Simple Solvent Evaporation Method Research Articles

Development of eutectics of pioglitazone with citric acid and its effect on crystallite properties and dissolution.

Eutectics of pioglitazone were developed using citric acid (CA) as the co-former, and the effect on crystallite properties and dissolution has correspondingly been studied. Pioglitazone-citric acid eutectics (PC1, PC2, PC3, and PC4) in different molar ratios (3:1, 3:2, 1:1, and 3:4 respectively) were prepared by simple solvent evaporation method. Difference in dislocation density and strain value of the eutectics were observed, and the maximum strain value of PC1 might be due to the highest deformation activity compared to PC2, PC3, and PC4. Carbonyl-thiazolidine or carboxyl-pyridine weak bond formation might be the reason of producing eutectics of PGZ-CA rather than cocrystal with a docking score of - 2.2 Kcal/M. Likewise, lowest particle size was found with PC1 rather than that of pure PGZ and other eutectics. PC1 demonstrated highest dissolution of drug (68 %) rather than other eutectics (54 to 61 %) and PGZ (44 %) after 360 min.

Full colour luminescence tuning including white light from a mixed lanthanide activated metal-organic complex

In an attempt, metal–organic compounds of rare earth ions with 2,6-pyridinedicarboxylic acid (H2pydc) were synthesized and characterized. This paper summarizes the synthesis, characterization, and multicolour luminescence behaviour of a europium and terbium co-doped metal–organic compound (MOC) of formula [Y1.972Eu0.013Tb0.014(pydcH)6]·3H2O, 1 {H2pydc = 2,6-pyridinedicarboxylic acid}. The synthesis was performed by simple solvent evaporation method. We have also synthesized a pure yttrium based compound [Y2(pydcH)6]·3H2O, 1a following a similar procedure. The powder XRD patterns indicated that 1 and 1a were new materials; the patterns being entirely consistent with the simulated XRD pattern generated based on the structure of pure Eu compound determined using the single-crystal XRD. Compound 1 was well characterized by SEM, IR, TGA, EDX, and EDX elemental mapping analysis. Compound 1 showed different colour upon the variation of the excitation wavelength from 260 nm to 385 nm.

A novel noble-metal-free FeS2/Mn0.5Cd0.5S heterojunction for enhancing photocatalytic H2 production activity: Carrier separation, light absorption, active sites

BackgroundThe development of efficient and noble-metal-free photocatalysts is greatly essential for photocatalytic hydrogen production. However, the photocatalytic activity of a single photocatalyst is usually limited for various reasons. MethodsHerein, FeS2/Mn0.5Cd0.5S (FSMCS) heterojunctions were constructed by a simple solvent evaporation method. The morphological characterizations revealed a raspberry-like hollow microsphere structure for FeS2 and irregular granularity for Mn0.5Cd0.5S. Photoluminescence (PL) and electrochemical experiments indicated that the FSMCS composite effectively facilitated the separation of photogenerated electron-hole pairs. The UV–vis diffuse reflectance spectrum (DRS) showed that, in FSMCS composite, the visible light absorption range was effectively expanded to the full visible light. Significant findingsExcellent photocatalytic activity in FSMCS heterojunctions without loading noble metals because FeS2 could serve an active site for hydrogen production. The optimum FSMCS composite had excellent photocatalytic hydrogen production activity (6.1 mmol·g−1·h−1), which was 5.6 and 2.3 times higher than that of the pristine Mn0.5Cd0.5S (1.1 mmol·g−1·h−1) and Mn0.5Cd0.5S-1 %Pt (2.7 mmol·g−1·h−1). Meanwhile, in four round-robin tests, the activity of the 5FSMCS photocatalyst did not significantly decrease. This work proved that combining Mn0.5Cd0.5S and non-precious metal cocatalysts to construct heterojunctions is a promising strategy for photocatalytic hydrogen production.

