Ball Milling Method Research Articles

Prediction of wear properties of CaO and MgO doped stabilized zirconia ceramics produced with different pressing methods using adaptive neuro fuzzy inference systems

AbstractThe present paper describes the fabrication and wear behaviour of CaO and MgO added stabilized zirconia (ZrO2) ceramics produced by powder metallurgy method were examined and modelling with artificial neural networks was studied using the experimental data obtained. CaO/MgO added stabilized zirconia ceramics were fabricated by using a combined method of ball milling, cold pressing ‐ cold isostatic pressing and sintering. CaO and MgO in different amounts (0–8 %mole) were mixed with zirconia. These mixtures were prepared by mechanical alloying method. The green compacts were sintered at 1600 °C. The wear experimental results obtained were converted into data suitable for modelling with artificial neural networks. Wear Load, wear time, CaO and MgO data were used as artificial neural networks input variables. The amount of wear according to the pressing method was taken as the output variables of artificial neural networks. An artificial neural networks was established for the prediction of wear properties of zirconia pressed using the adaptive neuro fuzzy inference systems (ANFIS) learning technique. As a result, a high R2 value of 0.9187 for cold pressing samples and 0,9449 for cold isostatic pressing samples was achieved based on the approach of comparing the success of the model with the test data set and the result produced.

Fabrication of ZnO-quantum dot hybrid nanocomposites with enhanced light scattering and emission characteristics for micro LED display applications

Herein, a facile method is reported to fabricate a color conversion layer comprised of zinc oxide nanoparticles (ZnO NPs) and quantum dots (QDs) for micro-light emitting diode (μ-LED) displays. Further, 11-mercaptoundecanoic acid (MUA)-treated ZnO NPs (ZnO@MUA NPs) are synthesized via a high-energy ball milling method, which bypasses the need for complex synthesis processes and enables functional groups to attach to the surface, thereby facilitating the formation of ZnO@MUA NPs-QD hybrid composites (ZQCs). The particle size, surface characteristics, elemental composition, and binding energy are analyzed to elucidate the reaction mechanism and to confirm that the fabricated ZQC exhibits a chemically bonded structure. To ascertain the optimal molar concentration for incorporating the QDs, parameters such as QD bonding efficiency, quantity of bonded QDs, interparticle distance, and absolute photoluminescence quantum yield (PLQY) are evaluated as functions of molar concentration. As a result, the optimal molar concentration is found to be 1930 nM, giving a bonding efficiency of 96.8 %, along with the bonded QDs of 1.51 × 1011 per a unit area of 1 mm2 of ZnO NPs and a PLQY of 64.8 %. Furthermore, comprehensive optical analyses are performed to assess the potential of the ZQC as a color conversion material for μ-LED displays, in comparison to the use of pristine QDs and silica NP-QD composites.

Composite xNiFe2O4/(1-x)SrFe12O19 oxygen carriers for chemical looping reforming of bioethanol coupled with water splitting to coproduce syngas and hydrogen

Sr–Fe oxides are suitable oxygen carriers (OCs) with excellent cyclic stability. However, the moderate redox activity causes a deficiency in H2 yield in chemical looping reforming coupled with water splitting (CLR-WS) process. Herein, we designed and prepared the composite xNiFe2O4/(1-x)SrFe12O19 OCs by ball milling method, which exhibited both high redox activity and high cyclic stability during reactions. A series of characterizations showed that the introduction of NiFe2O4 promoted the oxygen vacancy formation and the release of lattice oxygen, facilitating the reforming of bioethanol in fuel reactor (FR). During CLR-WS process, a high carbon conversion of 79.20 % and a H2 yield of 13.23 mmol/g OC were achieved by 3Ni7Sr OC at 800 °C, outperforming that of the conventional SrFe12O19 OC. Moreover, the severe carbon deposition and sintering issues inherent to NiFe2O4 were avoided due to the presence of Sr. All Sr-containing composite OCs showed H2 purity exceeding 99.26 % and excellent cycling stability with no apparent activation of oxygen transport capacity over 3000 min redox reactions.

