An Explosive Bomb-Inspired Method to Prepare Collapsed and Ruptured Fe2 O3 /Nitrogen-Doped Carbon Capsules as Catalyst Support.

Compared with integrated capsules, ruptured ones have better mass diffusion and transport properties due to large gaps in the shells. However, most studies focus on integrated capsules, whereas little attention has been paid to the ruptured counterparts. Herein, an explosive bomb-inspired method was employed to prepare collapsed and ruptured Fe2 O3 /nitrogen-doped carbon (CR-Fe2 O3 /NC) capsules by using polystyrene (PS) nanoparticles (NPs) as a hard template, and polypyrrole (PPy) with embedded Prussian blue (PB) NPs as the shell. During pyrolysis, PB is converted into Fe2 O3 , and PPy is carbonized to form NC. Importantly, the PS core decomposes into gas molecules, leading to high pressure inside of the capsule, which explodes the thin shell into pieces. The roles of shell thickness and amount of Fe2 O3 on determining the spherical or collapsed, and integrated or ruptured morphology were revealed. Taking advantage of structural merits, including large gaps, thin shells, low density, and high surface area, CR-Fe2 O3 /NC capsules were used as supports for Pd NPs. These capsules exhibited better catalytic activity than that of integrated ones. Due to the magnetic properties, they could be reused at least five times.

Mediating peroxymonosulfate activation path in Fenton-like reaction via doping different metal atoms into g-C3N5.

Peroxymonosulfate (PMS) could be activated by either radical path or non-radical path, how to rationally mediate these two routines was an important unresolved issue. This work has introduced a simple way to address this problem via metal atom doping. It was found that Fe-doped nitrogen-rich graphitic carbon nitride (Fe-C3N5) exhibited high activity towards PMS activation for tetracycline degradation, and the degradation rate was 3.14 times higher than that of Co-doped nitrogen-rich graphitic carbon nitride (Co-C3N5). Radical trapping experiment revealed the contributions of reactive species over two catalysts were different. Electron paramagnetic resonance analysis further uncovered the non-radical activation path played a dominated role on Fe-C3N5 surface, while the radical activation path was the main routine on Co-C3N5 surface. Density functional theory calculations, X-ray photoelectron spectroscopy analysis, and electrochemical experiments provided convincing evidence to support these views. This study supplied a novel method to mediate PMS activation path via changing the doped metal atom in g-C3N5 skeleton, and it allowed us to better optimize the PMS activation efficiency.

An interfacial C-S bond bridged S-scheme ZnS/C3N5 for photocatalytic H2 evolution: Opposite internal-electric-field of ZnS/C3N4, increased field strength, and accelerated surface reaction.

An interfacial C-S bond bridged ZnS/C3N5 heterojunction was constructed for photocatalytic H2 evolution. Different from traditional type-II ZnS/C3N4 heterojunction, the electron transfer followed S-scheme pathway, due to opposite internal-electric-field (IEF) directions in these two heterojunctions. The C-S bond formation was carefully investigated, and they were susceptive to the preparation temperatures. In photocatalytic reaction, C-S bond was functioned as the "high-speed channel" for electron separation and transfer, and the IEF strength in ZnS/C3N5 was 1.86 × 108 V/m, 2.6 times higher than that in ZnS/C3N4. Moreover, the C-S bond also altered the surface molecular structure of ZnS/C3N5, and hence the surface reaction was accelerated via improving H2O adsorption and activation behaviors. Benefiting from the S-scheme pathway, enhanced IEF strength, and accelerated surface reaction, the photocatalytic H2 production over ZnS/C3N5 reached up to 20.18 mmol/g/h, 3.2 and 2.5 times higher than those of ZnS/C3N4 and ZnS/C3N5-300 without C-S bond.

Internal-electric-field induced high efficient type-I heterojunction in photocatalysis-self-Fenton reaction: Enhanced H2O2 yield, utilization efficiency and degradation performance.

