Photosynthesis System Research Articles

Dynamic Characteristics of Soil Respiration in Park Green Spaces in Qingdao City

Urban green spaces play an essential role in maintaining the carbon cycle and mitigating climate change in urban ecosystems. In order to gain more carbon sinks from urban green ecosystems, it is essential to determine the carbon sequestration statuses and soil respiration rates of dominant green spaces, especially park green spaces. However, in comparison to natural ecosystems, the dynamic characteristics of soil respiration in artificial park green spaces remain unclear. This study investigated the soil respiration rates for three forest communities (dominated by Prunus serrulata var. lannesiana, Cedrus deodara, Ginkgo biloba, respectively), a shrub community (dominated by Aucuba japonica var. variegata) and a lawn community (dominated by Poa pratensis) in the Qingdao Olympic Sculpture and Culture Park. We used the CRIAS-3 portable photosynthesis system in combination with the SRC-1 soil respiration chamber to measure the soil respiration rate from July 2022 to June 2023 and analyzed the dynamic variations in the soil respiration rate for these specific plant communities. Our results showed that the diurnal variation in soil respiration presented a unimodal curve for the five plant communities, and it peaked at midday or in the early afternoon. They also exhibited a significant seasonal difference in the soil respiration rate, which was characterized by higher rates in summer and lower rates in winter. The lawn community exhibited significantly higher soil respiration rates compared to the woody plant community. The mean annual soil respiration rate (RS) was, respectively, 2.88 ± 0.49 µmol·m−2·s−1, 1.94 ± 0.31 µmol·m−2·s−1, 1.43 ± 0.21 µmol·m−2·s−1, 1.24 ± 0.14 µmol·m−2·s−1 and 1.05 ± 0.11 µmol·m−2·s−1 for the lawn community, Ginkgo biloba community, Prunus serrulata var. lannesiana community, shrub community and Cedrus deodara community. The soil temperature at a 10 cm depth (T10) accounted for 67.39–86.76% of the variation in the soil respiration rate, while the soil volumetric water content at a 5 cm depth (W5) accounted for 9.29–44.01% of the variation for the five plant communities. The explained variance for both T10 and W5 ranged from 67.8% to 87.6% for the five plant communities. The Q10 values for the five different communities ranged from 1.97 to 2.75. Based on these findings, this paper concludes that the factors influencing the soil respiration process in urban green spaces are more complicated in comparison to natural ecosystems, and it is essential to comprehensively analyze these driving factors and key controlling factors of soil respiration across urban green spaces in future studies.

Exogenous hydrogen sulfide increased Nicotiana tabacum L. resistance against drought by the improved photosynthesis and antioxidant system

Drought stress is an abiotic stressor that impacts photosynthesis, plant growth, and development, leading to decreased crop yields. Sodium hydrosulfide (NaHS), an exogenous additive, has demonstrated potential regulatory effects on plant responses to polyethylene glycol-induced drought stress in tobacco seedlings. Compared to the control, drought stress induced by 15 g/L PEG-6000 significantly reduced several parameters in tobacco seedlings: shoot dry weight (22.83%), net photosynthesis (37.55%), stomatal conductance (33.56%), maximum quantum yield of PSII (Fv/Fm) (11.31%), photochemical quantum yield of PSII (ΦPSII) (25.51%), and photochemical quenching (qP) (18.17%). However, applying NaHS, an H2S donor, mitigated these effects, ultimately enhancing photosynthetic performance in tobacco seedlings. Furthermore, optimal NaHS concentration (0.4 mM) effectively increased leaf stomatal aperture, relative water content (RWC) and root activity, as well as facilitated the absorption of N, K, Mg and S. It also enhanced the accumulation of soluble sugar and proline content to maintain osmotic pressure balance under drought stress. Compared to drought alone, pretreatment with NaHS also bolstered the antioxidant defense system in leaves, leading to 22.93% decrease in hydrogen peroxide (H2O2) content, a 22.19% decrease in malondialdehyde (MDA) content and increased activities of ascorbate peroxidase (APX) by 28.13%, superoxide dismutase (SOD) by 17.07%, peroxidase (POD) by 46.99%, and catalase (CAT) by 65.27%. Consequently, NaHS protected chloroplast structure and attenuated chlorophyll degradation, thus mitigating severe oxidative damage. Moreover, NaHS elevated endogenous H2S levels, influencing abscisic acid (ABA) synthesis and the expression of receptor-related genes, collaboratively participating in the response to drought stress. Overall, our findings provide valuable insights into exogenous NaHS’s role in enhancing tobacco drought tolerance. These results lay the foundation for further research utilizing H2S-based treatments to improve crop resilience to water deficit conditions.

