Higher CO2 Production Research Articles

Water process/treatment by a S-scheme Fe2O3/TiO2 heterojunction photocatalyst for excellent antibiotic degradation/CO2 reduction/H2 production; process optimization and mechanistic insights

A facile synthesis approach was employed to fabricate a binary Fe2O3/TiO2 nanocomposite (FeTi4-400) for enhanced photocatalytic hydrogen (H2) production, cephalexin degradation and CO2 reduction under visible light irradiation. Compared to pristine TiO2, FeTi4-400 exhibited improved visible light absorption and promoted charge carrier separation, leading to increased H2 production rate and CO2 conversion into CH4 and CO. This improvement can be attributed to the formation of an S-scheme heterojunction, along with the desirable properties of FeTi4-400, including visible light activity, high surface area, and strong CO2 adsorption. The photocatalyst achieved a maximum H2 production rate of 649 μmol/g·h−1, exceeding that of pure TiO2. Similarly, the highest CO production rate of 16.44 μmol/g·h−1 was attained with FeTi4-400. Furthermore, FeTi4-400 achieved excellent cephalexin degradation (96 %) under optimal conditions, with a degradation rate constant of 0.01 min−1. A plausible cephalexin degradation pathway over FeTi4-400 is proposed. Transient photocurrent measurements and EIS analysis corroborated a significant enhancement in photocatalytic activity for FeTi4-400, attributed to the efficient separation of photogenerated electron-hole pairs. Stability studies demonstrated consistent cephalexin degradation by FeTi4-400 over five consecutive cycles without noticeable photocatalyst deactivation. This work presents a novel strategy for fabricating low-cost, efficient, and readily synthesized nanomaterials for applications in solar energy conversion and environmental remediation.

Preparation of conductive bimetallic phthalocyanine with acceptor and their electrocatalytic properties for CO2 reduction

Abstract In order to develop a catalyst for electrochemical CO2 reduction with high power efficiency, we prepared molecular crystals with 2 types of metal phthalocyanine. Charge transfer complexes with acceptor were selected as the molecular crystal system to reduce the electrical resistance. Various bimetallic phthalocyanine systems consisting of cobalt phthalocyanine and another metal phthalocyanine were obtained as highly conductive separated stacked charge transfer complexes with iodine as an acceptor. The obtained catalysts for CO2 reduction were evaluated using gas diffusion electrodes. The catalysts containing the bimetallic phthalocyanine system of cobalt and copper phthalocyanines showed higher CO2 reduction current and higher CO production, indicating that the CO2 reduction on cobalt phthalocyanine is enhanced by the H2 formation reaction on copper phthalocyanine.

Insights into the influence of anions on the syngas production behavior of bio-wastes during molten salt thermal treatment

Thermal treatment of bio-wastes in molten nitrate at low temperatures has emerged as an efficient approach for producing syngas. Molten salt facilitates the thermal conversion of bio-wastes due to its superior heat transfer and catalytic properties. To enhance the depolymerisation of macromolecules in bio-wastes for the production of high-quality syngas, molten NaNO3-NaNO2 with varying anion ratios was employed in this study, and the effects of these anions on bio-wastes with diverse properties were thoroughly investigated. The results indicated that NO3− tended to be significantly involved in the cleavage of carbonyl groups and C–C/CC bonds, which dominated the high CO2 production. NO2− tended to be significantly involved in the cleavage of ether and C–C/CC bonds, which dominated the high CO production. The elevated NO2− ratio in molten salt significantly facilitated the depolymerisation of bio-wastes, increasing the yield of combustible gases (CO, CH4, H2) while decreasing CO2 yield in the syngas. This resulted in a notable enhancement of the lower heating value (LHV) of syngas, reaching up to 11.55 MJ/Nm3. This behavior also led to the formation of substantial quantities of nitro-phenols and amines containing nitro/nitroso groups in the tar. The nitrosation reaction of NO2− with bio-wastes was the primary factor in this process and took precedence over the nitrification of NO3−. This study elucidated the reaction pathways of NO3−/NO2− with bio-wastes and their contributions to the production of high-quality syngas at low temperature.

