Bismuth Oxychloride Nanosheets Research Articles

Heteropoly blue-modified ultrathin bismuth oxychloride nanosheets with oxygen vacancies for efficient photocatalytic nitrogen fixation in pure water

Photocatalytic nitrogen reduction is a promising green technology for ammonia synthesis under mild conditions. However, the poor charge transfer efficiency and weak N2 adsorption/activation capability severely hamper the ammonia production efficiency. In this work, heteropoly blue (r-PW12) nanoparticles are loaded on the surface of ultrathin bismuth oxychloride nanosheets with oxygen vacancies (BiOCl-OVs) by electrostatic self-assembly method, and a series of xr-PW12/BiOCl-OVs heterojunction composites have been prepared. Acting as a robust support, ultrathin two-dimensional (2D) structure of BiOCl-OVs inhibits the aggregation of r-PW12 nanoparticles, enhancing the interfacial contact between r-PW12 and BiOCl. More importantly, the existence of oxygen vacancies (OVs) provides abundant active sites for efficient N2 adsorption and activation. In combination of the enhanced light absorption and promoted photogenerated carriers separation of xr-PW12/BiOCl-OVs heterojunction, under simulated solar light, the optimal 7r-PW12/BiOCl-OVs exhibits an excellent photocatalytic N2 fixation rate of 33.53 µmol g-1h−1 in pure water, without the need of sacrificial agents and co-catalysts. The reaction dynamics is also monitored by in situ FT-IR spectroscopy, and an associative distal pathway is identified. Our study demonstrates that construction of heteropoly blues-based heterojunction is a promising strategy for developing high-performance N2 reduction photocatalysts. It is anticipated that combining of different defects with heteropoly blues of different structures might provide more possibilities for designing highly efficient photocatalysis systems.

Oxygen-defect bismuth oxychloride nanosheets for ultrasonic cavitation effect enhanced sonodynamic and second near-infrared photo-induced therapy of breast cancer

Sonodynamic therapy (SDT) relies heavily on the presence of oxygen to induce cell death. Its effectiveness is thus diminished in the hypoxic regions of tumor tissue. To address this issue, the exploration of ultrasound-based synergistic treatment modalities has become a significant research focus. Here, we report an ultrasonic cavitation effect enhanced sonodynamic and 1208 nm photo-induced cancer treatment strategy based on thermoelectric/piezoelectric oxygen-defect bismuth oxychloride nanosheets (BNs) to realize the high-performance eradication of tumors. Upon ultrasonic irradiation, the local high temperature and high pressure generated by the ultrasonic cavitation effect combined with the thermoelectric and piezoelectric effects of BNs create a built-in electric field. This facilitates the separation of carriers, increasing their mobility and extending their lifetimes, thereby greatly improving the effectiveness of SDT and NIR-Ⅱ phototherapy on hypoxia. The Tween-20 modified BNs (TBNs) demonstrate ∼88.6 % elimination rate against deep-seated tumor cells under hypoxic conditions. In vivo experiments confirm the excellent antitumor efficacy of TBNs, achieving complete tumor elimination within 10 days with no recurrences. Furthermore, due to the high X-ray attenuation of Bi and excellent NIR-Ⅱ absorption, TBNs enable precise cancer diagnosis through photoacoustic (PA) imaging and computed tomography (CT).

Bismuth oxychloride nanosheets anchored aramid separator with sponge-like structure for improved lithium-ion battery performance

Functional modification of inorganic particles is an effective approach to tackle the issue of Li+ transport and the lithium dendrites formation in lithium-ion batteries (LIBs). In this study, PMIA/BiOCl composite separators are prepared by nonsolvent induce phase separation (NIPS) method using P-type semiconductor bismuth oxychloride (BiOCl) functionalized poly (m-phenylene isophthalamide) (PMIA) separators. Compared with the polypropylene (PP) separator, PMIA has superior thermal stability and the addition of BiOCl further enhances its flame retardancy. And the prepared PMIA/BiOCl separator presents improved porosity (66.47 %), enhanced electrolyte uptake rate (863 %) and higher ionic conductivity (0.49 mS∙cm−1). Besides, the incorporation of BiOCl can anchor PF6- to the three-dimensional network skeleton of the PMIA/BiOCl separators, enabling the desolvation of Li+ and selectively facilitating Li+ transport (the Li+ transfer number is 0.79). Moreover, the uniform porous structure of the PMIA/BiOCl separators and the efficient transport of Li+ uniformly deposite Li+, and minimize the growth of lithium dendrites. Batteries assembled with PMIA/BiOCl separators have a discharge specific capacity of 124.4 mAh∙g−1 and capacity retention of 96.7 % after 200 cycles at 0.2C. Therefore, this work provides an effective route in the design strategy of separators for LIBs.

