Disinfection and post-disinfection conditions drive bacterial and viral evolution across the environment and host.

Water disinfection practices have long been established as a critical engineering intervention for controlling pathogen transmission and safeguarding individual and public health. However, recent discoveries have unveiled the significant role disinfection and post-disinfection play in accelerating the development of resistance to disinfectants and antimicrobial drugs within bacterial and viral communities in the environment. This phenomenon, in turn, may facilitate the emergence of persistent microbes and those with new genetic characteristics. These microbes may thrive in host environments with increased infectivity and resistance, posing challenges to current medical treatments and jeopardizing human health. In this perspective, we illuminate the intricate interplay between aquatic environments, microbes, and hosts and how microbial virulence evolves across the environment and host under the pressure of disinfection and post-disinfection conditions. We aim to draw attention to the previously overlooked potential risks associated with disinfection in driving the virulence evolution of bacteria and viruses, establish connections between pathogens in diverse environments and hosts within the overarching framework of the One Health concept, and ultimately provide guidelines for advancing future water disinfection technologies to effectively curb the spread of infectious diseases.

Fe-Fe Double-Atom Catalysts for Murine Coronavirus Disinfection: Nonradical Activation of Peroxides and Mechanisms of Virus Inactivation.

Peroxides find broad applications for disinfecting environmental pathogens particularly in the COVID-19 pandemic; however, the extensive use of chemical disinfectants can threaten human health and ecosystems. To achieve robust and sustainable disinfection with minimal adverse impacts, we developed Fe single-atom and Fe-Fe double-atom catalysts for activating peroxymonosulfate (PMS). The Fe-Fe double-atom catalyst supported on sulfur-doped graphitic carbon nitride outperformed other catalysts for oxidation, and it activated PMS likely through a nonradical route of catalyst-mediated electron transfer. This Fe-Fe double-atom catalyst enhanced PMS disinfection kinetics for inactivating murine coronaviruses (i.e., murine hepatitis virus strain A59 (MHV-A59)) by 2.17-4.60 times when compared to PMS treatment alone in diverse environmental media including simulated saliva and freshwater. The molecular-level mechanism of MHV-A59 inactivation was also elucidated. Fe-Fe double-atom catalysis promoted the damage of not only viral proteins and genomes but also internalization, a key step of virus lifecycle in host cells, for enhancing the potency of PMS disinfection. For the first time, our study advances double-atom catalysis for environmental pathogen control and provides fundamental insights of murine coronavirus disinfection. Our work paves a new avenue of leveraging advanced materials for improving disinfection, sanitation, and hygiene practices and protecting public health.

Transformation of Graphitic Carbon Nitride by Reactive Chlorine Species: "Weak" Oxidants Are the Main Players.

Graphitic carbon nitride (g-C3N4) nanomaterials hold great promise in diverse applications; however, their stability in engineering systems and transformation in nature are largely underexplored. We evaluated the stability, aging, and environmental impact of g-C3N4 nanosheets under the attack of free chlorine and reactive chlorine species (RCS), a widely used oxidant/disinfectant and a class of ubiquitous radical species, respectively. g-C3N4 nanosheets were slowly oxidized by free chlorine even at a high concentration of 200-1200 mg L-1, but they decomposed rapidly when ClO· and/or Cl2•- were the key oxidants. Though Cl2•- and ClO· are considered weaker oxidants in previous studies due to their lower reduction potentials and slower reaction kinetics than ·OH and Cl·, our study highlighted that their electrophilic attack efficacy on g-C3N4 nanosheets was on par with ·OH and much higher than Cl·. A trace level of covalently bonded Cl (0.28-0.55 at%) was introduced to g-C3N4 nanosheets after free chlorine and RCS oxidation. Our study elucidates the environmental fate and transformation of g-C3N4 nanosheets, particularly under the oxidation of chlorine-containing species, and it also provides guidelines for designing reactive, robust, and safe nanomaterials for engineering applications.