Highly stable and electron-rich Ni single atom catalyst for directed electroreduction of CO2 to CO

Transition metal-nitrogen-carbon (M−N−C) are considered as promising candidates for the electrochemical conversion of inert CO2 into high value-added CO products. However, previous reports have focused on Ni single-atom sites (Ni SAs) and the role of Ni nanoparticles (Ni NPs) in CO2 electroreduction reaction (CO2RR) has been overlooked. Herein, we prepared a series of Ni, N-codoped porous carbon (NiNC-T, T represents the temperature) catalysts by combining Ni phthalocyanine pyrolysis and acid etching strategy, which either contain only Ni SAs or both Ni SAs and Ni NPs. Notably, the NiNC-1100 catalyst with both Ni SAs and Ni NPs exhibited 99 % CO faradaic efficiency (FECO) at −0.66 V versus reversible hydrogen electrode (vs. RHE) and FECO above 98 % over a wide potential range (−0.66 V ∼ −1.06 V). Moreover, the FECO of NiNC-1100 remained above 95 % after 100 h of continuous electrocatalysis, which was significantly superior to that of the most advanced Ni single atom electrocatalysts. The systematic characterization results showed that the introduction of Ni NPs can promote the adsorption and activation of CO2 by increasing the electron cloud density of Ni SAs, thus enhancing the CO2RR catalytic performance.

Fabrication of a Partial Encapsulation Architecture on S-Scheme Heterojunctions toward Durable Selective Photocatalytic CO2 Reduction.

It remains a challenging issue to achieve durably stable photocatalytic CO2 reduction over heterojunctions owing to their inherent structural assembly features. Herein, a unique partial encapsulation architecture is fabricated on the 3D/2D CoWO4/C3N5 heterojunction by embedding CoWO4 microspheres on C3N5 nanosheets, which achieves efficient, durable, stable, and selective photocatalytic CO2 reduction. For the optimal 5%-CoWO4/C3N5 heterojunction, the yield of selective CO2 reduction to CO is 7.70 and 3.82 times higher than those of CoWO4 and C3N5 in 4 h, respectively, and it maintains a stable CO generation rate within 20 cycles over 80 h. A series of characterization experiments and density functional theory calculations reveal that the structural stability is reinforced significantly via strong interfacial interaction owing to the unique partial encapsulation architecture fabricated on the 3D/2D CoWO4/C3N5 heterojunction, the separation efficiency of photogenerated carriers is improved by inducing a built-in electric field and triggering the S-scheme charge-transport path, and the high CO product selectivity is attributed to the much lower free energy required for the generation path of CO compared to that for CH4.

Anion Effect in Electrochemical CO2 Reduction: From Spectators to Orchestrators.

The electrochemical CO2 reduction reaction (eCO2RR) offers a pathway to produce valuable chemical fuels from CO2. However, its efficiency in aqueous electrolytes is hindered by the concurrent H2 evolution reaction (HER), which takes place at similar potentials. While the influence of cations on this process has been extensively studied, the influence of anions remains largely unexplored. In this work, we study how eCO2RR selectivity and activity on a gold catalyst are affected by a wide range of inorganic and carboxylate anions. We utilize in situ differential electrochemical mass spectrometry (DEMS) for real-time product monitoring coupled with molecular dynamics (MD) simulations. We show that anions significantly impact eCO2RR kinetics and eCO2RR selectivity. MD simulations reveal a new descriptor─free energy of anion physisorption─where weakly adsorbing anions enable favorable CO2 reduction kinetics, despite the negative charge carried by the electrode surface. By leveraging these fundamental insights, we identify propionate as the most promising anion, achieving nearly 100% Faradaic efficiency while showing high CO production rates that are comparable to those in bicarbonate. These insights underscore the vital role of anion selection in achieving a highly efficient eCO2RR in aqueous electrolytes.