Construction of BiOCl/reduced graphene oxide nanocomposites heterojunction with abundant oxygen vacancies for efficient photocatalytic organic pollutant removal

Precisely manipulating defects in semiconductor is an effective way to improve their photocatalytic activity. In this work, bismuth oxychloride (BiOCl)/reduced graphene oxide (RGO) nanocomposites with abundant oxygen vacancies (OVs) are successfully constructed by a facile solvothermal method. BiOCl nanosheets are uniformly distributed on the RGO with superior conductivity. The RGO served as a pivotal charge transmission bridge substantially accelerates the transfer of photogenerated charge carriers, resulting in the improvement of the charge separation efficiency. The abundant oxygen vacancies in BiOCl/RGO nanocomposites increase light harvesting and enhance the adsorption of O2 to promote the formation of superoxide free radicals (·O2−). By virtue of these merits, the unique BiOCl/RGO nanocomposite shows excellent degradation efficiency. When the mass ratio of RGO was 2 %, 99.07 % of 20 mg/L(100 mL) methyl orange (MO) was removed after 80 min, which was much higher than that of pure BiOCl.

Pyro-phototronic effect enhanced the performance of TiO2 NRs/BiOCl//PEDOS heterojunction for a UV photodetector

This study presents the construction of an organic–inorganic heterojunction ultraviolet (UV) photodetector (PD) through face-to-face assembly. The synergistic effects of bismuth oxychloride (BiOCl) and titanium dioxide nanorods (TiO2 NRs) improve carrier transport efficiency and enhance the performance of the UV photodetector. The combination of BiOCl with TiO2 NRs generates a pyro-phototronic effect and increases the surface oxygen vacancies of TiO2 NRs, resulting in enhanced carrier transport efficiency, increased transient photocurrent, and reduced dark current in TiO2-based UV photodetectors. The enhanced photosensitivity of chloride (Cl) ions bound to selenium (Se) ions promotes easy electron injection from poly (3,4-ethylene dioxyselenophene) (PEDOS) into BiOCl, leading to accelerated electron transfer and a shortened response time. Compared to TiO2 NRs/BiOCl//TiO2 NRs/BiOCl, the TiO2 NRs/BiOCl//PEDOS heterojunction exhibits a fast photoresponse with a rise time of 0.0802 s and a fall time of 79.8 ms. The responsivity is significantly improved from 11.0 mA/W to 108.8 mA/W (a 10-fold enhancement), and the detectivity is increased from 0.67 × 1011 Jones to 1.25 × 1011 Jones at 365 nanomaterials (0 V). These findings provide valuable insights into the mechanism by which BiOCl nanosheets enhance the photodetection performance of devices, contributing to the advancement of UV photodetector technology.

Copper-doped bismuth oxychloride nanosheets assembled into sphere-like morphology for improved photocatalytic inactivation of drug-resistant bacteria

The devastating microbiological contamination as well as emerging drug-resistant bacteria has posed severe threats to the ecosystem and public health, which propels the continuous exploitation of safe yet efficient disinfection products and technology. Here, copper doping engineered bismuth oxychloride (Cu-BiOCl) nanocomposite with a hierarchical spherical structure was successfully prepared. It was found that due to the exposure of abundant active sites for the adsorption of both bacteria cells and molecular oxygen in the structure, the obtained Cu-BiOCl with nanosheets assembled into sphere-like morphology exhibited remarkable photocatalytic antibacterial effects. In particular, compared to the pure BiOCl, composite Cu-BiOCl possessed improved antibacterial effects against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Methicillin-resistant Staphylococcus aureus (MRSA). The combination of physicochemical characterizations and theoretical calculations has revealed that copper doping significantly promoted the light absorbance, inhibited the recombination of electron-hole pairs, and enhanced molecular oxygen adsorption, which resulted in more generation of active species including reactive oxygen species (ROS) and h+ to achieve superior photocatalytic bacterial inactivation. Finally, transcriptome analysis on MRSA pinpointed photocatalytic inactivation induced by Cu-BiOCl may retard largely the development of drug-resistance. Therefore, the built spherical Cu-BiOCl nanocomposite has provided an ecofriendly, economical and robust strategy for the efficient removal of drug-resistant bacteria with promising potentials for environmental and healthcare utilizations.

