Li Zhenbang, Liu Pu, Yang Guowei
State Key Laboratory of Optoelectronic Materials and Technologies Nanotechnology Research Center School of Materials Science & Engineering Sun Yat-sen University Guangzhou 510275 Guangdong P. R. China.
Glob Chall. 2019 Dec 9;4(2):1900066. doi: 10.1002/gch2.201900066. eCollection 2020 Feb.
Hydrogen energy is considered to be a critical environmentally friendly and widely sourced renewable energy source that can be used as an alternative to fossil fuels. At present, the preparation of hydrogen (H) mainly depends on traditional fossil fuels. In order to achieve sustainable development of environmental protection, great attention has been paid to the preparation of H by electrocatalysis, photocatalysis, and photoelectrochemistry. Here, it is reported for the first time that a novel active catalyst for the hydrogen evolution reaction, consisting of all-2D amorphous nanosheets/2D crystal layer heterojunction structure and without any noble metal (no precious metals are present in the preparation or measuring), is almost entirely fabricated by laser ablation in liquid (LAL) growth of amorphous cobalt sulfide on the surface of multilayered molybdenum disulfide. In acidic media, the amorphous cobalt sulfide nanosheets/multilayered molybdenum disulfide (a-CoS/MoS) catalyst exhibits fast hydrogen evolution kinetics with onset potential of -147 mV and a Tafel slope of 126 mV per decade, which is much better than only the amorphous cobalt sulfide and molybdenum disulfide layer. The high hydrogen evolution activity of the amorphous cobalt sulfide nanosheets/multilayered molybdenum disulfide hybrid is likely due to the unique electrocatalytic synergistic effects between hydrogen evolution-active amorphous cobalt sulfide nanosheets and layered crystal molybdenum disulfide materials, as well as the much-increased catalytic sites. This work provides a new general route based on all-2D amorphous nanosheets/2D crystal structure for designing and preparing novel layered materials with effectively manipulated catalytic properties and active functionality surface.
氢能被认为是一种至关重要的环境友好型且来源广泛的可再生能源,可作为化石燃料的替代品。目前,氢气(H)的制备主要依赖传统化石燃料。为实现环境保护的可持续发展,通过电催化、光催化和光电化学制备氢气受到了广泛关注。在此,首次报道了一种用于析氢反应的新型活性催化剂,它由全二维非晶纳米片/二维晶体层异质结结构组成,且不含任何贵金属(在制备或测量过程中不存在贵金属),几乎完全通过在多层二硫化钼表面进行液相激光烧蚀(LAL)生长非晶硫化钴来制备。在酸性介质中,非晶硫化钴纳米片/多层二硫化钼(a-CoS/MoS)催化剂表现出快速的析氢动力学,起始电位为-147 mV,塔菲尔斜率为每十倍126 mV,这比仅使用非晶硫化钴和二硫化钼层要好得多。非晶硫化钴纳米片/多层二硫化钼复合材料的高析氢活性可能归因于析氢活性非晶硫化钴纳米片与层状晶体二硫化钼材料之间独特的电催化协同效应,以及催化位点的大幅增加。这项工作基于全二维非晶纳米片/二维晶体结构提供了一条新的通用路线,用于设计和制备具有有效调控催化性能和活性功能表面的新型层状材料。