Herein, a type-I phosphorus-doped carbon nitride/oxygen-doped carbon nitride (P-C3N4/O-C3N4) heterojunction was designed for photocatalysis-self-Fenton reaction (photocatalytic H2O2 production and following Fenton reaction). In P-C3N4/O-C3N4, the photoinduced charge carriers were effectively separated with the help of internal-electric-field near the interface, ensuring the high catalytic performance. As a result, the production rate of H2O2 in an air-saturated solution was 179 µM·h-1, about 7.2, 2.5, 2.5 and 2.1 times quicker than that on C3N4, P-C3N4, O-C3N4, and phosphorus and oxygen co-doped C3N4, respectively. By taking advantage of the cascade mode in photocatalysis-self-Fenton reaction, H2O2 utilization efficiency was remarkably improved to 77.7%, about 9.0 times higher than that of traditional homogeneous Fenton reaction. Befitting from the superior yield and utilization efficiency, the degradation performance of P-C3N4/O-C3N4 was undoubtedly superior than other photocatalysts. This work well addressed two bottlenecks in traditional Fenton reaction: source of H2O2 and their low utilization efficiency, and the findings were beneficial to understand the mechanism and advantage of the photocatalysis-self-Fenton system in environmental remediation.

Construction of Z-scheme heterojunction by coupling Bi2Sn2O7 and BiOBr with abundant oxygen vacancies: Enhanced photodegradation performance and mechanism insight.

Promoting charge migration and enhancing redox ability of photogenerated carriers are important for the development of highly efficient semiconductor-based photocatalyst. Here, BiOBr/Bi2Sn2O7 heterojunction with oxygen vacancies (OVs) was constructed by homogeneously depositing Bi2Sn2O7 nanoparticles on the Vo-BiOBr surface. The experimental results manifested that Vo-BiOBr/Bi2Sn2O7 displayed better performance for rhodamine B, ciprofloxacin, and tetracycline degradation than counterparts without OVs. The characterization results proved OVs played the essential role for enhanced performance via improving the separation efficiency of charge carriers, increasing the visible light harvest, and lowering conduction band position. Moreover, mechanism study revealed that an inner electric field was built at the interface, leading to a Z-scheme path of photogenerated electron. This study provided an efficient strategy for designing highly efficient photocatalyst for solving environmental pollution.

A stable lanthanum-based metal-organic framework as fluorescent sensor for detecting TNP and Fe3+ with hyper-sensitivity and ultra-selectivity.

A new Lanthanum-based luminescent metal-organic framework, {[La(H2O)4(HL)]·H2O} (1), has been successfully synthesized by employing 3,3',5,5'-azodioxybenzenetetracarboxylic acid (H4L) as a rigid organic linker through the solvothermal reactions. 1 exhibits a two-dimensional (2D) layered structure and a three-dimensional (3D) supramolecular structure is formed by hydrogen bonds between the layers. Stability studies indicate that 1 has good chemical stability and thermostability. Meanwhile, the Ksv values for TNP is 4.61 × 104 M-1 with the LOD of 4.13 × 10-6 M and the Ksv value for Fe3+ is 1.22 × 104 M-1 with the LOD of 1.72 × 10-5 M, respectively, which demonstrated that 1 exhibits high sensitivity and excellent selectivity for the detection of TNP and Fe3+via fluorescence quenching. Significantly, 1 shows high regenerability after five recycling progress for sensing Fe3+. The possible mechanisms associated with the luminescent quenching are discussed in detail through some relevant experiments and tests, as well as the DFT calculations. Based on the above excellent properties of 1, it will have extremely potential to be used as a dual functional sensor for both detecting TNP and Fe3+ in aqueous solution, simultaneously.

Z-scheme Fe2(MoO4)3/Ag/Ag3PO4 heterojunction with enhanced degradation rate by in-situ generated H2O2: Turning waste (H2O2) into wealth (•OH).

Ag3PO4-based photocatalysts have been deeply studied in environmental remediation; however, two problems limited their further application: photocorrosion and quenching effect by in-situ generated H2O2. To addressed these two questions simultaneously, Fe2(MoO4)3 was coupled with Ag3PO4 to construct Z-scheme Fe2(MoO4)3/Ag/Ag3PO4 heterojunction driven by internal-electric-field. The rhodamine B degradation rate of heterojunction was 254 and 7.0 times higher than those of Fe2(MoO4)3 and Ag3PO4, respectively. The outstanding photoactivity was due to the high visible-light harvest, low interface resistance, high separation efficiency of charge carriers, long lifetime of hole (h+) and electron (e-), well-preserved oxidation potential of h+, and especially photocatalytic produced H2O2 inside the system. The in-situ generated H2O2 was fully activated to be •OH on the Fe2(MoO4)3 surface via a Fenton reaction, leading to the elimination of quenching effect on h+ and e-, and generation of more •OH. Additionally, in Z-scheme heterojunction, e- transferred from Ag3PO4 to Fe2(MoO4)3, avoiding the accumulation on Ag3PO4 surface, and hence suppressing the photocorrosion. As a result, 91.2% of degradation efficiency remained after 5 cycles. This paper provides a new method to simultaneously increase the degradation rate by utilizing the in-situ generated H2O2 and improve the stability of Ag3PO4 via constructing a Z-scheme heterojunction.

