ZINC BATTERY ELECRTOLYTE ADDITIVE

Abstract

An electrolyte additive is provided. The additive is a quaternary ammonium or phosphonium salt effective to suppress hydrogen evolution and metal dendrite formation during operation of a zinc electrochemical cell such as a zinc-air battery. A zinc battery cell is also provided, which contains an effective amount of the electrolyte additive.

Claims

1. A composition, comprising: ##STR00027## wherein, N/P is a central nitrogen atom having a +1 charge; wherein R.sup.1 is selected from the group consisting of 2 methylene-chlorobenzene, 3 methylene-bromobenzene, 2-methylene-bromobenzene, 4-methylene-cyanobenzene, 3-methylene-cyanobenzene, 2-methylene-cyanobenzene, 1 methylene-2,4-dimethylbenzene, 1-methylene-3,4-dimethylbenzene, 1-methylene-2,5-dimethylbenzene, 3 -methylene-benzoic acid, 2-methylene-benzoic acid, 2-methylene-phenol, 3-methylene-phenol, and 2 methylene-anisole; and wherein [An]− is a counter anion.

2. The composition of claim 1, wherein N/P is phosphorous and R1 is methylene benzene.

3. The composition of claim 1, wherein the counter anion is selected from chloride, bromide, iodide, fluoride, hydroxide, nitrate, nitrite, sulphate, sulphite, phosphate, perchlorate, or any combination thereof.

4. A composition, comprising: ##STR00028## wherein, N/P is a central phosphorous atom having a +1 charge; wherein R.sup.1 is selected from the group consisting of 3-methylene-toluene, 2-methylene-toluene, 3-methylene-chlorobenzene, 2-methylene-chlorobenzene, 4-methylene-bromobenzene, 3-methylene-bromobenzene, 2-methylene-bromobenzene, 4-methylene-cyanobenzene, 3-methylene-cyanobenzene, 2-methylene-cyanobenzene, 1-methylnaphthalene, 1-methylene-2,6-dimethylbenzene, 1-methylene-2,4-dimethylbenzene, 1-methylene-3,4-dimethylbenzene, 1-methylene-2,5-dimethylbenzene, 1-methylene-3,5-dimethylbenzene, 1-methylene-2,6-dichlorobenzene, 4-methylene-benzoic acid, 3-methylene-benzoic acid, 2-methylene-benzoic acid, 2-methylene-phenol, 3-methylene-phenol, 4-methylene-phenol, 4-methylene-anisole, 3-methylene-anisole, 2-methylene-anisole; and wherein [An]− is a counter anion.

5. The composition of claim 4, wherein R1 is methylene benzene.

6. The composition of claim 4, wherein the counter anion is selected from chloride, bromide, iodide, fluoride, hydroxide, nitrate, nitrite, sulphate, sulphite, phosphate, perchlorate, or any combination thereof.

Description

III. BRIEF DESCRIPTION OF THE DRAWINGS

[0010] The invention may take physical form in certain parts and arrangement of parts, embodiments of which will be described in detail in this specification and illustrated in the accompanying drawings which form a part hereof, wherein like reference numerals indicate like structure, and wherein:

[0011] FIG. 1 is a photograph of electrodeposited zinc in a control cell containing no additive after operating the cell for 1500 s;

[0012] FIG. 2 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % Benzyltrimethylammonium Hydroxide after operating the cell for 1500 s;

[0013] FIG. 3 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % Benzyltributylammonium Chloride after operating the cell for 1500 s;

[0014] FIG. 4 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % Dibenzyldimethylammonium Chloride after operating the cell for 1500 s;

[0015] FIG. 5 is a photograph of electrodeposited zinc in a cell containing 0.01 wt % Dibenzyldimethylammonium Chloride after operating the cell for 1500 s;

[0016] FIG. 6 is a photograph of electrodeposited zinc in a cell containing 0.1 wt % Dibenzyldimethylammonium Chloride after operating the cell for 1500 s;

[0017] FIG. 7 is .sup.1H NMR data for 1-(Trimethylammonium methyl)naphthalene chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % 1-(Trimethylammonium methyl)naphthalene chloride after operating the cell for 1500 s;

