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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Interface charge induced self-assembled (Co(OH)2)4@La(OH)3 heterojunction derived from Co4-MOF@La(HCO2)3 to boost oxygen evolution reaction

Le Gao,Yawen Li,Guifang Li,Jiaqi Huo,Lishan Jia

Interface engineering as an effective material modification method can regulate local corresponding interfacial geometry and electronic structures, thus enabling a higher intrinsic activity for the oxygen evolution reaction (OER). Herein, we carefully designed p-p heterojunction precursor Co4-MOF@La(HCO 2 ) 3 with internal electric field through electrostatic adherence, which then in-situ transformed into p-p type heterojunction electrocatalyst (Co(OH) 2 )4@La(OH) 3 under KOH activation strategy. The one-step in-situ conversion of (Co(OH) 2 )4@La(OH) 3 generated the interface with significant difference in metal atomic radius and exhibits fascinating nanostructures, which enhances the specific surface area and increases the number of active sites compared with the parent material. Impressively, the obtained material (Co(OH) 2 )4@La(OH) 3 demonstrates satisfying electrocatalytic activity in OER with a low overpotential of only 233 mV to reach a current density of 20 mA cm −2 , and excellent stability for 50 h at 10 mA cm −2 in alkaline medium. In-situ Raman technique indicates that multivalent Co centers are the true active sites during the OER process. Based on density functional theory (DFT) calculation results, La atoms possess empty d orbitals, which are beneficial to facilitate charge transfer from Co to La at the heterojunction interface. Meanwhile, the introduction of La atoms changes the coordinated environment around the adjacent atoms at the interface, which induces the upshift of the d-band center for Co atoms and increases the binding strength of the adsorbed oxygen intermediate.

CAS / MDL: 100-21-0
研究领域: 材料科学 · 电化学 · 能源转换与存储
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Desalination and Water Treatment · 2024 · IF 1

Photocatalytic degradation of bagasse pulp wastewater with La-TiO2/Al2O3 as a catalyst

Lihuan Mo,Peiqi Lyu,Zhen Yang,Jie Gong,Kai Liu,Jun Li

Bagasse pulp wastewater has restricted and disturbed the bagasse pulp industry all the time. In this paper, photocatalytic oxidation technology (O 3 +UV+TiO 2 ) was applied to bagasse pulp wastewater treatment. TiO 2 was prepared into a composite photocatalyst (La-TiO 2 /Al 2 O 3 ) to improve the treatment effect. p-Chlorophenol was chosen as a target compound to evaluate the catalytic activity and study the preparation process of La-TiO 2 /Al 2 O 3 . La-TiO 2 /Al 2 O 3 was finally used in the treatment of real bagasse pulp wastewater with photocatalytic oxidation technology. Under an optimum experiment conditions, chemical oxygen demand (COD) and total organic carbon removal rate of bagasse pulp wastewater reached 80.2% and 77.1%, respectively, and AOX dropped to 2.9 mg/L. Most organic pollutants in the wastewater had been removed. Additionally, in the reusability study, COD removal was maintained at 70.5% at 7th reuse. These findings of present study revealed that La-TiO 2 /Al 2 O 3 held great potential in the practical photocatalytic degradation application of industrial organic wastewater.

研究领域: 环境科学 · 化学工程 · 材料科学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Thermoelectric enhancement achieved by Y and La Co-doping in n-type Mg3.2Sb1.5Bi0.5

Yu Jiang,Marhoun Ferhat,Wenhao Fan,Shaoping Chen,Yachao Wang,Jie Chen,Rasha Abdullah Ahmed Al-Yusufi,Chaochao Dun

Additional cation doping is one of the potential strategies to enhance the thermoelectric (TE) performance of Mg 3 Sb 2 -based materials with precise regulation of interaction between cations and the host. In this work, using Mg 3 Sb 1.5 Bi 0.5 as an example, we confirmed that co-doping rare-earth elements with Y and La is capable to simultaneously improve its power factor and suppress the thermal conductivity : Y is an effective n -type dopant to regulate the optimal carrier concentration, while La doping can modulate the band structure and increase the effective mass that related to the improved Seebeck coefficient . A promising power factor of 18.3 μW cm -1 K -2 is obtained after co-doping. Meanwhile, the lattice thermal conductivity is dramatically reduced to 0.39 W m -1 K -1 at 750 K thanks to the extra defect scattering introduced by Y and La. As a result, a peak figure of merit ( zT ) of 1.76 and a competitive average zT of 1.1 among 300–750 K are achieved in Mg 3.2 Y 0.04 La 0.01 Sb 1.5 Bi 0.5 . The synergistic effect stemming from dual-cations doping provides profound insights for controllable host-dopant design and modulation toward high-efficient n-type TE materials .