A simple and green method to prepare non-typical yolk/shell nanoreactor with dual-shells and multiple-cores: Enhanced catalytic activity and stability in Fenton-like reaction.

Nowadays, non-typical yolk/shell structure has drawn much attentions due to the better catalytic performance than traditional counterparts (one yolk/one shell). In this study, ZIF-67 @Co2SiO4/SiO2 yolk/shell structure was prepared in one-step at room temperature, in which ZIF-67 was served as the hard-template, H2O was served as etchant and tetraethyl orthosilicat was served as the raw material for Co2SiO4/SiO2. After calcination, the non-typical CoxOy @Co2SiO4/SiO2 yolk/shell nanoreactor with Co2SiO4/SiO2 dual-shells and CoxOy multiple-cores was obtained. On the one hand, more active sites were exposed on multiple-cores surface and better protection were provided by dual-shells. On the other hand, the sheet-like Co2SiO4 inner shell not only extended the travel path and retention time of pollutants trapped in cavity, but also separated the multiple-cores from aggregation. Therefore, the nanoreactor displayed the outstanding catalytic activity and recyclability in Fenton-like reaction. Metronidazole (20 mg/L) was completely degraded after 30 min, rhodamine B (50 mg/L) and methyl orange (20 mg/L) were removed even within 5.0 min. Catalytic mechanism indicated that 1O2 greatly contributed to the pollutant degradation. This paper presented a simple, versatile, green and energy-saving method for non-typical yolk/shell nanoreactor, and it could inspire to prepare other catalysts with high activity and stability for environmental remediation.

Partially oxidized MXenes-derived C-TiO2/Ti3C2 coupled with Fe-C3N4 as a ternary Z-scheme heterojunction: Enhanced photothermal and photo-Fenton performance.

Photo-Fenton reaction combining the photocatalytic reaction and Fenton reaction showed excellent degradation performance. However, it highly demanded the catalysts to display outstanding activity in these two reactions. Herein, Fe-doped carbon nitride/MXenes-derived C-TiO2/Ti3C2 (Fe-C3N4/Ti3C2/C-TiO2) was prepared via two steps: Fe-C3N4 and Ti3C2 were assembled via face-to-face attachment, following by in-situ partial oxidation of Ti3C2 to C-TiO2. DFT predicted a Z-scheme charge transfer routine via metallic Ti3C2 as bridge, which was verified by EPR and radical trapping experiments. Additionally, PDOS calculation revealed the charge density around the doped-Fe atoms was remarkably increased, leading to better H2O2 activation, which was experimentally confirmed by high yield of •OH. Moreover, Fe-C3N4/Ti3C2/C-TiO2 possessed the high photothermal effect to accelerate the surface reaction. By taking advantage of these merits, the degradation rate of Fe-C3N4/Ti3C2/C-TiO2 was at least 4.2 times higher than the reference catalysts. Our work provided an insight toward the g-C3N4/TiO2-based photo-Fenton catalysts with high performance.

Preparation of double-yolk egg-like nanoreactor: Enhanced catalytic activity in Fenton-like reaction and insight on confinement effect.