[0018] FIG. 8 is .sup.1H NMR data for 4-(Trimethylammonium methyl)benzonitrile Chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % 4-(Trimethylammonium methyl)benzonitrile Chloride after operating the cell for 1500 s;

[0019] FIG. 9 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % 4-(Trimethylammonium methyl)anisole Chloride after operating the cell for 1500 s;

[0020] FIG. 10 is a photograph of electrodeposited zinc in a cell containing 0.5 wt % 4-(Trimethylammonium methyl)anisole Chloride after operating the cell for 1500 s;

[0021] FIG. 11 is a photograph of electrodeposited zinc in a cell containing 0.1 wt % 4-(Trimethylammonium methyl)anisole Chloride after operating the cell for 1500 s;

[0022] FIG. 12 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % 4-(Trimethylammonium methyl)-1,2,6-trimethoxybenzene after operating the cell for 1500 s;

[0023] FIG. 13 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % (4-Methylbenzyl)trimethylammonium Chloride after operating the cell for 1500 s;

[0024] FIG. 14 is .sup.1H NMR data for (2-Methylbenzyl)trimethylammonium Chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % (2-Methylbenzyl)trimethylammonium Chloride after operating the cell for 1500 s;

[0025] FIG. 15 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % (4-Chlorobenzyl)trimethylammonium Chloride after operating the cell for 1500 s;

[0026] FIG. 16 is .sup.1H NMR data for (2-Chlorobenzyl)trimethylammonium Chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % (2-Chlorobenzyl)trimethylammonium Chloride after operating the cell for 1500 s;

[0027] FIG. 17 is .sup.1H NMR data for (4-Bromobenzyl)trimethylammonium Bromide in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % (4-Bromobenzyl)trimethylammonium Bromide after operating the cell for 1500 s;

[0028] FIG. 18 is .sup.1H NMR data for Benzyltrimethylphosphonium Chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % Benzyltrimethylphosphonium Chloride after operating the cell for 1500 s;

[0029] FIG. 19 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % (2-Hydroxybenzyl)trimethylammonium Iodide after operating the cell for 1500 s;

[0030] FIG. 20 is .sup.1H NMR data for (3-Methylbenzyl)trimethylammonium Chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % (3-Methylbenzyl)trimethylammonium Chloride after operating the cell for 1500 s;

[0031] FIG. 21 is .sup.1H NMR data for 4-(Trimethylammonium)benzoic acid Bromide in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % 4-(Trimethylammonium methyl)benzoic acid Bromide after operating the cell for 1500 s;

[0032] FIG. 22 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % 3-(Trimethylammonium methyl)anisole Chloride after operating the cell for 1500 s;

[0033] FIG. 23 is a photograph of electrodeposited zinc in a cell containing 1.0 wt % Benzalkonium Chloride after operating the cell for 1500 s;

[0034] FIG. 24 is .sup.1H NMR data for (2,6-Dimethylbenzyl)trimethylammonium Chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % (2,6-Dimethylbenzyl)trimethylammonium;

[0035] FIG. 25 is a photograph of electrodeposited zinc in a cell containing 25 wt % Benzyltrimethylammonium chloride after operating the cell for 1500 s;

[0036] FIG. 26 is .sup.1H NMR data for (2,6-Dichlorobenzyl)trimethylammonium chloride in D.sub.2O;

[0037] FIG. 27 is .sup.1H NMR data for (3,4-Dimethylbenzyl)trimethylammonium chloride in D.sub.2O with an inlay photograph of electrodeposited zinc in a cell containing 1.0 wt % (3,4-Dimethylbenzyl)trimethylammonium chloride after operating the cell for 1500 s;

[0038] FIG. 28 is .sup.1H NMR data for (4-Hydroxybenzyl)trimethylammonium Iodide in D.sub.2O;

[0039] FIG. 29 is a photograph of electrodeposited zinc in a cell containing 15 wt % 4-(Trimethylammoniummethyl)anisole chloride after operating the cell for 1500 s;

[0040] FIG. 30 is a photograph of electrodeposited zinc in a cell containing 15 wt % (4-Methylbenzyl)trimethylammonium chloride after operating the cell for 1500 s;

[0041] FIG. 31 is a photograph of electrodeposited zinc in a cell containing 0.1 wt % (4-Methylbenzyl)trimethylammonium chloride after operating the cell for 1500 s; and

[0042] FIG. 32 is a schematic view of a general zinc-based battery in accordance with one or more embodiments of the invention.

