Sort:
Issue
Research progress and challenges in chip atomic layer polishing
Journal of Tsinghua University (Science and Technology) 2025, 65(2): 215-232
Published: 15 February 2025
Abstract PDF (22 MB) Collect
Downloads:38
Significance

This review highlights the progress and challenges in chip atomic layer polishing. Chips are fundamental to the modern information society. According to Moore's Law, the chip feature size is shrinking and approaching the physical limit. At the same time, advanced packaging technologies such as hybrid bonding continuously evolve. These create pressing needs to develop atomic layer polishing, a technique that enables extremely precise material removal at the atomic layer level, to achieve surfaces with atomic-level precision for demanding processes such as photolithography and bonding. Currently, chemical mechanical polishing (CMP) is the only key technology in chip manufacturing capable of simultaneously achieving local and global planarization of the wafer surface, with the potential to realize atomic layer polishing. This review provides a systematic summary of the mechanisms and processes of CMP for chip substrate surfaces and interconnect heterogeneous surfaces.

Progress

Significant progress has been made in the controlled removal with a single atomic layer precision at the microscopic level and in the CMP with surface roughness close to the theoretical limit at the macroscopic level for the monocrystalline silicon substrate. These advances highlight the extreme precision processing capability of CMP for the wafer surface. Furthermore, ongoing developments in multi-field assisted CMP and energy particle beam polishing hold promise for enabling atomic layer polishing for new substrates like GaN, SiC and diamond. In the case of interconnect heterogeneous surfaces, two material removal modes in CMP are summarized from a tribological perspective based on the interactions between the abrasive and material surfaces: mechanical plowing and chemical bonding. Copper, cobalt, and nickel are mainly removed through the mechanical plowing mode, while tantalum, ruthenium, and titanium are mainly removed through chemical bonding. According to this foundation, control principles and methods for achieving equivalent removal of heterogeneous surfaces are proposed based on different material removal modes. In the mechanical plowing material removal mode, corrosion and its impact on the mechanical strength of the material surface can be adjusted through the modulation of the effects of oxidation, complexation, and corrosion inhibition, as well as their synergistic effects. This approach allows for controlling the material removal rate (MRR). In the chemical bonding material removal mode, the number of reactive sites and their influence on interfacial chemical bonds can be regulated through the adjustment of pH, oxidation, and ionic strength, along with their synergistic effects, thus controlling the MRR. According to these control principles, a systematic summary of the planarization processes for interconnect heterogeneous surfaces, such as copper/tantalum, copper/cobalt, and copper/ruthenium, is provided. Finally, based on existing research progress, it is proposed to leverage the synergistic effects of mechanical, chemical, and electrical/optical/plasma/energy beams to confine chemical reactions and mechanical-chemical reactions to the surface atomic layer, to achieve atomic layer polishing. Specifically, for the mechanical plowing material removal mode, the focus is on designing the molecular structures of chemical additives to precisely modulate the effects of oxidation, complexation, and corrosion inhibition. This approach confines the corrosion behavior to the outermost atomic layer while controlling the mechanical action of the abrasive to enable precise, controllable atomic layer removal. For the chemical bonding material removal mode, the investigation focuses on confining chemical bonding reactions to the outermost atomic layer, weakening back bonds, and simultaneously controlling the mechanical action of the abrasive to disrupt chemical bonds between the outermost and sub-surface atoms, thus achieving controlled atomic layer removal.

Conclusions and Prospects

This review highlights the growing demand for atomic-level manufacturing of high-end chips and the development of atomic layer polishing. It provides a systematic summary of the mechanisms, progress, and challenges in atomic layer polishing, with the aim of offering critical theoretical and technical support for the atomic-level manufacturing of advanced chips. The findings from this research have potential applications in key areas such as high-end optical components and superlubricity devices.

