Surface Of Quantum Dots Research Articles

Detection of C6H6, CO2, and H2S gases on arsenic (As) and cobalt (Co) doped quantum dots (QDs) nanostructured materials

Abstract Gas sensors exhibit significant potential due to their widespread use in various applications, such as food packaging, indoor air quality assessment, and real-time monitoring of man-made gas emissions to mitigate global warming. The utilization of nanostructured materials for sensor and adsorbent surfaces has seen remarkable growth over time, though substantial efforts are still needed to develop more efficient adsorbents. Consequently, this study investigates the viability of metal-doped quantum dots (QDs) as prospective gas-sensing and adsorption materials. Density functional theory (DFT) calculations employing the 6-311 + G(d,p) basis set and three functionals (B3LYP, B3LYP-GD3(BJ), and ɷB97XD) were utilized for this investigation. Three environmentally and health-significant gases (C6H6, CO2, and H2S) were chosen as adsorbates on arsenic (As) and cobalt (Co) functionalized QDs to assess the performance and sensing capabilities of resulting QD surfaces. The analysis encompassed computation of adsorption energy, thermodynamic properties, non-covalent interactions, natural bond orbital analysis, and other topological aspects for both the surfaces and gases. The outcomes indicate that the GP_As functionalized surface exhibits a lower energy gap, rendering it more reactive and sensitive toward the respective gases (C6H6, CO2, and H2S). Moreover, the calculated adsorption energies of the investigated systems indicate thermodynamic favorability and spontaneity. Notably, our findings suggest that QD_As surfaces possess superior adsorption potential for H2S compared to the other gases examined; nonetheless, all studied QD surfaces demonstrate significant adsorption capacities for C6H6, CO2, and H2S gases.

Ultrasensitive electrochemiluminescence biosensor based on dual quenching effects of silver nanoclusters and multiple cycling amplification for detection of ATP

In this work, an electrochemiluminescence (ECL) biosensor based on dual ECL quenching effects of silver nanoclusters (Ag NCs) and multiple cycling amplification was designed to achieve ultrasensitive detection of ATP. The specific recognition of target ATP to aptamer initiated multiple cycling amplification, and a small amount of target was converted into a large number of DNA product chains (S1) by amplification. After S1 opened hairpin DNA 2 (HP2), Ag NCs approached the surface of CdS quantum dots (QDs) modified-electrode by complementary DNA, resulting in a significant decrease of ECL intensity from CdS QDs. The quenching principle is as follows. Firstly, the absorption spectrum of Ag NCs overlaps well with the ECL emission spectrum of CdS QDs, leading to effective ECL resonance energy transfer (ECL-RET); Secondly, Ag NCs could catalyze electrochemical reduction of K2S2O8, leading to consumption of ECL co-reactant and reducing ECL of QDs. The double-ECL quenching achieved ultrasensitive biosensing detection of ATP with a wide range from 1 aM to 1 pM. This present work reported new principle of double-quenching QDs ECL by Ag NCs, and developed a novel ECL biosensor by combining with multiple cycle amplification technique, which has great contribution to the development of QDs ECL and biosensing applications.

DNA‐Programmed (De)Hybridization of Near‐Infrared Photosensitized UCNP‐QDs‐GNPs Nanoprobes for MicroRNA Imaging and Image‐Guided Cancer Therapy

AbstractAccurate and sensitive analysis of cancer‐associated microRNAs in living tissue is of great significance for the early diagnosis and treatment of cancer. Herein, a hierarchical nanoprobe denoted as UCNP‐QDs‐GNPs is delicately designed, where a near‐infrared (NIR) absorptive upconversion nanoparticle (UCNP) serves as the core, broad‐absorptive and bright emissive quantum dots (QDs) and emission‐quencher gold nanoparticles (GNPs) surround as satellites for microRNA imaging and image‐guided cancer therapy. Through the programmed assembly of heterobivalent DNA‐conjugated QDs with DNA‐modified GNPs and UCNPs, the well‐defined nanostructured UCNP‐QDs‐GNPs are generated with quenched fluorescence. Upon encountering the microRNA‐21 target, GNPs underwent catalytic disassembly, resulting in the concurrent recovery and amplification of fluorescence from QDs and UCNPs, which enabled sensitive imaging and quantification of microRNA‐21 within living cells. Furthermore, dithiol‐constituted aggregation‐induced emission (AIE) photosensitizers bonded on the surface of QDs, are effectively photosensitized by the QDs. The NIR excitation harvested by UCNPs is therefore efficiently transferred to QDs and subsequently converged on the AIE photosensitizers, boosting photodynamic activity for image‐guided therapy in deep‐seated tumors. The DNA‐programmed (de)hybridization strategy, facilitating the conversion of NIR excitation into imaging signals and photodynamic activity, offers a promising avenue for the early theranostics of malignancies.

