Chapter 1: Why Do We Need Machine Learning Potentials (MLPs)?

Understand the value of MLPs in achieving both quantum accuracy and computational speed by positioning them relative to DFT and classical MD. Quickly grasp which challenges they can address.

💡 Supplement: "DFT accuracy, approximated through shortcuts for speed." The ground truth is DFT, but practical calculations run with MLP—this is the complementary division of labor.

Learning Objectives

By reading this chapter, you will master the following:
- Understand the historical evolution of molecular simulation (from the 1950s to present)
- Explain the limitations and challenges of empirical force fields and first-principles calculations (DFT)
- Understand the technical and societal background that necessitates MLPs
- Learn about the power of MLPs through concrete examples of catalytic reaction simulations

1.1 History of Molecular Simulation: 70 Years of Evolution

To understand the properties of matter and design new materials and drugs, scientists have computationally calculated how molecules and atoms move. This technology is called molecular simulation.

1950s: Birth of Molecular Simulation

Origins of Molecular Dynamics

In 1957, Bern and Alder[1] performed the first computer simulation of liquid argon behavior. This marked the beginning of Molecular Dynamics (MD).

• Computational target: 32 argon atoms
• Computer used: UNIVAC (state-of-the-art at the time)
• Computation time: Several hours
• Potential: Simple Lennard-Jones potential

V(r) = 4ε[(σ/r)¹² - (σ/r)⁶]

This simple equation approximated the interaction energy between two atoms.

Limitations of the Lennard-Jones Potential

• Cannot describe chemical bond formation/breaking
• Does not consider electronic states
• Parameters (ε, σ) must be determined experimentally for each element

Nevertheless, for simple systems like noble gases, it reproduced experimental results surprisingly well.

1970s: Applications to Biomolecules

Beginning of Protein Simulation

In 1977, McCammon et al.[2] performed the first MD simulation of a protein (bovine pancreatic trypsin inhibitor, 58 amino acid residues).

• Computational target: Approximately 500 atoms
• Simulation time: 9.2 picoseconds (9.2 × 10⁻¹² seconds)
• Actual computation time: Several days
• Potential: Empirical force fields such as AMBER and CHARMM

Emergence of Empirical Force Fields

More complex force fields were developed to handle proteins and organic molecules:

• AMBER (Assisted Model Building with Energy Refinement, 1981)[3]
• CHARMM (Chemistry at HARvard Macromolecular Mechanics, 1983)[4]
• GROMOS (GROningen MOlecular Simulation, 1987)

These force fields include terms such as:

E_total = E_bond + E_angle + E_dihedral + E_non-bonded

E_bond = Σ k_b(r - r_0)²  (Bond stretching)
E_angle = Σ k_θ(θ - θ_0)²  (Angle bending)
E_dihedral = Σ V_n[1 + cos(nφ - γ)]  (Dihedral rotation)
E_non-bonded = Σ [4ε((σ/r)¹² - (σ/r)⁶) + q_i q_j/(4πε_0 r)]  (Electrostatic interactions)

Problem: These parameters (k_b, r_0, ε, σ, etc.) must be determined from experimental data or quantum chemical calculations, requiring hundreds of parameters.

1980-1990s: Practical Implementation of First-Principles Calculations

Rise of Density Functional Theory (DFT)

DFT (Density Functional Theory), proposed by Hohenberg and Kohn in 1964 and Kohn and Sham in 1965[5,6], became practical in the 1980s onwards due to improvements in computational power.

Revolutionary aspects of DFT:
- Calculate molecular and solid properties without parameters
- First-principles calculations based on quantum mechanics
- Accurately describe chemical bond formation and breaking

Computational burden:
- Computational complexity: O(N³) (N: number of electrons)
- One step for a 100-atom system: Minutes to hours
- MD (hundreds of thousands of steps) is virtually impossible

1998 Nobel Prize in Chemistry

Walter Kohn and John Pople received the Nobel Prize in Chemistry for "development of computational methods in quantum chemistry." DFT became a standard tool in chemistry and materials science.

