High-efficiency Synthesis Research Articles

High efficient synthesis of benzyl lactate through waste PLA alcoholysis by protic ionic salt

Benzyl lactate (BL) is a critical reagent in pharmaceutical and chemical synthesis due to its versatility. Traditional synthesis of BL was constrained by the high cost and low yield, thereby hindering the feasibility of large-scale production. Here, we reported a novel synthesis strategy for BL by utilizing the alcoholysis of waste polylactic acid (PLA) by benzyl alcohol with the protic ionic salt, HTBD-OAc, as the catalyst. The gram-scale experiments achieved a 94.9 % yield, and the robustness of this reaction was evidenced by the yield maintaining 92.5 % across six recycling experiments. More impressively, kilogram-scale synthesis facilitated a complete conversion of PLA to BL, achieving an unprecedented yield of 98.7 % at 180 °C within two hours. The exceptional catalytic efficiency of this reaction is attributed to the synergistic functions between the HTBD+ cation and OAc− anion in the catalyst HTBD-OAc. This study heralds a significant stride towards the sustainable and scalable production of high-purity benzyl lactate, paving the way for extended industrial applicability for this essential compound.

High-efficient synthesis of straw-derived carbon quantum dots for facilitating methanogenic performance in high-load co-digestion of food waste and excess sludge

Anaerobic digestion (AD), as a crucial technology for organic waste resource recovery, faces the challenge of low efficiency in converting high-load organic substance into biogas. In this study, high-load AD system with food waste and excess sludge as co-substrates was constructed. The effect and mechanism of carbon quantum dots (CQD) derived from straw in promoting the performance of AD systems have been studied. The oxidation pretreatment of straw with H2O2 and acetic acid increased the yield of hydrothermal synthesis CQD to approximately 40%. The effect of different CQD on CH4 yield performance was further explored. The cumulative CH4 yield performance of the fermenter was improved after adding CQD. The CQD synthesized from pretreated straw and the nitrogen-doped CQD synthesized using Chlorella as the nitrogen source showed competitive promotion performance, increasing cumulative CH4 yield by 17.71% and 8.87%, respectively. These CQD can effectively accelerate the degradation of dissolved organic matter and thus improve the CH4 yield performance, with the most significant effect of CQD synthesized from pretreated straw. Electrochemical analysis and the correlation analysis between microorganisms and performance parameters showed that these CQD established an electron conductive network to enhance the electron transfer of the system. This well conductive conditions enriched hydrogenotrophic methanogenic (Methanosarcina), electroactive bacteria (Clostridium_sensu_stricto_1), and hydrolytic-acidifying bacteria (norank_f__Bacteroidetes_vadinHA17). This study significantly enhanced the yield of straw-derived CQD through green methods, and deeply revealed the potential promoting mechanisms of biomass-derived CQD by investigating the correlation between system performance and microorganisms in high-load AD systems

Multi-omics profiling reveals the molecular mechanism of Bifidobacterium animalis BB04 in co-culture with Wickerhamomyces anomalus Y-5 to induce bifidocin A synthesis.

Bacteriocin is a kind of natural substance that can effectively inhibit bacteria, but its production usually limited by environment. Co-culture is a strategy to stimulate bacteriocin production. Bifidocin A produced by Bifidobacterium animalis BB04, is a novel bacteriocin with a broad-spectrum antimicrobial active of foodborne bacteria. In order to enhance bifidocin A production, bacteriocin-inducing strains were screened firstly in co-cultivation. Then, the molecular mechanism of co-cultural induction was investigated by transcriptomic and proteomic analysis. Finally, the key inducing metabolites were identified by using targeted metabolomic technology. The results showed that Wickerhamomyces anomalus Y-5 in co-cultivation could significantly enhance bifidocin A production, with a 3.00-fold increase compared to mono-culture. The induction may not depend on direct contact with cells and may instead be attributed to be continuous exposure to inducing substances at specific concentration. In co-cultivation, W. anomalus Y-5 up-regulated Hxk2 and Tap42 to activate Glucose-cAMP and Tor and HOG-MAPK pathway, stimulated the expression of the retrograde gene, produced glutamine and glycerol to maintain activity. During this process, glutamine, inosine, guanosine, adenine, uracil, fumaric acid and pyruvic acid produced by W. anomalus Y-5 could induce the synthesis of bifidocin A. In conclusion, W. anomalus Y-5 in co-cultivation induced the synthesis of bifidocin A by regulating various signaling pathways to produce inducing substances. These findings establish a foundation for high-efficient synthesis of bifidocin A and provide a new perspective into the industrial production of bacteriocin.