Improving oxygen resistance of hydrogen storage alloys with graphite or nickel coating

A series of graphite- and Ni-coated hydrogen storage alloys were prepared with simple ball-mill method, and their hydrogen storage behaviors were characterized and compared with bare alloys. The results showed that the oxygen resistance of the graphite-coated materials increased, while the hydrogen storage kinetics decreased significantly. For the Ni-coated materials, oxygen resistance was noticeably improved and excellent oxygen resistance was achieved with sufficient Ni loading, while the hydrogen storage capacity and kinetics were also maintained or even improved. Our results show that the elemental coating method is an effective method to improve the oxygen resistance of hydrogen storage alloys, which brings about new insights into the design of these materials.

Mxene-supported NbVH nanoparticles as efficient catalysts for reversible hydrogen storage in magnesium borohydride

Bimetallic niobium vanadium hydride nanoparticles (NbVH NPs) anchored on Ti3C2 were synthesized using a facile ball milling method as an effective catalyst for the dehydrogenation kinetics and reversibility of Mg(BH4)2. It was found that the onset dehydrogenation temperature of the Mg(BH4)2 + 30NbVH NPs@Ti3C2 composite was 105.7 °C and released 9.07 wt% of hydrogen at 330 °C, while undoped Mg(BH4)2 only released 4.2 wt% of H2 from 248 °C to 330 °C. Additionally, the Mg(BH4)2 + 30NbVH NPs@Ti3C2 composite achieved remarkable hydrogen release of over 9.44 wt% at a temperature as low as 230 °C, indicating unexpected dehydrogenation kinetics. In the reversible hydrogen desorption tests, Mg(BH4)2 + 30NbVH NPs@Ti3C2 released 5.98 wt% of H2 in the 2nd cycle at 250 °C and maintained a reversible capacity of 4.35 wt% after 10 cycles, demonstrating a remarkable enhancement in reversibility. The enhancement in the dehydrogenation kinetics of Mg(BH4)2 could be attributed to the greatly reduced activation energies from 343 kJ·mol−1 and 138.3 kJ·mol−1 to 103.7 kJ·mol−1 and 124 kJ·mol−1. Investigations on the evaluation of catalyst and Mg(BH4)2 during reversible hydrogen storage have revealed that NbVH NPs actually acted as a “bidirectional hydrogen pump”, facilitating both the hydrogen release and uptake from Mg(BH4)2. This strategy of multi-component hydrides may show a new way to design effective catalysts for solid-state hydrogen storage materials.

Characterization of bamboo shoot cellulose nanofibers modified by TEMPO oxidation and ball milling method and its application in W/O emulsion

It has rarely been reported that the modification of bamboo shoot nanofibers by oxidation combined with physical and applied in food emulsions. In this study, the combination of 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO)-mediated oxidation and the ball milling technique was employed to prepare bamboo shoot cellulose nanofibers (TOCNF) for W/O emulsions. A comparative study of the properties and structures of CNF prepared only by ball milling and TOCNF prepared by oxidation-ball milling was carried out, and a preliminary structural and rheological study of their application to emulsions was carried out. The results showed that TOCNF had higher water holding, swelling, and oil holding properties, cholesterol and glucose adsorption capacity than CNF. The combination of oxidative pretreatment and ball milling resulted in a dense entangled network structure, uniform particle size distribution, and high zeta potential value of TOCNF. The higher crystallinity of the TOCNF (68%) resulted in improved thermal stability. In addition, compared with the CNF-stabilized emulsion, with TOCNF dispersion as the internal aqueous phase, the emulsion droplets had a more uniform particle size distribution (6.61 ± 3.59 μm), higher gel strength, and thixotropic resilience of up to 71.24%. Thus, TEMPO oxidation combined with the ball milling method can be an effective means to improve nanofibers and provide a theoretical basis for expanding the application of bamboo shoot cellulose resources in the food colloid field.

