoflower morphology increases the electrochemical active surface area, boosting current densities. This design achieved a formate FE of 91.27% at −0.9 V vs RHE and a current density of 80.12 mA cm–2, outperforming many existing Cu@Bi electrocatalysts. This success is due to the innovative surface design and the distinct structural features of the hollow fiber electrodes.

CAS / MDL: 7727-54-0 872-50-4
研究领域: 材料科学 · 电化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Binder-free Bi@MXene film with 3D sandwich structure for highly hybrid capacitive deionization

Meng Xu,Zhiyou Tan,Yilong Tian,Feng Gong,Kebing Yi,Zhike He,Xinghu Ji

Developing anode materials significantly enhances the desalination performance of hybrid capacitive deionization (HCDI). Bismuth exhibits high selectivity for chloride ion removal. However, the sluggish kinetics and poor cycling stability of bismuth present considerable challenges for its application in high-capacitance deionization. In this study, we successfully prepared a binder-free Bi@MXene film electrode for chloride storage by employing an electrostatic self-assembly strategy to anchor Bi nanospheres into MXene layers. The bismuth nanospheres, as the pillars of MXene network, improve the self-stacking problem of Ti 3 C 2 T X layers. And MXene layers effectively mitigate the volume expansion of bismuth nanospheres through the spatial confinement effect. Benefiting from three-dimentional sandwich structure of Bi@MXene film, the HCDI system exhibits outstanding salt adsorption capacity (113.4 mg·g −1 ), excellent adsorption rate (4.2 mg·g −1 ·min −1 ) and a good desalination capacity retention of 84.6 % following 50 cycles at 100 mA·g −1 . The development of this composite material provides insights for the design of efficient and stable chloride storage electrodes.

研究领域: 材料科学 · 环境工程
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Visible-to-Near-Infrared Mechanoluminescence in Bi-Activated Spinel Compounds for Multiple Information Anticounterfeiting

Zhicong Chen,Peishan Shao,Puxian Xiong,Yao Xiao,Bingjun Liu,Zhiduo Wang,Sheng Wu,Dongliang Jiang,Kang Chen,Jiulin Gan,Dongdan Chen,Zhongmin Yang

Mechanoluminescence (ML) is the nonthermal luminescence generated in the process of force-to-light conversion, which has broad prospects in stress sensing, wearable devices, biomechanics, and multiple information anticounterfeiting. Multivalence emitter ions utilize their own self-reduction process to realize multiband ML without introducing another dopant, such as Eu3+/Eu2+, Sm3+/Sm2+, and Mn4+/Mn2+. However, self-reduction-induced ML in bismuth-activated materials has rarely been reported so far. In this work, a novel visible-to-near-infrared (vis–NIR) ML induced by the self-reduction of Bi3+ to Bi2+ in the spinel-type compound (MgGa2O4) is reported. The photoluminescence (PL) spectra, PL excitation (PLE) spectra, and PL lifetime curves demonstrate that Bi3+/Bi2+ ions are the main luminescence centers. Notably, the possible self-reduction model is proposed, where a magnesium vacancy (VMg″) is considered as the driving force for the self-reduction of Bi3+ to Bi2+. Furthermore, an oxygen vacancy (VO••) is confirmed by electron paramagnetic resonance (EPR) spectroscopy. Combined with thermoluminescence (TL) glow curves and ML spectra, a plausible trap-controlled ML mechanism is illustrated, where electron–hole (VO••/VMg″) pairs play a significant role in capturing electrons and holes. It is worth noting that the proof-of-concept dual-mode electronic signature application is implemented based on the flexible ML film, which improves the capabilities of signature anticounterfeiting for high-level security applications. Besides, multistimulus-responsive luminescence behaviors of the ML film are realized under the excitation of a 254 nm UV lamp, thermal disturbance, 980 nm laser, and mechanical stimuli. In general, this study provides new insights into designing vis–NIR ML materials toward wider application possibilities.

