Anode active material and method of preparing the same
US-2015380733-A1 · Dec 31, 2015 · US
US10529975B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10529975-B2 |
| Application number | US-201514814881-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 31, 2015 |
| Priority date | Dec 15, 2014 |
| Publication date | Jan 7, 2020 |
| Grant date | Jan 7, 2020 |
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One embodiment includes forming surface-modifying phases on a surface of a functional electrode via atomic layer deposition and controlling the chemistry of constituent phases, the crystalline nature of the constituent phases and the thickness of the surface-modifying phase via the atomic layer deposition such that the thickness is between about 2 nm to about 200 nm. The surface-modifying phases enhances the performance of electrocatalytic activity of the functional electrode and the device.
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Therefore, at least the following is claimed: 1. A method, comprising: forming a surface-modifying phase on a surface of a functional electrode via atomic layer deposition; controlling the chemistry of the surface modifying phase, the crystalline nature of the surface modifying phase and thickness of the surface-modifying phase via the atomic layer deposition, the thickness being controlled to be within a range of about 2 nm to about 200 nm; establishing a nano-grained porous ionic conductor surface network on the surface of the functional electrode which increases a triple phase boundary density of the functional electrode; and wherein the surface-modifying phase enhances a performance of electrocatalytic activity of the functional electrode. 2. The method of claim 1 , further comprising applying one or more thermal treatments to the surface-modifying phase. 3. The method of claim 1 , wherein the surface-modifying phase comprises at least one of: (1) a plurality of discrete nano-particles of an ionic conductor, (2) a plurality of discrete nano-particles of an electrocatalyst, (3) a continuous nano-scale porous single phase ionic conductor network, (4) a continuous nano-scale porous single-phase electrocatalyst, or (5) a nano-composite scaffold composed of multiple phases selected from the above (1)-(4). 4. The method of claim 3 , wherein the ionic conductors may comprise at least one of: pure ZrO 2 , doped ZrO 2 , pure CeO 2 , doped CeO 2 , pure LaGaO 3 , doped LaGaO 3 , pure Ba 2 In 2 O 5 , doped Ba 2 In 2 O 5 , BaZrO 3 , or doped BaZrO 3 . 5. The method of claim 3 , wherein the continuous nano-scale porous single phase ionic conductor network may comprise at least one of: pure ZrO 2 , doped ZrO 2 , pure CeO 2 , doped CeO 2 , BaZrO 3 , doped BaZrO 3 , pure LaGaO 3 , doped LaGaO 3 , pure Ba 2 In 2 O 5 , or doped Ba 2 In 2 O 5 . 6. The method of claim 3 , wherein discrete nano-particles of an electrocatalyst may comprise at least one of: cobalt oxide, ferrite, La x Sr 1-x MnO 3 (LSM), La x Sr 1-x CoO 3 (LSC), La x Sr 1-x Co y Fe 1-y MnO 3 (LSCF), Pt, Ru Pd, or Pt—Ru alloy. 7. The method of claim 3 , wherein the nano-composite scaffold comprises a nano-ionic conductor network and a nano catalyst. 8. The method of claim 3 , wherein the nano-composite scaffold comprises a nano electrocatalyst network and a nano catalyst. 9. The method of claim 1 , wherein the surface modifying phase comprises a plurality of phases, and wherein forming the surface-modifying phase further comprises: depositing a first surface-modifying phase comprising a plurality of isolated and discrete particles, a porous connected network, and a continuous layer of an electrocatalyst; and depositing a second surface-modifying phase comprising an electrolyte over the first surface-modifying phase, wherein the second surface-modifying phase fills in one or more gaps in the first surface-modifying phase. 10. The method of claim 1 , wherein the surface modifying phase comprises a plurality of phases, and wherein forming the surface-modifying phase further comprises: depositing a first surface-modifying phase comprising an ionic conductor; and depositing a second surface-modifying phase over the first surface-modifying phase, the second surface-modifying phase comprising a plurality of isolated and discrete particles of an electrocatalyst. 11. The method of claim 1 , wherein the thickness is between about 2 nm to about 100 nm. 12. The method of claim 1 , wherein the thickness is between about 2 nm to about 40 nm. 13. The method of claim 1 , wherein the thickness is between about 2 nm to about 20 nm.
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