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In recent studies, iron-containing Fenton nanocatalysts have demonstrated significant promise for clinical use due to their effective antitumor activity and low cytotoxicity. A new approach was reported in this work utilizing cation exchange synthesis to fabricate FeMnO x nanoparticles (NPs) that boost Fenton reactions and responses to the tumor microenvironment (TME) for chemodynamic therapy (CDT) and chemotherapy (CT). Within the TME, the redox metal pair of Fe 2+ /Mn 2+ helps break down endogenous hydrogen peroxide (H 2 O 2 ) into very harmful hydroxyl radicals (•OH) while simultaneously deactivating glutathione (GSH) to boost CDT performance. To further enhance the therapeutic potential, FeMnO x NPs were encapsulated with thioketal-linked camptothecin (CPT-TK-COOH), a reactive oxygen species (ROS)-responsive prodrug, achieving a high CPT-loading capacity of up to 51.1%. Upon ROS generation through the Fenton reaction, the prodrug TK linkage was disrupted, releasing 80% of the CPT payload within 48 h. Notably, FeMnO x @CPT exhibited excellent dual-modal imaging capabilities, enabling magnetic resonance and fluorescence imaging for image-guided therapy. In vitro studies showed the cytocompatibility of FeMnO x NPs using MDA-Mb-231 and 4T1 cells, but in the presence of H 2 O 2 , they induced significant cytotoxicity, resulting in 80% cell death through CDT and CT effects. Upon intravenous administration, FeMnO x @CPT displayed remarkable tumor accumulation, which enhanced tumor suppression in xenografts through improved CDT and CT effects. Moreover, no significant adverse effects were observed in the FeMnO x NP-treated animals. In the current study, the FeMnO x @CPT anticancer platform, with its boosted •OH-producing capability and ROS-cleavable drug release, has been validated utilizing in vitro and animal studies, suggesting its capacity as a viable strategy for clinical trials.

Recently, intercalation pseudocapacitance has received significant interest as an abnormal charge storage mechanism owing to the battery-like intercalation energy storage into the bulk electrodes and the fast charge storage kinetics of electrochemical capacitors. However, intercalation pseudocapacitance of molybdenum-based polyoxometalates (POMs) for high-performance Zn ion battery (ZIB) cathodes is yet to be exploited. Herein, we demonstrate the fast and reversible intercalation pseudocapacitance of vanadium-substituted Keggin-type molybdenum-based POMs (XPMoV), where H of HPMoV is replaced by X cations (X = Li, Na, K, or Rb). This cation exchange allows cation-exchanged XPMoV to exhibit the morphological evolution into an anisotropic rodlike structure and to achieve a pillar effect on the improved chemical and structural integrity. Despite the micron-size rod morphology and the contracted lattice of (100) plane, the intercalation pseudocapacitance kinetics of XPMoV was dominated by the fast surface-confined electrochemistry and became highly reversible after the 1st cycle activation process by co-intercalation of Li + and Zn 2+ ions. Therefore, the ZIB with the KPMoV cathode delivered a high rate capability of 74.0 mAh g -1 at 20,000 mA g -1 and 87% capacity retention over 2000 cycles at 1000 mA g -1 , far exceeding HPMoV and other Mo-based cathodes. This study paves the way to design the fast and reversible intercalation pseudocapacitance of POMs and the cation exchange chemistry into the improved (electro)chemical and structural integrity.

Prussian blue (PB) and its analogues are considered as promising cathode materials for sodium-ion batteries (SIBs) owing to their low cost and high capacity. However, it is still a huge challenge to avoid obvious capacity decay during cycling due to the structural collapse. Herein, we design a method to replace parts of Fe ion sites in PB with Ni ions to prepare fluffy-like nickel PB (PB-Ni) by cationic solution immersion, which improves cycling stability for sodium storage. The content of Ni in PB-Ni is explored by regulating the soaking time in the Ni-containing solution, which results in different effects on the electrochemical performance as cathodes of SIBs. Especially, PB-Ni-1d (soaking in NiCl 2 solution for 1 day) exhibits an initial capacity of 114.2 mA h g -1 at 50 mA g -1 and a stable cycling performance of 800 cycles at 300 mA g -1 . Furthermore, the reversible phase transformation and small volume variation for PB-Ni-1d are revealed by in situ X-ray diffraction characterization. The nickel hexacyanoferrate in outer layer maintains the cubic phase to stabilize the crystal structure. The cation-exchange strategy provides a facile idea to fabricate high-quality PB cathodes with superior stability for high-performance SIBs.