2D Ultrathin Iron Doped Bismuth Oxychloride Nanosheets with Rich Oxygen Vacancies for Enhanced Sonodynamic Therapy.

Sonodynamic therapy (SDT) combines ultrasound and sonosensitizers to produce toxic reactive oxygen species (ROS) for cancer cell killing. Due to the high penetration depth of ultrasound (US), SDT breaks the depth penetration barrier of conventional photodynamic therapy for the treatment of deeply seated tumors. A key point to enhance the therapeutic efficiency of SDT is the development of novel sonosensitizers with promoted ability for ROS production. Herein, ultrathin Fe-doped bismuth oxychloride nanosheets with rich oxygen vacancies and bovine serum albumin coating on surface are designed as piezoelectric sonosensitizers (BOC-Fe NSs) for enhanced SDT. The oxygen vacancies of BOC-Fe NSs provide electron trapping sites to promote the separation of e- -h+ from the band structure, which facilitates the ROS production under the ultrasonic waves. The piezoelectric BOC-Fe NSs create a built-in field and the bending bands, further accelerating the ROS generation with US irradiation. Furthermore, BOC-Fe NSs can induce ROS generation by a Fenton reaction catalyzed by Fe ion with endogenous H2 O2 in tumor tissues for chemodynamic therapy. The as-prepared BOC-Fe NSs efficiently inhibited breast cancer cell growth in both in vitro and in vivo tests. The successfully development of BOC-Fe NSs provides a new nano-sonosensitiser option for enhanced SDT for cancer therapy.

Manganese oxide-modified bismuth oxychloride piezoelectric nanoplatform with multiple enzyme-like activities for cancer sonodynamic therapy

Sonodynamic therapy (SDT) is considered as a new-rising strategy for cancer therapeutics, but the inefficient production of reactive oxygen species (ROS) by current sonosensitizers seriously hinders its further applications. Herein, a piezoelectric nanoplatform is fabricated for enhancing SDT against cancer, in which manganese oxide (MnOx) with multiple enzyme-like activities is loaded on the surface of piezoelectric bismuth oxychloride nanosheets (BiOCl NSs) to form a heterojunction. When exposed to ultrasound (US) irradiation, piezotronic effect can remarkably promote the separation and transport of US-induced free charges, and further enhance ROS generation in SDT. Meanwhile, the nanoplatform shows multiple enzyme-like activities from MnOx, which can not only downregulate the intracellular glutathione (GSH) level, but also disintegrate endogenous hydrogen peroxide (H2O2) to generate oxygen (O2) and hydroxyl radicals (•OH). As a result, the anticancer nanoplatform substantially boosts ROS generation and reverses tumor hypoxia. Ultimately, it reveals remarkable biocompatibility and tumor suppression in a murine model of 4 T1 breast cancer under US irradiation. This work provides a feasible pathway for improving SDT using piezoelectric platforms.

Third-order optical nonlinearity and passively Q-switching operation with BiOCl nanosheets at 1.3 µm.

In this contribution, we measured the third-order nonlinear optical response of bismuth oxychloride (BiOCl) nanosheets with the open-aperture (OA) and the closed-aperture (CA) Z-scan techniques with a variable excitation intensity at 1.34 µm. The effective nonlinear absorption coefficient βeff and the nonlinear refractive index n2 of the prepared BiOCl nanosheets with abundant oxygen vacancies were obtained under the excitation intensity. The third-order nonlinear optical susceptibility |χ(3)| was 1.64 × 10-9 esu. The nonlinear optical features of BiOCl enabled it as a superb saturable absorber for pulse laser generation. As a consequence, we demonstrated the first passively Q-switched Nd:GdVO4 laser with the BiOCl saturable absorber, producing a shortest pulse duration of 543 ns and a highest repetition rate of 227 kHz, leading to a maximum pulse energy of 74 nJ. Our findings show that BiOCl nanosheets with oxygen vacancies have large nonlinear optical sensitivities and can be exploited to generate optical pulses.