Peroxymonosulfate (PMS)-based Fenton-like reaction is an effective technique for the pollutant degradation, and the Co-based metal organic frameworks displayed the excellent activity for the PMS activation. Nevertheless, how to further improve the catalytic activity, suppress the leaching of toxic cobalt ions, and realize the rapid separation were still challenges for practical application. In this work, a novel solution was proposed: encapsulating Fe3O4 and Prussian blue analogue (PBA) into the polypyrrole (PPy) shell and constructing a "double-yolk egg-like" Fe3O4/PBA@PPy as a nanoreactor. In Fe3O4/PBA@PPy-10, the catalytic performance was remarkably enhanced with the help of confinement effect, and the degradation rate (0.38 L·min·mol-1) was 5.1 times than that of reference Fe3O4/PBA-10 (0.074 L·min·mol-1). In addition, the concentration of leached cobalt ions was reduced to only 0.174 mg/L by the protective function from the PPy shell. Moreover, the nanoreactor could be magnetically separated from the reaction solution due to the encapsulation of Fe3O4 nanospheres, and 84.5% of activity still preserved after the 4th cycle. The main active species involved in Fe3O4/PBA@PPy-10 system was 1O2, while that in reference Fe3O4/PBA-10 system was OH. Electron spin resonance analysis and radical trapping experiment revealed that the different catalytic mechanisms were attributed to the confinement effect inside the hollow cavity. This work not only presents a feasible way to prepare rarely-reported double-yolk egg-like nanoreactor, but also provides a new insight to solve the bottlenecks in Fenton-like reaction.

MoS2/FeS Nanocomposite Catalyst for Efficient Fenton Reaction.

Nanocomposites containing FeS as catalyst and MoS2 as cocatalyst have been synthesized toward efficient heterogeneous Fenton reaction. The deposition of FeS nanoparticles in situ on the surface of MoS2 nanosheets creates strong contact between the two components and generates a large number of exposed Mo6+ sites and sulfur vacancies, which contribute to the enhanced degradation rate by accelerating Fe3+/Fe2+ cycling and ensuring rapid electron transfer. In addition, the MoS2/FeS nanocomposite catalysts exhibit the best performance at near-neutral conditions (pH 6.5), which solves the challenges in conventional Fenton reactions such as leaching of metal ions, the formation of iron slurry, and the need of adjusting solution pH. Further, the nanocomposite can maintain high efficiency after many recycling experiments. It is believed that the MoS2/FeS nanocomposite represents an efficient heterogeneous Fenton catalyst that can greatly promote the performance of advanced oxidation processes (AOPs) for solving practical environmental issues.

Transforming type-II Fe2O3@polypyrrole to Z-scheme Fe2O3@polypyrrole/Prussian blue via Prussian blue as bridge: Enhanced activity in photo-Fenton reaction and mechanism insight.

Photo-Fenton reaction is a more effective technique for pollutant disposal than photocatalytic reaction. Herein, Fe2O3@polypyrrole/Prussian blue (Fe2O3@PPy/PB) with a hierarchical porous structure was prepared by a reactive-template method. After transforming typical type-II Fe2O3@PPy to Z-scheme Fe2O3@PPy/PB via PB as a bridge, the degradation rate was increased by 1.4 times in photocatalytic reaction and 4.0 times in photo-Fenton reaction due to higher visible-light harvest, enhanced separation efficiency of photoinduced charges, lower interface resistance, and especially well-preserved redox potentials of holes and electrons. Mechanism studies revealed that holes were quenched by H2O2, and this led to •O2- generation and efficient separation of electrons. Meanwhile, O2 was reduced by separated electrons, and this further increased •O2- yield. Therefore, the main radicals changed from hole in photocatalytic reaction to •O2- in the photo-Fenton reaction, leading to an increase as high as 12.1-fold enhancement in the degradation rate. Conversely, only H2O2 participated into photocatalytic reaction using Fe2O3@PPy while O2 was absent, resulting in merely 4.2-fold improvement. This manuscript gives a comprehensive understanding on mechanisms of type-II and Z-scheme heterojunctions in both photocatalytic and photo-Fenton reactions. Obviously, the outcomes are beneficial for designing catalysts with high photo-Fenton activity.

Improvement of the stability of colloidal gold superparticles by polypyrrole modification.

The colloidal gold superparticle (SP)/polypyrrole (PPy) core/shell composites were successfully prepared by oxidative polymerization of pyrrole monomer on the surface of poly(N-vinylpyrrolidone) (PVP)-grafted colloidal gold SPs. These core/shell composites showed strong catalytic activity and excellent stability. Control experiments indicated that the morphology and the thickness of PPy shell were controllable by adjusting the dosage of pyrrole monomer. Meaningfully, the resulting SP/PPy core/shell composites were quite stable in water, which could be stored for more than half a year without damaging their structures. As an example, we demonstrated the use of these composites as catalyst for the reduction of methylene blue (MB) dye with a reducing agent of sodium borohydride. The composites exhibited highly catalytic activity and long-term stability, implying promising applications of SP/PPy composites in catalysis.