Electrospun Nanofibrous Membranes for Controlling Airborne Viruses: Present Status, Standardization of Aerosol Filtration Tests, and Future Development.

The global COVID-19 pandemic has raised great public concern about the airborne transmission of viral pathogens. Virus-laden aerosols with small size could be suspended in the air for a long duration and remain infectious. Among a series of measures implemented to mitigate the airborne spread of infectious diseases, filtration by face masks, respirators, and air filters is a potent nonpharmacologic intervention. Compared with conventional air filtration media, nanofibrous membranes fabricated via electrospinning are promising candidates for controlling airborne viruses due to their desired characteristics, i.e., a reduced pore size (submicrometers to several micrometers), a larger specific surface area and porosity, and retained surface and volume charges. So far, a wide variety of electrospun nanofibrous membranes have been developed for aerosol filtration, and they have shown excellent filtration performance. However, current studies using electrospinning for controlling airborne viruses vary significantly in the practice of aerosol filtration tests, including setup configurations and operations. The discrepancy among various studies makes it difficult, if not impossible, to compare filtration performance. Therefore, there is a pressing need to establish a standardized protocol for evaluating the electrospun nanofibrous membranes' performance for removing viral aerosols. In this perspective, we first reviewed the properties and performance of diverse filter media, including electrospun nanofibrous membranes, for removing viral aerosols. Next, aerosol filtration protocols for electrospun nanofibrous membranes were discussed with respect to the aerosol generation, filtration, collection, and detection. Thereafter, standardizing the aerosol filtration test system for electrospun nanofibrous membranes was proposed. In the end, the future advancement of electrospun nanofibrous membranes for enhanced air filtration was discussed. This perspective provides a comprehensive understanding of status and challenges of electrospinning for air filtration, and it sheds light on future nanomaterial and protocol development for controlling airborne viruses, preventing the spread of infectious diseases, and beyond.

Vesicle-Cloaked Rotavirus Clusters are Environmentally Persistent and Resistant to Free Chlorine Disinfection.

Recent discovery of vesicle-cloaked virus clusters (i.e., viral vesicles) has greatly challenged the central paradigm of viral transmission and infection as a single virion. To understand the environmental transmission of viral vesicles, we used an in vivo model to investigate their environmental persistence and engineering control by disinfection. Murine rotavirus vesicles maintained both their integrity and infectivity after incubation in filtered freshwater and wastewater for at least 7 days, with 24.5-27.5% of the vesicles still intact at 16 weeks after exposure to both waters. Free chlorine disinfection at a dosage of 13.3 mg min L-1 did not decompose murine rotavirus vesicles, and it was much less effective in inactivating rotaviruses inside vesicles than free rotaviruses based on the quantification of rotavirus shedding in mouse stool and rotavirus replication in small intestines. Rotavirus vesicles may be more environmentally transmissible than free rotaviruses regardless of disinfection. Vesicle-mediated en bloc transmission could be responsible for vesicles' resistance to disinfection due to an increased multiplicity of infection and/or genetic recombination or reassortment to promote infection. Our work highlights the environmental, biological, and public health significance of viral vesicles, and the findings call for urgent action in advancing disinfection for pathogen control.

Environmental application of chlorine-doped graphitic carbon nitride: Continuous solar-driven photocatalytic production of hydrogen peroxide.

Solar-driven photocatalytic generation of H2O2 over metal-free catalysts is a sustainable approach for value-added chemical production. Here, we synthesized chlorine-doped graphitic carbon nitride (Cl-doped g-C3N4) through a solvothermal method to effectively produce H2O2 with a rate of 1.19 ± 0.06 µM min-1 under visible light irradiation, which was improved by 104 times compared to pristine g-C3N4. Continuous net production of H2O2 was realized at a rate of 2.78 ± 0.10 µM min-1 up to 54 h with isopropanol as the hole scavenger, whereas H2O2 production was only sustained for ~ 6 h without scavengers. Both molecular simulations and advanced spectroscopic characterizations elucidated that the Cl dopant increased the charge transfer rate, decreased the bandgap, and reduced the activation energy of the rate-limiting step of O2 reduction, all of which favored H2O2 production. This work implemented a novel metal-free photocatalyst for sustainable H2O2 production and elucidated the mechanism for promoting H2O2 production that can guide future photoreactive nanomaterial design.