研究领域: 材料科学 · 物理学
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CERAMICS INTERNATIONAL · 2021 · IF 4.527

Ultra-fast charge-discharge and high energy storage density realized in NaNbO3–La(Mn0.5Ni0.5)O3 ceramics

Jitong Wang,Xinru Nie,Zhanhui Peng,Xiaoping Lei,Pengfei Liang,Zupei Yang,Xiaolian Chao

Lead-free antiferroelectric (AFE) NaNbO 3 (NN) is one of promising materials for dielectric capacitors, but the recoverable energy-storage density and efficiency get restrained owing to huge remanent polarization and limited dielectric breakdown field strength . In this work, a variety of NN based lead-free bulk (1- x )NaNbO 3 - x La(Mn 0.5 Ni 0.5 )O 3 (abbreviated as (1- x )NN- x LMN, x  = 0, 0.05, 0.10, 0.15, 0.20) ceramics were designed using a solid-state synthesis method. Remarkably, an ultra-fast charge-discharge speed 47 ns and an acceptable recoverable energy-storage density W rec ~1.77 J/cm 3 with a high efficiency η  = 77% were obtained under the E b of 200 kV/cm at x  = 0.05. The superior energy storage performance is attributed to the regulation of domain size and voltage resistance by special ions substitution of A and B sites. This work not only proposes an efficient strategy to realize high recoverable energy-storage density and efficiency, but also provide an candidate material for application of advanced pulsed power capacitors.

CAS / MDL: 1313-13-9
研究领域: 材料科学 · 能源存储
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PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE · 2024 ·Vol. 221 ·期 12 ·2300874 · IF 1.9

Fe-La-Ce-ZSM-5 Zeolite for Adsorbing Congo Red

Jie Yang,Zhengkun Cai,Dong Li

In this experiment, ZSM-5 molecular sieves are prepared by hydrothermal synthesis and modified by impregnation with Fe, La, and Ce loading. X-ray diffraction, X-ray photon-electron spectroscopy, and scanning electron microscopy show that Fe, La, and Ce elements are successfully loaded onto the surface of the material, and the surface area of Fe-La-Ce-ZSM-5 is 241.66 m 2 g −1 . A systematic study on the adsorption of Congo red solution is carried out using Fe-La-Ce-ZSM-5 molecular sieves and it is found through the adsorption data that the adsorption process is more in line with Langmuir and the proposed second-order kinetic model, and the theoretical saturated adsorption capacity is 2669.19 mg g −1 . The adsorption process is recycled four times and still has more than 60 % removal performance for high-concentration Congo red solution. The results of this experiment show that Fe-La-Ce-ZSM-5 molecular sieves show excellent removal performance for Congo red dye in wastewater.

研究领域: 环境科学 · 材料科学 · 化学工程
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International Journal of Electrochemical Science · 2024 · IF 1.3

Phosphorus doping heterostructure La(OH)3@CuO @NF as an advanced electrocatalyst for the oxygen evolution reaction

Dandan Liang,Weili Hou,Ying Zhang,Jihua Shang,Haibo Ren,Yufeng Sun

Due to the prevailing energy shortages, the pursuit of new alternative energy sources is becoming increasingly urgent. Hydrogen production through water electrolysis has emerged as a crucial method. However, the sluggish four-electron reaction in the oxygen evolution reaction (OER) remains the primary rate-limiting step. In this study, we synthesized a heterostructure La(OH) 3 @CuO-P material on the nickel foam (NF) substrate. The experimental results demonstrate that after phosphating treatment, the heterostructure La(OH) 3 @CuO-P exhibits exceptional catalytic performance with only 215 mV overpotential, a Tafel slope value of 79.36 mV/dec, and a bilayer capacitance of 39.02 mF/cm 2 at a current density of 10 mA/cm 2 for OER in a 1 M KOH solution. These values are significantly superior compared to those obtained using heterostructure La(OH) 3 @CuO alone which showed an overpotential value of 365 mV at a current density of 10 mA/cm 2 . Moreover, during cyclic voltammetry testing for up to 500 cycles, La(OH) 3 @CuO-P also demonstrates relatively stable performance. Analyses suggest that composite heterostructure effectively addresses issues such as insufficient conductivity of La(OH) 3 and monomer aggregation tendency for CuO while maintaining excellent properties for each component. By incorporating P atoms as dopants, the interaction between La, Cu, and P atoms not only facilitates fine-tuning of the electronic structure and optimization of the adsorption free energy (-OH), but also promotes an increase in catalytic active sites through sample size reduction, thereby further augmenting the performance of the OER.