Construction of phosphorus-doped carbon nitride/phosphorus and sulfur co-doped carbon nitride isotype heterojunction and their enhanced photoactivity.

Photocatalysis was one of the most promising techniques for environmental remediation. Exploring photocatalysts with high efficiency, low cost and easy preparation was still an ongoing issue. In this work, phosphorus-doped carbon nitride/phosphorus and sulfur co-doped carbon nitride (P-C3N4/PS-C3N4) isotype heterojunction was prepared by a two-step calcination method. The composite displayed a sheet-like structure with a surface area of 23 m2/g. Compared with pure C3N4, band gaps of P-C3N4 and PS-C3N4 were only slightly modified during the heteroatom-doping process. Therefore, a well-matched band alignment was constructed, which not only improved the separation efficiency of photogenerated electron-hole pairs, but also well preserved the high oxidizability of holes on valance band and good reducibility of electrons on conduction band. Because of the similarity in physicochemical properties, the interface resistance between P-C3N4 and PS-C3N4 was low, which accelerated the electron transfer and prolonged the lifetime of charge carriers. Although the visible-light utilization was somewhat low in comparison with P-C3N4 and PS-C3N4, by taking advantage of above merits, P-C3N4/PS-C3N4 displayed the high photocatalytic activity in rhodamine B degradation, and the reaction rate constant was 0.183 min-1, about 8.7 and 4.0 times higher than those of P-C3N4 and PS-C3N4. Besides high catalytic activity, isotype heterojunction displayed good recyclability, since 95.3% of catalytic activity was maintained after the 5th cycle. The method presented here was facile, economic and environmentally benign, thus it was highly attractive for the application in environmental remediation.

Fabrication of flexible superhydrophobic films by lift-up soft-lithography and decoration with Ag nanoparticles.

Superhydrophobic films with excellent flexibility have been fabricated by combining the lift-up soft-lithography technique and chemical reduction of [Ag(NH(3))(2)](+) ions to Ag nanoparticles (NPs) on the surface of silica spheres which are patterned on the polydimethylsiloxane (PDMS) films. Scanning electron microscopy (SEM) images reveal the presence of raspberry-like hierarchical structures on the PDMS films. The influence of the amount of Ag NPs and the size of the silica spheres on the wettability of the soft films is investigated carefully. Because PDMS films are elastomeric materials, our superhydrophobic films offer great flexibility. The resulting films can be easily transferred from one substrate surface to another without destroying their superhydrophobicity. These flexible and superhydrophobic films can be used repeatedly to satisfy a wide range of applications.

One-step preparation of reduced graphene oxide aerogel loaded with mesoporous copper ferrite nanocubes: A highly efficient catalyst in microwave-assisted Fenton reaction.

Heterogeneous Fenton reaction is an attractive method for degradation of organic pollutants due to its high efficiency and non-selectivity and it also causes no secondary pollution. However, low degradation rate and poor recyclability of the catalysts limit its applications for water purification. To overcome this, herein, copper ferrite/reduced graphene oxide (CF/rGO) aerogel was prepared by a one-step hydrothermal method, as a highly efficient catalyst for the microwave-assisted Fenton reaction (MAFR). Under optimal conditions (500 W of microwave power, 600 µL of H2O2, 15 mg of catalyst, and 30 mg/L of RhB), the degradation efficiency of CF/rGO aerogel at 1.0 min (95.7%) was higher than that of reference samples at 3.0 min. Thermodynamical study showed the activation energy, enthalpy change, entropy change, and Gibbs free energy change were 0.73 kJ/mol, -49.5 kJ/mol, -0.135 kJ/mol·K, and -6.8 kJ/mol, respectively, indicating that MAFR was an endothermic and non-spontaneous process.Radical trapping experiments showed that OH, O2-, and h+ played a combined role in RhB degradation. Besides high catalytic activity, CF/rGO aerogel also displayed good reusability, showing removal efficiency of 87.4% after 5 cycles. The high efficiency, good reusability, and simple process make CF/rGO aerogel a promising catalyst for wastewater treatment.

Preparation of reduced graphene oxide nanosheet/FexOy/nitrogen-doped carbon layer aerogel as photo-Fenton catalyst with enhanced degradation activity and reusability.