Flexible semitransparent perovskite solar cells (ST-PSCs) have great potential for use in high-density energy systems, such as building or vehicle integrated photovoltaics, considering the great features of PSC devices, including high performance, light weight, thin-film processability, and high near-infrared transmittance. Despite numerous efforts toward achieving efficiency and flexibility in ST-PSCs, the realization of high-performance and operational stability in ST-PSCs still require further development. Herein, we demonstrated the development of highly efficient, stable, and flexible ST-PSCs using polyimide-integrated graphene electrodes via a lamination-assisted bifacial cation exchange strategy. A high-quality perovskite layer was obtained through the cation exchange reaction using the lamination process, and ST-PSCs with 15.1% efficiency were developed. The proposed ST-PSC device also demonstrated excellent operational stability, mechanical durability, and moisture stability owing to the chemically inert and mechanically robust graphene electrodes. This study provides an effective strategy for developing highly functional ST-perovskite optoelectronic devices with high-performance and long-term operational stability.

Indium phosphide (InP) quantum dots (QDs) have demonstrated great potential for light-emitting diode (LED) application because of their excellent optical properties and nontoxicity. However, the over performance of InP QDs still lags behind that of CdSe QDs, and one of main reasons is that the Zn traps in InP lattices can be formed through the cation exchange in the ZnSe shell growth process. Herein, we realized highly luminescent InP/ZnSe/ZnS QDs by constructing Se-rich shielding layers on the surfaces of InP cores, which simultaneously protect the InP cores from the invasion of Zn 2+ into InP lattices and facilitate the ZnSe shell growth via the reaction between Zn 2+ precursors and Se 2- shielding layers. The as-synthesized green InP/ZnSe/ZnS QDs had a high photoluminescence quantum yield (PLQY) of up to 87%. The fabricated QLEDs present a peak external quantum efficiency of 6.2% with an improved efficiency roll-off at high luminance, which is 2 times higher than that of control devices.

Dual-mode luminescent nanomaterials have outstanding performance in biosensing and multistage anticounterfeiting. Herein, we report the tuning of optical attributes of lanthanide-doped nanoparticles (NPs) via simultaneous binary cation exchange. We show that cation exchange of NaYF 4 :Yb/Er (18/2 mol %)@NaLnF 4 (Ln = Y and Gd) NPs with a combination of Ce 3+ and Tb 3+ enables the resultant nanoparticles to exhibit both upconversion and downshifting emissions upon excitation at 980 and 254 nm, respectively. We find that in addition to introducing downshifting emission attributes, the use of Tb 3+ ions allows conservation of the integrity of the parent core@shell NPs by decreasing the dissociation tendency caused by Ce 3+ ions during the cation exchange. The upconversion color output can be tuned from green to red and blue by changing lanthanide combinations in the core NPs. This work not only provides an effective strategy for the optical tuning of lanthanide-doped NPs but also builds a platform for probing the difference in the reactivity nature of lanthanides.

Nontoxic tin-based perovskite solar cells (Sn-PSCs) as a promising alternative to toxic Pb-PSCs have drawn great attention in recent years for their environmental friendliness and unique optoelectronic properties. However, both the efficiency and long-term stability of Sn-PSCs are considerably inferior to those of Pb-based ones. One of the main reasons is the difficulty in obtaining high-quality Sn-perovskite films due to the rapid crystallization of Sn-perovskites, which also results in poor device reproducibility. Here, we report a novel cation exchange strategy to prepare high-quality formamidinium tin triiodide (FASnI 3 ) perovskite films with a better controlled crystallization process and improved reproducibility, which allows easy access to smooth and pinhole-free perovskite films with oriented crystal growth, enlarged grain size, and reduced trap-state density. The corresponding Sn-PSCs show excellent photovoltaic performance with a champion efficiency of 9.11%, comparable to the best results reported for FASnI 3 -PSCs, and the devices also demonstrate outstanding long-term stability without encapsulation. Our results offer a practical strategy for fabricating Sn-PSCs with superb performance and stability.