An open‐source LED lamp for use with the LI‐6800 photosynthesis system

AbstractPremiseControlling light flux density during carbon dioxide assimilation measurements is essential in photosynthesis research. Commercial lamps are expensive and are based on monochromatic light‐emitting diodes (LEDs), which deviate significantly in their spectral distribution compared to sunlight.Methods and ResultsUsing LED‐emitted white light with a color temperature similar to sunlight, we developed a cost‐effective lamp compatible with the LI‐6800 Portable Photosynthesis System. When coupled with customized software, the lamp can be controlled via the LI‐6800 console by a user or Python scripts. Testing and calibration show that the lamp meets the quality needed to estimate photosynthesis parameters.ConclusionsThe lamp can be built using a basic electronics lab and a 3D printer. Calibration instructions are supplied and only require equipment commonly available at plant science laboratories. The lamp is a cost‐effective alternative to perform photosynthesis research coupled with the popular LI‐6800 photosynthesis measuring system.

Novel Inorganic-Organic Dual-Photosensitizing Dinuclear-Metal Self-Assembly System for Efficient Artificial Photosynthesis without Sacrificial Electron Donors.

Owing to the unique synergistic effect, dinuclear-metal-molecule-catalysts (DMCs) show excellent performance in catalytic fields. However, for overall photocatalytic CO2 reaction (CO2RR), it is still a challenge to construct well-matched photosensitizer (PS) components for DMCs-based photocatalysts. Inorganic-quantum-dot PS possesses capacities of multiple exciton generation and catalyzing water oxidation but is incompatible with DMCs. In contrast, organic PS can be covalently linked with DMCs but inescapable of using sacrificial electron donors. For overall photocatalytic CO2RR, organic-inorganic dual-photosensitizing system might be a promising candidate. Herein, we employed covalent-linking and electrostatic-driven approaches to construct the self-assembly of pyrene-sensitized Co2L DMCs (Py-Co2L) and perovskite (PVK) quantum dots, i.e., PVK@[Py-Co2L]. Using H2O as an electron donor, PVK@[Py-Co2L] realized 105.24 μmol·g-1·h-1 CO yield in photocatalytic CO2RR, much higher than PVK (15.44 μmol·g-1·h-1) and PVK@Co2L (32.30 μmol·g-1·h-1), ascribing to the efficient photogenerated charge separation and transfer. The experimental results and theoretical investigations demonstrated that the pyrene linked on Co2L boosted the electron delivery from PVK to DMCs. Besides, this strategy could also be extended to the photocatalytic H2 evolution coupled with alcohol oxidation. As a proof-of-concept, our work lightens the integration of DMCs, organic and inorganic PS components, promoting the development of photocatalysis without sacrificial electron donors.

