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BiOCl
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY · 2026 · IF 7.1

Dual-field synergy in oxygen-vacancy-rich g-C3N4/BiOCl/PVDF membranes for enhanced piezo-photocatalytic antibiotic degradation

Yining Zhang,Jiahao Gan,Mengyang Xu,Jinze Li,Xiang Liu,Zhengyu Chen,Aigang Zhang,Pengwei Huo

Dual-electric-field coupling of the S-scheme g-C 3 N 4 /BiOCl heterojunction and β-PVDF piezo-polarization modulates oxygen-vacancy energy levels for efficient charge separation. • An oxygen-vacancy-rich g-C 3 N 4 /BiOCl photocatalyst is integrated into a porous PVDF membrane, achieving stable immobilization and rapid mass transport. • The multifunctional membrane delivers a high piezo-photocatalytic rate of 0.04012 min −1 and 98.21 % tetracycline removal under light-mechanical coupling. • The composite membrane exhibits excellent recyclability and enables synergistic piezo-photocatalytic purification for antibiotic-contaminated wastewater. Oxygen vacancies (O Vs ) play an important role in photocatalysis, but exploiting O Vs in heterostructures to achieve efficient electron trapping and directional transport remains challenging. In this study, oxygen-vacancy-rich 2D/2D g-C 3 N 4 /BiOCl nanosheets were prepared via a simple hydrothermal method and immobilized on a porous β-PVDF matrix through a freeze-assisted phase inversion process, forming a flexible piezo-photocatalytic membrane. The results indicate that the built-in electric field of the g-C 3 N 4 /BiOCl heterojunction and the piezoelectric polarization field of PVDF jointly regulate the electronic behavior near O Vs . These two electric fields overlap around the defect sites and favorably modulate the defect energy levels, thereby enhancing the ability of O Vs to capture electrons. This dual-field regulation deepens the defect potential wells, prolongs electron residence time, and suppresses carrier recombination. The piezoelectric field also provides a directional driving force that guides electron transport along the interface and promotes the generation of reactive oxygen species. Using tetracycline as the target pollutant, the g-C 3 N 4 /BiOCl/PVDF-50 % membrane exhibited the highest piezo–photocatalytic activity, with an apparent rate constant of 0.04012 min −1 . Overall, this study elucidates the synergistic mechanism among the piezoelectric field, the heterojunction electric field, and O Vs , and provides an effective strategy for designing high performance flexible piezo-photocatalytic materials. Oxygen‑vacancy‑rich g‑C 3 N 4 /BiOCl nanosheets embedded in a flexible β‑PVDF membrane construct dual electric fields by combining an S‑scheme built‑in field with piezoelectric polarization under mechanical vibration. This dual‑field superposition deepens defect potential wells, facilitates directional charge separation, and enhances defect‑mediated O 2 activation, thereby enabling efficient piezophotocatalytic degradation of tetracycline in aqueous solution. Download: Download high-res image (148KB) Download: Download full-size image

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Discover Materials · 2025 ·Vol. 5 ·期 1 ·1-13 · IF 5.1

Carbon quantum dots modified 3D flower-like BiOCl nanostructures with enhanced visible light photocatalytic degradation of rhodamine B

Li Jiaxin,Li Xinyuan,Li Xia

In this work, a series of carbon quantum dot (CQDs) modified three-dimensional flower-like BiOCl microspheres were synthesized using a simple solvothermal method.A multitude of techniques like XRD, TEM, XPS, BET, XPS UV–vis, PL and EPR were employed to investigate the morphology, structure, optical and electronic properties as well as photocatalytic performance of the samples. The BC-1.5 photocatalyst displays the he best-performing photocatalytic degradation rate of 99% for Rhodamine B (RhB) degradation under visible-light irradiation within 30 min. The photoactivity is 5.3 times of that of the bare BiOCl. This unique three-dimensional flower-like structure can provide a large number of reaction sites and stronger internal light reflection, which can enhance the absorption of photons. Meanwhile, CQDs enable faster charge transfer and more effective separation of photogenerated charge carriers, thereby increasing the degradation rate. The mechanism of photocatalysis was further proposed, and the charge transfer and active substances formed during photocatalysis were unfolded. This study provides a new opportunity for rational design of efficient photocatalysts in environmental remediation.