The development of novel electrocatalysts, especially Pt-free electrocatalysts, is of great significance for evolving hydrogen fuel cells. Two-dimensional materials have many advantages, such as large specific surface area, abundant active edges, and adjustable electronic structure, which provide broad prospects for studying high-performance electrocatalysts. In this paper, Cu 2- x S@Au 2 S@Au nanoplates (NPs) were synthesized by cation exchange, which showed good catalytic performance toward the hydrogen evolution reaction (HER). Dark-field microscopy can help observe the process of cation exchange in real time to precisely control the synthesis of the composite materials. The synthesized Cu 2- x S@Au 2 S@Au nanoplates (NPs) exhibited greatly enhanced plasmonic emission, resulting in accelerated chemical conversion and improved HER efficiency. Under 532 nm laser excitation, the overpotential of the HER shifted from 152 to 96 mV at a current density of -10 mA cm -2 . The plasmonic nanocatalysts show exciting prospects in the field of new energy resources.

Perovskite quantum dots (PQDs) have expanded the scalability of perovskite materials by their high crystallinity, band-gap tunability, and surface ligand-driven functionalities in the colloidal state across optoelectronics as well as photovoltaics. To improve PQD performance in applications, however, defect control has emerged as a major challenge given the increased PQD surface area. Herein, we have developed a heterostructured PQD solar cell by combining CsPbI 3 and FAPbI 3 (FA, formamidinium) PQD layers to introduce a multinary PQD layer based on a solid-state A-site cation-exchange strategy. A heterostructure, including the solid-state diffusion-driven multinary PQD layer, creates an internally graded heterojunction for more efficient charge extraction. The best PQD cell achieves a power conversion efficiency (PCE) of 16.07% with negligible hysteresis. Furthermore, this architecture offers significantly enhanced stability with reduction of trap-assisted recombination as compared to cells of a monocompositional PQD layer. The unencapsulated device retains a 96% PCE after 1000 h in ambient storage.

NASICON-type oxide Li 1+ x Al x Ti 2- x (PO 4 ) 3 (LATP) is expected to be a promising solid electrolyte (SE) for all-solid-state batteries (ASSBs) owing to its high ion conductivity and chemical stability. However, its interface properties with electrodes on the atomic scale remain unclear, but it is crucial for rational control of the ASSBs performance. Herein, we focused on the LATP SE with x = 0.17 and investigated the electron and ion transfer behaviors at the interfaces with the Li metal negative electrode and the LiCoO 2 (LCO) positive electrode via explicit interface models and density functional theory calculations. Ti reduction was found at the LATP/Li interface. For the LATP/LCO interface, the results indicated the Li-ion transfer from LCO to LATP upon contact until a certain electric double layer is formed under equilibrium, in which LCO is partially reduced. Co-Ti exchange was also found to be favorable where the Li ion moves with Co 3+ to LATP. We also explored the possible interfacial processes during annealing by simulating the oxygen removal effect and found that oxygen vacancy can be more easily formed in the LCO at the interface. It implies that partial Li ions move back to LCO for the local charge neutrality. We also demonstrated higher Li chemical potential around the LATP/LCO interfaces, leading to the dynamical Li-ion depletion upon charging. The calculation results and the deduced mechanisms well explain the experimental results so far and provide insights into the interfacial electron and ion transfer upon contact, during annealing, and charging.

PbSe colloidal quantum dots (CQDs) are widely used in solar cells because of their tunable band gap, solution processability, and efficient multiple exciton generation effect. The most efficient PbSe CQD solar cells use high-temperature-processed ZnO as the electron transport layer (ETL), limiting their applications in flexible photovoltaics. Currently, low-temperature solution-processed SnO 2 has been demonstrated as an efficient ETL for high-efficient PbS CQD and perovskite solar cells because of less parasitic light absorption and higher electron mobility. Herein, we introduce low-temperature solution-processed SnO 2 as ETL for PbSe CQD solar cells, and fabricate the PbSe CQD absorber layer with a one-step spin-coating method. The champion device with the structure of FTO (SnO 2 :F)/SnO 2 /PbSe-PbI 2 /PbS-EDT (1,2-ethanedithiol)/Au achieves a high open-circuit voltage of 577.1 mV, a short-circuit current density of 24.87 mA  cm -2 , a fill factor of 67%, and an impressive power conversion efficiency of 9.67%. Our results pave the way for the development of low-temperature flexible PbSe CQD solar cells.

