In the face of growing water scarcity, it is critical to understand the potential of saltwater desalination as a long-term water supply option. Recent studies have highlighted the promise of new membrane materials that could desalinate water while exhibiting far greater permeability than conventional reverse osmosis (RO) membranes, but the question remains whether higher permeability can translate into significant reductions in the cost of desalinating water. Here, we address a critical question by evaluating the potential of such ultra-permeable membranes (UPMs) to improve the performance and cost of RO. By modeling the mass transport inside RO pressure vessels, we quantify how much a tripling in the water permeability of a membrane would reduce the energy consumption or the number of required pressure vessels for a given RO plant. We find that a tripling in permeability would allow for 44% fewer pressure vessels or 15% less energy for a seawater RO plant with a given capacity and recovery ratio. Moreover, a tripling in permeability would result in 63% fewer pressure vessels or 46% less energy for brackish water RO. However, we also find that the energy savings of UPMs exhibit a law of diminishing returns due to thermodynamics and concentration polarization at the membrane surface. Broader contextThe development of affordable, reliable and energy-efficient technologies for converting saltwater into fresh water is one of the most important research goals of this century. Yet the best technology available today, reverse osmosis (RO), remains costly. Recent advances in materials research suggest that new membranes could reject salt while permeating water much faster than nonporous RO membranes. However, considerable confusion exists regarding the likelihood that future RO systems will continue to become smaller, more productive or more energy-efficient. Given the critical importance of water technology research for human development goals, it is essential to carefully evaluate what future RO systems can and cannot achieve on the basis of more permeable membranes. Beginning with fundamental transport equations and extending to applied engineering scenarios, we demonstrate that membranes with 3x higher permeability could reduce the energy consumption of RO by 15-46% for seawater and brackish water respectively, or alternatively reduce the number of pressure vessels by 44-63%. Given many recent advances in the design of RO membranes, this work highlights the likely development of a new generation of desalination plants with higher throughput and a smaller spatial footprint than what is achievable today. Motivation and research questionThe orders-of-magnitude increase in permeability that UPMs could potentially enable require an in-depth assessment of the physical mechanisms that occur at the membrane's surface.
Graphene oxide (GO) and reduced GO (rGO) are the only variants of graphene that can be manufactured at the kilogram scale, and yet the widely accepted model for their structure has largely relied on indirect evidence. Notably, existing high-resolution transmission electron microscopy (HRTEM) studies of graphene oxide report long-range order of sp(2) lattice with isolated defect clusters. Here, we present HRTEM evidence of a different structural form of GO, where nanocrystalline regions of sp(2) lattice are surrounded by regions of disorder. The presence of contaminants that adsorb to the surface of the material at room temperature normally prevents direct observation of the intrinsic atomic structure of this defective GO. To overcome this, we use an in situ heating holder within an aberration-corrected TEM (AC-TEM) to study the atomic structure of this nanocrystalline graphene oxide from room temperature to 700 °C. As the temperature increases to above 500 °C, the adsorbates detach from the GO and the underlying atomic structure is imaged to be small 2-4 nm crystalline domains within a polycrystalline GO film. By combining spectroscopic evidence with the AC-TEM data, we support the dynamic interpretation of the structural evolution of graphene oxide.
Colloidal quantum dots (CQDs) are highly versatile nanoscale optoelectronic building blocks, but despite their materials engineering flexibility, there is a considerable lack of fundamental understanding of their electronic structure as they couple within thin films. By employing a joint experimental-theoretical study, we reveal the impact of connectivity in CQD assemblies, going beyond the single CQD picture. High-resolution transmission electron microscopy (HR-TEM) demonstrates connectivity motifs across different CQD sizes and length scales and provides the necessary perspective to build robust computational models to systematically study the achievable degree of connectivity in these materials. We focused on state-of-the-art surface ligand treatments, taking into account both the degree of connectivity and nanocrystal orientation, and performed ab initio simulations within the phonon-assisted hopping regime. Importantly, both the TEM studies and our simulation results revealed morphological and electronic defects that could dramatically reduce optoelectronic performance, and yet would not have been captured within a single CQD model that neglects connectivity. We calculate carrier mobility in the presence of such defect states and conclude that the best-achievable CQD assemblies for optoelectronics will require a modest degree of fusing via the {001} facet, followed by atomic ligand passivation to generate a clean band gap and unprecedentedly high charge transport.
Abstract-Water desalination has a central role to play in the global challenge for sustainable water supply in the 21 st century. But while the membranes employed in reverse osmosis (RO) have benefited from substantial improvements over the past 25 years, several recent advances in materials suggest that new membranes with dramatically higher water permeability will become available in the future. After providing an overview of the importance of membranes for sustainable water production, we describe some of the most exciting novel approaches for water desalination based on nanomaterials. In particular, graphene, a single-layer sheet of carbon with remarkable mechanical and electronic properties, can be patterned with nanometer-sized pores, to act as an ultra-thin filtration membrane. Drawing from our group's research at MIT, we will share some of our key findings about the potential impact of nanomaterials as membranes for water desalination in the 21 st century.
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