Assembly of root-associated bacterial community and soil health in cadmium-contaminated soil affected by nano/bulk-biochar compost associations

Biochar (BC) has been proven effective in promoting the production of safety food in cadmium (Cd)-polluted soil and the impact can be further enhanced through interaction with compost (CM). However, there existed unclear impacts of biochar with varying particle sizes in conjunction with compost on microbiome composition, rhizosphere functions, and soil health. Hence, in this study, two bulk-biochar derived from wood chips and pig manure were fabricated into nano-biochar using a ball-milling method. Subsequently, in a field experiment, the root-associated bacterial community and microbial functions of lettuce were evaluated in respond to Cd-contaminated soil remediated with nano/bulk-BCCM. The results showed that compared to bulk-BCCM, nano-BCCM significantly reduced the Cd concentration in the edible part of lettuce and the available Cd in the soil. Both nano-BCCM and bulk-BCCM strongly influenced the composition of bacterial communities in the four root-associated niches, and enhanced rhizosphere functions involved in nitrogen, phosphorus, and carbon cycling, as well as the relative abundance and biodiversity of keystone modules in rhizosphere soil. Furthermore, soil quality index analysis indicated that nano-BCCM exhibited greater potential than bulk-BCCM in maintaining soil health. The data revealed that nano-BCCM could regulate the Cd concentration in lettuce shoot by promoting microbial biodiversity of keystone modules in soil-root continuum and rhizosphere bacterial functions. These findings suggest that nano-biochar compost associations can be a superior strategy for enhancing microbial functions, maintaining soil health, and ensuring crop production safety in the Cd-contaminated soil compared to the mix of bulk-biochar and compost.

Study on the microwave absorption properties of FeCoNiCrMn/PLA 3D printed composites

The work in this paper is dedicated to the study of wave-absorbing materials for applications in extremely harsh environmental conditions such as seawater and oil. In this paper, FeNiCrMn high-entropy alloy material with corrosion resistance and polylactic acid (PLA) material with high strength and high modulus were used to prepare more environmentally adaptable FeNiCrMn/PLA electromagnetic(EM) microwave-absorbing materials by two-step method of ball milling and melt extrusion.The physical phases, microscopic morphology, EM parameters and mechanical performance of FeCoNiCrMn/PLA composites were characterized using XRD, SEM, Vector Network Analyzer and Universal Testing Machine respectively. The microwave-absorbing properties of FeCoNiCrMn/PLA composites were investigated, and the effects of their components and micro-morphology on the microwave-absorbing and mechanical performance were discussed. The results show that when the FeCoNiCrMn content reaches 25 wt% and the thickness is 4.5 mm, the minimum reflection loss of FeCoNiCrMn/PLA composites reaches −24.58 dB, and the effective microwave-absorbing bandwidth is 2.51 Ghz. The maximum tensile strength and elongation at break of the composites could reach 23.83 MPa and 7.12 %, respectively. The microwave-absorbing ability of FeCoNiCrMn composites is mainly due to their rich EM loss mechanisms, including dielectric losses such as dipole polarization, interface polarization, defect-induced polarization, etc., as well as magnetic losses such as natural resonance, exchange resonance, and eddy current losses. Finally, the wide-angle microwave-absorbing characteristics of FeCoNiCrMn/PLA 3D-printed composites were investigated, the results showed that the composites with FeCoNiCrMn content of 25 wt% had Radar Cross Section (RCS) values lower than −10 dBm² within the microwave incidence angle of −90° < θ < −6° and 6° < θ < 90°, which indicated that the composites had wide-angle microwave-absorbing capability. The materials have microwave-absorbing properties along with a certain degree of mechanical strength, and at the same time have good environmental adaptability. The FeCoNiCrMn/PLA composite wire can be used in FDM technology to prepare structural microwave absorbers, realizing the integration of “material-design-manufacturing”, which has a broad application prospect in the field of EM microwave absorption and 3D printing.