Processes of Metal Oxides Catalyst on Conversion of Spent Coffee Grounds into Rich-Synthesis Gas by Gasification

Spent coffee grounds (SCGs), a waste product of the coffee industry, present a significant untapped resource for fuel production. This study aims to optimize the gasification of SCG using various metal catalysts (NiO, MnO2, Al2O3, and Fe2O3) to maximize syngas yield. SCG samples were gasified at different temperatures (800 °C, 900 °C, 1000 °C) and analyzed using Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TG-DTA), and Fourier Transform Infrared (FTIR) spectroscopy to evaluate catalyst performance and reaction mechanisms. The findings indicated that utilizing mixing techniques for physical contact to introduce catalysts led to a uniform distribution of catalyst particles throughout the sample. The decomposition rate of the gasification experiment after adding the catalyst was 24% faster than that of the pure SCGs. In the gasification experiment, the MnO2 catalyst showed the highest CO production, which was 71% higher than that of NiO under the same conditions. At this temperature, MnO2 generated around 171% more CO than at 800 °C, surpassing the yields observed with other catalysts. The study concludes that Mn emerged as the most promising catalyst, significantly improving both CO and CH4 yields. Selecting the appropriate metal catalyst and optimizing operational temperatures are crucial for enhancing the efficiency of SCG gasification.

Well-designed V2AlC MAX supported g-C3N4/TiO2 Z-scheme heterojunction for photocatalytic CO2 reduction through bi-reforming to produce CO and CH4

Well-designed V2AlC MAX supported g-C3N4/TiO2 Z-scheme heterojunction was synthesized and tested for photocatalytic CO2 reduction through bi-reforming under UV and visible light in batch and continuous photoreactors. Compared to V2AlC/g-C3N4, V2AlC/TiO2 produced 2.17 times more CO and 6.40 times more CH4, along with H2. The highest CO production of 14644 μmol g−1 h−1 was obtained over V2AlC-g-C3N4/TiO2 composite at a selectivity of 20.21 %. Similarly, CH4 and H2 production of 56567 and 1253 μmol g−1 h−1 was obtained, which were 11.11 and 169.9 folds higher for CH4 and 2.77 and 2.32 folds higher for H2 production compared to using g-C3N4/TiO2 and V2AlC/TiO2, respectively. The efficient generation and separation of charge carriers were achieved by the Z-scheme heterojunction of g-C3N4/TiO2 with V2AlC MAX cocatalysts, which led to a greatly increased photocatalytic activity. Using a continuous process, the production of CO was decreased by 1.12 folds, whereas the production of methane disappeared and the reaction pathway was the conversion of CO2 to CO. Using methanol with UV light resulted in higher production of protons and hydrogen, achieving the highest quantum efficiency. The stability study further confirmed the continuous evolution of CO, CH4, and H2 over four cycles.

Experimental Study on Coal Oxidation and Temperature Rise Under Reciprocating Air Leakage

ABSTRACT Reciprocating air leakage often occurs in the goaf of coal mines because of changes in internal or external pressure. However, its impact on the spontaneous combustion of coal in the goaf is uncertain. Therefore, a comparative study of constant air leakage and reciprocating air leakage was carried out using a self-built system. The results indicate that reciprocating air leakage promotes coal oxidation and produces higher CO levels compared to constant air leakage. Further investigation was carried out to examine the effect of air leakage rate and reciprocating half-cycle (referred to as half-cycle hereafter) on coal oxidation and temperature rise. The results show that there is a linear relationship between resistance and air leakage rate in the coal oxidation heating space; however, the half-cycle length has little effect on resistance. The influence of a fixed air leakage rate on temperature and CO concentration does not always increase, with the maximum value achieved at 1.2 m3/h. Shorter half-cycles result in higher temperatures and CO concentrations. Gradually increasing air leakage rates and shortening half-cycles can promote coal oxidation and temperature rise and lead to higher CO production compared to previous scenarios. Additionally, the effect of using four different air leakage rates or half-cycle lengths is greater than that of using two. These research findings offer a theoretical foundation for preventing and controlling coal spontaneous combustion in goafs under complex air leakage conditions.