Synthesis of ruthenium-doped molybdenum disulfide quantum dots for Fe3+ detection

This research successfully achieved a high-efficiency synthesis of Ruthenium-doped molybdenum disulfide quantum dots (Ru-MoS2 QDs) with a yield of 27 wt%. The obtained Ru-MoS2 QDs possess blue fluorescence and quantum yield of 2.56 %. Moreover, these Ru-MoS2 QDs demonstrated exceptional selectivity and an impressively low detection limit of 0.55 μM for Fe3+ ions, highlighting their considerable promise for future applications in sensitive detection methodologies.

Novel Bioproduction of 1,6-Hexamethylenediamine from l-Lysine Based on an Artificial One-Carbon Elongation Cycle.

1,6-hexamethylenediamine (HMD) is an important precursor for nylon-66 material synthesis, while research on the bioproduction of HMD has been relatively scarce in scientific literature. As concerns about climate change, environmental pollution, and the depletion of fossil fuel reserves continue to grow, the significance of producing fundamental chemicals from renewable sources is becoming increasingly prominent. In recent investigations, the bioproduction of HMD from adipic acid has been reported but with lingering challenges concerning costly raw materials and low yields. Here, we have undertaken the reconstruction of the HMD synthetic pathway within Escherichia coli, which was constituted with l-lysine α-oxidase (Raip), LeuABCD, α-ketoacid decarboxylase (KivD), and transaminases (Vfl), leveraging a carbon chain extension module and a metabolic pathway of transaminase-decarboxylase cascade catalysis within the strain WD20, which successfully produce 46.7 ± 2.0 mg/L HMD. To increase the cascade activity and create a higher tolerance to external environmental disturbance for l-lysine to convert into HMD, another two enzymes d-alanine aminotransferase (Dat) and alpha-ketoacid decarboxylase (KdcA) were introduced into WD21 to provide flux flexibility for α-ketoacid metabolization, which was named "Smart-net metabolic engineering" in our research, and high-efficiency synthesis of HMD utilizing l-lysine as the substrate has been successfully achieved. Finally, we established a + 1C bioconversion multienzyme cascade catalyzing up to 65% conversion of l-lysine to HMD. Notably, our fermentation process yielded an impressive 213.5 ± 8.7 mg/L, representing the highest reported yield to date for the bioproduction of HMD from l-lysine.

Highly efficient CuNi-ZrO2 nanocomposites for selective hydrogenation of levulinic acid to γ-valerolactone.

CuNi-ZrO2 nanocomposites were prepared by a simple coprecipitation technique of copper, nickel and zirconium ions with potassium carbonate. The structures of the nanocomposites were characterized by N2 physical adsorption, XRD, H2-TPR and STEM-EDS. The Cu0.05Ni0.45-ZrO2 nanocomposite showed outstanding catalytic performance in hydrogenation of levulinic acid (LA) to γ-valerolactone (GVL), especially NaOH solution (0.5 mol L-1) as a solvent. 100% LA conversion and > 99.9% GVL selectivity are achieved over Cu0.05Ni0.45-ZrO2 catalyst at 200 °C, 3 MPa for 1.5 h. Characterization results suggest that the excellent reactivity of the Cu0.05Ni0.45-ZrO2 may be due to a better reducibility of nickel oxide in the CuONiO-ZrO2, dispersion of Ni in the Cu0.05Ni0.45-ZrO2 compared to nickel oxide in the NiO-ZrO2 and Ni in the Ni0.5-ZrO2 and promotion of OH-. The results demonstrate that the Cu0.05Ni0.45-ZrO2 nanocomposite has potential to realize high efficiency and low-cost synthesis of liquid fuels from biomass.

