Yuan Hefeng, Wei Shiwei, Tang Bin, Ma Zizai, Li Jinping, Kundu Manab, Wang Xiaoguang
Laboratory of Advanced Materials and Energy Electrochemistry, Institute of New Carbon Materials, Taiyuan University of Technology, Taiyuan, 030600, P.R. China.
Shanxi Key Laboratory of Gas Energy Efficient and Clean Utilization, Taiyuan, Shanxi, 030024, P.R. China.
ChemSusChem. 2020 Jul 22;13(14):3662-3670. doi: 10.1002/cssc.202000784. Epub 2020 Jun 4.
The development of highly active and efficient nonprecious-metal electrocatalysts for the oxygen evolution reaction is important for the design of renewable energy production and storage devices. In this work, highly dense, ultrathin Co-Ni boride nanoflakes supported on a 3 D CoNi skeleton are fabricated in situ by a simple one-step, high-temperature, solid-state boronation process. As a result of the induced high electroactive surface area and low charge transfer resistance, CoNiB-700 exhibits high catalytic activity at an overpotential of 262 (η ) and 284 mV (η ) to deliver current densities of 10 and 20 mA cm , respectively, with a Tafel slope of 58 mV dec in an alkaline medium towards the oxygen evolution reaction. DFT calculations show that the Ni-regulated Co-B compound has a lower rate-determining energy barrier for the *OOH intermediate than the mono-Co-B compound, which facilitates the production of more active catalytic sites for an accelerated surface charge-transfer process for the oxygen evolution reaction.
开发用于析氧反应的高活性和高效非贵金属电催化剂对于可再生能源生产和存储设备的设计至关重要。在这项工作中,通过简单的一步高温固态硼化过程原位制备了负载在三维CoNi骨架上的高密度超薄钴镍硼纳米片。由于诱导产生的高电活性表面积和低电荷转移电阻,CoNiB-700在262 mV(η10)和284 mV(η20)的过电位下分别表现出高催化活性,以在碱性介质中朝向析氧反应提供10和20 mA cm-2的电流密度,塔菲尔斜率为58 mV dec-1。密度泛函理论计算表明,与单钴硼化合物相比,镍调控的钴硼化合物对*OOH中间体具有更低的速率决定能垒,这有利于产生更多活性催化位点,以加速析氧反应的表面电荷转移过程。