过电位
塔菲尔方程
电催化剂
分解水
析氧
电解质
化学工程
电化学
材料科学
电极
氧化锡
氧化物
催化作用
无机化学
可逆氢电极
化学
工作电极
冶金
物理化学
光催化
工程类
生物化学
作者
Adil Mehboob,NULL AUTHOR_ID,Awais Ahmad,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,Adnan Raza Altaf,NULL AUTHOR_ID,Muftah H. El‐Naas
标识
DOI:10.1016/j.rineng.2024.102516
摘要
The ultimate goal of the hydrogen economy is to develop an efficient and cost-effective electrocatalyst that can accelerate hydrogen synthesis from water without or with little additional energy. This study describes a unique surface modified electrodeposited nano-sized tungsten oxide (WO3) as an intriguing bi-functional electrocatalyst for OER in alkaline and HER in acidic conditions. The nano-WO3 was synthesized hydrothermally and electrodeposited on a fluorinated tin oxide (FTO) electrode. The highly uniform distribution of the WO3@FTO catalyst results in negligible charge transfer resistance, a large electroactive surface area, and increased water-splitting potential. During oxygen evolution reaction (OER), electrodeposited WO3@FTO initiates water splitting at an overpotential (η) of just 240 mV and represents a turnover frequency (TOF) of 0.59 sec−1. These results are comparable to previously reported electrocatalysts. Under an alkaline electrolyte, a current density of 15 mA/cm2 remained constant for several hours, indicating the high stability and durability of the electrodeposited WO3@FTO electrode. The electrode also performed well in hydrogen evolution reactions (HER). A Tafel slope of 46 mV/dec and −28 mV/dec was found for OER and HER, respectively, indicating an enhanced kinetics rate of reaction taking place at the electrode surface. Furthermore, in acidic conditions, the electrode represents a lower HER overpotential of 104 mV. The work provides a significant understanding of electrodeposited WO3@FTO electrodes and their role in electrochemical water splitting.
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