Reversible epitaxial electrodeposition of metals in battery anodes

Zheng, Jingxu; Zhao, Qing; Tang, Tian; Yin, Jiefu; Quilty, Calvin D.; Renderos, Genesis D.; Liu, Xiaotun; Deng, Yue; Wang, Lei; Bock, David C.; Jaye, Cherno; Zhang, Duhan; Takeuchi, Esther S.; Takeuchi, Kenneth J.; Marschilok, Amy C.; Archer, Lynden A.

doi:10.1126/science.aax6873

Cited by 1,364 publications

(1,151 citation statements)

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“…To circumvent this obstacle, Zheng et al. proposed the concept of reversible epitaxial electrodeposition . Graphene was found to be a favorable substrate with similar lattice match to nucleate homogenous Zn deposit.…”

Section: Figurementioning

confidence: 99%

Constructing a Super‐Saturated Electrolyte Front Surface for Stable Rechargeable Aqueous Zinc Batteries

Yang,

Chang,

Qiao

et al. 2020

Angew Chem Int Ed

667

490

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Rechargeable aqueous zinc batteries (RAZB) have been re‐evaluated because of the superiority in addressing safety and cost concerns. Nonetheless, the limited lifespan arising from dendritic electrodeposition of metallic Zn hinders their further development. Herein, a metal–organic framework (MOF) was constructed as front surface layer to maintain a super‐saturated electrolyte layer on the Zn anode. Raman spectroscopy indicated that the highly coordinated ion complexes migrating through the MOF channels were different from the solvation structure in bulk electrolyte. Benefiting from the unique super‐saturated front surface, symmetric Zn cells survived up to 3000 hours at 0.5 mA cm−2, near 55‐times that of bare Zn anodes. Moreover, aqueous MnO2–Zn batteries delivered a reversible capacity of 180.3 mAh g−1 and maintained a high capacity retention of 88.9 % after 600 cycles with MnO2 mass loading up to 4.2 mg cm−2.

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Section: Figurementioning

confidence: 99%

Constructing a Super‐Saturated Electrolyte Front Surface for Stable Rechargeable Aqueous Zinc Batteries

Yang,

Chang,

Qiao

et al. 2020

Angew Chem Int Ed

667

490

View full text Add to dashboard Cite

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“…[ 2–7 ] Among them, aqueous zinc batteries have aroused extensive interest and attention, which benefits from many advantages of zinc anode, including high theoretical capacity (820 mAh g −1 ), appropriate redox potential (−0.762 V vs the standard hydrogen electrode (SHE)), and intrinsic safety in aqueous system. [ 8–20 ] Inspired by conventional Li + storage reaction, intercalation reaction of transition metal oxides are employed to storage Zn 2+ in the mild aqueous solution. For example, Zn 0.25 V 2 O 5 · n H 2 O, [ 9 ] Prussian blue analogue, [ 15 ] VO 2 , [ 17 ] MnO 2 , [ 18 ] Zn 3 V 2 O 7 (OH) 2 ·2H 2 O, [ 19 ] CuV 2 O 6 [ 20 ] have been used as cathodes for zinc batteries.…”

Section: Figurementioning

confidence: 99%

Binding Zinc Ions by Carboxyl Groups from Adjacent Molecules toward Long‐Life Aqueous Zinc–Organic Batteries

et al. 2020

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storage. [2][3][4][5][6][7] Among them, aqueous zinc batteries have aroused extensive interest and attention, which benefits from many advantages of zinc anode, including high theoretical capacity (820 mAh g −1 ), appropriate redox potential (−0.762 V vs the standard hydrogen electrode (SHE)), and intrinsic safety in aqueous system. [8][9][10][11][12][13][14][15][16][17][18][19][20] Inspired by conventional Li + storage reaction, intercalation reaction of transition metal oxides are employed to storage Zn 2+ in the mild aqueous solution. For example, Zn 0.25 V 2 O 5 ·nH 2 O, [9] Prussian blue analogue, [15] VO 2 , [17] MnO 2 , [18] Zn 3 V 2 O 7 (OH) 2 ·2H 2 O, [19] CuV 2 O 6 [20] have been used as cathodes for zinc batteries. However, the hydrated Zn 2+ and H + usually result in large volumetric change and serious structural collapse of these inorganic compounds with the insertion of a large amount of hydrated Zn 2+ , [21][22][23][24][25] showing significant capacity fading and limited cycle life. In recent years, the organic compounds containing carbonyl groups have been employed to store Li + and Na + through reversible coordination reaction (i.e., the CO/C-O-Li + /Na + conversion), and thus many batteries based on organic electrodes were proposed by using monovalent ion (Li + /Na + ) as charge carrier. [26][27][28][29][30][31] Then, it was demonstrated that such coordination reaction can also be used to store divalent ions (e.g., Mg 2+ and Zn 2+ ), which evoked the enthusiasm for developing divalent ion batteries using organic electrode. [32][33][34][35][36][37] Very recently, Chen's group reported the first Zn-organic (C 4 Q//Zn) battery with high energy and long life. [38] Chen and co-workers work indicates that it should be a good choice for building zinc batteries to use organics as the alternative to inorganic host materials to store Zn 2+ . However, many organics with carbonyl groups (CO) and/or their reduced products (C-O-) suffer from the inherent instability and solubility in electrolyte. [39][40][41][42][43] It is well known that the solubility can lead to the crossover of electrode active materials between cathode and anode. As a result, expensive ion exchange membranes generally are required to prevent the crossover. [38] Furthermore, owing to the inevitable presence of H + in mild aqueous electrolyte (e.g., aqueous ZnSO 4 electrolyte generally shows a pH value of 4-5), H + can also react with carbonyl groups of organic compounds before or in parallel with the storage of Zn 2+ , which might aggravate the poor cycle life arising from the inherent The newly emerged aqueous Zn-organic batteries are attracting extensive attention as a promising candidate for energy storage. However, most of them suffer from the unstable and/or soluble nature of organic molecules, showing limited cycle life (≤3000 cycles) that is far away from the requirement (10 000 cycles) for grid-scale energy storage. Here, a new aqueous zinc battery is proposed by using sulfur heterocyclic quinone dibenzo[b,i]thianthrene-5,7,12,1...

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“…Beneting from the above advantages, many of the recent innovations in water splitting have been achieved through electrodeposition, which has generated unprecedented interest. [24][25][26][27] Although some excellent review articles on electrodeposition have been published, they mainly focus on alloys, batteries, or photoelectrodes. 18,21,28 The latest progress on metal (hydro)oxide OER electrocatalysts prepared via electrodeposition has rarely been reviewed.…”

Section: Introductionmentioning

confidence: 99%