| 查看: 569 | 回复: 4 | |||
| 【奖励】 本帖被评价3次,作者jjf_sxnu增加金币 3 个 | |||
| 当前主题已经存档。 | |||
[资源]
【共享资料】How to handle a SCF convergence fail (Link 502)
|
|||
|
I find so many friends encounter the problem about a difficult SCF convergence. I find a completely resolution in a book, now paste it here to share with everybody. 1. Try a dfferent initial guess. Many programs have several dfferent initial guess procedures, often based on semiempirical calculations. 2. For an open-shell system, try converging the closed-shell ion of the same molecule and then use that as an initial guess for the open-shell calculation. Adding electrons may give more reasonable virtual orbitals, but as a general rule, cations are easier to converge than anions. 3. Another initial guess method is to first run the calculation with a small basis set and then use that wave function as the initial guess for a larger basis set calculation. 4. Try level shifting. This will usually work with the default parameters or not at all. 5. If the SCF is approaching but not reaching the convergence criteria, relax or ignore the convergence criteria. This is usually done for geometry optimizations that do not converge at the initial geometry. Geometry optimizations often converge better as they approach the equilibrium geometry. 6. Some programs use reduced-accuracy integrals to speed the SCF. Using full integral accuracy may be necessary for systems with di¨use functions, long-range interactions, or low-energy excited states. Turning o¨ incremental Fock matrix formation may also be necessary for these systems. 7. For DFT calculations, use a finer integration grid. 8. Try changing the geometry. First, slightly shorten a bond length. Then, slightly extend a bond length and next shift the conformation a bit. 9. Consider trying a different basis set. 10. Consider doing the calculation at a di¨erent level of theory. This is not always practical, but beyond this point the increased number of iterations may make the computation time as long as that occurring with a higher level of theory anyway. 11. Turn off the DIIS extrapolation. Give the calculation more iterations along with this. 12. Give the calculation (with DIIS) more SCF iterations. This seldom helps, but the next option often uses so many iterations that it is worth a try. 13. Use a forced convergence method. Give the calculation an extra thousand iterations or more along with this. The wave function obtained by these methods should be tested to make sure it is a minimum and not just a stationary point. This is called a stability test. 14. See if the software documentation suggests any other ways to change the DIIS method. You may have to run hundreds of calculations to become experienced enough with the method to know what works when and by how much to adjust it. ENJOY !!! [ Last edited by jjf_sxnu on 2008-5-20 at 16:01 ] |
» 收录本帖的淘帖专辑推荐
VASP |
» 猜你喜欢
推荐几个靠谱的文献网站?
已经有1人回复
求助火焰封管的时候管子炸了
已经有1人回复
物理化学论文润色/翻译怎么收费?
已经有246人回复
夏威夷大学生物胶体与界面实验室诚招全奖博士生和博士后
已经有1人回复
求助立方晶体In(OH)3的CIF卡片
已经有2人回复
请问四氢呋喃溶解的聚合物用甲醇沉淀时,如何使沉淀过程加速?
已经有2人回复
[电子教材]天津大学物理化学(第七版)上、下册
已经有1人回复
半透性容器进行高湿或者低湿研究
已经有0人回复
阴离子交换膜电解二氧化碳还原
已经有0人回复
2楼2008-05-20 08:32:08
3楼2008-05-20 23:18:46
4楼2008-05-21 19:16:23













回复此楼