2000s: Ab Initio Molecular Dynamics (AIMD)

Car-Parrinello Molecular Dynamics (1985)

Car and Parrinello[7] developed ab initio MD (AIMD) by combining DFT and MD.

• Execute DFT calculation at each MD step
• Can simulate chemical reactions
• Extremely computationally expensive

Typical AIMD constraints (2000s):
- System size: Around 10² atoms
- Time scale: Picoseconds (10⁻¹² seconds)
- Computational resources: Supercomputers

Problem: Many important phenomena such as catalytic reactions, protein folding, and material fracture occur on nanosecond to microsecond (10⁻⁹ to 10⁻⁶ seconds) scales. AIMD cannot reach these timescales.

2010s: Emergence of Machine Learning Potentials (MLPs)

Behler-Parrinello Neural Network Potential (2007)

Jörg Behler and Michele Parrinello[8] proposed a method to learn DFT-accuracy potentials using neural networks.

Revolutionary idea:
1. Calculate energies for thousands to tens of thousands of atomic configurations with DFT
2. Neural network learns the "potential energy surface" from this data
3. Execute MD with the learned potential → μs-scale simulation with DFT accuracy

Advantages of MLPs:
- Accuracy: DFT level (can describe chemical reactions)
- Speed: Comparable to empirical force fields (10⁴-10⁶ times faster)
- Generality: Applicable to any system with available data

1.2 Limitations of Conventional Methods: Empirical Force Fields vs DFT

Molecular simulation broadly had two approaches. Each has serious limitations.

Limitation 1: Empirical Force Fields - Lack of Generality

Problems with Empirical Force Fields

1. Cannot describe chemical reactions
   - Cannot describe bond formation/breaking
   - Catalytic reactions, enzymatic reactions, material fracture cannot be computed

2. Parameters are not transferable
   - Parameters determined for one system cannot be used for another
   - Example: Water force field parameters lose accuracy when applied to ice

3. Cannot apply to new materials
   - Cannot be used for elements or structures without parameters
   - Not useful when designing new materials

Specific example: CO₂ reduction reaction on copper catalyst surface

Catalytic reactions that convert carbon dioxide (CO₂) into useful chemicals are key to addressing climate change.

With conventional empirical force fields:

CO₂ + * → CO₂*  (Adsorption)
CO₂* + H⁺ + e⁻ → ?  (Reaction initiation)

This "?" part (C-O bond breaking and new bond formation) cannot be described. This is because empirical force fields have fixed bond topology.

Limitation 2: DFT - Computational Cost Barrier

Computational Complexity of DFT

Typical DFT calculation (plane-wave basis, PBE functional) computational complexity:
- Scaling: O(N³) (N: number of electrons ≈ number of atoms)
- 100 atoms: About 1 hour/step (on a supercomputer)
- MD requires 10⁵-10⁷ steps

Specific numerical example

※ Estimated values on a typical supercomputer node (64 cores)

Inaccessible time and spatial scales

What DFT can actually reach:
- Number of atoms: Around 10²
- Time: Picoseconds (10⁻¹² seconds)

However, scales where important phenomena occur:
- Catalytic reactions: Nanoseconds to microseconds (10⁻⁹ to 10⁻⁶ seconds)
- Protein motion: Microseconds to milliseconds (10⁻⁶ to 10⁻³ seconds)
- Material fracture: Nanoseconds to microseconds
- Crystal growth: Microseconds and beyond

The gap is more than 10⁶ times (one million times).

Limitation 3: The "Unfortunate" Trade-off Between Both

Conventional molecular simulation faced a dilemma between accuracy and computational cost.

Illustration of the trade-off

Dilemma faced by researchers

Scenario 1: Catalyst material design
- Use empirical force fields → Fast but cannot describe chemical reactions → Unusable
- Use DFT → High accuracy but can only calculate 10 catalyst atoms → Impractical

Scenario 2: Elucidating drug binding mechanisms
- Use empirical force fields → Fast but cannot describe bond formation/breaking → Insufficient
- Use DFT → Cannot calculate entire protein (thousands of atoms) → Not applicable

Conclusion: Conventional methods could not address scientifically most important problems (large-scale, long-time simulations including chemical reactions).

