To alleviate the scarcity of clean water, solar steam generation, which utilizes the green and abundant resources of Earth, has attracted considerable attention and been recognized as a sustainable technology to purify seawater and wastewater.
Herein, the recent advances in realizing highly efficient cellulose-based solar evaporators for alleviating the global water crisis are summarized. Fresh water scarcity is one of most threatening issues for sustainable development. Solar steam generation, which harnesses the abundant sunlight, has been recognized as a sustainable approach to harvest fresh water. In contrast to synthetic polymeric materials that can pose serious negative environmental impacts, cellulose-based materials, owing to their biocompatibility, renewability, and sustainability, are highly attractive for realizing solar steam generators. The molecular and macromolecular features of cellulose and the physicochemical properties of extracted cellulose nanoparticles (cellulose nanocrystals and cellulose nanofibrils) and natural cellulose materials (wood and bacterial nanocellulose) that make them attractive as supporting substrate materials in solar steam generators are briefly discussed. Recent progress in designing highly efficient cellulose-based solar evaporators, including utilizing the extracted cellulose nanoparticles via bottom-up assembly (cellulose nanofibrils), natural cellulose materials with intrinsic hierarchical structure (wood and bacterial nanocellulose), and commercial planar cellulose substrates (air-laid paper, cellulose paper and cotton fabric) is reviewed. The outstanding challenges that need to be addressed for these materials and devices to be utilized in the real-world and in overcoming global water crisis are also briefly highlighted.
This study demonstrates a simple, stable, and scalable polydopamine (PDA) coated PVDF membrane for highly efficient solar-driven membrane distillation.
Nanotechnology has driven scientific advances in catalytic materials and processes over the past few decades. Unique physicochemical and electronic properties that emerge when materials are engineered from the bulk to the nanoscale have been exploited for a wide range of applications, including environmental remediation such as catalytic pollutant destruction. Recent advances in the catalytic synthesis of fuels and value-added chemicals explore the properties of materials, noble and transition metal catalysts in particular, when they are engineered to be below nanoscale and at the single-atom limit. In addition to the maximized efficiency of atomic utilization due to size reduction, significantly reduced costs and the potential to achieve highly selective catalysis are particularly appealing to the environmental application of single-atom catalysts, overcoming certain limitations that the field has been unable to address with nanotechnology. This critical review, built upon a comprehensive discussion of fundamental properties, synthesis methods, and application examples, evaluates in depth the opportunities and challenges of single-atom catalysts as new frontier materials for environmental remediation applications beyond nanomaterials.
In this study, we loaded Pd catalysts onto a reduced graphene oxide (rGO) support in an atomically dispersed fashion [i.e., Pd single-atom catalysts (SACs) on rGO or Pd 1 /rGO] via a facile and scalable synthesis based on anchor-site and photoreduction techniques. The as-synthesized Pd 1 /rGO significantly outperformed the Pd nanoparticle (Pd nano ) counterparts in the electrocatalytic hydrodechlorination of chlorinated phenols. Downsizing Pd nano to Pd 1 leads to a substantially higher Pd atomic efficiency (14 times that of Pd nano ), remarkably reducing the cost for practical applications. The unique single-atom architecture of Pd 1 additionally affects the desorption energy of the intermediate, suppressing the catalyst poisoning by Cl − , which is a prevalent challenge with Pd nano . Characterization and experimental results demonstrate that the superior performance of Pd 1 /rGO originates from (1) enhanced interfacial electron transfer through Pd−O bonds due to the electronic metal−support interaction and (2) increased atomic H (H*) utilization efficiency by inhibiting H 2 evolution on Pd 1 . This work presents an important example of how the unique geometric and electronic structure of SACs can tune their catalytic performance toward beneficial use in environmental remediation applications.
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