Process for producing lithium batteries having an ultra-high energy density

Abstract

A process for producing a lithium battery, comprising: (A) Preparing a plurality of conductive porous layers, wet anode layers, and wet cathode layers; (B) Stacking a desired number of porous layers and wet anode layers in an alternating manner to form an anode electrode having a thickness no less than 100 μm; (C) Placing a porous separator layer in contact with the anode electrode; (D) Stacking a desired number of porous layers wet cathode layers in an alternating manner to form a cathode electrode in contact with the porous separator, wherein the cathode electrode has a thickness no less than 100 μm; and (F) Assembling and sealing the anode electrode, separator, and cathode electrode in a housing to produce the lithium battery. The consolidated anode or cathode layer is preferably thicker than 300 more preferably thicker than 400 μm, and further more preferably greater than 500 μm.

We claim: 
     
         1 . A process for producing a lithium metal battery, said process comprising:
 (A) preparing a plurality of electrically conductive porous layers, and a plurality of wet cathode layers of a cathode active material and an optional conductive additive mixed with a liquid electrolyte, wherein said conductive porous layers contain interconnected conductive pathways and at least 80% by volume of pores;   (B) preparing an anode electrode having an anode current collector that has two opposed primary surfaces wherein at least one of the two primary surfaces is deposited with a layer of lithium metal or lithium alloy having at least 50% by weight of lithium element in said alloy;   (C) placing a porous separator layer in contact with said anode electrode;   (D) stacking and consolidating a desired number of said porous layers and a desired number of said wet cathode layers in an alternating manner to form a cathode electrode in contact with said porous separator, wherein said cathode electrode has a thickness no less than 100 μm; wherein said step (D) is conducted before or after step (B); and   (E) assembling and sealing said anode electrode, porous separator, and cathode electrode in a housing to produce said lithium battery;   wherein said cathode active material has a material mass loading no less than 15 mg/cm 2  for an organic or polymer material or no less than 30 mg/cm 2  for an inorganic and non-polymer material in said cathode electrode.   
     
     
         2 . The process of  claim 1 , wherein said cathode active material comprises a lithium intercalation compound or lithium-absorbing compound selected from an inorganic material, an organic or polymeric material, a metal oxide/phosphate/sulfide, or a combination thereof. 
     
     
         3 . The process of  claim 2 , wherein said metal oxide/phosphate/sulfide is selected from a lithium cobalt oxide, lithium nickel oxide, lithium manganese oxide, lithium vanadium oxide, lithium-mixed metal oxide, lithium iron phosphate, lithium manganese phosphate, lithium vanadium phosphate, lithium mixed metal phosphate, transition metal sulfide, or a combination thereof. 
     
     
         4 . The process of  claim 2 , wherein said inorganic material is selected from sulfur, sulfur compound, lithium polysulfide, transition metal dichalcogenide, a transition metal trichalcogenide, or a combination thereof. 
     
     
         5 . The process of  claim 2 , wherein said inorganic material is selected from TiS 2 , TaS 2 , MoS 2 , NbSe 3 , MnO 2 , CoO 2 , an iron oxide, a vanadium oxide, or a combination thereof. 
     
     
         6 . The process of  claim 2 , wherein said metal oxide/phosphate/sulfide contains a vanadium oxide selected from the group consisting of VO 2 , Li x VO 2 , V 2 O 5 , Li x V 2 O 5 , V 3 O 8 , Li x V 3 O 8 , Li x V 3 O 7 , V 4 O 9 , Li x V 4 O 9 , V 6 O 13 , Li x V 6 O 13 , their doped versions, their derivatives, and combinations thereof, wherein 0.1<x<5. 
     
     
         7 . The process of  claim 2 , wherein said metal oxide/phosphate/sulfide is selected from a layered compound LiMO 2 , spinel compound LiM 2 O 4 , olivine compound LiMPO 4 , silicate compound Li 2 MSiO 4 , tavorite compound LiMPO 4 F, borate compound LiMBO 3 , or a combination thereof, wherein M is a transition metal or a mixture of multiple transition metals. 
     