Synthesis of metal-phenanthroline-modified hypercrosslinked polymer for enhanced CO2 capture and conversion via chemical and photocatalytic methods under ambient conditions

Catalytic conversion of CO2 into valuable chemicals is a promising approach to mitigate the greenhouse effect and alleviate energy shortages. Hypercrosslinked polymers (HCPs) offer a scalable and stable platform for this conversion, but they often suffer from low CO2 adsorption and activation capabilities, necessitating high temperatures and pressures for effectiveness. To overcome these limitations, nitrogen-based CO2-philic active sites have been integrated into the structure of HCPs, enhancing CO2 attraction and leading to superior adsorption performance. The incorporation of cobalt ions further bolsters CO2 affinity, with HCP-PNTL-Co-B achieving the highest observed adsorption heat of 33.0 kJ·mol-1 alongside a substantial 2.0 mmol·g-1 CO2 uptake. These modified HCPs exhibit higher yields and reaction rates in cycloaddition reactions with cocatalyst tetrabutylammonium bromide at room temperature and atmospheric pressure, while HCP-1,10-phenanthroline (PNTL)-Co-B demonstrates a higher CO production rate (2,173 μmol·g-1·h-1) and selectivity (84%) in photocatalytic reduction reaction. This research has successfully achieved outstanding carbon dioxide capture and conversion performance at room temperature and atmospheric pressure by introducing CO2-philic active sites and cobalt ions into HCPs via facile one-step polymerization. This study provides a new method to design highly efficient organic catalysts for CO2 conversion.

Photocatalytic performance of metal poly(heptazine imide) for carbon dioxide reduction

Poly(heptazine imide) (PHI), a carbon nitride polymer, is a highly efficient visible-light-driven photocatalytic material. We aimed to improve its photocatalytic performance for CO2 conversion. We prepared M-PHIs by encapsulating different metals (M = K, Li, Rb, and Na) and H-PHIs, in which the metal of each M-PHI was ion-exchanged with a proton. We evaluated their photocatalytic activities for CO2 conversion and found that Na-PHI and H-PHI, prepared from Na-PHI (H-PHI(NaCl)), showed more than twice the CO production efficiency of melon and other PHIs.The high CO production efficiency of Na-PHI and H-PHI(NaCl) was attributed to their extremely smaller particle size compared with those of the other PHIs. By closely examining the synthesis conditions of Na-PHI, we have identified a method to intentionally synthesize M-PHI with small particle size. These results provide a new strategy for highly efficient CO2 conversion using PHI.

Electrochemical Conversion of Bicarbonate Using Proton Exchange Membrane-Based Electrolyzer

Direct electrochemical conversion of captured carbon dioxide (CO2) is gaining interest as an efficient method for capturing and utilizing CO2, eliminating the need for energy-intensive CO2 separation process.[1] The integrated electrolyzer with bicarbonate feed operates on the principle of spontaneous reduction of CO2 released from bicarbonate within the electrolyzer. The key to the on-site decomposition of bicarbonate into CO2 is to acidify the bicarbonate within the electrolyzer through the deliberately generated pH gradient. Bipolar membrane has been extensively used to generate pH gradient and acidify the bicarbonate feed.[2] However, the high ionic resistivity of bipolar membrane and slow kinetic of water dissociation reaction can result in a high operation cell voltage.In this study, we demonstrate proton exchange membrane based-bicarbonate electrolyzer which produces carbon monoxide from bicarbonate feedstock with high CO production selectivity and low cell voltage that are comparable to the conventional gas fed CO2 electrolyzer. To achieve highly selective CO production selectivity, a nickel single atom catalyst (Ni SAC) where the atomically dispersed nickel active sites decorated on the nitrogen doped carbon was prepared and utilized. Ni-SAC showed high CO production selectivity even in bicarbonate feed electrolyzer. To further improve the performance of this integrated electrolyzer, significant attention was given to the optimization of electrode structures. Due to the complexity of the reaction environment within the integrated electrolzyer, the performance of the electrolyzer is heavily dependent on the porosity of electrodes and distribution of catalyst on the electrodes. By optimizing the fabrication of electrodes with Ni-SACs, the optimal catalyst coated electrode showed high CO production selectivity over 90% with current density of 100 mA/cm2 at low operating cell potential of 3 V.