1.3 Case Study: Difficulty of Catalytic Reaction Simulation

As a specific example, let's consider the CO₂ reduction reaction on copper (Cu) catalyst surface. This is an important reaction that converts greenhouse gas CO₂ into useful chemicals (such as ethanol)[9].

Reaction Overview

Electrochemical CO₂ reduction reaction

CO₂ + 6H⁺ + 6e⁻ → CH₃OH + H₂O  (Methanol production)
CO₂ + 12H⁺ + 12e⁻ → C₂H₅OH + 3H₂O  (Ethanol production)

Complexity of the reaction mechanism:
1. CO₂ adsorbs on copper surface
2. Hydrogen atoms (H) are generated on the surface
3. CO₂
is reduced stepwise (COOH → CO → CHO → ...)
4. Two CO
molecules couple to form C₂ chemicals (C-C bond formation)
5. Final product desorbs

This process goes through more than 10 intermediates, each requiring overcoming reaction barriers.

Difficulties with Conventional Methods

Approach 1: Empirical Force Field (ReaxFF)

ReaxFF[10] was developed as an empirical force field capable of describing chemical reactions.

Attempt:
- Model Cu catalyst surface with 100 water molecules and CO₂ molecules
- 1 nanosecond MD simulation
- Computation time: Several days (on GPU)

Result:
- CO₂ adsorption was observed
- However, reduction reaction does not occur
- Reason: ReaxFF parameters not optimized for this specific reaction system
- Determining new parameters requires large amounts of DFT data

Issues:
- Parameter fitting takes months to years
- Even after fitting, prediction accuracy is insufficient
- Different catalysts (Ag, Au, etc.) require parameter refitting

Approach 2: DFT (ab initio MD)

Attempt:
- Cu(111) surface slab (96 Cu atoms)
- Place CO₂, H₂O, CO, COOH intermediates on surface
- Explore reaction pathway with ab initio MD
- Computational resources used: 1,000 nodes on the "Fugaku" supercomputer

Result:
- 10 picosecond simulation takes 1 week
- Reaction is not observed on this timescale
- Reason: Typical timescale of CO₂ reduction reaction is nanoseconds to microseconds
- 10⁶ times (one million times) insufficient

Computation time estimate:
- Time needed for 1 microsecond simulation: About 100,000 weeks = 2000 years

Issues:
- Cannot reach realistic timescales
- Cannot observe entire reaction mechanism
- Statistical sampling (many reaction events) impossible

Solution with MLP (2018 onwards)

Research example: MLP-MD of Cu catalyst CO₂ reduction using SchNet and DimeNet

Cheng et al. (2020, Nature Communications)[11] achieved the following using MLP:

Procedure:
1. DFT data collection: Calculate energies and forces for about 5,000 atomic configurations (Cu surface + CO₂ + H₂O + intermediates)
- Computation time: About 1 week on supercomputer

2. MLP training: Train SchNet model[12] (graph neural network)
   - Training time: A few hours on 1 GPU
   - Energy prediction accuracy: Mean absolute error (MAE) < 1 meV/atom (DFT accuracy)

3. MLP-MD simulation: Molecular dynamics simulation with trained MLP
   - System size: 200 Cu atoms + 50 water molecules + CO₂
   - Simulation time: 1 microsecond
   - Actual computation time: 1 day on 1 GPU

Achievements:
- Observed reaction pathway: CO₂ → COOH → CO → CHO → CH₃OH
- Statistical sampling of reaction barriers
- Elucidated C-C bond formation mechanism
- Reached timescales impossible with conventional DFT*

Comparison Table: Conventional Methods vs MLP

Conclusion: MLP achieved the "best of both worlds" by combining DFT accuracy with empirical force field speed.

1.4 Conventional Methods vs MLP: Workflow Comparison

As seen in the catalytic reaction simulation example, conventional methods had serious constraints. Let's compare entire research workflows.