Formulation and evaluation of dabigatran loaded microballoons for prolonged drug release

The objective of the present investigation was to formulate microballoons loaded with dabigatran in the polymeric core for achieving sustained release and hence improved bioavailability. Microballoons loaded with dabigatran in the polymer shell were prepared by simple solvent evaporation method using either ethyl cellulose alone or a blend of ethyl cellulose with HPMC/PVP-K30/Eudragit S100/Methyl cellulose in a fixed ratio. The percent yield of the microballoons ranged from 38.7 to 62.4% with highest yield obtained in F3. The particle size was measured using optical microscopy and the particles were observed to be spherical in shape. The particle size ranged from 28.50 ± 16.378 µm (F3) to 48.14 ± 16.748 µm (F1). The angle of repose ranged from 26.37° to 28.09° and the Carr’s index and Hausner’s ratio were in between 6.38 to 19.95 and 1.07 to 1.25 respectively. It was found that all the formulations exhibited buoyancy in the range of 61.42 to 71.71% over a period of 8h. This suggests that the formulations were able to float for sufficient time and would be able to control the release of dabigatran for longer duration. The in vitro drug release study depicted that the highest amount of drug was released from F3 (66.79%) while the lowest was released from F1 (50.27%) at the end of 8 hours of study.

Dual-Function Platform Based on Postsynthetic Functionalization of a Water-Stable Hydrogen-Bonded Organic Framework: Ratiometric Sensing of Nicotine and Cotinine and Dynamic Anticounterfeiting for Information Encryption.

Nicotine and its major metabolite cotinine are widely used as markers of tobacco smoke abstinence as well as indicators of active smoking levels and the assessment of passive inhalation of tobacco smoke in nonsmokers. Therefore, using an easy-to-prepare sensing platform that can provide a rapid, highly sensitive response for the simultaneous detection of salivary nicotine levels and urinary cotinine levels is especially crucial for helping heavy cigarette smokers quit smoking and protecting public health. Hydrogen-bonded organic frameworks, as a novel class of porous crystalline materials, show immense potential for functional modification and optical sensing. Herein, a new HOF was prepared by a simple solvent evaporation method, and a dual-emitting material Eu(bpy)@HOF-215(1) was obtained by the postsynthetic modification of HOF by lanthanide luminescent complexes, which maintains favorable structural stability and introduces the characteristic emitting of Eu, allowing use as a ratiometric fluorescent sensor for salivary nicotine and urinary cotinine, with a limit of detection of nicotine of 0.045 μM in saliva and a limit of detection of cotinine of 0.591 μM in urine. Furthermore, luminescent inks based on HOF-215 have been fabricated based on the photoresponse variations of 1 to NIC and COT, which enables the multilevel encryption and decryption of information, in a dynamic and recyclable process. This work not only synthesizes a novel blue HOF but also provides a representative successful case of a dual-function platform for simultaneous application to ratiometric sensing and dynamic anticounterfeiting.

Strongly bonded CFx@S composite assisting the long-cycle stability of Li-S battery

Lithium‑sulfur battery (LSB) has drawn extensive concentration for its high energy density. Nevertheless, the “shuttle effect” of polysulfides leads to inferior sulfur utilization and short service life. Herein, CFx@S composites with a strongly bonded interface of S and CFx have been prepared by a simple solvent evaporation method. The research shows that CFx in the composites will be preferentially discharged to form F-doped carbon (F@C) conductive network and LiF, which improve the electronic and ionic conductivities of electrodes, separately. Numerous polar sites on F@C cooperate with the polar LiF to adsorb polysulfides effectively and then inhibit the “shuttle effect”. The robust F@C conductive network and the SEI film enhanced by LiF can work together to relieve the volumetric dilatation of S in the charge/discharge cycles. Profiting by the above-mentioned merits, even the as-prepared 10-CFx@S composite loads a sulfur content as high as 87.6 %, it manifests an excellent rate capability and stable cycling performance. Under a high current of 1600 mAh g−1, 10-CFx@S delivered a high capacity of 573 mAh g−1 in the initial discharge, and it remained as 334 mAh g−1 after 800 cycles with an average capacity decay of 0.052 % per cycle. This research supplies an easy and feasible approach to promote the performances of LSB.

Preparation and laser response of graphene oxide complexes for typical polynitramine energetic materials

The conflict between polynitramine energetic materials’ high energy density and its safety has been a challenge in its safe and efficient application. GO has been demonstrated to be promising materials for the regulation of energetic materials’ performance with various advanced preparation methods. However, the thermal-based performance of GO-based polynitramine energetic composites haven’t been deeply investigated. In this work, the GO@RDX and GO@CL-20 composites were obtained with the simple solvent evaporation method. GO-based polynitramine energetic composites’ structure was identified with SEM, PXRD, IR, and XPS, its thermal based performance was investigated with DSC, activation energy, and laser initiation system. This work could provide basis for the design of novel energetic composites with excellent comprehensive performance.