Low Rh doping accelerated HER/OER bifunctional catalytic activities of nanoflower-like Ni-Co sulfide for greatly boosting overall water splitting

Facile synthesis of high-efficiency and stable bifunctional electrocatalyst is essential for producing clean hydrogen in energy storage systems. Herein, low Rh-doped flower-like Ni3S2/Co3S4 heterostructures were facilely prepared on porous nickel foam (labeled Rh-Ni3S2/Co3S4/NF) by a hydrothermal method. The correlation of the precursors types with the morphological structures and catalytic properties were rigorously investigated for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in the control groups. The low Rh doping within the catalyst played important role in boosting the catalytic characteristics. The resulting catalyst showed the smaller overpotentials of 197 and 78 mV to drive a current density of 10 mA cm−2 for the OER and HER in alkaline electrolyte, respectively. And the potential only required 1.71 V to drive a current density of 100 mA cm-2 in a water splitting device. It reflects excellent overall water splitting of the home-made Rh-Ni3S2/Co3S4/NF. This strategy shed some constructive light for preparing transition metal sulfide-based electrocatalysts in water splitting devices.

High-efficiency synthesis of B@Mg@KNO3 by solvent extraction enhances the ignition and energy release performance of B

Boron (B) is widely acknowledged as the preferred fuel for rocket ramjets. Nevertheless, the presence of boron oxide (B2O3) on the surface of boron impedes the interaction between the oxidized component and the internal active component B, leading to challenges in ignition and constraints on reactivity and combustion efficiency. To mitigate these issues, high-energy materials featuring a B@Mg@KNO3 coating structure were efficiently and expeditiously prepared using a solvent extraction method. The B@Mg@KNO3 material distributes magnesium inside and outside the B shell, while KNO3 serves as the load layer. The addition of the load layer facilitates closer contact between Mg and the oxidizer, reducing the diffusion distance between oxygen and fuel. As a result, the ignition energy of B is reduced, and the energy release characteristic of B is improved through multi-effect coordination. In comparison with the B/KNO3 sample, the heat release of B@Mg@KNO3 increased by 113.1 %, the ignition temperature decreased by 50 °C, and the ignition energy decreased by 62.5 % as indicated by the ignition test. The flame temperature increased by 51.8 %, the combustion efficiency of B@Mg@KNO3 increased by 23.92 %, and the apparent activation energy decreased by 109.6 kJ/mol. Consequently, B@Mg@KNO3 is anticipated to expedite the application and advancement of boron-based rocket ramjet engines.

Acetal-thiol Click-like Reaction: Facile and Efficient Synthesis of Dynamic Dithioacetals and Recyclable Polydithioacetals.

Dithioacetals are heavily used in organic, material and medical chemistries, and exhibit huge potential to synthesize degradable or recyclable polymers. However, the current synthetic approaches of dithioacetals and polydithioacetals are overwhelmingly dependent on external catalysts and organic solvents. Herein, we disclose a catalyst- and solvent-free acetal-thiol click-like reaction for synthesizing dithioacetals and polydithioacetals. High conversion, higher than acid catalytic acetal-thiol reaction, can be achieved. High universality was confirmed by monitoring the reactions of linear and cyclic acetals (including renewable bio-sourced furan-acetal) with aliphatic and aromatic thiols, and the reaction mechanism of monomolecular nucleophilic substitution (SN1) and auto-protonation (activation) by thiol was clarified by combining experiments and density functional theory computation. Subsequently, we utilize this reaction to synthesize readily recyclable polydithioacetals. By simple heating and stirring, linear polydithioacetals with w of ~110 kDa were synthesized from acetal and dithiol, and depolymerization into macrocyclic dithioacetal and repolymerization into polydithioacetal can be achieved; through reactive extrusion, a semi-interpenetrating polymer dynamic network with excellent mechanical properties and continuous reprocessability was prepared from poly(vinyl butyral) and pentaerythritol tetrakis(3-mercaptopropionate). This green and high-efficient synthesis method for dithioacetals and polydithioacetals is beneficial to the sustainable development of chemistry.

Facile synthesis of zeolite catalyst from lithium slag efficiently activates peroxymonosulfate for tetracycline degradation: •O2- and the electron transfer

Iron is the most suitable candidate for activating peroxymonosulfate (PMS) for organic degradation. To realize the effective separation and recycling of iron catalysts, it is urgent to explore a low-cost and excellent supporter. In this study, a zeolite catalyst (CAN) with both supporter and catalyst functions was synthesized in one step using lithium slag (LS, containing iron), and used to degrade tetracycline (TC) wastewater. The results showed that the electron transfer of iron and sulfur in CAN promotes the decomposition of PMS. The CAN/PMS system exhibited great removal efficiency (89.5 %, 0.083 min−1) and relatively lower activation energy (15.31 kJ/mol) toward TC. And •O2- plays a crucial role in the degradation. The CAN also represented great catalytic stability and reusability. This study revealed a new approach for the synthesis of high efficiency and low-cost catalysts and the tetracycline degradation.