Waterborne Human Pathogenic Viruses in Complex Microbial Communities: Environmental Implication on Virus Infectivity, Persistence, and Disinfection.

Waterborne human pathogenic viruses challenge global health and economy. Viruses were long believed to transmit among hosts as individual, free particles. However, recent evidence indicates that viruses also transmit in populations, so-called en bloc transmission, by either interacting with coexisting bacteria, free-living amoebas, and other higher organisms through endosymbiosis and surface binding, or by being clustered inside membrane-bound vesicles or simply self-aggregating with themselves. En bloc transmission of viruses and virus-microbiome interactions could enable viruses to enhance their infectivity, increase environmental persistence, and resist inactivation from disinfection. Overlooking this type of transmission and virus-microbiome interactions may underestimate the environmental and public health risks of the viruses. We herein provide a critical perspective on waterborne human pathogenic viruses in complex microbial communities to elucidate the environmental implication of virus-microbiome interactions on virus infectivity, persistence, and disinfection. This perspective also provides insights on advancing disinfection and sanitation guidelines and regulations to protect the public health.

Photosensitized Electrospun Nanofibrous Filters for Capturing and Killing Airborne Coronaviruses under Visible Light Irradiation.

To address the challenge of the airborne transmission of SARS-CoV-2, photosensitized electrospun nanofibrous membranes were fabricated to effectively capture and inactivate coronavirus aerosols. With an ultrafine fiber diameter (∼200 nm) and a small pore size (∼1.5 µm), optimized membranes caught 99.2% of the aerosols of the murine hepatitis virus A59 (MHV-A59), a coronavirus surrogate for SARS-CoV-2. In addition, rose bengal was used as the photosensitizer for membranes because of its excellent reactivity in generating virucidal singlet oxygen, and the membranes rapidly inactivated 97.1% of MHV-A59 in virus-laden droplets only after 15 min irradiation of simulated reading light. Singlet oxygen damaged the virus genome and impaired virus binding to host cells, which elucidated the mechanism of disinfection at a molecular level. Membrane robustness was also evaluated, and in general, the performance of virus filtration and disinfection was maintained in artificial saliva and for long-term use. Only sunlight exposure photobleached membranes, reduced singlet oxygen production, and compromised the performance of virus disinfection. In summary, photosensitized electrospun nanofibrous membranes have been developed to capture and kill airborne environmental pathogens under ambient conditions, and they hold promise for broad applications as personal protective equipment and indoor air filters.

Radical-Driven Decomposition of Graphitic Carbon Nitride Nanosheets: Light Exposure Matters.

Understanding the transformation of graphitic carbon nitride (g-C3N4) is essential to assess nanomaterial robustness and environmental risks. Using an integrated experimental and simulation approach, our work has demonstrated that the photoinduced hole (h+) on g-C3N4 nanosheets significantly enhances nanomaterial decomposition under •OH attack. Two g-C3N4 nanosheet samples D and M2 were synthesized, among which M2 had more pores, defects, and edges, and they were subjected to treatments with •OH alone and both •OH and h+. Both D and M2 were oxidized and released nitrate and soluble organic fragments, and M2 was more susceptible to oxidation. Particularly, h+ increased the nitrate release rate by 3.37-6.33 times even though the steady-state concentration of •OH was similar. Molecular simulations highlighted that •OH only attacked a limited number of edge-site heptazines on g-C3N4 nanosheets and resulted in peripheral etching and slow degradation, whereas h+ decreased the activation energy barrier of C-N bond breaking between heptazines, shifted the degradation pathway to bulk fragmentation, and thus led to much faster degradation. This discovery not only sheds light on the unique environmental transformation of emerging photoreactive nanomaterials but also provides guidelines for designing robust nanomaterials for engineering applications.