研究领域: 材料科学 · 环境修复 · 纳米技术 · 物理化学
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CERAMICS INTERNATIONAL · 2025 ·Vol. 51 ·期 24 ·41304-41311 · IF 5.6

Significantly enhanced energy storage performance of PMMA polymer by filling an ultralow content of ultrathin 2D BiOCl nanosheets

Chunran Wu,Wei Li,Shijie Hao,Wen Dai,Lingni Yang,Jiawei She,Qing Zhang,Fenglin Wang,Xingyu Chen,Haijun Mao,Weijun Zhang,Hu Ye,Yujiu Zhou,Zhuofeng Liu

Polymer nanocomposites with high energy density hold great promise for the future miniaturization of dielectric capacitors in modern electronics. However, their performance is limited by the poor dispersion of inorganic fillers and severe interfacial electric field distortion. To address the above challenges, ultrathin two-dimensional (2D) BiOCl nanosheets are employed as the nanofiller for the first time, achieving excellent energy storage performance for the PMMA-based nanocomposites. Remarkably, the nanocomposite film with 0.5 wt% 2D BiOCl exhibits an outstanding energy storage density of 13.28 J/cm 3 and charge-discharge efficiency of 86.11 %, which is 108 % and 13.4 % higher than that of the pristine PMMA . Furthermore, the underlying enhancement mechanism is elucidated by finite element simulations. This work highlights the exceptional potential of 2D BiOCl as a novel nanofiller for designing high-performance polymer nanocomposites.

CAS / MDL: 10035-06-0 7647-14-5
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CHEMICAL PHYSICS LETTERS · 2024 · IF 2.8

In-situ constructing oxygen-enriched vacancies BiOCl with 3D flower-structure for exceptional visible-light-driven photocatalytic properties

Jingyu Sun,Fengyi You,Yuan Fang,Lie Ding,Peiyan Wang,Chengsheng Ge,Liyong Ding

Bismuth oxychloride (BiOCl), emerging as a novel environmentally friendly nanomaterial, possesses considerable potential for photocatalytic degradation of organic wastewater. However, inadequate active sites and inhibited electron separation efficiency severely hinder its visible-light photocatalytic activity. To address this issue, herein we present a facile approach to in-situ construct BiOCl three-dimensional (3D) flower-structure (BOC-F) with oxygen-enriched vacancies for abundant active sites and effective electron separation efficiency through morphology control and vacancy engineering. The visible photocatalytic activity of BOC-F and BiOCl with 2D flaky-structure (BOC-S) was assessed through a systematic examination of the degradation efficiencies of tetracycline hydrochloride (TC-HCl) and rhodamine B (RhB). Under visible light irradiation, BOC-F exhibited superior visible photocatalytic activity, effectively degrading tetracycline hydrochloride (TC-HCl) (20 mg/L) and rhodamine B (RhB) (200 mg/L) within 90 min and 20 min of light exposure, respectively. The findings elucidate that BOC-F, possessing a 3D flower structure, manifests a heightened concentration of oxygen vacancies in contrast to BOC-S, consequently yielding excellent performance. Moreover, The ESR test showed that singlet oxygen ( 1 O 2 ) and hole (h + ) were two main active species in the photocatalytic degradation of BOC-F. This work not only furnishes a facile method for constructing oxygen-rich vacancies in BiOCl but also provides fresh insights into the potential for enhancing the visible photocatalytic properties of Bi-based materials through vacancy engineering.

研究领域: 环境科学 · 材料科学
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RSC Advances · 2011 ·Vol. 1 ·期 8 ·1542-1553 · IF 0

Well-crystallized square-like 2D BiOCl nanoplates: mannitol-assisted hydrothermal synthesis and improved visible-light-driven photocatalytic performance

Jinyan Xiong,Gang Cheng,Guangfang Li,Fan Qin,Rong Chen

Well-crystallized square-like bismuth oxychloride (BiOCl) nanoplates were successfully synthesized by a facile and environmentally friendly hydrothermal process in mannitol solution. The product was characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), Raman spectroscopy, UV–vis diffuse reflection spectroscopy (DRS) and nitrogen adsorption. It was found that mannitol played a key role in the formation of square-like BiOCl nanoplates and the possible growth mechanism was also discussed. The photocatalytic activity of prepared BiOCl nanoplates was determined by the degradation of Rhodamine B (RhB) under visible light irradiation. The square-like BiOCl nanoplates exhibited excellent visible-light-driven photocatalytic efficiency, which was much higher than that of commercial BiOCl and TiO2 (anatase). The remarkable visible-light photocatalytic activity was mainly attributed to the synergistic effect of the layered structure and the strong adsorption of RhB dye upon the BiOCl nanoplates, which might allow more efficient transport of the injected electrons. A possible dye-sensitized photocatalytic degradation process (photosensitization pathway) was proposed.