Efficient synthesis of high-purity carbon dots via self-polymerization driven bottom-up growth for high-selectivity sensing and high-efficiency separation

Carbon dots (CDs) have attracted extensive interest due to their exceptional optical properties and facile synthesis processes. However, achieving high-efficiency synthesis of high-purity CDs with high yield remains an unresolved critical issue. Herein, we report a facile and versatile self-polymerization-driven bottom-up growth strategy for efficient fabrication of high-purity CDs. As a proof-of-concept demonstration, dopamine and its four analogues were used as the self-polymerizable precursors for self-driven synthesis of fluorescent CDs with high-purity. By employing a mixed-solvent system and rationally regulating periodate oxidation process, the highly controllable self-polymerization processes and efficient solvothermal-assisted production of polydopamine and polyphenols derived CDs were readily achieved. Further integrating high molecular weight membrane dialysis, we successfully obtained the highly purified polydopamine-derived CDs with high yield of 21.1 % and quantum yield of 3.6 %, confirmed by nuclear magnetic resonance, capillary electrophoresis and other types of high-resolution characterization techniques. The formation and luminescence mechanisms of the self-polymerized CDs were also elucidated through comparative analysis of their morphological features and elemental compositions. We also demonstrated the broad universality of this self-polymerization driven bottom-up strategy by utilizing by employing four other phenolic compounds, including l-dopa, gallic acid, catechol, and pyrogallol, as readily accessible precursors for high-yield synthesizing highly purified fluorescent CDs. Moreover, the enormous application potential of the high-purity CDs for high-selectivity sensing and high-efficiency electrochromatographic separation was thoroughly demonstrated.

Low temperature and high efficiency synthesis of boron nitride nanosheets (BNNSs) and its application in SiO2 microwave-transparent composites

In this study, Zn8B3H3O14 nanosheets were synthesized through a one-step coprecipitation process and employed as both a boron source and substrate templates for the fabrication of boron nitride nanosheets (BNNSs), which were synthesized efficiently at low temperatures by the borate nitration method using ammonia as the nitrogen source. The thickness of the synthesized BNNSs ranged from 3 to 10 nm with a flake dimension of about 2.56 μm. The prepared BNNSs using this method realized 98.8% boron source utilization and single batch yields up to gram level. In addition, BNNSs/SiO2 microwave-transparent composites were prepared to investigate the potential for large-scale applications of the BNNSs produced by using this method. The composites demonstrated a remarkable increase in bending strength and fracture toughness, reaching 122.02 MPa and 2.31 MPa·m1/2, respectively, with the addition of only 0.5 wt% BNNSs. Compared with SiO2 without BNNSs, the fracture toughness of the composites is increased by 106%. A novel crack plugging strong toughening mechanism of BNNSs is proposed. Simultaneously, the composites exhibit exceptional microwave-transparent properties, with dielectric constants below 4 in the real part and below 0.03 in the imaginary part. Therefore, this study has successfully achieved the low-temperature and efficient synthesis of micron-scale BNNSs, laying the groundwork for their large-scale application.

Design and synthesis of APN and 3CLpro dual-target inhibitors based on STSBPT with anticoronavirus activity.

Coronaviruses (CoVs) have continuously posed a threat to human and animal health. However, existing antiviral drugs are still insufficient in overcoming the challenges caused by multiple strains of CoVs. And methods for developing multi-target drugs are limited in terms of exploring drug targets with similar functions or structures. In this study, four rounds of structural design and modification on salinomycin were performed for novel antiviral compounds. It was based on the strategy of similar topological structure binding properties of protein targets (STSBPT), resulting in the high-efficient synthesis of the optimal compound M1, which could bind to aminopeptidase N and 3C-like protease from hosts and viruses, respectively, and exhibit a broad-spectrum antiviral effect against severe acute respiratory syndrome CoV 2 pseudovirus, porcine epidemic diarrhea virus, transmissible gastroenteritis virus, feline infectious peritonitis virus and mouse hepatitis virus. Furthermore, the drug-binding domains of these proteins were found to be structurally similar based on the STSBPT strategy. The compounds screened and designed based on this region were expected to have broad-spectrum and strong antiviral activities. The STSBPT strategy is expected to be a fundamental tool in accelerating the discovery of multiple targets with similar effects and drugs.

