Zhi Lihua, Tu Jibing, Li Jiaxuan, Li Min, Liu Jiacheng
Key Laboratory of Bioelectrochemistry & Environmental Analysis of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, PR China.
Key Laboratory of Bioelectrochemistry & Environmental Analysis of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, PR China.
J Colloid Interface Sci. 2022 Jun 15;616:379-388. doi: 10.1016/j.jcis.2022.02.066. Epub 2022 Feb 18.
With the increasing energy and environmental crisis, exploring convenient and general strategies for constructing of highly active, stable, and cost-effective bifunctional electrocatalysts for overall water splitting are exceedingly desirable yet still challenging. Herein, 3D hierarchical mesoporous cobalt phosphide embedded N-doped carbon nanoflowers (CoP@NCNFs) are successfully constructed with ultrathin nanosheets by phosphatingof the cobalt coordination polymer nanoflowers (CoCPNFs). By virtue of their unique architecture and particular composition, the obtained CoP@NCNFs reveal extraordinary performance with ultralow overpotentials and small Tafel slopes for both OER (291 mV at 10 mA cm; 75 mV dec) and HER (166 mV at 10 mA cm; 76 mV dec) in alkaline medium. In particular, CoP@NCNFs can act as both anode and cathode to perform overall water splitting, and the assembled device only needs a cell voltage as low as 1.59 V to achieve the current density of 10 mA cm. Simultaneously, the CoP@NCNFs also exhibit admirable durability (at least 15 h) throughout the water splitting process. These remarkable electrocatalytic performances could be attributed to the synergistic effect of highlyactive CoP NPs and conductive mesoporous N-doped carbon nanosheets, which effectively improved the surface contact between catalyst and electrolyte, mass diffusion, and stability.
随着能源和环境危机的日益加剧,探索便捷通用的策略来构建用于全水解的高活性、稳定且经济高效的双功能电催化剂极具吸引力,但仍具有挑战性。在此,通过对钴配位聚合物纳米花(CoCPNFs)进行磷化处理,成功制备出由超薄纳米片组成的三维分级介孔磷化钴嵌入氮掺杂碳纳米花(CoP@NCNFs)。凭借其独特的结构和特殊的组成,所制备的CoP@NCNFs在碱性介质中对析氧反应(OER,在10 mA cm时过电位为291 mV;Tafel斜率为75 mV dec)和析氢反应(HER,在10 mA cm时过电位为166 mV;Tafel斜率为76 mV dec)均展现出优异的性能,过电位极低且Tafel斜率较小。特别地,CoP@NCNFs可同时作为阳极和阴极进行全水解,所组装的器件仅需1.59 V的电池电压就能实现10 mA cm的电流密度。同时,CoP@NCNFs在整个水解过程中还表现出令人称赞的耐久性(至少15小时)。这些卓越的电催化性能可归因于高活性CoP纳米颗粒与导电介孔氮掺杂碳纳米片的协同效应,这有效地改善了催化剂与电解质之间的表面接触、质量扩散以及稳定性。