Continuous photocatalysis via photo-charging and dark-discharging for sustainable environmental remediation: Performance, mechanism, and influencing factors.

Continuous photocatalysis via photo-charging and dark-discharging presents a paradigm shift in conventional photocatalysis with the requirement of continuous illumination to maintain the catalytic activity. This is expected to meet the ever-increasing demand for sustainable development of energy and environment driven by natural day-night cycles. Substantial advances in continuous photocatalysis for various environmental applications under light-dark cycles have been witnessed during the last decade. However, there lacks a systematic and critical review on basic but important information of continuous photocatalysis for environmental remediation, challenging robust scientific progress of this technology towards potential practical use. Here, the general description of continuous photocatalysis involving energy storage mechanisms (hole and electron storage) and characterizations (electron storage behaviors, release behaviors and storage capacity) has been first introduced. Importantly, the remediation performance and mechanism of continuous photocatalysis for environmental applications are qualitatively and quantitatively demonstrated, including chemical pollutant oxidation and reduction, microbial pathogen inactivation, and multifunctional treatment. In addition, key factors influencing its remediation performance are analyzed, for the first time, from both operational and environmental views. The ample opportunities in the field of continuous photocatalysis for sustainable environmental remediation are also pointed out, calling for more efforts to fill current knowledge gaps in the future.

Fe-based single-atom catalysis for oxidizing contaminants of emerging concern by activating peroxides.

We prepared a single-atom Fe catalyst supported on an oxygen-doped, nitrogen-rich carbon support (SAFe-OCN) for degrading a broad spectrum of contaminants of emerging concern (CECs) by activating peroxides such as peroxymonosulfate (PMS). In the SAFe-OCN/PMS system, most selected CECs were amenable to degradation and high-valent Fe species were present for oxidation. Moreover, SAFe-OCN showed excellent performance for contaminant degradation in complex water matrices and high stability in oxidation. Specifically, SAFe-OCN, with a catalytic center of Fe coordinated with both nitrogen and oxygen (FeNxO4-x), showed 5.13-times increased phenol degradation kinetics upon activating PMS compared to the catalyst where Fe was only coordinated with nitrogen (FeN4). Molecular simulations suggested that FeNxO4-x, compared to FeN4, was an excellent multiple-electron donor and it could potential-readily form high-valent Fe species upon oxidation. In summary, the single-atom Fe catalyst enables efficient, robust, and sustainable water and wastewater treatment, and molecular simulations highlight that the electronic nature of Fe could play a key role in determining the activity of the single-atom catalyst.

Emerging Pathogenic Unit of Vesicle-Cloaked Murine Norovirus Clusters is Resistant to Environmental Stresses and UV254 Disinfection.

An individual virion was long believed to act as an independent infectious unit in virology, until the recent discovery of vesicle-cloaked virus clusters which has greatly challenged this central paradigm. Vesicle-cloaked virus clusters (also known as viral vesicles) are phospholipid-bilayer encapsulated fluid sacs that contain multiple virions or multiple copies of viral genomes. Norovirus is a global leading causative agent of gastroenteritis, and the reported prevalence of vesicle-cloaked norovirus clusters in stool has raised concerns whether the current disinfection, sanitation, and hygiene practices can effectively control environmental pollution by these pathogenic units. In this study, we have demonstrated that vesicle-cloaked murine norovirus (MNV-1) clusters were highly persistent under temperature variation (i.e., freeze-thaw) and they were partially resistant to detergent decomposition. MNV-1 vesicles were 1.89-3.17-fold more infectious in vitro than their free virus counterparts. Most importantly, MNV-1 vesicles were up to 2.16-times more resistant to UV254 disinfection than free MNV-1 at a low viral load in vitro. Interestingly, with the increase of the viral load, free MNV-1 and MNV-1 vesicles showed equivalent resistance to UV254 disinfection. We show that the increased multiplicity of infection provided by vesicles is in part responsible for these attributes. Our study, for the first time, sheds light on the environmental behavior of vesicle-cloaked virus clusters as unique emerging pathogenic units. Our study highlights the need to revisit current paradigms of disinfection, sanitation, and hygiene practices for protecting public health.