Use of rice straw nano-biochar to slow down water infiltration and reduce nitrogen leaching in a clayey soil

Biochar exhibits numerous advantages in enhancing the soil environment despite a few limitations due to its lower surface energy. Nanomodified biochar combines the advantages of biochar and nanoscale materials. However, its effects on water infiltration and N leaching in a clayey soil remain unclear. Therefore, this study prepared rice straw nano-biochar by a ball milling method, and investigated its physicochemical properties and effects of bulk biochar and nano-biochar at various addition rates (0 %, 0.5 %, 1 %, 2 %, 3 %, and 5 %) on wetting peak migration, cumulative infiltration, water absorption and retention, and N leaching. The results showed that, compared with bulk biochar, nano-biochar presented a more abundant pore structure with an increase in specific surface area of approximately 1.5 times, accompanied by a 20 % increase in acid functional groups. Compared with those for clayey soil without biochar addition, the wetting front migration time was increased by 10.2 %–123.9 % and 17.0 %–257.9 %, and the cumulative infiltration volume at 60 min was decreased by 26.0 %–48.4 % and 14.1 %–62.4 % for bulk biochar and nano-biochar, respectively. The parameter S of Philip model and the parameter a of Kostiakov model for nano-biochar were lower than those for bulk biochar, whereas the parameter b of Kostiakov model was greater, indicating that nano-biochar decreased initial soil infiltration rate and increased attenuation degree of the infiltration rate. Nano-biochar increased water absorption by 8.03 % and subsequently enhanced water retention capacity relative to bulk biochar. In addition, bulk biochar and nano-biochar reduced NH4+-N leaching by 3.0 %–13.1 % and 5.7 %–39.2 %, respectively, and NO3−-N leaching by 2.7 %–3.6 % and 9.0 %–43.3 %, respectively, by decreasing N concentration and leachate volume relative to those with no biochar addition. This study provides new knowledge for nano-biochar application in a clayey soil.

Amorphous Boron Nitride Nanosheet‐Based Solid State Electrolytes with High Ionic Conductivity

AbstractAmorphous boron nitride nanosheets, with natural electrical insulation, outstanding chemical stability and mechanical properties, are introduced as a matrix to be incorporated with lithium bis (trifluoromethanesulfonyl) imide (LiTFSI) and polymer polyvinylidene fluoride‐hexafluoropropylene copolymer (PVDF‐HFP), for constructing a novel composite solid‐state electrolyte by a simple solution‐casting method. Amorphous boron nitride nanosheets are produced via a combination method of ball milling and pure water exfoliation. The obtained composite solid‐state electrolyte containing 40 % (mass fraction) PVDF‐HFP shows a high lithium ion conductivity (1.936×10−3 S cm−1) and lithium ion transference number (0.47), and a wide electrochemical stability window (5 V) at room temperature. The LiFePO4/Li based all solid‐state battery, consisting of the composite solid electrolyte (40 % PVDF‐HFP), delivers a capacity of 128.1 mAh g−1, a Coulombic efficiency of 99.79 % after 500 cycles and a capacity retention rate of 94.5 % at 1.0 C and 25 °C. The composite solid electrolyte (40 % PVDF‐HFP) can maintain flat and stable stripping/plating plateaus for over 800 hours in symmetrical cells. The amorphous boron nitride nanosheets with high lithium ion conductivity are employed to construct solid‐state electrolytes, which is important significant for the development of high energy density, high safety, and long cycle life all‐solid‐state lithium‐ion batteries.

Metal ion-crosslinked thermoconductive sugar-functionalized graphene fluoride-based cellulose papers with enhanced mechanical properties and electrical insulation

