IP Library Granted Patent US 12683153
Granted Patent B2
US 12683153 · App. 17/933,657 · Granted Jul 14, 2026

Method of fabricating nanoporous Zn anodes and the applications in Zn batteries

Inventors: Qing Chen (Hong Kong, CN); Liangyu Li (Hong Kong, CN); Yung Chak Anson Tsang (Hong Kong, CN)
Assignee: The Hong Kong University of Science and Technology
H01M4/42H01M10/26H01M2300/0014
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Quick Facts
Patent No.
US 12683153
App. No.
17/933,657
Granted
Jul 14, 2026
Kind
B2
Abstract

A method of making a free-standing nanoporous Zn is provided. The method includes compacting a predetermined amount of Zn compound precursor into a form of an anode; controlling a thickness of the Zn compound precursor to obtain desirable porosity; and reducing the Zn compound precursor in an electrochemical cell having an electrolyte at a predetermined volage against a reference electrode to obtain a nanoporous Zn anode. The nanoporous Zn includes continuous metal ligaments and pores each having a uniform width of around a few hundred nanometers. The nanoporous Zn may serve as an anode in a rechargeable Zn battery having the nanoporous Zn anode coupled to a conductive substrate, a physical block, an electrolyte, a reference electrode, and a cathode electrode, to deliver a high areal capacity and a long cycle life.

Claims (13)

1 . A method of making a free-standing nanoporous Zn, comprising:

compacting a predetermined amount of Zn compound precursor into a form of an anode;

controlling a thickness of the Zn compound precursor to adjust porosity; and

electrochemically reducing the Zn compound precursor to metallic zinc by applying a controlled reduction voltage against a reference electrode, thereby converting the Zn compound precursor to a free-standing nanoporous metallic Zn anode.

2 . The method of claim 1 , wherein the Zn compound precursor is selected from zinc oxide, zinc carbonate, zinc chloride, zinc acetate, and combinations of any of them.

3 . The method of claim 2 , wherein the Zn compound precursor further comprises an additive selected from carbon black, carbon fiber, bismuth oxide, tin oxide, and calcium hydroxide.

4 . The method of claim 1 , wherein the compacting a predetermined amount of Zn compound precursor comprises compacting the predetermined amount of Zn compound precursor onto a conductive substrate.

5 . The method of claim 4 , wherein the conductive substrate is a Sn-plated Cu foam or a copper foam/foil.

6 . The method of claim 1 , wherein the controlling a thickness of the Zn compound precursor comprises configuring a physical block that is a rigid perforated plate to control the thickness of the Zn compound precursor to adjust porosity.

7 . The method of claim 6 , wherein the physical block is made of a material selected from polyproplene, high-density polyethylene, and acrylic resin.

8 . The method of claim 1 , wherein the electrolyte is an alkaline solution of potassium hydroxide.

9 . The method of claim 1 , wherein the controlled reduction voltage is in a range between −1.55 V and −1.6 V.

10 . The method of claim 1 , wherein the electrolyte is an alkaline solution of sodium hydroxide or lithium hydroxide.