CAS / MDL: 10031-43-3 10277-43-7
研究领域: 材料科学 · 电催化
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Polymers · 2023 ·Vol. 15 ·期 1 ·248 · IF 5

Controllable Preparation of Superparamagnetic Fe3O4@La(OH)3 Inorganic Polymer for Rapid Adsorption and Separation of Phosphate

Yao Lu,Xuna Jin,Xiang Li,Minpeng Liu,Baolei Liu,Xiaodan Zeng,Jie Chen,Zhigang Liu,Shihua Yu,Yucheng Xu

Superparamagnetic Fe3O4particles have been synthesized by solvothermal method, and a layer of dense silica sol polymer is coated on the surface prepared by sol-gel technique; then La(OH)3covered the surface of silica sol polymer in an irregular shape by controlled in situ growth technology. These magnetic materials are characterized by TEM, FT-IR, XRD, SEM, EDS and VSM; the results show that La(OH)3nanoparticles have successfully modified on Fe3O4surface. The prepared Fe3O4@La(OH)3inorganic polymer has been used as adsorbent to remove phosphate efficiently. The effects of solution pH, adsorbent dosage and co-existing ions on phosphate removal are investigated. Moreover, the adsorption kinetic equation and isothermal model are used to describe the adsorption performance of Fe3O4@La(OH)3. It was observed that Fe3O4@La(OH)3exhibits a fast equilibrium time of 20 min, high phosphate removal rate (>95.7%), high sorption capacity of 63.72 mgP/g, excellent selectivity for phosphate in the presence of competing ions, under the conditions of phosphate concentration 30 mgP/L, pH = 7, adsorbent dose 0.6 g/L and room temperature. The phosphate adsorption process by Fe3O4@La(OH)3is best described by the pseudo-second-order equation and Langmuir isotherm model. Furthermore, the real samples and reusability experiment indicate that Fe3O4@La(OH)3could be regenerated after desorption, and 92.78% phosphate removing remained after five cycles. Therefore, La(OH)3nanoparticles deposited on the surface of monodisperse Fe3O4microspheres have been synthesized for the first time by a controlled in-situ growth method. Experiments have proved that Fe3O4@La(OH)3particles with fast separability, large adsorption capacity and easy reusability can be used as a promising material in the treatment of phosphate wastewater or organic pollutants containing phosphoric acid functional group.Keywords:superparamagnetic;Fe3O4@La(OH)3inorganic polymer;phosphate adsorption

研究领域: 材料科学 · 环境科学
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Materials Advances · 2023 ·Vol. 4 ·期 3 ·940-947 · IF 5

Construction of a La-ZnIn2S4/MIL-125(Ti) heterojunction for highly efficient photocatalytic degradation of aflatoxin B1

Xiaobing Yang,Junjie Pan,Bingcong Xing,Wenjie Lei,Yingchun Fu,Kejun Cheng

Nowadays, aflatoxin B1 (AFB1) contamination is considered as one of the most common food safety issues for humans and animals. As one of the most advanced oxidation techniques, photocatalytic degradation can break down organic contaminants into nontoxic and harmless materials efficiently. In this paper, we explored the degradation efficiency of AFB1 by ZnIn2S4. To promote the photocatalytic degradation efficiency of AFB1, ZnIn2S4 was coupled with MIL-125(Ti) and then doped with La [this hybrid is denoted as La-ZnIn2S4/MIL-125(Ti)] to effectively convert it via photocatalytic generation of superoxide radicals (˙O2− and ˙OH) and achieve much enhanced photocatalytic performance, which is demonstrated by degrading 97.6% of AFB1. According to the transient photocurrent responses, the doping of La and coupling with MIL-125(Ti) can highly improve the efficient separation of the photoinduced electron–hole pairs on ZnIn2S4, leading to the effective conversion of OH− and O2 into ˙O2− and ˙OH, respectively, during the photodegradation process. This strategy of coupling with MOFs and doping with rare earth elements provides a facile and efficient method for degrading food pollutants produced by aflatoxins.

