Bio-Inspired Ultrathin Perfect Absorber for High-Performance Photothermal Conversion.

Ultrathin perfect absorber (UPA) enables efficient photothermal conversion (PC) in renewable chemical and energy systems. However, it is challenging so far to obtain efficient absorption with thickness significantly less than the wavelength, especially considering the common view that an ultrathin film can absorb at most 50% of incident light. Here, a highly light-absorbing and mechanically stable UPA is reported by learning from the honeycomb mirror design of the crab compound eyes. With the hollow apertures enclosed by the self-supporting ultrathin film of reduced graphene oxide and gold nanoparticles, the absorber achieves spoof-plasmon enhanced broadband absorption in solar spectrum and low radiative decay in infrared. Specifically, a strong absorption (87%) is realized by the apertures with cross-section thickness of 1/20 of the wavelength, which is 7.3 times stronger than a planar counterpart with the identical material. Its high PC efficiency up to 64%, with hot-electron temperature as high as 2344 K, is also experimentally demonstrated. Utilizing its low thermal mass nature, a high-speed visible-to-infrared converter is constructed. The absorber can enable high-performance PC processes for future interfacial catalysis and photon-detection.

Effect of mechanical-chemical modification on adsorption of beryllium by calcite.

The treatment of beryllium wastewater has become a major problem in industry. In this paper, CaCO3 is creatively proposed to treat beryllium-containing wastewater. Calcite was modified by an omnidirectional planetary ball mill by a mechanical-chemical method. The results show that the maximum adsorption capacity of CaCO3 for beryllium is up to 45 mg/g. The optimum treatment conditions were pH = 7 and the amount of adsorbent was 1 g/L, and the best removal rate was 99%. The concentration of beryllium in the CaCO3-treated solution is less than 5 µg/L, which meets the international emission standard. The results show that the surface co-precipitation reaction between CaCO3 and Be (II) mainly occurs. Two different precipitates are generated on the used-CaCO3 surface; one is the tightly connected Be (OH)2 precipitation, and the other is the loose Be2(OH)2CO3 precipitation. When the pH of the solution exceeds 5.5, Be2+ in the solution is first precipitated by Be (OH)2. After CaCO3 is added, CO32- will further react with Be3(OH)33+ to form Be2(OH)2CO3 precipitation. CaCO3 can be considered as an adsorbent with great potential to remove beryllium from industrial wastewater.

Low-Grade Waste Heat Enables Over 80 L m- 2 h-1 Interfacial Steam Generation Based on 3D Superhydrophilic Foam.

Clean water scarcity and energy shortage have become urgent global problems due to population growth and human industrial development. Low-grade waste heat (LGWH) is a widely available and ubiquitous byproduct of human activities worldwide, which can provide effective power to address the fresh water crisis without additional energy consumption and carbon emissions. In this regard, 3D superhydrophilic polyurethane/sodium alginate (PU/SA) foam and LGWH-driven interfacial water evaporation systems are developed, which can precipitate over 80 L m-2  h-1 steam generation from seawater and has favorable durability for purification of high salinity wastewater. The excellent water absorption ability, unobstructed water transport, and uniform thin water layer formed on 3D skeletons of PU/SA foam ensure the strong heat exchange between LGWH and fluidic water. As a result, the heat-localized PU/SA foam enables the efficient energy utilization and ultrafast water evaporation once LGWH is introduced into PU/SA foam as heat flow. In addition, the precipitated salt on PU/SA foam can be easily removed by mechanical compression, and almost no decrease in water evaporation rate after salt precipitation and removal for many times. Meanwhile, the collected clean water has high rejection of ions of 99.6%, which meets the World Health Organization (WHO) standard of drinking water. Above all, this LGWH-driven interfacial water evaporation system presents a promising and easily accessible solution for clean water production and water-salt separation without additional energy burden for the society.

Adsorptive removal of beryllium by Fe-modified activated carbon prepared from lotus leaf.

Lotus leaf was used as raw material to prepare HNO3-activated carbon with 1.5:1 (HNO3:lotus leaf) (wt:wt) impregnation. Then, the activated carbon was modified by Fe(NO3)3 to obtain Fe-activated carbon (Fe-AC). The adsorption test results show that Fe-AC maximum saturated adsorption capacity (Qm) is 45.68 mg/g when the Fe(NO3)3 loading is 5% of the total activated carbon, pH = 6, and the temperature is 35 ℃. The adsorption effect of Fe-AC under neutral conditions is better than that under alkaline and acidic conditions. The modified activated carbon has better adsorption selectivity. The obtained material (Fe-AC) was characterized by N2 adsorption-desorption isotherm, SEM, FT-IR, BET, XRD, XPS, and pHpzc. The total pore volume, specific surface area, and zero charges of modified activated carbon were increased. The types of modified functional groups were reduced, and the iron reacted with the functional groups, providing ion exchange sites for the adsorption of beryllium. The adsorption thermodynamics showed that the adsorption process was spontaneous and endothermic. The adsorption mechanism of Fe-AC to beryllium is mainly chemical adsorption.

Moisture adsorption-desorption full cycle power generation.

Environment-adaptive power generation can play an important role in next-generation energy conversion. Herein, we propose a moisture adsorption-desorption power generator (MADG) based on porous ionizable assembly, which spontaneously adsorbs moisture at high RH and desorbs moisture at low RH, thus leading to cyclic electric output. A MADG unit can generate a high voltage of ~0.5 V and a current of 100 µA at 100% relative humidity (RH), delivers an electric output (~0.5 V and ~50 µA) at 15 ± 5% RH, and offers a maximum output power density approaching to 120 mW m-2. Such MADG devices could conduct enough power to illuminate a road lamp in outdoor application and directly drive electrochemical process. This work affords a closed-loop pathway for versatile moisture-based energy conversion.