Hollow-structured semiconductor nanocrystals (NCs) have aroused tremendous research interest because of their compelling structure-related properties that can facilitate the development of many important applications including solar water splitting. However, the creation of multicomponent semiconductor NCs (such as I-III-VI 2 and I 2 -II-IV-VI 4 semiconductors) possessing a hollow architecture still remains a great challenge because of the difficulty in balancing the reactivities of multiple precursors. In this study, we report an effective strategy to prepare hollow CuInS 2 nanododecahedrons featuring high uniformity in morphology and composition, based on the Kirkendall effect driven by the cation exchange between Cu + and In 3+ using Cu 2- x S nanododecahedrons as templates. The unequal diffusion rates of cations result in an inward flux of vacancies favorably along the (0 16 0) facets of Cu 2- x S dodecahedrons, forming a Cu 2- x S@CuInS 2 core-shell intermediate with striped voids in the core region. Optical absorption studies and photoelectrochemical measurements imply that the increase in the hollowing degree of the NCs benefits enhanced light harvesting and separation of photogenerated charge carriers. As a result, the obtained hollow CuInS 2 nanododecahedrons present a high activity in photocatalytic hydrogen evolution, much superior to previously reported CuInS 2 photocatalysts with different architectures. We envision that the multifarious morphologies attainable for the Cu 2- x S NC templates and the advantages of Cu + for cation exchange can make this method adaptable to a vast variety of previously intractable structures and compositions.

Cancer stem cells, which are a population of cancer cells sharing common properties with normal stem cells, have strong self-renewal ability and multi-lineage differentiation potential to trigger tumor proliferation, metastases, and recurrence. From this, targeted therapy for cancer stem cells may be one of the most promising strategies for comprehensive treatment of tumors in the future. We design a facile approach to establish the colon cancer stem cells-selective fluorescent probe based on the low-density lipoprotein (LDL) and the novel AgGa x In (1- x) S 2 quantum dots (AGIS QDs). The AGIS QDs with a high crystallinity are obtained for the first time via cation-exchange protocol of Ga 3+ to In 3+ starting from parent AgInS 2 QDs. Photoluminescence peak of AGIS QDs can be turned from 502 to 719 nm by regulating the reaction conditions, with the highest quantum yield up to 37%. Subsequently, AGIS QDs-conjugated LDL nanocomposites (NCs) are fabricated, in which a cationic polyelectrolyte was used as a coupling reagent to guarantee the electrostatic self-assembly. The structural integrity and physicochemical properties of the LDL-QDs NCs are found to be maintained in vitro, and the NCs exhibit remarkable biocompatibility. The LDL-QDs can be selectively delivered into cancer stem cells that overexpress LDL receptor, and three-dimensional imaging of cancer stem cells is realized. The results of this study not only demonstrate the versatility of nature-derived lipoprotein nanoparticles, but also confirm the feasibility of electrostatic conjugation using cationic polyelectrolyte, allowing reseachers to design nanoarchitectures for targeted diagnosis and treatment of cancer.

Currently, it is of great challenge to achieve cation exchange in CsPbX 3 (X = Cl, Br, I) perovskite nanocrystals (NCs) on account of rigid Pb 2+ octahedral coordination protected by six halogen anions (PbX 6 4- octahedrons and enable fast Mn-to-Pb cation exchange at room temperature in a few seconds. Importantly, Cl concentration rather than Mn one is demonstrated to be a dominant factor for cation exchange, where different Mn 6 4- octahedrons and enable fast Mn-to-Pb cation exchange at room temperature in a few seconds. Importantly, Cl concentration rather than Mn one is demonstrated to be a dominant factor for cation exchange, where different Mn 2+ /Cl - salts can be adopted as Mn/Cl sources and Cl-to-Cl or Cl-to-Br anion exchange is the necessary prerequisite. Such a facile synthesizing method can lead to the feasibility of tuning emissive colors for the Mn-doped CsPb(Cl/Br) 3 NCs by controlling both cation and anion exchanges and open a new way to replace Pb 2+ in CsPbX 3 NCs by other nontoxic metal elements.

Though 2D transition metal dichalcogenides have attracted a lot of attention in energy-storage applications, the applications of NbSe 2 for Li storage are still limited by the unsatisfactory theoretical capacity and uncontrollable synthetic approaches. Herein, a controllable oil-phase synthetic route for preparation of NbSe 2 nanoflowers consisted of nanosheets with a thickness of ∼10 nm is presented. Significantly, a part of NbSe 2 can be further replaced by orthorhombic CoSe 2 nanoparticles via a post cation exchange process, and the predominantly 2D nanosheet-like morphology can be well-maintained, resulting in the formation of CoSe 2 -decorated NbSe 2 (denoted as CDN) nanosheets. More interestingly, the CDN nanosheets exhibit excellent lithium-ion battery performance. For example, it achieves a highly reversible capacity of 280 mAh g -1 at 10 A g -1 and long cyclic stability with specific capacity of 364.7 mAh g -1 at 5 A g -1 after 1500 cycles, which are significantly higher than those of reported pure NbSe 2 .

