水电解析氢电催化剂的高通量研究

R. K. Putri, B. Hayden, A. Prasetya, Sihana
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摘要

本文对碱水电解用析氢电催化剂进行了研究。水电解制氢需要开发新型电催化剂,以降低阴极析氢过电位,使水电解更具竞争力和效率。优化水分解电催化剂的另一种方法可能是通过在氧化物载体上支持纳米颗粒来修饰金属电催化行为。开发碱性电解液析氢反应电催化剂材料,可获得更稳定的析氢反应。采用高通量物理气相沉积(HT PVD)方法在TiO2电催化剂上合成了铂。利用Pt在TiO2上的电化学测量,研究了该电催化剂在碱性电解液中析氢反应的特性和稳定性。在450℃下退火6小时后,XRD证实TiO2为无定形和锐钛矿相。非晶型和锐钛型TiO2的厚度均为200 nm。在碱性电解质(0.5 M NaOH)中,使用循环伏安法和电位步进对10 × 10 E-chem阵列进行电化学测量,发现Pt在无定形TiO2和Pt在锐钛矿TiO2上的电催化行为相似。无论是非晶相还是锐钛矿相,TiO2中铂的粒径越大,电流越大。析氢反应开始于低于-0.8 V vs RHE的电位。析氢反应的电位向低电位转移。铂的粒径越大,析氢电位越低。Pt在tio2上是碱性水电解析氢反应的稳定电催化剂。这是因为析氢反应发生在低电位下。锐钛矿型TiO2比非晶型TiO2更稳定,因此,在碱水电解中,Pt在锐钛矿型TiO2 - 2 -上的析出氢反应优于Pt在非晶型TiO2 - 2上的析出氢反应。
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HIGH THROUGHPUT STUDIES OF HYDROGEN EVOLUTION ELECTROCATALYST FOR WATER ELECTROLYSIS
This thesis presents a study of hydrogen evolution electrocatalyst for alkaline water electrolysis. Hydrogen production through the electrolysis of water requires the development of new electrocatalysts in order to reduce the hydrogen evolution over-potential of the cathode in order to make water electrolysis more competitive and efficient. An alternative approach in the optimisation of water splitting electrocatalyst may Be the modification of the metal electrocatalytic behaviour by supporting nano-particles on oxide support. Development of the electrocatalyst material for hydrogen evolution reaction in alkaline electrolyte may obtain more stable hydrogen evolution reaction.Pt on TiO2 electrocatalyst has been synthesized by applying high throughput Physical Vapor Deposition (HT PVD) method. Electrochemistry measurements of Pt on TiO2 have been used to study the characteristic and stability of the electrocatalyst for hydrogen evolution reaction in alkaline electrolyte for water electrolysis. XRD confirmed that the phase of TiO2 were amorphous and anatase after annealing for 6 hours at the temperature of 450oC. The thicknesses of TiO2 both for amorphous and anatase were 200 nm.Similar electrocatalytic behavior are presented both for Pt on amorpous TiO2 and Pt on anatase TiO2 from electrochemistry measurements using cyclic voltammetry and potential step on the 10 x 10 E-chem arrays in alkaline electrolyte (0.5 M NaOH). Higher currents are seen in the larger particle size of platinum in TiO2 both for amorphous and anatase phase. The hydrogen evolution reaction starts at the potential below -0.8 V vs RHE. The potential for hydrogen evolution reaction is shifted to the low potential. Larger particle size of platinum shows lower potential of hydrogen evolution reaction.Pt on TiO­2 tends to be a stable electrocatalyst for hydrogen evolution reaction in alkaline water electrolysis. It is because hydrogen evolution reaction occurs at low potential. Anatase phase of TiO­2 is more stable than amorphous TiO2, hence, Pt on anatase TiO­2­ could be better than Pt on amorphous TiO­2 for hydrogen evolution reaction in alkaline water electrolysis.
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