Colloidal one-pot synthesis and characterization of Glycine capped Al(x) doped ZnS QDs for efficient UV light assisted photo-degradation of Stilbene 420 dye

In thisstudy, successful synthesis and characterization of undoped and Al-doped ZnS quantum dots (QDs) capped with bio-friendly glycine (ZnSAl/Gly) are described. The synthesis is accomplished through a one-pot colloidal co-precipitation process, followed by the characterization of QDs using various analytical techniques.X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HR-TEM) showed the formation of cubic-faced ZnS QDs, with the crystal size decreasing as the amount of Al doping increased. A ZnS phase layer on the QDs surface was also demonstrated by Fourier-transform infrared spectroscopy (FTIR) measurements. Field emission scanning electron microscopy with energy dispersive X-ray spectroscopy (FESEM-EDS) analysis was employed to examine the stoichiometry and shape of the synthesized QDs. Thermogravimetric analysis (TGA) showed a remarkable stability of Al-doped ZnS QDs over an extended period, enhancing their potential for a variety of applications. Measurements of the absorption band edge in the UV–Visible range demonstrated that Al ions were successfully incorporated into the ZnS lattice, causing a substantial red shift. This change, which caused the energy band gap to rise from 3.2 eV (ZnS/Gly) to 4.42 eV (ZnSAl1%/Gly), was attributed to the size confinement effect. The degradation of the Stilbene-420 dye under UV irradiation served as a test for the photodegradation capability of the synthesized QDs. The photodegradation efficiency of Al doping ranged from 60 % to 92 %, showing the induction of a significant number of crystalline structures with rising Al concentration. The Al-doped ZnS/Gly QDs are highly catalytic and photoactive, and they show great promise in the field of photoluminescence, medical and biological areas. Their potential for use as effective catalysts in waste water treatment methods is also remarkable.

Surface Reconstructions in II-VI Quantum Dots.

Although density functional theory (DFT) calculations have been crucial in our understanding of colloidal quantum dots (QDs), simulations are commonly carried out on QD models that are significantly smaller than those generally found experimentally. While smaller models allow for efficient study of local surface configurations, increasing the size of the QD model will increase the size or number of facets, which can in turn influence the energetics and characteristics of trap formation. Moreover, core-shell structures can only be studied with QD models that are large enough to accommodate the different layers with the correct thickness. Here, we use DFT calculations to study the electronic properties of QDs as a function of size, up to a diameter of ∼4.5 nm. We show that increasing the size of QD models traditionally used in DFT studies leads to a disappearance of the band gap and localization of the HOMO and LUMO levels on facet-specific regions of the QD surface. We attribute this to the lateral coupling of surface orbitals and the formation of surface bands. The introduction of surface vacancies and their a posteriori refilling with Z-type ligands leads to surface reconstructions that widen the band gap and delocalize both the HOMO and LUMO. These results show that the surface geometry of the facets plays a pivotal role in defining the electronic properties of the QD.

Stability and photocurrent enhancement of photodetectors by using core/shell structured CsPbBr3/TiO2 quantum dots and 2D materials.

Ultra-stable CsPbBr3 perovskite quantum dots (QDs) were prepared, and the performance of the photodetector fabricated from them was enhanced by 2D material incorporation. This multi-component photodetector appears to have good stability in the ambient utilization environment. All inorganic CsPbBr3 QDs are potential candidates for application in photodetection devices. However, QDs have several issues such as defects on the QD surface, degradation under environmental conditions, and unfavorable carrier mobility limiting the high performance of the photodetectors. This work addresses these issues by fabricating a core/shell structure and introducing 2D materials (MXenes, Ti3C2Tx) into the device. Here, three types of photodetectors with QDs only, QDs with a core/shell structure, and QDs with a core/shell structure and MXenes are fabricated for systematic study. The CsPbBr3/TiO2 photodetector demonstrated a two times photocurrent enhancement compared to bare QDs and had good device stability after TiO2 shell coating. After introducing Ti3C2Tx into CsPbBr3/TiO2, a significant photocurrent enhancement from nanoampere (nA) to microampere (μA) was observed, revealing that MXenes can improve the photoelectric response of perovskite materials significantly. Higher photocurrent can avoid signal interference from environmental noise for better practical feasibility. This study provides a systematic understanding of the photocurrent conversion of perovskite quantum dots that is beneficial in advancing optoelectronic device integration, especially for flexible wearable device applications.

