Le Shi

MXene Ti3C2: An Effective 2D Light-to-Heat Conversion Material

MXene, a new series of 2D material, has been steadily advancing its applications to a variety of fields, such as catalysis, supercapacitor, molecular separation, electromagnetic wave interference shielding. This work reports a carefully designed aqueous droplet light heating system along with a thorough mathematical procedure, which combined leads to a precise determination of internal light-to-heat conversion efficiency of a variety of nanomaterials. The internal light-to-heat conversion efficiency of MXene, more specifically Ti3C2, was measured to be 100%, indicating a perfect energy conversion. Furthermore, a self-floating MXene thin membrane was prepared by simple vacuum filtration and the membrane, in the presence of a rationally chosen heat barrier, produced a light-to-water-evaporation efficiency of 84% under one sun irradiation, which is among the state of art energy efficiency for similar photothermal evaporation system. The outstanding internal light-to-heat conversion efficiency and great light-to-water evaporation efficiency reported in this work suggest that MXene is a very promising light-to-heat conversion material and thus deserves more research attention toward practical applications.

Microwave-Assisted Self-Doping of TiO2 Photonic Crystals for Efficient Photoelectrochemical Water Splitting

In this article, we report that the combination of microwave heating and ethylene glycol, a mild reducing agent, can induce Ti(3+) self-doping in TiO2. A hierarchical TiO2 nanotube array with the top layer serving as TiO2 photonic crystals (TiO2 NTPCs) was selected as the base photoelectrode. The self-doped TiO2 NTPCs demonstrated a 10-fold increase in visible-light photocurrent density compared to the nondoped one, and the optimized saturation photocurrent density under simulated AM 1.5G illumination was identified to be 2.5 mA cm(-2) at 1.23 V versus reversible hydrogen electrode, which is comparable to the highest values ever reported for TiO2-based photoelectrodes. The significant enhancement of photoelectrochemical performance can be ascribed to the rational coupling of morphological and electronic features of the self-doped TiO2 NTPCs: (1) the periodically morphological structure of the photonic crystal layer traps broadband visible light, (2) the electronic interband state induced from self-doping of Ti(3+) can be excited in the visible-light region, and (3) the captured light by the photonic crystal layer is absorbed by the self-doped interbands.

Rational design of a bi-layered reduced graphene oxide film on polystyrene foam for solar-driven interfacial water evaporation

Solar-driven water evaporation has been emerging as a highly efficient way for utilizing solar energy for clean water production and wastewater treatment. Here we rationally designed and fabricated a bi-layered photothermal membrane with a porous film of reduced graphene oxide (rGO) on the top and polystyrene (PS) foam at the bottom. The top porous rGO layer acts as a light absorber to harvest and convert light efficiently to thermal energy and the bottom PS layer, which purposefully disintegrates water transport channels, acts as an excellent thermal barrier to minimize heat transfer to the nonevaporative bulk water. The optimized bi-layered membrane was able to produce water evaporation rate as high as 1.31 kg m−2 h−1 with light to evaporation conversion efficiency as high as 83%, which makes it a promising photothermal material in the literature. Furthermore, the experiments and theoretical simulation were both conducted to examine the relationship between the overall energy efficiency and the depth of the photothermal material underwater and the experimental and simulations results coincided with each other. Therefore, this work provides systematic evidence in support of the concept of the interfacial heating and shines important light on practical applications of solar-driven processes for clean water production.

A highly flexible and washable nonwoven photothermal cloth for efficient and practical solar steam generation

Solar-driven water evaporation is emerging as a promising solar-energy utilization process. In the present work, a highly stable, flexible and washable nonwoven photothermal cloth is prepared by electrospinning for efficient and durable solar steam evaporation. The cloth is composed of polymeric nanofibers as the matrix and inorganic carbon black nanoparticles encapsulated inside the matrix as light absorbing components. The photothermal cloth with an optimized carbon loading shows desirable underwater black properties, absorbing 94% of the solar spectrum and giving rise to a state-of-the-art solar energy utilization efficiency of 83% during the pure water evaporation process. Owing to its compositions and special structural design, the cloth possesses anti-photothermal-component-loss properties and is highly flexible, mechanically strong, and chemically stable in various harsh environments such as strong acid, alkalis, organic solvents and salty water. It can be hand-washed more than 100 times without degrading its performance and thus offers a potential mechanism for foulant cleaning during practical solar steam generation and distillation processes. The results of this work stimulate more research in durable photothermal materials aiming at real world applications.