TEAOH-assisted cost-effective preparation of SSZ-13 using L zeolite as Al source

Developing an economical and high-efficiency synthesis pathway of SSZ-13 zeolite is of great significance for the ammonia selective catalytic reduction of nitrogen oxides (NH3-SCR of NOx) reactions. Herein, SSZ-13 zeolite were synthesized using L zeolite as the aluminum source in the presence of a mixed structure directing agent (SDA) composed of N,N,N, trimethtyl-1-adamantammonium hydroxide (TMAdaOH) and tetraethylammonium hydroxide (TEAOH). This synthesis strategy aims to accelerate the crystallization rate through interzeolite transformation, while less expensive TEAOH can play a cooperative structure-directing role, thus reducing the consumption of expensive TMAdaOH template. The results showed that pure SSZ-13 zeolites with high crystallinity can be obtained from L zeolite within 12 h at 160 ℃ under low TMAdaOH/SiO2 ratio of 0.05 (too low to carry out the synthesis on its own in the current synthesis system) in the presence of TEAOH. Moreover, the crystallization mechanism was also investigated by XRD, FT-IR, SEM and TG-DTG techniques. It was proposed that the crystallization of SSZ-13 occurs through the formation of SSZ-13 nuclei under the direction of TMAdaOH and promotion of TEAOH, subsequently TMAdaOH was incorporated in the framework to further induce the crystal growth of SSZ-13. Especially, the zeolite crystal size can be modulated by the amount of TEAOH added. In addition, After Cu2+ exchange, the obtained Cu-SSZ-13 sample exhibits superior catalysis performance in the NH3-SCR of NOx reaction, and the NOx conversion rate remained over 90 % across a broad range from 200 to 600 °C, demonstrating its significant application potentials in NOx removal from diesel vehicle exhausts.

Utilization of ovalbumin and visible light irradiation for efficient and eco‐friendly production of AgNPs composite

Silver nanoparticles (AgNPs) are one of the most widely used antimicrobial agents. However, due to the potential problems of environmental pollution and high energy consumption, a green and efficient synthesis strategy of AgNPs is urgently required. Ovalbumin (OVA) is the most abundant protein in egg whites, and its extraction process is simple and productive. This paper reported a new green synthesis method of AgNPs by using OVA as an assistant accompanying with a visible light irradiation. Together with the reduction of silver ions, the uniformly dispersed OVA‐AgNPs nanocomposite could be formed within 30 min under xenon light irradiation by simple mixing AgNO3 and OVA in aqueous solution. The detailed mechanism study showed that tyrosine residue and peptide bonds in OVA played a major role in the reduction and stability of silver ions. In addition, in vitro antibacterial experiments indicated that 10 mg/L of OVA‐AgNPs, the minimum inhibitory concentration, has a good antimicrobial effect on both Gram‐positive and Gram‐negative bacteria, fungi, and some drug‐resistant bacteria species within 4 h of treatment, mainly due to the disruption of the structure of bacterial cell and the balance of reactive oxygen species. This work provides a new way for the green and efficient synthesis of AgNPs and shows good prospects for the applications in the field of biomedical materials and functional nanomaterials.

One-step high efficiency synthesis of zeolite from fly ash by mechanochemical method as a low-cost adsorbent for cadmium removal

The hydrothermal synthesis of zeolite from fly ash is a time-consuming process with a low conversion rate. Mechanochemical activation is commonly employed as a green and moderate pre-treatment process for surface modification purposes. This study proposes a one-step high efficiency synthesis of zeolite from fly ash using the mechanochemical method. The ball milling modification is conducted simultaneously with the zeolite synthesis process, reducing the overall synthesis time to a significant extent (3 h being determined as the optimal synthesis time). The findings reveal that P1 zeolite can be effectively synthesized under the following conditions: a sodium hydroxide concentration of 2 mol L−1, a synthesis temperature of 130 °C and a ball milling frequency of 30 Hz. Moreover, the synthesized zeolite exhibits a maximum Cd2+ adsorption capacity of 130.68 mg/g at pH= 5, following pseudo-second-order kinetics and Langmuir adsorption isotherm. This study not only simplifies the production process and saves energy but also yields zeolite with smaller particle sizes and higher purity. By utilizing the mechanochemical method, the disposal of solid waste can be made environmentally friendly, convenient, and economically beneficial.