CO2 Electroreduction by Engineering the Cu2O/RGO Interphase

In the present investigation, Cu2O-based composites were successfully prepared through a multistep method where cubic Cu2O nanoparticles (CU Cu2O) have been grown on Reduced Graphene Oxide (RGO) nanosheets. The structural and morphological properties of the materials have been studied through a comprehensive characterization, confirming the coexistence of crystalline Cu2O and RGO. Microscopical imaging revealed the intimate contact between the two materials, affecting the size and the distribution of Cu2O nanoparticles on the support. The features of the improved morphology strongly affected the electrochemical behavior of the composites, increasing the activity and the faradaic efficiencies towards the electrochemical CO2 reduction reaction process. CU Cu2O/RGO 2:1 composite displayed selective CO formation over H2, with higher currents compared to pristine Cu2O (−0.34 mA/cm2 for Cu2O and −0.64 mA/cm2 for CU Cu2O/RGO 2:1 at the voltage of −0.8 vs. RHE and in a CO2 atmosphere) and a faradaic efficiency of 50% at −0.9 V vs. RHE. This composition exhibited significantly higher CO production compared to the pristine materials, indicating a favorable *CO intermediate pathway even at lower voltages. The systematic investigation on the effects of nanostructuration on composition, morphology and catalytic behavior is a valuable solution for the formation of effective interphases for the promotion of catalytic properties providing crucial insights for future catalysts design and applications.

A highly stable TiO2/covalent organic framework heterojunction photocatalyst boosting charge transfer for visible-light-driven CO2 reduction

In this study, we present a novel heterojunction photocatalyst (TiO2-TTCOF) boosting charge transfer for visible-light-driven CO2 to CO conversion without photosensitizer or sacrificial agents. The 10% TiO2-TTCOF heterojunction photocatalyst is able to catalyze CO2 conversion, resulting in a highest CO production rate of 139.1 μmol g−1 with a selectivity of 96% and O2 production rate of 73.1 μmol g−1. Additionally, time-resolved fluorescence decay spectra confirmed the heterostructure between TTCOF and TiO2 can promote photoelectron transfer. The ATR-IFTS spectra indicated the photocatalytic reaction pathway.

Longitudinal modeling of residual carbon dioxide and residual feed intake in the Nordic Red dairy cattle