IV. DETAILED DESCRIPTION OF THE INVENTION

[0043] Embodiments of the invention include organic electrolyte additives that improve zinc battery performance by both selectively preventing dendrite formation and preventing hydrogen evolution side reactions without hindering cell efficiency. Embodiments may include quaternary nitrogen and/or quaternary phosphorous compounds substituted with a variety of linear and/or cyclic organic groups.

[0044] Formula I illustrates an embodiment of the invention comprising a central nitrogen or phosphorous atom with a charge of +1, denoted herein as “N/P.sup.+” or as an “N/P.sup.+ center”. The N/P.sup.+ center is bonded to four R groups R.sup.1, R.sup.2, R.sup.3, and R.sup.4. The structure shown in Formula I is not intended to illustrate isomers or stereochemical structures, but rather is intended to encompass all isomeric forms with the same atom-to-atom connectivity.

##STR00001##

[0045] R.sup.1 is selected from the following radicals, where “yl” or “methylene” refers to the position of the radical electron available for bonding with an N/P+ center: methyl benzene, 4-methylene-toluene, 3-methylene-toluene, 2-methylene-toluene, 4-methylene-chlorobenzene, 3-methylene-chlorobenzene, 2-methylene-chlorobenzene, 4-methylene-bromobenzene, 3-methylene-bromobenzene, 2-methylene-bromobenzene, 4-methylene-iodobenzene, 3-methylene-iodobenzene, 2-methylene-iodobenzene, 4-methylene-cyanobenzene, 3-methylene-cyanobenzene, 2-methylene-cyanobenzene, 4-methylene-anisole, 3-methylene-anisole, 2-methylene-anisole, 1-methylnaphthalene, 1-methylene-2,6-dimethylbenzene, 1-methylene-2,4-dimethylebenzene, 1-methylene-3,4-dimethylbenzene, 1-methylene-2,5-dimethylbenzene, 1-methylene-3,5-dimethylbenzene, 1-methylene-2,4,6-trimethylbenzene, 1-methylene-3,4,5-trimethoxybenzene, 1-methylene-2,6-dichlorobenzene, 4-methylene-nitrobenzene, 4-methylene-benzoic acid, 3-methylene-benzoic acid, 2-methylene-benzoic acid, 2-methylene-phenol, 3-methylene-phenol, and 4-methylene-phenol.

[0046] With continuing reference to Formula I, the radicals R.sup.2, R.sup.3, and R.sup.4 may be independently selected from R.sup.1, methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, n-octyl, n-decyl, n-dodecyl, n-tetradecyl, n-hexadecyl, or n-octadecyl. Radicals R.sup.2, R.sup.3, and R.sup.4 may be independently selected from linear and non-linear alkyls from C1 to C25.

[0047] Embodiments conforming to Formula I may include a sufficient amount of counter anion [An] to produce a neutral species. The anion [An] may be, for example and without limitation, chloride, bromide, iodide, fluoride, hydroxide, nitrate, nitrite, sulphate, sulphite, phosphate, perchlorate, or any combination thereof. The person having ordinary skill in the art will readily appreciate that the anion has less or no influence on performance of the electrolyte additives of the present invention. Accordingly, a wide variety of anions are within the scope of the invention, and the foregoing list is meant only to be illustrative.

[0048] Referring now to the drawings wherein the showings are for purposes of illustrating embodiments of the invention only and not for purposes of limiting the same, FIG. 1 is a photograph showing dendrite growth using 4M KOH, 0.1M ZnO, and water with no additives suppressing dendrite growth. Plating was conducted at −1.6V relative to a Hg/HgO reference electrode for 1500 seconds. FIG. 1 shows dendrite growth after 1500 seconds. This serves as a control against which dendrite suppression additives are compared in subsequent tests. Each experimental run is conducted under the same conditions as the control run, namely, in 4M KOH electrolyte, 0.1M ZnO, and water at −1.6V relative to a Hg/HgO reference electrode for 1500 seconds. The results are summarized in Table I.

