首页|Pt掺杂对Ti/SnO2-Sb-Nd纳米球状电极性能的影响

Pt掺杂对Ti/SnO2-Sb-Nd纳米球状电极性能的影响

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采用一步水热法成功制备出不同Pt掺杂量下Ti/SnO2-Sb-Nd-Pt纳米球状电极,通过SEM、XRD和XPS表征电极表面的形貌、结构和化学组成,LSV、CV和加速寿命(ALT)测试电极的电化学性能和稳定性,并通过降解硝基苯(NB)能力验证电极催化活性。结果表明,Pt掺杂不会改变电极的SnO2晶型结构,适量Pt掺杂可以使电极表面涂层更加均匀致密,提高电极稳定性,但降低了涂层中吸附氧含量,使得电极催化活性降低。掺杂1。5%Pt后,电极ALT由28。0 min延长至78。2 h,虽然NB去除率由96。53%降至80。61%,但在电极实际使用寿命内,NB理论降解总量由62。6 mg/cm2增至8 754。1 mg/cm2。显示了该电极具有良好的应用潜力,为开发高效、稳定的电极材料提供了参考。
Effect of Pt doping on properties of Ti/SnO2-Sb-Nd nano-spherical electrodes
Using one-step hydrothermal synthesis to successfully prepare Ti/SnO2-Sb-Nd-Pt nanosphere electrodes with different Pt doping amounts.SEM,XRD and XPS were applied to characterize the surface morphology,structure and chemical composition of the electrodes,respectively.The electrochemical activi-ty and stability of the electrodes were characterized via LSV,CV and accelerated service life test(ALT).The performance for NB degradation was also studied.Results showed that an appropriate amount of Pt doping formed a uniform and compact coating on the electrode surface,which improved the stability of the electrode.Although the Pt doping did not change the crystal structure of SnO2,it also reduced the adsorbed oxygen content in the coating and reduced the catalytic activity of the electrode.After 1.5%Pt doping,the ALT of the electrodes was extended from 28.0 min to 78.2 h;although the NB removal rate decreased from 96.53%to 80.61%,the total amount of theoretical degradation of NB in the actual serv-ice life increased from 62.6 mg/cm2 to 8 754.1 mg/cm2.These findings reveal good application potential for the electrodes and provide a reference for developing efficient and stable electrode materials.

Ti/SnO2-Sb-Nd electrodePt dopingcharacterizationelectrocatalytic performancestability

李阳、丁家正、谢文玉、李长刚、梁家豪

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广东石油化工学院环境科学与工程学院广东省石油化工污染控制工程技术研究中心,广东茂名 525000

中国石油大学(北京)重质油国家重点实验室,北京 102249

Ti/SnO2-Sb-Nd电极 Pt掺杂 表征 电催化性能 稳定性

国家自然科学基金面上项目茂名市科技计划项目广东石油化工学院人才引进项目

222784342022S041RC-XJ2022000702

2024

应用化工
陕西省石油化工研究设计院 陕西省化工学会

应用化工

CSTPCD北大核心
影响因子:0.411
ISSN:1671-3206
年,卷(期):2024.53(9)