Li Chengjun, Wang Zengting, Tian Shuangshuang, Zhang Ying
School of Detroit Green Technology, Hubei University of Technology, Wuhan 430068, China.
Hubei Engineering Research Center for Safety Monitoring of New Energy and Power Grid Equipment, Hubei University of Technology, Wuhan 430068, P. R. China.
ACS Omega. 2023 Jul 25;8(31):28769-28777. doi: 10.1021/acsomega.3c03569. eCollection 2023 Aug 8.
The detection of sulfur hexafluoride (SF) decomposition components has become one of the best ways to diagnose early latent insulation faults in gas-insulated equipment, which can effectively prevent sudden accidents by identifying such faults. In this paper, we by first-principles theory investigated the adsorption and sensing behaviors of four typical SF decomposition components (HS, SO, SOF, and SOF) on the pristine Pd-doped MoTe monolayer. The adsorption energy, work function, recovery time, charge density difference, density of state, and band structure of the adsorption structures are obtained as well as analyzed. The results indicate that the Pd dopant prefers to be trapped at the T site, with a binding energy of -2.25 eV. The Pd-MoTe chemisorbs the remaining gases except SOxF, with the adsorption capacity ranking as SOF > SO > HS. The adsorption of gas molecules reduces the bandgap of Pd-MoTe, thereby increasing conductivity. On the other hand, the recovery time of the Pd-MoTe monolayer material at a temperature of 398 K demonstrates its excellent gas desorption performance toward four decomposition gases. The research results provide a theoretical basis for Pd-MoTe to detect SF decomposition components, thus, promoting the stable operation of the power system.
六氟化硫(SF₆)分解组分的检测已成为诊断气体绝缘设备早期潜伏绝缘故障的最佳方法之一,通过识别此类故障可有效预防突发事故。本文基于第一性原理理论,研究了四种典型的SF₆分解组分(H₂S、SO₂、SOF₂和SO₂F₂)在原始掺钯碲化钼单层上的吸附和传感行为。获得并分析了吸附结构的吸附能、功函数、恢复时间、电荷密度差、态密度和能带结构。结果表明,钯掺杂剂倾向于捕获在T位,结合能为-2.25 eV。钯-碲化钼对除SOₓF外的其余气体进行化学吸附,吸附能力排序为SOF₂>SO₂>H₂S。气体分子的吸附降低了钯-碲化钼的带隙,从而提高了导电性。另一方面,钯-碲化钼单层材料在398 K温度下的恢复时间表明其对四种分解气体具有优异的气体解吸性能。研究结果为钯-碲化钼检测SF₆分解组分提供了理论依据,从而促进电力系统的稳定运行。