The Quest for Two-Dimensional MBenes: From Structural Evolution to Solar-Driven Hybrid Systems for Water-Fuel-Energy Generation and Phototherapy.

The field of 2D materials has advanced significantly with the emergence of MBenes, a new material derived from the MAX phases family, a novel class of materials that originates from the MAX phases family. Herein, this article explores the unique characteristics and morphological variations of MBenes, offering a comprehensive overview of their structural evolution. First, the discussion explores the evolutionary period of 2D MBenes associated with the several techniques for synthesizing, modifying, and characterizing MBenes to tailor their structure and enhance their functionality. The focus then shifts to the defect chemistry of MBenes, electronic, catalytic, and photothermal properties which play a crucial role in designing multifunctional solar-driven hybrid systems. Second, the recent advancements and potentials of 2D MBenes in solar-driven hybrid systems e.g. photo-electro catalysis, hybrid solar evaporators for freshwater and thermoelectric generators, and phototherapy, emphasizing their crucial significance in tackling energy and environmental issues, are explored. The study further explores the fundamental principles that regulate the improved photocatalytic and photothermal characteristics of MBenes, highlighting their promise for effective utilization of solar energy and remediation of the environment. The study also thoroughly assesses MBenes' scalability, stability, and cost effectiveness in solar-driven systems. Current insights and future directions allow researchers to utilize MBenes for sustainable and varied applications. This review regarding MBenes will be valuable to early researchers intrigued with synthesizing and utilizing 2D materials for solar-powered water-energy-fuel and phototherapy systems.

Hierarchical Ti3C2/BiVO4 microcapsules for enhanced solar-driven water evaporation and photocatalytic H2 evolution.

Desalination processes frequently require a lot of energy to generate freshwater and energy, which depletes resources. Their reliance on each other creates tension between these two vital resources. Herein, hierarchical MXene nanosheets and bismuth vanadate (Ti3C2/BiVO4)-derived microcapsules were synthesized for a photothermal-induced photoredox reaction for twofold applications, namely, solar-driven water evaporation and hydrogen (H2) production. For this purpose, flexible aerogels were fabricated by introducing Ti3C2/BiVO4 microcapsules in the polymeric network of natural rubber latex (NRL-Ti3C2/BiVO4), and a high evaporation rate of 2.01 kg m-2 h-1 was achieved under 1-kW m-2 solar intensity. The excellent performance is attributed to the presence of Ti3C2/BiVO4 microcapsules in the polymeric network, which provides balanced hydrophilicity and broadband sun absorption (96 %) and is aimed at plasmonic heating with microscale thermal confinement tailored by heat transfer simulations. Notably, localized plasmonic heating at the catalyst active sites of the Ti3C2/BiVO4 heterostructure promotes enhanced photocatalytic H2 production evolved after 4 h of reaction is 9.39 µmol, which is highly efficient than pure BiVO4 and Ti3C2. This method turns the issue of water-fuel crisis into a collaborative connection, presenting avenues to collectively address the anticipated demand rather than fostering competition.

Multi-Walled CNTs/BiVO4 Heterostructures for Solar-Driven Evaporation System and Efficient Photocatalytic Activity against Oxytetracycline.

Developing a sustainable environment requires addressing primitive water scarcity and water contamination. Antibiotics such as oxytetracycline (OTC) may accumulate in the environment and in the human body, increasing the risks to the ecosystem. The treatment of polluted water and the production of potable water can be achieved in a variety of ways, including photodegradation, solar distillation, and filtration. Freshwater supplies can be increased by implementing energy-efficient technologies for the production of clean water. Solar water evaporation combined with photocatalytic degradation and sterilization offers a promising avenue for integration into the clean water and energy production fields. The present study reports the synthesis of a 3D solar steam generator comprised of BiVO4 and carbon nanotubes (CNT) nanocomposite decorated over a cigarette filter as the light-to-heat conversion layer for solar steam generation. The BiVO4@CNT-based 3D solar evaporator over the hydrophilic cellulosic fibers of the cigarette filter endowed excellent evaporation rates (2.36 kg m-2 h-1) under 1 kW m-2 solar irradiation, owing to its superior hydrophilicity and broadband solar absorption (96%) equipped with localized heating at microscale thermal confinement optimized by the minimum thermal conductivity of the overall system. Furthermore, the BiVO4@CNT composite exhibited a heightened photo activity up to 83% of the photodegradation of oxytetracycline (OTC) antibiotic due to the inhibition of charge recombination from the industrial effluents. This approach transforms the water-energy nexus into a synergistic bond that offers opportunities to meet expected demand, rather than being competitive.