Photocatalytic graphitic carbon nitride-chitosan composites for pathogenic biofilm control under visible light irradiation.

Photocatalysis holds promise for inactivating environmental pathogens. Visible-light-responsive composites of carbon-doped graphitic carbon nitride and chitosan with high reactivity and processability were fabricated, and they can control pathogenic biofilms for environmental, food, biomedical, and building applications. The broad-spectrum biofilm inhibition and eradication of the photocatalytic composites against Staphylococcus epidermidis, Pseudomonas aeruginosa PAO1, and Escherichia coli O157: H7 under visible light irradiation were demonstrated. Extracellular polymeric substances in Escherichia coli O157: H7 biofilms were most resistant to photocatalytic oxidation, which led to reduced performance for biofilm removal. 1O2 produced by the composites was believed to dominate biofilm inactivation. Moreover, the composites exhibited excellent performance for inhibiting biofilm development in urine, highlighting the promise for inactivating environmental biofilms developed from multiple bacterial species. Our study provides fundamental insights into the development of new photocatalytic composites, and elucidates the mechanism of how the photocatalyst reacts with a microbiological system.

Development of Electrospun Nanofibrous Filters for Controlling Coronavirus Aerosols.

Airborne transmission of SARS-CoV-2 plays a critical role in spreading COVID-19. To protect public health, we designed and fabricated electrospun nanofibrous air filters that hold promise for applications in personal protective equipment (PPE) and the indoor environment. Due to ultrafine nanofibers (∼300 nm), the electrospun air filters had a much smaller pore size in comparison to the surgical mask and cloth masks (a couple of micrometers versus tens to hundreds of micrometers). A coronavirus strain served as a SARS-CoV-2 surrogate and was used to generate aerosols for filtration efficiency tests, which can better represent SARS-CoV-2 in comparison to other agents used for aerosol generation in previous studies. The electrospun air filters showed excellent performance by capturing up to 99.9% of coronavirus aerosols, which outperformed many commercial face masks. In addition, we observed that the same electrospun air filter or face mask removed NaCl aerosols equivalently or less effectively in comparison to the coronavirus aerosols when both aerosols were generated from the same system. Our work paves a new avenue for advancing air filtration by developing electrospun nanofibrous air filters for controlling SARS-CoV-2 airborne transmission.

3D printed photoreactor with immobilized graphitic carbon nitride: A sustainable platform for solar water purification.

Solar-energy-enabled photocatalysis is promising for sustainable water purification. However, photoreactor design, especially immobilizing nano-sized photocatalysts, remains a major barrier preventing industrial-scale application of photocatalysis. In this study, we immobilized photocatalytic graphitic carbon nitride on chitosan to produce g-C3N4/chitosan hydrogel beads (GCHBs), and evaluated GCHB photoreactivity for degrading phenol and emerging persistent micropollutants in a 3D printed compound parabolic collector (CPC) reactor. The CPC photocatalytic system showed comparable performance with slurry reactors for sulfamethoxazole and carbamazepine degradation under simulated sunlight, and it maintained the performance for contaminant removal in real water samples collected from water/wastewater treatment plants or under outdoor sunlight irradiation. Global drinking water production was estimated for the CPC system, and it holds promise for small-scale sustainable water treatment, including, but not limited to, the production of high-quality potable water for single houses, small communities, rural areas, and areas impacted by natural disasters in both developed and developing countries.