[0049] With respect to the control results shown in FIG. 1, prominent dendrite growth is clearly visible. Although the control rapidly evolves hydrogen, the bubbles form so quickly over the entire surface that they do not adhere to the dendrites. Accordingly, very few if any hydrogen bubbles are visible in FIG. 1. In contrast FIGS. 2-18 all show suppression of hydrogen evolution to some degree, which may be complete hydrogen suppression or partial hydrogen suppression. Where hydrogen suppression is complete, no bubbles form on the plated zinc surface so the associated figure shows no hydrogen bubbles. However, where hydrogen evolution is partially suppressed large slow-forming hydrogen bubbles are visible in the associated figure adhering to the plated zinc.

TABLE-US-00001 TABLE I Suppression of Dendrite Formation by Additives Amount Hydrogen Dendrite Additive (wt %) Suppressed Suppressed Figure No additive (control) 0 No No Fig. 1 Benzyltrimethylammonium Hydroxide 1.0 Partial Yes Fig. 2 [00002] Benzyltributylammonium Chloride (BTBAC) 1.0 Partial Yes Fig. 3 [00003] Dibenzyldimethylammonium Chloride 1.0 Partial Yes Fig. 4 (DBDMAC) [00004] Dibenzyldimethylammonium Chloride 0.01 No Partial Fig. 5 (DBDMAC) Dibenzyldimethylammonium Chloride 0.1 Partial Yes Fig. 6 (DBDMAC) 1-(Trimethylammonium methyl)naphthalene 1.0 No Partial Fig. 7 Chloride (TMAMNC) [00005] 4-(Trimethylammoniummethyl)benzonitrile 1.0 Yes Partial Fig. 8 Chloride (TMAMBC) [00006] 4-(Trimethylammoniummethyl)anisole 1.0 Yes Yes Fig. 9 Chloride [00007] 4-(Trimethylammoniummethyl)anisole 0.5 Partial Yes Fig. 10 Chloride 4-(Trimethylammoniummethyl)anisole 0.1 Partial Partial Fig. 11 Chloride 4-(Trimethylammoniummethyl)-1,2,6- 1.0 Partial Yes Fig. 12 trimethoxybenzene [00008] (4-Methylbenzyl)trimethylammonium Chloride 1.0 Partial Yes Fig. 13 [00009] (4-Methylbenzyl)trimethylammonium 15 Yes Yes Fig. 30 chloride (4-Methylbenzyl)trimethylammonium 0.1 Partial Partial Fig. 31 chloride (2-Methylbenzyl)trimethylammonium Chloride 1.0 Partial Yes Fig. 14 [00010] (4-Chlorobenzyl)trimethylammonium Chloride 1.0 Partial Partial Fig. 15 [00011] (2-Chlorobenzyl)trimethylammonium Chloride 1.0 No Partial Fig. 16 [00012] (4-Bromobenzyl)trimethylammonium Bromide 1.0 Partial Yes Fig. 17 [00013] Benzyltrimethylphosphonium Chloride 1.0 No Partial Fig. 18 [00014] (2-Hydroxybenzyl)trimethylammonium Iodide 1.0 Partial Partial Fig. 19 [00015] (3-Methylbenzyl)trimethylammonium Chloride 1.0 Partial Yes Fig. 20 [00016] 4-(Trimethylammoniummethyl)benzoic acid 1.0 Partial Partial Fig. 21 Bromide [00017] 3-(Trimethylammoniummethyl)anisole 1.0 Partial Partial Fig. 22 Chloride [00018] Benzalkonium Chloride 1.0 Partial Yes Fig. 23 [00019] (2,6-Dimethylbenzyl)trimethylammonium 1.0 No Partial Fig. 24 Chloride [00020] Benzyltrimethylammonium Hydroxide 25 Yes Yes Fig. 25 (BTMAH) [00021] (2,6-Dichlorobenzyl)trimethylammonium 1.0 Partial No Fig. 26 Chloride [00022] (3,4-Dimethylbenzyl)trimethylammonium 1.0 Yes Yes Fig. 27 Chloride [00023] (4-Hydroxybenzyl)trimethylammonium Iodide 1.0 Partial Partial Fig. 28 [00024] 4-(Trimethylammoniummethyl)anisole 15 Yes Yes Fig. 29 Chloride [00025]

[0050] Dibenzylimethylammonium chloride (DBDMAC) preparation and performance.

