过电位
钴
材料科学
石墨烯
电催化剂
磷化物
无机化学
碳化
纳米颗粒
吸附
化学工程
电极
催化作用
碳纤维
金属
纳米技术
电化学
物理化学
冶金
化学
复合数
有机化学
复合材料
工程类
扫描电子显微镜
作者
Guixiang Li,Jiayuan Yu,Jin Jia,Linjing Yang,Lili Zhao,Weijia Zhou,Hong Liu
标识
DOI:10.1002/adfm.201801332
摘要
Abstract Development of electrocatalysts for hydrogen evolution reaction (HER) with low overpotential and robust stability remains as one of the most serious challenges for energy conversion. Herein, a serviceable and highly active HER electrocatalyst with multilevel porous structure (Co‐Co 2 P nanoparticles@N, P doped carbon/reduced graphene oxides (Co‐Co 2 P@NPC/rGO)) is synthesized by Saccharomycete cells as template to adsorb metal ions and graphene nanosheets as separating agent to prevent aggregation, which is composed of Co‐Co 2 P nanoparticles with size of ≈104.7 nm embedded into carbonized Saccharomycete cells. The Saccharomycete cells provide not only carbon source to produce carbon shells, but also phosphorus source to prepare metal phosphides. In order to realize the practicability and permanent stability, the binderless and 3D electrodes composed of obtained Co‐Co 2 P@NPC/rGO powder are constructed, which possess a low overpotential of 61.5 mV (achieve 10 mA cm −2 ) and the high current density with extraordinary catalytic stability (1000 mA cm −2 for 20 h) in 0.5 m H 2 SO 4 . The preparation process is appropriate for synthesizing various metal or metal phosphide@carbon electrocatalysts. This work may provide a biological template method for rational design and fabrication of various metals or metal compounds@carbon 3D electrodes with promising applications in energy conversion and storage.
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