石墨氮化碳
三元运算
催化作用
氮化物
化学工程
材料科学
氮化碳
碳纤维
氢
化学
无机化学
纳米技术
复合数
有机化学
复合材料
图层(电子)
光催化
计算机科学
工程类
程序设计语言
作者
Qihang He,Lei Wang,Feng Xiao,Rong Su,Yu Jiang,Lichuan Chen,Zeyi Wang,Bin Jia,Ping He,Chao Chen,Yali Zeng,Yun Zhou,Bin Tang
标识
DOI:10.1016/j.ijhydene.2024.01.111
摘要
The design of advanced noble-metal-free electrocatalysts with high activity and good stability for the hydrogen evolution process (HER) is both appealing and challenging. Herein, cauliflower-like Co–B–P nanoparticles anchored on multi-layered g-C3N4 nanosheets (Co–B–P/g-C3N4) are fabricated by a facile electroless deposition method at room temperature. The effect of P/B ratios on electrocatalytic performance of ternary Co–B–P/g-C3N4 catalysts for HER is fully investigated in 1.0 M KOH solution. Due to both the synergetic effect among P, B and Co, and the support of multi-layered g-C3N4 nanosheets, ternary Co–B–P/g-C3N4 catalyst exhibits satisfactory electrocatalytic HER performances. The onset overpotential for the best ternary Co–B–P/g-C3N4 catalyst is only 93 mV, whereas it is 173 mV for binary Co–B/g-C3N4 catalyst. When current density achieves 10 mA cm−2 and 40 mA cm−2, the required overpotentials for ternary Co–B–P/g-C3N4 catalyst are 174 mV and 226 mV, respectively, which are much lower than those of binary Co–B/g-C3N4 catalyst (261 mV and 327 mV). Furthermore, the stability test indicates that ternary Co–B–P/g-C3N4 catalyst possesses a favorable long-term electrochemical stability under alkaline condition. The satisfactory electrocatalytic performances of as-prepared ternary Co–B–P/g-C3N4 catalyst suggest that it is a promising candidate to substitute noble-metal based catalysts for HER.
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