Novel strategies for enhancing energy metabolism and wastewater treatment in algae-bacteria symbiotic system through carbon dots-induced photogenerated electrons: The definitive role of accelerated electron transport

The nitrogen removal efficiency of the algae-bacteria symbiotic system (ABSS) remains challenging due to competition for light capture and insufficient electron donors in aquaculture wastewater. To overcome this bottleneck issue, we first identified and reported the introduction of photogenerated electrons into ABSS by coupling them with carbon dots (CDs). The energy metabolism (21.52 %-56.25 %) and pollutant degradation efficiency (89.36 %-96.42 %) of ABSS/CDs surpassed the biochemical limit observed in traditional ABSS. Notably, the addtion of CDs facilitated an opening of the plastoquinone-pool (PQ-pool) valve and accelerated electron transfer rates, enabling photogenerated electrons to selectively target light-harvesting complexs as activation sites, thereby mobilizing photosynthesis and respiratory system activity to enhance nicotinamide adenine dinucleotide reduced (NADH) and adenosine triphosphate (ATP) production while promoting tricarboxylic acid (TCA) and Calvin cycle processes. In simulated swine wastewater treatment, ABSS/CDs achieved higher removal rates for the chemical oxygen demand (COD), total nitrogen (TN) and ammonium-nitrogen (NH4+-N) (100 %, 99.23 % and 98.62 % respectively) compared to pure culture systems alone. Network-based analysis revealed that ABSS/CDs improved microbial community structure stability within the photobioreactor while demonstrating efficient coupling between fungi, nitrifying bacteria, and denitrifying bacteria for enhanced performance in nitrogen removal processes. The upregulation of nitrogen metabolism and PQ-pool genes maintains efficient electron transport rates and contributes to nitrogen removal. This study expands our understanding of the physiological aptitudes of ABSS and provides valuable insights into applying CDs photoelectrons for enhanced wastewater treatment.

Morphophysiological adaptations and fragrance profile analysis of two relocated orchid species

This study investigates the morpho-physiological adaptations and fragrance profiles of 2 relocated orchid species, Cattleya aclandiae x Brassavola Little star (V1) and Dendrobium var. Meesangnil (V2), following their translocation from Nagercoil to Coimbatore, India. The research aims to elucidate the mechanisms underlying successful acclimatization of these fragrant orchids to a new environment, with implications for horticulture, conservation and therapeutic applications. Comprehensive analyses were conducted on vegetative growth parameters, flowering characteristics, physiological responses and volatile organic compound (VOC) profiles. Morphological assessments revealed distinct adaptive strategies between the 2 species, with Dendrobium exhibiting superior vertical growth (39.13 cm) and leaf production (9 leaves/plant), while Cattleya developed larger leaves (30.483 cm length, 7.178 cm breadth) and longer internodes (5.061 cm). Flowering characteristics also differed significantly, with Cattleya demonstrating earlier spike emergence and floret opening. Physiological analyses using a CI-340 Handheld Photosynthesis System showed higher photosynthetic rates, transpiration rates and stomatal conductance in Dendrobium, suggesting a more resource-acquisitive strategy. Gas chromatography-mass spectrometry (GC-MS) analysis identified unique VOC profiles for each species, with 30 compounds detected in both varieties, including notable compounds such as n-Hexadecanoic acid, Octadecanoic acid and beta-Sitosterol. The study also explored potential applications in therapeutic horticulture, highlighting the diverse sensory and educational value of these orchid species. This comprehensive analysis of morphological, physiological and biochemical adaptations provides valuable insights into orchid acclimation processes and their potential for conservation and horticultural applications, contributing to our understanding of plant adaptability in the face of environmental changes and offering a foundation for future studies on orchid biology, ecology and therapeutic uses.