CAS / MDL: 81-88-9
研究领域: 材料科学 · 环境科学
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Near-infrared-driven enhanced β-NaYF4:Yb3+, Tm3+@BiOCl heterostructured upconversion composites for efficient degradation of organic contaminants

Jinyuan Zhang,Tong Liu,Tian Shi,Zhiyuan Cheng,Fuhua Gao,Da Cai,Shenghong Yang,Yueli zhang

Constructing comprehensive performance-enhanced heterostructured composite using the synergistic effect of complementary advantages between heterogeneous materials has always been challenging. In this work, highly stable β-NaYF 4 :Yb 3+ , Tm 3+ @BiOCl (NYF@BiOCl) heterostructured upconversion composites were successfully prepared using a two-step hydrothermal method. Compared to NYF/BiOCl mechanical mixtures, NYF@BiOCl with intimate interface show a higher photocatalytic degradation rate of rhodamine B (RhB) aqueous solutions, achieving 99.9% in 18 min and 98% in 2 h under simulated sunlight and near-infrared (NIR) light, respectively. The construction of heterostructures has a broad-spectrum response, which improves the utilization of sunlight and achieves efficient photocatalytic degradation of organic contaminants. Upconversion luminescence mechanism, spectral overlap, and Förster resonance energy transfer (FRET) explain the high photocatalytic activity of NYF@BiOCl. Meanwhile, NYF@BiOCl exhibits good universality to efficiently degrade other organic contaminants (methyl orange (MO), methylene blue (MB), bisphenol A (BPA), p-chlorophenol (4-CP)). This study demonstrates the potential of synergistic effects between heterogeneous materials. It Enhanced the photocatalytic activity of the NYF@BiOCl heterostructured composites driven by NIR light, providing a new strategy for energy-efficient and degradation of hazardous organic contaminants to alleviate environmental pollution.

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RSC Advances · 2023 ·Vol. 13 ·期 7 ·4729-4745 · IF 3.9

Crystal facet and Na-doping dual engineering ultrathin BiOCl nanosheets with efficient oxygen activation for enhanced photocatalytic performance

Kunyu Chen,Yiwei Huang,Meina Huang,Yanqiu Zhu,Ming Tang,Renjie Bi,Meiping Zhu

Photocatalytic oxidation (PCO) based on semiconductors offers a sustainable and promising way for environmental remediation. However, the photocatalytic performance currently suffers from weak light-harvesting ability, rapid charge combination and a lack of accessible reactive sites. Ultrathin two-dimensional (2D) materials are ideal candidates to overcome these problems and become hotpots in the research fields. Herein, we demonstrate an ultrathin (<4 nm thick) Na-doped BiOCl nanosheets with {001} facets (Na-BOC-001) fabricated via a facile bottom-up approach. Because of the synergistic effect of highly exposed active facets and optimal Na doping on the electronic and crystal structure, the Na-BOC-001 showed an upshifted conduction band (CB) with stronger reduction potential for O2 activation, more defective surface for enhanced O2 adsorption, as well as the highest visible-light driven charge separation and transfer ability. Compared with the bulk counterparts (BOC-010 and BOC-001), the largest amount of active species and the best photocatalytic performance for the tetracycline hydrochloride (TC) degradation were achieved for the Na-BOC-001 under visible-light irradiation, even though it had slightly weaker visible-light absorption ability. Moreover, the effect of the Na doping and crystal facet on the possible pathways for TC degradation was investigated. This work offers a feasible and economic strategy for the construction of highly efficient ultrathin 2D materials.

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JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS · 2022 · IF 4.383

In-situ preparation of Cu-BiOCl/Bi2O3-C-dots composite and excellent performance for photocatalytic bisphenol A degradation

Bing Xiao,Minghao Xu,Bin Lu,Yun Wang,Hui Liu,Rufen Chen

Economical elimination of organic pollutants from waste water has be paid more attention owing to its environmental and ecological significance. In this study, an easily achievable process to in-situ fabricate copper and co-modified Z-scheme BiOCl/Bi 2 O 3 heterojunction was proposed. The study on the formation mechanism indicated that the introduction of copper ions is favorable for the formation of Bi-based catalyst with flaky morphology while the addition C-dots makes the nanosheets loosely be packed and intercrossed each other. The composite exhibited a high degradation efficiency for Bisphenol A (BPA) and 91% of BPA was removal within 35 min under xenon lamp irradiation. The excellent photocatalytic performance was attributed to the synergistic effect of the in-situ formation Z-scheme BiOCl/β-Bi 2 O 3 heterojunction, multiple charge transfer channels including Cu 2+ /Cu + and C-dots, and efficient charge separation. The electron paramagnetic resonance (EPR) analysis and quenching tests revealed that O 2 •− play a main role in degradation of BPA. Based on the experimental results, the photo-catalytic mechanism is proposed and the degradation path of BPA is revealed.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Preparation, characterization and photodegradation mechanism of 0D/2D Cu2O/BiOCl S-scheme heterojunction for efficient photodegradation of tetracycline