     
         8 . The process of  claim 2 , wherein said organic material or polymeric material is selected from poly(anthraquinonyl sulfide) (PAQS), a lithium oxocarbon, 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), poly(anthraquinonyl sulfide), pyrene-4,5,9,10-tetraone (PYT), polymer-bound PYT, quino(triazene), redox-active organic material, tetracyanoquinodimethane (TCNQ), tetracyanoethylene (TCNE), 2,3,6,7,10,11-hexamethoxytriphenylene (HMTP), poly(5-amino-1,4-dyhydroxy anthraquinone) (PADAQ), phosphazene disulfide polymer ([(NPS 2 ) 3 ]n), lithiated 1,4,5,8-naphthalenetetraol formaldehyde polymer, hexaazatrinaphtylene (HATN), hexaazatriphenylene hexacarbonitrile (HAT(CN) 6 ), 5-benzylidene hydantoin, isatine lithium salt, pyromellitic diimide lithium salt, tetrahydroxy-p-benzoquinone derivatives (THQLi 4 ), N,N′-diphenyl-2,3,5,6-tetraketopiperazine (PHP), N,N′-diallyl-2,3,5,6-tetraketopiperazine (AP), N,N′-dipropyl-2,3,5,6-tetraketopiperazine (PRP), a thioether polymer, a quinone compound, 1,4-benzoquinone, 5,7,12,14-pentacenetetrone (PT), 5-amino-2,3-dihydro-1,4-dyhydroxy anthraquinone (ADDAQ), 5-amino-1,4-dyhydroxy anthraquinone (ADAQ), calixquinone, Li 4 C 6 O 6 , Li 2 C 6 O 6 , Li 6 C 6 O 6 , or a combination thereof. 
     
     
         9 . The process of  claim 8 , wherein said thioether polymer is selected from poly[methanetetryl-tetra(thiomethylene)] (PMTTM), poly(2,4-dithiopentanylene) (PDTP), a polymer containing poly(ethene-1,1,2,2-tetrathiol) (PETT) as a main-chain thioether polymers, a side-chain thioether polymer having a main-chain consisting of conjugating aromatic moieties, and having a thioether side chain as a pendant, poly(2-phenyl-1,3-dithiolane) (PPDT), poly(1,4-di(1,3-dithiolan-2-yl)benzene) (PDDTB), poly(tetrahydrobenzodithiophene) (PTHBDT), poly[1,2,4,5-tetrakis(propylthio)benzene] (PTKPTB, or poly[3,4(ethylenedithio)thiophene] (PEDTT). 
     
     
         10 . The process of  claim 2 , wherein said organic material contains a phthalocyanine compound selected from copper phthalocyanine, zinc phthalocyanine, tin phthalocyanine, iron phthalocyanine, lead phthalocyanine, nickel phthalocyanine, vanadyl phthalocyanine, fluorochromium phthalocyanine, magnesium phthalocyanine, manganous phthalocyanine, dilithium phthalocyanine, aluminum phthalocyanine chloride, cadmium phthalocyanine, chlorogallium phthalocyanine, cobalt phthalocyanine, silver phthalocyanine, a metal-free phthalocyanine, a chemical derivative thereof, or a combination thereof. 
     
     
         11 . The process of  claim 1 , wherein said cathode active material contains a lithium intercalation compound or lithium-absorbing compound selected from a metal carbide, metal nitride, metal boride, metal dichalcogenide, or a combination thereof. 
     
     
         12 . The process of  claim 1 , wherein said cathode active material contains a lithium intercalation compound or lithium-absorbing compound selected from an oxide, dichalcogenide, trichalcogenide, sulfide, selenide, or telluride of niobium, zirconium, molybdenum, hafnium, tantalum, tungsten, titanium, vanadium, chromium, cobalt, manganese, iron, or nickel in a nanowire, nanodisc, nanoribbon, or nanoplatelet form. 
     
     
         13 . The process of  claim 1 , wherein said cathode active material contains a lithium intercalation compound or lithium-absorbing compound selected from nanodiscs, nanoplatelets, nano-coating, or nanosheets of an inorganic material selected from: (a) bismuth selenide or bismuth telluride, (b) transition metal dichalcogenide or trichalcogenide, (c) sulfide, selenide, or telluride of niobium, zirconium, molybdenum, hafnium, tantalum, tungsten, titanium, cobalt, manganese, iron, nickel, or a transition metal; (d) boron nitride, or (e) a combination thereof; wherein said discs, platelets, or sheets have a thickness less than 100 nm. 
     
     
         14 . The process of  claim 1 , wherein said cathode active material contains a lithium intercalation compound or lithium-absorbing compound contains nanodiscs, nanoplatelets, nano-coating, or nanosheets of a lithium intercalation compound selected from: (i) bismuth selenide or bismuth telluride, (ii) transition metal dichalcogenide or trichalcogenide, (iii) sulfide, selenide, or telluride of niobium, zirconium, molybdenum, hafnium, tantalum, tungsten, titanium, cobalt, manganese, iron, nickel, or a transition metal; (iv) boron nitride, or (v) a combination thereof, wherein said discs, platelets, coating, or sheets have a thickness less than 100 nm.