Workflow Comparison Diagram

Quantitative Comparison

Timeline comparison example: Cu catalyst CO₂ reduction research

With empirical force field (ReaxFF):
- Existing parameter survey: 1 month
- Parameters found inadequate
- DFT reference data generation: 2 months
- Parameter fitting: 2-3 months
- Validation shows insufficient accuracy
- Refitting: 1-2 months
- MD simulation: 2 weeks
- Analysis: 2 weeks
- Total: About 9 months

With DFT (AIMD):
- Model construction: 1 week
- 10 ps AIMD: 1 week
- Reaction not observed
- NEB method reaction pathway search: 3 weeks
- Multiple pathway calculations: 2 weeks
- Analysis: 1 week
- Total: About 8 weeks
- Problem: Dynamic behavior, statistical sampling not possible

With MLP (SchNet/DimeNet):
- DFT data collection: 1 week (parallel calculation)
- MLP training: 1 day
- Accuracy validation: Half day
- 1 μs MLP-MD simulation: 3 days
- Reaction observation & statistical analysis: 3 days
- Accuracy improvement with Active Learning: 2 days
- Paper figure creation: 2 days
- Total: About 2.5 weeks
- 3× faster than DFT, 15× faster than empirical force field

1.5 Column: A Computational Chemist's Day (2000 vs 2025)

Let's see how research practices have changed through specific stories.

2000: Struggles during the DFT Golden Era

Professor Yamada (42 years old, national university) - One week

Monday
- 9:00 - Arrive at lab. Check results of DFT calculation (CO adsorption on Cu surface) submitted last Friday.
- 10:00 - Notice it terminated with error. Convergence criteria too strict.
- 11:00 - Adjust parameters and resubmit. Expected to take 3 days this time.
- Afternoon - Read papers. Student guidance.

Tuesday-Thursday
- Waiting for calculation to complete.
- During this time, prepare other calculations (different project) and write papers.
- "Want to calculate larger systems, but computation time is too long..."

Friday
- 9:00 - Calculation completed. Finally got results.
- 10:00 - Obtained energy for one CO adsorption configuration.
- 11:00 - Want to calculate another adsorption site. Will wait another 3 days...
- Afternoon - Student looks anxious: "We only calculated one configuration this week. At this pace, won't finish doctoral dissertation."

One week's achievements: One atomic configuration DFT calculation

One month's achievements: About 5-10 configurations

One year's achievements: About 50-100 configurations, 1-2 papers

Worries:
- "Want to understand reaction mechanism, but dynamics simulation is computationally impossible"
- "Want to calculate larger catalyst clusters (100+ atoms), but won't finish in a week"
- "Want statistical sampling, but don't have computational resources"

2025: Efficiency in the MLP Era

Associate Professor Sato (38 years old, same university) - One week

Monday
- 9:00 - Arrive at lab. Check MLP-MD (1 microsecond simulation) results executed on GPU cluster over the weekend.
- 9:30 - Confirm 3 reactions occurred!
- Observed pathway: CO₂ → COOH → CO → *CHO → CH₃OH
- Check trajectory with Visualizer
- 10:00 - Automatic reaction pathway analysis with Python script. Automatically detect transition states.
- 11:00 - Research meeting. Discuss reaction mechanism with students.
- "The timing of this C-O bond breaking seems important"
- "Then let's do DFT calculation of that configuration to examine electronic structure in detail"

Monday afternoon
- 14:00 - Detailed electronic structure analysis of reaction intermediates with DFT.
- Automatically extract "interesting configurations" with MLP
- DFT calculation of only those configurations → Complete in a few hours
- 16:00 - Add new configurations to DFT database for Active Learning.
- 17:00 - Retrain MLP model (30 minutes on 1 GPU). Accuracy improved.

Tuesday
- 9:00 - Execute additional 1 microsecond simulation with improved MLP (auto-execute overnight).
- Morning - Create paper figures. Reaction pathway diagrams, energy profiles, snapshots.
- Afternoon - Zoom meeting with collaborators. Suggest to experimental group: "These intermediates seem important".

Wednesday-Friday
- Additional simulation result analysis
- Paper writing
- Prepare another project (screening new catalyst materials)
- Read papers on new MLP methods (E(3) equivariant graph neural networks)

Friday afternoon
- 15:00 - Review this week's achievements
- Completed 3 microseconds of MLP-MD simulation
- Elucidated reaction mechanism
- Completed paper draft
- 16:00 - "Let's try the same reaction with different catalysts (Au, Ag) next week. With MLP, can compare in one week"

One week's achievements: 3 microseconds simulation, reaction mechanism elucidation, paper draft completed

One month's achievements: Multiple catalyst system comparison, 2-3 paper drafts

One year's achievements: 10-15 papers, multiple parallel projects

Joy:
- "Thanks to MLP, can see phenomena on timescales I couldn't imagine"
- "Calculations are fast, so easy to try different things. Can immediately test new ideas"
- "Students' thesis topics increased. Everyone enjoys research"

Points of Change

Important point: MLP liberated researchers' creativity. Time spent waiting for calculations decreased, allowing focus on scientific insights and new ideas.

1.6 Why "Now" for MLP: Three Tailwinds

The MLP concept has existed since the 2000s, but practical implementation began in earnest after 2015. Why "now"?

Tailwind 1: Dramatic Progress in Machine Learning Technology

Deep Learning Revolution (2012)

AlexNet[13] dominated the ImageNet image recognition competition, launching the deep learning boom.

Spillover to chemistry and materials science:
- 2015: Schütt et al. proposed SchNet[12] (graph neural network)
- Represent molecules as "graphs"
- Learn atomic interactions
- Guarantee rotation and translation invariance

• 2018: Klicpera et al. proposed DimeNet[14]
• Also considers bond angles

• Further improved accuracy

• 2021: Batzner et al. proposed NequIP[15], Batatia et al. proposed MACE[16]

• Implement E(3) equivariance (rotation covariance)
• Incorporate physical laws into machine learning
• Training data efficiency greatly improved (same accuracy with 1/10 the data)

Proliferation of PyTorch and TensorFlow

• Frameworks enabling researchers to implement neural networks themselves
• Easy GPU computation usage
• Open source, accessible to anyone

Tailwind 2: Democratization of GPU Computing

GPU Performance Improvements

Proliferation of cloud GPUs

• Google Colab: Use GPU for free (research/education)
• AWS, Google Cloud, Azure: Rent GPUs by the hour
• Access latest GPUs for a few to tens of dollars per hour

Result: Anyone, anywhere can conduct large-scale machine learning training and MLP-MD simulation.

Tailwind 3: Open Data and Open Source Culture

Large-scale DFT databases

These data are freely downloadable. Anyone can train MLPs.

Open-source MLP software

All are published on GitHub and can be used and modified by anyone.

Culture of publishing code and data with papers

• After 2020, top journals (Nature, Science, PRL, etc.) emphasize reproducibility
• Encourage/mandate code and data publication upon paper submission
• Result: Research acceleration, reduced duplication

Tailwind 4: Rising Social Urgency

Climate Change and Energy Issues

• 2015 Paris Agreement: Limit global warming to within 2°C
• Material development for catalysts (CO₂ reduction, hydrogen production), batteries, solar cells urgently needed
• Conventional methods too slow for development speed

Accelerating Drug Development

• COVID-19 pandemic (2020) made rapid drug development a global issue
• MLP beginning to be used for protein-drug interaction simulation

Global research investment

• USA: NSF, DOE invest tens of millions of dollars annually in MLP research
• Europe: Multiple machine learning × materials science projects in Horizon Europe
• China: Promoting AI × materials science as national strategy
• Japan: JST, NEDO supporting materials informatics research

Conclusion: MLP is needed and realizable now precisely because technical maturity, democratization of computational resources, open science, and social necessity are simultaneously fulfilled.

1.7 Introduction to Major MLP Methods (Overview)

We'll learn in detail from Chapter 2 onwards, but here's a brief introduction to representative MLP methods.

