过电位
析氧
分解水
催化作用
X射线光电子能谱
材料科学
纳米线
钴
电化学
拉曼光谱
过渡金属
化学工程
制氢
氮化物
纳米技术
电极
化学
光催化
冶金
物理化学
光学
物理
工程类
生物化学
图层(电子)
作者
Chengming Long,Sirui Liu,Di Wang,Zhaoqi Lu,Qiulan Zhang,Qiong Gao,Mingyi Zhang,Xinzhi Ma
标识
DOI:10.1021/acsanm.4c03220
摘要
Photoelectrochemical hydrogen production technology holds promise for directly and swiftly generating green hydrogen, which is pivotal for human welfare; however, it faces challenges posed by the energetically sluggish oxygen evolution reaction (OER). Cobalt-based nitrides are considered excellent photoelectrochemically active in the OER (PEOER) catalysts, and their conductivity and photoconversion efficiency remain relatively low. This paper presents the fabrication of Ni-alloyed Co 4 N nanowire arrays on carbon cloth ((Co 1– x Ni x ) 4 N NWAs/CC) as PEOER catalysts. By analyzing advanced in situ Raman and X-ray photoelectron spectroscopy (XPS) results, we discovered that Ni not only enhances the conductivity of the catalyst but, more importantly, also creates more photoexcited Co 2+ OER centers and favors its reconstruction to CoOOH to charge PEOER. Furthermore, nitrogen plays a critical role in transforming pyridinic nitrogen into other forms of nitrogen to stabilize the catalyst’s structure. These advantages endow (Co 0.74 Ni 0.26 ) 4 N NWAs/CC with remarkable PEOER enhancement (988%), which drives the standard current density of 10 mA cm –2 with only a 283 mV overpotential along with good durability. This research provides insights into the PEOER mechanisms of cobalt-based transition metal nitrides, providing a way for designing next-generation PEOER catalysts.
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