Facile engineering of CoS/rGO heterostructures on carbon cloth for efficient all-pH hydrogen evolution reaction and alkaline water electrolysis

IF 10.7 2区 材料科学 Q1 CHEMISTRY, PHYSICAL
Yuxian Chen, Jiayi Rong, Qiaolin Fan, Meng Sun, Qiuyi Deng, Zhonghua Ni, Xiao Li, Tao Hu
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Abstract

Developing a cost-effective and commercially viable catalyst from non-noble metals that exhibits superior performance in both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) presents a significant challenge due to the distinct electrocatalytic mechanisms involved in each process. Herein, we engineered a three-dimensional, self-supporting heterostructure on carbon cloth (CC) using facile two-step electrodeposition, consisting of reduced graphene oxide (rGO) and cobalt sulfide (CoS), aimed at enhancing the efficiency of overall water electrolysis. The porous rGO network promoted the anchoring and vertical growth of CoS nanosheets, while the heterojunction between rGO and CoS enhanced the catalyst's stability remarkably. The CoS/rGO@CC catalyst exhibited extremely low overpotentials for both HER (η10=76.3 mV) and OER (η10=290.4 mV), maintaining these stable overpotentials for more than 24 hours, matching the performance of leading electrocatalysts based on noble metals. Moreover, by utilizing CoS/rGO@CC as both cathode and anode, we achieved overall water splitting with just 744 mV @10 mA cm-2. Theoretical calculations validated the synergistic effect of rGO and CoS nanosheets on enhancing HER and OER processes. Additionally, experimental data highlighted the CoS/rGO@CC catalyst's exceptional HER catalytic ability across varied pH levels, which provides a promising strategy to design low-cost and high-performance electrocatalysts for other energy-related applications.
碳布上 CoS/rGO 异质结构的简易工程设计,用于高效全 pH 氢进化反应和碱性水电解
由于氢进化反应(HER)和氧进化反应(OER)的电催化机理各不相同,因此从非贵金属中开发出一种在氢进化反应和氧进化反应中均表现出卓越性能的、具有成本效益和商业可行性的催化剂是一项重大挑战。在此,我们采用简便的两步电沉积法在碳布(CC)上设计了一种由还原氧化石墨烯(rGO)和硫化钴(CoS)组成的三维自支撑异质结构,旨在提高整体水电解效率。多孔的 rGO 网络促进了 CoS 纳米片的锚定和垂直生长,而 rGO 和 CoS 之间的异质结合则显著提高了催化剂的稳定性。CoS/rGO@CC 催化剂表现出极低的 HER(η10=76.3 mV)和 OER(η10=290.4 mV)过电位,这些稳定的过电位可维持 24 小时以上,与基于贵金属的领先电催化剂性能相当。此外,通过将 CoS/rGO@CC 同时用作阴极和阳极,我们实现了仅 744 mV @10 mA cm-2 的整体水分离。理论计算验证了 rGO 和 CoS 纳米片在增强 HER 和 OER 过程中的协同效应。此外,实验数据还突显了 CoS/rGO@CC 催化剂在不同 pH 值条件下卓越的 HER 催化能力,这为设计用于其他能源相关应用的低成本、高性能电催化剂提供了一种前景广阔的策略。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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