Feed utilization efficiency is an important trait in dairy production playing a significant role in reducing feed costs and lowering methane emission. One of the metrics used to measure feed efficiency in dairy cows is residual feed intake (RFI). This metric requires routine measurement of feed intake. Since there is a positive high correlation between heat production and carbon dioxide (CO2) production on the one hand and heat production and efficiency on the other hand, residual carbon dioxide (RCO2) might be a useful metric to improve feed efficiency. The objectives of this study were to model the trajectories of RCO2 and RFI as well as to estimate their repeatabilities and correlations at different stages of lactation. Daily CO2 output and feed intake were recorded from 46 primiparous Nordic Red dairy cows using two Greenfeed Emissions Monitoring™ systems from 2 to 305 days in milk (DIM). Edited data comprised 5 995 daily averages. To calculate predicted values of CO2 and DM intake (DMI), prediction models were developed by fitting multiple regression models to observations. Subsequently, RCO2 and RFI were calculated by subtracting predicted values of CO2 and DMI from their corresponding actual observations. A random regression bivariate model was fitted to estimate repeatabilities and animal correlations within lactation at different DIMs between RCO2 and RFI traits. The model fitted included fixed effects of year-month of recording, lactation month, fixed regressions as well as random regressions for the animal effect. The residual variance was considered to be heterogeneous. Repeatabilities and animal correlations of RCO2 and RFI between selected DIM (for every 30 DIM i.e., 6, 36,…, 246 and 276) were calculated. Repeatability of RCO2 was high at the beginning of lactation (0.72 at DIM 6) and decreased around the peak of milk production (0.27 at DIM 96) and again increased gradually toward the end of lactation. Similarly, RFI also had high repeatability at the beginning (0.86 at DIM 6); however, it decreased in mid-lactation (0.37 at DIM 156) and then increased toward the end of lactation. Animal correlations between RCO2 and RFI were moderate to high on the same DIM and ranged from 0.37 to 0.88. Overall, we found that animals with higher CO2 production than expected also consume more DMI than expected, but the moderate correlation between RCO2 and RFI found in this study calls for more research to assess the potential of RCO2 to become a new feed efficiency metric.

Comprehensive evaluation of low-temperature oxidation characteristics of low-rank bituminous coal and oil shale

The coexistence of coal and oil shale mining conditions exacerbates the complexity of coal spontaneous combustion (CSC) prevention, so conducting in-depth research on the spontaneous combustion characteristics of coal, oil shale, and their mixed samples is necessary. A programmed heating system simulated the low-temperature oxidation process of bituminous coal and oil shale under different air volumes. It was found that CO concentration, C2H4 concentration, and Graham's fire coefficient (R1, R2) can be used as indicator gases to predict the CSC process. Compared with oil shale and mixed samples, bituminous coal has a higher CO production rate, oxygen consumption rate, heat release intensity, and lower apparent activation energy during the slow oxidation stage. Meanwhile, bituminous coal also has lower peak values of minimum float coal thickness, lower limit oxygen concentration, and maximal air leakage intensity, which means that bituminous coal in the goaf is more prone to oxidation. However, the abundant free hydrogen bonds in oil shale can stabilize the hydrogen-deficient functional groups of bituminous coal, which weakens the oxidation ability of the mixed sample during the accelerated oxidation stage. In addition, the increased air volume fraction increases the oxygen adsorption efficiency of the mixed sample throughout the low-temperature oxidation process, which means that the M70 sample has a higher CSC risk. The results have enriched the research on the spontaneous combustion characteristics of coal, oil shale, and mixed samples, which may strengthen the management and control of CSC in coal and oil shale co-mining mines.

Polyarene Oxides with Tunable Quinone Units for Photocatalytic CO2 Reduction: A Simple Strategy toward Effective and Selective Catalysts.

The photocatalytic transformation of carbon dioxide (CO2) into valuable chemicals is a challenging process that requires effective and selective catalysts. However, most polymer-based photocatalysts with electron donor-acceptor (D-A) structures are synthesized with a fixed D-A ratio by using expensive monomers. Herein, we report a simple strategy to prepare polyarene oxides (PAOs) with quinone structural units via oxidation treatment of polyarene (PA). The resultant PAOs show tunable D-A structures and electronic band positions depending on the degree of oxidation, which can catalyze the photoreduction of CO2 with water under visible light irradiation, generating CO as the sole carbonaceous product without H2 generation. Especially, the PAO with an oxygen content of 17.6% afforded the highest CO production rate of 161.9 μmol g-1 h-1. It is verified that the redox transformation between quinone and phenolic hydroxyl in PAOs achieves CO2 photoreduction coupled with water oxidation. This study provides a facile way to access conjugated polymers with a tunable D-A structure and demonstrates that the resultant PAOs are promising photocatalysts for CO2 reduction.