Enhancing the performance of PbS:CsPbBr3 bulk-heterojunction photodetectors by treating with imidazolium-based ionic liquids.

All-inorganic lead halide perovskites and quantum dots (QDs) have gained significant attention since their emergence, owing to their immense potential for applications in optoelectronic devices. Here, enhanced-performance broadband photodetectors based on the bulk-heterostructure of a CsPbBr3 perovskite and PbS colloidal quantum dots (CQDs) are presented, and 1-ethyl-3-methylimidazolium tetrafluoroborate ([EMIM]BF4) ionic liquids as a dual-purpose additive were introduced in the blended film to regulate the surface of QDs by facilitating surface passivation, adjusting energy levels, and coupling with longer alkyl chains as compared to iodide ions (I-). As a result, a superior-quality bulk-heterostructure based photodetector with long-term stability was obtained, showing outstanding performance in photodetection across the visible to near-infrared wavelength range, demonstrating a high photoresponsivity of 22.4 A W-1 with a response time of 16.2 ms and a specific detectivity of 1.58 × 1014 Jones under 405 nm illumination. Thus, this work provides a novel modification strategy for PbS:CsPbBr3 as a promising material for novel optoelectronics.

Probing surface interactions in CdSe quantum dots with thiocyanate ligands.

Surface chemistry dictates the optoelectronic properties of semiconductor quantum dots (QDs). Tailoring these properties relies on the meticulous selection of surface ligands for efficient passivation. While long-chain organic ligands boast a well-understood passivation mechanism, the intricacies of short inorganic ionic ligands remain largely unexplored. This study sheds light on the surface-passivation mechanism of short inorganic ligands, particularly focusing on SCN- ions on CdSe QDs. Employing steady-state and time-resolved infrared spectroscopic techniques, we elucidated the surface-ligand interactions and coordination modes of SCN--capped CdSe QDs. Comparative analysis with studies on CdS QDs unveils intriguing insights into the coordination behavior and passivation efficacy of SCN- ions on Cd2+ rich QD surfaces. Our results reveal the requirement of both surface-bound (strong binding) and weakly-interacting interfacial SCN- ions for effective CdSe QD passivation. Beyond fostering a deeper understanding of surface-ligand interactions and highlighting the importance of a comprehensive exploration of ligand chemistries, this study holds implications for optimizing QD performance across diverse applications.

Graphene quantum dot surface ligand and Co and Pt double-doping-engineered Co/Co3O4 nanozyme displaying superior performance to horseradish peroxidase and choline oxidase for the efficient degradation of rhodamine B without an activator

Nanozymes show great potential in organic degradation because of their good stability and low cost.

Development of a new phosphorescence sensor based on surface molecularly imprinted Mn-doped ZnS quantum dots for detection of melamine in milk products

This paper presents a novel room temperature phosphorescence sensor (IMIPs-ZnS QDs RTP sensor) based on inorganic surface molecularly imprinted polymers and Mn-doped ZnS quantum dots (QDs) for the rapid detection of trace melamine (MEL) in commercial milk products. The surface of Mn-ZnS QDs was modified with 3-(mercaptopropyl) trimethoxy silane (MPTS). Then, MEL, 3-aminopropyltriethoxysilane (APTES) and tetraethoxysilane (TEOS) were used as a template/target molecule, functional monomer, and cross-linker, respectively. IMIPs-ZnS QDs RTP sensor was characterized using spectrofluorimeter, UV–Vis spectrophotometer, FT-IR, transmission electron microscope (TEM), and X-ray photoelectron spectrometer (XPS).Detection time and linear range for IMIPs-ZnS QDs RTP sensor were 30 min and 4.0–79.2 µM with a correlation coefficient value of 0.9946, respectively. Furthermore, LOD and LOQ values were calculated using Stern-Volmer equation as 0.29 and 0.97 µM, respectively. Thus, IMIPs-ZnS QDs RTP sensor was successfully applied for the detection of MEL residue in milk samples. Recovery values were in the range of 88.62–90.22 % with relatively high precision values (0.57–0.92 % RSD). Our findings indicate that the developed IMIPs-ZnS QDs RTP sensor exhibits high sensitivity and selectivity towards the MEL in milk sample containing potentially relatively high number of interfering compounds.