Thermally conductive papers with electrical insulation and mechanical robustness are essential for efficient thermal management in modern electronics. In this study, we introduced a metal ion-assisted interfacial crosslinking strategy to strengthen sugar-functionalized graphene fluoride (SGF) and cellulose nanofibers (CNF) by hydrogen bonding and metal ion crosslinking that leads to simultaneous enhancements in thermal conductivity and mechanical properties. The facile sugar-assisted ball-milling exfoliation method was developed to achieve the exfoliation of graphite fluoride and hydroxyl group functionalization on the surface of graphene fluoride. Thanks to the good dispersibility of the SGF sheets in water, the flexible SGF/CNF composite papers with hydrogen bonding were prepared via vacuum-assisted filtration. We introduced hydrogen bonding and metal ion crosslinking into SGF/CNF papers to obtain densely packed composite papers. Ca2+ or Al3+ ion-crosslinked SGF/ CNF papers exhibited superior thermal and mechanical properties owing to hydrogen bonding and metal ion crosslinking. SGF/CNF-Ca2+ and SGF/CNF-Al3+ papers at 50 wt% of SGF yield in-plane thermal conductivities of 72.93 and 75.02 W m–1 K–1, and tensile strengths of 121.5 and 135.7 MPa, respectively. A thermal percolation value was observed at 12.6 vol% of SGF filler content. In addition, the SGF/CNF papers exhibited electrical insulation properties. These remarkable characteristics of the metal ion-crosslinked SGF/CNF papers are attributed to the densely packed structures caused by the strong interfacial interactions from hydrogen bonding as well as metal ion-crosslinking that could promote phonon transport. High-performance metal ion-crosslinked SGF/CNF papers with these fascinating advantages offer great potential for the thermal management of flexible electronics.

Al–B4C-(Gd, Gd2O3) composite materials: Synthesis and characterization for neutron shielding applications

In this study, Al–20%B4C-x%Gd and Al–20%B4C-x%Gd2O3 (x = 1, 3, 5) composite powders were prepared using a high-energy planetary ball milling method to enhance the physical properties of Al–B4C neutron shielding composites. The prepared powders were subjected to uniaxial cold compaction at 500 MPa, resulting in cylindrical specimens. Subsequently, the specimens were sintered in a tube furnace at 600 °C for 1 h under an Ar atmosphere to prevent oxidation. The microstructure of the resulting composites was characterized using X-ray diffraction (XRD) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM/EDX). Archimedes density, hardness, and corrosion tests were performed on the compacted samples. Moreover, the composite's thermal and fast neutron absorption rates were calculated using the MCNP6.2 simulation code. The neutron equivalent dose rate was experimentally determined using the Am–Be neutron source. The simulation results demonstrated that the composite materials containing Gd exhibited the highest thermal neutron absorption rate, while those containing Gd2O3 demonstrated the highest fast neutron absorption rate. This research contributes valuable insights into the design and utilization of neutron-absorbing materials with suitable mechanical properties.

Tightly confined tellurium nanocrystals in few-layer expanded graphite with Te–C bonds toward highly reversible zinc storage

Tellurium (Te) has great potential as high-performance cathode materials for aqueous zinc-ion batteries (AZIBs) owing to high electronic conductivity and volumetric capacity. Nevertheless, its poor utilization and large volume expansion result in insufficient rate and cycle performances, thereby, impeding practical application. Herein, a kind of Te/carbon composite was prepared via a ball-milling method, in which Te nanocrystals were tightly confined in few-layer expanded graphite (EG) with Te–C bonds (denoted as Te@EG). In addition to maintaining structural stability, such unique nanocomposite shows abundant electrochemically active sites and efficient charge transfer channels, which is beneficial to the utilization of Te. More importantly, the Te–C bonds between Te nanocrystals and EG can enhance the adsorption of Zn2+ and reduce the Zn2+ migration barrier, which contributes to promoting electrochemical kinetics. Consequently, the Te@EG cathode for the AZIBs exhibits sufficient specific capacity (412 mAh g–1 at 0.1 A g–1), high-rate performance (284 mAh g–1 at 3 A g–1), and reliable cycling stability (94% capacity retention at 1 A g–1 after 500 cycles). Furthermore, the soft-packaged Zn//Te@EG battery delivers excellent flexibility and cycling stability. This study offers a perspective on rational design of Te-based cathodes for practical AZIBs.

