Chinnadurai Deviprasath, Rajendiran Rajmohan, Kandasamy Prabakar
Department of Electrical Engineering, Pusan National University, 2 Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea.
Department of Electrical Engineering, Pusan National University, 2 Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea.
J Colloid Interface Sci. 2022 Jan 15;606(Pt 1):101-112. doi: 10.1016/j.jcis.2021.07.145. Epub 2021 Aug 4.
Transition metal sulfides have been intensively investigated as an effective catalyst for overall water splitting application due to their inexorable bifunctional oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) activity. However, the chalcogenides are oxidised during the OER process and hence limit the stability of the electrocatalyst. The synthesized materials should have a higher oxidation state corresponding to the active species in order to improve the stability. In this study, we have employed a one-step chemical bath deposition (CBD) route to synthesis bimetallic copper nickel sulfide (CuNiS) electrocatalyst. We have accomplished a superior OER electrocatalytic activity with a lower overpotential of 337 mV at 10 mA/cm current density and a small Tafel slope of 43 mV/dec. Also, we have achieved an excellent HER activity with a very low overpotential of 99 mV at 10 mA/cm and a Tafel slope of 63 mV/dec. The constructed electrolyzer attained a lower cell voltage of only 1.55 V to reach the current density of 10 mA/cm The stability test carried at a high current density of 200 mA/cm for 50 h showed less than 5% increase in Ni active species at the surface ensure the stable performance nature. Thus, this work provides a promising methodology for the synthesis of bimetallic sulfides for enhanced electrocatalytic water splitting with exceptional reliability.
过渡金属硫化物因其不可避免的双功能析氧反应(OER)和析氢反应(HER)活性,作为用于全水分解应用的有效催化剂受到了广泛研究。然而,硫族化物在OER过程中会被氧化,从而限制了电催化剂的稳定性。为了提高稳定性,合成材料应具有与活性物种相对应的更高氧化态。在本研究中,我们采用一步化学浴沉积(CBD)路线合成了双金属硫化铜镍(CuNiS)电催化剂。我们实现了优异的OER电催化活性,在10 mA/cm²电流密度下过电位较低,为337 mV,塔菲尔斜率较小,为43 mV/dec。此外,我们还实现了出色的HER活性,在10 mA/cm²时过电位极低,为99 mV,塔菲尔斜率为63 mV/dec。构建的电解槽在达到10 mA/cm²电流密度时,电池电压仅为1.55 V。在200 mA/cm²的高电流密度下进行50小时的稳定性测试表明,表面镍活性物种的增加不到5%,确保了稳定的性能。因此,这项工作为合成双金属硫化物提供了一种有前景的方法,用于增强电催化水分解并具有出色的可靠性。