Quercus acutissima exhibits more adaptable water uptake patterns in response to seasonal changes compared to Pinus massoniana

BackgroundSeasonal precipitation variability significantly affects water use in forests; however, whether water uptake is adapted to changes in precipitation, particularly whether it could affect the coexistence of tree species, has rarely been quantified in forest systems. MethodIn this study, dual stable isotopes and the Li-6400 portable photosynthesis system were used to determine the water sources of a mixed conifer (Pinus massoniana) and broadleaf (Quercus acutissima) forest and changes in hydraulic characteristics during the dry and wet seasons in a southern hilly region of China. ResultsAlthough the hydraulic characteristics of P. massoniana were lower than those of Q. acutissima, it maintained a stable water source from the deep soil layer and a higher stomatal conductance (Gs), leading to a higher transpiration rate (Tr) during the growing seasons. Q. acutissima mainly absorbed water from deeper soil layers in the dry season and took up from shallow soil layers in the wet season. Its Gs values exhibited sensitivity to precipitation, while it maintained a lower Tr value during the growing seasons. The excessive water-use strategy observed in P. massoniana may confer weak drought-tolerance during higher frequency and more intense extreme precipitation events, whereas Q. acutissima may exhibit better ecological adaption to precipitation changes. ConclusionsThe overlap of water niches in mixed forests did not appear to affect the coexistence of tree species. The present study provides insights into reforestation and water management in the southern hilly regions of China.

Identification and Evaluation of Diploid and Tetraploid Passiflora edulis Sims.

Passiflora edulis Sims (2n = 18) is a perennial plant with high utilization values, but its spontaneous polyploidy in nature has yet to be seen. Thus, this study aims to enhance our understanding of polyploidy P. edulis and provide rudimentary knowledge for breeding new cultivars. In this study, colchicine-induced tetraploid P. edulis (2n = 36) was used as experimental material (T1, T2, and T3) to explore the variances between it and its diploid counterpart in morphology, physiology, and biochemical characteristics, and a comparison of their performance under cold stress was conducted. We measured and collected data on phenotype parameters, chlorophyll contents, chlorophyll fluorescence, photosynthesis, osmotic substances, and antioxidant enzymes. The results showed that tetraploid P. edulis exhibited a shorter phenotype, more giant leaves, darker leaf color, and longer and fewer roots. Moreover, the physiological and biochemical analysis indicated that the tetraploid P. edulis had better photosynthesis systems and higher chlorophyll fluorescence parameters than the diploid P. edulis. Additionally, the tetraploid P. edulis had higher activity of antioxidant enzymes (SOD, POD, CAT) and lower MDA content to maintain better resistance in low temperatures. Overall, we conclude that there were apparent differences in the morphological, physiological, and biochemical traits of the tetraploid and diploid P. edulis. The tetraploid plants showed better photosynthesis systems, higher osmotic substance content, and antioxidant enzyme activity than the diploid, even under cold stress. Our results suggest that tetraploids with more abundant phenotype variation and better physiological and biochemical traits may be used as a new genetic germplasm resource for producing new P. edulis cultivars.

GO promotes detoxification of nicosulfuron in sweet corn by enhancing photosynthesis, chlorophyll fluorescence parameters, and antioxidant enzyme activity

Although graphene oxide (GO) has extensive recognized application prospects in slow-release fertilizer, plant pest control, and plant growth regulation, the incorporation of GO into nano herbicides is still in its early stages of development. This study selected a pair of sweet corn sister lines, nicosulfuron (NIF)-resistant HK301 and NIF-sensitive HK320, and sprayed them both with 80 mg kg–1 of GO-NIF, with clean water as a control, to study the effect of GO-NIF on sweet corn seedling growth, photosynthesis, chlorophyll fluorescence, and antioxidant system enzyme activity. Compared to spraying water and GO alone, spraying GO-NIF was able to effectively reduce the toxic effect of NIF on sweet corn seedlings. Compared with NIF treatment, 10 days after of spraying GO-NIF, the net photosynthetic rate (A), stomatal conductance (Gs), transpiration rate (E), photosystem II photochemical maximum quantum yield (Fv/Fm), photochemical quenching coefficient (qP), and photosynthetic electron transfer rate (ETR) of GO-NIF treatment were significantly increased by 328.31%, 132.44%, 574.39%, 73.53%, 152.41%, and 140.72%, respectively, compared to HK320. Compared to the imbalance of redox reactions continuously induced by NIF in HK320, GO-NIF effectively alleviated the observed oxidative pressure. Furthermore, compared to NIF treatment alone, GO-NIF treatment effectively increased the activities of superoxide dismutase (SOD), guaiacol peroxidase (POD), catalase (CAT), and ascorbate peroxidase (APX) in both lines, indicating GO induced resistance to the damage caused by NIF to sweet corn seedlings. This study will provides an empirical basis for understanding the detoxification promoting effect of GO in NIF and analyzing the mechanism of GO induced allogeneic detoxification in cells.

