Zia Misbah, Ahmad Zahoor, Munawar Khurram S, Khattak Zafar A K, Raza Hamid, Idrees Hira, Younus Hussain A, Shaheen Muhammad Ashraf, Ahmad Nazir
Institute of Chemistry, University of Sargodha Sargodha-40100 Pakistan.
Department of Chemistry, Faculty of Science, University of Engineering and Technology Lahore Pakistan.
RSC Adv. 2025 Sep 10;15(39):32667-32678. doi: 10.1039/d5ra04999g. eCollection 2025 Sep 5.
The catalytic activation of small molecules is an excellent approach for scientific and technological developments. The production of green hydrogen and fine chemicals through water splitting and carbon dioxide fixation, respectively, is highly effective and eco-friendly; it can meet the requirements for energy economy and sustainability. Transition metal-derived nanomaterials are considered very efficient catalysts. Herein, we developed a metal oxides@carbon (NCC) nanocomposite derived from a bimetallic (Ni/Co) MOF as a multifunctional catalyst. The NCC catalyst was successfully investigated for CO fixation, oxygen evolution, and hydrogen evolution reactions. The NCC nanocomposite catalyst shows a noticeable CO cycloaddition to epoxide efficiency of 74-99.9% at 50-100 °C under 1.97 atm in 24 h. NCC exhibits low overpotentials ( ) for an alkaline (1 M KOH) medium OER and HER, , 310 and 200 mV with Tafel slopes of 76 and 117 mV dec, respectively. Similarly, for an acidic (0.1 M HSO) medium HER, = 118 mV and Tafel slope = 47 mV dec. High electron conductivity with very low charge transfer resistance is observed ( /Ω = 0.55 for the OER, 8.13 for the HER, and 0.824 for the HER). Bulk electrolysis revealed stable performance for 10-15 h at in each case without any major changes in the structural morphology of NNC. These results show the synergy of the active sites for achieving superior catalytic properties, presenting NCC as a suitable candidate for sustainable energy applications.
小分子的催化活化是推动科技发展的一种卓越方法。分别通过水分解和二氧化碳固定来生产绿色氢气和精细化学品,具有高效且环保的特点;能够满足能源经济和可持续发展的需求。过渡金属衍生的纳米材料被认为是非常高效的催化剂。在此,我们开发了一种源自双金属(Ni/Co)金属有机框架的金属氧化物@碳(NCC)纳米复合材料作为多功能催化剂。成功研究了NCC催化剂用于二氧化碳固定、析氧和析氢反应。NCC纳米复合催化剂在50 - 100°C、1.97个大气压下24小时内,二氧化碳与环氧化物环加成的效率达到74 - 99.9%,表现显著。在碱性(1 M KOH)介质的析氧反应和析氢反应中,NCC的过电位较低,分别为310和200 mV,塔菲尔斜率分别为76和117 mV dec⁻¹。同样,在酸性(0.1 M H₂SO₄)介质的析氢反应中,η = 118 mV,塔菲尔斜率 = 47 mV dec⁻¹。观察到其具有高电子导电性和非常低的电荷转移电阻(析氧反应时R/Ω = 0.55,析氢反应时R/Ω = 8.13,另一个析氢反应时R/Ω = 0.824)。整体电解表明,在每种情况下,NNC在10 - 15小时内性能稳定,其结构形态没有任何重大变化。这些结果表明活性位点之间的协同作用实现了优异的催化性能,使NCC成为可持续能源应用的合适候选材料。