Converting solar energy into concentrated heat is very appealing for various applications. Polypyrrole (PPy) is known to possess excellent photothermal property with low thermal conductivity, and thus is an ideal candidate for solar–thermal energy conversion. However, solar–thermal materials based on PPy or other conducting polymers still exhibit limited energy conversion efficiency due to the lack of effective light‐trapping schemes. Here, it is demonstrated that multilayer PPy nanosheets with spontaneously formed surface structures such as wrinkles and ridges via sequential polymerization on paper substrates can dramatically enhance broadband and wide‐angle light absorption across the full solar spectrum, leading to an impressive solar–thermal conversion efficiency of 95.33%. The intriguing solar–thermal properties and structural features of multilayer PPy nanosheets can be used for solar heating and photoactuators. Meanwhile, when used for solar steam generation, the measured efficiency could achieve ≈92% under one sun irradiation. The hierarchically multilayer structure is mechanically flexible and robust, holding great potential for practical solar energy utilization. This study provides a simple and straightforward approach toward engineering light‐weight and thermally insulating polymers into efficient solar–thermal materials for emerging solar energy‐related applications. 相似文献
The use of abundant solar energy for regeneration and desalination of water is a promising strategy to address the challenge of a global shortage of clean water. Progress has been made to develop photothermal materials to improve the solar steam generation performance. However, the mass production rate of water is still low. Herein, by a rational combination of photo‐electro‐thermal effect on an all‐graphene hybrid architecture, solar energy can not only be absorbed fully and transferred into heat, but also converted into electric power to further heat up the graphene skeleton frame for a much enhanced generation of water vapor. As a result, the unique graphene evaporator reaches a record high water production rate of 2.01–2.61 kg m?2 h?1 under solar illumination of 1 kW m?2 even without system optimization. Several square meters of the graphene evaporators will provide a daily water supply that is enough for tens of people. The combination of photo‐electro‐thermal effect on graphene materials offers a new strategy to build a fast and scalable solar steam generation system, which makes an important step towards a solution for the scarcity of clean water. 相似文献
Solar steam generation is emerging as a promising technology, for its potential in harvesting solar energy for various applications such as desalination and sterilization. Recent studies have reported a variety of artificial structures that are designed and fabricated to improve energy conversion efficiencies by enhancing solar absorption, heat localization, water supply, and vapor transportation. Mushrooms, as a kind of living organism, are surprisingly found to be efficient solar steam‐generation devices for the first time. Natural and carbonized mushrooms can achieve ≈62% and ≈78% conversion efficiencies under 1 sun illumination, respectively. It is found that this capability of high solar steam generation is attributed to the unique natural structure of mushroom, umbrella‐shaped black pileus, porous context, and fibrous stipe with a small cross section. These features not only provide efficient light absorption, water supply, and vapor escape, but also suppress three components of heat losses at the same time. These findings not only reveal the hidden talent of mushrooms as low‐cost materials for solar steam generation, but also provide inspiration for the future development of high‐performance solar thermal conversion devices. 相似文献
Photothermal steam generation promises decentralized water purification, but current methods suffer from slow water evaporation even at high photothermal efficiency of ≈98%. This drawback arises from the high latent heat of vaporization that is required to overcome the strong and extensive hydrogen bonding network in water for steam generation. Here, light-to-vapor conversion is boosted by incorporating chaotropic/kosmotropic chemistries onto plasmonic nanoheater to manipulate water intermolecular network at the point-of-heating. The chaotropic-plasmonic nanoheater affords rapid light-to-vapor conversion (2.79 kg m−2 h−1 kW−1) at ≈83% efficiency, with the steam generation rate up to 6-fold better than kosmotropic platforms or emerging photothermal designs. Notably, the chaotropic-plasmonic nanoheater also lowers the enthalpy of water vaporization by 1.6-fold when compared to bulk water, signifying that a correspondingly higher amount of steam can be generated with the same energy input. Simulation studies unveil chaotropic surface chemistry is crucial to disrupt water hydrogen bonding network and suppress the energy barrier for water evaporation. Using the chaotropic-plasmonic nanoheater, organic-polluted water is purified at ≈100% efficiency, a feat otherwise challenging in conventional treatments. This study offers a unique chemistry approach to boost light-driven steam generation beyond a material photothermal property. 相似文献
With recent progress in photothermal materials, organic small molecules featured with flexibility, diverse structures, and tunable properties exhibit unique advantages but have been rarely applied in solar-driven water evaporation owing to limited sunlight absorption resulting in low solar–thermal conversion. Herein, a stable croconium derivative, named CR-TPE-T, is designed to exhibit the unique biradical property and strong π–π stacking in the solid state, which facilitate not only a broad absorption spectrum from 300 to 1600 nm for effective sunlight harvesting, but also highly efficient photothermal conversion by boosting nonradiative decay. The photothermal efficiency is evaluated to be 72.7% under 808 nm laser irradiation. Based on this, an interfacial-heating evaporation system based on CR-TPE-T is established successfully, using which a high solar-energy-to-vapor efficiency of 87.2% and water evaporation rate of 1.272 kg m−2 h−1 under 1 sun irradiation are obtained, thus making an important step toward the application of organic-small-molecule photothermal materials in solar energy utilization. 相似文献
As a renewable and environment-friendly technology for seawater desalination and wastewater purification, solar energy triggered steam generation is attractive to address the long-standing global water scarcity issues. However, practical utilization of solar energy for steam generation is severely restricted by the complex synthesis, low energy conversion efficiency, insufficient solar spectrum absorption and water extraction capability of state-of-the-art technologies. Here, for the first time, we report a facile strategy to realize hydrogen bond induced self-assembly of a polydopamine (PDA)@MXene microsphere photothermal layer for synergistically achieving wide-spectrum and highly efficient solar absorption capability (≈ 96% in a wide solar spectrum range of 250–1,500 nm wavelength). Moreover, such a system renders fast water transport and vapor escaping due to the intrinsically hydrophilic nature of both MXene and PDA, as well as the interspacing between core-shell microspheres. The solar-to-vapor conversion efficiencies under the solar illumination of 1 sun and 4 sun are as high as 85.2% and 93.6%, respectively. Besides, the PDA@MXene photothermal layer renders the system durable mechanical properties, allowing producing clean water from seawater with the salt rejection rate beyond 99%. Furthermore, stable light absorption performance can be achieved and well maintained due to the formation of ternary TiO2/C/MXene complex caused by oxidative degradation of MXene. Therefore, this work proposes an attractive MXene-assisted strategy for fabricating high performance photothermal composites for advanced solar-driven seawater desalination applications.