Two-photon upconversion photoluminescence in CsPbBr3 nanoplates

The utilization of solar energy by light conversion processes in both natural and artificial photosynthesis systems has become a pivotal means of sustaining a consistent power supply for our daily lives and production. In general, these reactions rely on the visible spectra region where the sun produces abundant energy according to the black body's emission. Further expanding the adoption of the near-infrared (NIR) spectral region through upconversion has become an intelligent strategy to improve the entire utilization rate of solar energy. In this work, the two-photon upconversion (TPUC) properties were discovered in CsPbBr3 nanoplates (NPs) emitted at 450 nm, and a sub-gap energy level was observed to serve as the center to facilitate the upconversion process. The excitation threshold for TPUC is drastically lower than that for the two-photon absorption, another nonlinear upconversion path that requires strengthened excitation power. Moreover, a significant negative correlation between the excitation threshold for TPUC in the CsPbBr3 NPs and the exciton binding energy was unveiled, which could be attributed to the enhanced quantum confinement effects. Our work paved the way for a feasible way to expand the utilization of the NIR spectral region in light conversion applications.

Construction of An Artificial Photosynthesis System with A Single CdS QDs-Ferritin Hybrid Molecule.

Establishing artificial photosynthesis systems in a simple but effective manner to mitigate the greenhouse effect and address the energy crisis remains challenging. The combination of photocatalysis technology with bioengineering is an emerging field with great potential to construct such artificial photosynthesis systems, but so far, it has barely been explored in this area. Herein, an artificial photocatalysis platform is constructed with high CO2 conversion and H2O splitting capability by integration of CdS QDs into the intra-subunit interface of H-type ferritin (Marsupenaeus japonicus), a natural ferroxidase through protein interface redesign. The crystal structure of the synthesized CdS QDs with engineered ferritin molecules as bio-templates confirmed the design at an atomic level. Notably, upon absorbing desirable visible light (≈420nm), such a single CdS-ferritin hybrid molecule is able to selectively catalyze the reduction of CO2 into HCOOH (≈90%), meanwhile catalyzing the oxidation of H2O into O2 in an aqueous environment. The O2 production rate reached to 180µmolg-1h-1, and the HCOOH output hit almost 800µmolg-1h-1. This work advances the utilization of the four-helix bundle structure for crafting artificial photosynthesis systems, facilitating the seamless integration of bioengineering and photocatalysis technology.

Bioinspired octanuclear copper cubane complex as an efficient molecular electrocatalyst for water oxidation

Water oxidation catalysts (WOCs) with excellent activity and stability are highly desired. Numerous efforts have been dedicated to develop WOCs mimicking the cubic structure and activity of Mn4CaO5 cluster in oxygen-evolving center (OEC) of photosynthesis system II (PSII). Herein, a octanuclear Cu cluster [Cu8(dpy{OH}O)8(OAc)4]4+ (1, dpy{OH}O− = the monoanion of the hydrated, gem-diol form of di-2-pyridyl ketone) that contains two Cu4O4 cubic fragments with bioinspired structure mimicking the Mn4CaO5 cluster of OEC of natural PSII is developed as efficient homogeneous catalyst for electrochemical water oxidation under near neutral condition for the first time. It exhibits outstanding water oxidation catalytic activity via accelerating oxygen evolution with onset overpotential of 730 mV and appreciable turnover frequency of 20.1 s−1. Collective experiments together confirmed the homogeneity and stability of cluster 1 under long-term water oxidation catalytic cycle. Kinetic study reveals the water nucleophilic attack (WNA) catalytic mechanism occurs on the coordination unsaturated Cu center of the cluster. This work provides the inspiration of the development of robust bioinspired catalyst for electrochemical water oxidation.