Lead halide perovskite nanocrystals (NCs) as promising optoelectronic materials are intensively researched. However, instability is one of the biggest challenges needed to overcome before fulfill their practical applications. To improve their stability, we present a postsynthetic controlled phase transformation of CsPbBr 3 toward CsPbBr 3 /Rb 4 PbBr 6 core/shell structure triggered by rubidium oleate treatment. The resulting core/shell NCs show exceptional photostability both in solution and on-chip. The solution of CsPbBr 3 /Rb 4 PbBr 6 NCs can remain over 90% of the initial emission photoluminescence quantum yields after 42 h of intense light-emitting diodes illumination (450 nm, 175 mW/cm 2 ), which is even better than the conventional CdSe/CdS quantum dots whose emission drop to 50% after 18 h under the same condition. We believe that the exceptional photostability should be resulted from the protection of the robust Rb 4 PbBr 6 shell on CsPbBr 3 NCs.

Luminescent metal-organic frameworks (MOFs) (typically dye-encapsulated MOFs) are considered as one kind of interesting downconversion materials for white-light-emitting diodes (LEDs), but their quantum efficiency (QE) is not sufficient and thus needs to be significantly enhanced for practical applications. In this study, we successfully synthesized a series of Rh@bio-MOF-1 (Rh = rhodamine) with an internal QE as high as ∼79% via a solvothermal reaction followed by cation exchanges. The high efficiency of the Rh@bio-MOF-1 composites was attributable to the high intrinsic luminescent efficiency of the selected Rh dyes, the confinement effect in the bio-MOF-1 host, and the uniform particle morphology. The emission maximum could be continuously tuned from 550 to 610 nm by controlling the species and concentration of encapsulated dye molecules, showing great color tunability of the dye-encapsulated MOFs. The emission lifetime of ∼7 ns was 1 or 2 magnitude orders shorter than that of Ce 3+ - or Eu 2+ -doped inorganic phosphors, allowing for visible light communication (VLC). White LEDs, fabricated by using the synthesized Rh@bio-MOF-1 composite and inorganic phosphors of green (Ba,Sr) 2 SiO 4 :Eu 2+ and red CaAlSiN 3 :Eu 2+ , exhibited a high color rendering index of 80-94, a luminous efficacy of 94-156 lm/W, and an excellent stability in color point against drive current. The Rh@bio-MOF-1 composites with tunable colors, short emission lifetime, and high QE are expected to be used for smart white LEDs with multifunctions of both lighting and VLC.

In this study, we report the fabrication of nanocomposites made of titanate nanosheets immobilized in a solid matrix of regenerated silk fibroin as novel heavy-metal-ion removal systems. The capacity of these nanocomposite films to remove lead, mercury, and copper cations from water was investigated, and as shown by the elemental quantitative analysis performed, their removal capacity is 73 mmol/g for all of the ions tested. We demonstrate that the nanocomposites can efficiently retain the adsorbed ions, with no release of titanate nanosheets occurring even after several exposure cycles to ionic solutions, eliminating the risk of release of potentially hazardous nanosubstances to the environment. We also prove that the introduction of sodium ions in the nanocomposite formulation makes the materials highly selective toward the lead ions. The developed biopolymer nanocomposites can be potentially used for the efficient removal of heavy-metal-ion pollutants from water and, thanks to their physical and optical characteristics, offer the possibility to be used in sensor applications.