2D MXenes Embedded Perovskite Hydrogels for Efficient and Stable Solar Evaporation.

Solar evaporation is a facile and promising technology to efficiently utilize renewable energy for freshwater production and seawater desalination. Here, the fabrication of self-regenerating hydrogel composed of 2D-MXenes nanosheets embedded in perovskite La 0.6Sr 0.4Co 0.2Fe 0.8O3- δ (LSCF)/polyvinyl alcohol hydrogels for efficient solar-driven evaporation and seawater desalination is reported. The mixed dimensional LSCF/Ti3C2 composite features a localized surface plasmonic resonance effect in the polymeric network of polyvinyl alcohol endows excellent evaporation rates (1.98 kg m-2 h-1) under 1 k Wm-2 or one sun solar irradiation ascribed by hydrophilicity and broadband solar absorption (96%). Furthermore, the long-term performance reveals smooth mass change (13.33 kg m-2) during 8 h under one sun. The composite hydrogel prompts the dilution of concentrated brines and redissolves it back to water (1.2 g NaCl/270 min) without impeding the evaporation rate without any salt-accumulation. The present research offers a substantial opportunity for solar-driven evaporation without any salt accumulation in real-life applications.

Recent Progress and Perspective of an Evolving Carbon Family From 0D to 3D: Synthesis, Biomedical Applications, and Potential Challenges.

A variety of imaging techniques are available for detecting biological processes with sufficient penetration depth and temporal resolution. However, inflammation, cardiovascular, and cancer-related disorders might be difficult to diagnose with typical bioimaging methods because of the lack of resolution in the imaging of deep tissues. Therefore, nanomaterials are the most promising candidate to overcome this hurdle. This review is on the utilization of carbon-based nanomaterials (CNMs), ranging from zero-dimension (0D) to three-dimension (3D), in the development of fluorescence (FL) imaging, photoacoustic imaging (PAI), and biosensing for the early detection of cancer. Nanoengineered CNMs, such as graphene, carbon nanotubes (CNTs), and functional carbon quantum dots (QDs), are being further studied for multimodal biometrics and targeted therapy. CNMs have many advantages over conventional dyes in FL sensing and imaging, including clear emission spectra, long photostability, low cost, and high FL intensity. Nanoprobe production, mechanical illustrations, and diagnostic therapeutic applications are the key areas of focus. The bioimaging technique has facilitated a greater understanding of the biochemical events underlying multiple disease etiologies, consequently facilitating disease diagnosis, evaluation of therapeutic efficacy, and drug development. This review may lead to the development of interdisciplinary research in bioimaging and sensing as well as possible future concerns for researchers and medical physicians.

Strontium-Cobaltite-Based Perovskite (SrCoO3) for Solar-Driven Interfacial Evaporation Systems for Clean Water Generation.