CAS / MDL: 62-55-5 1162-65-8
研究领域: 食品安全 · 环境科学 · 材料科学
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CATALYSIS LETTERS · 2024 · IF 2.3

SrTiO3: La/Cr hollow cube decorated with plasmonic Co for efficient photocatalytic hydrogen production

Sun Xiaoqin,Zhang Zehua,Yun Sining

Plasmonic-driven photocatalyst have outstanding solar driven surface plasmon resonance (SPR) characteristics, and it is a prospective approach to improve photocatalytic performance. Herein, plasmonic Co metal decorated SrTiO 3 : La/Cr hollow cubes was developed and constructed by template-free hydrothermal method. The photocatalyst possesses the merits of the hollow structure with large specific surface area and strong light absorption. The intimate contact between Co and SrTiO 3 : La/Cr promotes the interfacial charge transfer. Co-SrTiO 3 : La/Cr manifests the superior photocatalytic performance toward water splitting for hydrogen evolution compared with that of other cocatalyst. And the H 2 evolution exceeds 210 μmol·g −1 ·h −1 under the optimum of the amount of 1.25wt% Co NPs. The mechanism of the enhanced performance comes from the improvement of light absorption in the visible-light region induced by SPR, as well as the efficient interfacial separation and transport of charge carriers on the photocatalyst facilitated by the local electromagnetic fields of plasmonic Co metal. Graphical Abstract

CAS / MDL: 13548-38-4
研究领域: 材料科学 · 能源科学 · 纳米技术
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2022 ·Vol. 29 ·期 56 ·84166-84179 · IF 5.19

Promoting effect of Fe/La loading on γ-Al2O3 catalyst for hydrolysis of carbonyl sulfur

Gao Panting,Li Yuran,Lin Yuting,Chang Liping,Zhu Tingyu

Catalytic hydrolysis of carbonyl sulfur (COS) from blast furnace gas is one of the keys to achieving ultra-low emission in the iron–steel industry. To improve the COS hydrolysis activity on γ-Al 2 O 3 catalyst at low temperature, catalysts with Fe or La as the active component were prepared by the impregnation method, the physical and chemical properties of the catalyst were characterized by ICP, XRF, XRD, BET, and TPD. The hydrolysis activity of COS and sulfur resistance ability on various catalysts were investigated in a fixed bed reactor combined with gas chromatography. The results show that the addition of Fe or La improves the COS hydrolysis activity due to the increase in alkaline sites on the catalyst surface. The roles of various alkaline sites on catalysts have been recognized. The weak alkaline center is the reaction site of COS hydrolysis, the middle and strong alkaline centers are the adsorption and oxidation sites of H 2 S. The Fe/Al 2 O 3 catalyst has higher hydrolytic activity and oxidative capacity for H 2 S removal due to forming more sulfate species on Fe. The La/Al 2 O 3 catalyst has higher hydrolysis efficiency in that H 2 S rapidly desorbs from the catalyst surface to the gas phase, and then, the activity of reaction sites is recovered. This provides an idea for the preparation of sulfur-resistant catalysts.

研究领域: 环境科学 · 催化化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Rare earth La single atoms supported MoO3-x for efficient photocatalytic nitrogen fixation

Xiufan Liu,Yani Luo,Cancan Ling,Yanbiao Shi,Guangming Zhan,Hao Li,Huayu Gu,Kai Wei,Furong Guo,Zhihui Ai,Lizhi Zhang

Herein, we demonstrate that the rare-earth La single catalyst with multi-shell characteristic is an excellent choice for this purpose. By merit of its unsaturated orbitals of La, the single La atom strongly bonds with the two-coordinated lattice oxygen on the oxygen-deficient MoO 3−x to form O 2c -La-O 2c coordination. This robust metal-support interaction frees single atoms from detachment or aggregation, and prevents catalyst from deactivation. Meanwhile, the occupied 5d orbitals of La back-donate electrons to the 2π* molecular orbitals of adsorbed N 2 that substantially activate the inert N N bond towards successive hydrogenation. And single La atom could optimize the electron property of the MoO 3−x support to promote photocatalytic nitrogen fixation. Without any sacrificial agents, this single atom La catalyst with a well-designed coordination structure delivers an impressive NH 3 production rate of 209.0 μmol h 1 g 1 under visible light, outperforming most reported single atom photocatalysts.

研究领域: 材料科学 · 催化化学 · 环境科学
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ACS Omega · 2021 · IF 3.512

Preparation and Electrochemical Characterization of La and Al Co-doped NCM811 Cathode Materials

Mingyu Zhang,Chaoyong Wang,Junkai Zhang,Gang Li,Li Gu

LiNi0.8Co0.1Mn0.1O2 (NCM811) became a research hot point because of its low cost, environmental friendliness, and excellent electrochemical performance. However, Li+/Ni2+ intermixing is an essential factor affecting its applicability. Doping could be an important method to improve the electrochemical performance of NCM811-based cathode materials. In this work, La and Al co-doped NCM811 was prepared by a solid-state method. Results from X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS) and electrochemical performance were discussed in depth. These showed that when La and Al doping concentrations were 1 and 0.5%, the samples showed the best performance. The as-improved performances were mainly attributed to the reduced Li+/Ni2+ intermixing, suppressed phase transition, and decreased potential polarization and impedance.

研究领域: 材料科学 · 电化学
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