Voorhoeve R J, Johnson D W, Remeika J P, Gallagher P K
Science. 1977 Mar 4;195(4281):827-33. doi: 10.1126/science.195.4281.827.
In a time of growing need for catalysts, perovskites have been rediscovered as a family of catalysts of such great diversity that a broad spectrum of scientific disciplines have been brought to bear in their study and application. Because of the wide range of ions and valences which this simple structure can accommodate, the perovskites lend themselves to chemical tailoring. It is relatively simple to synthesize perovskites because of the flexibility of the structure to diverse chemistry. Many of the techniques of ceramic powder preparation are applicable to perovskite catalysts. In their own right, they are therefore of interest as a model system for the correlation of solid-state parameters and catalytic mechanisms. Such correlations [See figure in the PDF file] have recently been found between the rate and selectivity of oxidation-reduction reactions and the thermodynamic and electronic parameters of the solid. For commercial processes such as those mentioned in the introduction, perovskite catalysts have not yet proven to be practical. Much of the initial interest in these catalysts related to their use in automobile exhaust control. Current interest in this field centers on noble metalsubstituted perovskites resistant to S poisoning for single-bed, dual-bed, and three-way catalyst configurations. The formulations commercially tested to date have shown considerable promise, but long-term stability has not yet been achieved. A very large fraction of the elements that make up presently used commercial catalysts can be incorporated in the structure of perovskite oxides. Conversely, it is anticipated that perovskite oxides, appropriately formulated, will show catalytic activity for a large variety of chemical conversions. Even though this expectation is by no means a prediction of commercial success in the face of competition by existing catalyst systems, it makes these oxides attractive models in the study of catalytic chemical conversion. By appropriate formulation many desirable properties can be tailored, including the valence state of transition metal ions, the binding energy and diffusion of O in the lattice, the distance between active sites, and the magnetic and conductive properties of the solid. Only a very small fraction of possible perovskite formulations have been explored as catalysts. It is expected that further investigation will greatly expand the scope of perovskite catalysis, extend the understanding of solid-state parameters in catalysis, and contribute to the development of practical catalytic processes.
在对催化剂需求不断增长的时代,钙钛矿作为一类具有高度多样性的催化剂被重新发现,众多科学学科都参与到其研究与应用之中。由于这种简单结构能够容纳种类繁多的离子和化合价,钙钛矿适合进行化学剪裁。钙钛矿的合成相对简单,因为其结构对多样化学性质具有灵活性。许多陶瓷粉末制备技术都适用于钙钛矿催化剂。因此,就固态参数与催化机理的关联而言,它们本身就是一个很有研究价值的模型体系。最近已发现氧化还原反应的速率和选择性与固体的热力学及电子参数之间存在这样的关联(见PDF文件中的图)。对于引言中提到的那些商业过程,钙钛矿催化剂尚未被证明具有实用性。最初对这些催化剂的诸多兴趣都与它们在汽车尾气控制中的应用有关。目前该领域的研究重点是用于单床、双床和三效催化剂配置的抗硫中毒的贵金属取代钙钛矿。迄今为止经过商业测试的配方已显示出相当大的前景,但尚未实现长期稳定性。构成目前使用的商业催化剂的很大一部分元素都可以纳入钙钛矿氧化物的结构中。相反,可以预期,经过适当配方设计的钙钛矿氧化物将对多种化学转化表现出催化活性。尽管面对现有催化剂体系的竞争,这种预期绝不是商业成功的预测,但它使这些氧化物成为催化化学转化研究中具有吸引力的模型。通过适当的配方设计,可以定制许多理想的性能,包括过渡金属离子的价态、氧在晶格中的结合能和扩散、活性位点之间的距离以及固体的磁性和导电性。作为催化剂被探索的钙钛矿配方只有极小一部分。预计进一步的研究将极大地扩展钙钛矿催化的范围,加深对催化过程中固态参数的理解,并有助于开发实际的催化工艺。