材料科学
接受者
纳米技术
光电子学
结晶学
凝聚态物理
物理
化学
作者
Priyanka Ray,Ankit Sharma,Peeyush Pandey,Ameer Suhail,Nageswara Rao Peela,Mohammad Qureshi
标识
DOI:10.1021/acsami.5c12080
摘要
Designing a non-noble metal based heterojunction electrocatalyst with outstanding catalytic activity and long-term stability is essential for efficient oxygen evolution reaction (OER). Herein, we have strategically designed a NiTe/CeO2 heterojunction based on a donor-acceptor approach, wherein CeO2 functions as the electron donor and NiTe as the electron acceptor. Kelvin probe force microscopy (KPFM) measurements revealed that the work functions of NiTe and CeO2 facilitate the charge transfers upon interfacial coupling between NiTe and CeO2. This interfacial synergy induces the formation of a built-in electric field at the heterojunction, which effectively modulates the surface electronic structure of NiTe through strong interfacial interactions with CeO2, achieving an overpotential of 263 mV at 10 mA cm-2 and a Tafel slope of 81 mV dec-1 for the OER. The formation of the heterojunction led to an increased electrochemical active surface area (a Cdl value of 10.5 μF cm-2) and a reduced charge-transfer resistance (1 Ω), which results in improved turnover frequency (3 s-1) as compared to the bare counterpart. Through the distribution of relaxation time (DRT) analysis, the extracted time constants corresponding to different relaxation processes reveal an enhanced charge-transfer kinetics across the interfaces, enhancing OER kinetics.
科研通智能强力驱动
Strongly Powered by AbleSci AI