Antibacterial properties of antimicrobial peptide HHC36 modified polyetheretherketone.

Polyetheretherketone (PEEK) is considered to be a new type of orthopedic implant material due to its mechanical properties and biocompatibility. It is becoming a replacement for titanium (Ti) due to its near-human-cortical transmission and modulus of elasticity. However, its clinical application is limited because of its biological inertia and susceptibility to bacterial infection during implantation. To solve this problem, there is an urgent need to improve the antibacterial properties of PEEK implants. In this work, we fixed antimicrobial peptide HHC36 on the 3D porous structure of sulfonated PEEK (SPEEK) by a simple solvent evaporation method (HSPEEK), and carried out characterization tests. We evaluated the antibacterial properties and cytocompatibility of the samples in vitro. In addition, we evaluated the anti-infection property and biocompatibility of the samples in vivo by establishing a rat subcutaneous infection model. The characterization test results showed that HHC36 was successfully fixed on the surface of SPEEK and released slowly for 10 days. The results of antibacterial experiments in vitro showed that HSPEEK could reduce the survival rate of free bacteria, inhibit the growth of bacteria around the sample, and inhibit the formation of biofilm on the sample surface. The cytocompatibility test in vitro showed that the sample had no significant effect on the proliferation and viability of L929 cells and had no hemolytic activity on rabbit erythrocytes. In vivo experiments, HSPEEK can significantly reduce the bacterial survival rate on the sample surface and the inflammatory reaction in the soft tissue around the sample. We successfully loaded HHC36 onto the surface of SPEEK through a simple solvent evaporation method. The sample has excellent antibacterial properties and good cell compatibility, which can significantly reduce the bacterial survival rate and inflammatory reaction in vivo. The above results indicated that we successfully improved the antibacterial property of PEEK by a simple modification strategy, making it a promising material for anti-infection orthopedic implants.

Study on g-C3N4/BiVO4 Binary Composite Photocatalytic Materials

Recent studies have shown that the composite of semiconductor photocatalytic materials and g-C3N4 can effectively inhibit photocatalytic carrier recombination and enhance the adsorption performance of the composite photocatalytic materials, so that the composite photocatalyst has stronger photocatalytic activity. In this paper, three kinds of graphitic carbon nitride photocatalyst g-C3N4 with different morphologies were prepared using the same precursor system by the chemical cracking method. After characterization and application, the sample with the most significant photocatalytic activity was selected and the g-C3N4/BiVO4 heterostructure was synthesized by the simple solvent evaporation method, then the photocatalytic experiment was carried out. The results show that, when the content of BiVO4 in the composite sample is 1%, the photocatalytic activity of RhB was the highest, and the degradation rate could reach 90.4%. The kinetic results showed that the degradation of RhB was consistent with the quasi-primary degradation kinetic model. The results of the photocatalytic cycle experiment show that the photocatalytic performance remains unchanged and stable after four photocatalytic cycles. The existence of a g-C3N4/BiVO4 binary heterojunction was confirmed by UV/Visible diffuse reflection (UV-DRS) and photoluminescence (PL) experiments. Owing to the Z-type charge process between BiVO4 and g-C3N4, efficient carrier separation was achieved, thus enhancing the photocatalytic capacity. This work provides a new idea for the study of heterojunction photocatalytic materials based on g-C3N4.

Temperature-responsive binary superlattices prepared by the selective solvent evaporation of O/W microemulsion composed of gold nanoparticles and surfactants.

Binary nanoparticle superlattices (BNSLs) are one of the important classes of nanomaterial architectures for a wide range of potential applications because they can provide synergistically enhanced properties depending on the morphology and spatial arrangement of nanoparticles (NPs). However, although many studies have been conducted on the fabrication of BNSLs, there are still several challenges in achieving BNSLs with a three-dimensional lattice due to their complicated synthesis, hindering their practical applications. Herein, we report the fabrication of temperature-sensitive BNSLs in complexes of gold nanoparticles (AuNPs), Brij 58 surfactant, and water via a two-step evaporation method. The surfactant was utilized for two different purposes, i.e., surface modification of the AuNPs to control their interfacial energy and as a template material for the formation of the superlattice. Depending on the size and concentration of the AuNPs, the mixture of AuNPs and surfactant self-assembled into three types of BNSLs, including CaF2, AlB2, and NaZn13, which were sensitive to temperature. This study is the first demonstration of the temperature- and particle size-dependent control of BNSLs in the bulk state without the covalent functionalization of NPs via a simple two-step solvent evaporation method.

Solvation and Stabilization of Superior Alanate Nanostructures

NaAlH4 and LiAlH4 are promising materials for hydrogen storage due to their high hydrogen density (7.4 and 10.5 mass%, respectively). However, their practical application is hampered from the slow hydrogen kinetics and poor reversibility. To improve the hydrogen properties of alanates, the alternative core–shell strategy has been proposed. In this respect, a simple solvent evaporation method is presented to synthesize the alanate core. In this approach, NaAlH4 and LiAlH4 are stabilized by solvation and electrostatic forces, respectively, through the addition of ionic salts. Remarkably, it is found that the size of the alanate nanoparticles can be tuned by varying the concentration of the introduced ion. More importantly, the partial substitution of Na+ and Li+ with cations of higher electronegativity enables the release of hydrogen at much lower temperatures.

A Red-Emitting Hybrid Manganese Halide Perovskite C5H5NOMnCl2·H2O Featuring One-Dimensional Octahedron Chains.

Herein, we successfully synthesized a new organic-inorganic hybrid manganese halide perovskite C5H5NOMnCl2·H2O, in which organic molecules, water molecules (through O atoms), and Cl atoms coordinate with Mn atoms to form deformed [MnO3Cl3] octahedrons. Then, octahedrons form a chain through edge sharing, resulting in a 1D-chain single crystal structure. The high-quality C5H5NOMnCl2·H2O single crystal prepared by a simple solvent evaporation method produced bright red emission at 656 nm attributed to the d-d transition of Mn2+. Also, it has a photoluminescence quantum yield (PLQY) of 24.2%. Photoluminescence excitation and absorption spectra were both featured with multiple bands and were in good agreement with the Mn2+ 3d energy levels. The photoluminescence decay spectrum showed an average lifetime of 0.466 ms, which further proves the d-d transition mechanism. The C5H5NOMnCl2·H2O single crystal had a direct band gap of 1.43 eV. Moreover, a red light LED with a CCT of 1857 K was obtained based on the C5H5NOMnCl2·H2O powder, indicating its promising application in red-emitting LED.

Surfactant Induced Synthesis of LiAlH4 and NaAlH4 Nanoparticles for Hydrogen Storage

LiAlH4 and NaAlH4 are considered to be promising hydrogen storage materials due to their high hydrogen density. However, their practical use is hampered by the lack of hydrogen reversibility along with poor kinetics. Nanosizing is an effective strategy to enable hydrogen reversibility under practical conditions. However, this has remained elusive as the synthesis of alanate nanoparticles has not been explored. Herein, a simple solvent evaporation method is demonstrated to assemble alanate nanoparticles with the use of surfactants as a stabilizer. More importantly, the roles of the surfactants in enabling control over particle size and morphology was determined. Surfactants with long linear carbon chains and matching the hard character of alanates are more prone to lead to the formation of small particles of ~10 nm due to steric hindrance. This can result in significant shifts in the temperature for hydrogen release.

All-Inorganic Luminescent Ternary Cadmium Halide Cs7Cd3Br13 with Two Types of Cd-Centered Polyhedrons.

All-inorganic metal halides comprise a class of semiconductor material with a wide range of applications. In these materials, cadmium-related materials have excellent optical properties in the field of binary quantum dots. However, ternary cadmium halides have not attracted much attention until now. Here, we successfully synthesize a ternary all-inorganic cesium cadmium bromide, Cs7Cd3Br13, and obtained its acicular single crystals through a simple solvent evaporation method. Cadmium atoms are found to be coordinated with bromine atoms in two different polyhedrons including isolated [CdBr4]2- tetrahedrons and corner-shared [CdBr6]4- octahedral chains in the unit cells of Cs7Cd3Br13. Optical properties are then measured and the needlelike single crystals are found to have an orange emission at 630 nm upon 365 nm UV light with a photoluminescence quantum yield (PLQY) of 9.85%. The orange luminescence with large Stokes shift (255 nm) and broad full width at half-maximum (fwhm = 147 nm) is derived from self-trapped excitons, and it is further evidenced by temperature-variable photoluminescence spectra. The PL decay spectrum shows the lifetime of Cs7Cd3Br13 is 1.26 μs. Finally, DFT calculation reveals that Cs7Cd3Br13 has a direct band gap with a value of 3.09 eV.

In situ construction of a Te/CsPbBr3 heterojunction for self-powered photodetector.

In this study, CsPbBr3 particles were prepared by a simple solvent evaporation method in ambient environment; the p–n heterojunction formed by CsPbBr3 particles on the surface of a single long Te wire was used to construct a high-performance Te/CsPbBr3 photodetector. Compared with CsPbBr3 PDs, the Te/CsPbBr3 photodetector showed improved photocurrent, and exhibited characteristics of excellent self-powered performance, broad-spectrum response (UV-visible), and ultra-fast response speed (trise = 0.09 ms). In addition, under zero bias and upon 540 nm light irradiation, the device had good responsivity (0.35 mA W−1), high photosensitivity (up to 100 on/off ratio), and a detectivity of 1.42 × 1010 Jones. This study provides insight into the possibility of manufacturing high-performance self-powered photodetectors through a simple in situ construction of heterojunctions.

Facile and Scalable Synthesis and Self-Assembly of Chitosan Tartaric Sodium.

Chitosan-based nanostructures have been widely applied in biomineralization and biosensors owing to its polycationic properties. The creation of chitosan nanostructures with controllable morphology is highly desirable, but has met with limited success yet. Here, we report that nanostructured chitosan tartaric sodium (CS-TA-Na) is simply synthesized in large amounts from chitosan tartaric ester (CS-TA) hydrolyzed by NaOH solution, while the CS-TA is obtained by dehydration-caused crystallization. The structures and self-assembly properties of CS-TA-Na are carefully characterized by Fourier-transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (1H-NMR), X-ray diffraction (XRD), differential scanning calorimeter (DSC), transmission electron microscopy (TEM), a scanning electron microscope (SEM) and a polarizing optical microscope (POM). As a result, the acquired nanostructured CS-TA-Na, which is dispersed in an aqueous solution 20–50 nm in length and 10–15 nm in width, shows both the features of carboxyl and amino functional groups. Moreover, morphology regulation of the CS-TA-Na nanostructures can be easily achieved by adjusting the solvent evaporation temperature. When the evaporation temperature is increased from 4 °C to 60 °C, CS-TA-Na nanorods and nanosheets are obtained on the substrates, respectively. As far as we know, this is the first report on using a simple solvent evaporation method to prepare CS-TA-Na nanocrystals with controllable morphologies.

High performance membranes containing zeolitic imidazolate framework‐8 and polysulfone for CO2 removal from CH4

AbstractBACKGROUNDNatural gas is essential for the world's supply of energy due to its economic viability and environmental sustainability in producing adequate amounts of clean energy. However, the removal of CO2 as an undesirable impurity remains challenging in natural gas purification. In this work, high performance dense mixed matrix membranes (MMMs) containing a low loading (<2 wt%) of zeolitic imidazolate framework 8 (ZIF‐8) and polysulfone (PSF) were prepared via simple solvent evaporation method and single solvent for the removal of CO2 from CH4.RESULTSSignificant enhancements in CO2 permeability and CO2/CH4 ideal selectivity were obtained for the resultant MMMs as compared to the neat PSF membrane. The highest CO2 permeability of 33.57 Barrer and CO2/CH4 ideal selectivity of 39.03 were achieved for a PSF membrane loaded with 1 wt% of ZIF‐8; these values were 514% and 161% higher than those obtained for the neat PSF membrane, respectively. Furthermore, MMM embedded with 1 wt% of ZIF‐8 demonstrated CO2 plasticization pressure up to 16 bar, which is equivalent to an 100% increment of the value obtained for the neat PSF membrane.CONCLUSIONOverall, MMMs fabricated in this work demonstrated a significant improvement of CO2 separation from CH4 compared to the PSF‐based MMMs reported in the literature, where most of the reported MMMs contain high loading of fillers up to 30 wt%. Therefore, the MMMs fabricated in this work are ready to be further exploited for application in gas separation industries. © 2021 Society of Chemical Industry (SCI).

Flexible phase change materials obtained from a simple solvent-evaporation method for battery thermal management

In the advanced battery thermal management (BTM) strategy of phase change material (PCM) cooling, composite PCM (CPCM) is commonly obtained by a melting-blending method, which requires a preparation temperature as high as 150–200 °C to melt the polymer component. Herein, we prepare a new kind of flexible CPCM (FCPCM) through a simple solvent-evaporation method under room temperature by carefully selecting an ethylene-vinyl acetate (EVA) copolymer as the flexible polymer component. As prepared, the obtained EVA-based FCPCM possesses suitable thermo-physical properties and an excellent flexibility at room temperature, which can effectively reduce the thermal contact resistance, and therefore delivers an outstanding temperature-control performance in BTM applications. For example, during a harsh cyclic working environment, the battery module cooled by EVA-FCPCM plates shows a much lower maximum temperature and temperature difference at 50.0 and 3.7 °C, respectively, 8.1 and 4.8 °C lower than the battery module cooled by traditional rigid CPCM plates, respectively. This new and mild strategy adopting solvent-evaporation instead of melting-blending is believed to greatly simplify the preparation procedure, and thereby promotes the engineering applications.

Preparation, High-Density Spherical, and Low Sensitivity of RDX/NC/PMMA Composite Particles

In order to reduce the mechanical sensitivity of cyclotrimethylenetrinitramine (RDX) and improve its energy density, spherical RDX/PMMA/NC composite particles were prepared by spray drying method, selecting polymethyl methacrylate (PMMA, hydrocarbon binder) with excellent mechanical properties and nitrocellulose (NC, energy-containing binder) with higher density as the desensitizing shell material, RDX as the core material. PMMA/NC composite particles of the same component were prepared by a simple solvent evaporation method at the same time. Structural characterizations and thermal stability of the composites were systematically studied by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimeter (DSC), respectively. Moreover, the safety performance has been qualitatively tested and analyzed through impact sensitivity and friction sensitivity. The results show that the addition of NC/PMMA binder would not change the original crystal structure of RDX, and the RDX/NC/PMMA composites fabricated by spray drying presented spherical particles with uniform distribution and smooth surface. The Tp0 of RDX/NC/PMMA composite particles increased from 220.3°C to 228.2°C, improving the thermal decomposition performance. The H50 rose from 29.32 cm to 84.3 cm, and the probability of friction explosion decreased from 96% to 8%, significantly enhancing the safety performance. In short, the RDX/NC/PMMA composites prepared via the spray drying method and the improvement of their performance have positive significance for the development of explosives in pursuit of high energy and low sensitivity.

Anions mediated amino-type Cd-MOFs catalysts for efficient photocatalytic hydrogen evolution

Photocatalytic water splitting can be used to directly transfer solar energy into chemical energy with highly efficiency. Metal-organic frameworks (MOFs) materials are well known on the advantages of high design flexibility and metal center functionalization. In this study, a series of Cd-centered MOFs were successfully fabricated by a simple solvent evaporation method based on the different anion mediated pyridyl leucine derivatives. Single-crystal X-Ray diffraction showed the isostructural 3D chiral coordination networks of three Cd-MOFs with helical chains connected by the adjacent carboxylate groups. Within the helical coordination chains, the formate (For) and acetate (OAc) anions adopted chelate modes in Cd-LFor and Cd-LOAc, whereas the chloride worked as a monodetate ligand in Cd-LCl. Powder X-ray diffraction (PXRD), Thermogravimetric analysis, UV–vis spectra, Photocurrent-time test (I-t) and Mott-Schottky (MS) curves were carried out to characterize and analysis these Cd-MOFs. All the samples exhibit photocatalytic activity for hydrogen generation in aqueous solution of Na2S/Na2SO3 upon irradiation at full light. The photocurrent time test showed that Cd-LCl showed a higher photocurrent intensity than those of Cd-LFor and Cd-LOAc, which proved the lower electron-hole recombination and correspondingly higher hydrogen production photocatalysis active. The highest H2 production rate reached 17242 ​μmol ​g−1 ​h−1 for Cd-LCl. In the photocatalytic reaction, the hydrogen production rate was stable without significant decrease, indicating that the material had no significant deactivation and had good photocatalytic activity.