Deciphering the photoactive species-directed antibacterial mechanism of bismuth oxychloride with modulated nanoscale thickness

As an environmentally benign disinfection strategy, photocatalytic bacterial inactivation using nanoparticles involves photogenerated reactive species that cause cellular oxidative stress. Rationalising the structural performance of photocatalysts for the practical uses such as wastewater treatment has attracted significant attention; however, the contribution of reactive species to their photocatalytic antibacterial activities at the molecular and transcriptomic levels remains unclear. In this study, nontoxic bismuth oxychloride (BiOCl) photocatalysts with different nanoscale thicknesses, including nanosheets (Ns, ∼5.4 nm), nanoplates (Np, ∼1.8 nm), and ultra-nanosheets (Uns, ∼1.1 nm), were synthesised under hydrothermal conditions. Among the three samples, BiOCl Uns exhibited the most effective photocatalytic degradation efficiency with the calculated apparent rate constant of 0.0294 min−1, ∼4 times faster than that of Ns, whereas BiOCl Ns possessed the most pronounced bactericidal effect (5.4 log inactivation). Such findings indicate the distinct role of the photoactive species responsible for photocatalytic bacterial inactivation. Moreover, transcriptome analysis of Escherichia coli after photocatalytic treatment revealed that the underlying photocatalytic antibacterial mechanism at the genetic expression level involves cellular component biosynthesis, energy metabolism, and material transportation. Notably, the differences between BiOCl Ns and BiOCl Uns were significantly enriched in purine metabolism. Therefore, the cost-effective preparation of BiOCl nanosheets with nanoscale thickness-modulated photocatalytic antibacterial activity has remarkable potential for sustainable environmental and biomedical applications.

Significant enhancement in hydrogen evolution rate of 2D bismuth oxychloride lamellar membrane photocatalyst with cellulose nanofibers

Photocatalytic hydrogen evolution (PHE) is a sustainable alternative for generating green and clean energy. However, it requires the use of nanoscale photocatalysts, whose applicability is limited by their poor reusability and proton release from water molecules. Herein, a porous two-dimensional lamellar membrane (2DLM) photocatalyst was fabricated from bismuth oxychloride (BiOCl) nanosheets (BNs) and cellulose nanofibers (CNFs) via layer-by-layer self-assembly. The hybridization of the CNFs with the BNs improved the PHE rate of the resulting BiOCl/CNFs membrane (BCM). The optimal PHE rate was observed for a CNF content of 3.2 wt% and was 4.7-times that of raw BNs dispersed in an aqueous solution alone and 1.85-times that of the BiOCl membrane (BM). Moreover, the PHE rate remained unchanged even after 10 discontinuous cycles for a total time of 60 h. Comprehensive experimental characterization and molecular dynamics simulations confirmed that the introduction of the CNFs effectively regulated the hydrogen bond network of the confined water molecules, thus improving the efficiency of the conversion of H2O into H2. Meanwhile, the optimization of the nanochannel sizes of the BNs by the hybridized CNFs accelerated water transport within the nanochannels. The 2DLM also showed excellent mechanical strength, flexibility, and translucence. This strategy of fabricating 2DLMs using a nanosheet photocatalyst and CNFs not only results in improved PHE performance but also should also aid the development of stable and reusable photocatalysts for other industrial applications.

Two-Dimensional Mixed Lead/Bismuth Oxychloride Based Materials As Anodes for Sodium-Ion Batteries

The continuous pursuit on building low cost and sustainable batteries to efficiently harvest renewable energy from intermittent sources is ever expanding. The research on Na-ion technology has gained significant interest due to inexpensive and broad availability of precursor materials. Until now, various Na-ion anodes including carbonaceous materials such hard carbon, alloy-based materials such as Bi, Pb, Sb and Sn based systems and conversion materials have been explored1. Along this line, the recent chase on two dimensional (2D) materials such as chalcogenides, MXenes and van der Waals types oxyhalide heterostructures, have become more intense due to their excellent electrical and structural properties 2. Among them, 2D Sillén-type metal oxyhalide heterostructures (MOX), due to their unique layered structure consisting of anionic sheets interleaved with cationic layers have gain particular interest as electrode materials. BiOCl is one such candidate with fluorite-like layers, [Bi2O2]2+ intergrown with halide Cl– anions, have been studied as anode in rechargeable batteries. However, its application is mainly challenged by rapid capacity decay originating from particle pulverization and unstable solid electrolyte interphase (SEI).In this work, 2D layered mixed lead bismuth oxychloride nanosheets (BiOCl4 and PbBiO2Cl 3) were synthesized by new rapid room temperature chemical precipitation route. In former anode, the electrolyte engineering approach has been used to enhance the cycling stability of BiOCl and at the same time, its electrochemical (de)sodiation mechanism is also clarified through in-operando XRD studies, which reveals the reversible formation of Bi ↔ NaBi ↔ cubic-Na3Bi phases. On the other hand, the later anode, i.e., 2D-PbBiO2Cl was further investigated with the combined in-operando XRD and ex-situ TEM, XPS studies, which reveal a distinct (de)sodiation process of the 2D-PbBiO2Cl in comparison with reported Na-(Pb/Bi) phase diagram. This 2D heterostructure demonstrated stable sodium storage performance (~250 mAh g–1 for 250 cycles at 100 mA g–1). Henceforth, the detailed understanding of formation process of these two structures (BiOCl and PbBiO2Cl) at room temperature using material characterizations and electrochemical studies combined with operando findings will be discussed to comprehend the reversible storage mechanism of 2D-MOX type heterostructures as anodes in SIBs.