Reducing the Open-Circuit Voltage Loss of PbS Quantum Dot Solar Cells via Hybrid Ligand Exchange Treatment.

The interface VOC loss between the active layer and the hole transport layer (HTL) of lead sulfide colloidal quantum dot (PbS-CQD) solar cells is a significant factor influencing the efficiency improvement of PbS colloidal quantum dot solar cells (PbS-CQDSCs). Currently, the most advanced solar cells adopt organic P-type HTLs (PbS-EDT) via solid-state ligand exchange with 1,2-ethanedithiol (EDT) on the CQD top active layer. However, EDT is unable to altogether remove the initial ligand oleic acid from the quantum dot surface, and its high reactivity leads to cracks in the HTL film caused by volume contractions, which inevitably results in significant VOC loss. These flaws prompted this research to develop a method involving hybrid organic ligand exchange using 3-mercaptopropionic acid (MPA) and 1,2-EDT (PbS-Hybrid) to overcome these drawbacks of VOC loss. The results indicated that the new exchange strategy improved the quality of the HTL film and benefited from the enhanced passivation of the quantum dot surface and better alignment of energy levels, and the average VOC of PbS-Hybrid devices is increased by approximately 25 mV compared to control devices. With the enhanced VOC, the average power conversion efficiency (PCE) of the devices is improved by 10%, with the highest PCE reaching 13.24%.

Synthesis and characterization of CIS/CISe core–shell structured quantum dots in green systems

I–III–VI2 group compounds, such as CuInSe2 (CISe), and CuInS2 (CIS) quantum dots (QDs), are promising for photovoltaic applications by virtue of their excellent photoelectric properties and low toxicity. Considering that the surface of QDs with smaller sizes tends to have a larger density of defect states, inorganic shell layer modification is beneficial to passivate the surface defects and enhance the optical properties and quantum efficiency of QDs. In this study, a novel core–shell structure was constructed by growing a CISe shell layer with a narrower band gap on the surface of CIS nanocrystals with a wider band gap through a green and simple method. The components and properties of the core–shell QDs were analyzed by different characterization methods (XRD, TEM, EDS, UV–Vis, Raman, and fluorescence spectroscopy). The prepared CIS/CISe core–shell QDs with increased size and good coating effects exhibited high absorbance and extended carrier lifetime while showing quantum effects associated with the CISe shell layer, as well as a promising application in the field of solar cells.

Aromatic ammonium salts ligand engineering-assisted CsPbBr3 quantum dots enable electroluminescent solar cell

All-inorganic perovskite quantum dots (QDs) have gained significant attention for their excellent optoelectronic properties, making them promising materials for applications in light-emitting diodes (LEDs) and solar cells (SCs), but it is still a challenge to balance colloidal stability of QDs and conductivity of QD films. To address the issue, an effective surface ligand engineering method has been employed by using phenethylammonium bromide (PEABr) to passivate the surface defects of QDs while enhancing the charge transport and injection in QD films. The results indicate that PEABr ligand has successfully been adsorbed onto the surface of CsPbBr3 QDs to passivate the vacancy defects, significantly enhance the electronic coupling between QDs. Systematically experimental studies show that PEABr post-treatment improves the PLQY (85 %) and stability of QDs with enhanced the carrier transport in QD film. Thanks to enhanced optoelectronic performance, the fabricated devices exhibited excellent photovoltaic (PV) and electroluminescent (EL) performance, and the CsPbBr3 QD SC had a PCE of 2.00 % while exhibiting a maximum luminance (Lmax) of 1512 cd cm−2, thus realizing high-performance electroluminescent solar cell.

Interfacial Passivation Engineering for Highly Efficient Quantum Dot Light-Emitting Diodes via Aromatic Amine-Functionalized Dipole Molecules.

Blue quantum dot (QD) light-emitting diodes (QLEDs) exhibit unsatisfactory operational stability and electroluminescence (EL) properties due to severe nonradiative recombination induced by large numbers of dangling bond defects and charge imbalance in QD. Herein, dipolar aromatic amine-functionalized molecules with different molecular polarities are employed to regulate charge transport and passivate interfacial defects between QD and the electron transfer layer (ETL). The results show that the stronger the molecular polarity, especially with the -CF3 groups possessing a strong electron-withdrawing capacity, the more effective the defect passivation of S and Zn dangling bonds at the QD surface. Moreover, the dipole interlayer can effectively reduce electron injection into QD at high current density, enhancing charge balance and mitigating Joule heat. Finally, blue QLEDs exhibit a peak external quantum efficiency (EQE) of 21.02% with an operational lifetime (T50 at 100 cd m-2) exceeding 4000 h.