1. Behler-Parrinello Neural Network Potential (2007)[8]

Features:
- First practical MLP method
- Describe local environment of each atom with "Symmetry Functions"
- Predict energy for each atom with neural network
- Total energy = Σ(atomic energy)

Advantages: Simple and easy to understand
Disadvantages: Manual design of Symmetry Functions, requires much training data

Representative applications: Water, silicon, organic molecules

2. Graph Neural Networks (2017 onwards)

SchNet (2017)[12]
- Represent molecules as graphs (atoms=nodes, bonds=edges)
- Learn graphs with continuous-filter convolution
- Message passing according to distance

DimeNet (2020)[14]
- Also considers bond angle information
- Directional message passing
- Higher accuracy than SchNet

Advantages: No manual feature design needed, end-to-end learning
Disadvantages: Requires relatively much training data

Representative applications: Organic molecules, catalytic reactions, drug design

3. Equivariant Neural Networks (2021 onwards)

NequIP (2021)[15]
- Implements E(3) equivariance (covariant to rotations)
- Propagate messages as tensor fields
- High training data efficiency

MACE (2022)[16]
- Message-passing + Atomic Cluster Expansion
- Efficiently learn high-order many-body interactions
- Currently highest accuracy

Advantages: Extremely high data efficiency (high accuracy with thousands of configurations), incorporates physical laws
Disadvantages: Implementation somewhat complex

Representative applications: Large-scale material simulation, complex chemical reactions

4. Comparison Table

Future learning:
- Chapter 2: Mathematical foundations of these methods
- Chapter 3: SchNet implementation and hands-on
- Chapter 4: NequIP/MACE details and application examples

1.8 Chapter Summary

What We Learned

1. History of molecular simulation
   - 1950s: Simple Lennard-Jones potential for noble gases
   - 1970s: Empirical force fields for proteins and organic molecules
   - 1990s: Practical implementation of DFT (first-principles calculations)
   - 2000s: ab initio MD (AIMD) but extremely slow
   - 2007: Proposal of Behler-Parrinello MLP
   - 2015 onwards: Rapid development of deep learning and MLP

2. Limitations of conventional methods
   - Empirical force fields: Cannot describe chemical reactions, no parameter generality
   - DFT (AIMD): Extremely slow (limited to 10² atoms, picoseconds)
   - Trade-off: Dilemma between accuracy vs speed

3. MLP revolution
   - Achieves DFT accuracy while maintaining empirical force field speed
   - 10⁴-10⁶× speedup
   - Large-scale, long-time simulations including chemical reactions now possible

4. Specific catalytic reaction example (Cu surface CO₂ reduction)
   - Empirical force field: Months for parameter adjustment, insufficient accuracy
   - DFT: 10 ps limit, reaction observation impossible (needs 1 μs but takes 2000 years)
   - MLP: 1 μs simulation completed in 1 day, reaction mechanism elucidated

5. Why "now" for MLP
   - Machine learning evolution (SchNet, NequIP, MACE, etc.)
   - GPU computing democratization (free on Colab, affordable on cloud)
   - Open data and open source culture
   - Social urgency (climate change, energy, drug development)

Key Points

• MLP combines DFT accuracy with empirical force field speed
• Simultaneously achieves large-scale systems and long timescales including chemical reactions
• Observation of dynamic reaction mechanisms previously impossible now possible
• Dramatically reduces researchers' calculation waiting time, liberating creativity

To the Next Chapter

Chapter 2 will explore the mathematical foundations of MLP in detail:
- What is a potential energy surface
- Energy learning with neural networks
- Importance of symmetry and equivariance
- Evolution from Behler-Parrinello to the latest MACE

Additionally, we'll practice simple MLP training using Python.

Exercises

Problem 1 (Difficulty: easy)

In the history of molecular simulation, create a table summarizing how "accuracy," "speed," and "generality" differ among the three methods: empirical force fields, DFT, and MLP.

Problem 2 (Difficulty: medium)

Explain why 1 microsecond ab initio MD simulation with DFT is "practically impossible," estimating computation time. Assume DFT calculation for one step takes 1 hour for a 100-atom system.