研究领域: 材料科学 · 光学
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Advanced Science · 2024 ·Vol. 11 ·期 28 ·2401730 · IF 14.3

Bi Nanospheres Embedded in N-Doped Carbon Nanowires Facilitate Ultrafast and Ultrastable Sodium Storage

Qian Yao,Cheng Zheng,Kejun Liu,Mingyue Wang,Jinmei Song,Lifeng Cui,Di Huang,Nana Wang,Shi Xue Dou,Zhongchao Bai,Jian Yang

Sodium ion batteries (SIBs) are considered as the ideal candidates for the next generation of electrochemical energy storage devices. The major challenges of anode lie in poor cycling stability and the sluggish kinetics attributed to the inherent large Na + size. In this work, Bi nanosphere encapsulated in N-doped carbon nanowires (Bi@N-C) is assembled by facile electrospinning and carbonization. N-doped carbon mitigates the structure stress/strain during alloying/dealloying, optimizes the ionic/electronic diffusion, and provides fast electron transfer and structural stability. Due to the excellent structure, Bi@N-C shows excellent Na storage performance in SIBs in terms of good cycling stability and rate capacity in half cells and full cells. The fundamental mechanism of the outstanding electrochemical performance of Bi@N-C has been demonstrated through synchrotron in-situ XRD, atomic force microscopy, ex-situ scanning electron microscopy (SEM) and density functional theory (DFT) calculation. Importantly, a deeper understanding of the underlying reasons of the performance improvement is elucidated, which is vital for providing the theoretical basis for application of SIBs.

研究领域: 材料科学 · 电化学
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REACTIVE & FUNCTIONAL POLYMERS · 2020 · IF 3.333

Bi-functionalized ionic liquid porous copolymers for CO2 adsorption and conversion under ambient pressure

Liwei Sun,Jingyi Luo,Ming Gao,Shaokun Tang

Developing solid materials with high CO 2 adsorption capacity and catalytic activity has been a hotspot due to the greenhouse effect. In this work, bi-functionalized ionic liquid 1-vinyl-3-methoxyethyl imidazolium glycinate ([VMOEim][Gly]) was copolymerized with crosslinker divinylbenzene (DVB) to obtain bi-functionalized ionic liquid porous copolymers P( n DVB-[VMOEim][Gly]) and HP( n DVB-[VMOEim][Gly]). These copolymers possess loose stack of small particles or laminates, and they contain mesopores and a small number of micropores. For HP(0.6DVB-[VMOEim][Gly]), surface area reaches up to 508 m 2 ·g −1 and the initial decomposition temperature is about 180 °C. Then these porous copolymers were applied for CO 2 adsorption at 25 °C and cycloaddition reaction of CO 2 with epichlorohydrin under ambient pressure and cocatalyst-free condition. The maximum CO 2 capture capacity is 64.5 mg/g with HP(0.6DVB-[VMOEim][Gly]) as adsorbent. The effects of catalyst type, catalyst dosage, reaction time and temperature on the yield of cyclic carbonate were also investigated. The optimum conditions are 4 wt% of HP(0.6DVB-[VMOEim][Gly]) (based on the epichlorohydrin) as catalyst at 130 °C for 10 h, and the yield of 4-(chloromethyl)-1,3-dioxolan-2-one can reach 94%. Furthermore, the catalytic activity of HP(0.6DVB-[VMOEim][Gly]) maintains and the yield is 91% after five-cycle experiment. The mechanism of cycloaddition reaction was also discussed.

研究领域: 材料科学 · 环境科学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2020 · IF 4.939

Hydrogen generation from splitting water with Al–Bi(OH)3 composite promoted by NaCl

Chen Chen,Xu Guan,Hongbo Wang,Shijie Dong,Ping Luo

In this paper, a novel Al–Bi(OH) 3 system hydrogen-generating material is investigated. Hydrolysis experiments show that the hydrolysis properties of the Al–10 wt% Bi(OH) 3 composite are significantly improved by doping with sodium chloride, and the Al–10 wt% Bi(OH) 3 –5 wt% NaCl composite has a low activation energy (10.4 kJ mol −1 ). With the further optimization of milling time, the hydrogen yield of Al–10 wt% Bi(OH) 3 –5 wt% NaCl composite reaches 1000 mL g −1 in 1 min. X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, energy-dispersive spectroscopy and thermogravimetric analysis are applied to characterize the composite and explore the hydrolysis mechanism. The characterization results show that the activation of aluminum mainly comes from three factors: (1) The formation of alumina during ball milling plays an important role in preventing the agglomeration between Al–Bi, Al–Al and Bi–Bi; (2) Bismuth generated during ball milling can form micro-galvanic cell with aluminum to promote the corrosion of aluminum; (3) Sodium chloride as a grinding aid contributes to crush aluminum powder , and chloride ions facilitate the corrosion of aluminum in the hydrolysis process . In addition, the drying method and initial water temperature have a great influence on by-products. The composite is expected to be used in mobile emergency fuel cell due to its rapid hydrogen production capacity.