Dual-template engineering of triple-layered nanoarray electrode of metal chalcogenides sandwiched with hydrogen-substituted graphdiyne

Hybrid nanostructures integrating electroactive materials with functional species, such as metal-organic frameworks, covalent organic frameworks, graphdiyne etc., are of significance for both fundamental research and energy conversion/storage applications. Here, hierarchical triple-layered nanotube arrays, which consist of hydrogen-substituted graphdiyne frameworks seamlessly sandwiched between an outer layer of nickel–cobalt co-doped molybdenum disulfide nanosheets and an inner layer of mixed cobalt sulfide and nickel sulfide (Co9S8/Ni3S2), are directly fabricated on conductive carbon paper. The elaborate triple-layered structure emerges as a useful hybrid electrode for energy conversion and storage, in which the organic hydrogen-substituted graphdiyne middle layer, with an extended π-conjugated system between the electroactive nanomaterials, provides built-in electron and ion channels that are crucial for performance enhancement. This dual-template synthetic method, which makes use of microporous organic networks to confine a self-template, is shown to be versatile and thus provides a promising platform for advanced nanostructure-engineering of hierarchical multi-layered nanostructures towards a wide range of electrochemical applications.Multi-shelled nanomaterials offer interesting electrochemical properties, but have been limited in composition. Here the authors use dual templating to integrate electroactive metal chalcogenide layers with hydrogen-substituted graphdiyne, achieving electrocatalytic activity for hydrogen evolution.

Harvesting Water from Air: Using Anhydrous Salt with Sunlight

Atmospheric water is an abundant alternative water resource, equivalent to 6 times the water in all rivers on Earth. This work screens 14 common anhydrous and hydrated salt couples in terms of their physical and chemical stability, water vapor harvesting, and release capacity under relevant application scenarios. Among the salts screened, copper chloride (CuCl2), copper sulfate (CuSO4), and magnesium sulfate (MgSO4) distinguish themselves and are further made into bilayer water collection devices, with the top layer being the photothermal layer, while the bottom layer acts as a salt-loaded fibrous membrane. The water collection devices are capable of capturing water vapor out of the air with low relative humidity (down to 15%) and releasing water under regular and even weakened sunlight (i.e., 0.7 kW/m2). The work shines light on the potential use of anhydrous salt toward producing drinking water in water scarce regions.

Solar Evaporator with Controlled Salt Precipitation for Zero Liquid Discharge Desalination

A sustainable supply of clean water is essential for the development of modern society, which has become increasingly dependent on desalination technology since 96.5% of the water on Earth is salt water. Thousands of desalination plants are producing massive waste brine as byproduct, and the direct discharge of brine raises serious concerns about its ecological impact. The concept of zero liquid discharge (ZLD) desalination is regarded as the solution, but the current ZLD technologies are hampered by their intensive use of energy and high cost. In this work, a 3D cup shaped solar evaporator was fabricated to achieve ZLD desalination with high energy efficiency via solar distillation. It produces solid salt as the only byproduct and uses sunlight as the only energy source. By rationally separating the light absorbing surface from the salt precipitation surface, the light absorption of the 3D solar evaporator is no longer affected by the salt crust layer as in conventional 2D solar evaporators. Therefore, it can be operated at an extremely high salt concentration of 25 wt % without noticeable water evaporation rate decay in at least 120 h. This new solar evaporator design concept offers a promising technology especially for high salinity brine treatment in desalination plants to achieve greener ZLD desalination as well as for hypersaline industrial wastewater treatment.