Attention on semiconductor nanocrystals have been largely focused because of their unique optical and electrical properties, which can be applied as light absorber and luminophore. However, the band gap and structure engineering of nanomaterials is not so easy because of their finite size. Here we demonstrate an approach for preparing ternary AgInS2 (AIS), quaternary AgZnInS (AZIS), AgInS2/ZnS and AgZnInS/ZnS nanocompounds based on cation exchange. First, pristine Ag2S quantum dots (QDs) with different sizes were synthesized in one-pot, followed by the partial cation exchange between In(3+) and Ag(+). Changing the initial ratio of In(3+) to Ag(+), reaction time and temperature can control the components of the obtained AIS QDs. Under the optimized conditions, AIS QDs were obtained for the first time with a cation disordered cubic phase and high photoluminescence (PL) quantum yield (QY) up to 32% in aqueous solution, demonstrating the great potential of cation exchange in the synthesis for nanocrystals with excellent optical properties. Sequentially, Zn(2+) ions were incorporated in situ through a second exchange of Zn(2+) to Ag(+)/In(3+), leading to distinct results under different reaction temperature. Addition of Zn(2+) precursor at room temperature produced AIS/ZnS core/shell NCs with successively enhancement of QY, while subsequent heating could obtain AZIS homogeneous alloy QDs with a successively blue-shift of PL emission. This allow us to tune the PL emission of the products from 483 to 675 nm and fabricate the chemically stable QDs core/ZnS shell structure. Based on the above results, a mechanism about the cation exchange for the ternary nanocrystals of different structures was proposed that the balance between cation exchange and diffusion is the key factor of controlling the band gap and structure of the final products. Furthermore, photostability and in vitro experiment demonstrated quite low cytotoxicity and remarkably promising applications in the field of clinical diagnosis.

Mn3O4@CoMn2O4 nanoparticles (NPs) were produced at low temperature and ambient atmosphere using a one-pot two-step synthesis protocol involving the cation exchange of Mn by Co in preformed Mn3O4 NPs. Selecting the proper cobalt precursor, the nucleation of CoxOy crystallites at the Mn3O4@CoMn2O4 surface could be simultaneously promoted to form Mn3O4@CoMn2O4-CoxOy NPs. Such heterostructured NPs were investigated for oxygen reduction and evolution reactions (ORR, OER) in alkaline solution. Mn3O4@CoMn2O4-CoxOy NPs with [Co]/[Mn] = 1 showed low overpotentials of 0.31 V at -3 mA·cm(-2) and a small Tafel slope of 52 mV·dec(-1) for ORR, and overpotentials of 0.31 V at 10 mA·cm(-2) and a Tafel slope of 81 mV·dec(-1) for OER, thus outperforming commercial Pt-, IrO2-based and previously reported transition metal oxides. This cation-exchange-based synthesis protocol opens up a new approach to design novel heterostructured NPs as efficient nonprecious metal bifunctional oxygen catalysts.

We report the fabrication and utilization of elastomeric polymer nanocomposite foams for the efficient removal of Pb2+ and Hg2+ heavy metal ions from polluted water. The polydimethylsiloxane (PDMS) foams are properly modified in order to become hydrophilic and allow the polluted water to penetrate in their volume. The ZnSe colloidal nanocrystals (NCs) that decorate the surface of the foams, act as active components able to entrap the metal ions. In this way, after the dipping of the nanocomposite foams in water polluted with Pb2+ or Hg2+, a cation exchange reaction takes place, and the heavy metal ions are successfully removed. The removal capacity for the Pb2+ ions exceeds 98% and the removal of Hg2+ ions approaches almost 100% in the studied concentrations region of 20-40 ppm. The reaction is concluded after 24 h, but it should be noticed that after the first hour, more than 95% of both the metal ions is removed. The color of the foams changes upon heavy metal ions entrapment, providing thus the opportunity of an easy detection of the presence of the ions in water. Taking into account that the fabricated foams provide good elastic properties and resistance to heat, they can be used in different conditions of water remediation.

We report a novel nanocrystals (NCs) sorbent, which shows an extraordinary adsorption capacity to aqueous Hg(2+) based on cation exchange and allows for the utmost removal of mercury from water. The NCs sorbent was synthesized by direct coating ZnS NCs on the surface of the α-Al2O3 nanoparticles. The as-prepared ZnS NCs sorbent can efficiently remove over 99.9% Hg(2+) in 1 min, and lower the Hg(2+) concentration from 297.5 mg/L (ppm) to below 1.0 μg/L (ppb) within 5 min. The saturated adsorption capacity of ZnS NCs for Hg(2+) is about 2000 mg/g, which is close to the theoretic saturated adsorption capacity. The mechanism of Hg(2+) removal by ZnS NCs sorbent, the influences of pH value and other cations on Hg(2+) removal were investigated, respectively. Meanwhile, it is found the size-dependent cation exchange plays a critical role in the removal of Hg(2+) by ZnS NCs. Small size ZnS NCs shows better performance than the big size ZnS NCs in the adsorption capacity and adsorption rate for Hg(2+). Furthermore, the mercury adsorbed by the ZnS NCs sorbent is readily recycled by extraction with aqueous sodium sulfide.