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表面剪裁调控的CoP双功能氧电催化用于可充电锌空气电池和水分解

Surface Tailoring-Modulated Bifunctional Oxygen Electrocatalysis with CoP for Rechargeable Zn-Air Battery and Water Splitting.

作者信息

Kumar Mopidevi Manikanta, Aparna C, Nayak Amit Kumar, Waghmare Umesh V, Pradhan Debabrata, Raj C Retna

机构信息

Functional Materials and Electrochemistry Lab Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal 721302, India.

Theoretical Sciences Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru, Karnataka 560064, India.

出版信息

ACS Appl Mater Interfaces. 2024 Jan 24;16(3):3542-3551. doi: 10.1021/acsami.3c17349. Epub 2024 Jan 12.

Abstract

The transition metal phosphide (TMP)-based functional electrocatalysts are very promising for the development of electrochemical energy conversion and storage devices including rechargeable metal-air batteries and water electrolyzer. Tuning the electrocatalytic activity of TMPs is one of the vital steps to achieve the desired performance of these energy devices. Herein, we demonstrate the modulation of the bifunctional oxygen electrocatalytic activity of nitrogen-doped carbon-encapsulated CoP (CoP@NC) nanostructures by surface tailoring with ultralow amount (0.56 atomic %) of Ru nanoparticles (2.5 nm). The CoP at the core and the Ru nanoparticles on the shell have a facile charge transfer interaction with the encapsulating NC. The strong coupling of Ru with CoP@NC boosts the electrocatalytic performance toward oxygen reduction (ORR), oxygen evolution (OER), and hydrogen evolution (HER) reactions. The surface-tailored catalyst requires only 35 mV to deliver the benchmark current density of 10 mA·cm for HER. A small potential gap of 620 mV between ORR and OER is achieved, making the catalyst highly suitable for the development of rechargeable zinc-air batteries (ZABs). The homemade ZAB delivers a specific capacity of 780 mA·hg and peak power density of 175 mW·cm with a very small voltaic efficiency loss (1.1%) after 300 cycles. The two-electrode water splitting cell (CoP@NC-Ru||CoP@NC-Ru) delivers remarkably low cell voltage of 1.47 V at the benchmark current density. Stable current density of 25 mA·cm for 25 h without any significant change is achieved. Theoretical studies support the charge transfer interaction-induced enhanced electrocatalytic activity of the surface-tailored nanostructure.

摘要

基于过渡金属磷化物(TMP)的功能电催化剂对于包括可充电金属空气电池和水电解槽在内的电化学能量转换和存储装置的发展非常有前景。调节TMP的电催化活性是实现这些能量装置所需性能的关键步骤之一。在此,我们展示了通过用超低含量(0.56原子%)的钌纳米颗粒(2.5纳米)进行表面修饰来调节氮掺杂碳包覆CoP(CoP@NC)纳米结构的双功能氧电催化活性。核心处的CoP和壳层上的钌纳米颗粒与包覆的NC具有便捷的电荷转移相互作用。Ru与CoP@NC的强耦合提高了对氧还原(ORR)、析氧(OER)和析氢(HER)反应的电催化性能。表面修饰的催化剂在HER时仅需35 mV就能达到10 mA·cm的基准电流密度。ORR和OER之间实现了620 mV的小电位差,使得该催化剂非常适合用于可充电锌空气电池(ZAB)的开发。自制ZAB在300次循环后具有780 mA·hg的比容量和175 mW·cm的峰值功率密度,且电压效率损失非常小(1.1%)。两电极水分解电池(CoP@NC-Ru||CoP@NC-Ru)在基准电流密度下的电池电压低至1.47 V。实现了25 mA·cm的稳定电流密度持续25小时且无任何显著变化。理论研究支持了电荷转移相互作用诱导的表面修饰纳米结构增强的电催化活性。

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