One-step hydrothermal synthesis of CeVO4/bentonite nanocomposite as a dual-functional photocatalytic adsorbent for the removal of methylene blue from aqueous solutions

Cerium vanadate/modified bentonite (CeVO4/mbt) nanocomposite with different composition percentages was synthesized through a simple one-step hydrothermal method at 180 ℃, and then its photocatalytic activity was evaluated by decolorizing methylene blue (MB) in an aqueous solution under light exposure. In order to increase the surface area as an important parameter in photocatalytic processes, bentonite was modified by ball mill method. The structural and optical properties of the synthesized composites were determined by XRD, FT-IR, DRS, FESEM, EDS, and BET measurements. XRD and EDS results confirmed the successful synthesis of pure CeVO4. FESEM images and EDS mapping showed a proper distribution of rice-like CeVO4 nanoparticles on bentonite. The removal efficiency of MB with only 0.1 g of CeVO4/mbt nanocomposite in 15 min was about 99%, which is significant compared to neat bentonite and pure CeVO4 with efficiency of 30% and 57%. The mentioned nanocomposite followed the first-order kinetics, had a reaction rate constant equal to 0.1483 min–1, and showed acceptable stability in five consecutive cycles.

Enhanced Hard Magnetic Performance for MnBi Green Powders

Mn55Bi45 melt - spun ribbons were prepared by using the melt-spinning technique followed by annealing in Ar/5%H2 gas mixture. The in-situ formation of ferromagnetic phase (denoted as LTP) of MnBi was observed by the multi-section cycled Differential Scanning Calorimetry (DSC) method. It was found that, the optimal annealing temperature range for forming MnBi LTP is 250 – 280 oC. The prolonging annealing time increases the content of MnBi LTP leading to the increase of saturation magnetization Ms but paid by the drop of the intrinsic coercivity iHc. The MnBi green powders were prepared by the Low Energy Ball Milling method (LEBM) in N2 liquid. The maximum energy product of MnBi green powders is estimated about 10.8 MGOe.

Optimizing interfacial modification for enhanced performance of Na3V2(PO4)3 cathode in sodium-ion batteries

A novel cathode material, Na3V2(PO4)3C@CNT (NVP/C@CNT), was designed and synthesized by a low-temperature solid-phase drying ball milling method. The nanoparticles are covered by an amorphous carbon layer, and simultaneously enveloped and embedded by carbon nanotubes on the surface. Consequently, a carbon network consisting of carbon nanotubes and amorphous carbon layers is formed in the material. Notably, no phase transition during the intercalation process of sodium ions, confirming the stable crystal structure, which ensures the stability and reversibility of the large-capacity cathode in the large-volume change. The addition of CNTs can regulate the size of NVP particles, increase the contact area between NVP and electrolyte, leading to an enhancement in the sodium ion diffusion coefficient. The NVP/C@CNT electrode exhibits a capacity of 114.5 mA h g−1 at 0.1 C. After 2650 cycles, the discharge capacity retention rate is 98.2 % at 10 C. Even at 20 C, the discharge capacity is still 93.3 mA h g−1 after 2710 cycles, with a retention rate of 99.5 %. This work provides a feasible approach for the design of low-cost, long-life, high-performance cathode materials for sodium-ion batteries.

Microstructure Analysis and Powder Bed Fusion of Inconel 738 Powder Materials Mixed with Nano-Sized Ceramic Powders

Powder materials strengthened by oxide dispersion are generally made by in-situ method; direct oxide dispersing in matrix powders during atomization. There is also ex-situ method; oxides dispersing by mixing with matrix powders. In this study powder mixtures (Inconel 738 matrix powder + SiO2 powder + Al2O3 powder) were mechanically manufactured by ex-situ process, a lowenergy ball milling method. Then, specimens of the as-mill powders were manufactured by laser powder bed fusion (L-PBF) method and spark plasma sintering (SPS) process. The microstructures of each prepared specimen were compared according to process variables. SEM, EDS, XRD, and Electron Backscatter Diffraction (EBSD) analyses were applied in this study.

Clean water harvesting and power generation by solar-absorbing Germanium@k-carrageenan evaporator demonstrating superior energy conversion

The deterioration of climate exacerbates the freshwater crisis. Solar-thermal interfacial evaporation, using sunlight as a driving energy source, is a promising approach to provide an effective solution to freshwater shortages. However, the low energy conversion efficiency and expensive evaporator manufacturing are still to be resolved. Herein, a strategy of clean water harvesting by solar-absorbing germanium@k-carrageenan (Ge@CA) evaporator demonstrating superior energy conversion is proposed. The Ge nanoparticles exhibit a significant solar absorption of 92.33% to achieve efficient solar-thermal conversion. The CA hydrogel provides three-dimensional water transmission channels to the evaporating surface. Meanwhile, the Ge nanoparticles can be fabricated by a facile ball-milling method. The CA as a cheap biomass can be easily interacted with KCl to obtain the porous hydrogel. Taking the advantages of Ge nanoparticles and CA hydrogel, the Janus-type Ge@CA hydrogel evaporator can achieve an evaporation rate of 2.88 kg m−2·h−1 and a solar-vapor conversion efficiency of 82.65% under 1 sun irradiation. Furthermore, the evaporator can produce thermoelectricity with the output voltage of 140.95 mV and the short-circuit current of 13.32 mA, yielding a power of 1.17 W m−2. This reported solar device has huge potential for cutting-edge solar harvesting and usage.

Effect of ball milling time on Sr0.7Sm0.3Fe0.4Co0.6O2.65 perovskites and their application as semiconductor layers in dye-sensitized solar cells

The practical utilization of TiO2 as a semiconductor in dye-sensitized solar cells (DSSCs) has been set back by poor visible light absorption, high charge carrier recombination, and low electrical conductivity, which reduce the power conversion efficiency (PCE) and sustainability of the device. In this respect, perovskites with excellent properties, such as large surface area, good optical properties, high electrical conductivity, and superior electrochemical stability, have recently emerged as promising alternatives capable of overcoming the drawbacks of TiO2. Herein, Sr0.7Sm0.3Fe0.4Co0.6O2.65 (SSFC) perovskites were prepared via the ball milling method at various milling times of 0, 5, and 10 h, and the obtained samples were denoted by SSFC-0, SSCF-5, and SSCF-10, respectively. Increasing the ball milling time led to a significant reduction in nanoparticle size and agglomeration, which, in turn, increased the surface area and electrical conductivity of the samples. As a consequence, the SSFC-10 perovskite exhibited the smallest average particle sizes (18.9 nm) with the largest surface area (61.8 m2 g−1) and minimum defects, which allowed for efficient electron transport, resulting in the best electrical conductivity of 49.8 S cm−1. Ultimately, DSSCs fabricated using SSFC-10 semiconductor layers achieved an optimum PCE of 6.01 %, which is an improvement of 8.67 %, 1.1 %, and 6.56 % for SSFC-0 (3.69 %), SSFC-5 (4.96 %), and TiO2 (5.64 %), respectively. Thus, varying the ball milling time can be used as an effective technique to tailor the physicochemical properties of SSFC to suit desired applications, particularly the fabrication of highly efficient and sustainable DSSC semiconductor layers.

Visible‐Light Photoreforming of Biomass Derivatives through MBi2O4‐P25 Heterostructures: Study of the Influence of Metals (M = Cu, Ni, Zn, Co)

AbstractIn this work, MBi2O4‐P25 (M = Cu, Ni, Co, Zn) composites are successfully synthesized by a simple ball milling method by varying some parameters (rotation speed, rotation time, metal/TiO2 ratio) to optimize the preparation conditions. The noble metal‐free TiO2‐based photocatalysts are used to carry out the partial oxidation of glucose and glycerol with the simultaneous H2 production under simulated solar light irradiation. Starting from glucose, 2.6 mmol of H2 are obtained with a conversion of 34%, along with arabinose, formic acid and gluconic acid as main intermediates. By using glycerol, 3.2 mmol of H2 are produced, with 17% conversion and the production of dihydroxyacetone and glycolic acid. The composites exhibit higher activity than pure P25 and CuBi2O4 (CBO). The produced H2 amount is comparable to that reported in the literature by using Pt–TiO2 photocatalysts. This study offers a paradigm for the future design of bifunctional photocatalysts for simultaneous noble metal‐free H2 production and biomass valorization under environmentally friendly conditions with a possible scale up of the process.