Solar-driven evaporation technology is often used in areas with limited access to clean water, as it provides a low-cost and sustainable method of water purification. Avoiding salt accumulation is still a substantial challenge for continuous desalination. Here, an efficient solar-driven water harvester that consists of strontium-cobaltite-based perovskite (SrCoO3) anchored on nickel foam (SrCoO3@NF) is reported. Synced waterways and thermal insulation are provided by a superhydrophilic polyurethane substrate combined with a photothermal layer. The structural photothermal properties of SrCoO3 perovskite have been extensively investigated through state-of-the-art experimental investigations. Multiple incident rays are induced inside the diffuse surface, permitting wideband solar absorption (91%) and heat localization (42.01 °C @ 1 sun). Under 1 kW m-2 solar intensity, the integrated SrCoO3@NF solar evaporator has an outstanding evaporation rate (1.45 kg/m2 h) and solar-to-vapor conversion efficiency (86.45% excluding heat losses). In addition, long-term evaporation measurements demonstrate small variance under sea water, illustrating the system's working capacity for salt rejection (1.3 g NaCl/210 min), which is excellent for an efficient solar-driven evaporation application compared to other carbon-based solar evaporators. According to the findings of this research, this system offers significant potential for producing fresh water devoid of salt accumulation for use in industrial applications.

Biomass-Printed Hybrid Solar Evaporator Derived from Bio-polluted Invasive Species, a Potential Step toward Carbon Neutrality.

Biomass-based photothermal conversion is of great importance for solar energy utilization toward carbon neutrality. Herein, a hybrid solar evaporator is innovatively designed via UV-induced printing of pyrolyzed Kudzu biochar on hydrophilic cotton fabric (KB@CF) to integrate all parameters in a single evaporator, such as solar evaporation, salt collection, waste heat recovery for thermoelectricity, sieving oil emulsions, and water disinfection from microorganisms. The UV-induced printed fabric demonstrates stronger material adhesion as compared to the conventional dip-dry technique. The hybrid solar evaporator gives an enhanced evaporation rate (2.32 kg/m2 h), and the complementary waste heat recovery system generates maximum open-circuit voltage (Vout ∼ 143.9 mV) and solar to vapor conversion efficiency (92%), excluding heat losses under one sun illumination. More importantly, 99.98% of photothermal-induced bacterial killing efficiency was achieved within 20 min under 1 kW m-2 using the hyperthermia effect of Kudzu biochar. Furthermore, numerical heat-transfer simulations were performed successfully to analyze the enhanced interfacial heat accumulation (75.3 °C) and heat flux distribution of the thermoelectric generators under one sun. We firmly believe that the safe use of bio-polluted invasive species in hybrid solar-driven evaporation systems eases the environmental pressure toward carbon neutrality.

Nanocomposite-Enhanced Efficient Evaporation System for Solar-Driven Seawater Desalination-An Optimized Design for Clean Water Production.

Solar-driven evaporation is a promising technology for desalinating seawater and wastewater without mechanical or electrical energy. The approaches to obtaining fresh water with higher evaporation efficiency are essential to address the water-scarcity issue in remote sensing areas. Herein, we report a highly efficient solar evaporator derived from the nanocomposite of anatase TiO2/activated carbon (TiO2/AC), which was coated on washable cotton fabric using the dip-dry technique for solar water evaporation. The ultra-black fabric offers enhanced solar absorption (93.03%), hydrophilic water transport, and an efficient evaporation rate of 1.65 kg/m2h under 1 kW m-2 or one sun solar intensity. More importantly, the sideways water channels and centralized thermal insulation of the designed TiO2/AC solar evaporator accumulated photothermal heat at the liquid and air interface along with an enhanced surface temperature of 40.98 °C under one sun. The fabricated solar evaporator desalinated seawater (3.5 wt%) without affecting the evaporation rates, and the collected condensed water met the standard of drinking water set by the World Health Organization (WHO). This approach eventually enabled the engineering design groups to develop the technology pathways as well as optimum conditions for low-cost, scalable, efficient, and sustainable solar-driven steam generators to cope with global water scarcity.

Interfacial Photothermal Heat Accumulation for Simultaneous Salt Rejection and Freshwater Generation; an Efficient Solar Energy Harvester.