Xinxin Yuan,Jieyi Yang,Yiyang Yao,Hui Shen,Yue Meng,Bo Xie,Zheming Ni,Shengjie Xia

Single-phase photocatalysts exhibit low performance of photocatalytic degradation of pollutants, which is mainly due to the fact that most intrinsic photocatalysts can only produce one active species for degradation reactions. In order to solve this problem, the 0D/2D Cu 2 O/BiOCl S-scheme heterojunction was successfully constructed through a facile hydrothermal route. The obtained 0D/2D Cu 2 O/BiOCl displays high catalytic activity for tetracycline (TC) photodegradation, and 90.3% of TC was photodegraded within 80 min, which is much better than that by pure Cu 2 O and BiOCl. The excellent photocatalytic activity can be ascribed to the formation of S-scheme heterostructures, which enables the photocatalyst to generate superoxide radicals and hydroxyl radicals, and at the same time, makes the oxidation potential more positive and the reduction potential more negative. It is further proved by the results of experimental characterization and theoretical calculation show that the built-in electric field between Cu 2 O and BiOCl is a key factor in inducing the path of S-scheme electron transmission. In addition, the effects of various reaction conditions, including catalyst dosage, pH value and reaction temperature, on the photodegradation of tetracycline were discussed in detail. The intermediates and degradation path were also discussed in detail by liquid chromatography-mass spectrometry.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Ni2+-assisted catalytic one-step synthesis of Bi/BiOCl/Bi2O2CO3 heterojunction with enhanced photocatalytic activity under visible light

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 DISPERSION SCIENCE AND TECHNOLOGY · 2021 · IF 2.262

The synthesis and enhanced photocatalytic activity of heterostructure BiOCl/TiO2 nanofibers composite for tetracycline degradation in visible light

Sarenqiqige Bao,Haiou Liang,Chunping Li,Jie Bai

Heterojunction of TiO2 nanoparticles and BiOCl nanosheets grown on the carbon nanofibers (CNFs) were prepared by simply process that combine of electrospinning, solvothermal, and calcine. The photocatalytic activity of the as-obtained samples was evaluated by photodegradation of tetracycline (TC) in visible light irradiation (λ ≥ 420 nm). Compared with CNFs and TiO2/CNFs, BiOCl/TiO2/CNFs composites performed the best photocatalytic degradation performance (82%) and good stability. Moreover, the degradation rates of Norfloxacin, Ciprofloxacin, and Oxytetracycline are all more than 90%. Finally, trapping experiments were carried out, and a possible photocatalytic degradation mechanism was proposed.

CAS / MDL: 79603-03-5
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Enhanced N2 photofixation activity of flower-like BiOCl by in situ Fe(III) doped as an activation center

Zhengfeng Shen,Feifei Li,Jiangrui Lu,Zhidan Wang,Rui Li,Xiaochao Zhang,Changming Zhang,Yawen Wang,Yunfang Wang,Zhiping Lv,Jianxin Liu,Caimei Fan

Photocatalytic nitrogen fixation has been considered to be a safe, green, eco-friendly, and sustainable technology. However, photoinduced activation of inert dinitrogen is an important factor hindering the development of this technology. Herein, in-situ Fe 3+ doped flower-like BiOCl with highly active sites exposure was prepared by a solvent thermal method, which has excellent performance of N 2 photofixation. Compared with virgin BiOCl with no nitrogen fixation activity, Fe-BiOCl reached 30 μmol·L −1 ·h −1 ammonia evolution rate under simulated sunlight without any sacrificial reagent. Characterization results demonstrated that the enhancement of N 2 photofixation capacity was mainly attributed to the in-situ doped Fe 3+ in BiOCl, the doped Fe 3+ not only acts as a reaction center for N 2 activation also as an “electron transfer bridge” trapping and migrating electrons from BiOCl to N 2 molecules. Furthermore, the transformation of crystal facets from virgin BiOCl (0   0   1) to Fe-BiOCl (1   1   0) and (1   0   2) is more conducive for the exposure and accessibility of iron reactive sites. This work developed a potential strategy by in-situ introducing Fe 3+ active sites in BiOCl semiconductor substrate, which establishes a good basis for the application of semiconductor catalysts in nitrogen fixation.

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