Design, Synthesis, and Herbicidal Activity of Natural Naphthoquinone Derivatives Containing Diaryl Ether Structures.

Photosynthesis system II (PS II) is an important target for the development of bioherbicides. In this study, a series of natural naphthoquinone derivatives containing diaryl ether were designed and synthesized based on the binding model of lawsone and PS II D1. Bioassays exhibited that most compounds had more than 80% inhibition of Portulaca oleracea and Echinochloa crusgalli roots at a dose of 100 μg/mL and compounds B4, B5, and C3 exhibited superior herbicidal activities against dicotyledonous and monocotyledon weeds to commercial atrazine. In particular, compound B5 exhibited excellent herbicidal activity at a dosage of 150 g a.i./ha. In addition, compared with atrazine, compound B5 causes less damage to crops. Molecular docking studies revealed that compound B5 effectively interacted with Pisum sativum PS II D1 via diverse interaction models, such as π-π stacking and hydrogen bonds. Molecular dynamics simulation studies and chlorophyll fluorescence measurements revealed that compound B5 acted on PS II. This is the first report of natural naphthoquinone derivatives targeting PS II and compound B5 may be a candidate molecule for the development of new herbicides targeting PS II.

Novel furan-containing linear polymer with strong built-in electric field for H2O2 photosynthesis

Using oxygen and water as raw materials, the photocatalytic production of H2O2 is a promising pathway. However, the limited charge separation efficiency represents a significant challenge in the photocatalysis field, as it impedes the generation of H2O2. Herein, a novel highly crystalline linear polymer has been synthesized here by bridging the strongly electronegative furan group with a diphenyl group, in order to adjust its molecular dipole moment to construct an intrinsic electric field to optimize photocatalytic performance. The optimal sample exhibited the best H2O2 synthesis rate of 2686 μmol·g−1·h−1 under pure water conditions, which is the best-performing linear conjugated polymer reported to date for H2O2 photosynthesis system. Importantly, the large internal dipole moment within furan-diphenyl linear polymer, together with the ordered crystalline structure induced robust built-in electric field, can facilitate migration and separation of photogenerated charge carriers. Manipulating molecular dipoles to enhance the built-in electric field can significantly improve photocatalytic activity, providing a new perspective for the rational design of functional linear conjugated polymers in green chemistry and sustainable production.

Enhanced inhibitory efficiency against toxic bloom forming Raphidiopsis raciborskii by Streptomyces sp. HY through triple algicidal modes: Direct and indirect attacks combined with bioflocculation

Raphidiopsis raciborskii (R. raciborskii) forms harmful cyanobacterial blooms globally, and poses a great threat to the safety of drinking water and public health. There is a great need to develop eco-friendly biological alternative measures to mitigate mass blooms of R. raciborskii. However, previous rare studies on algicidal microorganisms against R. raciborskii restricted this aim. Recently, an algicidal bacterium Streptomyces sp. HY (designated HY) was identified with flavones producing ability, and could remove up to 98.73 % of R. raciborskii biomass within 48 h by directly attacking the cyanobacterium and release of algicidal substances (i.e., flavonoids) with a inoculum ratio of 5 %. Algicidal rate of HY was enhanced by 88.05 %, 89.33 % under dark and light, and full-light conditions respectively, when compared with the dark condition. Its algicidal substances were stable in a broad range of temperature (−80–55 °C) and pH (3−11) conditions, and all treated groups exhibited ≈ 100 % algicidal rate at day 3. HY treatment disrupted the photosynthesis system and triggered serious oxidative stress resulting in severe morphological injury. Thereby, HY treatment significantly affected expression levels of several essential genes (i.e., psbA, psaB, rbcL, ftsZ, recA, grpE), and simultaneously inhibited the biosynthesis and release of cylindrospermopsin. Yet, HY treatment didn’t show any toxicity to zebrafish test embryos. Such results indicate that HY is a promising algicidal candidate strain to control global R. raciborskii blooms, and holds great promises for an effective biological measure to sustain water safety.

Atomically Precise Regulation of the N-Heterocyclic Microenvironment in Triazine Covalent Organic Frameworks for Coenzyme Photocatalytic Regeneration.

Artificial photosynthesis represents a sustainable strategy for accessing high-value chemicals; however, the conversion efficiency is significantly limited by its difficulty in the cycle of coenzymes such as NADH. In this study, we report a series of isostructural triazine covalent organic frameworks (COFs) and explore their N-substituted microenvironment-dependent photocatalytic activity for NADH regeneration. We discovered that the rational alteration of N-heterocyclic species, which are linked to the triazine center through an imine linkage, can significantly regulate both the electron band structure and planarity of a COF layer. This results in different separation efficiencies of the photoinduced electron-hole pairs and electron transfer behavior within and between individual layers. The optimal COF catalyst herein achieves an NADH regeneration capacity of 89% within 20 min, outperforming most of the reported nanomaterial photocatalysts. Based on this, an artificial photosynthesis system is constructed for the green synthesis of a high-value compound, L-glutamate, and its conversion efficiency significantly surpasses the enzymatic approach without the NADH photocatalytic cycle. This work offers new insights into the coenzyme regeneration by means of regulating the distal heterocyclic microenvironment of a COF skeleton, holding great potential for the green photosynthesis of important chemicals.

Anisotropic Dual S‐Scheme Heterojunctions Mimic Natural Photosynthetic System for Boosting Photoelectric Response

AbstractThe design of heterojunctions that mimic natural photosynthetic systems holds great promise for enhancing photoelectric response. However, the limited interfacial space charge layer (SCL) often fails to provide sufficient driving force for the directional migration of inner charge carriers. Drawing inspiration from the electron transport chain (ETC) in natural photosynthesis system, we developed a novel anisotropic dual S‐scheme heterojunction artificial photosynthetic system composed of Bi2O3−BiOBr−AgI for the first time, with Bi2O3 and AgI selectively distributed along the bicrystal facets of BiOBr. Compared to traditional semiconductors, the anisotropic carrier migration in BiOBr overcomes the recombination resulting from thermodynamic diffusion, thereby establishing a potential ETC for the directional migration of inner charge carriers. Importantly, this pioneering bioinspired design overcomes the limitations imposed by the limited distribution of SCL in heterojunctions, resulting in a remarkable 55‐fold enhancement in photoelectric performance. Leveraging the etching of thiols on Ag‐based materials, this dual S‐scheme heterojunction is further employed in the construction of photoelectrochemical sensors for the detection of acetylcholinesterase and organophosphorus pesticides.

Anisotropic Dual S-Scheme Heterojunctions Mimic Natural Photosynthetic System for Boosting Photoelectric Response.

The design of heterojunctions that mimic natural photosynthetic systems holds great promise for enhancing photoelectric response. However, the limited interfacial space charge layer (SCL) often fails to provide sufficient driving force for the directional migration of inner charge carriers. Drawing inspiration from the electron transport chain (ETC) in natural photosynthesis system, we developed a novel anisotropic dual S-scheme heterojunction artificial photosynthetic system composed of Bi2O3-BiOBr-AgI for the first time, with Bi2O3 and AgI selectively distributed along the bicrystal facets of BiOBr. Compared to traditional semiconductors, the anisotropic carrier migration in BiOBr overcomes the recombination resulting from thermodynamic diffusion, thereby establishing a potential ETC for the directional migration of inner charge carriers. Importantly, this pioneering bioinspired design overcomes the limitations imposed by the limited distribution of SCL in heterojunctions, resulting in a remarkable 55-fold enhancement in photoelectric performance. Leveraging the etching of thiols on Ag-based materials, this dual S-scheme heterojunction is further employed in the construction of photoelectrochemical sensors for the detection of acetylcholinesterase and organophosphorus pesticides.

