Highly asymmetrically configured single atoms anchored on flame-roasting deposited carbon black as cathode catalysts for ultrahigh power density Zn-air batteries

IF 22.2 Q1 CHEMISTRY, MULTIDISCIPLINARY EnergyChem Pub Date : 2024-09-01 DOI:10.1016/j.enchem.2024.100134
Yu-Chieh Ting , Chih-Chieh Cheng , Fan-Yu Yen , Guan-Ru Li , Shao-I Chang , Chih-Heng Lee , Hsin-Yi Tiffany Chen , Shih-Yuan Lu
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Abstract

Iron group element-based single atom (SA) catalysts are highly regarded as promising alternatives to commercial Pt/C for catalysis of oxygen reduction reaction (ORR). For applications in rechargeable zinc-air batteries (ZABs), achieving the necessary high catalytic efficiency of the SAs toward oxygen evolution reaction (OER) however remains a significant challenge. Here, highly asymmetrically configured Fe SAs created with N,S co-coordination and anchored on flame-roasting deposited carbon black (CB), Fe-N3S1/CB, are developed, achieving outstanding bifunctional oxygen catalytic efficiency, with an ultra-small potential gap of 0.661 V at 10 mA cm-2 (ΔE10), outperforming the (Pt/C+RuO2) composite catalyst (0.697 V). With a newly proposed binder-free composite air cathode design, the Fe-N3S1/CB based ZAB achieves an ultrahigh power density of 365.7 mW cm-2 at a current density of 511.3 mA cm-2, largely outperforming the (Pt/C+RuO2) based ZAB (225.9 mW cm-2 at 344.7 mA cm-2). Furthermore, the Fe-N3S1/CB based ZAB demonstrates excellent long-term stability, with only 8.2 % decay in round-trip efficiency over 1000 (333.3 h) charge-discharge cycles at 10 mA cm-2. Density functional theory calculations elucidate that incorporation of sulfur into the coordination sphere of Fe facilitates the electrochemical dehydroxylation step for ORR and accelerates the electrochemical O2 desorption step for OER, thereby reducing the corresponding free energy differences on Fe SAs for largely enhanced catalytic efficiency.
1. A large size hetero-atom element, sulfur, is introduced to create highly asymmetrically configured Fe single atoms for enhancements in catalytic efficiency toward both oxygen reduction reaction and oxygen evolution reaction, and a binder-free composite air cathode design is proposed to improve electrochemical performances of zinc-air batteries.
2. An ultra-small potential gap of 0.661 V at 10 mA cm-2 (ΔE10) is achieved for the air cathode, and an ultrahigh discharge power density of 365.7 mW cm-2 at a current density of 511.3 mA cm-2 is acquired for the zinc-air battery.
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锚定在火焰焙烧沉积炭黑上的高度不对称配置单原子作为超高功率密度锌-空气电池的阴极催化剂
以铁族元素为基础的单原子(SA)催化剂在催化氧还原反应(ORR)方面被认为是商用铂/钯(Pt/C)的理想替代品。然而,要在可充电锌-空气电池(ZABs)中实现单原子催化剂对氧进化反应(OER)所需的高催化效率,仍然是一项重大挑战。本文开发了高度不对称配置的铁质 SAs(Fe-N3S1/CB),这种 SAs 具有 N、S 共配位,并锚定在火焰焙烧沉积的炭黑(CB)上,实现了出色的双功能氧催化效率,在 10 mA cm-2 时具有 0.661 V 的超小电位差(ΔE10),优于(Pt/C+RuO2)复合催化剂(0.697 V)。通过新提出的无粘结剂复合空气阴极设计,基于 Fe-N3S1/CB 的 ZAB 在 511.3 mA cm-2 的电流密度下实现了 365.7 mW cm-2 的超高功率密度,大大超过了基于(Pt/C+RuO2)的 ZAB(在 344.7 mA cm-2 下为 225.9 mW cm-2)。此外,基于 Fe-N3S1/CB 的 ZAB 还具有出色的长期稳定性,在 10 mA cm-2 的条件下,经过 1000 次(333.3 h)充放电循环后,往返效率仅下降 8.2%。密度泛函理论计算阐明,在铁的配位层中加入硫元素可促进 ORR 的电化学脱羟步骤,并加速 OER 的电化学 O2 解吸步骤,从而减少铁 SA 上的相应自由能差,在很大程度上提高催化效率。引入大尺寸异质原子元素硫,创造出高度不对称配置的铁单质原子,从而提高氧还原反应和氧进化反应的催化效率,并提出一种无粘结剂的复合空气阴极设计,以改善锌-空气电池的电化学性能。空气阴极在 10 mA cm-2 条件下实现了 0.661 V 的超小电位差(ΔE10),锌空气电池在 511.3 mA cm-2 电流密度条件下获得了 365.7 mW cm-2 的超高放电功率密度。
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来源期刊
EnergyChem
EnergyChem Multiple-
CiteScore
40.80
自引率
2.80%
发文量
23
审稿时长
40 days
期刊介绍: EnergyChem, a reputable journal, focuses on publishing high-quality research and review articles within the realm of chemistry, chemical engineering, and materials science with a specific emphasis on energy applications. The priority areas covered by the journal include:Solar energy,Energy harvesting devices,Fuel cells,Hydrogen energy,Bioenergy and biofuels,Batteries,Supercapacitors,Electrocatalysis and photocatalysis,Energy storage and energy conversion,Carbon capture and storage
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