当前位置: X-MOL 学术J. Power Sources › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Facile formation of 2D Co2[email protected]3O4 microsheets through in-situ toptactic conversion and surface corrosion: Bifunctional electrocatalysts towards overall water splitting
Journal of Power Sources ( IF 8.1 ) Pub Date : 2017-11-15 , DOI: 10.1016/j.jpowsour.2017.11.028
Lihua Yao , Nan Zhang , Yin Wang , Yuanman Ni , Dongpeng Yan , Changwen Hu

Exploring efficient non-precious electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is crucial for many renewable energy conversion processes. In this work, we report that 2D Co2[email protected]3O4 microsheets can be prepared through an in-situ toptactic conversion from single-crystal β-Co(OH)2 microplatelets, associated with a surface phosphatization and corrosion process. The resultant Co2[email protected]3O4 2D hybrid materials can further serve as self-supported bifunctional catalytic electrodes to drive the overall water splitting for HER and OER simultaneously, with low overpotentials and high long-term stability. Furthermore, a water electrolyzer based on Co2[email protected]3O4 hybrid as both anode and cathode is fabricated, which achieves 10 mA cm−2 current at only 1.57 V during water splitting process. Therefore, this work provides a facile strategy to obtain 2D Co2P-based micro/nanostructures, which act as low-cost and highly active electrocatalysts towards overall water splitting application.



中文翻译:

通过原位拓扑转换和表面腐蚀可轻松形成2D Co 2 [受电子邮件保护] 3 O 4微片:双功能电催化剂可实现整体水分解

对于氢气释放反应(HER)和氧气释放反应(OER)而言,探索有效的非贵金属电催化剂对于许多可再生能源转化过程至关重要。在这项工作中,我们报告说可以通过单晶β - Co(OH)2片的原位拓扑转换与表面磷化和腐蚀过程相关联来制备2D Co 2 [受电子邮件保护] 3 O 4微片。生成的Co 2 [受电子邮件保护] 3 O 42D杂化材料还可以用作自支撑双功能催化电极,以同时驱动HER和OER的总水分解,且超电势低且长期稳定性高。此外,制造了基于Co 2 [电子邮件保护] 3 O 4杂化物作为阳极和阴极的水电解槽,该水电解槽在分水过程中仅1.57 V即可实现10 mA cm -2的电流。因此,这项工作为获得基于2 Co 2 P的微/纳米结构提供了一种简便的策略,该结构可作为低成本和高活性的电催化剂,适用于整个水分解应用。

更新日期:2017-11-15
down
wechat
bug