Coordinated responses of rice (Oryza sativa) to the stresses of benzotriazole ultraviolet stabilizers (BZT-UVs): Antioxidative system, photosynthetic activity, and metabolic regulation

Massive use of plastic products has caused their accumulation in soils, releasing large amounts of endogenous plastic additives (e.g., benzotriazole ultraviolet stabilizers, in short BZT-UVs) into terrestrial ecosystems. However, their plant toxicity is little known. Herein, we investigated the occurrence of BZT-UVs in contaminated farmland and selected three BZT-UV congeners to explore their toxic effects on the antioxidant, photosynthetic, and metabolic perturbation on rice (Oryza sativa). Results showed that the mean concentrations of ∑BZT-UVs in soil and plant samples were 180.7 ng/g dw and 156.4 ng/g dw, respectively. UV-P, UV-327 and UV-328 were the dominant BZT-UV congeners in both of soils and plants. Three BZT-UV congeners caused oxidative damages to rice in a dose-dependent manner, especially for UV-328. Functional genes involved in chlorophyll synthetases was inhibited by over 50 % under the stress of BZT-UVs, whereas those responsible for chlorophyll degradation were obviously promoted. The chlorophyll content was thus decreased, leading to a weakened photosynthesis system and an unbalanced carbon metabolism. The transcriptome and metabolome proved that the flux of carbohydrate metabolism and amino acid metabolism were obviously promoted in plants induced by BZT-UVs, which could inhibit the growth of rice. These findings offered insights into the coordinated responses of plants and advanced our understanding of potential ecological risks of BZT-UVs to terrestrial ecosystems.

Boosted Charge Transfer for Highly Efficient Photosynthesis of H2O2 over Z‐Scheme I−/K+ Co‐Doped g‐C3N4/Metal–Organic‐Frameworks in Pure Water under Visible Light

AbstractPhotocatalytic oxygen reduction reaction (ORR) is an environmentally friendly and cost‐effective approach for H2O2 synthesis. However, the current photosynthesis system suffers from sluggish kinetics, rapid recombination of photoexcited charge carriers, and weak redox potentials, resulting in unsatisfactory solar‐to‐chemical conversion efficiency. Herein, a Z‐scheme heterojunction (UiO/IKCN) is constructed through coupling I−/K+ co‐doped g‐C3N4 (IKCN) with NH2‐UiO‐66, a typical metal‐organic framework material. Under visible light irradiation, the optimal UiO/IKCN exhibits exceptional H2O2 production rates in pure water (13.3 mM g−1 h−1) and in isopropanol solution (72.6 mM g−1 h−1), that is 48.4 times higher than pristine CN in isopropanol (1.5 mM g−1 h−1). A high apparent quantum yield of 10.28% at 420 nm is achieved by UiO/IKCN, surpassing most previously reported values. The dominating role of two‐electron ORR in H2O2 photosynthesis is elucidated in detail. The significantly enhanced photocatalytic activity can be attributed to the facilitated charge separation and Z‐scheme charge transfer, which are unambiguously verified by stable‐state surface photovoltage, transient photoluminescence, femtosecond transient absorption spectroscopy, in‐situ irradiated X‐ray photoelectron spectroscopy, and density functional theory calculations. This study represents the first exploration of H2O2 production using NH2‐UiO‐66 and provides insights into the rational design of Z‐scheme heterojunction for highly efficient photosynthesis.