Photocatalytic degradation of trihalomethanes and haloacetonitriles on graphitic carbon nitride under visible light irradiation.

Trihalomethanes (THMs) and haloacetonitriles (HANs), most common disinfection by-products in drinking water, pose adverse environmental impacts and potential risks to human health. There is a pressing need to develop innovative, economically feasible, and environmentally benign processes to control these persistent contaminants. In this paper, visible-light-responsive graphitic carbon nitride (g-C3N4) samples were synthesized to degrade the THMs and HANs and the photocatalytic degradation mechanism was explored. The results indicated that a carbon-doped g-C3N4 with an optimum dopant content (MCB0.07) displayed the best photocatalytic activity for the total trihalomethanes (TTHM) and total haloacetonitriles (THAN), with the reaction rate constant of 11.6 and 10.4 (10-3 min-1), respectively. MCB0.07 demonstrated a high THMs and HANs removal efficiency under visible light irradiation and could be reused. According to scavenger tests of the selected reactive species and X-ray photoelectron spectroscopy, holes play a dominant role for both THMs and HANs degradation on the MCB0.07. The degradation of HANs by holes proceeded mainly through breakage of the CC bond in the CCN group. The THMs degradation was achieved through hydrogen abstraction or/and dehalogenation. The brominated-THMs/HANs were more photosensitive than their chlorinated analogous and were less stable than bromo-chloro-THMs/HANs. This study sheds light on the mechanism of the photocatalytic degradation of THMs and HANs under visible light irradiation by carbon-doped g-C3N4. Furthermore, it could provide insights for engineering applications and contaminant control in drinking water purification.

Acquisition of time-frequency localized mechanical properties of biofilms and single cells with high spatial resolution.

Biofilms are a cluster of bacteria embedded in extracellular polymeric substances (EPS) that contain a complex composition of polysaccharides, proteins, and extracellular DNA (eDNA). Desirable mechanical properties of the biofilms are critical for their survival, propagation, and dispersal, and the response of mechanical properties to different treatment conditions also sheds light on biofilm control and eradication in vivo and on engineering surfaces. However, it is challenging yet important to investigate mechanical behaviors of biofilms with a high spatial resolution because biofilms are very heterogeneous. Moreover, biofilms are viscoelastic, and their time-dependent mechanical behavior is difficult to capture. Herein, we develop a powerful technique that combines the high spatial resolution of an atomic force microscope (AFM) with a rigorous history-dependent viscoelastic analysis to deliver highly spatial-localized biofilm properties within a wide time-frequency window. By exploiting the use of static force spectroscopy in combination with an appropriate viscoelastic framework, we highlight the intensive amount of time-dependent information experimentally available that has been largely overlooked. It is shown that this technique provides a detailed nanorheological signature of the biofilms even at the single-cell level. We share the computational routines that would allow any user to perform the analysis from experimental raw data. The detailed localization of mechanical properties in space and in time-frequency domain provides insights into the understanding of biofilm stability, cohesiveness, dispersal, and control.

Graphitic carbon nitride (g-C3N4)-based photocatalysts for water disinfection and microbial control: A review.

Microbial contamination in drinking water is of great concern around the world because of high pathogenic risks to humans. Semiconductor photocatalysis has aroused an increasing interest as a promising environmental remediation technology for water disinfection and microbial control. Among various photocatalysts, graphitic carbon nitride (g-C3N4), as a fascinating two-dimensional conjugated polymer consisting of low-cost, earth-abundant elements, has drawn broad attention as a robust, metal-free, and visible-light-active material in the fields of both environmental remediation and solar energy conversion. Photocatalytic applications of g-C3N4-based nanomaterials for water splitting, hydrogen production, carbon dioxide reduction, and pollutant degradation have been extensively investigated and systematically reviewed. In contrast, their antimicrobial properties have been explored more recently due to the complex structure and unique metabolism of living microorganisms compared with chemicals. The corresponding rapidly increasing research efforts in the last five years have inspired us to conduct the review. This review is the first to comprehensively summarize the progress in design and antimicrobial performance of g-C3N4-based photocatalysts for water disinfection and microbial control, involving not only bacteria but also viruses and microalgae. Moreover, the underlying inactivation mechanisms of photocatalysts for microorganisms are evaluated to provide further understanding of g-C3N4-based advanced disinfection processes. In addition, some exciting future opportunities and challenges at the forefront of this research platform are pointed out. It is expected that this review can pave a new avenue for the development of a facile, cost-effective, environmental-friendly, and sustainable disinfection alternative.