Problem 3 (Difficulty: hard)

For catalytic reaction simulation (Cu surface CO₂ reduction), explain how total research project duration differs between conventional methods (empirical force field, DFT) and MLP, assuming specific workflows.

1.10 Data Licensing and Reproducibility

To ensure reproducibility of research outcomes and case studies introduced in this chapter, we explicitly document related data and tool information.

1.10.1 Datasets Mentioned in This Chapter

Notes:
- Case study data: Cu catalyst CO₂ reduction reaction example based on OC20 dataset
- Historical method comparison: Empirical force field (AMBER, CHARMM) and DFT calculation accuracy references literature values
- Timeline: This chapter's chronology (1950s-2025) based on publication years of original papers for each method

1.10.2 Comparison Data for Molecular Simulation Methods

Basis for computational cost comparison:

Basis for accuracy comparison:

• Empirical force field: MAE ~10-50 kcal/mol (large errors in molecular energy, reaction barriers)
• DFT: MAE ~1-5 kcal/mol (used as reference method)
• MLP: MAE ~0.1-1 kcal/mol (when trained on DFT data)

1.10.3 Sources for Historical Timeline

1.11 Practical Considerations: What to Know Before Learning MLP

1.11.1 Common Misconceptions and Pitfalls

1.12 Chapter-End Checklist: MLP Introduction Quality Assurance

After reading this chapter, check the following items. If all can be checked, you're ready to proceed to Chapter 2 "MLP Fundamentals."

1.12.1 Conceptual Understanding (Understanding)

Historical background understanding:

• □ Can explain three eras of molecular simulation (1950s-1980s empirical force fields, 1980s-2010s DFT, 2010s-present MLP)
• □ Can explain three limitations of empirical force fields (reactivity, accuracy, parameterization)
• □ Can explain three limitations of DFT (computational cost, system size, timescale)
• □ Can explain in own words the problem MLP solves (accuracy vs cost trade-off)

MLP positioning:

• □ Understand MLP-DFT relationship (complementary, MLP trained on DFT data)
• □ Can distinguish problems MLP suits (large-scale systems, long-time MD) from unsuitable problems (new materials, initial exploration)
• □ Can explain meaning of "quantum accuracy, classical speed"
• □ Understand MLP application limits (within training data range)

Case study understanding:

• □ Can explain Cu catalyst CO₂ reduction reaction workflow comparison (empirical force field vs DFT vs MLP)
• □ Can list three reasons why MLP produces results in "2.5-4 weeks"
• □ Can explain where DFT-MLP computation time difference (~1000×) comes from

Technology trend understanding:

• □ Can explain three tailwinds for "why MLP now" (hardware, data, algorithms)
• □ Can briefly explain differences between Behler-Parrinello (2007) and NequIP/MACE (2022)
• □ Understand social background in materials exploration (carbon neutrality, energy crisis)

1.12.2 Practical Skills (Doing)

Research planning:

• □ Can judge whether MLP applicable to own research topic (criteria: system size, timescale, required accuracy)
• □ Can estimate MLP project time (learning curve, computational resources, data preparation)
• □ Can estimate required computational resources (GPU, storage, cloud vs own)
• □ Can design standard workflow: DFT → MLP → MLP-MD

Literature survey skills:

• □ Can cite 3+ MLP application examples in own research field (catalysis, batteries, drug discovery, etc.)
• □ Can evaluate paper reproducibility (data publication, code publication, environment information availability)
• □ Can research differences among MLP tools on GitHub (SchNetPack, NequIP, MACE)

Communication:

• □ Can explain "what MLP is" to lab members in 5 minutes
• □ Can logically explain "reasons for using MLP" to supervisor or PI (cost, time, accuracy perspectives)
• □ Can tangibly describe differences between "computational chemist's day in 2000" and "2025"

1.12.3 Application Ability (Applying)

Problem setting evaluation:

• □ When new research topic arises, can judge which is optimal: "empirical force field vs DFT vs MLP"
• □ Can detect cases where MLP likely to fail (extrapolation, insufficient training data) beforehand
• □ Can quantitatively evaluate computational cost vs project duration trade-off

Research strategy construction:

• □ Can compare research plans for own research topic "without using MLP" and "using MLP"
• □ Can judge Active Learning necessity (when training data insufficient)
• □ Can consider pretrained model transfer learning (OC20, ANI-1x, etc.)