Embedding Cu3P quantum dots onto BiOCl nanosheets as a 0D/2D S-scheme heterojunction for photocatalytic antibiotic degradation

The development of highly efficient photocatalysts is vital for solvinge the problem of environmental pollution. In this study, a novel zero-/two-dimensional (0D/2D) S-scheme heterojunction was fabricated by integrating 0D copper phosphide (Cu3P) quantum dots (QDs) with a size in the range of 3–8 nm onto 2D bismuth oxychloride (BiOCl) nanosheets using a self-assembly tactic. The Cu3P/BiOCl presented intimate interface contact and high photocatalytic activity for the degradation of antibiotics (tetracycline hydrochloride (TC), oxytetracycline, ofloxacin). The optimal sample exhibited the highest photocatalytic TC degradation, with a total removal rate of 86% after 6 min under full-spectrum irradiation, which was higher than that of compared to individual BiOCl. The improved activity of the Cu3P/BiOCl heterojunction was attributed to the enhanced separation of the photogenerated carriers due to the S-scheme mode which can promote the recombination of useless photogenerated carriers and maintain photogenerated carriers with stronger redox potentials for photocatalytic reaction. In addition, employing Cu3P QDs and BiOCl nanosheets to construct an S-scheme composite can offer abundant active sites for antibiotic degradation. In brief, this study demonstrates that Cu3P QDs are an effective cocatalyst for degrading organic pollutants, which provides novel inspiration for the future design of green recycling photocatalysts for wastewater remediation.

Polymer-coated BiOCl nanosheets for safe and regioselective gastrointestinal X-ray imaging.

Bismuth-based compounds are considered to be the best candidates for computed tomography (CT) imaging of gastrointestinal (GI) tract due to high X-ray absorption. Here, we report the introduction of polymer-coated bismuth oxychloride (BiOCl) nanosheets for highly efficient CT imaging in healthy mice and animal with colitis. We demonstrate simple, low cost and fast aqueous synthesis protocol which provides gram-quantity yield of chemically stable BiOCl nanosheets. The developed contrast gives 2.55-fold better CT enhancement compared to conventional contrast with negligible in vivo toxicity. As a major finding we report a regioselective CT imaging of GI tract by using nanoparticles coated with differentially charged polymers. Coating of nanoparticles with a positively charged polymer leads to their fast accumulation in small intestine, while the coating with negatively charged polymers stimulates prolonged stomach retention. We propose that this effect may be explained by a pH-controlled aggregation of nanoparticles in stomach. This feature may become the basis for advancement in clinical diagnosis of entire GI tract.

Enhanced photocatalytic ammonia generation from water and nitrogen by decorating BiOCl nanosheets with CoOOH oxygen evolution reaction cocatalyst

Photocatalytic synthesis of ammonia from N2 and water consists of N2 reduction and water oxidation, but most research is focused only on the N2 reduction. Here, we demonstrated a strategy to improve ammonia generation by enhancing water oxidation through an oxygen evolution reaction (OER) cocatalyst. We employed cobalt oxyhydroxide as an OER cocatalyst for a well-known nitrogen reduction photocatalyst bismuth oxychloride (BiOCl). A series of cobalt-doped BiOCl (Co–BiOCl) nanoplatelets were synthesized through a combination of coprecipitation and hydrothermal synthesis with systematic variation in the percentage of added cocatalyst. The formation of a few atom clusters of cobalt oxyhydroxide was verified via X-ray diffraction, X-ray photoelectron spectroscopy, electron microscopy, Raman, and infrared spectroscopy. A 4.6-fold improvement in the ammonia production rate was realized with 5% Co–BiOCl. OER from water using Co–BiOCl was performed and correlated well with the ammonia generation. Enhancing water oxidation by loading of an OER cocatalyst points a promising and applicable method for better N2 fixation photocatalyst design.