[0051] N,N-dimethylbenzylamine (2 g, 14.8 mmol) is diluted into 10 mL of acetonitrile and stirred under air. Benzylchloride (2.06 g, 1.87 mL, 16.3 mmol) is added at once and the reaction is heated to 78° C. to reflux for 3 hours. The solution is concentrated under reduced pressure to a colorless viscous oil. The desired product is recrystallized from acetone. A white/colorless crystal solid of 3.50 g is collected (90.4% yield) and its structure is confirmed by .sup.1H NMR. The dendrite suppressive effect of this additive is shown in FIGS. 4-6. Full dendrite suppression occurs at 1 wt % and 0.1 wt %, and partial suppression is observed at 0.01 wt %. Hydrogen evolution is partially suppressed at 1 wt % and 0.1 wt %. No hydrogen suppression is observed at 0.01 wt %.

[0052] 1-(Trimethylammonium methyl)naphthalene chloride preparation and performance.

[0053] To a 100 mL flask is added 10 mL of a 13% solution of trimethylamine in tetrahydrofuran (1.16 g, 19.7 mmol). The solution is stirred under air at room temperature. 1-(Chloromethyl)naphthalene (3.80 g, 3.22 mL, 21.5 mmol) is added in four quick portions and the reaction is heated to 60° C. for 3 hours. The reaction is then cooled to room temperature and white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 3.10 g of white fluffy powder is collected (67% yield), and the desired product structure is confirmed by .sup.1H NMR. The partial dendrite suppressive effect of this additive is shown in FIG. 7. 1-(Trimethylammonium methyl)naphthalene chloride promotes, rather than suppresses, hydrogen evolution.

[0054] 4-(Trimethylammoniummethyl)benzonitrile chloride preparation and performance.

[0055] To a 100 mL flask is added 10 mL of a 13% solution of trimethylamine in tetrahydrofuran (1.16 g, 19.7 mmol). The solution is stirred under air at room temperature. 4-(Chloromethyl)benzonitrile (2.70 g, 17.8 mmol) is added in quick portions and the reaction is heated to 60° C. for 2 hours. The reaction is then cooled to room temperature and white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 2.80 g of white fluffy powder is collected (75% yield), and the desired product structure is confirmed by .sup.1H NMR. The partial dendrite suppressive effect of this additive is shown in FIG. 8. This additive strongly suppresses hydrogen evolution.

[0056] 4-(Trimethylammoniummethyl)anisole chloride preparation and performance.

[0057] To a 100 mL flask is added 20 mL of a 13% solution of trimethylamine in tetrahydrofuran (2.32 g, 39.4 mmol) and this is stirred under air at room temperature. (4-Methoxybenzyl)chloride (5.59 g, 4.84 mL, 35.7 mmol) is added in quick portions and the reaction is heated to 60° C. for 3 hours. The reaction is then cooled to room temperature and white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 7.08 g of white fluffy powder is collected (92% yield) and the desired product structure is confirmed by .sup.1H NMR. The dendrite suppressive effect of this additive is shown in FIGS. 9-11. Dendrite suppression is complete under the test conditions at 1 wt % and 0.5 wt %, and partial at 0.1 wt %. Hydrogen evolution is fully suppressed at 1.0 wt % and partially suppressed at 0.5 wt % and 0.01 wt %.

[0058] An analogous method is used to synthesize 3-(trimethylammoniummethyl)anisole chloride, as well as similar 4-(trimethylammoniummethyl)-1,2,6-trimethoxybenzene. FIG. 12 shows that 4-(trimethylammoniummethyl)-1,2,6-trimethoxybenzene fully suppresses dendrite formation under the test conditions at 1.0 wt %, and partially suppresses hydrogen evolution. FIG. 22 shows that 3-(trimethylammoniummethyl)anisole chloride fully suppresses hydrogen evolution and dendrite formation.

[0059] (4-Methylbenzyl)trimethylammonium chloride preparation and performance.