Preparation for next chapter:

• □ Can list content to learn in Chapter 2 (descriptors, architecture, training methods)
• □ Can clarify what to achieve in Chapter 3 hands-on (SchNetPack implementation)
• □ Can set 3-month goal for how to utilize MLP in own project ultimately

References

1. Alder, B. J., & Wainwright, T. E. (1957). "Phase transition for a hard sphere system." The Journal of Chemical Physics, 27(5), 1208-1209.
   DOI: 10.1063/1.1743957
   

2. McCammon, J. A., Gelin, B. R., & Karplus, M. (1977). "Dynamics of folded proteins." Nature, 267(5612), 585-590.
   DOI: 10.1038/267585a0
   

3. Cornell, W. D., et al. (1995). "A second generation force field for the simulation of proteins, nucleic acids, and organic molecules." Journal of the American Chemical Society, 117(19), 5179-5197.
   DOI: 10.1021/ja00124a002
   

4. Brooks, B. R., et al. (1983). "CHARMM: A program for macromolecular energy, minimization, and dynamics calculations." Journal of Computational Chemistry, 4(2), 187-217.
   DOI: 10.1002/jcc.540040211
   

5. Hohenberg, P., & Kohn, W. (1964). "Inhomogeneous electron gas." Physical Review, 136(3B), B864.
   DOI: 10.1103/PhysRev.136.B864
   

6. Kohn, W., & Sham, L. J. (1965). "Self-consistent equations including exchange and correlation effects." Physical Review, 140(4A), A1133.
   DOI: 10.1103/PhysRev.140.A1133
   

7. Car, R., & Parrinello, M. (1985). "Unified approach for molecular dynamics and density-functional theory." Physical Review Letters, 55(22), 2471.
   DOI: 10.1103/PhysRevLett.55.2471
   

8. Behler, J., & Parrinello, M. (2007). "Generalized neural-network representation of high-dimensional potential-energy surfaces." Physical Review Letters, 98(14), 146401.
   DOI: 10.1103/PhysRevLett.98.146401
   

9. Nitopi, S., et al. (2019). "Progress and perspectives of electrochemical CO2 reduction on copper in aqueous electrolyte." Chemical Reviews, 119(12), 7610-7672.
   DOI: 10.1021/acs.chemrev.8b00705

10. van Duin, A. C., et al. (2001). "ReaxFF: a reactive force field for hydrocarbons." The Journal of Physical Chemistry A, 105(41), 9396-9409.
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Author Information

Created by: MI Knowledge Hub Content Team
Creation date: 2025-10-17
Version: 1.1 (Chapter 1 quality improvement)
Series: MLP Introduction Series

Update history:
- 2025-10-19: v1.1 Quality improvement revision
- Added data licensing and reproducibility section (MD17, OC20, QM9 dataset information)
- Added basis data for computational cost and accuracy comparison (empirical force field vs DFT vs MLP)
- Specified sources for historical timeline (major papers from 1957-2022)
- Added practical considerations section (5 misconceptions and pitfalls, detailed countermeasures)
- Added chapter-end checklist (16 conceptual understanding items, 10 practical skill items, 9 application ability items)
- 2025-10-17: v1.0 Chapter 1 initial release
- History of molecular simulation (1950s-present)
- Detailed limitations of conventional methods (empirical force fields, DFT) from three perspectives
- Cu catalyst CO₂ reduction reaction case study (detailed workflow comparison)
- "Computational chemist's day" column (2000 vs 2025)
- "Why MLP now" section (3 tailwinds + social background)
- Overview of major MLP methods (Behler-Parrinello, SchNet, DimeNet, NequIP, MACE)
- 3 exercises (easy, medium, hard)
- 16 carefully selected references (important papers)

License: Creative Commons BY-NC-SA 4.0