School of Chemical Engineering, The University of Adelaide , Adelaide, SA 5005, Australia.
Acc Chem Res. 2017 Apr 18;50(4):915-923. doi: 10.1021/acs.accounts.6b00635. Epub 2017 Feb 16.
Developing cost-effective and high-performance electrocatalysts for renewable energy conversion and storage is motivated by increasing concerns regarding global energy security and creating sustainable technologies dependent on inexpensive and abundant resources. Recent achievements in the design and synthesis of efficient non-precious-metal and even non-metal electrocatalysts make the replacement of noble metal counterparts for the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR) with earth-abundant elements, for example, C, N, Fe, Mn, and Co, a realistic possibility. It has been found that surface atomic engineering (e.g., heteroatom-doping) and interface atomic or molecular engineering (e.g., interfacial bonding) can induce novel physicochemical properties and strong synergistic effects for electrocatalysts, providing new and efficient strategies to greatly enhance the catalytic activities. In this Account, we discuss recent progress in the design and fabrication of efficient electrocatalysts based on carbon materials, graphitic carbon nitride, and transition metal oxides or hydroxides for efficient ORR, OER, and HER through surface and interfacial atomic and molecular engineering. Atomic and molecular engineering of carbon materials through heteroatom doping with one or more elements of noticeably different electronegativities can maximally tailor their electronic structures and induce a synergistic effect to increase electrochemical activity. Nonetheless, the electrocatalytic performance of chemically modified carbonaceous materials remains inferior to that of their metallic counterparts, which is mainly due to the relatively limited amount of electrocatalytic active sites induced by heteroatom doping. Accordingly, coupling carbon substrates with other active electrocatalysts to produce composite structures can impart novel physicochemical properties, thereby boosting the electroactivity even further. Although the majority of carbon-based materials remain uncompetitive with state-of-the-art metal-based catalysts for the aforementioned catalytic processes, non-metal carbon hybrids have already shown performance that typically only conventional noble metals or transition metal materials can achieve. The idea of hybridized carbon-based catalysts possessing unique active surfaces and macro- or nanostructures is addressed herein. For metal-carbon couples, the incorporation of carbon can effectively compensate for the intrinsic deficiency in conductivity of the metallic components. Chemical modification of carbon frameworks, such as nitrogen doping, not only can change the electron-donor character, but also can introduce anchoring sites for immobilizing active metallic centers to form metal-nitrogen-carbon (M-N-C) species, which are thought to facilitate the electrocatalytic process. With thoughtful material design, control over the porosity of composites, the molecular architecture of active metal moieties and macromorphologies of the whole catalysts can be achieved, leading to a better understanding structure-activity relationships. We hope that we can offer new insight into material design, particularly the role of chemical composition and structural properties in electrochemical performance and reaction mechanisms.
为了解决全球能源安全问题并创造依赖廉价丰富资源的可持续技术,开发用于可再生能源转换和存储的高性价比和高性能电催化剂的需求日益增长。最近在设计和合成高效的非贵金属甚至非金属电催化剂方面取得的成就使得用丰富的地球元素(例如 C、N、Fe、Mn 和 Co)替代贵金属来实现析氢反应(HER)、析氧反应(OER)和氧还原反应(ORR)成为可能。已经发现,表面原子工程(例如杂原子掺杂)和界面原子或分子工程(例如界面键合)可以为电催化剂诱导新颖的物理化学性质和强协同效应,为极大地提高催化活性提供了新的有效策略。在本综述中,我们讨论了通过表面和界面原子和分子工程,基于碳材料、石墨相氮化碳和过渡金属氧化物或氢氧化物设计和制造高效电催化剂的最新进展,用于高效的 ORR、OER 和 HER。通过具有显著不同电负性的一种或多种元素的杂原子掺杂对碳材料进行原子和分子工程处理,可以最大程度地调整其电子结构并诱导协同效应以提高电化学活性。尽管经过化学修饰的碳质材料的电催化性能仍然不如其金属对应物,但这主要是由于杂原子掺杂所诱导的电催化活性位点的数量相对有限。因此,将碳基底与其他活性电催化剂结合以产生复合结构可以赋予新颖的物理化学性质,从而进一步提高电活性。尽管大多数碳基材料在上述催化过程中仍不及最先进的金属基催化剂具有竞争力,但非金属碳杂化物已经表现出通常只有传统的贵金属或过渡金属材料才能达到的性能。本文介绍了具有独特活性表面和宏观或纳米结构的混合碳基催化剂的想法。对于金属-碳偶联物,碳的掺入可以有效地弥补金属成分固有的导电性不足。对碳框架进行化学修饰,例如氮掺杂,不仅可以改变供电子特性,还可以引入固定活性金属中心的锚固位点,形成金属-氮-碳(M-N-C)物种,这被认为有助于电催化过程。通过精心的材料设计,可以控制复合材料的孔隙率、活性金属部分的分子结构和整个催化剂的宏观形态,从而更好地理解结构-活性关系。我们希望能够为材料设计提供新的见解,特别是化学成分和结构特性在电化学性能和反应机制中的作用。