Visible-Light-Responsive Photocatalyst of Graphitic Carbon Nitride for Pathogenic Biofilm Control.

Pathogenic biofilms raise significant health and economic concerns, because these bacteria are persistent and can lead to long-term infections in vivo and surface contamination in healthcare and industrial facilities or devices. Compared with conventional antimicrobial strategies, photocatalysis holds promise for biofilm control because of its broad-spectrum effectiveness under ambient conditions, low cost, easy operation, and reduced maintenance. In this study, we investigated the performance and mechanism of Staphylococcus epidermidis biofilm control and eradication on the surface of an innovative photocatalyst, graphitic carbon nitride (g-C3N4), under visible-light irradiation, which overcame the need for ultraviolet light for many current photocatalysts (e.g., titanium dioxide (TiO2)). Optical coherence tomography and confocal laser scanning microscopy (CLSM) suggested that g-C3N4 coupons inhibited biofilm development and eradicated mature biofilms under the irradiation of white light-emitting diodes. Biofilm inactivation was observed occurring from the surface toward the center of the biofilms, suggesting that the diffusion of reactive species into the biofilms played a key role. By taking advantage of scanning electron microscopy, CLSM, and atomic force microscopy for biofilm morphology, composition, and mechanical property characterization, we demonstrated that photocatalysis destroyed the integrated and cohesive structure of biofilms and facilitated biofilm eradication by removing the extracellular polymeric substances. Moreover, reactive oxygen species generated during g-C3N4 photocatalysis were quantified via reactions with radical probes and 1O2 was believed to be responsible for biofilm control and removal. Our work highlights the promise of using g-C3N4 for a broad range of antimicrobial applications, especially for the eradication of persistent biofilms under visible-light irradiation, including photodynamic therapy, environmental remediation, food-industry applications, and self-cleaning surface development.

Visible-light-driven, water-surface-floating antimicrobials developed from graphitic carbon nitride and expanded perlite for water disinfection.

Waterborne pathogens, especially bacteria and viruses, pose significant health risks to the public, calling for the development of a sustainable, efficient, and robust disinfection strategy with reduced energy footprint and minimized byproduct formation. Here, we developed a sustainable photocatalytic composite for antimicrobial applications by integrating visible-light-responsive graphitic carbon nitride (g-C3N4) with low-density porous expanded perlite (EP) mineral, and g-C3N4/EP-520 showed a high specific surface area of 45.3 m2/g and optimum performance for disinfection. g-C3N4/EP-520 achieved 8-log inactivation of E. coli and MS2 under 180 and 240 min visible-light irradiation without stirring, respectively. Water quality parameters were found to influence the disinfection performance of g-C3N4/EP-520: MS2 inactivation was promoted with the increase of dissolved oxygen (DO), proton concentration, salinity (NaCl), and hardness (Ca2+). Importantly, g-C3N4/EP-520 could fully inactivate MS2 in a real source water sample with prolonged light irradiation, and negligible activity loss was observed in recycle use, demonstrating its viability and robustness for waterborne pathogen removal. Antimicrobial mechanisms of g-C3N4/EP-520 were systemically evaluated by radical scavenger addition, and revealed that the inactivation behavior was dependent on the type of microorganisms. Microscopic analyses confirmed that the destruction of bacterial cells and viral particles, leading to the inactivation of microorganisms.