In this manuscript, a novel reduced graphene oxide nanosheet/FexOy/nitrogen-doped carbon layer (rGS/FexOy/NCL) aerogel with FexOy NPs sandwiched between rGS and NCL was prepared via a two-step method. Their catalytic performance was evaluated in a photo-Fenton degradation of rhodamine B. It was found that rGS/FexOy/NCL aerogel represented higher degradation activity than the sum of rGS/NCL support and FexOy NPs, suggesting synergistic effect was established between support and reactive species. The degradation activity was investigated on the basis of aerogel usage, FexOy loading, H2O2 dosage, pH value and RhB concentration. To test stability and reusability, leaching experiments, cyclic experiments and structural analysis were carried out. Based on inhibitor experiment and intermediate detection, a possible catalytic mechanism and degradation pathway of RhB were proposed.

One-step preparation of nanobeads-based polypyrrole hydrogel by a reactive-template method and their applications in adsorption and catalysis.

In this manuscript, nanobeads-based polypyrrole (PPy) hydrogel was prepared by a reactive-template method in one-step. Fe3O4 nanoparticles were selected as reactive-templates, which not only acted as the oxidants to initiate polymerization of pyrrole monomer, but also guided the growth of polymer chains. No surfactants were involved in whole preparation procedure, leading to a superior purity of products. Because PPy hydrogels were obtained by cross-linking individual nanobeads, they have bridged nano-dimension and macro-dimension together; thus displayed a three-dimensional hierarchical porous structure. By taking advantage of structural merits, PPy hydrogels exhibited large surface area and plenty of interconnected channels, which made them act as good candidates for adsorbents of rhodamine B (RhB). During the adsorption experiment, their adsorption kinetics were carefully investigated. In comparison tests, their equilibrium adsorption capacities were higher than that of referenced PPy (R-PPy) hydrogels prepared by a classical oxidation polymerization. In addition to be used as adsorbent, PPy hydrogels could serve as support to load Pd nanoclusters. During the catalytic reduction of RhB with NaBH4 as reducing agent under the same Pd loadings, PPy/Pd hydrogels displayed better catalytic activity than that of R-PPy/Pd hydrogels, and their rate constant and turnover frequency was 12 and 4.8 times higher than that of the latter.

Preparation of SiO2@polystyrene@polypyrrole sandwich composites and hollow polypyrrole capsules with movable SiO2 spheres inside.

In this paper, we describe a flexible method for preparing conducting building blocks: SiO2@polystyrene@polypyrrole sandwich multilayer composites and hollow polypyrrole (PPy) capsules with movable SiO2 spheres inside. First, SiO2@polystyrene (PS) core/shell composites were synthesized, and then SiO2@PS@PPy sandwich multilayer composites were prepared by chemical polymerization of pyrrole monomer on the surface of SiO2@PS composites. Furthermore, hollow polypyrrole capsules with movable SiO2 spheres inside were obtained after removal of the middle PS layer. The diameter of sandwich multilayer composites could easily be controlled by adjusting the dosage of pyrrole monomer. The conductivities of composites increased with the increase of PPy content. After the insulating PS layer was selectively etched, the conductivities of hollow capsules with movable SiO2 spheres inside were much higher than those of the corresponding sandwich multilayer composites.

Preparation of Magnetically Recyclable Yolk/Shell Fex Oy /PdPt@CeO2 Nanoreactors with Enhanced Catalytic Activity.

Noble metal nanoparticles (NPs) have recently received considerable attention from researchers working in the field of catalysis. However, the development of new methods allowing these materials to reach their maximum catalytic properties remains challenging. Nanoreactors could lead to dramatic improvements in activity with the help of the intrinsic confinement effect. In this study, we designed a series of yolk/shell Fex Oy /PdPt@CeO2 composites, where the Fex Oy NPs acted as a movable core, allowing for the uniform distribution of the PdPt alloys on the inner surface of the CeO2 shell. The high porosity and existence of hollow voids in the CeO2 shell allowed these Fex Oy /PdPt@CeO2 composites to be used as nanoreactors in catalytic reactions. As well this confinement effect, we identified two structural features that led to enhanced catalytic activity, including (i) the replacement of monometallic NPs with a bimetallic PdPt alloy and (ii) the replacement of a chemically inert support with a reactive CeO2 shell. The resulting nanoassembled catalysts displayed higher activities toward the catalytic reduction of dyes than the reference samples. Moreover, these catalysts were readily recovered and reused because of the magnetic Fex Oy core.