4.8 Article

Mesoporous LixMn2O4 Thin Film Cathodes for Lithium-Ion Pseudocapacitors

Journal

ACS NANO
Volume 10, Issue 8, Pages 7572-7581

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.6b02608

Keywords

LiMn2O4; pseudocapacitor; lithium-ion battery; high rate; mesoporous; cathode; nanocrystal templated

Funding

  1. U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences [DE-SC001342]
  2. DOE [DE-SC0014213]
  3. Office of Naval Research
  4. National Science Foundation [0840531]
  5. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  6. Division Of Chemistry
  7. Direct For Mathematical & Physical Scien [0840531] Funding Source: National Science Foundation
  8. U.S. Department of Energy (DOE) [DE-SC0014213] Funding Source: U.S. Department of Energy (DOE)

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Charge storage devices with high energy density and enhanced rate capabilities are highly sought after in today's mobile world. Although several high-rate pseudocapacitive anode materials have been reported, cathode materials operating in a high potential range versus lithium metal are much less common. Here, we present a nanostructured version of the well-known cathode material, LiMn2O4. The reduction in lithium-ion diffusion lengths and improvement in rate capabilities is realized through a combination of nanocrystallinity and the formation of a 3-D porous framework. Materials were fabricated from nanoporous Mn3O4 films made by block copolymer templating of preformed nanocrystals. The nano porous Mn3O4 was then converted via solid-state reaction with LiOH to nanoporous LixMn2O4 (1 < x < 2). The resulting films had a wall thickness of similar to 15 nm, which is small enough to be impacted by inactive surface sites. As a consequence, capacity was reduced by about half compared to bulk LiMn2O4, but both charge and discharge kinetics as well as cycling stability were improved significantly. Kinetic analysis of the redox reactions was used to verify the pseudocapacitive mechanisms of charge storage and establish the feasibility of using nanoporous LixMn2O4 as a cathode in lithium-ion devices based on pseudocapacitive charge storage.

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