Department of Materials Science and Engineering & Materials Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
Department of Chemical & Biomedical Engineering, FAMU-FSU College of Engineering, Florida State University (FSU) , Tallahassee, Florida 32310, United States.
ACS Nano. 2017 May 23;11(5):5103-5112. doi: 10.1021/acsnano.7b02060. Epub 2017 May 12.
Large-area (∼cm) films of vertical heterostructures formed by alternating graphene and transition-metal dichalcogenide (TMD) alloys are obtained by wet chemical routes followed by a thermal treatment at low temperature. In particular, we synthesized stacked graphene and WMoS alloy phases that were used as hydrogen evolution catalysts. We observed a Tafel slope of 38.7 mV dec and 96 mV onset potential (at current density of 10 mA cm) when the heterostructure alloy was annealed at 300 °C. These results indicate that heterostructures formed by graphene and WMoS alloys are far more efficient than WS and MoS by at least a factor of 2, and they are superior compared to other reported TMD systems. This strategy offers a cheap and low temperature synthesis alternative able to replace Pt in the hydrogen evolution reaction (HER). Furthermore, the catalytic activity of the alloy is stable over time, i.e., the catalytic activity does not experience a significant change even after 1000 cycles. Using density functional theory calculations, we found that this enhanced hydrogen evolution in the WMoS alloys is mainly due to the lower energy barrier created by a favorable overlap of the d-orbitals from the transition metals and the s-orbitals of H; with the lowest energy barrier occurring for the WMoS alloy. Thus, it is now possible to further improve the performance of the "inert" TMD basal plane via metal alloying, in addition to the previously reported strategies such as creation of point defects, vacancies and edges. The synthesis of graphene/WMoS produced at relatively low temperatures is scalable and could be used as an effective low cost Pt-free catalyst.
大面积(~cm)的垂直异质结构薄膜是通过湿化学方法合成,然后在低温下进行热处理得到的。这些异质结构由交替的石墨烯和过渡金属二卤化物(TMD)合金组成。特别地,我们合成了堆叠的石墨烯和 WMoS 合金相,它们被用作析氢催化剂。我们观察到,当异质结构合金在 300°C 下退火时,其 Tafel 斜率为 38.7 mV dec 和 96 mV 的起始电位(在 10 mA cm 的电流密度下)。这些结果表明,由石墨烯和 WMoS 合金形成的异质结构比 WS 和 MoS 至少高效 2 倍,并且优于其他报道的 TMD 体系。这种策略提供了一种廉价且低温的合成方法,能够替代析氢反应(HER)中的 Pt。此外,合金的催化活性在长时间内是稳定的,即即使经过 1000 次循环,催化活性也不会发生显著变化。通过密度泛函理论计算,我们发现 WMoS 合金中这种增强的析氢作用主要归因于过渡金属的 d 轨道和 H 的 s 轨道之间有利的重叠所产生的较低的能量势垒;在 WMoS 合金中,能量势垒最低。因此,除了先前报道的如形成点缺陷、空位和边缘等策略外,通过金属合金化进一步提高“惰性”TMD 基面的性能现在是可能的。在相对较低的温度下合成的石墨烯/WMoS 具有可扩展性,可作为一种有效的低成本无 Pt 催化剂。