Assembling an S-type heterojunction comprising vacancy-rich CeO2-x and CuBi2O4 for improved photocatalytic oxidation of gaseous toluene

The exploration of highly efficient methods for degrading VOCs, with concurrent low energy consumption and lasting reusability, holds significant appeal. In this regard, an S-type CuBi2O4/CeO2-x heterojunction with the robust interfacial interactions is presented as an active photocatalyst for the efficient decomposition of gaseous toluene under full-spectrum irradiation. The optimal sample CC15 effectively degrades gaseous toluene at a high concentration of 1800 ppm within 2 h, achieving a notable CO2 yield of 87.05 %, and a TOC (total organic carbon) removal rate of 89.33 %. Furthermore, CuBi2O4/CeO2-x exhibits exceptional stability, maintaining its 100 % degradation capability over 32 cycles for nearly 64 h. Comparative characterization reveals that the superior performance derives from an abundance of oxygen vacancies and effective pre-adsorption capabilities, which facilitate rapid adsorption of VOCs on the catalyst surface, thereby increasing the likelihood of degradation reactions. Additionally, the formation of an S-type heterojunction, valence pairing between Bi3+ and Ce3+/4+ ions, and strong interfacial interactions serve as the primary pathways for the efficient separation of photogenerated carriers, contributing to the high CO2 production rate and prolonged cycle stability. The present investigation underscores the significant potential of vacancy-rich S-type heterojunctions and interfacial interactions between composite components, offering excellent activity and long-term availability for VOCs removal.

Downsizing Porphyrin Covalent Organic Framework Particles Using Protected Precursors for Electrocatalytic CO2 Reduction.

Covalent organic frameworks (COFs) are promising electrocatalyst platforms owing to their designability, porosity, and stability. Recently, COFs with various chemical structures are developed as efficient electrochemical CO2 reduction catalysts. However, controlling the morphology of COF catalysts remains a challenge, which can limit their electrocatalytic performance. Especially, while porphyrin COFs show promising catalytic properties, their particle size is mostly large and uncontrolled because of the severe aggregation of crystallites. In this work, a new synthetic methodology for rationally downsized COF catalyst particles is reported, where a tritylated amine is employed as a novel protected precursor for COF synthesis. Trityl protection provides high solubility to a porphyrin precursor, while its deprotection proceeds in situ under typical COF synthesis conditions. Subsequent homogeneous nucleation and colloidal growth yield smaller COF particles than a conventional synthesis, owing to suppressed crystallite aggregation. The downsized COF particles exhibit superior catalytic performance in electrochemical CO2 reduction, with higher CO production rate and faradaic efficiency compared to conventional COF particles. The improved performance is attributed to the higher contact area with a conductive agent. This study reveals particle size as an important factor for the evaluation of COF electrocatalysts and provides a strategy to control it.

Enhanced biodegradable polyester film degradation in soil by sequential cooperation of yeast-derived esterase and microbial community.

The degradation of biodegradable plastics poses a significant environmental challenge and requires effective solutions. In this study, an esterase derived from a phyllosphere yeast Pseudozyma antarctica (PaE) enhanced the degradation and mineralization of poly(butylene succinate-co-adipate) (PBSA) film in soil. PaE was found to substitute for esterases from initial degraders and activate sequential esterase production from soil microbes. The PBSA film pretreated with PaE (PBSA-E) rapidly diminished and was mineralized in soil until day 55 with high CO2 production. Soil with PBSA-E maintained higher esterase activities with enhancement of microbial abundance, whereas soil with inactivated PaE-treated PBSA film (PBSA-inact E) showed gradual degradation and time-lagged esterase activity increases. The fungal genera Arthrobotrys and Tetracladium, as possible contributors to PBSA-film degradation, increased in abundance in soil with PBSA-inact E but were less abundant in soil with PBSA-E. The dominance of the fungal genus Fusarium and the bacterial genera Arthrobacter and Azotobacter in soil with PBSA-E further supported PBSA degradation. Our study highlights the potential of PaE in addressing concerns associated with biodegradable plastic persistence in agricultural and environmental contexts.