电催化剂
材料科学
纳米笼
电池(电)
开路电压
化学工程
催化作用
阴极
金属
电解质
电化学
无机化学
物理化学
电极
冶金
化学
电压
有机化学
功率(物理)
工程类
物理
量子力学
作者
Junxing Han,Xiaoyi Meng,Liang Lu,Juanjuan Bian,Zhipeng Li,Chunwen Sun
标识
DOI:10.1002/adfm.201808872
摘要
Abstract Highly efficient non‐noble metal electrocatalysts are vital for metal–air batteries and fuel cells. Herein, a noble‐metal–free single‐atom Fe‐N x ‐C electrocatalyst is synthesized by incorporating Fe‐Phen complexes into the nanocages in situ during the growth of ZIF‐8, followed by pyrolysis at 900 °C under inert atmosphere. Fe‐Phen species provide both Fe 2+ and the organic ligand (Phen) simultaneously, which play significant roles in preparing single‐atom catalysts. The obtained Fe‐N x ‐C exhibits a half‐wave potential of 0.91 V for the oxygen reduction reaction, higher than that of commercial Pt/C (0.82 V). As a cathode catalyst for primary zinc–air batteries (ZABs), the battery shows excellent electrochemical performances in terms of the high open‐circuit voltage (OCV) of 1.51 V and a high power density of 96.4 mW cm −2 . The rechargeable ZAB with Fe‐N x ‐C catalyst and the alkaline electrolyte shows a remarkable cycling performance for 300 h with an initial round‐trip efficiency of 59.6%. Furthermore, the rechargeable all‐solid‐state ZABs with the Fe‐N x ‐C catalyst show high OCV of 1.49 V, long cycle life for 120 h, and foldability. The single‐atom Fe‐N x ‐C electrocatalyst may function as a promising catalyst for various metal–air batteries and fuel cells.
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