二进制数
尿素
路径(计算)
理论(学习稳定性)
分解水
材料科学
金属
等离子体
曲面(拓扑)
能量(信号处理)
计算机科学
化学工程
化学
催化作用
工程类
冶金
数学
机器学习
物理
有机化学
统计
程序设计语言
算术
光催化
量子力学
几何学
作者
Swapnil R. Patil,Rakesh Kulkarni,Sourabh B. Ghode,Jungmin Kim,Qazi Muhammad Saqib,Muhammad Noman,Chandrashekhar S. Patil,Youngbin Ko,Sangrak Bae,Yoon‐Young Chang,Janardhan Reddy Koduru,Kolleboyina Jayaramulu,Nilesh R. Chodankar,Jinho Bae
标识
DOI:10.1021/acsaem.4c02919
摘要
This study introduces an advanced Cu2MnS2 ctenophore-like nanostructured electrocatalyst, synthesized through a hydrothermal process and enhanced via argon (Ar) plasma activation (Cu2MnS2-Ar) to improve its performance in overall water splitting (OWS) and urea oxidation reactions (UORs). Plasma activation generates reactive species that modify the material’s surface, increasing its conductivity, electroactive sites, and surface energy, all contributing to enhanced catalytic activity. The Cu2MnS2-Ar catalyst exhibits impressive performance in hydrogen evolution (HER) and oxygen evolution (OER) reactions, with overpotentials of 0.012 and 0.026 V at 10 and 300 mA/cm2, respectively, much lower than the untreated Cu2MnS2 catalyst, which shows 0.308 and 0.309 V. More importantly, the developed cell with the Cu2MnS2-Ar electrocatalyst demonstrates an exceptional overpotential of 1.47 and 1.37 V at 50 mA/cm2 for the OWS and UOR and, notably, which is much smaller than the noble metal-based catalyst. Conversely, our developed cell exhibits outstanding performance by achieving cell voltages of 1.59 V even under demanding industrial conditions (60 °C). The stability of the Cu2MnS2-Ar catalyst was further evaluated using time series analysis (TSA) and long short-term memory (LSTM) modeling, which accurately predicts the electrocatalytic behavior, confirming the effectiveness of the modeling technique in understanding the catalyst’s performance.
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