研究领域: 材料科学 · 化学工程
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2019 ·Vol. 103 ·期 1 ·183-192 · IF 3.094

Controllable ultra-broadband visible and near-infrared photoemissions in Bi-doped germanium-borate glasses

Xueyun Liu,Cuimei Cheng,Xiaoman Li,Qing Jiao,Shixun Dai

The design of functional materials with tunable broadband luminescence performance is still of great interest in the fields of lighting, solar cells, tunable lasers, and optical amplifiers. Here, via a melt-quenching method, a series of bismuth (Bi)-doped germanium-borate glasses with composition of 40GeO 2 –25B 2 O 3 –25Gd 2 O 3 –10La 2 O 3 – x Bi 2 O 3 have been prepared, in which multiple Bi active centers can be stabilized simultaneously. Dual-modulating modes of visible (380-750 nm) and near-infrared (NIR) (1000-1600 nm) broadband photoemissions were effectively controlled under flexible excitation scheme. Photoluminescence (PL) spectra at low temperature 10-298 K were appropriately employed to interpret such an unusual wide visible emission band. To further illustrate the origin of NIR component, transmission electron microscopy (TEM) measurement was carried out. It is demonstrated experimentally that the visible emission mainly originates from the collective contribution of the 3 P 1 / 3 P 0 1 S 0 transitions of Bi 3+ , while the broadband NIR luminescence should be related to the formation of low valent Bi + and (or) Bi 0 centers. This work may help to enhance the knowledge of the complex luminescence mechanism for the Bi species and it also enables such transparent glass materials to be a promising candidate for the multifunctional tunable light source.

研究领域: 材料科学 · 光学工程
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COLLOIDS AND SURFACES B-BIOINTERFACES · 2019 · IF 3.973

Bi-layered electrospun nanofibrous membrane with osteogenic and antibacterial properties for guided bone regeneration

Meifei Lian,Binbin Sun,Zhiguang Qiao,Kai Zhao,Xiaojun Zhou,Qianqian Zhang,Duohong Zou,Chuanglong He,Xiuyin Zhang

Guided bone regeneration (GBR) membranes have the potential to prevent the invasion of epithelial and connective tissues as well as to maintain a stable space for facilitating the ingrowth of regenerative bone tissue. However, the bioactivity and regeneration potential of currently available membranes still need to be improved. In this study, a novel bi-layered membrane with both osteogenic and antibacterial functions was developed for GBR applications. The loose layer (LL) of the membrane was composed of conjugated electrospun poly (lactic-co-glycolic acid) (PLGA)/gelatin nanofibers incorporating dexamethasone-loaded mesoporous silica nanoparticles ( [email protected] ), while the dense layer (DL) of the membrane consisted of traditionally electrospun PLGA nanofibers loaded with the broad-spectrum antibiotic doxycycline hyclate (DCH). Morphological results showed that the LL ( [email protected] /PLGA/Gel) membrane exhibited a porous and loosely packed structure, which was beneficial for cell adhesion and infiltration, while the DL (DCH/PLGA) membrane remained dense enough to act as a barrier. In vitro drug release tests indicated that both DEX and DCH followed a favorable sustained release profile. The cell viability evaluation suggested that the electrospun membranes possessed good cytocompatibility. Furthermore, in vitro osteogenesis analyses demonstrated that the [email protected] /PLGA/Gel composite membrane possessed an enhanced osteoinductive capacity for rat bone marrow stem cells (BMSCs), which was verified by the increased alkaline phosphatase (ALP) activity, the enhanced calcium deposition, and the upregulated osteocalcin (OCN) expression. In vitro antimicrobial experiments revealed the effective antibacterial potency of the DCH/PLGA membrane. In conclusion, the prepared nanocarrier-incorporated bi-layered composite membrane with combined osteogenic and antibacterial properties may be a promising candidate for GBR application.