Open Access Research Article Issue
Running-in behavior of a H-DLC/Al2O3 pair at the nanoscale
Friction 2021, 9(6): 1464-1473
Published: 23 November 2020
Abstract PDF (1.8 MB) Collect
Downloads:27

Diamond-like carbon (DLC) film has been developed as an extremely effective lubricant to reduce energy dissipation; however, most films should undergo running-in to achieve a super-low friction state. In this study, the running-in behaviors of an H-DLC/Al2O3 pair were investigated through a controllable single-asperity contact study using an atomic force microscope. This study presents direct evidence that illustrates the role of transfer layer formation and oxide layer removal in the friction reduction during running-in. After 200 sliding cycles, a thin transfer layer was formed on the Al2O3 tip. Compared with a clean tip, this modified tip showed a significantly lower adhesion force and friction force on the original H-DLC film, which confirmed the contribution of the transfer layer formation in the friction reduction during running-in. It was also found that the friction coefficient of the H-DLC/Al2O3 pair decreased linearly as the oxygen concentration of the H-DLC substrate surface decreased. This phenomenon can be explained by a change in the contact surface from an oxygen termination with strong hydrogen bond interactions to a hydrogen termination with weak van der Waals interactions. These results provide new insights that quantitatively reveal the running-in mechanism at the nanoscale, which may help with the design optimization of DLC films for different environmental applications.

Open Access Review Article Issue
Role of interfacial water in adhesion, friction, and wear—A critical review
Friction 2021, 9(1): 1-28
Published: 12 September 2020
Abstract PDF (1.6 MB) Collect
Downloads:118

Surficial water adsorption and interfacial water condensation as natural phenomena that can alter the contact status of the solid interface and tribological performances are crucial in all length scales, i.e., from earthquakes to skating at the macroscale level and even to micro/nano-electromechanical systems (M/NEMS) at the microscale/nanoscale level. Interfacial water exhibits diverse structure and properties from bulk water because of its further interaction with solid surfaces. In this paper, the evolutions of the molecular configuration of the adsorbed water layer depending on solid surface chemistry (wettability) and structure, environmental conditions (i.e., relative humidity and temperature), and experimental parameters (i.e., sliding speed and normal load) and their impacts on tribological performances, such as adhesion, friction, and wear, are systematically reviewed. Based on these factors, interfacial water can increase or reduce adhesion and friction as well as facilitate or suppress the tribochemical wear depending on the water condensation kinetics at the interface as well as the thickness and structure of the involved interfacial water.

Open Access Short Communication Issue
Water-based superlubricity in vacuum
Friction 2019, 7(2): 192-198
Published: 04 April 2018
Abstract PDF (4.8 MB) Collect
Downloads:56

This study achieved water-based superlubricity with the lubrication of H3PO4 solution in vacuum (highest vacuum degree <10-4 torr) for the first time by performing a pre-running process in air before running in vacuum. The stable water-based superlubricity was sustainable in vacuum (0.02 torr) for 14 h until the test was stopped by the user for non-experimental factor. A further analysis suggested that the superlubricity may be attributed to the phosphoric acid-water network formed in air, which can efficiently lock water molecules in the liquid lubricating film even in vacuum owing to the strong hydrogen bond interaction. Such capability to lock water is strongly affected by the strength of hydrogen bond and environmental conditions. The realization of water-based superlubricity with H3PO4 solution in vacuum can lead to its application in space environment.

Open Access Research Article Issue
Running-in process of Si–SiOx/SiO2 pair at nanoscale—Sharp drops in friction and wear rate during initial cycles
Friction 2013, 1(1): 81-91
Published: 26 March 2013
Abstract PDF (799.3 KB) Collect
Downloads:22

Using an atomic force microscope, the running-in process of a single crystalline silicon wafer coated with native oxide layer (Si–SiOx) against a SiO2 microsphere was investigated under various normal loads and displacement amplitudes in ambient air. As the number of sliding cycles increased, both the friction force Ft of the Si–SiOx/SiO2 pair and the wear rate of the silicon surface showed sharp drops during the initial 50 cycles and then leveled off in the remaining cycles. The sharp drop in Ft appeared to be induced mainly by the reduction of adhesion-related interfacial force between the Si–SiOx/SiO2 pair. During the running-in process, the contact area of the Si–SiOx/SiO2 pair might become hydrophobic due to removal of the hydrophilic oxide layer on the silicon surface and the surface change of the SiO2 tip, which caused the reduction of friction force and the wear rate of the Si–SiOx/SiO2 pair. A phenomenological model is proposed to explain the running-in process of the Si–SiOx/SiO2 pair in ambient air. The results may help us understand the mechanism of the running-in process of the Si–SiOx/SiO2 pair at nanoscale and reduce wear failure in dynamic microelectromechanical systems (MEMS).

Total 5
1/11GOpage