Fabrication of shaping catalyst SO42−/SnO2-RC for high efficient and continuous synthesis of trimethylolpropane oleate in fixed bed reactor

Fabrication of shaping catalyst SO42−/SnO2-RC for high efficient and continuous synthesis of trimethylolpropane oleate in fixed bed reactor

Laser-Induced Electron Synchronization Excitation for Photochemical Synthesis and Patterning Graphene-Based Electrode.

Micro-supercapacitors (MSCs) represent a pressing requirement for powering the forthcoming generation of micro-electronic devices. The simultaneous realization of high-efficiency synthesis of electrode materials and precision patterning for MSCs in a single step presents an ardent need, yet it poses a formidable challenge. Herein, a unique shaped laser-induced patterned electron synchronization excitation strategy has been put forward to photochemical synthesis RuO2 /reduced graphene oxide (rGO) electrode and simultaneously manufacture the micron-scale high-performance MSCs with ultra-high resolution. Significantly, the technique represents a noteworthy advancement over traditional laser direct writing (LDW) patterning and photoinduced synthetic electrode methods. It not only improves the processing efficiency for MSCs and the controllability of laser-induced electrode material but also enhances electric fields and potentials at the interface for better electrochemical performance. The resultant MSCs exhibit excellent area and volumetric capacitance (516mFcm-2 and 1720Fcm-3 ), and ultrahigh energy density (0.41Whcm-3 ) and well-cycle stability (retaining 95% capacitance after 12000 cycles). This investigation establishes a novel avenue for electrode design and underscores substantial potential in the fabrication of diverse microelectronic devices.

Fast synthesis of high-entropy oxides for lithium-ion storage

High-entropy oxides (HEOs) have been considered conspicuous battery materials due to their tunable properties and stable crystal structure. In this work, several kinds of high entropy oxides (HEOs) are prepared by an ultra-fast Joule heating method in several seconds. This simple and effective method enhances the efficiency of near four orders of magnitude than that of the common sintering methods. As anode materials of lithium-ion batteries (LIBs), they have considerable rate capacity and cycling stability. For example, quinary (MgCoNiCuZn)O HEO delivers a high capacity of ∼150 mAh g−1 even at ultrahigh current density of 10 A g−1 and cycle stability up to 2,600 cycles. By in-situ transmission electron microscopy, the full lithiation/de-lithiation process is tracked down to the atomic scale in real time, observing the distinct reaction dynamics and structural evolutions in rock-salt-type (MgCoNiCuZn)O during cycling. Conversion/alloying reaction kinetics are identified by the disappearance of the original rock-salt phase and the formation of polyphase with the intercalation of lithium-ions. While upon de-lithiation, the post-lithiation polyphase state can be recovered to the original rock-salt-structured (MgCoNiCuZn)O. Our work provides valuable guidelines to high-efficient synthesis and mathematical understanding of lithium storage mechanisms of HEOs for next-generation long-life energy storage.

High-efficient synthesis of NaBH4 by solid-phase electrolysis process on a core-shell-type cathode

NaBH4 is a promising hydrogen storage material, while faced with enormous difficulties for scale-up application due to regeneration issues. In this study, a highly efficient and economical strategy for the electrosynthesis of NaBH4 from hydrolysis by-product NaB(OH)4 has been proposed. By fabricating solid-phase electrodes with NaB(OH)4 and electrocatalyst etc., the mass transfer process of B(OH)4- at the cathode surface was remarkably improved, thus reducing the resistance of the cathodic reaction. Meanwhile, XPS, FTIR, and CV analyses were combined to reveal the reaction path and control steps of B(OH)4- reduction to BH4− in the electrocatalytic system. The formation of NaBH4 and intermediates (BH(OH)3-, BH2(OH)2-, and BH3(OH)-) is the gradual replacement of (OH)- in NaB(OH)4 by H−. Furthermore, this study reveals that PbO has a suitable hydrogen evolution overpotential and excellent selective catalytic activity. The current efficiency for NaBH4 synthesis via solid-phase electrolysis was up to 68.12 % by systematically regulating various factors.