Water scarcity has emerged as an intense global threat to humanity and needs prompt attention from the scientific community. Solar-driven interfacial evaporation and seawater desalination are promising strategies to resolve the primitive water shortage issue using renewable resources. However, the fragile solar thermal devices, complex fabricating techniques, and high cost greatly hinder extensive solar energy utilization in remote locations. Herein, we report the facile fabrication of a cost-effective solar-driven interfacial evaporator and seawater desalination system composed of carbon cloth (CC)-wrapped polyurethane foam (CC@PU). The developed solar evaporator had outstanding photo-thermal conversion efficiency (90%) with a high evaporation rate (1.71 kg m-2 h-1). The interfacial layer of black CC induced multiple incident rays on the surface allowing the excellent solar absorption (92%) and intensifying heat localization (67.37 °C) under 1 kW m-2 with spatially defined hydrophilicity to facilitate the easy vapor escape and validate the efficacious evaporation structure using extensive solar energy exploitation for practical application. More importantly, the long-term evaporation experiments with minimum discrepancy under seawater conditions endowed excellent mass change (15.24 kg m-2 in consecutive 8 h under 1 kW m-2 solar irradiations) and promoted its operational sustainability for multi-media rejection and self-dissolving potential (3.5 g NaCl rejected from CC@PU surface in 210 min). Hence, the low-cost and facile fabrication of CC@PU-based interfacial evaporation structure showcases the potential for enhanced solar-driven interfacial heat accumulation for freshwater production with simultaneous salt rejection.

Erratum: Arshad, N., et al. Super Hydrophilic Activated Carbon Decorated Nanopolymer Foam for Scalable, Energy Efficient Photothermal Steam Generation, as an Effective Desalination System. Nanomaterials 2020, 10, 2510.

The authors wish to make the following corrections to this paper [...].

Nanoenabled Photothermal Materials for Clean Water Production.

Solar-powered water evaporation is a primitive technology but interest has revived in the last five years due to the use of nanoenabled photothermal absorbers. The cutting-edge nanoenabled photothermal materials can exploit a full spectrum of solar radiation with exceptionally high photothermal conversion efficiency. Additionally, photothermal design through heat management and the hierarchy of smooth water-flow channels have evolved in parallel. Indeed, the integration of all desirable functions into one photothermal layer remains an essential challenge for an effective yield of clean water in remote-sensing areas. Some nanoenabled photothermal prototypes equipped with unprecedented water evaporation rates have been reported recently for clean water production. Many barriers and difficulties remain, despite the latest scientific and practical implementation developments. This Review seeks to inspire nanoenvironmental research communities to drive onward toward real-time solar-driven clean water production.

Green thin film for stable electrical switching in a low-cost washable memory device: proof of concept.

Low-cost and washable resistive switching (RS) memory devices with stable retention and low operational voltage are important for higher speed and denser non-volatile memories. In the case of green electronics, pectin has emerged as a suitable alternative to toxic metal oxides for resistive switching applications. Herein, a pectin-based thin film was fabricated on a fluorine-doped tin oxide glass substrate for RS mechanism. The presence of sp3-C groups with low binding energy corresponds to tunable charged defects and the oxygen vacancies confirmed by the O 1s spectra that plays a decisive role in the resistive switching mechanism, as revealed by X-ray photoemission spectroscopy (XPS). The surface morphology of the pectin film shows homogeneous growth and negligible surface roughness (38.98 ± 9.09). The pectin film can dissolve in DI water (10 minutes) owing to its ionization of carboxylic groups, that meet the trends of transient electronics. The developed Ag/pectin/FTO-based memory cell exhibits stable and reproducible bipolar resistive switching behavior along with an excellent ON/OFF ratio (104) and negligible electrical degradation was observed over 30 repeated cycles. Hence, it appears to be a valuable application for green electronics. Indeed, biocompatible storage devices derived from natural pectin are promising for high-density safe applications for information storage systems, flexible electronics, and green electronics.

Super Hydrophilic Activated Carbon Decorated Nanopolymer Foam for Scalable, Energy Efficient Photothermal Steam Generation, as an Effective Desalination System.