Ultrathin bismuth oxychloride nanosheet for enhanced potassium storage

Ultrathin bismuth oxychloride nanosheets have been realized as anodes with outstanding performance in potassium ion batteries. It can deliver a capacity of 196.8 mAh g−1 after 50 cycles and 151.8 mA h g−1 after 100 cycles at 50 mA g−1 due to the two-dimensional nature, which facilitates the electron transport and ion diffusion, and achieves continuous conductive matrix. Our results provide distinct insights into electrode design for energy storage devices.

Ultrathin 2D bismuth oxychloride nanosheets as novel catalytic interfaces for detection of biomolecules

We introduce highly stable 2D layered bismuth oxychloride nanosheets as the catalytic interfaces to bind important biomedical analytes. Transmission electron and atomic force microscopy revealed the prepared nanosheets possess perfect square morphology possessing average lateral size of 200 nm, and thickness around 3–4 nm. We specifically demonstrated characteristics for the binding of uric acid. When these sheets were employed to functionalize microchips, the limit of detection was achieved as low as 0.38 µM (S/N = 3). We further investigated that the modified devices determined successfully uric acid in human blood sample. This is the first study where ultrathin nanostructures are integrated with microchips. This work establishes the potential of ultrathin graphene-like nanosheets to design smart and effective interfaces for label-free binding of molecules of clinical and pharmacology significance.

Bismuth telluride functionalized bismuth oxychloride used for enhancing antibacterial activity and wound healing efficacy with sunlight irradiation.

Bacterial infection can lead to chronic non-healing wounds and serious tissue damage. The wound healing process could be accelerated through bacterial inactivation using some semiconductor nanomaterials with the irradiation of light. Herein, we develop sunlight triggered bismuth telluride-bismuth oxychloride heterostructure nanosheets as antibacterial agents for promoting wound healing, in which bismuth telluride can effectively narrow the bandgap of bismuth oxychloride, resulting in more sunlight absorption and higher antibacterial activity. In fact, the bandgap of bismuth oxychloride has been narrowed from 3.25 eV to 2.37 eV as proved by ultraviolet-visible diffuse reflectance spectroscopy. With simulated sunlight irradiation, bismuth telluride-bismuth oxychloride nanosheets could effectively produce reactive oxygen species and inhibit the growth of both Gram-positive and Gram-negative bacteria. In vivo experiments further confirmed the excellent wound healing capability of bismuth telluride-bismuth oxychloride nanosheets. This work may provide a facile strategy for designing sunlight triggered bacterial inactivation agents.

Fabrication of Bismuth Oxychloride Nanosheets Decorated with Chitosan and Phytic Acid for Improvement of Flexible Poly(vinyl chloride) Flame Retardancy

Fabrication of Bismuth Oxychloride Nanosheets Decorated with Chitosan and Phytic Acid for Improvement of Flexible Poly(vinyl chloride) Flame Retardancy

Intermediate excited state suppression and upconversion enhancement of Er3+ ions by carbon-doping boosting photocarrier separation in bismuth oxychloride nanosheets

Low luminescence efficiency of rare-earth ions dopedupconversion (UC) nanomaterials is still a major limitation for their applications.Here, based on bismuth oxychloride nanosheets that show efficient photocarriers separation due to combining spontaneous polarization and layered semiconductor, we report a new carbon heterovalent doping strategy for efficient UC luminescence enhancement by suppressing the intermediate excited states of Er3+ ions. The first-principles calculations and photoelectrochemical characterizations provide evidences that the replacement of C ions for Cl strengthen the spontaneous polarization and inter electric field (IEF) of bismuth oxychloride nanosheets, which further improve the photocarriers separation efficiency. Under 808 or 980 nm excitation, the emission intensity of 4I13/2 energy level of Er3+ ions (1550 nm) increase slightly with C doping, but the its decay time and the visible UC emission are improved tremendously at the same time. We show that the recombination rate of intermediate excited state electrons of Er3+ ions with the ground state is inhibited by the enhanced IEF, which promotes the energy reabsorption transition to upper energy levels, thus enhancing the visible UC emission. This work not only may provide a new insight into the method for engineering of UC emissions but also deepen the understanding for layered semiconducting material to modify the transition of Lanthanide ions.