[0060] To a 100 mL flask is added 10 mL of a 13% solution of trimethylamine in tetrahydrofuran (1.16 g, 19.7 mmol). The solution is stirred under air at room temperature. 4-Methylbenzyl chloride (2.75 g, 2.6 ml, 19.5 mmol) is added in quick portions and the reaction is heated to 60° C. for 3 hours. The reaction is then cooled to room temperature and white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 2.92 g of white fluffy powder is collected (75% yield) and the desired product structure is confirmed by .sup.1H NMR. FIG. 13 shows that 1 wt % (4-methylbenzyl)trimethylammonium chloride fully suppresses dendrite formation under the test conditions, and partially suppresses hydrogen evolution. FIG. 30 shows that 15 wt % (4-methylbenzyl)trimethylammonium chloride fully suppresses dendrite formation and hydrogen evolution under the test conditions. FIG. 31 shows that 0.1 wt % (4-methylbenzyl)trimethylammonium chloride partially suppresses dendrite formation, and less effective in suppressing hydrogen evolution than higher tested concentrations of this additive.

[0061] (3,4-dimethylbenzyl)trimethylammonium chloride preparation and performance.

[0062] To a 100 mL flask is added 10.0 ml of a 13% solution of trimethylamine in tetrahydrofuran (1.16 g, 19.6 mmol). The solution is stirred under air at room temperature. 3,4-Dimethylbenzyl chloride (2.75 g, 17.8 mmol) is added in quick portions and the reaction is heated to 60° C. for 4 hrs. The reaction is then cooled to room temperature and white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 2.75 g of white fluffy powder are collected (73% yield) and the desired product structure is confirmed by .sup.1H NMR as shown in FIG. 27. Also shown in FIG. 27 is an inlay photo showing that 1.0 wt % (3,4-dimethylbenzyl)trimethylammonium chloride fully suppresses dendrite formation and fully suppresses hydrogen evolution under the test conditions.

[0063] An analogous method is used to synthesize other isomers of this product, namely, (2-methylbenzyl)trimethylammonium chloride and (3-methylbenzyl)trimethylammonium chloride, as well as (2,4-dimethylbenzyl)trimethylammonium chloride, (2,5-dimethylbenzyl)trimethylammonium chloride, (2,6-dimethylbenzyl)trimethylammonium chloride, (3,5-dimethylbenzyl)trimethylammonium chloride, and (2,4,6-trimethylbenzyl)trimethylammonium chloride. FIG. 14 shows that 1 wt % (2-methylbenzyl)trimethylammonium chloride fully suppresses dendrite formation, and partially suppresses hydrogen evolution. FIG. 20 shows that 1 wt % (3-methylbenzyl)trimethylammonium chloride partially suppresses dendrite formation, and partially suppresses hydrogen evolution, under the test conditions.

[0064] (4-Chlorobenzyl)trimethylammonium chloride preparation and performance.

[0065] To a 100 mL flask is added 10 mL of a 13% solution of trimethylamine in tetrahydrofuran (1.16 g, 19.7 mmol). The solution is stirred under air at room temperature. 4-Chlorobenzyl chloride (2.86 g, 17.8 mmol) is added in quick portions and the reaction is heated to 60° C. for 3 hours. The reaction is then cooled to room temperature and the white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 3.17 g of white fluffy powder are collected (82% yield) and the desired product structure is confirmed by .sup.1H NMR. FIG. 15 shows that 1 wt % (4-chlorobenzyl)trimethylammonium chloride partially suppresses dendrite formation, and hydrogen evolution, under the test conditions.

[0066] An analogous method is used to synthesize (2-chlorobenzyl)trimethylammonium chloride, (3-chlorobenzyl)trimethylammonium chloride, (2-bromobenzyl)trimethylammonium bromide, (3-bromobenzyl)trimethylammonium bromide, and (4-bromobenzyl)trimethylammonium bromide, with the later three using reagent bromobenzyl bromide in place of chlorobenzyl chloride. Similarly, iodobenzyl chlorides are used in an analogous method to produce (2-iodobenzyl)trimethylammonium chloride, (3-bromobenzyl)trimethylammonium chloride, and (4-iodobenzyl)trimethylammonium chloride. FIG. 16 shows that (2-chlorobenzyl)trimethylammonium chloride does not suppress dendrite formation under the test conditions, but does partially suppress hydrogen evolution. FIG. 17 shows that 1 wt % (4-bromobenzyl)trimethylammonium bromide fully suppresses dendrite formation under the test conditions, and partially suppress hydrogen evolution.

[0067] Benzyltrimethylphosphonium chloride preparation and performance.