Manipulation of hot-carrier cooling dynamics in CsPbBr3 quantum dots via site-selective ligand engineering.

Prolonging the lifetime of photoinduced hot carriers in lead-halide perovskite quantum dots (QDs) is highly desirable because it can help improve the photovoltaic conversion efficiency. Ligand engineering has recently become a promising strategy to achieve this; nevertheless, mechanistic studies in this field remain limited. Herein, we propose a new scenario of ligand engineering featuring Pb2+/Br- site-selective capping on the surface of CsPbBr3 QDs. Through joint observations of temperature-dependent photoluminescence, ultrafast transient absorption, and Raman spectroscopy of the two contrasting model systems of CsPbBr3 QDs (i.e., capping with organic ligand only vs hybrid organic/inorganic ligands), we reveal that the phononic regulation of Pb-Br stretching at the Br-site (relative to Pb-site) leads to a larger suppression of charge-phonon coupling due to a stronger polaronic screening effect, thereby more effectively retarding the hot-carrier cooling process. This work opens a new route for the manipulation of hot-carrier cooling dynamics in perovskite systems via site-selective ligand engineering.

Assessing the Steric Impact of Surface Ligands on the Proteolytic Turnover of Quantum Dot-Peptide Conjugates.

Proteases are important biomarkers and targets for the diagnosis and treatment of disease. The advantageous properties of semiconductor quantum dots (QDs) have made these nanoparticles useful as probes for protease activity; however, the effects of QD surface chemistry on protease activity are not yet fully understood. Here, we present a systematic study of the impact of sterics on the proteolysis of QD-peptide conjugates. The study utilized eight proteases (chymotrypsin, trypsin, endoproteinase Lys C, papain, endoproteinase Arg C, thrombin, factor Xa, and plasmin) and 41 distinct surface chemistries. The latter included three molecular weights of each of three macromolecular ligands derived from dextran and polyethylene glycol, as well as anionic and zwitterionic small-molecule ligands, and an array of mixed coatings of macromolecular and small-molecule ligands. These surface chemistries spanned a diversity of thicknesses, densities, and packing organization, as characterized by gel electrophoresis, capillary electrophoresis, dynamic light scattering, and infrared spectroscopy. The macromolecular ligands decreased the adsorption of proteases on the QDs and decelerated proteolysis of the QD-peptide conjugates via steric hindrance. The properties of the QD surface chemistry, rather than the protease properties, were the main factor in determining the magnitude of deceleration. The broad scope of this study provides insights into the many ways in which QD surface chemistry affects protease activity, and will inform the development of optimized nanoparticle-peptide conjugates for sensing of protease activity and resistance to unwanted proteolysis.

An ′On‐off‐on′ Fluorescence Sensor Based on CdSe Quantum Dots for the Selective Detection of Cd2+

AbstractIn this work, an “on‐off‐on” nanoprobe for specific detection of Cd2+ was constructed using N‐acetyl‐l‐cysteine (NAC)‐modified CdSe quantum dots (QDs). The prepared CdSe QDs exhibit characteristic green fluorescence. The adsorbed S2− on the surface of CdSe QDs leads to dangling bonds and causes the fluorescence quenching of QDs, where the fluorescence of the system turns “off“. When Cd2+ exists, it can react with the adsorbed S2− to form CdS shell, resulting in the fluorescence enhancement of CdSe QDs, where the fluorescence of the system turns “on”. Due to the similar lattice structure between CdSe and CdS, CdSe/CdS can be produced by shell deposition, while self‐nucleation of metal sulfide is observed in the presence of other metal ions. Thus, the developed nanoprobe shows high selectivity for Cd2+. Under the optimum sensing conditions, the fluorescence sensing signal of CdSe QDs depends linearly on the Cd2+ in the range of 0.2–9 μM. The limit of detection (LOD) and limit of quantification (LOQ) of this nanoprobe is 27 nM and 90 nM, respectively. Furthermore, the proposed nanoprobe can monitor Cd2+ in drinking water with a recovery rate between 95.82 % and 102.00 %, indicating its good practicability and applicability for real sample analysis.

Multivalent Display of Erythropoietin on Quantum Dots Enhances Aquaporin-4 Expression and Water Transport in Human Astrocytes In Vitro.

In mammalian cells, growth factor-induced intracellular signaling and protein synthesis play a critical role in cellular physiology and homeostasis. In the brain's glymphatic system (GS), the water-conducting activity of aquaporin-4 (AQPN-4) membrane channels (expressed in polarized fashion on astrocyte end-feet) mediates the clearance of wastes through the convective transport of fluid and solutes through the perivascular space. The glycoprotein erythropoietin (EPO) has been shown to induce the astrocyte expression of AQPN-4 via signaling through the EPO receptor and the JAK/STAT signaling pathway. Here, we self-assemble EPO in a multivalent fashion onto the surface of semiconductor quantum dots (QDs) (driven by polyhistidine-based self-assembly) to drive the interaction of the bioconjugates with EPOR on human astrocytes (HA). This results in a 2-fold augmentation of JAK/STAT signaling activity and a 1.8-fold enhancement in the expression of AQPN-4 in cultured primary HA compared to free EPO. This translates into a 2-fold increase in the water transport rate in HA cells as measured by the calcein AM water transport assay. Importantly, EPO-QD-induced augmented AQPN-4 expression does not elicit any deleterious effect on the astrocyte viability. We discuss our results in the context of the implications of EPO-nanoparticle (NP) bioconjugates for use as research tools to understand the GS and their potential as therapeutics for the modulation of GS function. More generally, our results illustrate the utility of NP bioconjugates for the controlled modulation of growth factor-induced intracellular signaling.

Colloidal InSb Quantum Dots for 1500nm SWIR Photodetector with Antioxidation of Surface.

III-V quantum dots (QDs) have emerged as significant alternatives to Cd- and Pb-based QDs, garnering notable attention over the past two decades. However, the understanding of III-V QDs, particularly in the short wave-infrared (SWIR) region, remains limited. InAs QDs are widely recognized as the most prominent SWIR QDs, but their absorption beyond 1400nm presents various challenges. Consequently, InSb QDs with relatively narrower bandgaps have been investigated; however, research on their device applications is lacking. In this study, InSb QDs are synthesized with absorption ranging from 1000 to 1700nm by introducing Cl- ions to enhance QD surface stability during synthesis. Additionally, it coated InAs and ZnSe shells onto the InSb QDs to validate photoluminescence in the SWIR region and improve photostability. Subsequently, these QDs are employed in the fabrication of photodetector devices, resulting in photodetection above 1500nm using Pb-free QDs. The photodetection device exhibited an external quantum efficiency (EQE) of 11.4% at 1370nm and 6.3% at 1520nm for InSb core QDs, and 4.6% at 1520nm for InSb/InAs core/shell QDs, marking the successful implementation of such a device. In detail, the 1520nm for InSb core device showed a dark current density(JD ) value of: 1.46 × 10-9 A/cm2 , responsivity(R): 0.078 A/W, and specific detectivity based on the shot noise(Dsh *): 3.6×1012 Jones at 0V.

Stepwise−Process−Controlled Ligand Management Strategy for Efficient and Stable Perovskite Quantum Dot Solar Cells

CsPbI3 perovskite quantum dots (QDs) have attracted much attention in the field of solar cells because of their excellent photovoltaic properties. Conventional modification of long−chain insulating ligands can ensure good dispersion and film−forming stability of QDs, but the limitations of their low defect passivation ability and poor charge transport ability will make them fail to achieve high efficiency in the corresponding solar cell devices. In this study, by introducing “Benzylphosphonic acid” short−chain ligands to the surface of CsPbI3 QDs, the ligands were re−administered on the surface during the preparation of the CsPbI3 QDs as well as during the film−forming process. The strong coordination ability of Benzenephosphonic acid can effectively passivate defects on the surface of CsPbI3 QDs and inhibit non−radiative recombination and phase transition. Meanwhile, this short−chain ligand can effectively promote the charge exchange between adjacent QDs and improve the electrical transport properties of the film. The efficiency of the Benzylphosphonic acid−modified CsPbI3 QDs solar cell reaches 13.91% compared to the unmodified device (PCE of 11.4%). The storage stability and operation stability of the device are also significantly improved. (The efficiency remains at 91% of the original for 800 h of atmospheric storage; the efficiency remains at 92% of the original for 200 h of continuous light exposure.) The present strategy realizes the simultaneous improvement of photovoltaic properties and stability of CsPbI3 QD solar cells and also provides a reference for surface ligand engineering to realize highly efficient and stable perovskite quantum dot solar cells.