研究领域: 生物材料 · 组织工程 · 再生医学 · 药学 · 材料科学
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OPTICAL MATERIALS · 2024 · IF 3.8

Preparation and electrochromism of amorphous Bi-doped TiO2 film for aqueous-based electrochromic device

Bo Zhang,Hui Wang,Zhuohua Liu,Naiye Zhao,Qiquan Zou,Yuanyuan Tian

Amorphous Bi–TiO 2 films with improved electrochromic properties have been successfully fabricated by a facile sol-gel spin-coating technology. The influence of dopant bismuth (Bi) content and sol amount on the electrochromic performance of Bi–TiO 2 films was studied. The optimized Bi–TiO 2 films show outstanding electrochromic properties, including wide transmittance modulation (ΔT = 74.26 % at 640 nm), short switching times (2.6 s/3 s for bleaching and coloring), and large coloration efficiency (52.77 cm 2  C −1 ). A proton-based electrochromic device was prepared by the amorphous Bi–TiO 2 film as the electrochromic film and Cu sheet as the counter electrode. The prepared device has a small operating potential range (1.0 V) in aqueous electrolyte due to the excellent electrochromic performance and high proton activity for the amorphous Bi–TiO 2 film. In addition, the device shows excellent performance (ΔT = 67.41 %, 2.5 s/3.9 s for bleaching and coloring), providing an important reference value for the development of high-efficiency electrochromic device.

研究领域: 材料科学 · 电化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Porous bi-functional ionic liquid-grafted metal–organic framework for diluted CO2 cycloaddition reaction

Liwei Sun,Lipeng Wang,Meilin Yin,Shaokun Tang

Direct utilization of low-concentration CO 2 is of importance to mitigate the global warming and reduce energy consumption. Herein, a new bi-functional ionic liquid-grafted material was fabricated for CO 2 /N 2 selectivity and diluted CO 2 cycloaddition reaction. Following the preparation of 1-carboxymethyl-3-methoxy ethyl-imidazolium chloride ([CmMOEim]Cl) containing carboxyl and ether group, MIL-53(Al) was used for directly chemical grafting of the ionic liquid to obtain [CmMOEim]Cl@MIL-53(Al). CO 2 capture capacity of [CmMOEim]Cl@MIL-53(Al) reached up to 70 cm 3 CO 2 /g sorbent at 25 °C and 0.1 MPa, which was higher than that of two individual components. Cyclopropyl carbonate of 97 % yield was obtained at 110 °C, 3 MPa of initial 50 vol% CO 2 /N 2 pressure and 4 h with 2.4 wt% [CmMOEim]Cl@MIL-53(Al)-0.4 under solventless and co-catalyst-free condition. Various terminal cyclocarbonates were synthesized with above 90 % yield. In addition, the heterogeneous catalyst was separated from reaction system by simple centrifugation and the yield of cyclopropyl carbonate was higher than 90 % after 12 cycles owing to the chemical grafting of [CmMOEim]Cl on MIL-53(Al).

研究领域: 化学工程 · 材料科学 · 环境科学
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JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS · 2024 · IF 2.5

Influence of Bi doping on the structure and electromagnetic wave absorption for LaFeO3 perovskite

Liang Yan,Yujing Zhang,Yilin Zhang,Rui Liu,Chuyang Liu,Fan Wu,Xuefei Miao,Er Liu,Xiaoling Peng,Jing Li,Shan Tao,Feng Xu

LaFeO 3 perovskite has possessed great potential in the field of microwave absorption considering its outstanding dielectric and magnetic properties. In this work, Bi-doped LaFeO 3 powders (BLFO) were prepared by a simple solid state reaction method. The results have demonstrated that the crystalline of LaFeO 3 and the lattice oxygen are increased with the additionally introduced Bi. As a result, the samples could exhibit the strongest microwave absorption with the minimum reflection loss (RL min ) of −39.48 dB and the effective absorption band (EAB) of 3.63 GHz (10.28–13.91 GHz) at a filling ratio of 60 wt%. The excellent microwave absorption properties are ascribed to the enhanced conductive loss, polarization relaxation and the co-existed magnetic loss. Moreover, the optimum sample exhibits the radar cross-section values below −10 dBm 2 across a wide angular range of −90° to 90° with a thickness of 2.5 mm. Therefore, this work opens up a feasible and effective way for modulating the electromagnetic properties of perovskite materials as potential microwave absorbents.

研究领域: 材料科学 · 电磁学
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