Clean water scarcity is still an intense, prolonged global issue that needs to be resolved urgently. The solar steam generation has shown great potential with a high energy conversion efficiency for clean water production from seawater and wastewater. However, the high evaporation rate of water cannot be preserved due to the inevitable fouling of solar absorbers. Herein, a self-floatable and super hydrophilic solar-driven steam generator composed of activated carbon coated melamine foam (ACM). The deposited ACM photothermal layer exhibits outstanding solar absorption (92%) and an efficient evaporation rate of 1.27 kg m-2 h-1, along with excellent photothermal conversion efficiency (80%) as compared to commercially available primitive solar stills. The open porous assembly of melamine foam equipped with 80% flexibility (0.8 MPa) enabled smooth water transport and sustain heat accumulation within the matrix. The thermal insulation of ACM is 10 times greater than pure water. Moreover, open porous assembly of designed solar-powered steam generator rejects salt ions as well as volatile organic compounds efficiently. The low-cost and facile fabrication of photothermal based water production presents a potential solution to single step drinking water supply from various resources of the sea, the lakes and mixtures of emulsified oil and industrial wastewater.

Low-cost green recyclable biomaterial for energy-dependent electrical switching and intact biofilm with antibacterial properties.

A highly cost-effective recycled biomaterial extracted from lime peel has been made biocompatible and has been coated on a commercial fluorine-doped tin oxide (FTO) substrate of glass using the spin coating method. Structural, morphologic, electronic, and antibacterial measurements were thoroughly characterized as a green biomaterial thin film using X-rays (XRD), PL, FTIR, Raman, SEM, HRTEM, AFM, I-V, and antibacterial diffusion techniques. The comprehensive analysis of structures of recyclable waste in the form of lime peel extract (LPE) as thin films showed the crystalline cellulose structure that corresponds to the lattice fringe (0.342 nm) exposed by HRTEM. The K+1 interstitial active sites or vacancies in LPE/FTO thin films are confirmed by the PL spectra that show important evidence about conduction mechanisms, and hence facilitates Ag+1 ion migration from the top to the bottom electrode. The AFM investigations revealed the minor surface roughness (169.61 nm) of the LPE/FTO film, which controls the current leakage that is associated with surface defects. The designed memory cell (Ag/LPE/FTO) exhibits stable, reproducible electrical switching under low operational voltage and is equipped with excellent retention over 5 × 103 s. Furthermore, owing to presence of flavonoids and their superior antioxidant nature, lime peel extract powder shows tremendous antimicrobial activity against gram-positive and Gram-negative bacterial strains.

Biomaterial-Induced Stable Resistive Switching Mechanism in TiO2 Thin Films: The Role of Active Interstitial Sites/Ions in Minimum Current Leakage and Superior Bioactivity.

Leakage of current in oxide layers is the main issue for higher speed and denser resistive random-access memory. Defect engineering played a substantial role in meeting this challenge by doping or producing controlled interstitial defects or active sites. These controlled active sites enabled memory cells to form a stable and reproducible conduction filament following an electrochemical metallization model. In this study, a defect-abundant lime peel extract (LPE)-mediated anatase TiO2 thin film was fabricated using a simple hydrothermal route. The detailed structural and morphological analysis of the bioactive anatase TiO2-LPE thin film reveals the homogeneous growth of TiO2 flowers and distinct features in terms of controlled defects as compared to simple anatase TiO2. These interstitial defects (Ti+3 and Ti+4) behave as active sites for cation migrations along highly conductive K1+ ions because of the mediation of LPE. The defect-free surface reveals slight surface roughness (4.8 nm) that successfully minimizes leakage of current. The strategy enabled a reliable conductive bridge filament, which can replicate with no more electric degradation. The Ag/TiO2-LPE/FTO-based memory cell demonstrates reproducible bipolar resistive switching along with a high ON/OFF ratio (>105), excellent endurance (1.5 × 103 cycles), and long-term retention (105 s) without any electrical degradation. Furthermore, green-synthesized TiO2-LPE nanoparticles have shown superior antibacterial activity as compared to other green syntheses of different plants or fruits against the toxic microorganisms present in inorganic media.