[0068] To a 100 mL flask is added 10 mL of a 1M solution of trimethylphosphine in tetrahydrofuran (1.52 g, 20, ml, 20 mmol). The solution is stirred under nitrogen at room temperature. Benzylchloride (2.52 g, 2.3 ml, 20.0 mmol) is added in quick portions and the reaction is heated to 60° C. for 3 hours. The reaction is then cooled to room temperature and white precipitates are collected by brief suction filtration. About 1.80 g of white fluffy powder is collected (44% yield) and the desired product structure is confirmed by .sup.1H NMR. FIG. 18 shows that 1 wt % benzyltrimethylphosphonium chloride partially suppresses dendrite formation, but does not suppress hydrogen evolution, under the test conditions.

[0069] (2-Hydroxybenzyl)trimethylammonium iodide preparation and performance.

[0070] To a 100 mL flask is added 2-[(Dimethylamino)methyl]phenol (2.45 g, 16.2 mmol) and tetrahydrofuran (25 mL). The clear solution is cooled to 0° C. by an ice bath under air and with magnetic stirring. To this solution iodomethane (3.45 g, 24.3 mmol) is added dropwise. After stirring for 20 minutes the ice bath is removed and the reaction proceeds at room temperature for 3 hours as a viscous oil forms at the bottom of the flask. The solvents are removed from the reaction by reduced pressure (Rotavap) to a mass of orange/brown amorphous solid measuring 4.6 g (94% yield). The desired product structure is confirmed by .sup.1H NMR. FIG. 19 shows that 1 wt % (2-hydroxybenzyl)trimethylammonium iodide partially suppresses dendrite formation, and partially suppresses hydrogen evolution, under the test conditions.

[0071] 4-(Trimethylammoniummethyl)benzoic acid bromide preparation.

[0072] To a 100 mL flask is added 8.0 mL of a 13% solution of trimethylamine in tetrahydrofuran (0.92 g, 15.6 mmol) is diluted in 30 mL acetonitrile. The solution is stirred under air at room temperature. Then, 4-(bromomethyl)benzoic Acid (3.36 g, 15.6 mmol) is added in quick portions and the reaction is heated to 80° C. for 3 hrs. The reaction is then cooled to room temperature and white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 4.10 g of white solids are collected (95.6% yield) and the desired product structure is confirmed by .sup.1H NMR. FIG. 21 shows that 1 wt % 4-(Trimethylammoniummethyl)benzoic acid bromide partially suppresses dendrite formation, and partially suppresses hydrogen evolution, under the test conditions.

[0073] (2,6-Dimethylbenzyl)trimethylammonium chloride preparation.

[0074] To a 100 mL flask is added 9.1 mL of a 13% solution of trimethylamine in tetrahydrofuran (1.05 g, 17.8 mmol). The solution is stirred under air at room temperature. 2,6-Dimethylbenzyl chloride (2.5 g, 16.2 mmol) is added in quick portions and the reaction is heated to 60° C. for 3 hrs. The reaction is then cooled to room temperature and the white precipitates are collected by suction filtration and washed with additional tetrahydrofuran. About 3.05 g of white fluffy powder are collected (88% yield) and the desired product structure is confirmed by .sup.1H NMR. FIG. 24 shows that 1.0 wt % (2,6-Dimethylbenzyl)trimethylammonium chloride partially suppresses dendrite formation, but does not suppress hydrogen evolution, under the test conditions.

[0075] FIG. 23 shows that 1.0 wt % Benzalkonium Chloride is effective in fully suppressing dendrite formation and hydrogen evolution under the test condition. The tested additive is a mixture having the following formula, where R.sup.5=C.sub.nH.sub.2n+1 where 8≤n≤18:

##STR00026##

[0076] FIG. 32 shows a schematic view of a zinc-battery cell 100. The cell includes a zinc anode 102 in communication with a cathode 108 through an electrolyte 104. A porous separator 110 such as a membrane may be interposed between the cathode 108 and the electrolyte 104. The person having ordinary skill in the art will readily appreciate that the cathode may comprise a wide variety of known materials such as without limitation, air and carbon.

[0077] It will be apparent to those skilled in the art that the above methods and apparatuses may be changed or modified without departing from the general scope of the invention. The invention is intended to include all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof.

[0078] Having thus described the invention, it is now claimed: