4.8 Article

Diversity-oriented synthesis of polymer membranes with ion solvation cages

Journal

NATURE
Volume 592, Issue 7853, Pages 225-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03377-7

Keywords

-

Funding

  1. Joint Center for Energy Storage Research (JCESR), an Energy Innovation Hub - US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences
  2. Office of Science, Office of Basic Energy Sciences of the US DOE [DE-AC02-05CH11231]
  3. Center for Gas Separations Relevant to Clean Energy Technologies, an Energy Frontier Research Center - US DOE, Office of Science, Basic Energy Sciences [DE-SC0001015]
  4. DOE Office of Science User Facility [DE-AC0205CH11231]
  5. DOE's Office of Biological and Environmental Research
  6. Pacific Northwest National Laboratory
  7. Advanced Research Projects Agency-Energy Integration and Optimization of Novel Ion Conducting Solids (IONICS) programme [DE-AR0000774]
  8. DOE Vehicle Technologies Office

Ask authors/readers for more resources

A diversity-oriented synthetic strategy has been developed to identify microporous polymer membranes that feature solvation cages for lithium ions, showing higher ionic conductivity and cation transference number. These membranes have potential applications as anode-stabilizing interlayers in high-voltage lithium metal batteries.
Microporous polymers feature shape-persistent free volume elements (FVEs), which are permeated by small molecules and ions when used as membranes for chemical separations, water purification, fuel cells and batteries(1-3). Identifying FVEs that have analyte specificity remains a challenge, owing to difficulties in generating polymers with sufficient diversity to enable screening of their properties. Here we describe a diversity-oriented synthetic strategy for microporous polymer membranes to identify candidates featuring FVEs that serve as solvation cages for lithium ions (Li+). This strategy includes diversification of bis(catechol) monomers by Mannich reactions to introduce Li+-coordinating functionality within FVEs, topology-enforcing polymerizations for networking FVEs into different pore architectures, and several on-polymer reactions for diversifying pore geometries and dielectric properties. The most promising candidate membranes featuring ion solvation cages exhibited both higher ionic conductivity and higher cation transference number than control membranes, in which FVEs were aspecific, indicating that conventional bounds for membrane permeability and selectivity for ion transport can be overcome(4). These advantages are associated with enhanced Li+ partitioning from the electrolyte when cages are present, higher diffusion barriers for anions within pores, and network-enforced restrictions on Li+ coordination number compared to the bulk electrolyte, which reduces the effective mass of the working ion. Such membranes show promise as anode-stabilizing interlayers in high-voltage lithium metal batteries.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available