Effective utilization of abundant solar energy for desalination of seawater and purification of wastewater is one of sustainable techniques for production of clean water, helping relieve global water resource shortage. Herein, we fabricate a vertically aligned reduced graphene oxide/Ti3C2Tx MXene (A-RGO/MX) hybrid hydrogel with aligned channels as an independent solar steam generation device for highly efficient solar steam generation. The vertically aligned channels, generated by a liquid nitrogen-assisted directional-freezing process, not only rapidly transport water upward to the evaporation surface for efficient solar steam generation, but also facilitate multiple reflections of solar light inside the channels for efficient solar light absorption. The deliberate slight reduction endows the RGO with plenty of polar groups, decreasing the water vaporization enthalpy effectively and hence accelerating water evaporation efficiently. The MXene sheets, infiltrated inside the A-RGO hydrogel on the basis of Marangoni effect, enhance light absorption capacity and photothermal conversion performance. As a result, the A-RGO/MX hybrid hydrogel achieves a water evaporation rate of 2.09 kg·m−2·h−1 with a high conversion efficiency of 93.5% under 1-sun irradiation. Additionally, this photothermal conversion hydrogel rapidly desalinates seawater and purifies wastewater to generate clean water with outstanding ion rejection rates of above 99% for most ions.
利用太阳能实现光蒸气转化是一项极具前景的技术,可应用于海水脱盐和淡水制备等领域.然而,从工业的角度来看,制备低成本、高效率的光热材料仍具有挑战性.本文利用聚离子液体(PIL)和氧化镍(Ni O)作为复合催化剂,实现了聚丙烯(PP)的可控碳化,并制备了镍/碳纳米材料(Ni/CNM).研究结果表明,加入微量的PIL可实现对Ni/CNM形貌和织态结构的调控.Ni/CNM由杯状碳纳米管(CS-CNT)和梨形镍纳米颗粒组成,二者在太阳光吸收上的协同作用使得Ni/CNM具有优异的光热转换性能.此外,Ni/CNM具有较高的比表面积和丰富的微/介/大孔,其构建的三维多孔网络可为水和蒸气的高效传输提供通道.光吸收高、水传输快和热导率低等优势,使Ni/CNM的水蒸发速率高达1.67 kg m^-2h^-1,光-蒸气转换效率高达94.9%,且重复使用10次后性能依然保持稳定.该材料同时适用于染料废水、海水和油/水乳化液等水质的纯化.其中,海水中金属离子的去除效率高达99.99%,染料去除率>99.9%.更重要的是,材料的光蒸气转换性能优于最新报道的碳基光热材料.此工作不仅提出了一种可将废弃聚合物转化为先进的金属/碳杂化物的可持续方法,同时也有助于太阳能利用和海水淡化领域的进一步研究. 相似文献
Photothermal hydrogels featuring broadband light absorption abilities and highly hydrated networks provide an appealing mass-energy transfer platform for water evaporation by using solar energy. However, the targeted delivery of solar heat energy to power the water evaporation process remains challenging. Herein, enlightened by metal-phenolic coordination chemistry and camouflaged architecture, photothermal hydrogels with dual-mechanism vaporization structure are tactfully designed via a rational interfacial engineering and integration strategy to enable near-µm heat confinement and highly efficient light-to-heat conversion ability. The spectrum-tailored liquid metal droplet (LMGAs-FeIII) and optimized carbon-wrapped silver nanowire sponge (Ag@C750) are integrally built as photothermal promotors/channels and jointly embedded into a highly hydratable poly(vinyl alcohol) hydrogel, denoted as PALGH, to synergistically boost water molecule activation and interfacial vaporization behavior by triggering robust photothermal performance. As a result, under one sun irradiation, the all-embracing PALGH hydrogel evaporation system achieves a brine evaporation rate to a high level of 3.47 kg m−2 h−1, and >19 L m−2 clean water of PALGH is ideally delivered daily when purifying natural seawater. This work offers not only a rational design principle to create sophisticated photothermal materials but also replenishes insight into solar heat generation and water transportation in a cross-media system. 相似文献
Recent advances in five key areas of materials technology are discussed. Structural and non-structural composites, electrically-conducting
polymers, materials obtained by rapid quenching, new developments in hydraulic cements and photothermal solar energy conversion
are reviewed. 相似文献